| P.O.Box 2345, Beijing 100023,China | World J Gastroenterol 2003 Mar 15;9(3):615-618 |
| Email: wjg@wjgnet.com | WJG ISSN 1007-9327 CN 14-1219/ R |
| http:// www.wjgnet.com | Copyright © 2003 by The WJG Press |
Crohn's
disease and risk of fracture: does thyroid disease play a role?Nakechand Pooran, Pankaj Singh, Simmy Bank
Nakechand Pooran, Pankaj Singh,
Simmy Bank, Division of Gastroenterology
Albert Einstein College of Medicine - Long Island Jewish Medical Center, New
Hyde Park, New York, USA
Correspondence to: Simmy
Bank, M.D., FRCP, Division of Gastroenterology, Long Island Jewish Medical
Center, New Hyde Park, NY 11040, USA. simmybank@lij.edu
Telephone: +1-718-4704692
Fax: +1-718-3430128
Received:
2002-10-05 Accepted: 2002-11-04
Abstract
AIM: To assess the role of thyroid
disease as a risk for fractures in Crohn's patients.
METHODS: A
cross-sectional study was conducted from 1998 to 2000. The study group consisted
of 210 patients with Crohn抯 disease.
A group of 206 patients without inflammatory bowel disease served as controls.
Primary outcome was thyroid disorder. Secondary outcomes included use of
steroids, immunosuppressive medications, surgery and incidence of fracture.
RESULTS: The
prevalence of hyperthyroidism was similar in both groups. However, the
prevalence of hypothyroidism was lower in Crohn's patients
(3.8 % vs 8.2 %, P=0.05). Within the Crohn's
group, the use of immunosuppressive agents
(0 % vs 11 %), steroid usage (12.5 % vs 37 %), small bowel surgery
(12.5 % vs 28 %) and large bowel surgery (12.5 % vs 27 %) were
lower in the hypothyroid subset as compared to the euthyroid subset. Seven (3.4
%) Crohn's patients
suffered fracture, all of whom were euthyroid.
CONCLUSION: Thyroid
disorder was not found to be associated with Crohn's disease
and was not found to increase the risk for fractures. Therefore, screening for
thyroid disease is not a necessary component in the management of Crohn's
disease.
Pooran N, Singh P, Bank S. Crohn's disease
and risk of fracture: does thyroid disease play a role? World J Gastroenterol
2003; 9(3): 615-618
http://www.wjgnet.com/1007-9327/9/615.htm
INTRODUCTION
Recent studies have shown that patients
with Crohn's disease
have decreased bone density[1,2] that predisposes to an increased
risk of fracture[3,4]. A chronic inflammatory state with the release
of inflammatory cytokines, steroid usage and malnutrition is the proposed
mechanism. The co-existence of other medical conditions, which are independently
associated with osteoporosis, will further increase the risk of fracture in
patients with Crohn's disease.
Thyroid disorder is associated with changes in bone metabolism and is an
important cause of osteoporosis[5-7]. Thyroid disorder has also been
reported in patients with underlying inflammatory bowel disease (IBD)[8-12].
One study showed altered thyroid physiology and anatomy in patients with IBD[9]
and suggests that it may be important to investigate the association between
thyroid disorders and Crohn's
disease. If patients with Crohn's
disease have a higher prevalence of thyroid
disease, then screening and treatment of the thyroid disease may reduce the risk
of fractures in the Crohn's
disease population. Secondly, it has been
reported that the presence of hyperthyroidism makes the treatment of
inflammatory bowel disease more difficult[10,13] and, therefore,
correcting the thyroid disorder may have an impact on treatment response.
We compared the
prevalence of hypothyroidism and hyperthyroidism in patients with Crohn's
disease and those without Crohn's
disease. To investigate whether co-existing thyroid
dysfunction has an impact on the treatment of Crohn's
disease, we compared the use of immunosuppressive
medications and surgical procedures for the underlying Crohn's
disease in patients with and without co-existing thyroid
dysfunction.
