Ejaculatory dysfunction in men with diabetes mellitus

Abstract

Diabetes mellitus (DM) is a metabolic disorder that is characterized by elevated blood glucose levels due to absolute or relative insulin deficiency, in the background of β-cell dysfunction, insulin resistance, or both. Such chronic hyperglycemia is linked to long-term damage to blood vessels, nerves, and various organs. Currently, the worldwide burden of DM and its complications is in increase. Male sexual dysfunction is one of the famous complications of DM, including abnormal orgasmic/ejaculatory functions, desire/libido, and erection. Ejaculatory dysfunction encompasses several disorders related to DM and its complications, such as premature ejaculation, anejaculation (AE), delayed ejaculation, retrograde ejaculation (RE), ejaculatory pain, anesthetic ejaculation, decreased ejaculate volume, and decreased force of ejaculation. The problems linked to ejaculatory dysfunction may extend beyond the poor quality of life in diabetics as both AE and RE are alleged to alter the fertility potential of these patients. However, although both diabetes patients and their physicians are increasingly aware of diabetic ejaculatory dysfunction, this awareness still lags behind that of other diabetes complications. Therefore, all these disorders should be looked for thoroughly during the clinical evaluation of diabetic men. Besides, introducing the suitable option and/or maneuvers to treat these disorders should be tailored according to each case. This review aimed to explore the most important findings regarding ejaculatory dysfunction in diabetes from pre-clinical and clinical perspectives.

Key Words: Diabetes mellitus, Ejaculation, Anejaculation, Retrograde ejaculation, Semen

Core Tip: Male sexual dysfunction is a famous complication of diabetes mellitus (DM), including abnormal orgasmic/ejaculatory function, desire/libido, and erection. DM-related ejaculatory dysfunction encompasses several disorders such as premature ejaculation, anejaculation (AE), delayed ejaculation, retrograde ejaculation (RE), ejaculatory pain, anesthetic ejaculation, decreased ejaculate volume, and decreased force of ejaculation. The problems linked to ejaculatory dysfunction may lead to poor quality of life as both AE and RE are alleged to alter their fertility potential. All these disorders should be looked for thoroughly during the clinical evaluation of diabetic men.

INTRODUCTION

Ejaculation is a complex, coordinated sequence of mechanisms and reflexes compared to erection. It requires coordinated innervation of the sympathetic and parasympathetic systems in addition to somatic innervation. In essence, it is intermediated by a multifaceted neural control system including sensory receptors, afferent pathways, cerebral sensory areas, cerebral motor centers, spinal motor centers, and efferent pathways. Likewise, this process comprises complex neurochemical interplay between central serotonergic and dopaminergic neurons, with involvement of cholinergic, adrenergic, oxytocinergic, and gamma-aminobutyric acidergic neurons[1]. However, ejaculation entails two diverse sequential coordinated phases, seminal emission and ejaculation proper, each of them involving diverse anatomic structures[2].

The sympathetic nervous system is accountable for bladder neck closure and emission, whereas the somatic nervous system is accountable for the contraction of the pelvic muscles and the bulbourethral and ischiocavernosal muscles[3]. Additionally, the external urinary bladder sphincter as well as the perineal periurethral muscles are under somatic control[4]. Emission process is characterized by closure of the bladder neck and contraction of smooth muscles across the seminal tract aiming of propulsion of the ejaculate constituents into the posterior urethra where they are mixed with spermatozoa to form seminal fluid[5]. This phase is activated by augmented sexual arousal and the peripheral sex-related stimuli. The sympathetic centers, found within the intermediolateral and the intermediomedial cell columns in lamina VII of segments T₁₂-L₂, supply the smooth muscles of the male accessory glands, seminal tract, and urinary bladder neck[6]. Before emission, there are secretions from the distal epididymis, seminal vesicles (SVs), and the prostate supporting emission. Neural control of those secretions is mediated by the cholinergic post-ganglionic, sympathetic, and parasympathetic fibers, derived from the pelvic plexus[6-8]. The emission phase is under the cerebral control and can be affected by the physical or visual erotic stimulation[9].

The ejaculation proper phase follows emission and refers to the relaxation of the external urinary sphincter followed by repetitive contractions of the bulbospongiosus, ischiocavernosus, and the pelvic striated muscles leading to expulsion of seminal fluid out of the urethra[10]. Motor neurons controlling the pelvic and perineal striated muscles are situated in the ventral horn of segments S₂-S₄ in Onuf's nucleus[11]. Both emission and ejaculation proper occur in coherence to bring normal antegrade ejaculation. Although the precise trigger for the ejection phase is not yet known, it is believed that the filling of the posterior urethra urges the urethral-muscular reflex boosted by sensory inputs-somatosensory, visceral sensory, or proprioceptive-to the spinal control center might trigger the onset of ejection. Harmonization between autonomic and somatic neurons for emission as well as ejection is supposed to be controlled by a group of lumbar spinothalamic interneurons called “spinal ejaculation generator (SEG)''[12]. In rats, these interneurons are situated in lamina X and the medial part of lamina VII of the gray matter in the L₃-L₄[13]. In humans, neurohistologic data, in addition to the clinical observations, have established the existence of SEG in L₃-L₅ segments[14].

Exact knowledge on hormonal control of ejaculation is still lacking. Studies have shown an oxytocin surge during male sexual activity, peaking during or soon after ejaculation[15]. Additionally, oxytocin's contractile effect concerning the seminal tract in humans appears to be weaker than in the animal models[16]. Moreover, estrogens have been demonstrated to take part in the peripheral regulation of epididymal contractility[17]. Furthermore, prolactin was also noted to increase around orgasm with oxytocin suggesting that it may serve as a neuroendocrine reproductive reflex for peripheral reproductive organs[18,19]. Androgens are deeply elaborated in the ejaculation process[20]. The effects of androgens are not limited to the fact that the development of the epididymis, vas deferens, and SVs is dependent on androgens, but also, spinal nuclei elaborated in the control of ejaculation, such as the nucleus of the bulbocavernosus nerve, are androgen-dependent[21], as are the muscles of the pelvic floor[22,23]. However, the dynamic and complex interplay among androgens, growth factors, and genes in the ejaculatory process is less well understood.

