Wu Ruicheng, Luo Peiyi, Luo Min, Li Xiaoyu, Zhong Xin, He Qiang, Zhang Jie, Zhang Yangchang, Xiong Yang, Han Ping
Department of Urology, West China Hospital, Sichuan University, Chengdu, China.
Department of Nephrology, West China Hospital of Sichuan University, Chengdu, China.
Front Genet. 2022 Jul 26;13:920510. doi: 10.3389/fgene.2022.920510. eCollection 2022.
It is not clarified whether the elevation of adiponectin is the results of kidney damage, or the cause of kidney function injury. To explore the causal association of adiponectin on estimated glomerular filtration rate (eGFR) and chronic kidney disease (CKD), this study was performed. The genetic association of adiponectin were retrieved from one genome-wide association studies with 39,883 participants. The summary-level statistics regarding the eGFR (133,413 participants) and CKD (12,385 CKD cases and 104,780 controls) were retrieved from the CKDGen consortium in the European ancestry. Single-variable Mendelian randomization (MR), bilateral and multivariable MR analyses were used to verify the causal association between adiponectin, eGFR, and CKD. Genetically predicted adiponectin reduces the risk of CKD (OR = 0.71, 95% CI = 0.57-0.89, = 0.002) and increases the eGFR ( = 0.014, 95% CI = 0.001-0.026, = 0.034) by the inverse variance weighting (IVW) estimator. These findings remain consistent in the sensitivity analyses. No heterogeneity and pleiotropy were detected in this study ( for MR-Egger 0.617, for global test > 0.05, and for Cochran's Q statistics = 0.617). The bilateral MR identified no causal association of CKD on adiponectin (OR = 1.01, 95% CI = 0.96-1.07, = 0.658), nor did it support the association of eGFR on adiponectin (OR = 0.86, 95% CI = 0.68-1.09, = 0.207) by the IVW estimator. All the sensitivity analyses reported similar findings ( > 0.05). Additionally, after adjusting for cigarette consumption, alcohol consumption, body mass index, low density lipoprotein, and total cholesterol, the ORs for CKD are 0.70 (95% CI = 0.55-0.90, = 0.005), 0.75 (95% CI = 0.58-0.97, = 0.027), 0.82 (95% CI = 0.68-0.99, = 0.039), 0.74 (95% CI = 0.59-0.93, = 0.011), and 0.79 (95% CI = 0.61-0.95, = 0.018), respectively. : Using genetic data, this study provides novel causal evidence that adiponectin can protect the kidney function and further reduce the risk of CKD.
脂联素升高是肾脏损伤的结果还是肾功能损害的原因尚不清楚。为了探究脂联素与估计肾小球滤过率(eGFR)和慢性肾脏病(CKD)之间的因果关系,进行了本研究。从一项有39883名参与者的全基因组关联研究中获取脂联素的基因关联数据。关于eGFR(133413名参与者)和CKD(12385例CKD病例和104780名对照)的汇总统计数据来自欧洲血统的CKDGen联盟。采用单变量孟德尔随机化(MR)、双向和多变量MR分析来验证脂联素、eGFR和CKD之间的因果关系。通过逆方差加权(IVW)估计器,基因预测的脂联素可降低CKD风险(OR = 0.71,95%CI = 0.57 - 0.89,P = 0.002)并增加eGFR(P = 0.014,95%CI = 0.001 - 0.026,P = 0.034)。这些发现在敏感性分析中保持一致。本研究未检测到异质性和多效性(MR - Egger的P = 0.617,全局检验的P > 0.05,Cochran's Q统计量的P = 0.617)。双向MR未发现CKD与脂联素之间的因果关系(OR = 1.01,95%CI = 0.96 - 1.07,P = 0.658),也不支持IVW估计器得出的eGFR与脂联素之间的关联(OR = 0.86,95%CI = 0.68 - 1.09,P = 0.207)。所有敏感性分析均报告了相似的结果(P > 0.05)。此外,在调整吸烟、饮酒、体重指数、低密度脂蛋白和总胆固醇后,CKD的OR分别为0.70(95%CI = 0.55 - 0.90,P = 0.005)、0.75(95%CI = 0.58 - 0.97,P = 0.027)、0.82(95%CI = 0.68 - 0.99,P = 0.039)、0.74(95%CI = 0.59 - 0.93,P = 0.011)和0.79(95%CI = 0.61 - 0.95,P = 0.018)。结论:本研究利用基因数据提供了新的因果证据,表明脂联素可保护肾功能并进一步降低CKD风险。