MATERIALS AND METHODS
Study design and subjects
A retrospective
cross-sectional study was conducted at this hospital from 1998 to 2000. The
study group included 210 patients with Crohn's
disease admitted to the hospital or referred to the
endoscopy suite for endoscopic procedures. A control group comprised of 206
consecutive patients who did not have inflammatory bowel disease and who were
referred for either screening colonoscopy or esophagogastroduodenoscopy (EGD).
Data collection
Medical records of patients
were reviewed to extract information regarding their baseline demographic
information, diagnosis and extent of Crohn's
disease, presence of thyroid disease and use of either
steroid or immunosuppressive agents. The diagnosis of Crohn's
disease was made either endoscopically or radiographically.
A history of other medical diagnoses (e.g. rheumatoid arthritis, chronic
obstructive pulmonary disease) where the potential use of steroids or
immunosuppressive agents may be a confounding factor was also recorded. Sample
size was calculated based on a reference value of 1 % of thyroid dysfunction in
the general population. To detect the difference of 5 % between the two groups
with power of 0.8 and a two sided alpha error of 0.05, more than 200 patients
were required in both the groups.
Outcome
The primary outcome was the
presence of hypothyroidism or hyperthyroidism. Secondary outcomes included the
use of immunosuppressive medications and surgery for the Crohn's
disease. Thyroid disorder was considered present if the
patient had a prior diagnosis of thyroid disorder and was taking thyroid
medication (thyroxine, propylthiouracil, methimazole) or had an abnormal thyroid
stimulating hormone (TSH) level.
Statistical analysis
Descriptive statistics were
reported as proportions, means ?standard deviation or median and range.
Comparison between groups was done using the Pearson chi-square test for
categorical variable (or the Fisher exact test if appropriate) and two-sided
student t-test for continuous variables (SPSS for Windows, release 10.0,
Chicago, IL). P<0.05 was considered significant.
RESULTS
Demographic and clinical characteristics
There were 210 patients with Crohn's
disease and 206 controls. The two groups
were matched for age (49.24 yr. vs 48.58 yr., P=0.68), sex (88
males/122 females vs 91 males/133 females, P=0.29), and race (153
whites/1 black/34 others vs 118 whites/14 blacks/36 others, P=0.34).
The groups differed in body mass index (24.35 kg/m2 vs 27.46
kg/m2, P=0.001). (Table 1).
Table 1 Comparison
of baseline characteristics and thyroid status in patients with Crohn's
disease and control group
| Case (n=210) | Control (n=206) | P | |
| Age (years) | 49.24?3.71 | 48.58?8.43 | 0.68 |
| Sex (M/F) | 88/122 | 91/113 | 0.29 |
| Body Mass Index (kg/cm2) | 24.35 | 27.46 | 0.001 |
| Race (white/black/others) | 153/1/34 | 118/14/36 | 0.34 |
| Steroid use | 75 (35.7%) | None | _ |
| Immunosuppressive therapy | 22 (10.4%) | None | _ |
| Hypothyroidism | 8 (3.8%) | 17 (8.2%) | 0.05 |
| Hyperthyroidism | 2 (0.01%) | None | 0.25 |
Primary outcome - thyroid
dysfunction
In the Crohn's
group there were 8 (3.8 %) cases of hypothyroidism and 2
(0.01 %) cases of hyperthyroidism. The control population had 17 (8.2 %) cases
of hypothyroidism and 0 (0 %) case of hyperthyroidism. The difference in
hypothyroidism showed borderline significance (P=0.05) while
hyperthyroidism was not significant (P=0.25) (Figure 1).
Figure
1 (PDF) Bar graph showing the
prevalence of thyroid disorder in patients with Crohn's disease
and in the control group.
Secondary outcome - use of
immunosuppressives and surgery
Patients with Crohn's
disease were divided into those with hypothyroidism and
those without any thyroid disorder. There was clinically higher use of
immunosuppressive agents (0 % vs 11 %, P=0.59), steroid usage
(12.5 % vs 37 %, P=0.15), small bowel surgery (12.5 % vs 28
%, P=0.34) and large bowel surgery (12.5 % vs 27 %, P=0.38)
in Crohn's patients
with hypothyroidism in comparison to those who were euthyroid. This difference
however, was not statistically significant. (Table 2, Figure 2).