Diabetes mellitus (DM) is a metabolic disorder characterized by chronic hyperglycemia due to defects in insulin secretion and/or action[24]. The worldwide burden of DM and its complications are presently in an increase. DM is usually associated with long-term dysfunction of blood vessels, nerves, and several organs including the epididymis, vas deferens (VD), SV, prostate, and urethra[25-29]. Although both diabetes patients and their physicians are increasingly aware of diabetic ejaculatory dysfunction, this awareness still lags behind that of other diabetes complications. The problems linked to the ejaculatory dysfunction may extend beyond the poor quality of life in diabetics. Because anejaculation (AE) and retrograde ejaculation (RE) are believed to alter the fertility potential of patients[25,30]. Thus, the careful diagnosis and timely management of these cases together are of extreme importance. Therefore, this narrative review aims to explore the most important findings regarding ejaculatory dysfunction in diabetes from pre-clinical and clinical perspectives.

METHODS

We searched the PUBMED/MEDLINE, Scopus, Academic Search Complete database, Google Scholar, Cochrane Library, EMBASE, ProQuest, and CINAHL databases from inception to December 2020, for relevant studies. The literature search included these terms (with synonyms and closely related words): type 1 and type 2 diabetes mellitus; or hyperglycemia; or insulin resistance; and ejaculatory dysfunction; or premature ejaculation (PE); or delayed ejaculation (DE); or AE; or RE; or ejaculatory pain (EP); or anesthetic ejaculation; or spontaneous ejaculation (SE); or sexual dysfunction; or male sexual function; or epididymis; or VD; or SVs; or prostate; bladder neck; or urethra. The search was not limited by study design but restricted to English-language periodicals. Further studies were recognized by examining the reference lists of all retrieved articles.

ANIMAL STUDIES

In an attempt to understand the influence of DM on ejaculatory function, we have identified 18 studies (Table 1) reporting on the association between experimental DM and ejaculatory dysfunction. Generally, it seems that ejaculatory dysfunction after experimental DM is inexplicable because it ranges from PE, normal ejaculatory performance, to AE. Although the duration of the diabetic state seems to be the major determinant of the development of ejaculatory dysfunction, other factors such as dissimilar animal species and strains, with a diversity of metabolic pathways, different models for inducing DM, small experimental groups, nuances in laboratory technique that may affect the results, and selection of outcome measures of the ejaculatory function. Nonetheless, the following different observations were noted: (1) 3 studies showed no sexual performance difference between diabetic and control rats[31-33]; (2) prolonged ejaculation latency (EL) was reported in 9 studies suggesting DE[34-42]. Notably, in 1 study diabetic rats showed a significantly decreased amount of secretions stored in the seminal vesicle indicating that streptozotocin (STZ)-induced diabetic might affect the cholinergic nerve endings that are situated at the rich glandular epithelium[38]; (3) 0% ejaculations (rats did not achieve ejaculation) was noted in 4 reports suggesting AE[43-46]; and (4) reduced EL was reported in 2 reports suggesting PE[47,48]. These findings suggest not only that ejaculatory dysfunction in diabetic animals is variable but also may indicate that the dysfunction may occur during the early stage following experimental diabetes and becomes poorer as it progresses[34,38]. Additionally, early insulin replacement had been demonstrated to prevent ejaculatory dysfunction suggesting that insulin may play a role in controlling of seminal emission[34,37,38]. However, once the dysfunction occurs; delayed insulin replacement cannot restore normal ejaculatory function suggesting that long-term exposure to the hyperglycemia may lead to an irreversible ejaculatory dysfunction[34,38]. In this respect, it appears that insulin replacement may only delay rather than prevent changes in copulatory behavior[34].

Table 1 Ejaculatory behavior in diabetic animals.

Ref.	Animal model	Effects observed on ejaculatory function	Type of treatment and response
Sach et al[31], 1982	STZ-induced diabetic rats	No sexual performance difference between diabetic and control rats.
Clark[32], 1995	STZ-induced diabetic rats	No sexual performance difference between diabetic and control rats.
Scarano et al[33], 2006	STZ-induced diabetic rats	No sexual performance differences in EL after 15 d.
Steger et al[34], 1990	STZ-induced diabetic rats	Prolonged EL (DE or AE)	Delayed insulin replacement (4 wk) cannot prevent ejaculatory dysfunction.
Murray et al[35], 1992	Diabetic BB/WOR rats	Prolonged EL (DE or AE) after 28 wk
McVary et al[36], 1997	Diabetic BB/WOR rats	Prolonged EL (DE or AE) after 40 wk, reduced number of ejaculations.
		No differences regarding serum testosterone, FSH, and LH.
Ebiko et al[37], 2006	STZ-induced diabetic rats	Deteriorated spontaneous seminal emission after 5 wk.	Early insulin replacement can prevent ejaculatory dysfunction.
		In 15 and 30 wk, occurrence of SSE was almost completely suppressed.
Yonezawa et al[38], 2009	Streptozotocin (STZ)-induced diabetic rats	Deteriorated spontaneous seminal emission after 5 wk.	Early insulin replacement can prevent ejaculatory dysfunction. Once dysfunction occurs, insulin cannot restore it.
		Decreased ejaculated semen and decreased seminal vesicle fluid.
Suresh et al[39], 2012	STZ-induced diabetic rats	Prolonged EL suggesting DE. -Low serum testosterone.	Mucuna pruriens showed recovery of EL.
De et al[40], 2016	STZ-induced diabetic rats	Prolonged EL suggesting DE. -Low serum testosterone.	l-Norvaline (arginase inhibitor) reduced EL.
Shi et al[41], 2017	STZ-induced diabetic rats	Prolonged EL suggesting DE.	Lycium barbarum polysaccharide reduced EL.
Li et al[42], 2019	STZ-induced diabetic rats	Prolonged EL at 62 d suggesting DE.	No effect of vitexin (herb) on EL.
Lert-Amornpat et al[43], 2016	STZ-induced diabetic rats	Lack of copulatory behavior suggesting AE.	Kaempferia parviflora (herb) showed recovery of EL.
Fernández-Collazo et al[44], 1970	Rats with subtotal pancreatectomy	They did not AE.
Hassan et al[45], 1993	STZ-induced diabetic rats	Rats exhibited AE in diabetics. -Low serum testosterone.	Sabeluzole treatment was beneficial to correct dysfunction.
Pontes et al[46], 2011	STZ-induced diabetic rats	Lack of the sperms ejaculated into the uterus. -Low serum testosterone.	Testosterone supplement did not restore ejaculatory function.
Ghaheri et al[47], 2018	STZ-induced diabetic rats	Shorten EL after 28 d suggesting PE.	Stevia Bertoni extract improved EL.
Minaz et al[48], 2019	STZ-induced diabetic rats	Shorten EL after 8 wk suggesting PE. -Low serum testosterone.	Inhibition of soluble epoxide hydrolase prolonged EL.

