Department of Hygiene and Epidemiology, University of Ioannina School of Medicine, Ioannina, Greece.
Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
Eur J Gastroenterol Hepatol. 2024 Oct 1;36(10):1171-1179. doi: 10.1097/MEG.0000000000002810. Epub 2024 Aug 19.
The breadth and validity of the associations of nongenetic risk factors with celiac disease (CeD) are elusive in the literature. We aimed to evaluate which of these associations have strong epidemiological credibility and assessed presence and extent of potential literature biases. We systematically searched PubMed until April 2024 for systematic reviews and meta-analyses of studies examining associations between putative risk factors and CeD. Each association was categorized in five evidence grades (convincing, highly suggestive, suggestive, weak, and not statistically significant) based on broadly used criteria for evaluating quality of evidence in observational studies. Five eligible publications were included, describing 15 meta-analytic associations on seven nongenetic risk factors, three of which were nominally significant ( P < 0.05). None of the associations received a strοng or highly suggestive evidence. One meta-analytic association received suggestive evidence, namely any infections during childhood and adulthood for a higher risk of CeD (OR, 1.37; 95% CI, 1.2-1.56; P =3.77 × 10 -6 ). Two meta-analyses reported weak evidence, pertaining to current smoking for a lower risk of CeD (OR, 0.52; 95% CI, 0.32-0.84; P =7.84 × 10 -3 ) and use of antibiotics for a higher risk (OR, 1.2; 95% CI, 1.04-1.38; P 14.8 × 10 -3 ). The rest of the meta-analyses did not report statistically significant results, and pertained to breastfeeding, time of gluten introduction, rotavirus vaccination, and cesarean section. No association of nongenetic risk factors for CeD received high levels of evidence. The evidence was suggestive for the association of any infections during childhood and adulthood with higher risk of CeD. More and prospective future research is warranted.
非遗传因素与乳糜泻(CeD)之间关联的广度和有效性在文献中难以捉摸。我们旨在评估这些关联中有哪些具有强烈的流行病学可信度,并评估潜在文献偏倚的存在和程度。我们系统地在 PubMed 上搜索了截至 2024 年 4 月的系统评价和荟萃分析研究,以检查潜在风险因素与 CeD 之间的关联。根据广泛用于评估观察性研究证据质量的标准,将每个关联分为五个证据等级(令人信服、高度提示、提示、弱和无统计学意义)。有 5 篇合格的出版物,描述了 7 个非遗传风险因素的 15 个荟萃分析关联,其中 3 个具有名义显著性(P <0.05)。没有一个关联得到强烈或高度提示的证据。一个荟萃分析关联得到了提示性证据,即儿童期和成年期的任何感染都会增加 CeD 的风险(OR,1.37;95%CI,1.2-1.56;P =3.77×10 -6 )。两项荟萃分析报告了弱证据,涉及当前吸烟可降低 CeD 的风险(OR,0.52;95%CI,0.32-0.84;P =7.84×10 -3 )和使用抗生素可增加风险(OR,1.2;95%CI,1.04-1.38;P <0.001)。其余的荟萃分析没有报告统计学上显著的结果,涉及母乳喂养、谷蛋白引入时间、轮状病毒疫苗接种和剖腹产。没有非遗传因素与 CeD 的关联得到了高水平的证据。有证据表明,儿童期和成年期的任何感染与 CeD 的风险增加有关。需要进行更多和前瞻性的未来研究。