Published online May 7, 2008. doi: 10.3748/wjg.14.2639
Revised: January 17, 2008
Published online: May 7, 2008
Irritable bowel syndrome (IBS) is a highly prevalent gastrointestinal disorder characterized by abdominal pain and discomfort in association with altered bowel habits. It is estimated to affect 10%-15% of the Western population, and has a large impact on quality of life and (in)direct healthcare costs. IBS is a multifactorial disorder involving dysregulation within the brain-gut axis, and it is frequently associated with gastrointestinal motor and sensory dysfunction, enteric and central nervous system irregularities, neuroimmune dysregulation, and post-infectious inflammation. As with other functional medical disorders, the treatment for IBS can be challenging. Conventional therapy for those with moderate to severe symptoms is largely unsatisfactory, and the development of new and effective drugs is made difficult by the complex pathogenesis, variety of symptoms, and lack of objective clinical findings that are the hallmark of this disorder. Fortunately, research advances over the past several decades have provided insight into potential mechanisms responsible for the pathogenesis of IBS, and have led to the development of several promising pharmaceutical agents. In recent years there has been much publicity over several of these new IBS medications (alosetron and tegaserod) because of their reported association with ischemic colitis and cardiovascular disease. While these agents remain available for use under restricted prescribing programs, this highlights the need for continued development of safe and effective medication for IBS. This article provides a physiologically-based overview of recently developed and frequently employed pharmaceutical agents used to treat IBS, and discusses some non-pharmaceutical options that may be beneficial in this disorder.
- Citation: Hammerle CW, Surawicz CM. Updates on treatment of irritable bowel syndrome. World J Gastroenterol 2008; 14(17): 2639-2649
- URL: https://www.wjgnet.com/1007-9327/full/v14/i17/2639.htm
- DOI: https://dx.doi.org/10.3748/wjg.14.2639
Irritable bowel syndrome (IBS) is one of the most common functional gastrointestinal disorders affecting Western countries, with rates estimated as high as 10%-15% in the general population[1–3]. IBS is a heterogeneous condition broadly characterized by recurrent abdominal pain and discomfort with altered bowel habits and no detectable structural abnormalities. In addition to constipation and/or diarrhea, frequently reported symptoms include abdominal pain and cramps, flatulence, fecal urgency, straining, a sense of incomplete evacuation and relief of pain or discomfort upon defecation.
IBS can be classified according to the predominant bowel symptoms: IBS with constipation predominant features (IBS-C), IBS with diarrhea predominant features (IBS-D), and IBS with alternating symptoms of diarrhea and constipation (IBS-A). While the exact pathophysiology of IBS is unclear, dysregulation within the brain-gut axis and interactions between genetics, psychosocial factors, post-inflammatory changes[8–10], and motor and sensory dysfunction all likely play a role.
While only a fraction of IBS patients seek medical care, this condition accounts for up to 20% of all referrals to gastroenterologists. IBS has widespread economic ramifications in terms of both healthcare utilization and indirect costs incurred as a result of absenteeism from work. Moreover, IBS is a cause of substantial morbidity and is associated with a lower health care-related quality of life. It is clear that effective drugs for IBS are greatly needed.
IBS is a chronic, recurring condition with a wide range of symptoms. Therefore, the general goal of treatment is to alleviate the symptoms of abdominal pain, altered bowel transit (diarrhea or constipation) and any associated symptoms such as bloating and fecal incontinence. The treatment approach should be individualized, and will depend on the intensity of symptoms and the degree of other comorbid conditions. As with other functional medical disorders, the cornerstone of successful management revolves around establishing an effective patient-physician relationship. The physician should be non-judgmental, listen actively to determine the patient’s needs and concerns, and encourage the patient to participate in their medical care. Well-established physician relationships and positive interactions with health care providers have been shown to be associated with fewer IBS-related follow-up visits and a lower utilization of health care resources.
The majority of IBS patients are successfully managed in the primary care setting. These patients typically have mild symptoms and respond well to dietary and lifestyle modifications, education, and reassurance about their disease. Gut-directed medical therapy (anticholinergics, antispasmodics and newer IBS-specific agents) is used more frequently in patients with moderate to severe symptoms and is occasionally accompanied by the use of low dose tricyclic antidepressants (TCAs) and/or other psychiatric medications. The most severe, and smallest percentage of IBS cases, are often refractory to standard treatment and are likely to be seen at tertiary specialty centers. These patients will often require mental health providers, psychotropic medications, and may need frequent appointments with primary care providers to offer ongoing support throughout treatment.
In all cases of IBS, it is important to establish realistic and consistent treatment goals. Patients should be aware that a single drug is not likely to eradicate all symptoms, and that time, patience, and “trial and error” use of medications will be required. Additionally, physicians should educate patients about their diagnosis and provide reassurance that though this condition is a real medical disorder, it is a benign process that portends a normal life expectancy. In a long-term prognostic study of IBS, Owens and colleagues found that less than 10% of IBS patients developed an organic gastrointestinal disease, and that patients with IBS had survival rates not different from expected. Misconceptions about the causes, diagnosis and treatment of IBS are common among patients. In a recent questionnaire-based study of 636 IBS patients, 80% believed their condition developed as a result of anxiety, nearly two-thirds believed diet was responsible for IBS, and one in seven patients believed that IBS leads to cancer. Education about the possible mechanisms of IBS may dispel some of these misconceptions and it will help lay a foundation for the use of pharmacologic interventions if needed.
Physicians should be aware of other comorbidities that may worsen symptoms, and as with all chronic conditions, a detailed history about environmental stressors, social or emotional disturbances, impaired daily functioning, and underlying psychiatric conditions should be collected. This may help determine why the patient is seeking medical care and it could help uncover any potential hidden agendas.
Serotonin (5-hydroxytryptophan) is the most important neurotransmitter (NT) in the pathogenesis of IBS. It is a paracrine signaling molecule found extensively throughout the gastrointestinal tract (approximately 90% of all body stores) that modulates key functions such as motility, sensation, blood flow, and secretion[24–27]. Serotonin is stored primarily in enterochromaffin cells (90%) and in neurons of the enteric motor system (10%). Its release is triggered by luminal distension and chemical signals, and it binds to receptors located on enteric motor neurons, peripheral afferents, and within central nervous system domains that control appetite, mood and sexual function. The majority of serotonin receptors are G protein-coupled, with the exception of the 5-HT3 receptor, which is a ligand-gated ion channel. 5-HT3 and 5-HT4 appear to be the most important NTs in IBS. 5-HT3 receptors modulate visceral pain, aid in peristalsis, and its receptors within the CNS appear to influence the emotional component of visceral stimulation[28–31]. 5-HT4 is important in gastric emptying, colonic secretions, facilitating the peristaltic reflex, and it contracts or relaxes smooth muscle depending upon its location within the alimentary tract. Serotonin levels and its activity on receptors are in part regulated by the serotonin reuptake transporter (SERT). Coates et al recently demonstrated that patients with IBS have decreased levels of SERT mRNA and protein expression in intestinal epithelial cells when compared to healthy volunteers. Furthermore, polymorphisms within the SERT promoter region have been shown to be associated with the IBS-D phenotype, and findings from a recent study suggest that their existence may influence the response to a 5-HT3 antagonist in female IBS-D patients. While the exact role of serotonin signaling in the pathophysiology of IBS remains to be fully elucidated, pharmacotherapy directed at modulating its activity has proven to be an effective way of treating many IBS symptoms.
Antagonism of the 5-HT3 receptor results in slower small bowel and colonic transit times, a reduction in intestinal secretion, increased stool firmness, and an increase in colonic compliance. There is also data suggesting that antagonism of this receptor in the amygdala, dorsal pons and ventral striatum may be responsible for perceived improvement in visceral pain, though the exact mechanism is unclear.
Alosetron is a selective 5-HT3 receptor antagonist initially approved by the Food and Drug Administration (FDA) in 2000 for use in female patients with IBS-D who fail in conservative treatment. Approval of this medication was based on several large randomized controlled-trials that found alosetron (1 mg po twice daily) was more effective than placebo in controlling abdominal pain and discomfort in IBS-D[40–43]. Alosetron was associated with a statistically significant decrease in the percentage of days with urgency, and it led to firmer stools and a decrease in stool frequency. Clinical improvement was noted throughout the treatment period and usually occurred within 1-4 wk of therapy; symptoms returned to baseline following discontinuation of the medication. The most frequently reported adverse event was mild to moderate constipation which was self-limited and responded well to cessation of therapy. A meta-analysis by Cremonini in 2003 examined six randomized controlled-trails of alosetron and calculated a combined odds ratio of 1.8 for the adequate relief of pain [95% confidence interval (95% CI), 1.57-2.10] and the NNT of 7 patients in order to compare its relieving effect with placebo (95% CI, 5.74-9.43).
