Systematic reviews and meta-analyses
Global Prevalence of Celiac Disease: Systematic Review and Meta-analysis

https://doi.org/10.1016/j.cgh.2017.06.037Get rights and content

Background & Aims

Celiac disease is a major public health problem worldwide. Although initially it was reported from countries with predominant Caucasian populations, it now has been reported from other parts of the world. The exact global prevalence of celiac disease is not known. We conducted a systematic review and meta-analysis to estimate the global prevalence of celiac disease.

Methods

We searched Medline, PubMed, and EMBASE for the keywords celiac disease, celiac, celiac disease, tissue transglutaminase antibody, anti-endomysium antibody, endomysial antibody, and prevalence for studies published from January 1991 through March 2016. Each article was cross-referenced with the words Asia, Europe, Africa, South America, North America, and Australia. The diagnosis of celiac disease was based on European Society of Pediatric Gastroenterology, Hepatology, and Nutrition guidelines. Of 3843 articles, 96 articles were included in the final analysis.

Results

The pooled global prevalence of celiac disease was 1.4% (95% confidence interval, 1.1%–1.7%) in 275,818 individuals, based on positive results from tests for anti–tissue transglutaminase and/or anti-endomysial antibodies (called seroprevalence). The pooled global prevalence of biopsy-confirmed celiac disease was 0.7% (95% confidence interval, 0.5%–0.9%) in 138,792 individuals. The prevalence values for celiac disease were 0.4% in South America, 0.5% in Africa and North America, 0.6% in Asia, and 0.8% in Europe and Oceania; the prevalence was higher in female vs male individuals (0.6% vs 0.4%; P < .001). The prevalence of celiac disease was significantly greater in children than adults (0.9% vs 0.5%; P < .001).

Conclusions

In a systematic review and meta-analysis, we found celiac disease to be reported worldwide. The prevalence of celiac disease based on serologic test results is 1.4% and based on biopsy results is 0.7%. The prevalence of celiac disease varies with sex, age, and location. There is a need for population-based prevalence studies in many countries.

Section snippets

Methods

We conducted an extensive search on Medline, PubMed, and EMBASE with the following medical subject heading terms and keywords “celiac disease,” “celiac,” “coeliac disease,” “tissue transglutaminase antibody,” “anti-endomysium antibody,” “endomysial antibody,” and “prevalence.” Each one was cross-referenced with “Asia,” “Europe,” “Africa,” “South America,” “North America,” and “Australia.” Because the European Society of Gastroenterology, Hepatology and Nutrition released the first modern

Results

Our search found a total of 3843 articles in the database (Supplementary Figure 1). Of them, 3674 articles were excluded based on the titles or abstracts. Finally, full texts of 169 articles were assessed. Sixty-four additional studies were excluded based on the inclusion and exclusion criteria. Nine more studies were excluded for several reasons detailed in Supplementary Figure 1.4, 5, 22, 23, 24, 25, 26, 27, 28 Ultimately, 96 studies were included in the present meta-analysis (Supplementary

Discussion

The present meta-analysis showed that the pooled global seroprevalence of CD is 1.4% (95% CI, 1.1%–1.7%). The pooled global prevalence of biopsy-confirmed CD is 0.7% (95% CI, 0.5%–0.9%), with the highest prevalence in Europe (0.8%) and Oceania (0.8%), and the least prevalence in South America (0.4%). The present meta-analysis confirms that biopsy-confirmed CD is 1.5 times more common in females than in males, and approximately twice more common in children than in adults.

In our study, the

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    Conflicts of interest These authors disclose the following: Ciaran P. Kelly has acted as a scientific advisor to companies attempting to develop new management approaches for celiac disease including Celimmune, Cour Pharma, Immunogen X, and Takeda Pharmaceuticals, and also acts as the Principal Investigator on a research grant on celiac disease supported by Aptalis; Daniel Leffler is the medical director at Takeda Pharmaceuticals and has received research support/consultancy fees from Alba Therapeutics, Alvine Pharmaceuticals, INOVA Diagnostics, Genzyme, Coronado Biosciences, the Sidney Frank Foundation, and Pfizer; and Peter H. Green has received personal fees from ImmusanT outside of the submitted work. The remaining authors disclose no conflicts.

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