AE: Anejaculation; DE: Delayed ejaculation; EL: Ejaculation latency; FSH: Follicle stimulating hormone; LH: Luteinizing hormone; PE: Premature ejaculation; STZ: Streptozotocin.

The development of ejaculatory dysfunctions in animals is not limited to STZ-induced diabetic rats[34,37-40,43,45-48] but also have been demonstrated in STZ-induced diabetic mice[42,43], subtotal pancreatectomy-induced diabetic rats[44], and Bio Breeding Wistar Strain (BB/WOR) rats with spontaneous DM[35,36]. The major attributes of this latter strain (BB/WOR) are not only limited to the fact that its pathophysiology closely look like the development as well as the clinical features of type 1 diabetes in humans but also it lacks the artefactual end-organ changes seen with STZ such as angiopathy[36]. In other words, diabetic neuropathy is a prevailing feature of this model[49]. EL, the time of the first intromission until ejaculation, was the most frequently employed outcome measure to assess the ejaculatory function in these animal studies[34-36,39-43,47,48]. Other tools include spontaneous seminal emission test[37,38], measurement of seminal vesicle fluid[38], failure to recover spermatozoa in the female uterus[46], and numbers of ejaculations[36,43-45].

In the context of ejaculatory dysfunction associated with experimental DM, it would be of interest to review the potential effects of different therapeutic compounds to restore the ejaculatory function in STZ-induced diabetic mice. Nine studies were identified[39-43,45-48]. Animal studies have demonstrated that Mucuna pruriens[39], l-Norvaline (arginase inhibitor)[40], and Lycium barbarum polysaccharide[41] showed a reduction in the EL in those showing prolonged EL during the diabetic state. Additionally, both Kaempferia parviflora[43], and sabeluzole (benzothiazole derivative)[45], were found to be beneficial in correcting an ejaculatory condition. Moreover, Stevia Bertoni extracts and the soluble epoxide hydrolase inhibitor “trans-4-{4-[3-(4-trifluoromethoxyphenyl)-ureido] cyclohexyloxy} benzoic acid/t-TUCB”[47,48] showed prolongation of EL in those animals showing a reduction in EL. Unfortunately, both vitexin (bioactive flavonoids) and testosterone did not restore ejaculatory function in STZ-induced diabetic and mice, respectively. Finally, further experiments are needed to delineate better the effects of experimental diabetes on the ejaculatory function using a unified generally accepted easily measurable outcome measure.

ETIOPATHOPHOGENESIS OF DIABETIC EJACULATORY DYSFUNCTION

Animal studies assessed the effects of experimental diabetes on the end-organs of a seminal emission (epididymis, VD, SV, prostate, bladder neck, and urethra) have revealed that hyperglycemia is capable of altering the contractility of these organs either by modulating neurotransmitters release or by modifying the basal tone of the smooth muscle layers[50-52]. Interference with the normal function of these organs may therefore include central or peripheral mechanisms. Besides, these diabetes-associated changes may have general pathophysiological interest since ejaculatory dysfunction such as PE, DE, AE; or RE has been proven to be one of the complications of DM[25,27,28]. Moreover, animal models can deliver an important method to assess neural circuitry and molecular and cellular pathways in an organized setting. The following summarizes the major observations regarding the effects of experimental diabetes on the end-organs of seminal emission to understand the pathogenesis of diabetes-associated ejaculatory dysfunction: (1) Chronically STZ-diabetic rats and mice showed degenerative changes in the sympathetic supply of the VD leading to a decreased reaction to stimulation of their noradrenergic nerves and a supersensitivity to exogenous noradrenaline[50-54]. These findings suggest that a significant proportion of animals may have developed sympathetic neuropathy that may explain the prolongation of EL, reduction of the numbers of ejaculations, and the occurrence of AE; (2) The paravertebral thoracic ganglion cells of spontaneously diabetic BB rats exhibited a decreased number of synapses and the postganglionic fibers demonstrated increased glycogenosomes, axonal sequestration, and reduced axonal size suggesting an axonopathy in sympathetic nerves[49,53]. Additionally, this model showed a peripheral neuropathic change in both the hypogastric and motor pudendal nerve fibers suggesting that diabetic neuropathy is not only disturbed the emission phase but also may disrupt the ejection phase of the ejaculatory process[36]; (3) Reactive oxygen species (ROS) may be accountable for impaired sympathetic neurotransmission and the abnormal function of diabetic vas deferens in STZ-diabetic rats[54,55]; (4) There is evidence to suggest the presence of Ca channel hyperactivity in the smooth muscle of VD of STZ-induced diabetic rats possibly due to increased phosphatidylinositol turnover mediated by alpha 1-adrenoceptors[56,57]. These findings may reduce EL and explain the occurrence of PE; (5) Noradrenaline is the principal excitatory neurotransmitter in the internal urethral sphincter and augments closure of the bladder neck during ejaculation[58,59]. By principle, the combination of long-term diabetic sympathetic neuropathy in animals[37,38,49] and external urethral sphincter relaxation dysfunction[60] may result in RE; (6) It has been demonstrated that long-term diabetes is associated with changes in serotonergic transmission in the rat brain including changes in several types of 5-HT receptors[61,62]. Theoretically, 3, 5-HT receptor subtypes (5-HT1A, 5-HT1B, and 5-HT2C) were assumed to mediate 5-HT's modulating activity on the ejaculation process. PE is associated with decreased neurotransmission of serotonin, 5-HT_2C receptor hyposensitivity, and 5-HT_1A receptor hypersensitivity[63]. Accordingly, ejaculatory dysfunction due to changes in serotonergic transmission among diabetic animals could be anticipated; (7) There is adequate evidence to suggest that experimental diabetes in different animal models (STZ rats, spontaneously diabetic BB rats, BB/WOR diabetic rats, and spontaneously diabetic Torii rats) is associated with low testosterone levels[64-70]. The pathogenesis of hypogonadism in diabetic animal models may include impaired hypothalamic or pituitary signaling[34,71,72], deficiency of gonadotropic hormones, or blockade of their actions[73,74], and/or primary Leydig cell defect in steroidogenesis due to lack of stimulating effect of insulin[74-76]. In the light of the foregoing, it might be assumed that there is a link between low testosterone levels and ejaculatory dysfunction. However, it has been shown that testosterone supplement is not able to bring back ejaculatory function in induced diabetic rats[46,77] suggesting that the deficiency of testosterone was not related directly to the diabetes-induced ejaculatory dysfunction in this experimental model. Although expression of androgen receptors are demonstrated at different levels of the ejaculatory process such as the medial preoptic area of the hypothalamus[78], smooth muscles of the male genital tract[79], and in the spinal nucleus of the bulbocavernosus muscle[80], it is thought that testosterone plays a much superior role in libido than the ejaculatory process and the physiological capacity for ejaculation is less sensitive to testosterone reduction than that for the desire[81,82]. In support of this notion, it has been shown that testosterone levels as low as 0.2 ng/mL, can support ejaculatory behavior in rats[83]; (8) It is possible that diabetic ejaculatory dysfunction might be a reflection of decreased sexual desire[36,48]. Although the classic description of diabetic erectile dysfunction showed preserved desire[84], it has been shown that sexual desire (mount frequency) is notably decreased in diabetic rats[34,45,85-87], but this possibility was unlikely because of the absence of improved ejaculation behavior among diabetic rats after testosterone therapy despite the improvement of their libido (mount behavior)[77]; and (9) Lastly other factors that may participate in the pathogenesis of ejaculatory dysfunction in experimental diabetes may include decreased body and reproductive organs weight[45,77]. However, the relationship between these variables and diabetic ejaculatory dysfunction remains incompletely understood.