In late 2000, alosetron was withdrawn from the U.S. market over concerns regarding side-effects of severe constipation (approximately 70 cases), ischemic colitis (approximately 50 cases), and bowel perforation. Following substantial public pressure, it was re-introduced into the U.S. market in 2002 under a restricted prescribing program and further post-marketing studies are currently underway. In a recent placebo-controlled study, Krause and colleagues examined the safety and efficacy of alosetron at varying doses, and found that one of 250 patients developed self-limited ischemic colitis (0.5 mg daily). In a systematic review of post-marketing surveillance data, Chang and colleagues estimated the rate of ischemic colitis to be 1.1 per 1 000 patients. All cases of documented ischemic colitis were reversible and no-long-term sequelae were noted. These data suggest that the rate of adverse events is relatively low and that alosetron is a well-tolerated, effective medication that should be considered in the treatment of IBS-D. There are ongoing studies of alosetron in men.
Cilansetron is another 5-HT3 antagonist that has been used for treatment for men and women with IBS-D. Its mechanism of action is similar to alosetron and it has comparable bioavailability and metabolism. Two large phase III trials have shown that cilansetron is similar in efficacy to alosetron, but concerns over ischemic colitis and severe constipation led to the FDA denying approval in 2005[48–51].
Ramosetron is a potent 5-HT3 receptor antagonist that is effective in relieving chemotherapy-induced nausea and vomiting, and is currently being developed for IBS-D. Preliminary pharmacokinetic data suggest that it has a greater affinity, slower dissociation, and stronger antagonism at the 5-HT3 receptor than either alosetron or cilansetron. It also appears to be superior to both of these medications in inhibiting stress-induced defecation and stress-induced changes in colonic transit rates in rats. Data in human use are not available but can be anticipated in the near future.
5-HT4 receptors mediate the release of the excitatory NTs acetylcholine, substance P and calcitonin gene-related peptide which modulate peristalsis. Selective antagonism at this receptor has been postulated to provide symptomatic relief in patients suffering from IBS-D. In a study of 52 healthy subjects, Piboserod (SB207266), a selective 5-HT4 antagonist, was shown to block the effects of cisapride (5-HT4 agonist) and it tended to delay colonic transit times (P = 0.06). In a placebo-controlled study of 15 patients with IBS-D, Houghton and colleagues reported that 20 mg of SB207266 significantly improved orocecal transit times and demonstrated a non-statistical trend toward improved rectal sensitivity. Further studies with this class of medication are needed to confirm these results.
Activation of 5-HT4 receptors results in the release of excitatory neurotransmitters from enteric cholinergic neurons that function to modulate smooth muscle tone, electrolyte secretion and the peristaltic reflex. Tegaserod is a 5-HT4 agonist that was initially approved by the FDA for use in female patients with IBS-C, and in men and women under the age of 65 with chronic idiopathic constipation. It stimulates intestinal secretion of water and chloride and decreases the nociceptive response to rectal distension. Several large, randomized-trials have shown that tegaserod has a significant impact on a patient’s overall assessment of global relief, and that it statistically improves abdominal pain and bloating[59–62]. A 2004 Cochrane meta-analysis supported these results by concluding that tegaserod was associated with improvement in global relief of GI symptoms [relative risk (RR), 1.17; 95% CI, 1.08-1.27] and that it improved bowel consistency and frequency. The primary side-effect of tegaserod is diarrhea (NNH of 20 patients), but it is usually transient and resolves with ongoing treatment. Long-term use of tegaserod appears to be efficacious and re-treatment response rates appear to be similar to initial treatment. Recent data regarding the effect of tegaserod in men have shown that it accelerates colonic transit time, but improvement in bowel symptoms failed to reach statistical significance. In March 2007, Novartis voluntarily removed tegaserod from the U.S. and Canadian market as an FDA safety analysis of pooled data from 12 clinical trials demonstrated a statistical increase in the incidence of myocardial infarction, stroke and unstable angina. In July 2007, tegaserod was re-introduced to the U.S. market, but under a restricted investigational new drug (IND) protocol which limits its use to treatment of IBS-C and chronic idiopathic constipation in women under 55 years of age who meet specific guidelines. It continues to remain off market for general use.
Prucalapride is a new agent in a class of medications known as benzofurans. It is an agonist at the 5-HT4 receptor, and data have suggested that it enhances GI transit in patients with functional constipation compared to placebo. However, the clinical development of this drug remains unclear at this time based on the reported cases of intestinal carcinogenicity in animals.
Renzapride is a mixed agent that has shown promise for patients with IBS-C and with IBS-A. It is a full agonist of the 5-HT4 receptor and an antagonist of the 5-HT3 receptor. In a dose-ranging efficacy trial by Camilleri and colleagues, a statistically significant linear dose response to renzapride was observed for colonic transit and ascending colonic emptying time, but not for gastric emptying or small bowel transit time. No clinical or laboratory adverse events occurred during this study. In a dose-escalating pilot study of 17 patients, renzapride (2 mg twice daily) reduced overall gastrointestinal transit time and abdominal pain, increased the number of pain-free days and improved stool consistency. Adverse events were similar in drug and placebo groups. Further studies are underway.
Mosapride is a benzamide compound with prokinetic properties that possesses both 5-HT4 receptor agonist and 5-HT3 receptor antagonist properties. In a study of Parkinson’s patients, mosapride (15 mg/d) decreased colonic transit times and was associated with subjective improvements in bowel frequency. Additional data in animals and humans have shown that mosapride accelerates gastric emptying and decreases overall colonic transit, but does not appear to affect small bowel transit times. The primary side effect is mild diarrhea, but unlike cisapride, it does not seem to cause the electrophysiological abnormalities that could lead to Torsades de Pointes.
Another drug for the treatment of IBS-C is ATI-7505, a potent agonist of the 5HT4 receptor that is similar in chemical structure to the prokinetic agent, cisapride. It has been engineered to reduce the cardiovascular toxicity of cisapride and does not have P450 dependent clearance at therapeutic levels. Preliminary data from Camilleri and colleagues show that ATI-7505 accelerates overall colonic transit (10 mg three times daily), accelerates gastric emptying (20 mg three times daily), and loosens stool consistency. No safety issues were identified in this study.
Clonidine, an α2 agonist initially developed as an antihypertensive agent, has been found to increase colonic compliance, delay small bowel transit, and reduce colonic tone and sensitivity in response to distension[78–81]. In a small study of 44 IBS-D patients, clonidine was associated with a significant reduction in bowel dysfunction and an improvement in IBS symptoms (67% vs 46% of placebo), but it did not alter gastrointestinal transit times or gastric volumes. Relief was sustained throughout the 4-wk treatment protocol, and drowsiness, dizziness and dry mouth were the most frequently reported adverse events. Side-effects typically occurred when doses exceeded greater than 0.1 mg twice daily. This initial study suggests that α2 agonists may play a beneficial role in IBS-D, though unwanted hypotension may be a side-effect that precludes its chronic use. Further studies are warranted.
Octreotide, a somatostatin analogue, works by activating somatostatin type-2 receptors and has been shown to reduce visceral sensitivity in response to rectal distension. In healthy volunteers and in small numbers of IBS-D patients, octreotide administered in a 50 mg bolus was shown to prolong orocecal transit times and inhibit small bowel transit times. While these results suggest that octreotide may have benefits in patients with IBS-D, its intravenous preparation precludes daily use, and to date, no studies with oral somatostatin analogues exist for the treatment of IBS.
Opioid receptors are found throughout the enteric nervous system and on nociceptive pathways that conduct pain to the central nervous system. Altered bowel transit and visceral hypersensitivity are important components in IBS pathophysiology and peripherally-acting opioid receptors may be effective drug targets. Alvimopan is a peripherally acting &mgr;-opioid antagonist that is effective in treatment of post-operative ileus. In a study of 74 healthy volunteers, it normalized colonic transit delays induced by the administration of codeine, and alone was shown to accelerate colonic transit.
The κ-opioid agonist, asimadoline, exerts nociceptive properties on the GI tract at least in part by blocking Na receptor channels. It has been shown to decrease colonic tone during fasting and decrease colonic pain at low levels of distension. In a study of 20 IBS-C patients, asimadoline was shown to be effective in decreasing pain perception from colonic distension without affecting colonic compliance or tone.
More recently, a randomized, placebo-controlled trial by Szarka and colleagues showed that asimadoline (up to 1 mg four times daily) did not statistically improve abdominal pain when taken on an “as needed basis” compared to placebo. Further studies are needed to determine the efficacy of this medication.
