Metabolic dysfunction-associated fatty liver disease increases risk of chronic kidney disease: a systematic review and meta-analysis

Jianghua Zhou, Dan-Qin Sun, Giovanni Targher, Christopher D Byrne, Byung-wan Lee, Masahide Hamaguchi, Seung Up Kim, Xuhong Hou, Gian Paolo Fadini, Michio Shimabukuro, Masato Furuhashi, Ning-Jian Wang, Herbert Tilg, Ming-Hua Zheng
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Abstract

Background and aim Metabolic dysfunction-associated fatty liver disease (MAFLD) is an alternative description and classification of non-alcoholic fatty liver disease (NAFLD) that may have better utility than NAFLD in clinical practice. We performed a meta-analysis to quantify the magnitude of the association between MAFLD and risk of both prevalent and incident chronic kidney disease (CKD). Methods We systematically searched PubMed, Medline (OVID), Embase (OVID), Web of Science and Cochrane Library from database inception until 29 May 2022. We included observational studies examining the association between MAFLD and risk of CKD, defined by estimated glomerular filtration rate ≤60 mL/min/1.73 m 2 or presence of abnormal albuminuria. Meta-analysis was performed using random-effects models to obtain summary HRs or ORs with 95% CIs. Results Seventeen observational studies with aggregate data on 845 753 participants were included in meta-analysis. In the 7 cohort studies, the pooled random-effects HR for incident CKD in patients with MAFLD was 1.29 (95% CI 1.17 to 1.41, I 2 =87.0%). In the 10 cross-sectional studies, the pooled random-effects OR for prevalent CKD in patients with MAFLD was 1.35 (95% CI 1.11 to 1.64, I 2 =92.6%). Conclusion MAFLD is significantly associated with an increased prevalence and incidence of CKD. PROSPERO registration number CRD42022352366.
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代谢功能障碍相关的脂肪性肝病增加慢性肾脏疾病的风险:一项系统综述和荟萃分析
背景和目的代谢功能障碍相关脂肪性肝病(MAFLD)是非酒精性脂肪性肝病(NAFLD)的另一种描述和分类,在临床实践中可能比NAFLD有更好的效用。我们进行了一项荟萃分析,以量化MAFLD与流行和突发慢性肾脏疾病(CKD)风险之间的关联程度。方法系统检索PubMed、Medline (OVID)、Embase (OVID)、Web of Science和Cochrane Library从建库到2022年5月29日的数据库。我们纳入了观察性研究,以肾小球滤过率≤60ml /min/1.73 m2或存在异常蛋白尿来确定MAFLD与CKD风险之间的关系。采用随机效应模型进行meta分析,获得95% ci的总hr或or。meta分析纳入17项观察性研究,共纳入845753名受试者。在这7项队列研究中,MAFLD患者发生CKD的随机效应HR为1.29 (95% CI 1.17 ~ 1.41, i2 =87.0%)。在10项横断面研究中,MAFLD患者中流行CKD的合并随机效应OR为1.35 (95% CI 1.11至1.64,i2 =92.6%)。结论MAFLD与CKD患病率和发病率增高有显著相关性。普洛斯彼罗注册号CRD42022352366。
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