Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jun 17:8:674896.
doi: 10.3389/fmed.2021.674896. eCollection 2021.

Prevalence of Celiac Disease in Patients With Turner Syndrome: Systematic Review and Meta-Analysis

Affiliations

Prevalence of Celiac Disease in Patients With Turner Syndrome: Systematic Review and Meta-Analysis

Ghada S M Al-Bluwi et al. Front Med (Lausanne). .

Abstract

Introduction: Celiac disease (CD) is a multifactorial autoimmune disorder, and studies have reported that patients with Turner syndrome (TS) are at risk for CD. This systematic review and meta-analysis aimed to quantify the weighted prevalence of CD among patients with TS and determine the weighted strength of association between TS and CD. Methods: Studies published between January 1991 and December 2019 were retrieved from four electronic databases: PubMed, Scopus, Web of Science, and Embase. Eligible studies were identified and relevant data were extracted by two independent reviewers following specific eligibility criteria and a data extraction plan. Using the random-effects model, the pooled, overall and subgroup CD prevalence rates were determined, and sources of heterogeneity were investigated using meta-regression. Results: Among a total of 1,116 screened citations, 36 eligible studies were included in the quantitative synthesis. Nearly two-thirds of the studies (61.1%) were from European countries. Of the 6,291 patients with TS who were tested for CD, 241 were diagnosed with CD, with a crude CD prevalence of 3.8%. The highest and lowest CD prevalence rates of 20.0 and 0.0% were reported in Sweden and Germany, respectively. The estimated overall weighted CD prevalence was 4.5% (95% confidence interval [CI], 3.3-5.9, I 2, 67.4%). The weighted serology-based CD prevalence in patients with TS (3.4%, 95% CI, 1.0-6.6) was similar to the weighted biopsy-based CD prevalence (4.8%; 95% CI, 3.4-6.5). The strength of association between TS and CD was estimated in only four studies (odds ratio 18.1, 95% CI, 1.82-180; odds ratio 4.34, 95% CI, 1.48-12.75; rate ratio 14, 95% CI, 1.48-12.75; rate ratio 42.5, 95% CI, 12.4-144.8). Given the lack of uniformity in the type of reported measures of association and study design, producing a weighted effect measure to evaluate the strength of association between TS and CD was unfeasible. Conclusion: Nearly 1 in every 22 patients with TS had CD. Regular screening for CD in patients with TS might facilitate early diagnosis and therapeutic management to prevent adverse effects of CD such as being underweight and osteoporosis.

Keywords: Turner syndrome; celiac disease; meta-analysis; systematic review; weighted prevalence.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
PRISMA flow chart of study selection.
Figure 2
Figure 2
Forest plot of the meta-analysis of studies on celiac disease in patients with Turner syndrome. The diamond is centered on the summary prevalence estimate, and the width indicates the corresponding 95% confidence interval (CI).
Figure 3
Figure 3
Contour-enhanced Funnel plot (A) and Egger's publication bias plot (B) examining small-study effects on the pooled celiac disease prevalence among patients with Turner syndrome. The estimated bias coefficient is 0.346 with a standard error of 0.077, indicating a p-value of < 0.001.

References

    1. Holtmeier W, Caspary WF. Celiac disease. Orphanet J Rare Dis. (2006) 1:3. 10.1186/1750-1172-1-3 - DOI - PMC - PubMed
    1. Taylor AK, Lebwohl B, Snyder CL, Green PHR. Celiac Disease. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A. editors. GeneReviews [Internet]. Seattle, WA: University of Washington, Seattle; (2008).
    1. La Vieille S, Pulido OM, Abbott M, Koerner TB, Godefroy S. Celiac disease and gluten-free oats: a Canadian position based on a literature review. Can J Gastroenterol Hepatol. (2016) 2016:1870305. 10.1155/2016/1870305 - DOI - PMC - PubMed
    1. Guandalini S, Assiri A. Celiac disease: a review. JAMA Pediatr. (2014) 168:272–8. 10.1001/jamapediatrics.2013.3858 - DOI - PubMed
    1. Andren Aronsson C, Kurppa K, Agardh D. Gluten in infants and celiac disease risk. Expert Rev Gastroenterol Hepatol. (2016) 10:669–70. 10.1586/17474124.2016.1169922 - DOI - PubMed

Publication types

LinkOut - more resources