Corticotropin-releasing hormone (CRH) is a key mediator that regulates changes in colonic motility, visceral hypersensitivity, and autonomic function in response to stress. Stress is processed within the CNS and increases both ACTH and CRH secretion, the latter stimulates colonic motility and inhibits gastric emptying. Distension of the colon also activates CRH pathways in the brain, providing a plausible rationale for why visceral stimulation is perceived as anxiety or stress in some patients with IBS. Fukudo and colleagues demonstrated that administration of intravenous CRH was associated with exaggeration of colonic motility and increased ACTH secretion in IBS patients compared to healthy controls. More recently, α-Helical CRH (a non-selective CRH receptor antagonist) has been shown to significantly reduce abdominal pain and anxiety ratings induced by electrical stimulation of the rectum of IBS patients, but not of controls. Two CRH receptors appear important in the pathogenesis of IBS. Stimulation of the CRH-1 receptor is anxiogenic and associated with pro-inflammatory states, while CRH-2 receptors are involved in the inhibition of gastric emptying. CRH-1 antagonists are currently under development for clinical use in IBS.
Lubiprostone is a member of a new class of bicyclic fatty-acid derivatives known as prostones, and was approved by the FDA in 2006 for the treatment of chronic constipation. It acts on type-2 chloride channels located on the apical side of gastrointestinal epithelial cells, and increases secretion of electrolyte-rich fluid into the small intestine, promoting increased motility. Several studies have shown that in patients with chronic constipation, lubiprostone is effective in improving the spontaneous bowel movement and is associated with less bloating, straining and abdominal discomfort. The role of lubiprostone in IBS-C has recently been evaluated in a randomized, double-blinded placebo-controlled trial of approximately 200 patients. The results of this study showed an overall improvement in abdominal symptoms and bowel movement when compared to placebo and the most frequently reported side-effect was mild to moderate nausea. To date, no serious adverse events have been noted in clinical trials. Sucampo Pharmaceuticals submitted a supplemental New Drug Application to the FDA in September 2007 requesting approval for the use of lubiprostone in IBS-C. A decision is expected sometime in early 2008.
Cholecystokinin (CCK) is a neuropeptide released by duodenal and jejunal enterochromaffin cells that stimulates secretion of pancreatic enzymes and decreases gastric emptying in response to dietary fat. CCK1 receptors are distributed within enteric neurons and vagal afferents, and antagonism at this receptor has been postulated to stimulate gut motility in patients with IBS-C. A recent double-blinded study found that the CCK antagonist, dexloxiglumide (200 mg three times daily) had no significant effect on satisfactory relief of IBS, and that it did not alter transit times in IBS-C. Furthermore, two large phase III clinical studies of 1 400 women with IBS-C found no statistical improvement in the symptoms of abdominal pain, discomfort or altered bowel habits when compared to placebo. As a result, Forest Laboratories have discontinued development of this drug, though Rotta Research is pursuing additional placebo-controlled studies in Europe.
Substance P and neurokinin A are excitatory co-transmitters of cholinergic enteric neurons that have been well-linked to the pathophysiology of several neurologic and psychiatric disorders. Their receptors, neurokinin 1 (NK1) and NK2, play important roles in nociception and smooth muscle contraction, and the regulation of visceral sensitivity and mucosal inflammatory processes[104–107]. Clinical data is currently deficient. However, in one study of healthy volunteers using the selective NK2 antagonist nepadutant (MEN11420), IBS-like symptoms triggered by the infusion of neurokinin A were reduced. Saredutant (SR48968), another NK2 antagonist, is also being developed for the treatment of IBS, but clinical results are not yet available.
Antidepressants are frequently prescribed by gastroente-rologists for the treatment of IBS. Their mechanism in IBS is not completely understood, but has been postulated to relate to an ability to modulate central and peripheral pain perception, improve underlying psychiatric conditions, and possibly improve gut motility through modification of neurotransmitter activity. Unfortunately, randomized-controlled trials to date have largely been hindered by poor study design and methodological flaws, making it difficult to judge the therapeutic value of these agents[114–116]. Most studies provide little evidence that antidepressants are superior to placebo in improving specific IBS-related symptoms, but some do suggest that overall global well-being may be improved. In a recent meta-analysis evaluating 12 randomized-controlled trials, Jackson and colleagues concluded that tricyclic antidepressants are effective in improving global IBS symptoms (OR, 4.2; 95% CI, 2.3-7.9), and calculated an NNT of only 3 in order to see an effect. Fewer studies have been conducted with SSRIs. In one randomized-controlled trial comparing paroxetine (10-40 mg/d) to placebo, patients treated with the SSRI reported a significant improvement in overall well-being, but did not experience improvement in abdominal pain. Other studies with paroxetine have shown an improvement in abdominal pain and discomfort, and suggest that further studies with this class of medication are needed. While certain subgroups of IBS patients (particularly those with psychiatric comorbidities such as depression or anxiety) will likely benefit from the use of antidepressants, their use in other patients (particularly the elderly) should be met with caution as side-effects are common. Furthermore, the anticholinergic nature of some of these medications limits their use in patients with IBS-C. Antidepressants should not be used to relieve the target symptoms of IBS, and their use will not likely alter GI motility or physiology. Instead, antidepressants should be used as an adjunct in patients with moderate to severe IBS to help improve overall quality of life, well-being, and patient satisfaction with treatment.
Antispasmodic agents are believed to work in IBS based on their ability to decrease intestinal smooth muscle activity. There are two broad categories of antispasmodic agents: anticholinergics/antimuscarinic agents (e.g. hyoscyamine, dicyclomine, cimetropium) and direct smooth muscle relaxing agents (e.g. mebeverine, pinaverine, octylonium bromide). Most studies of smooth muscle relaxants have been hindered by poor study design, high drop-out rates, and low patient enrollment which have made assessment of their therapeutic value in IBS difficult[121–123]. In a recent meta-analysis, only octylonium bromide was found to have some benefit after excluding poor quality studies.
In a review of anticholinergic drugs, Schoenfield and colleagues found similar problems with study design, and based on the poor quality of trials and marginal data, concluded that any benefit observed with these agents was likely due to placebo effect. Additionally, their substantial side-effect profile makes these agents a suboptimal choice for IBS therapy.
Loperamide is one of the most frequently used drugs for IBS-D. It is a synthetic opioid that decreases intestinal transit, and increases intestinal water and ion absorption. Several RCTs have provided a good evidence that loperamide decreases stool frequency and improves stool consistency in IBS-D[124–126]. Loperamide does not appear to improve abdominal pain and should only be considered in cases of painless diarrhea.
Dextofisopam is a 2, 3 benzodiazepine that has been used outside of the U.S. for treatment of anxiety and autonomic and stress-related disorders. Unlike typical benzodiazepines which bind GABA receptors, dextofisopam binds 2, 3 benzodiazepine receptors. Results from a 12-wk placebo-controlled phase IIb trial showed that dextofisopam (200 mg twice daily) was associated with longer periods of overall relief from IBS symptoms than placebo during the treatment period (57% vs 43%). Stool frequency and consistency were also improved. Further trials are underway.
Small intestinal bacterial overgrowth (SIBO) has been proposed to be common in patients with IBS. Using lactulose breath tests (LBT), Pimental and colleagues showed that 78% of IBS patients had SIBO and that eradication with a seven-day course of neomycin was associated with a significant reduction in symptoms. However, these results are somewhat controversial, as both the accuracy of the LBT and its ability to gauge treatment response has been questioned[130–133]. More recently, Posserud and colleagues conducted a study of 162 IBS patients using cultures of jejunal aspirates to detect SIBO. They found that higher bacterial counts were present in IBS patients compared to placebo (43% vs 12%), but this finding was not related to small intestinal motility. Furthermore, using a standard definition of SIBO (> 105 bacteria/mL), there was no difference between IBS patients and healthy controls. Further research is needed in this area, including a better evaluation of the long-term effects of SIBO eradication.
The use of fiber and bulking agents remains a mainstay of therapy for patients with IBS-C, though their efficacy is controversial. The proposed mechanism for fiber is a decrease in intra-colonic pressures and an acceleration of oroanal transit though results from studies on transit times are conflicting. There have been a number of trials evaluating the effectiveness of fiber, but many have methodological limitations including small sample sizes, short follow-up periods, selection bias, and lack of well-defined endpoints. In a recent systematic review of 17 randomized controlled trials examining the role of fiber in the treatment of IBS, Bijkerk et al found only a minimal improvement in overall relief of IBS global symptoms (RR 1.33; 95% CI, 1.19-1.50), and found no evidence that fiber reduces abdominal pain. Furthermore, the effectiveness on individual symptoms was variable and insoluble fiber (corn, wheat bran) was found to actually worsen symptoms in some patients. In another meta-analysis of 13 placebo-controlled studies, fiber was found to improve global symptoms of IBS. But after exclusion of low-quality studies, the result did not reach statistical significance. Abnormal bacterial fermentation and disturbed gas handling may also cause bloating and abdominal pain and may worsen clinical outcome. The American College of Gastroenterology Functional Gastrointestinal Disorders Task Force currently recommends the use of fiber in patients with constipation, but does not recommend its use in IBS.