Ejaculatory dysfunctions are established complications found with variable prevalence in men with diabetes. There is also a substantial contribution of human studies to the pathogenesis of diabetic ejaculatory dysfunction. The factors that have been postulated to influence the development of ejaculatory dysfunctions in DM are summarized (Tables 2 and 3). However, there are limited data regarding the weight of each mechanism in participating in the pathogenesis of different ejaculatory dysfunctions in diabetes patients.

Table 2 Possible pathophysiological mechanisms underlying ejaculatory dysfunctions in diabetes mellitus (animal studies).

Ref.	Postulated mechanisms	Possible ejaculatory dysfunction
McVary et al[36], Yagihashi et al[49]	Pathologic changes in the nerve supply of seminal tract due to accumulation of AGE increased ROS (sympathetic neuropathy)	Prolongation of EL
Tomlinson et al[50], Longhurst et al[51]	Decreased number of synapses in thoracic ganglia	Reduction of the numbers of ejaculations
Kaschube et al[52], Kamata et al[53]	Axonopathy in postganglionic sympathetic fibers	Disturbed the emission phase
Güneş et al[54], Tsounapi et al[55]	Neuropathic changes in hypogastric nerve and motor pudendal nerve fibers	Disruption of the ejection phase
Tomlinson et al[50], Longhurst et al[51], Kaschube et al[52], Kamata et al[53], Güneş et al[54]	Hypersensitivity (supersensitivity) of seminal tract smooth muscles to exogenous noradrenaline	Reduction of EL
Sakai et al[56], Sakai et al[57]	Hyperactivity of Ca channels in smooth muscles	Reduction of EL
Ebiko et al[37], Yonezawa et al[38]Yagihashi et al[49], Torimoto et al[60]	Sympathetic neuropathy and external urethral sphincter relaxation dysfunction	Disruption of bladder neck closure
		Disruption of AE
Sandrini et al[61], Abraham et al[62]	Changes in serotonergic transmission	Reduction or prolongation of EL
Seethalakshmi et al[71], Wolfe et al[72]	Impaired hypothalamic or pituitary signaling	Decreased sexual performance
Oksanen et al[73], Sudha et al[74]	Deficiency of gonadotropic hormones or blockade of their actions	Decreased sexual performance
Ballester et al[75], Neirijnck et al[76]	Decrease in number and function of Leydig cells	Decreased sexual performance
Neirijnck et al[76]	Defective testicular steroidogenesis	Decreased sexual performance
Kühn-Velten et al[64], Anderson et al[65], Ricci et al[66], Murray et al[67], Cameron et al[68], Ohta et al[69], Nakane et al[70]	Reduced serum levels of LH and testosterone (T)	Decreased sexual performance
McVary et al[36], Minaz et al[48], Steger et al[85], Al-Roujayee et al[86], Kashif et al[87]	Reduced libido	Decreased sexual performance, decreased mount frequency, and reduced EL
Hassan et al[45], Steger et al[77]	Reduced reproductive organ weight	Exact Effects on ejaculation still unknown

AGE: Advanced glycation end products; Ca: Calcium; DE: Delayed ejaculation; EL: Ejaculation latency; FSH: Follicle stimulating hormone; LH: Luteinizing hormone; PE: Premature ejaculation; ROS: Reactive oxygen species; STZ: Streptozotocin; T: Testosterone.

Table 3 Possible pathophysiological mechanisms underlying ejaculatory dysfunctions in diabetes mellitus (human studies).

