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Issue Info: 
  • Year: 

    2004
  • Volume: 

    6
  • Issue: 

    13
  • Pages: 

    94-100
Measures: 
  • Citations: 

    1
  • Views: 

    1246
  • Downloads: 

    0
Abstract: 

Background&Objective: Studies about the prevalence of celiac disease (CD) in West-Asian countries are scarce and there is only one study on the prevalence of CD in healthy blood dOl}ors in Iran. The aim of this study is to determine the prevalence of CD in general population of the city of Sari in north of Iran. Materials&Methods: This was a descriptive study and the blood samples were obtained from 1438 person from general population (686 males, 752 females: mean age 35.5 range 18-66 year) of the Sari which were selected by stratified randomized sampling method during 2003. Total serum IgA was measured in all and IgA-deficient cases were excluded. From this study 1111 cases were analysed for IgA TISSUE TRANSGLUTAMINASE ANTIBODY (human tecombinant tTG). All persons who had a positive serology for tTG-Ab underwent small intestinal biopsy. The biopsy samples were classified according to modified Marsh criteria. Results: All of the samples had normal total IgA. Thirteen cases showed positive IgAtTG Ab (6 males and 7 females~ mean age 37.5 yrs). All subjects with positive serology except one of them were found to have small bowel biopsies compatible with gluten sensitive enteropathy. One of 13 had Marsh 0, 8/13 Marsh I, 3/13 Marsh II and 1/13 showed Marsh IIIa lesion. Conclusion: The minimum prevalence of gluten-sensitivity among general population in north of Iran is 1/120. This data confirms our study on healthy blood donors, which has published previously and is like of prevalence of celiac disease in western countries. So celiac disease is not a rare disease as it thought before in this area.

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Issue Info: 
  • Year: 

    2015
  • Volume: 

    13
Measures: 
  • Views: 

    144
  • Downloads: 

    56
Abstract: 

CELIAC DISEASE (CD) IS CHARACTERIZED BY A LIFE-LONG INTOLERANCE TO GLUTEN FROM BARELY OR RYE. THE CLASSICAL PRESENTATION OF CD INCLUDES GASTROIONTESTINAL SYMPTOMS AND AN INCREASED RISK FOR DEVELOPING OSTEOPOROSIS AND INTESTINAL LYMPHOMA ABOUT HALF OF THE CD PATIENTS DON’T SHOW THE TYPICAL GASTROINTESTINAL SYMPTOMS, SO THE PREVALENCE OF CD HAS BEEN UNDERESTIMATED FOR A LONG TIME...

Yearly Impact:   مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Issue Info: 
  • Year: 

    2014
  • Volume: 

    6
  • Issue: 

    3
  • Pages: 

    131-136
Measures: 
  • Citations: 

    0
  • Views: 

    420
  • Downloads: 

    250
Abstract: 

BACKGROUND: Recent guidelines have proposed that there is a correlation between TISSUE TRANSGLUTAMINASE (tTG) ANTIBODY titers and degrees of duodenal biopsy, and that duodenal biopsy can be omitted in some patients with high levels of tTG ANTIBODY. Using data of registered patients in a gastrointestinal clinic we aimed to assess the correlation between TISSUE TRANSGLUTAMINASE antibodies with duodenal histologic Marsh grading in Iranian patients with celiac disease.METHODS we retrospectively reviewed hospital files of registered patients in the gastrointestinal clinic of Firoozgar Hospital, Tehran, Iran. Demographic, laboratory, and histology data of those who had tTG titer and pathology reports of duodenal biopsy based on the modified Marsh classification were extracted and used for the study.RESULTS 159 patients with available tTG titer and pathology reports were enrolled in our study. Mean ±SD of the patients was 35.6±15.2 and 100 (62.9%) of them were women.133 out of 153 patients had villous atrophy (Marsh IIIa-IIIc). Anemia was the most common sign and bloating, abdominal pain, and diarrhea were the first three common symptoms in these patients. Mean tTG titers was significantly higher in patients graded as Marsh III (p for trend=0.003). Our results showed that tTG titer more than 9 folds higher than the kit’s cut-off value was about 97.2% sensitive for Marsh II and more duodenal damage.CONCLUSION: There was a correlation between tTG titers and degrees of duodenal damage in patients with celiac disease. Duodenal biopsy is not always necessary for diagnosing celiac disease and when tTG level is more than 9 folds higher than the manufacture’s recommended cut-off value it can be avoided. Meanwhile in case of high clinical suspicion, low tTG levels do not exclude diagnosis of celiac disease and further investigations including small intestinal biopsy should be considered.