The presence of low-grade inflammation and immune activation in some patients with IBS suggests that alterations in indigenous gut flora may play an important role in this disorder. Probiotics may work by helping restore both qualitative (i.e. depleted bifidobacteria species) and quantitative (i.e. small intestinal bacterial overgrowth) alterations in intestinal flora. Lactobacilli and bifidobacteria are two of the most frequently studied probiotics, and several trials have shown that their use is associated with improvement in IBS symptoms[145–148]. Niedzielin and colleagues demonstrated a complete resolution of abdominal pain in patients who took L. plantarum compared to approximately 50% of placebo controls. Other studies have shown that L. plantarum is associated with a decrease in bloating and may reduce global IBS symptom index scores. Post-infectious IBS may lead to abnormal immune activation and a persistent inflammatory state. The bifidobacterial species may be beneficial in this subset of IBS as it appears to possess immune-modulating activity through an ability to alter levels of IL-10 and IL-12.
To date, most studies assessing the efficacy of probiotics have been small, and it has been difficult to compare results across studies largely because of non-standardized formulations of probiotics. Nonetheless, data suggests that probiotics may be beneficial, and a good safety profile makes them a reasonable choice for IBS.
Two-thirds of IBS patients believe that their disorder is related to diet. They often complain of postprandial worsening of symptoms, and are intolerant to certain foods. Visceral hypersensitivity, motility disorders, gas-handling disturbances, and abnormal carbohydrate absorption are abnormalities that may explain some of these findings. However, presence of underlying psychological issues also affects the diet-related symptoms. In a recent pilot study of 20 IBS patients, Drisko and colleagues found that elimination and rotation diets based on the results of IgG and IgE food and mold panels led to a substantial improvement in stool frequency, abdominal pain, and quality-of-life scores. These results were sustained at the one year follow-up. Previous studies on elimination diets have produced more conflicting results, showing an effectiveness rate ranging from 15% to 71%. Nonetheless, dietary modification may be an option for patients who fail in the standard therapy.
The complex nature of IBS continues to pose a significant treatment challenge for patients and practitioners. Traditional medications such as antispasmodics, bulking agents, and antidepressants are frequently prescribed for IBS. But, they are seldom efficacious in patients with advanced symptoms. Fortunately, the recent efforts of basic scientists and clinician investigators have elucidated many of the neurotransmitters, effectors and neuroenteric interactions involved in the pathophysiology of IBS, and have led to the development of several new and promising therapeutic agents. Over the past years, the serotonergic medications, tegaserod and alosetron, have been proven to significantly improve patients’ overall quality of life and effectively manage many of the motor and sensory abnormalities in IBS. With more progress made in our understanding of IBS and more data obtained from phase III trials, we can expect to see several other classes of medications, such as CCK antagonists, NK antagonists, CRH antagonists, opioid-receptor agents and chloride channel activators, in the near future.
|1.||Drossman DA, Camilleri M, Mayer EA, Whitehead WE. AGA technical review on irritable bowel syndrome. Gastroenterology. 2002;123:2108-2131. [Cited in This Article: ]|
|2.||Cremonini F, Talley NJ. Irritable bowel syndrome: epidemiology, natural history, health care seeking and emerging risk factors. Gastroenterol Clin North Am. 2005;34:189-204. [Cited in This Article: ]|
|3.||Drossman DA, Li Z, Andruzzi E, Temple RD, Talley NJ, Thompson WG, Whitehead WE, Janssens J, Funch-Jensen P, Corazziari E. U.S. householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact. Dig Dis Sci. 1993;38:1569-1580. [Cited in This Article: ]|
|4.||Morris-Yates A, Talley NJ, Boyce PM, Nandurkar S, Andrews G. Evidence of a genetic contribution to functional bowel disorder. Am J Gastroenterol. 1998;93:1311-1317. [Cited in This Article: ]|
|5.||Levy RL, Jones KR, Whitehead WE, Feld SI, Talley NJ, Corey LA. Irritable bowel syndrome in twins: heredity and social learning both contribute to etiology. Gastroenterology. 2001;121:799-804. [Cited in This Article: ]|
|6.||Lydiard RB, Falsetti SA. Experience with anxiety and depression treatment studies: implications for designing irritable bowel syndrome clinical trials. Am J Med. 1999;107:65S-73S. [Cited in This Article: ]|
|7.||Whitehead WE, Crowell MD. Psychologic considerations in the irritable bowel syndrome. Gastroenterol Clin North Am. 1991;20:249-267. [Cited in This Article: ]|
|8.||Spiller RC. Inflammation as a basis for functional GI disorders. Best Pract Res Clin Gastroenterol. 2004;18:641-661. [Cited in This Article: ]|
|9.||Spiller R, Campbell E. Post-infectious irritable bowel syndrome. Curr Opin Gastroenterol. 2006;22:13-17. [Cited in This Article: ]|
|10.||O'Mahony L, McCarthy J, Kelly P, Hurley G, Luo F, Chen K, O'Sullivan GC, Kiely B, Collins JK, Shanahan F. Lactobacillus and bifidobacterium in irritable bowel syndrome: symptom responses and relationship to cytokine profiles. Gastroenterology. 2005;128:541-551. [Cited in This Article: ]|
|11.||Serra J, Azpiroz F, Malagelada JR. Impaired transit and tolerance of intestinal gas in the irritable bowel syndrome. Gut. 2001;48:14-19. [Cited in This Article: ]|
|12.||Kellow JE, Eckersley CM, Jones MP. Enhanced perception of physiological intestinal motility in the irritable bowel syndrome. Gastroenterology. 1991;101:1621-1627. [Cited in This Article: ]|
|13.||Drossman DA, Sandler RS, McKee DC, Lovitz AJ. Bowel patterns among subjects not seeking health care. Use of a questionnaire to identify a population with bowel dysfunction. Gastroenterology. 1982;83:529-534. [Cited in This Article: ]|
|14.||Thompson WG, Heaton KW, Smyth GT, Smyth C. Irritable bowel syndrome in general practice: prevalence, characteristics, and referral. Gut. 2000;46:78-82. [Cited in This Article: ]|
|15.||Hulisz D. The burden of illness of irritable bowel syndrome: current challenges and hope for the future. J Manag Care Pharm. 2004;10:299-309. [Cited in This Article: ]|
|16.||Leong SA, Barghout V, Birnbaum HG, Thibeault CE, Ben-Hamadi R, Frech F, Ofman JJ. The economic consequences of irritable bowel syndrome: a US employer perspective. Arch Intern Med. 2003;163:929-935. [Cited in This Article: ]|
|17.||Gralnek IM, Hays RD, Kilbourne A, Naliboff B, Mayer EA. The impact of irritable bowel syndrome on health-related quality of life. Gastroenterology. 2000;119:654-660. [Cited in This Article: ]|
|18.||Drossman DA, Thompson WG. The irritable bowel syndrome: review and a graduated multicomponent treatment approach. Ann Intern Med. 1992;116:1009-1016. [Cited in This Article: ]|
|19.||Drossman DA. Diagnosing and treating patients with refractory functional gastrointestinal disorders. Ann Intern Med. 1995;123:688-697. [Cited in This Article: ]|
|20.||Halpert A, Dalton CB, Palsson O, Morris C, Hu Y, Bangdiwala S, Hankins J, Norton N, Drossman D. What patients know about irritable bowel syndrome (IBS) and what they would like to know. National Survey on Patient Educational Needs in IBS and development and validation of the Patient Educational Needs Questionnaire (PEQ). Am J Gastroenterol. 2007;102:1972-82. [Cited in This Article: ]|