Ref.	Possible cause	Outcome
Premature ejaculation
Culha et al[88]	Anxiety	Among PE patients with DM, 15% had anxiety
Culha et al[88], Khan et al[89]	Depression	Among PE patients with DM, 16.9% had depression
		Depression score Significantly higher among diabetic-related PE patients
Khan et al[89], Malavige et al[90]	Genetic and racial factors	Long tri-nucleotide repeats of the androgen receptor are related to the lowest IELT (PE)
		Asian men reported higher diabetic PE than European counterparts
El-Sakka[91]	Diabetic condition, duration of MD	> 10 yr of diabetes were 2.7 times as likely to report diabetic-related PE
	Poor glycemic control	Poor glycemic control were 9.6 times as likely to report PE
El-Sakka[91], Majzoub et al[92]	Having diabetic-related -erectile dysfunction (ED) and Cardiovascular diseases	Significant association between PE and cardiovascular diseases
Malavige et al[93], Malavige et al[90]		ED showed a significantly higher incidence of PE
Olamoyegun et al[94]		ED was strongly associated with PE odds ratio = 4.4
El-Sakka[91]	Having diabetic –related neuropathy	It is not associated with PE
Khan et al[89]	Total serum testosterone	Significantly higher among type 2 diabetic-related PE patients
Owiredu et al[95]		It correlates negatively with short IELT among type 2 DM
Bellastella et al[96]		No significant difference in type 1 diabetes
Delayed ejaculation and anejaculation
Corona et al[97]	Depression	Severe depressive symptoms are associated with ejaculatory problems in DM
Ellenberg et al[25] , La Vignera et al[27] , Dinulovic et al[98]	Progressive autonomic neuropathy of the sympathetic nerves	Denervation leads to weak or loss of VD and SV peristaltic movements
Dunsmuir et al[99], Condorelli et al[100]		Abnormal inflammatory responses lead to alteration of the VD and SV peristaltic movements
La Vignera et al[101] , Pop-Busui et al[102]		Delayed /poor emission
		Absent emission
Haddad et al[26], Culver et al[103]	Calcification of vas deferens and seminal vesicles	Loss of their ability to contract as the smooth muscle is replaced by fibrotic, calcified tissue
Tsuno et al[104]		Delayed/poor emission
Hylmarova et al[29] , Corona et al[81]	Hypogonadism	No association between serum testosterone levels and ejaculation time in men self-reporting DE including diabetic patients
Paduch et al[82], Gianatti et al[105]
Morgentaler et al[106]		T replacement is not associated with improvement in DE or AE
Burke et al[107], Corona et al[108]	Low sexual desire	DM is significantly associated with low sexual desire
Corona et al[109]		DE and AE are associated with low sexual desire
Retrograde ejaculation
Klebanow et al[110]	Diabetic neuropathy (T10-L3)	Intact vasal and seminal vesicle contraction but incomplete simultaneous bladder neck closure leads to partial RE
Greene et al[111]		Intact vasal and seminal vesicle contraction and simultaneous complete lack of bladder neck closure leads to complete RE
Koyanagi[112]	External urethral sphincter relaxation dysfunction (triple parasympathetic-sympathetic-somatic innervation)	Lack of active external urethral sphincter relaxation leads to disruption of antegrade ejaculation
Cao et al[113]

AE: Anejaculation; DE: Delayed ejaculation; DM: Diabetes Mellitus; EL: Ejaculation latency; ED: Erectile dysfunction; PE: Premature ejaculation; SV: Seminal vesicle; VD: Vas deferens.

DIABETES-RELATED EJACULATORY DYSFUNCTIONS

Ejaculatory dysfunctions encompass several disorders related to DM and its complications, such as PE, DE, AE, RE, ejaculatory pain, anesthetic ejaculation, decreased ejaculate volume, and decreased force of ejaculation. Up to 40% of men with diabetes may complain of ejaculatory dysfunction[99]. Of these PE, DE, AE, and RE are the most common and the focus of this discussion[100-113].

PE

There is contradictory evidence concerning the prevalence of PE in diabetics, with one study reporting increased PE prevalence in diabetic men compared to healthy controls (78.8% vs 47.5%, P = 0.001)[92]. On the other hand, a study by the Italian Society of Andrology pointed out to a protecting effect of diabetes on PE (6.2% vs 8.4%, adjusted odds ratio = 0.6, P = 0.001)[114]. This low prevalence was endorsed to delayed emission caused by diabetic sympathetic neuropathy of nerve fibers innervating the organs of emission (VD, SV, prostate). However, with the well-known relation between erectile dysfunction (ED) and PE that recognizes ED as the significant comorbidity of PE[115] and a higher prevalence of ED among diabetics, we could speculate that diabetes might be considered a risk factor for PE. Anyway, most of the studies showed comparable prevalence between diabetic and non-diabetic persons[90,91,95,96]. Theoretically, diabetes-related PE is recognized to have a multi-factorial etiology (Tables 2 and 3). The lack of a significant difference in the prevalence of PE among men with/without diabetes might be attributed to socio-demographic factors, a multiplicity of different tools for measurement of PE such as self-reported PE, PE diagnostic tool (PEDT) score, self-reported, and stopwatch-recorded intravaginal ejaculation latency time (IELT) or to the presumed balance between the protective and detrimental factors inside the diabetes patients. Therefore, the true prevalence of PE in DM has not been firmly established. However, the PE subjects diagnosed with PEDT score or stopwatch IELT showed significant prevalence of diabetes[88,116] suggesting that DM is an important etiologic factor in acquired PE. Studies assessing whether PE in DM can be related to glycometabolic control and associated morbidities have also produced mixed results. While El-Sakka[91] and Malavige et al[93] have demonstrated that elongated duration of diabetes, poor metabolic control, and presence of cardiovascular disease are linked to increased risk of PE in type 2 DM, Other studies have found no such evidence in type 2 DM[92,97]. Additionally, in the subgroup of type 1 DM patients assessed for glucose variability, the PEDT score was associated with low blood glucose indices (r = 0.43; P = 0.01), but not with a standard deviation of blood glucose (r = 0.1, P = 0.6), mean amplitude of glycemic excursions (r = -0.1; P = 0.4), or high blood glucose indices (r = 0.1; P = 0.6) suggesting a link between glycemic excursions and PE[96]. This association between hypoglycemia and PE might be linked to increased adrenergic activity[117] or reduced serotoninergic activity[118]. Moreover, PE is known to be associated with diabetes-related ED as shown in different studies[91-93,97]. Likewise, one study suggests that 95% of Type 2 diabetes patients with PE also reported ED[91] indicating that ED is the principal risk factor of PE in type 2 DM. A vicious cycle probably exists between ED and PE with each condition being deteriorated by the other[93]. However, Culha et al[88] disputed these findings and have shown that simultaneously occurring different etiologic factors may be responsible for the development of DM-related PE. These factors include ED (20.75%), chronic prostatitis (18.87%), depression (16.98%), anxiety (15.09%), FSH–LH abnormality (7.55%), hyperprolactinemia (7.55%), and hyperthyroidism (1.89%). These latter findings still await confirmation.

According to the consensus of the International Society for Sexual Medicine, acquired PE (e.g., diabetes-related PE) is an ejaculation that always or nearly always occurs before or within about 3 min of vaginal penetration or, a significant and bothersome reduction in the latency time, associated with the incapability to delay ejaculation on all/nearly all vaginal penetrations, and negative personal consequences, as; distress, bother, frustration and/or avoidance of sexual intimacy[119]. Evaluation of diabetes-related PE includes a clinical history and careful physical examination focusing on all related symptoms, signs, and risk factors. A list of assessment steps that could be helpful in evaluating DM-related ejaculatory dysfunction is presented (Table 4). The most important dimensions in history taking include assessment of self-estimated IELT, subjective perceived control over ejaculation, existed distress by the condition, and the existence of an interpersonal difficulty owing to PE. Routine laboratory tests or neuro-physiological tests should merely directed by precise findings from either the history taking or physical examination[120].

