Su Qiang, Li Jian, Lu Yun, Wu Min, Liang Jiang, An Zhenxiang
The First Clinical Medical College of Guizhou University of Traditional Chinese Medicine, Guiyang, China.
The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang, China.
Front Nutr. 2024 Jul 10;11:1400713. doi: 10.3389/fnut.2024.1400713. eCollection 2024.
Evidence for anorexia and bulimia in relation to the risk of ulcerative colitis (UC) is limited and inconsistent. The objective of this research was to utilize bi-directional, two-sample Mendelian randomization (MR) analysis to predict the causal association between anorexia nervosa and bulimia nervosa with UC.
The genome-wide association studies (GWAS) provided data for anorexia and bulimia from the UK Biobank, utilizing single-nucleotide polymorphisms (SNP) as instrumental variables. Additionally, genetic associations with UC were collected from various sources including the FinnGen Biobank, the UK Biobank and the International Inflammatory Bowel Disease Genetics Consortium (IIBDGC). The main analytical approach utilized in this study was the inverse-variance-weighted (IVW) method. To evaluate horizontal pleiotropy, the researchers conducted MR-Egger regression and MR-PRESSO global test analyses. Additionally, heterogeneity was assessed using the Cochran's test.
This study found a negative association between genetically predicted bulimia (OR = 0.943, 95% CI: 0.893-0.996; = 0.034) and the risk of UC in the IIBDGC dataset, indicating that individuals with bulimia have approximately a 5.7% lower risk of developing UC. No association was observed in the other two datasets. Conversely, genetically predicted anorexia was not found to be causally associated with UC. In bi-directional Mendelian randomization, UC from the IIBDGC dataset was negatively associated with the risk of anorexia (OR = 0.877, 95% CI: 0.797-0.965; = 0.007), suggesting that UC patients have approximately a 12.3% lower risk of developing anorexia, but not causally associated with bulimia.
Genetically predicted bulimia may have a negative association with the onset of UC, while genetically predicted anorexia does not show a causal relationship with the development of UC. Conversely, genetically predicted UC may have a negative association with the development of anorexia.
关于神经性厌食症和神经性贪食症与溃疡性结肠炎(UC)风险之间关系的证据有限且不一致。本研究的目的是利用双向双样本孟德尔随机化(MR)分析来预测神经性厌食症和神经性贪食症与UC之间的因果关系。
全基因组关联研究(GWAS)提供了来自英国生物银行的神经性厌食症和神经性贪食症的数据,使用单核苷酸多态性(SNP)作为工具变量。此外,从包括芬兰生物银行、英国生物银行和国际炎症性肠病遗传学联盟(IIBDGC)等各种来源收集了与UC的遗传关联数据。本研究使用的主要分析方法是逆方差加权(IVW)方法。为了评估水平多效性,研究人员进行了MR-Egger回归和MR-PRESSO全局检验分析。此外,使用 Cochr an检验评估异质性。
本研究在IIBDGC数据集中发现遗传预测的神经性贪食症与UC风险之间存在负相关(OR = 0.943,95% CI:0.893 - 0.996;P = 0.034),表明患有神经性贪食症的个体患UC的风险大约低5.7%。在其他两个数据集中未观察到关联。相反,未发现遗传预测的神经性厌食症与UC存在因果关系。在双向孟德尔随机化中,IIBDGC数据集的UC与神经性厌食症风险呈负相关(OR = 0.877,95% CI:0.797 - 0.965;P = 0.007),表明UC患者患神经性厌食症的风险大约低12.3%,但与神经性贪食症无因果关系。
遗传预测的神经性贪食症可能与UC的发病呈负相关,而遗传预测的神经性厌食症与UC的发展未显示出因果关系。相反,遗传预测的UC可能与神经性厌食症的发展呈负相关。