Table 2 Comparison of medical and surgical treatment in patients with hypothyroidism and euthyroidism in Crohn's disease
| Hypothyroidism(n=8) | Euthyroid(n=201) | P | |
| Immunosuppresive medications | None | 22 (11%) | 0.59 |
| Steroid use | 1 (12.5%) | 74 (37%) | 0.15 |
| Small bowel surgery | 1 (12.5%) | 56 (28%) | 0.34 |
| Large bowel surgery | 1 (12.5%) | 54 (27%) | 0.38 |
Figure
2 (PDF) Bar
graph showing the usage of steroids, immunosuppressive agents, small bowel
surgery, large bowel surgery and fractures in Crohn's patients
with thyroid disorder and those without thyroid disorder.
DISCUSSION
Crohn's disease
is a chronic illness that is associated with a lower bone mineral density and a
higher incidence of fracture[1-4]. This results in increased
morbidity and mortality. Thyroid disorder may potentiate the risk of fracture.
The purpose of this study was to investigate whether thyroid disorder
contributed to this adverse event and if present, whether thyroid disorder has
an impact on the management of Crohn's
disease. We did not find a higher prevalence
of thyroid disease in our Crohn's
population when compared to a control group.
In fact, the prevalence of hypothyroidism was less in the Crohn's
group. Sub-group analysis of the Crohn's
group showed that there was lower usage of
steroids, immunosuppressive medications and surgery in those who were also
hypothyroid when compared to those who were euthyroid. There were 7 (3.4 %)
fractures in the Crohn's
population. All of the fractures occurred in
those who were euthyroid.
The prophylactic use of a
bisphosphonate has been shown to increase the bone mineral density in patients
with Crohn's disease[14].
However, the beneficial effect in lowering the incidence of fracture has not
been reported. Due to the lack of an effective prophylactic medication, it
becomes important to identify and treat any other co-existing illness that can
enhance bone loss and increase the risk of fracture. One common disease that is
linked to Crohn's and
has an impact on bone metabolism is thyroid disease[8-12].
In our study, we did not find a
difference in the prevalence of thyroid disease between patients with Crohn's
disease and our controls. These findings are
consistent with two prior studies[8,12]. Snook et al[8]
found a higher prevalence of thyroid disorder in patient with ulcerative
colitis, but not Crohn's
disease, when comparing patients with IBD to
the general population. Hammer et al[12] also found a higher
prevalence of thyroid disorder in the ulcerative colitis subset of their IBD
population when compared to the general population. The lack of association of
clinical thyroid disorder and Crohn's
disease is contradicted by the objective
findings of Jenerot et al[9]. They showed that patients with
IBD had a 35 % higher thyroid volume and were three times more likely to have an
enlarged thyroid. Their finding of thyroid enlargement may be secondary to
iodine deficiency, which has been reported in Crohn's
disease and is unrelated to functional
derangement of the thyroid[15]. When we subdivided our thyroid
disorder into hyperthyroid and hypothyroid, we did not find a difference in the
prevalence of hyperthyroid between those with Crohn's
disease and controls. Surprisingly, we found
a lower prevalence of hypothyroidism in the Crohn's
group as compared to controls.
Finding no difference in the
prevalence of hyperthyroidism between patients with Crohn's
disease and controls has clinical
significance. Hyperthyroidism is associated with accelerated bone turnover and
shortening of the normal bone remodeling cycle[6,7]. This results in
increased bone metabolism and osteoporosis. Since patients with Crohn's
disease do not have a higher prevalence of
hyperthyroidism, an elevation of thyroxine levels cannot be the basis for the
increased osteoporosis seen in this group of patients. Factors such as chronic
inflammation, prolonged steroid usage and malnutrition are the more likely
etiological agents for osteoporosis[16]. Thus, evaluating patients
with Crohn's disease
for hyperthyroidism should be done on clinical grounds and not as a screening
procedure.
Our finding of a lower
prevalence of hypothyroidism in our Crohn's population
as compared to our controls is similar to those of Hammer et al[12].