Table 4 Assessment steps in the evaluation of diabetes mellitus-related ejaculatory dysfunctions.

History
Asking about the period from vaginal intromission to ejaculation (intravaginal ejaculatory latency time).
Is the patient unable to advance his ejaculatory response?
Is the patient or his partner distressed or bothered by the situation?
Is the symptom occurring since the first sexual experience or occurring after a period of normal ejaculatory performance?
Onset and duration of the symptom.
Is the symptom occurring on every/almost every attempt and with every partner?
Presence or absence of premonitory ejaculatory sensation.
The duration of thrusting before the suspension of intercourse.
Reasons for delay of intercourse (e.g., fatigue, loss of erection, a sense of ejaculatory futility, or partner request).
Presence of post-coital self- or partner-assisted masturbation.
Psychogenic anejaculation/anorgasmia can be suspected when there is a history of nocturnal emission.
Patient's ability to get an erection, relax, sustain, and heighten sexual arousal.
Exclude anorgasmia by asking about lack of orgasm.
Whether orgasm is present but there is a lack of external ejaculation that may indicate retrograde ejaculate.
Feeling before ejaculation/orgasm: The inadequate combination of “friction and fantasy” may exacerbate DE.
Intercourse frequency.
Presence of other sexual dysfunctions such as ED (ability to initiate or maintain an erection), low libido.
Other symptoms of hypogonadism (such as lack of energy, depressed mood).
Masturbation habits
The life events/circumstances related to the complaint.
Sexual communication abilities.
Paraphilic inclinations/interests (may be related to DE and anejaculation).
Cultural or religious beliefs (if any).
History of a psychiatric disorder (may be the etiologic factor).
History of previous treatment for this symptom.
History of neurologic disorders, spinal cord injury, medical diseases, trauma, abdominal/pelvic operations, drug intake, or pelvic radiotherapy.
History of pelvic or testicular pain (may indicate inflammation).
History of dysuria, burning micturition, or any urinary symptom (indicate inflammation).
Clinical examination
Signs of diabetic complications and co-morbidities.
Signs of hypogonadism.
Rule out systemic disorders that contribute to ejaculation dysfunction as neurological impairment, endocrine/ urological diseases.
Examination for secondary sexual characteristics, penile and testicular abnormalities.
Examination of the epididymis, and vas deferens on each side.
PR examination to determine the prostate size, anal sphincter tone, and quality of the bulbocavernosus reflex.
The cremasteric reflex: measures intact L1-2 spinal segments, also mediating emission and psychogenic erection.
Perineal reflexes (bulbocavernosus and anal reflex) mediated by sacral segments, also mediating reflex erection (for intact S2–4 pathway).
Examination of pinprick and temperature sensations in the saddle area (perineal) and glans penis for healthy sacral cord segments.
Inability to feel testicular squeeze: measures the integrity of T11 to T12 spinal nerves via the sympathetic nervous system.
Examination of lower abdominal cutaneous reflex: measures intact Th11-12.
Penile biothesiometry.
Investigations
Blood levels of glucose, HbA1c, serum testosterone, thyrotropin, and prolactin to exclude other endocrine disorders.
Post-masturbation first-void urine if we suspect retrograde ejaculation to search for spermatozoa and fructose content to confirm retrograde ejaculate
Microbiological examination of expressed prostatic secretion and urine to verify or exclude associated genital infections.
Urine cytology to exclude bladder cancer
Serum prostate-specific antigen to exclude prostate cancer
Neurophysiologic investigations (bulbocavernosus evoked response and dorsal nerve somatosensory evoked-potentials): If there is clinical evidence of neurologic lesions. These tests are little used in clinical practice and usually do not affect management.
Trans-rectal ultrasound examination if we suspect ejaculatory duct obstruction, prostatic or seminal vesicle abnormalities or stones.
CT or MRI scans to assess pelvic anatomy if we suspect major pelvic lesions.

CT: Computed tomography; MRI: Magnetic resonance imaging.

In principle, scarce data are assessing the treatment of DM-related PE. Additionally, one should know that DM-related PE may be a heterogeneous group of patients. Hence, it is important to diagnose any associated comorbidity such as ED, depression, prostatitis, or hyperthyroidism as they should be treated first or at the same time as PE[120]. Therefore, the treatment may involve numerous interventions as per the kind of mechanism that would cause such condition: (1) The initial management for PE is controlling the patient’s blood glucose that in some cases may allow recover the normal ejaculatory function[91,93]; (2) Amelioration of glycemic variability would improve PE in type 1 diabetes patients[96]; (3) In cases of concomitant ED and PE, ED should receive phosphodiesterase type 5 inhibitors before, or at least at the same time as, PE[91,93,94]. The efficacy of the combined use of phosphodiesterase type 5 inhibitors and dapoxetine in males with comorbid PE and ED are supported by some studies[121-123]; (4) DM-related PE patients had a worse response to 30-60 mg oral dapoxetine treatment compared to non-diabetic PE patients. Poor treatment outcomes in diabetes patients may be attributed to DM-associated complications[123]; and (5) Various behavioral techniques (such as ‘squeeze’ technique or ‘stop-start’ program) may be beneficial in those associated with psychological factors or those patients uncomfortable with pharmacological therapy. However, the long-term success of these maneuvers is limited[120].

DE and AE

DE (also termed retarded ejaculation, inhibited ejaculation (IE), inadequate ejaculation, male orgasmic disorder, or primary impotentia ejaculationis,) was used to describe “a marked delay in or inability to achieve ejaculation”[124]. Current diagnostic criteria from the Diagnostic and Statistical Manual of Mental Disorders, 5^th edition, defines DE as either a marked delay in or a marked infrequency or absence of ejaculation on 75% to 100% of occasions for at least 6 mo of partnered sexual activity without the individual desiring delay and causing significant distress to the individual[125]. Therefore, the terminology DE aimed to describe all ejaculatory disorders that lead to a delay or absence of ejaculation (AE)[1]. Furthermore, the severity of DE was classified according to Kaplan criteria into mild and moderate forms and the most severe ones (AE or severe DE)[126]. For these reasons, both DE and AE will be discussed together in this section.