|21.||Owens DM, Nelson DK, Talley NJ. The irritable bowel syndrome: long-term prognosis and the physician-patient interaction. Ann Intern Med. 1995;122:107-112. [Cited in This Article: ]|
|22.||North CS, Hong BA, Alpers DH. Relationship of functional gastrointestinal disorders and psychiatric disorders: implications for treatment. World J Gastroenterol. 2007;13:2020-2027. [Cited in This Article: ]|
|23.||Lacy BE, Weiser K, Noddin L, Robertson DJ, Crowell MD, Parratt-Engstrom C, Grau MV. Irritable bowel syndrome: patients' attitudes, concerns and level of knowledge. Aliment Pharmacol Ther. 2007;25:1329-1341. [Cited in This Article: ]|
|24.||Greenwood-van Meerveld B. Importance of 5-hydroxy-tryptamine receptors on intestinal afferents in the regulation of visceral sensitivity. Neurogastroenterol Motil. 2007;19 Suppl 2:13-18. [Cited in This Article: ]|
|25.||Gershon MD. Review article: serotonin receptors and transporters -- roles in normal and abnormal gastrointestinal motility. Aliment Pharmacol Ther. 2004;20 Suppl 7:3-14. [Cited in This Article: ]|
|26.||Gershon MD. Review article: roles played by 5-hydroxy-tryptamine in the physiology of the bowel. Aliment Pharmacol Ther. 1999;13 Suppl 2:15-30. [Cited in This Article: ]|
|27.||Crowell MD. Role of serotonin in the pathophysiology of the irritable bowel syndrome. Br J Pharmacol. 2004;141:1285-1293. [Cited in This Article: ]|
|28.||Gershon MD. Serotonin and its implication for the management of irritable bowel syndrome. Rev Gastroenterol Disord. 2003;3 Suppl 2:S25-S34. [Cited in This Article: ]|
|29.||Gershon MD. 5-HT (serotonin) physiology and related drugs. Curr Opin Gastroenterol. 2000;16:113-120. [Cited in This Article: ]|
|30.||Bardhan KD, Bodemar G, Geldof H, Schutz E, Heath A, Mills JG, Jacques LA. A double-blind, randomized, placebo-controlled dose-ranging study to evaluate the efficacy of alosetron in the treatment of irritable bowel syndrome. Aliment Pharmacol Ther. 2000;14:23-34. [Cited in This Article: ]|
|31.||Houghton LA, Foster JM, Whorwell PJ. Alosetron, a 5-HT3 receptor antagonist, delays colonic transit in patients with irritable bowel syndrome and healthy volunteers. Aliment Pharmacol Ther. 2000;14:775-782. [Cited in This Article: ]|
|32.||Grider JR, Foxx-Orenstein AE, Jin JG. 5-Hydroxytryptamine4 receptor agonists initiate the peristaltic reflex in human, rat, and guinea pig intestine. Gastroenterology. 1998;115:370-380. [Cited in This Article: ]|
|33.||Hegde SS, Eglen RM. Peripheral 5-HT4 receptors. FASEB J. 1996;10:1398-1407. [Cited in This Article: ]|
|34.||Coates MD, Mahoney CR, Linden DR, Sampson JE, Chen J, Blaszyk H, Crowell MD, Sharkey KA, Gershon MD, Mawe GM. Molecular defects in mucosal serotonin content and decreased serotonin reuptake transporter in ulcerative colitis and irritable bowel syndrome. Gastroenterology. 2004;126:1657-1664. [Cited in This Article: ]|
|35.||Yeo A, Boyd P, Lumsden S, Saunders T, Handley A, Stubbins M, Knaggs A, Asquith S, Taylor I, Bahari B. Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women. Gut. 2004;53:1452-1458. [Cited in This Article: ]|
|36.||Camilleri M, Atanasova E, Carlson PJ, Ahmad U, Kim HJ, Viramontes BE, McKinzie S, Urrutia R. Serotonin-transporter polymorphism pharmacogenetics in diarrhea-predominant irritable bowel syndrome. Gastroenterology. 2002;123:425-432. [Cited in This Article: ]|
|37.||Delvaux M, Louvel D, Mamet JP, Campos-Oriola R, Frexinos J. Effect of alosetron on responses to colonic distension in patients with irritable bowel syndrome. Aliment Pharmacol Ther. 1998;12:849-855. [Cited in This Article: ]|
|38.||Berman SM, Chang L, Suyenobu B, Derbyshire SW, Stains J, Fitzgerald L, Mandelkern M, Hamm L, Vogt B, Naliboff BD. Condition-specific deactivation of brain regions by 5-HT3 receptor antagonist Alosetron. Gastroenterology. 2002;123:969-977. [Cited in This Article: ]|
|39.||Mayer EA, Berman S, Derbyshire SW, Suyenobu B, Chang L, Fitzgerald L, Mandelkern M, Hamm L, Vogt B, Naliboff BD. The effect of the 5-HT3 receptor antagonist, alosetron, on brain responses to visceral stimulation in irritable bowel syndrome patients. Aliment Pharmacol Ther. 2002;16:1357-1366. [Cited in This Article: ]|
|40.||Camilleri M, Mayer EA, Drossman DA, Heath A, Dukes GE, McSorley D, Kong S, Mangel AW, Northcutt AR. Improvement in pain and bowel function in female irritable bowel patients with alosetron, a 5-HT3 receptor antagonist. Aliment Pharmacol Ther. 1999;13:1149-1159. [Cited in This Article: ]|
|41.||Camilleri M, Northcutt AR, Kong S, Dukes GE, McSorley D, Mangel AW. Efficacy and safety of alosetron in women with irritable bowel syndrome: a randomised, placebo-controlled trial. Lancet. 2000;355:1035-1040. [Cited in This Article: ]|
|42.||Camilleri M, Chey WY, Mayer EA, Northcutt AR, Heath A, Dukes GE, McSorley D, Mangel AM. A randomized controlled clinical trial of the serotonin type 3 receptor antagonist alosetron in women with diarrhea-predominant irritable bowel syndrome. Arch Intern Med. 2001;161:1733-1740. [Cited in This Article: ]|
|43.||Lembo T, Wright RA, Bagby B, Decker C, Gordon S, Jhingran P, Carter E. Alosetron controls bowel urgency and provides global symptom improvement in women with diarrhea-predominant irritable bowel syndrome. Am J Gastroenterol. 2001;96:2662-2670. [Cited in This Article: ]|
|44.||Cremonini F, Delgado-Aros S, Camilleri M. Efficacy of alosetron in irritable bowel syndrome: a meta-analysis of randomized controlled trials. Neurogastroenterol Motil. 2003;15:79-86. [Cited in This Article: ]|
|45.||Chang L, Chey WD, Harris L, Olden K, Surawicz C, Schoenfeld P. Incidence of ischemic colitis and serious complications of constipation among patients using alosetron: systematic review of clinical trials and post-marketing surveillance data. Am J Gastroenterol. 2006;101:1069-1079. [Cited in This Article: ]|
|46.||Horton R. Lotronex and the FDA: a fatal erosion of integrity. Lancet. 2001;357:1544-1545. [Cited in This Article: ]|
|47.||Krause R, Ameen V, Gordon SH, West M, Heath AT, Perschy T, Carter EG. A randomized, double-blind, placebo-controlled study to assess efficacy and safety of 0.5 mg and 1 mg alosetron in women with severe diarrhea-predominant IBS. Am J Gastroenterol. 2007;102:1709-1719. [Cited in This Article: ]|
|49.||Chey WD, Cash BD. Cilansetron: a new serotonergic agent for the irritable bowel syndrome with diarrhoea. Expert Opin Investig Drugs. 2005;14:185-193. [Cited in This Article: ]|
|50.||Olden KW, Crowell MD. Cilansetron. Drugs Today (Barc). 2005;41:661-666. [Cited in This Article: ]|
|51.||Stacher G. Cilansetron. Solvay. Curr Opin Investig Drugs. 2001;2:1432-1436. [Cited in This Article: ]|
|52.||Rabasseda X. Ramosetron, a 5-HT3 receptor antagonist for the control of nausea and vomiting. Drugs Today (Barc). 2002;38:75-89. [Cited in This Article: ]|
|53.||Shi Y, He X, Yang S, Ai B, Zhang C, Huang D, Dong M, Liu P, Zhou S, Han X. Ramosetron versus ondansetron in the prevention of chemotherapy-induced gastrointestinal side effects: A prospective randomized controlled study. Chemotherapy. 2007;53:44-50. [Cited in This Article: ]|
|54.||Hirata T, Keto Y, Funatsu T, Akuzawa S, Sasamata M. Evaluation of the pharmacological profile of ramosetron, a novel therapeutic agent for irritable bowel syndrome. J Pharmacol Sci. 2007;104:263-273. [Cited in This Article: ]|
|55.||Funatsu T, Takeuchi A, Hirata T, Keto Y, Akuzawa S, Sasamata M. Effect of ramosetron on conditioned emotional stress-induced colonic dysfunction as a model of irritable bowel syndrome in rats. Eur J Pharmacol. 2007;573:190-195. [Cited in This Article: ]|