It is possible that since both Crohn's
disease and thyroid disorder have a possible
autoimmune etiology, treating Crohn's
disease with corticosteroids and immune
modulating agents may prevent the manifestation of an autoimmune thyroid
disorder. The difference in prevalence of hypothyroidism may also be the result
of a higher than expected prevalence of hypothyroidism in our control group. The
prevalence of hypothyroidism in population based studies varies from 0.5 % to 5
%[17-19], however, we had an 8 % prevalence of hypothyroidism in our
controls. This higher prevalence of hypothyroidism may be explained by the
availability of third generation assays for thyroid stimulating hormone (TSH)
and increased frequency of screening for thyroid disorder, leading to detection
of sub-clinical disease. There is also the possibility of a selection bias in
the control group. The controls included people who underwent screening
colonoscopy. Those persons are more likely to be health conscious and,
therefore, are more likely to visit a physician; thus, this would result in
increased screening for thyroid disease as compared to the general population.
In addition, the control group had a higher body mass index (BMI) as compared to
the Crohn's group.
BMI can act as a confounding factor as it is related to both hypothyroidism and
reflux symptoms. Hypothyroidism is associated with weight gain1[8,19].
Patients who have a higher BMI are more likely to have reflux symptoms[20,21]
and thus, are more likely to undergo EGD than the general population. Since our
controls included patients having EGD, it is possible that our controls
contained a higher percentage of people who are hypothyroid. This may be a
theoretical concern as a recent, well design; prospective study[22]
did not show an association between obesity and reflux symptoms.
There are concerns that the
presence of thyroid disease may have an impact on the management of IBD.
Moreover, there are case reports that suggest that thyroid disease needs to be
treated in order to successfully treat IBD[10,13]. We subdivided our
Crohn's disease
population into those who are euthyroid and those who had thyroid disease. The
two groups were compared with regard to steroid usage, use of immune modulating
agents, surgery for the management of Crohn's
and rate of fracture. There was a higher
rate of steroid usage, use of immune modulating agents, and both small and large
bowel surgeries in patients who were euthyroid. For instance, there were seven
fractures in the Crohn's
group, all of which occurred in patients who
were euthyroid. The differences, though clinically significant, were not
statistically significant. This is probably due to a small sample size. A larger
prospective, controlled study is needed to evaluate this issue. Hypothyroidism
is known to decrease metabolism and slow physiological functions. The presence
of hypothyroidism may act as endogenous disease modification in patients with
Crohn's disease.
Our study was limited by
retrospective data collection. This makes it difficult to evaluate and compare
disease severity index and extent of disease between Crohn's
disease patients who are euthyorid and those
who had a thyroid disorder present. It also makes it difficult to establish a
temporal relationship between thyroid disease and Crohn's
disease. Our results are based on the
assumption that patients who were characterized as euthyroid are actually
euthyroid. Symptoms may not suggest thyroid disease when it is mild and are
often atypical in the elderly[23-25]. Thus, it is possible that we
missed patients with subclinical thyroid disease.
In conclusion, patients
with Crohn's disease
do not have a higher prevalence of thyroid disease than the general population
and, therefore, routine screening for thyroid disease is not a necessary
component in the management of Crohn's
disease. However, it is apparent that thyroid disease has a
significant clinical impact on the course of Crohn's
disease, which needs to be studied in a prospective manner.
ACKNOWLEDGEMENT
The authors thank S.D. Rampertab,
M.D. for her critical comments on the manuscript.
REFERENCES
1
Silvennoinen JA, Karttunen TJ, Niemela SE, Manelius JJ, Lehtola JK. A
controlled study of bone mineral density in patients
with inflammatory bowel disease. Gut 1995; 37:
71-76
2
Andreassen H, Rungby J, Dahlerup JF, Mosekilde L. Inflammatory bowel
disease and osteoporosis. Scand J
Gastroenterol 1997; 32: 1247-1255
3
Vestergaard P, Krogh K, Rejnmark L, Laurberg S, Mosekilde L. Fracture
risk is increased in Crohn's disease, but
not
in ulcerative colitis. Gut 2000; 46:
176-181
4
Bernstein CN, Blanchard JF, Leslie W, Wajda A, Yu BN. The incidence of
fracture among patients with inflammatory
bowel disease. A population-based cohort study.