Overall, DE is the rarest and the least understood male sexual dysfunction. Its incidence in the general population rarely exceeds 3%[127,128]. There have been few attempts to study the prevalence of DE and AE in DM. While one study showed 0% prevalence among a series of 54 diabetes patients[129], another research demonstrated self-reported absent ejaculation and DE in 7.2 % and 0.36 % respectively among a total series of 276 diabetes patients[130]. However, sporadic cases were reported in literature either in the context of fertility evaluation[110,131] or as a sexual complaint[132]. It is thought that several pathophysiological factors may contribute to the development of DE and AE such as depression, progressive autonomic neuropathy, calcification of VD and SV, hypogonadism, or low sexual desire (Table 3).

Unfortunately, careful history is still the key there is no test to diagnose DE/AE[133]. It starts by excluding RE, genital tract obstruction, anorgasmia, and other sexual dysfunctions that may be misdiagnosed as DE/AE, such as ED, a subtly decreased libido, ejaculatory pain, the partner’s sexual dysfunction, sexual orientation conflicts, or paraphilic inclinations/interests (Table 4). A focused psychosexual evaluation is critical and typically begins by differentiating whether the complaint concerns DE/AE, the sensation of orgasm, or both. Attention should be given to identifying reversible factors such as poor glycemic control, hypogonadism low sexual desire, psychological factors, and genital infections. A focused clinical examination, laboratory tests, as well as radiologic imaging may help to diagnose these risk factors (Table 4). Sometimes the diagnosis of those risk factor(s) unfolds over time many clinical visits[134].

In this context, defining solid approaches for the treatment of DM-related DE/AE is difficult for a condition that the literature is restricted to case reports, case series, or small studies. It is assumed that intensive glycemic control may reduce the prevalence of diabetic autonomic dysfunction and might slow the deterioration of DM-related DE/AE; unfortunately, no article studying this effect has been published. If organic and iatrogenic reasons have been let off in DM-related DE/AE behavioral therapy may be considered[1]. Several drugs are recognized for the possible use in DE/AE. Those agents include; testosterone, amantadine, cyproheptadine, cabergoline, bupropion, yohimbine, buspirone, bethanechol, and others. Yet, no drug was approved for this indication[125]. Testosterone replacement therapy may be an appropriate option for DM-related DE/AE with decreased testosterone levels. However, in a clinical trial, in which diabetes is not an exclusion criterion, Paduch et al[82] reported that treatment of testosterone-deficient DE patients with a 2% solution of testosterone is not linked to improved perceived delay of ejaculation suggesting that testosterone deficiency is not the sole contributor to DE. Mechanistically, diabetic autonomic neuropathy is an important factor in the development of DM-related DE/AE that may affect neural systems at all levels of emission and ejection. Once diabetic autonomic neuropathy becomes clinically evident, there is no treatment to reverse it[135]. In the most severe cases, there may be a total lack of seminal emission leading to male infertility. If infertility is an issue, several approaches can be employed: (1) Assisted ejaculation by penile vibratory stimulation (PVS) is an option for sperm retrieval[136] because it is noninvasive and inexpensive[137]. However, DM patients frequently fail to obtain sperms by this method because it requires intact lumbosacral pathways[136,137]; (2) In cases in whom PVS fails, electroejaculation (EEJ) may be effective to retrieve spermatozoa[99,138]; and (3) If these procedures fail, surgical sperm retrieval can be tried through VD aspiration[139], percutaneous epididymal sperm aspiration (PESA)[140], or testicular sperm extraction (TESA)[141]. Using spermatozoa obtained by any of these procedures and utilizing intracytoplasmic sperm injection (ICSI), one can attain clinical pregnancy and live birth rates in DM-related AE. However, the fertilization rate and high-quality embryo rate in diabetic PE patients are lower than in non-diabetic PE patients[140].

RE

RE is unique in that it is almost exclusively organic in origin. Despite being a common type of ejaculatory dysfunction, it is responsible for only 0.3%–2% of infertility[142,143]. Specifically, young men with type 1 diabetes have a higher incidence of ejaculatory dysfunction estimated to be 5%-18% of cases due to diabetic neuropathy, which has been shown to cause male infertility[29,144,145].

RE is an ejaculation that is deposited into the posterior urethra but propelled backward into the urinary bladder. In the normal state, the bladder neck closes with high pressure under the sympathetic control during orgasm and the seminal bolus takes the route of least resistance, being antegrade. Diabetic neuropathy can interfere with the sympathetic fibers that provide for normal high-pressure bladder neck closure, causing a comparatively low-pressure route into the urinary bladder for semen[146].

Impairment of sympathetic innervation of the urinary bladder neck was supposed to be a cause of diabetic RE. Ibragimov et al[147] used the liquid profilometric technique to examine 3 groups of men: 8 patients with RE; 5 patients with DM without ejaculatory disorders; and 7 healthy subjects. Diabetic RE patients showed no elevation of the intraureteral pressure in the area of the inner sphincter of the urinary bladder, which evidenced its atony. In health the elevation of vesical pressure is usually accompanied by increased ureteral resistance, thus maintaining the stability of the positive pressure gradient and preventing the escape of urine. Correlation analysis revealed alterations of the interrelations between both intravesical and sphincter pressures in diabetes patients evidencing the disorders of somatic innervation of the outer ureteral sphincter being more pronounced in these patients.

DIAGNOSIS

RE can be partial or complete and the diagnosis is frequently suggested by the patient’s report of cloudy urine following orgasm confirmed by a post-ejaculatory urine analysis that reveals sperm, seminal fluid, or fructose[148]. McMahon[149] endorsed that the post-orgasmic urine should be centrifuged and visualizing of 10-15 sperm/high-power field could confirm RE diagnosis whereas Fedder et al[150] defined RE as > 1 million sperms in a post-ejaculatory urine sample.

TREATMENT STRATEGIES

Infertility is usually the main concern in RE patients as the combination of dry orgasm and infertility makes the condition upsetting to the patient and his partner[151]. Therefore, many lines of therapeutic approaches were advocated, either medical or surgical, with limited success rates.

Medical treatment

It is based either on increasing the sympathetic tone of the urinary bladder or on decreasing the parasympathetic activity but the onset of side effects and the lack of response should be considered. Several treatments were proposed with varied results[152-161] (Table 5).

Table 5 Studies involving medical treatment for reversal of diabetic retrograde ejaculation.