|56.||Bharucha AE, Camilleri M, Haydock S, Ferber I, Burton D, Cooper S, Tompson D, Fitzpatrick K, Higgins R, Zinsmeister AR. Effects of a serotonin 5-HT(4) receptor antagonist SB-207266 on gastrointestinal motor and sensory function in humans. Gut. 2000;47:667-674. [Cited in This Article: ]|
|57.||Houghton LA, Jackson NA, Whorwell PJ, Cooper SM. 5-HT4 receptor antagonism in irritable bowel syndrome: effect of SB-207266-A on rectal sensitivity and small bowel transit. Aliment Pharmacol Ther. 1999;13:1437-1444. [Cited in This Article: ]|
|58.||Prather CM, Camilleri M, Zinsmeister AR, McKinzie S, Thomforde G. Tegaserod accelerates orocecal transit in patients with constipation-predominant irritable bowel syndrome. Gastroenterology. 2000;118:463-468. [Cited in This Article: ]|
|59.||Muller-Lissner SA, Fumagalli I, Bardhan KD, Pace F, Pecher E, Nault B, Ruegg P. Tegaserod, a 5-HT(4) receptor partial agonist, relieves symptoms in irritable bowel syndrome patients with abdominal pain, bloating and constipation. Aliment Pharmacol Ther. 2001;15:1655-1666. [Cited in This Article: ]|
|60.||Novick J, Miner P, Krause R, Glebas K, Bliesath H, Ligozio G, Ruegg P, Lefkowitz M. A randomized, double-blind, placebo-controlled trial of tegaserod in female patients suffering from irritable bowel syndrome with constipation. Aliment Pharmacol Ther. 2002;16:1877-1888. [Cited in This Article: ]|
|61.||Kellow J, Lee OY, Chang FY, Thongsawat S, Mazlam MZ, Yuen H, Gwee KA, Bak YT, Jones J, Wagner A. An Asia-Pacific, double blind, placebo controlled, randomised study to evaluate the efficacy, safety, and tolerability of tegaserod in patients with irritable bowel syndrome. Gut. 2003;52:671-676. [Cited in This Article: ]|
|62.||Nyhlin H, Bang C, Elsborg L, Silvennoinen J, Holme I, Ruegg P, Jones J, Wagner A. A double-blind, placebo-controlled, randomized study to evaluate the efficacy, safety and tolerability of tegaserod in patients with irritable bowel syndrome. Scand J Gastroenterol. 2004;39:119-126. [Cited in This Article: ]|
|63.||Evans BW, Clark WK, Moore DJ, Whorwell PJ. Tegaserod for the treatment of irritable bowel syndrome. Cochrane Database Syst Rev. 2004;39:CD003960. [Cited in This Article: ]|
|64.||Quigley EM, Wald A, Fidelholtz J, Boivin M, Pecher E, Earnest D. Safety and tolerability of tegaserod in patients with chronic constipation: pooled data from two phase III studies. Clin Gastroenterol Hepatol. 2006;4:605-613. [Cited in This Article: ]|
|65.||Muller-Lissner S, Kamm MA, Musoglu A, Earnest DL, Dunger-Baldauf C, Shetzline MA. Safety, tolerability, and efficacy of tegaserod over 13 months in patients with chronic constipation. Am J Gastroenterol. 2006;101:2558-2569; quiz 2671. [Cited in This Article: ]|
|66.||Muller-Lissner S, Holtmann G, Rueegg P, Weidinger G, Loffler H. Tegaserod is effective in the initial and retreatment of irritable bowel syndrome with constipation. Aliment Pharmacol Ther. 2005;21:11-20. [Cited in This Article: ]|
|67.||Harish K, Hazeena K, Thomas V, Kumar S, Jose T, Narayanan P. Effect of tegaserod on colonic transit time in male patients with constipation-predominant irritable bowel syndrome. J Gastroenterol Hepatol. 2007;22:1183-1189. [Cited in This Article: ]|
|68.||Coremans G, Kerstens R, De Pauw M, Stevens M. Prucalopride is effective in patients with severe chronic constipation in whom laxatives fail to provide adequate relief. Results of a double-blind, placebo-controlled clinical trial. Digestion. 2003;67:82-89. [Cited in This Article: ]|
|69.||Kamm MA. Review article: the complexity of drug development for irritable bowel syndrome. Aliment Pharmacol Ther. 2002;16:343-351. [Cited in This Article: ]|
|70.||Camilleri M, McKinzie S, Fox J, Foxx-Orenstein A, Burton D, Thomforde G, Baxter K, Zinsmeister AR. Effect of renzapride on transit in constipation-predominant irritable bowel syndrome. Clin Gastroenterol Hepatol. 2004;2:895-904. [Cited in This Article: ]|
|71.||Tack J, Middleton SJ, Horne MC, Piessevaux H, Bloor JS, Meyers NL, Palmer RM. Pilot study of the efficacy of renzapride on gastrointestinal motility and symptoms in patients with constipation-predominant irritable bowel syndrome. Aliment Pharmacol Ther. 2006;23:1655-1665. [Cited in This Article: ]|
|72.||Liu Z, Sakakibara R, Odaka T, Uchiyama T, Uchiyama T, Yamamoto T, Ito T, Asahina M, Yamaguchi K, Yamaguchi T. Mosapride citrate, a novel 5-HT4 agonist and partial 5-HT3 antagonist, ameliorates constipation in parkinsonian patients. Mov Disord. 2005;20:680-686. [Cited in This Article: ]|
|73.||Mine Y, Yoshikawa T, Oku S, Nagai R, Yoshida N, Hosoki K. Comparison of effect of mosapride citrate and existing 5-HT4 receptor agonists on gastrointestinal motility in vivo and in vitro. J Pharmacol Exp Ther. 1997;283:1000-1008. [Cited in This Article: ]|
|74.||Inui A, Yoshikawa T, Nagai R, Yoshida N, Ito T. Effects of mosapride citrate, a 5-HT4 receptor agonist, on colonic motility in conscious guinea pigs. Jpn J Pharmacol. 2002;90:313-320. [Cited in This Article: ]|
|75.||Wei W, Ge ZZ, Lu H, Gao YJ, Hu YB, Xiao SD. Effect of mosapride on gastrointestinal transit time and diagnostic yield of capsule endoscopy. J Gastroenterol Hepatol. 2007;22:1605-1608. [Cited in This Article: ]|
|76.||Carlsson L, Amos GJ, Andersson B, Drews L, Duker G, Wadstedt G. Electrophysiological characterization of the prokinetic agents cisapride and mosapride in vivo and in vitro: implications for proarrhythmic potential? J Pharmacol Exp Ther. 1997;282:220-227. [Cited in This Article: ]|
|77.||Foxx-Orenstein AE, Camilleri M, Szarka LA, McKinzie S, Burton D, Thomforde G, Baxter K, Zinsmeister AR. Does co-administration of a non-selective opiate antagonist enhance acceleration of transit by a 5-HT4 agonist in constipation-predominant irritable bowel syndrome? A randomized controlled trial. Neurogastroenterol Motil. 2007;19:821-830. [Cited in This Article: ]|
|78.||Bharucha AE, Camilleri M, Zinsmeister AR, Hanson RB. Adrenergic modulation of human colonic motor and sensory function. Am J Physiol. 1997;273:G997-G1006. [Cited in This Article: ]|
|79.||Malcolm A, Camilleri M, Kost L, Burton DD, Fett SL, Zinsmeister AR. Towards identifying optimal doses for alpha-2 adrenergic modulation of colonic and rectal motor and sensory function. Aliment Pharmacol Ther. 2000;14:783-793. [Cited in This Article: ]|
|80.||Viramontes BE, Malcolm A, Camilleri M, Szarka LA, McKinzie S, Burton DD, Zinsmeister AR. Effects of an alpha(2)-adrenergic agonist on gastrointestinal transit, colonic motility, and sensation in humans. Am J Physiol Gastrointest Liver Physiol. 2001;281:G1468-G1476. [Cited in This Article: ]|
|81.||Malcolm A, Phillips SF, Camilleri M, Hanson RB. Pharmacological modulation of rectal tone alters perception of distention in humans. Am J Gastroenterol. 1997;92:2073-2079. [Cited in This Article: ]|
|82.||Camilleri M, Kim DY, McKinzie S, Kim HJ, Thomforde GM, Burton DD, Low PA, Zinsmeister AR. A randomized, controlled exploratory study of clonidine in diarrhea-predominant irritable bowel syndrome. Clin Gastroenterol Hepatol. 2003;1:111-121. [Cited in This Article: ]|
|83.||Schwetz I, Naliboff B, Munakata J, Lembo T, Chang L, Matin K, Ohning G, Mayer EA. Anti-hyperalgesic effect of octreotide in patients with irritable bowel syndrome. Aliment Pharmacol Ther. 2004;19:123-131. [Cited in This Article: ]|
|84.||Hasler WL, Soudah HC, Owyang C. Somatostatin analog inhibits afferent response to rectal distention in diarrhea-predominant irritable bowel patients. J Pharmacol Exp Ther. 1994;268:1206-1211. [Cited in This Article: ]|