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Issue Info: 
  • Year: 

    2016
  • Volume: 

    34
  • Issue: 

    379
  • Pages: 

    381-386
Measures: 
  • Citations: 

    1
  • Views: 

    3272
  • Downloads: 

    0
Abstract: 

Background: Alopecia areata (AA) is a common and asymptomatic disease which is characterized by rapid loss of hair in an area. Etiology of the disease is not fully understood. Several studies declare relationship between AA and celiac disease. This study aimed at evaluating the frequency distribution of celiac autoantibodies in patients with AA comparing to the control group.Methods: This study is a case-control study. 35 subjects entered in each group. Anti-TISSUE-trans-glutaminase IgA (Anti-tTg IgA) were tested in all subjects. And the result was reported as positive/negative. Finally the frequency distribution of these autoantibodies were compared between two groups.Findings: There was no significant difference between two groups based on gender and sex (P=0.151) and (P=0.621) respectively, via chi-square test analysis. Anti-tTg IgA was positive in one person (2.8%) In the case group. No one was positive in the control group, and therefor there is no significant difference between two groups (P=0.314) based on chi-square test. In the case group the most common form of AA was patchy, and the most common nail involvement was Pitting. 17.1% of patients had positive family history of AA.Conclusion: The study shows the frequency distribution of one of the celiac autoantibodies in patients with alopecia areata is not higher than normal population of the community of Isfahan. Therefore screening other autoantibodies such as Anti-Gliadin IgA and Anti-Gliadin IgG in these patients are recommended.

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Issue Info: 
  • Year: 

    2020
  • Volume: 

    11
  • Issue: 

    1
  • Pages: 

    00-00
Measures: 
  • Citations: 

    0
  • Views: 

    175
  • Downloads: 

    200
Abstract: 

Background: Although initially considered as a digestive tract disease, celiac disease (CD) can cause problems and complications in most other organs. Common serologic tests for the diagnosis of CD include anti-TISSUE TRANSGLUTAMINASE (tTG) and anti-endomysial Ab (EMA). A more recent test includes anti-deamidated gliadin peptide. Objectives: This study aimed to compare the values of TISSUE TRANSGLUTAMINASE and endomysial antibodies in A and G Immunoglobin subtypes in patients with a definitive diagnosis of CD. Methods: Patients suspected of CD referring to a Gastrointestinal Pediatric Clinic were evaluated for CD using IgG and IgA for TISSUE TRANSGLUTAMINASE and endomysial antibodies and total IgA. Endoscopy and biopsy were done based on the CD diagnosis protocol. The demographic data of children were recorded in a questionnaire and then analyzed. Results: Of the 54 patients diagnosed with CD, 29 were females and 25 were males. TTG-IgA had the highest positivity rate. Tests based on IgA were more positive than IgG tests. More than one test was positive in 81. 5% of the patients. All four tests were positive in 16 patients. In 18. 5 percent of patients, just one test was positive. In the latter group, TTG-IgA was positive in four patients. The coefficient of agreement between EMA-IgA and TTG-IgA was 0. 435, which was statistically significant. Conclusions: We suggest TISSUE TRANSGLUTAMINASE and endomysial antibodies in A and G Immunoglobin subtypes for the diagnosis of CD. In this method, the diagnostic sensitivity of CD is high and in the next step, endoscopy and sampling can increase the specificity value. If the tests are not available, preferable tests are IgA subtype antibodies.

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Issue Info: 
  • Year: 

    2025
  • Volume: 

    2
  • Issue: 

    2
  • Pages: 

    222-228
Measures: 
  • Citations: 

    0
  • Views: 

    8
  • Downloads: 

    0
Abstract: 

Background: Celiac disease (CD) is a chronic autoimmune disorder triggered by gluten, diagnosed primarily through serological tests measuring anti-TISSUE TRANSGLUTAMINASE antibodies (anti-tTG) alongside duodenal biopsy. We aimed to explore the relationship between anti-tTG levels and duodenal biopsy findings to improve diagnostic accuracy and management strategies for CD patients. Methods: This retrospective study analyzed 319 small intestine biopsy results from patients suspected of having celiac disease in Qom Province, central Iran between 2016 and 2023. Serum levels of anti-tTG IgA and IgG were measured by ELISA and compared with duodenal histopathology classified by Marsh criteria. Statistical analysis included one-way ANOVA and Tukey’s post hoc test. Results: Among 226 patients diagnosed with celiac disease, the mean anti-tTG IgA levels increased significantly with Marsh grade severity (Marsh I: 81±93 U/ml,Marsh II: 134. 5±97. 2 U/ml,Marsh IIIa: 146±121 U/ml,Marsh IIIb: 170±120. 2 U/ml,Marsh IIIc: 211. 5±116 U/ml,P<0. 002). Similarly, mean anti-tTG IgG levels rose with increasing Marsh grade (Marsh I: 20±30. 3 U/ml,Marsh II: 57. 3±70. 5 U/ml,Marsh IIIa: 57±79. 2 U/ml,Marsh IIIb: 71. 3±90. 7 U/ml,Marsh IIIc: 113. 5±98. 5 U/ml,P<0. 006). There was a statistically significant correlation between ANTIBODY titers and histopathological severity. Conclusion: Higher anti-tTG IgA and IgG ANTIBODY titers are significantly associated with greater duodenal TISSUE damage according to Marsh classification (P<0. 05). These findings highlight the clinical utility of serological testing not only for initial screening but also for predicting the severity of intestinal involvement in celiac disease. In patients with markedly elevated anti-tTG levels, the necessity for invasive biopsy may be reconsidered, supporting a more individualized diagnostic approach based on serological and histopathological correlation.

