Celiac disease among at-risk individuals in Saudi Arabia
1Department of Medical Microbiology and Parasitology, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. E-mail. aymansafi3@hotmail.com.
Insights
Celiac disease (CD) prevalence is significantly higher in at-risk Saudi Arabian populations compared to the general population. This meta-analysis highlights elevated seropositive (15.6%) and biopsy-proven (10.6%) CD rates in individuals with type-1 diabetes, short stature, and Down syndrome.
Area of Science:
- Gastroenterology and Hepatology
- Clinical Immunology
- Epidemiology
Background:
- Celiac disease (CD) is an autoimmune disorder triggered by gluten consumption.
- At-risk populations, including those with type-1 diabetes mellitus (DM), short stature (SS), and Down syndrome (DS), have a higher predisposition to CD.
- Understanding CD prevalence in these groups is crucial for timely diagnosis and management.
Purpose of the Study:
- To conduct a meta-analysis on the prevalence of celiac disease (CD) in at-risk populations within the Kingdom of Saudi Arabia (KSA).
- To compare the findings with a previously reported meta-analysis of CD prevalence in the general Saudi Arabian population.
Main Methods:
- A retrospective search of databases and journals for studies on CD in at-risk populations in KSA was performed.
- Data from sixteen relevant articles were analyzed using statistical software (SPSS Version 20) and Comprehensive Meta-Analysis (CMA).
- Prevalence was calculated for seropositive and biopsy-proven CD, with heterogeneity assessed using the I2 statistic.
Main Results:
- The meta-analysis revealed a seropositive CD prevalence of 15.6% (I2=80.353) and a biopsy-proven CD prevalence of 10.6% (I2=73.359) in at-risk populations.
- One study reported distinct figures of 18.4% for seroprevalence and 6.9% for biopsy-proven CD.
- The female-to-male ratio for CD was 1.9:1, consistent across both at-risk and normal populations.
Conclusions:
- The prevalence of both biopsy-proven (10.6%) and seropositive (15.6%) CD in at-risk Saudi Arabian populations is substantially higher than previously reported in the general population (1.4% and 2.7%).
- The consistent female-to-male ratio suggests similar disease patterns across different population groups.
- Further meta-analyses focusing on CD prevalence within specific at-risk subgroups (DM, SS, DS) in KSA are recommended.
Objectives:
To perform a meta-analysis for celiac diseases (CD) among at-risk populations in Kingdom of Saudi Arabia (KSA), as well as a comparison with our previously reported meta-analysis in the normal population.
Methods:
In March 2018, at King Abdulaziz University, Jeddah, KSA we commenced a retrospective comprehensive database and journal search for CD among at-risk populations in SA. Data from each of the relevant articles were analyzed using the Statistical Package for Social Science Version 20 (Armonk, NY: IBM Corp.). and the comprehensive meta-analysis program (CMA). The collected data were part of a retrospective literature review and analysis. Thus, a written ethical approval was not obtained before commencing the study. Results: Sixteen articles were found covering type-1 diabetes mellitus (DM), short stature (SS), and down syndrome (DS). Ages 1-50 years . The prevalence of seropositive-CD was 15.6% with high heterogeneity (I2=80.353), while prevalence of biopsy-proven CD was 10.6% with high heterogeneity (I2=73.359). Another article reported the CD prevalence in the at-risk population as 18.4% for the seroprevalence and 6.9% for the biopsy-proven CD. Anti-transglutaminase (anti-tTG) was used in 12 studies; in the remaining 4 studies (EMA in 2, ARA with AGA in one and no details given in one study). Conclusion: Both the prevalence of biopsy-proven CD (10.6%) and seroprevalence (15.6%) were higher than those we previously reported in the normal population (1.4% and 2.7%). The female-to-male ratio (1.9/1) of CD patients was the same in normal and at-risk populations in SA. Meta-analysis for prevalence of CD in DM, SS, and DS separately in SA is recommended.
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