|85.||O'Donnell LJ, Watson AJ, Cameron D, Farthing MJ. Effect of octreotide on mouth-to-caecum transit time in healthy subjects and in the irritable bowel syndrome. Aliment Pharmacol Ther. 1990;4:177-181. [Cited in This Article: ]|
|86.||von der Ohe MR, Camilleri M, Thomforde GM, Klee GG. Differential regional effects of octreotide on human gastrointestinal motor function. Gut. 1995;36:743-748. [Cited in This Article: ]|
|87.||Sternini C. Receptors and transmission in the brain-gut axis: potential for novel therapies. III. Mu-opioid receptors in the enteric nervous system. Am J Physiol Gastrointest Liver Physiol. 2001;281:G8-G15. [Cited in This Article: ]|
|88.||Delaney CP, Wolff BG, Viscusi ER, Senagore AJ, Fort JG, Du W, Techner L, Wallin B. Alvimopan, for postoperative ileus following bowel resection: a pooled analysis of phase III studies. Ann Surg. 2007;245:355-363. [Cited in This Article: ]|
|89.||Gonenne J, Camilleri M, Ferber I, Burton D, Baxter K, Keyashian K, Foss J, Wallin B, Du W, Zinsmeister AR. Effect of alvimopan and codeine on gastrointestinal transit: a randomized controlled study. Clin Gastroenterol Hepatol. 2005;3:784-791. [Cited in This Article: ]|
|90.||Delgado-Aros S, Chial HJ, Camilleri M, Szarka LA, Weber FT, Jacob J, Ferber I, McKinzie S, Burton DD, Zinsmeister AR. Effects of a kappa-opioid agonist, asimadoline, on satiation and GI motor and sensory functions in humans. Am J Physiol Gastrointest Liver Physiol. 2003;284:G558-G566. [Cited in This Article: ]|
|91.||Delvaux M, Beck A, Jacob J, Bouzamondo H, Weber FT, Frexinos J. Effect of asimadoline, a kappa opioid agonist, on pain induced by colonic distension in patients with irritable bowel syndrome. Aliment Pharmacol Ther. 2004;20:237-246. [Cited in This Article: ]|
|92.||Szarka LA, Camilleri M, Burton D, Fox JC, McKinzie S, Stanislav T, Simonson J, Sullivan N, Zinsmeister AR. Efficacy of on-demand asimadoline, a peripheral kappa-opioid agonist, in females with irritable bowel syndrome. Clin Gastroenterol Hepatol. 2007;5:1268-1275. [Cited in This Article: ]|
|93.||Tache Y, Monnikes H, Bonaz B, Rivier J. Role of CRF in stress-related alterations of gastric and colonic motor function. Ann N Y Acad Sci. 1993;697:233-243. [Cited in This Article: ]|
|94.||Fukudo S, Nomura T, Hongo M. Impact of corticotropin-releasing hormone on gastrointestinal motility and adrenocorticotropic hormone in normal controls and patients with irritable bowel syndrome. Gut. 1998;42:845-849. [Cited in This Article: ]|
|95.||Vale W, Spiess J, Rivier C, Rivier J. Characterization of a 41-residue ovine hypothalamic peptide that stimulates secretion of corticotropin and beta-endorphin. Science. 1981;213:1394-1397. [Cited in This Article: ]|
|96.||Fukudo S. Role of corticotropin-releasing hormone in irritable bowel syndrome and intestinal inflammation. J Gastroenterol. 2007;42 Suppl 17:48-51. [Cited in This Article: ]|
|97.||Sagami Y, Shimada Y, Tayama J, Nomura T, Satake M, Endo Y, Shoji T, Karahashi K, Hongo M, Fukudo S. Effect of a corticotropin releasing hormone receptor antagonist on colonic sensory and motor function in patients with irritable bowel syndrome. Gut. 2004;53:958-964. [Cited in This Article: ]|
|98.||Cuppoletti J, Malinowska DH, Tewari KP, Li QJ, Sherry AM, Patchen ML, Ueno R. SPI-0211 activates T84 cell chloride transport and recombinant human ClC-2 chloride currents. Am J Physiol Cell Physiol. 2004;287:C1173-C1183. [Cited in This Article: ]|
|99.||Camilleri M, Bharucha AE, Ueno R, Burton D, Thomforde GM, Baxter K, McKinzie S, Zinsmeister AR. Effect of a selective chloride channel activator, lubiprostone, on gastrointestinal transit, gastric sensory, and motor functions in healthy volunteers. Am J Physiol Gastrointest Liver Physiol. 2006;290:G942-G947. [Cited in This Article: ]|
|100.||Johanson JF, Ueno R. Lubiprostone, a locally acting chloride channel activator, in adult patients with chronic constipation: a double-blind, placebo-controlled, dose-ranging study to evaluate efficacy and safety. Aliment Pharmacol Ther. 2007;25:1351-1361. [Cited in This Article: ]|
|101.||Johanson JF WA, Ueno R. Efficacy and safety of lubiprostone in a subgroup of constipation patients diagnosed with irritable bowel syndrone with constipation (IBS-C). J Gastroenterol. 2006;101:S491. [Cited in This Article: ]|
|102.||Ueno R WA, Rivera E. Pooled analysis of the most frequent adverse events associated with the use of lubiprostone (abstract). J Gastroenterol. 2006;101:S489. [Cited in This Article: ]|
|103.||Cremonini F, Camilleri M, McKinzie S, Carlson P, Camilleri CE, Burton D, Thomforde G, Urrutia R, Zinsmeister AR. Effect of CCK-1 antagonist, dexloxiglumide, in female patients with irritable bowel syndrome: a pharmacodynamic and pharmacogenomic study. Am J Gastroenterol. 2005;100:652-663. [Cited in This Article: ]|
|104.||Holzer P. Tachykinins as targets of gastroenterological pharmacotherapy. Drug News Perspect. 1998;11:394-401. [Cited in This Article: ]|
|105.||Holzer P, Holzer-Petsche U. Tachykinins in the gut. Part I. Expression, release and motor function. Pharmacol Ther. 1997;73:173-217. [Cited in This Article: ]|
|106.||Holzer P, Holzer-Petsche U. Tachykinins in the gut. Part II. Roles in neural excitation, secretion and inflammation. Pharmacol Ther. 1997;73:219-263. [Cited in This Article: ]|
|107.||Holzer P, Lippe IT, Heinemann A, Bartho L. Tachykinin NK1 and NK2 receptor-mediated control of peristaltic propulsion in the guinea-pig small intestine in vitro. Neuropharmacology. 1998;37:131-138. [Cited in This Article: ]|
|108.||Lordal M, Navalesi G, Theodorsson E, Maggi CA, Hellstrom PM. A novel tachykinin NK2 receptor antagonist prevents motility-stimulating effects of neurokinin A in small intestine. Br J Pharmacol. 2001;134:215-223. [Cited in This Article: ]|
|109.||Clouse RE, Lustman PJ. Use of psychopharmacological agents for functional gastrointestinal disorders. Gut. 2005;54:1332-41. [Cited in This Article: ]|
|110.||Clouse RE. Antidepressants for functional gastrointestinal syndromes. Dig Dis Sci. 1994;39:2352-2363. [Cited in This Article: ]|
|111.||Mertz H, Fass R, Kodner A, Yan-Go F, Fullerton S, Mayer EA. Effect of amitriptyline on symptoms, sleep, and visceral perception in patients with functional dyspepsia. Am J Gastroenterol. 1998;93:160-165. [Cited in This Article: ]|
|112.||Gorard DA, Libby GW, Farthing MJ. Influence of anti-depressants on whole gut and orocaecal transit times in health and irritable bowel syndrome. Aliment Pharmacol Ther. 1994;8:159-166. [Cited in This Article: ]|
|113.||Gorard DA, Libby GW, Farthing MJ. 5-Hydroxytryptamine and human small intestinal motility: effect of inhibiting 5-hydroxytryptamine reuptake. Gut. 1994;35:496-500. [Cited in This Article: ]|
|114.||Heefner JD, Wilder RM, Wilson ID. Irritable colon and depression. Psychosomatics. 1978;19:540-547. [Cited in This Article: ]|
|115.||Steinhart MJ, Wong PY, Zarr ML. Therapeutic usefulness of amitriptyline in spastic colon syndrome. Int J Psychiatry Med. 1981;11:45-57. [Cited in This Article: ]|
|116.||Greenbaum DS, Mayle JE, Vanegeren LE, Jerome JA, Mayor JW, Greenbaum RB, Matson RW, Stein GE, Dean HA, Halvorsen NA. Effects of desipramine on irritable bowel syndrome compared with atropine and placebo. Dig Dis Sci. 1987;32:257-266. [Cited in This Article: ]|
|117.||Jackson JL, O'Malley PG, Tomkins G, Balden E, Santoro J, Kroenke K. Treatment of functional gastrointestinal disorders with antidepressant medications: a meta-analysis. Am J Med. 2000;108:65-72. [Cited in This Article: ]|