Ann Int Med 2000; 133: 759-799
5
Greenspan SL, Greenspan FS. The effect of thyroid hormone on skeletal
integrity. Ann Int Med 1999; 130: 750-758
6
Mosekilde L, Eriksen EF, Charles P. Effects of thyroid hormone on bone
and mineral metabolism. Endo Metabol Clin
NA 1990; 19: 35-63
7
Ross DS. Hyperthyroidism, thyroid hormone therapy, and bone. Thyroid
1994; 4: 319-326
8
Snook JA, de Silva HJ, Jewell DP. The association of autoimmune disorders
with inflammatory bowel disease. Q J
Med 1989; 72: 835-840
9
Jarnerot G, Kagedal B, von Schenck A, Trulove SC. The thyroid in
ulcerative colitis and Crohn's disease. V.
Triiodothyronine. Effect of corticosteroids and
influence of severe disease. .Acta Med Scand 1976; 199: 229-232
10
Bonapace ES, Srinivasan R. Simultaneous occurrence of inflammatory bowel
disease and thyroid disease. Am J
Gastroenterol 2001; 96: 1925-1926
11 Bianchi GP, Marchesini G, Gurli C, Zoli M. Thyroid involvement
in patients with active inflammatory bowel diseases. Ital
J Gastroenterol 1995; 27: 291-295
12 Hammer B, Ashurst P, Naish J. Diseases associated with
ulcerative colitis and Crohn抯 disease. Gut
1968; 9: 17-21
13 Modebe O. Autoimmune thyroid disease with ulcerative colitis.
Post Med J 1986; 62: 475-476
14 Haderslev KV, Tjellesen L, Sorensen HA, Staun M. Alendronate
increases lumbar spine bone mineral density in patients
with Crohn's disease.
Gastroenterol 2000; 119: 866-869
15 Janerot G. The thyroid in ulcerative colitis and Crohn's disease
I. Thyroid radioiodide uptake and urinary iodine excretion.
Acta Med Scand 1975; 197: 95
16 Andreassen H, Rungby J, Dahlerup JF, Mosekilde L. Inflammatory
bowel disease and osteoporosis. Scand J
Gastroenterol 1997; 32: 1247-1255
17 Sawin CT, Castelli WP, Hershman JM, McNamara P, Bacharach P. The
aging thyroid. Thyroid deficiency in the
framingham study. Arch Int Med 1985; 145:
1386-1388
18 Dale J, Daykin J, Holder R, Sheppard MC, Franklyn JA. Weight
gain following treatment of hyperthyroidism. Clin
Endo 2001; 55: 233-239
19 Pinkney JH, Goodrick SJ, Katz J, Johnson AB, Mohamed-Ali V,
Coppack SW. Leptin and the pituitary-thyroid axis: a
comparative study in obese, hypothyroid and
hhyperthyroid subjects. Clin Endo 1998; 49: 572-583
20 Wajed SA, Streets CG, Bremner CG, DeMeester TR. Elevated body
mass disrupts the barrier to gastroesophageal Reflux.
Arch Surg 2001; 136: 1014-1018
21 Wilson LJ, Ma W, Hirschowitz BI. Association of obesity with
hiatal hernia and esophagitis. Am J
Gastroenterol 1999; 94: 2840-2844
22 Langergren J, Bergstrom R, Nyren O. No relation between body
mass and gastro-oesophageal reflux symptoms in a
swedish population based study. Gut 2000; 47:
26-29
23 Evered DC, Ormston BJ, Smith PA, Hall R, Bird T. Grades of
hypothyroidism. Brit Med J 1973; 1: 657-662
24 Wenzel KW, Meinhold H, Raffenberg M, Adlkofer F, Schleusener H.
Classification of hypothyroidism in evaluating patients
after radioiodine therapy by serum cholesterol,
T3-uptake, total T4. Eur J Clin Invest 1974; 4: 141-148
25 Bahemuka M, Hodkinson HM. Screening for hypothyroidism in
elderly patients. Brit Med J 1975; 2: 601-603
Edited by Xu XQ