Yang Song, Jian Jun, Zhao Xiaojie, Wang Lei, Chen Zhiyuan, Liu Xiuheng
Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China; Institute of Urologic Disease, Renmin Hospital of Wuhan University, Wuhan, China.
J Cancer. 2024 Oct 21;15(20):6521-6530. doi: 10.7150/jca.100152. eCollection 2024.
Previous studies have indicated that there is an association between obesity and bladder cancer (BCa). However, the relationship between fat distribution, which is more representative of the risk of obesity, and BCa remains unclear. This study aimed to investigate the causal relationship between fat distribution and BCa, and the mediating role of circulating metabolites. The necessary data were obtained from a large Genome-Wide Association Studies (GWAS) database. Two-sample and two-step Mendelian randomization (MR) analyses were performed to investigate the association between fat distribution and BCa, as well as the mediating effect of circulating metabolites. The inverse variance weighted (IVW) method was the main analysis method. Heterogeneity tests, horizontal pleiotropy analyses, Mendelian randomization pleiotropy residual sum and outlier (MR-PRESSO) tests, and leave-one-out analyses were performed to assess the stability of the results. The IVW method indicated that abdominal subcutaneous adipose tissue adjusted for body mass index (BMI) and height (ASATadj) and abdominal subcutaneous/gluteofemoral adipose tissue (ASAT/GFAT) increased the risk of BCa. The odds ratio (OR) for ASATadj was 1.78 (95% CI=1.27-2.50, p=0.001) and that for ASAT/GFAT was 1.64 (95% CI=1.01-2.66, p=0.047). Furthermore, two-step MR analysis revealed that the effect of ASAT/GFAT on BCa was mediated by valine (proportion mediated: 7.13%, 95% CI = 3.57%-10.69%, p=0.045). Our research shows that, unlike most studies which focus on visceral fat, ASAT also impacts human health by increasing the risk of BCa, with the blood metabolite valine involved in this process. Monitoring and reducing ASAT accumulation can help reducce the disease burden of BCa.
以往的研究表明,肥胖与膀胱癌(BCa)之间存在关联。然而,更能代表肥胖风险的脂肪分布与BCa之间的关系仍不明确。本研究旨在探讨脂肪分布与BCa之间的因果关系以及循环代谢物的中介作用。必要的数据来自一个大型全基因组关联研究(GWAS)数据库。进行了两样本和两步孟德尔随机化(MR)分析,以研究脂肪分布与BCa之间的关联以及循环代谢物的中介作用。逆方差加权(IVW)方法是主要的分析方法。进行了异质性检验、水平多效性分析、孟德尔随机化多效性残差和离群值(MR-PRESSO)检验以及留一法分析,以评估结果的稳定性。IVW方法表明,调整体重指数(BMI)和身高后的腹部皮下脂肪组织(ASATadj)以及腹部皮下/臀股脂肪组织(ASAT/GFAT)会增加BCa的风险。ASATadj的比值比(OR)为1.78(95%CI=1.27-2.50,p=0.001),ASAT/GFAT的比值比为1.64(95%CI=1.01-2.66,p=0.047)。此外,两步MR分析显示,ASAT/GFAT对BCa的影响由缬氨酸介导(介导比例:7.13%,95%CI = 3.57%-10.69%,p=0.045)。我们的研究表明,与大多数关注内脏脂肪的研究不同,ASAT也会通过增加BCa风险来影响人类健康,血液代谢物缬氨酸参与了这一过程。监测和减少ASAT的积累有助于减轻BCa的疾病负担。