Ref.	Dosage	Ejaculation after	n	No. of successes	Ejaculate volume (ml)	Sperm count (106/m)	Sperm motility (%)
Brompheniramine
Andaloro et al[152]	16 mg/d p.o.	12 h	1	1	Unclear	Unclear	Unclear
Budd[153]	16 mg/d p.o.	3 d	1	1	Unclear	Unclear	Unclear
Chlorpheniramine + phenylpropanalamine
Stewart et al[154]	50 mg/d p.o.	Unclear	1	1	4.5	Normal	Normal
Ephedrine
Gilja et al[155]	50 mg/d p.o.	4 wk	17	3	Unclear	Unclear	Unclear
Arafa et al[156]	120 mg twice/d	14 d	23	11	Unclear	Unclear	Unclear
Shoshany et al[157]	60 mg/6 h the day before test + 2 doses on test day	At the test	6	4	1.5	Unclear	17.8
Imipramine
Brooks et al[158]	75 mg/d p.o.	1 wk	2	2	3	1.72	33
Okada et al[159]	25-150 mg/d	Unclear	7	3	Unclear	Unclear	Unclear
Gilja et al[155]	75 mg/d p.o.	4 wk	14	2	Unclear	Unclear	Unclear
Eppel et al[160]	50 mg/d p.o.	5 d	3	3	8	20	50
Arafa et al[156]	50 mg/d p.o	14 d	23	10	Unclear	Unclear	Unclear
Imramine + pseudoepherine
Arafa et al[156]	50 + 120 mg/d	14 d	23	16	Unclear	Unclear	Unclear
Amoxapine
Hibi et al[161]	50 mg/d	1 mo	1	1	0.2	213	53

Endourethral collagen injection

Kurbatov et al[145] analyzed the long-term outcome of endourethral injection of volume-forming material (VFM) of collagen type 2 into the bladder neck submucosa in 23 patients with RE secondary to type 1 DM with complete RE refractory to imipramine. These patients were randomized with a 1: 1 ratio into 2 groups; group A (endourethral collage type 2 injection) and group B (endourethral saline water injection). This technique included an endoscopic injection of VFM such as collagen into bladder neck submucosa. In group A, significant differences from baseline to 12 mo were detected relative to antegrade volume (mean difference: 0.71 mL), antegrade count (mean difference: 45.6 million/mL), antegrade total sperm motility (mean difference: 15.4%), and antegrade progressive sperm motility (mean difference: 8.4%). It was concluded that correcting RE in type 1 DM patients could be accomplished with the endourethral injection of collagen type 2.

SPERM RETRIEVAL

Beyond using standard sperm retrieval techniques such as; TESE and PESA, 3 methods of sperm retrieval were recognized for managing infertility in RE patients. These techniques include; centrifugation and resuspension of post-ejaculatory urine specimens, the Hotchkiss (or modified Hotchkiss) technique, as well as ejaculation on a full urinary bladder.

Centrifugation and resuspension: To improve the conditions for the sperm, the patient is asked to either increase their fluid intake or to take sodium bicarbonate to dilute or alkalize the urine. A post-orgasmic urine sample is collected by either introducing a catheter or spontaneous voiding. This sample is centrifuged and suspended in a medium such as bovine serum albumin, human serum albumin, Earle’s/Hank’s, phosphate-buffered medium. The resultant modified sperm mixture can be used in assisted reproductive techniques (ART) (Table 6)[162-165]. In their meta-analysis in couples with the male partner with RE, Jefferys et al[142] reported a 15% pregnancy rate/cycle (0%–100%) after using the centrifugation and resuspension method.

Table 6 Semen parameters of studies recovering sperms from alkalized urine in diabetic premature ejaculation patients.

Ref.	Medium installed	Post-masturbatory retrieval	No. of patients	Total sperm count (106)	Total sperm motility (%)	Pregnancies
Brassesco et al[163]	NaHCO3 4 g	Voiding	3	91	28	3
Templeton et al[162]	NaHCO3	Voiding	1	Unclear	2–21	0
Shangold et al[164]	NaHCO3 1.6 g	Voiding	1	30–240	0	5

Hotchkiss method: It involves emptying the urinary bladder before ejaculation by a catheter, washing out and instilling a small quantity of lactated Ringers to improve the ambient conditions of the bladder. The patient then ejaculates and the semen is retrieved by catheterization or voiding[166].

Modified Hotchkiss method: It involves a variance in the instillation medium. Pregnancy rates were 24%/cycle (0%–100%)[142]. Philippon et al[167] reported the largest series of births using frozen-thawed sperms retrieved from post-ejaculatory urine by a this technique that allows for successful association with sperm cryopreservation, leading to efficient management of couples with refractory RE with an average live birth rate/transfer of 28%.

Ejaculation on a full bladder: The patient is encouraged to ejaculate on a full urinary bladder and semen is suspended in Baker’s buffer[162].

EEJ

EEJ has been used to a restricted degree in diabetic men who have developed ejaculatory failure as a consequence of diabetic neuropathy. Gerig et al[131] described the experience of 2 male fertility programs using EEJ in managing men with ejaculatory failure secondary to DM. Overall, 29 EEJ procedures were performed in seven diabetic men with ejaculatory failure. Following EEJ, retrograde semen specimens retrieved from the urinary bladder contained a mean of 3444.5 million sperm (range 269.2-4996 million), mean sperm motility was 4% (range 0%-11%). Semen specimens were used for intrauterine insemination. It was concluded that EEJ can be successfully used to retrieve sperms from men with ejaculatory failure due to DM. That procedure requires general anesthesia, and the pregnancy rates after intrauterine insemination with the processed sperm were low. Therefore, AET could offer a practicable alternate, yielding higher success rates.

ICSI

ICSI-ART can greatly reduce the impact of sperm factors of infertility[167]. In cases of diabetic RE, TESA is combined with ICSI to treat infertility. Liu et al[168] assessed the effect of TESA-ICSI on first cycle ICSI-embryo transfer for type 2 diabetic patients in 1219 azoospermic patients or RE who were treated with TESA-ICSI classified into 2 groups; type 2 DM group (n = 54) and non-diabetic controls (n = 1165). There were no significant differences in clinical pregnancy, implantation, normal fertilization, or cleavage rates between these groups.

CONCLUSION

Ejaculatory dysfunction encompasses several disorders related to DM and its complications, such as PE, DE, AE, RE, ejaculatory pain, anesthetic ejaculation, decreased ejaculate volume, and decreased force of ejaculation. All these disorders should be looked for thoroughly during the clinical evaluation of diabetic men. Besides, introducing the suitable option and/or maneuvers to treat these disorders should be tailored according to each case.