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儿童肥胖与成年后炎症性肠病风险:一项孟德尔随机化研究。

Childhood obesity and risk of inflammatory bowel disease in adulthood: A Mendelian randomization study.

机构信息

Department of Gastroenterology and Hepatology, First Medical Center, Chinese PLA General Hospital, Beijing, China.

School of Medicine, Nankai University, Tianjin, China.

出版信息

Medicine (Baltimore). 2024 Nov 29;103(48):e40478. doi: 10.1097/MD.0000000000040478.

DOI:10.1097/MD.0000000000040478
PMID:39612455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11608687/
Abstract

It is well-known that childhood obesity is associated with various adult gastrointestinal diseases, inflammatory bowel disease (IBD) being no exception. However, previous epidemiological observational studies, while reporting a correlation between the 2, have left the question of a causal relationship inconclusive. This study aims to use a 2-sample Mendelian randomization (MR) analysis to assess the causal relationship between childhood obesity and IBD as well as its subtypes (ulcerative colitis [UC] and Crohn disease [CD]). Data on childhood obesity, IBD, and its subtypes (UC and CD) were sourced from IEU OpenGWAS (https://gwas.mrcieu.ac.uk/datasets/ieu-a-1096/) and IIBDGC (https://www.ibdgenetics.org/). The data were analyzed using the inverse variance weighted (IVW), MR-Egger, weighted median, simple mode, and weighted mode methods. The MR analysis indicates no causal relationship between childhood obesity and IBD or its subtypes (UC and CD). The consistency of the results across the IVW, MR-Egger, weighted median, simple mode, and weighted mode methods suggests the reliability of the findings. We found that childhood obesity is not causally related to IBD or its subtypes (UC and CD). This differs from prior studies. The observed discrepancies may be due to common biological or environmental confounding factors.

摘要

众所周知,儿童肥胖与各种成人胃肠道疾病有关,炎症性肠病(IBD)也不例外。然而,以前的流行病学观察性研究虽然报告了两者之间存在相关性,但对于因果关系的问题仍未得出明确结论。本研究旨在使用两样本孟德尔随机化(MR)分析来评估儿童肥胖与 IBD 及其亚型(溃疡性结肠炎[UC]和克罗恩病[CD])之间的因果关系。儿童肥胖、IBD 及其亚型(UC 和 CD)的数据来自 IEU OpenGWAS(https://gwas.mrcieu.ac.uk/datasets/ieu-a-1096/)和 IIBDGC(https://www.ibdgenetics.org/)。使用逆方差加权(IVW)、MR-Egger、加权中位数、简单模式和加权模式方法分析数据。MR 分析表明,儿童肥胖与 IBD 或其亚型(UC 和 CD)之间没有因果关系。IVW、MR-Egger、加权中位数、简单模式和加权模式方法的结果一致性表明了研究结果的可靠性。我们发现儿童肥胖与 IBD 或其亚型(UC 和 CD)之间没有因果关系。这与以前的研究不同。观察到的差异可能是由于共同的生物学或环境混杂因素所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/58f1c0061103/medi-103-e40478-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/c855fbd7360e/medi-103-e40478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/7de4df5caca9/medi-103-e40478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/4ac7d8980a93/medi-103-e40478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/58f1c0061103/medi-103-e40478-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/c855fbd7360e/medi-103-e40478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/7de4df5caca9/medi-103-e40478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/4ac7d8980a93/medi-103-e40478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b9/11608687/58f1c0061103/medi-103-e40478-g004.jpg

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本文引用的文献

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Separating the effects of life course adiposity on diabetic nephropathy: a comprehensive multivariable Mendelian randomization study. 分离生命历程肥胖对糖尿病肾病的影响:综合多变量孟德尔随机化研究。
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Circulating levels of cytokines and risk of inflammatory bowel disease: evidence from genetic data.
细胞因子循环水平与炎症性肠病风险:来自遗传数据的证据。
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The role of the gastrointestinal barrier in obesity-associated systemic inflammation.胃肠道屏障在肥胖相关系统性炎症中的作用。
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Does cardiovascular risk matter in IBD patients?炎症性肠病患者的心血管风险重要吗?
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Disruption of CerS6-mediated sphingolipid metabolism by FTO deficiency aggravates ulcerative colitis.FTO缺乏导致的CerS6介导的鞘脂代谢紊乱会加重溃疡性结肠炎。
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