Celiac Disease in Oman: A Tertiary Centre Experience

 
 

Tawfiq Taki Al-Lawati, Hashim Sadiq Al-Musawi

 
  DOI 10.5001/omj.2013.17  
 
 
 

Department of Child Health, Royal Hospital, Muscat, Sultanante of Oman.

Received: 21 Oct 2012          
Accepted: 09 Nov 2012

*Address correspondence and reprints request to: Tawfiq Taki Al-LawatiDepartment of Child Health, Royal Hospital, Muscat, Sultanante of Oman.
E-mail: 
roy-tawfiq@moh.gov.om
 
 
 
 

How to cite this article

Al-Lawati TT, Al-Musawi HS. Celiac Disease in Oman: A Tertiary Centre Experience. Oman Med J 2013 Jan; 28(1):70-72.

How to cite this URL

Al-Lawati TT, Al-Musawi HS. Celiac Disease in Oman: A Tertiary Centre Experience. Oman Med J 2013 Jan; 28(1):70-72. Available from http://www.omjournal.org/fultext_PDF.aspx?DetailsID=340&type=fultext

 
 


Abstract

Objective: To describe the frequency of encounter of celiac disease in Royal Hospital, Muscat, Oman.

Methods: Retrospective study of records of all adult and pediatric patients in Royal Hospital from the period of 1/4/2006 to 31/3/2012. Data regarding symptoms, anthropometry of the patients, haemoglobuin levels, liver and thyroid functions were retrieved. Diagnosis of celiac disease was established based on combination of serological detection of anti tissues transglutaminase (tTG) or anti endomysial antibodies (EMA) with duodenal biopsy.

Results: Only 9 children were identified in the hospital during the period of study. Two children were identified by screening protocol for Insulin Dependent Diabetes Melitus (IDDM) and one child from short stature workup. Six children presented with abdominal pain and diarrhea. Four children were severely wasted and stunted. No adult patients were identified with celiac disease. Anaemia was noted in 3 children and none had deranged thyroid functions.

Conclusion: Celiac disease is infrequently encountered in Royal Hospital and might be under diagnosed. The low rate of celiac disease in children with IDDM might indicate a different genetic composition. Awareness about celiac disease and family screening should be implemented in Oman.

Keywords: Celiac Disease; Arab Population; Oman.


Introduction

Celiac disease is an autosomal recessive autoimmune condition causing chronic inflammation of the small intestine triggered by ingestion of gluten. Clinical presentation of the disease could be either intestinal manifested mainly by abdominal pain and diarrhea or extra intestinal manifested by symptoms including rickets, dermatitis herpitoformis and infertility in adults. Celiac disease is ascertained by the presence of positive IgA of anti tissue transglutaminase (anti tTG) or anti endonysial anti bodies (anti EMA) in addition to histological changes on duodenal biopsy indicative of celiac disease with normal total serum IgA levels.1

The mass screening of four European populations reported in 2010 revealed a prevalence of 1%.2 Review of earlier studies conducted in Europe and United States indicates a prevalence ranging from 3 to 13 per 1000 children between the age of 2.5 to 15 years.2,3 Information about celiac disease among Arab populations is sparse and based on small scale studies. A single centre in Egypt reported a frequency of 0.53% among children attending a general pediatric clinic and rises to 6.4% in children with type 1 diabetes mellitus.4 At King Abdul Aziz Medical centre in Saudia Arabia, only 80 patients were diagnosed over a 5 year period.5 A more recent study in adult blood donors in Saudia Arabia reported a prevalence of 1.5% among blood donors.6 In India, the frequency of encounter of celiac disease in different areas ranged from 0.3%,7 to an encounter of 1%.8

Data on celiac disease in Oman is limited to two studies conducted at Sultan Qaboos University Hospital between 2003,and 2006.10 The screening of 51 adults with unexplained iron deficiency anemia attending Sultan Qaboos University Hospital by Fraser,9 revealed two cases of celiac disease based on anti EMA yielding a frequency of encounter of 3%. In 2006, Akinbami ascertained the disease among 13% out of 62 children with chronic diarrhea attending the same hospital.10

This study is aimed at updating information on celiac disease in Oman by providing a detailed review and description of the cases diagnosed in Royal Hospital as the main referral centre for work up of patients suspected to have celiac disease in Oman.

Methods

A descriptive study of cases of celiac diseases was conducted in March 2012 based on the retrospective review of the electronic records at Royal Hospital. Records of all adults and children diagnosed with celiac disease in the period of 1/4/2006 to 31/3/2012 were identified and included in the study. Data regarding presenting symptoms, age of diagnosis, anthropometric measures, liver functions, calcium profile and hemoglobuin were retrieved from the records.

Diagnosis of celiac disease was established by a combination of serological detection of anti tissues transglutaminase (tTG) or anti endomysial antibodies (EMA) and duodenal biopsy indicative of celiac disease.