|118.||Tabas G, Beaves M, Wang J, Friday P, Mardini H, Arnold G. Paroxetine to treat irritable bowel syndrome not responding to high-fiber diet: a double-blind, placebo-controlled trial. Am J Gastroenterol. 2004;99:914-920. [Cited in This Article: ]|
|119.||Masand PS, Gupta S, Schwartz TL, Virk S, Lockwood K, Hameed A, King M, Kaplan DS. Paroxetine in Patients With Irritable Bowel Syndrome: A Pilot Open-Label Study. Prim Care Companion J Clin Psychiatry. 2002;4:12-16. [Cited in This Article: ]|
|120.||Creed F, Fernandes L, Guthrie E, Palmer S, Ratcliffe J, Read N, Rigby C, Thompson D, Tomenson B. The cost-effectiveness of psychotherapy and paroxetine for severe irritable bowel syndrome. Gastroenterology. 2003;124:303-317. [Cited in This Article: ]|
|121.||Klein KB. Controlled treatment trials in the irritable bowel syndrome: a critique. Gastroenterology. 1988;95:232-241. [Cited in This Article: ]|
|122.||Lesbros-Pantoflickova D, Michetti P, Fried M, Beglinger C, Blum AL. Meta-analysis: The treatment of irritable bowel syndrome. Aliment Pharmacol Ther. 2004;20:1253-1269. [Cited in This Article: ]|
|123.||Schoenfeld P. Efficacy of current drug therapies in irritable bowel syndrome: what works and does not work. Gastroenterol Clin North Am. 2005;34:319-335, viii. [Cited in This Article: ]|
|124.||Cann PA, Read NW, Holdsworth CD, Barends D. Role of loperamide and placebo in management of irritable bowel syndrome (IBS). Dig Dis Sci. 1984;29:239-247. [Cited in This Article: ]|
|125.||Lavo B, Stenstam M, Nielsen AL. Loperamide in treatment of irritable bowel syndrome--a double-blind placebo controlled study. Scand J Gastroenterol Suppl. 1987;130:77-80. [Cited in This Article: ]|
|126.||Efskind PS, Bernklev T, Vatn MH. A double-blind placebo-controlled trial with loperamide in irritable bowel syndrome. Scand J Gastroenterol. 1996;31:463-468. [Cited in This Article: ]|
|127.||Leventer S, Raudibaugh K, Frissora C. The safety and efficacy of dextof-isopam in patients with diarrhea-predominant or alternating irritable bowel syndrome. Gastroenterology. 2005;128:A94. [Cited in This Article: ]|
|128.||Pimentel M, Chow EJ, Lin HC. Eradication of small intestinal bacterial overgrowth reduces symptoms of irritable bowel syndrome. Am J Gastroenterol. 2000;95:3503-3506. [Cited in This Article: ]|
|129.||Pimentel M, Chow EJ, Lin HC. Normalization of lactulose breath testing correlates with symptom improvement in irritable bowel syndrome. a double-blind, randomized, placebo-controlled study. Am J Gastroenterol. 2003;98:412-419. [Cited in This Article: ]|
|130.||Parisi G, Leandro G, Bottona E, Carrara M, Cardin F, Faedo A, Goldin D, Pantalena M, Tafner G, Verdianelli G. Small intestinal bacterial overgrowth and irritable bowel syndrome. Am J Gastroenterol. 2003;98:2572; author reply 2573-2574. [Cited in This Article: ]|
|131.||Riordan SM, McIver CJ, Walker BM, Duncombe VM, Bolin TD, Thomas MC. The lactulose breath hydrogen test and small intestinal bacterial overgrowth. Am J Gastroenterol. 1996;91:1795-1803. [Cited in This Article: ]|
|132.||O'Leary C, Quigley EM. Small bowel bacterial overgrowth, celiac disease, and IBS: what are the real associations? Am J Gastroenterol. 2003;98:720-722. [Cited in This Article: ]|
|133.||Hasler WL. Lactulose breath testing, bacterial overgrowth, and IBS: just a lot of hot air? Gastroenterology. 2003;125:1898-1900; discussion 1900. [Cited in This Article: ]|
|134.||Posserud I, Stotzer PO, Bjornsson ES, Abrahamsson H, Simren M. Small intestinal bacterial overgrowth in patients with irritable bowel syndrome. Gut. 2007;56:802-808. [Cited in This Article: ]|
|135.||Cann PA, Read NW, Holdsworth CD. What is the benefit of coarse wheat bran in patients with irritable bowel syndrome? Gut. 1984;25:168-173. [Cited in This Article: ]|
|136.||Camilleri M, Heading RC, Thompson WG. Clinical perspectives, mechanisms, diagnosis and management of irritable bowel syndrome. Aliment Pharmacol Ther. 2002;16:1407-1430. [Cited in This Article: ]|
|137.||Cook IJ, Irvine EJ, Campbell D, Shannon S, Reddy SN, Collins SM. Effect of dietary fiber on symptoms and rectosigmoid motility in patients with irritable bowel syndrome. A controlled, crossover study. Gastroenterology. 1990;98:66-72. [Cited in This Article: ]|
|138.||Ashraf W, Lof J, Jin G, Quigley EM. Comparative effects of intraduodenal psyllium and senna on canine small bowel motility. Aliment Pharmacol Ther. 1994;8:329-336. [Cited in This Article: ]|
|139.||Zuckerman MJ. The role of fiber in the treatment of irritable bowel syndrome: therapeutic recommendations. J Clin Gastroenterol. 2006;40:104-108. [Cited in This Article: ]|
|140.||Bijkerk CJ, Muris JW, Knottnerus JA, Hoes AW, de Wit NJ. Systematic review: the role of different types of fibre in the treatment of irritable bowel syndrome. Aliment Pharmacol Ther. 2004;19:245-251. [Cited in This Article: ]|
|141.||Haderstorfer B, Psycholgin D, Whitehead WE, Schuster MM. Intestinal gas production from bacterial fermentation of undigested carbohydrate in irritable bowel syndrome. Am J Gastroenterol. 1989;84:375-378. [Cited in This Article: ]|
|142.||Brandt LJ, Bjorkman D, Fennerty MB, Locke GR, Olden K, Peterson W, Quigley E, Schoenfeld P, Schuster M, Talley N. Systematic review on the management of irritable bowel syndrome in North America. Am J Gastroenterol. 2002;97:S7-S26. [Cited in This Article: ]|
|143.||Quigley EM. Bacterial flora in irritable bowel syndrome: role in pathophysiology, implications for management. J Dig Dis. 2007;8:2-7. [Cited in This Article: ]|
|144.||Quigley EM, Flourie B. Probiotics and irritable bowel syndrome: a rationale for their use and an assessment of the evidence to date. Neurogastroenterol Motil. 2007;19:166-172. [Cited in This Article: ]|
|145.||Halpern GM, Prindiville T, Blankenburg M, Hsia T, Gershwin ME. Treatment of irritable bowel syndrome with Lacteol Fort: a randomized, double-blind, cross-over trial. Am J Gastroenterol. 1996;91:1579-1585. [Cited in This Article: ]|
|146.||Niedzielin K, Kordecki H, Birkenfeld B. A controlled, double-blind, randomized study on the efficacy of Lactobacillus plantarum 299V in patients with irritable bowel syndrome. Eur J Gastroenterol Hepatol. 2001;13:1143-1147. [Cited in This Article: ]|
|147.||Nobaek S, Johansson ML, Molin G, Ahrne S, Jeppsson B. Alteration of intestinal microflora is associated with reduction in abdominal bloating and pain in patients with irritable bowel syndrome. Am J Gastroenterol. 2000;95:1231-1238. [Cited in This Article: ]|
|148.||O'Sullivan MA, O'Morain CA. Bacterial supplementation in the irritable bowel syndrome. A randomised double-blind placebo-controlled crossover study. Dig Liver Dis. 2000;32:294-301. [Cited in This Article: ]|
|149.||Chadwick VS, Chen W, Shu D, Paulus B, Bethwaite P, Tie A, Wilson I. Activation of the mucosal immune system in irritable bowel syndrome. Gastroenterology. 2002;122:1778-1783. [Cited in This Article: ]|
|150.||Hart AL, Lammers K, Brigidi P, Vitali B, Rizzello F, Gionchetti P, Campieri M, Kamm MA, Knight SC, Stagg AJ. Modulation of human dendritic cell phenotype and function by probiotic bacteria. Gut. 2004;53:1602-1609. [Cited in This Article: ]|
|151.||Addolorato G, Marsigli L, Capristo E, Caputo F, Dall'Aglio C, Baudanza P. Anxiety and depression: a common feature of health care seeking patients with irritable bowel syndrome and food allergy. Hepatogastroenterology. 1998;45:1559-1564. [Cited in This Article: ]|
|152.||Drisko J, Bischoff B, Hall M, McCallum R. Treating irritable bowel syndrome with a food elimination diet followed by food challenge and probiotics. J Am Coll Nutr. 2006;25:514-522. [Cited in This Article: ]|