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Issue Info: 
  • Year: 

    2010
  • Volume: 

    13
  • Issue: 

    4
  • Pages: 

    301-305
Measures: 
  • Citations: 

    0
  • Views: 

    434
  • Downloads: 

    367
Abstract: 

Background: The prevalence of celiac disease is common in Iran. The aim of the present study was to determine the prevalence of celiac disease in apparently healthy blood donors of Sistan and Balouchestan Province, southeastern Iran.Methods: Serum samples of 1600 consecutive apparently healthy blood donors at Zahedan Blood Donation Center were assayed for anti-TISSUE TRANSGLUTAMINASE (tTG) ANTIBODY. The levels of IgG antibodies against tTG were screened for all subjects with IgA deficiency. All subjects with positive anti-tTG IgA or IgG were offered upper gastrointestinal endoscopy and duodenal mucosal biopsies.Results: IgA deficiency was found in 28:1600 (1.8%) of the subjects, among whom 4 cases were positive for IgG-class tTG ANTIBODY. Meanwhile, 10 blood donors were positive for anti-tTG IgA ANTIBODY. With the exception of 2 subjects who had normal small bowel biopsies, the remainder of the subjects’ biopsy findings was compatible with celiac disease. The prevalence of celiac disease was found to be 0.88% (1/114) based on tTGA positivity.Conclusion: The prevalence of celiac disease among the southeastern Iranian population is high and comparable with other parts of Iran as well as many other countries.

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Author(s): 

MALEKZADEH R. | SHAKERI R.

Issue Info: 
  • Year: 

    2007
  • Volume: 

    65
  • Issue: 

    2
  • Pages: 

    1-11
Measures: 
  • Citations: 

    0
  • Views: 

    3527
  • Downloads: 

    0
Abstract: 

Background: Until a few decades ago, celiac disease was considered to be essentially a disease of European people and to be very rare in Middle Eastern countries. During the last two decades, having met the criteria for the WHO general screening, the advent and application of novel serological assays used to screen for celiac disease and the use of endoscopic small bowel biopsy have led to increasing numbers of diagnoses of celiac disease in western countries. With this new data, our knowledge on both the clinical pattern and epidemiology of celiac disease has increased, and is now known to be a relatively common autoimmune disorder. Studies performed in different parts of the developing world have shown that the prevalence of celiac disease in this area is similar to or even higher than those in western countries. In fact, celiac disease is known to be the most common form of chronic diarrhea in Iran. However, contrary to common belief, celiac disease is more than a pure digestive alteration. It is a protean systemic disease, and, with a 95 percent genetic predisposition, has a myriad of symptoms including gastrointestinal, dermatological, dental, neurological and behavioral that can occur at a variety of ages. Monosymptomatic, oligosymptomatic, atypical (without gastrointestinal symptoms), silent and latent forms of celiac disease have been identified. In this study we review the epidemiology of celiac disease based on the studies performed in Iran and discuss its pathogenesis, the role of antibodies in the diagnosis of celiac disease and the importance of its diagnosis and treatment in Iran.

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Journal: 

GASTROENTEROLOGY

Issue Info: 
  • Year: 

    1998
  • Volume: 

    115
  • Issue: 

    6
  • Pages: 

    1317-1321
Measures: 
  • Citations: 

    1
  • Views: 

    84
  • Downloads: 

    0
Keywords: 
Abstract: 

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Issue Info: 
  • Year: 

    2009
  • Volume: 

    11
  • Issue: 

    4
  • Pages: 

    442-444
Measures: 
  • Citations: 

    0
  • Views: 

    547
  • Downloads: 

    177
Abstract: 

Background: Autism is a heterogeneous condition and the possible pathogenic role of several different factors was postulated. Previous studies reported the existence of a linkage between autism and celiac disease (CD). The aim of this study was to determine the association between autism and CD by anti-gliadin (AGA), antiendomysial (AEA) and TISSUE TRANSGLUTAMINASE (tTG) antibodies.Methods: Thirty four consecutive autistic children (18 boys and 16 girls) aging 9.2±4.1 years (range 4-16 years) and thirty four age- and sex- matched healthy anonymous blood donors (18 boys and 16 girls) aging 10.8±4.0 years (range 4-16 years) were included. None of the patients and controls had symptoms (or positive family history) suggestive of specific gastrointestinal diseases. AGA and AEA antibodies (IgG and IgA), and IgA-tTG were detected by ELISA. The individuals with positive serology were offered duodenal biopsies.Results: IgG-AGA was found in 4 patients (11.8%) and 2 controls (5.9%), while IgA-AGA was found in none of the patients and controls. All patients presented normal values of IgG and IgA-AEA similar to the control group. There was no significant relationship between the levels of AGA and AEA antibodies and the severity of autism in the patient group. The levels of IgA-tTG in four patients (but no controls) were in the borderline range and two of them were found to have mild villous changes with chronic inflammatory cells. However, characteristic histological features of CD were absent.Conclusions: No evidence was found that children with autism were more likely to have celiac disease than children without autism.

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