Results

A total of 9 children with an established diagnosis of celiac diseases were identified (Table 1). Complete data were available for 8 children as one child was investigated in another hospital. Females (n: 6) outnumbered males (n: 3). The mean age of these children was 10.9 years (min: 3 years; max: 18 years). The mean age of diagnosis was 7 years (range: from 2-13 years). No adult patients were diagnosed with celic disease. Table 2 depicts the anthropometric data of children at the time of diagnosis. Four children were severely wasted and stunted at time of diagnosis. Clinical presentation was available for 8 children and it included diarrhea (n: 4), stunting (n: 2), and insulin dependent diabetes mellitus (n: 2), (Table 3). All children had endoscopy and biopsy in addition to serological testing for anti tTG or EMA with total IgA. Eight children had histological and serological evidence of celiac disease. Only one child had no histological evidence of celiac disease despite being strongly positive for anti tTG.

Table 1: Demographic data of patients.

t1

Three children had incomplete data on the hematological and biochemical tests at the time of diagnosis as they were investigated in other institutes. Three children had anemia and none had deranged liver or thyroid functions. (Table 4)

Table 2: Growth parameters at time of diagnosis.

t2

NA: Not Available

Table 3: Clinical presentation and means of diagnosis.

t3

IDDM: Insulin Dependent Diabetes Mellitus; FTT: Failure to Thrive

Table 4: Hematological and biochemical results of patients.

t4

Discussion

Oman is situated in the Arabic Peninsula with the Indian Ocean on the Eastern borders and Saudia Arabia and the rest of the Arab countries on the Westerns boarder. Gluten is commonly consumed by the Omani population as a staple diet. Bread and wheat are consumed on a daily basis including weaning foods of infants. This study describes the cases of celiac diseases in a tertiary hospital affiliated to the Ministry of Health in Muscat, the capital city. During six years, only 9 cases were diagnosed with celiac disease at this hospital. This number is similar to that reported by Akinbami in 2006 from Sultan Qaboos University Hospital.10 The data shows that celiac disease is not frequently encountered in the main tertiary hospitals in Oman.

The number of children under the age of 14 years in Oman is about 700,000, as estimated by the ministry of health annual report in 2010.11 Considering a prevalence of 0.5 to 1.5%, as reported in neighboring countries of India and Saudia Arabia, the number of celiac disease cases in children in Oman will be between 3500 to 10,000 children. With the crude birth rate of 58,000,11 at least 290 children should be diagnosed annually.

Frazer reported 3.3% prevalence in his cohort of adults with unexplained anemia.9 This is very high even compared to both the European populations and the reported data from Arab populations. Potential issues of low frequency of encounter of children with celiac disease might be related to the genetic variance in the Omani population, absence of screening programs of the siblings and possibly unawareness of the referring physicians with regards to the manifestations of the disease. Although there are no data from the rest of the Arabic Gulf countries, celiac disease is not frequently encountered in Kuwait, Bahrain or Qatar (personal communication).

On the other hand, the finding of an earlier study by Akinbami,10 of only 9 children over 7 years along with our study may indicate that the Omani population is different and the prevalence of celiac disease in this population is truly significantly low. This is further supported by the detection of only two children with celiac disease on screening for IDDM children over the 7 years. The reported incidence of celiac disease in patients with IDDM in Europe ranged from 4.4-11.1%,12 and upto 21% in Saudia Arabia.13 In a country with a high consanguinity rate, the frequency of encounter is expected to be higher. The consanguinity rate in Oman is about 50%.14

The vast difference in the prevalence of celiac disease in children with IDDM and the infrequent encounter of the disease in two major hospitals in Oman might indicate that the genetic predisposition of Omani population is different than the surrounding areas of the Gulf countries with regards to celiac disease.

The mean age of diagnosis at 7.1 years in the current study was very similar to the age of diagnosis in Finland at 7.2 years in a single centre study.15 The age of diagnosis at 7 would still be considered late as the disease sets in once gluten is introduced at the age of nearly 6 months. This also may explain why nearly 45% of the diagnosed children were severely stunted and wasted at the time of diagnosis, thus confirming late diagnosis. No obese children were identified. It is also important to note that no adults were diagnosed with celiac disease. This needs to be further studies as it might be an alarming negative finding.

Anemia was noted in 3 children at the time of diagnosis. It was not clear if anemia was related to celiac disease per se or is it primarily nutritional iron deficiency anemia. None of the children had elevated ALT or abnormal thyroid function tests.

Conclusion

The frequency of encounter of celiac disease in Royal Hospital is extremely low. The low frequency of encounter of celiac disease in Omani children with IDDM might indirectly point towards a low prevalence in the country in general. Inspite of this, there is probably some under diagnosis of the condition in the country as well for various reasons. Awareness of the disease should certainly be increased in the country.

Acknowledgements

The authors reported no conflict of interest and no funding was received on this work.


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