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MAFLD 和 NAFLD 对预测慢性肾脏病的发生。

MAFLD and NAFLD in the prediction of incident chronic kidney disease.

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon‑ro, Gangnam‑gu, Seoul, 06351, Republic of Korea.

Division of Endocrine and Metabolism, Department of Internal Medicine, CHA Bundang Medical Center, CHA University School of Medicine, 59 Yatap-ro, Bundang-gu, Seongnam, Gyeonggi-do, 14396, Republic of Korea.

出版信息

Sci Rep. 2023 Jan 31;13(1):1796. doi: 10.1038/s41598-023-27762-6.

Abstract

Whether metabolic dysfunction-associated fatty liver disease (MAFLD) can replace nonalcoholic fatty liver disease (NAFLD) is under debate. This study evaluated which definition better predicted incident chronic kidney disease (CKD). This was a 5.3-year (range, 2.8-8.3) retrospective cohort study of 21,713 adults who underwent at least two serial health examinations. Cox analyses were used to compare the risk of incident CKD among non-fatty liver disease (FLD) without metabolic dysregulation (MD; reference), non-FLD with MD, MAFLD-only, NAFLD-only, or both-FLD groups. Non-FLD with MD group (hazard ratio [HR] 1.23, 95% confidence interval [CI] 1.00-1.53), both-FLD group (HR 1.50, 95% CI 1.19-1.89), and MAFLD-only group (HR 1.97, 95% CI 1.49-2.60), but not NAFLD-only group (HR 1.06, 95% CI 0.63-1.79) demonstrated an increased risk of CKD. The increased risk of CKD was significant in MAFLD subgroups with overweight/obesity (HR 2.94, 95% CI 1.91-4.55), diabetes (HR 2.20, 95% CI 1.67-2.90), MD only (HR 1.50, 95% CI 1.19-1.89), excessive alcohol consumption (HR 2.71, 95% CI 2.11-3.47), and viral hepatitis (HR 2.38, 95% CI 1.48-3.84). The switch from NAFLD to MAFLD criteria may identify a greater number of individuals at CKD risk. The association was also significant in MAFLD patients with excessive alcohol consumption or viral hepatitis.

摘要

代谢相关脂肪性肝病(MAFLD)是否可以替代非酒精性脂肪性肝病(NAFLD)仍存在争议。本研究评估了哪种定义能更好地预测慢性肾脏病(CKD)的发生。这是一项对 21713 名至少进行过两次连续健康检查的成年人进行的 5.3 年(范围 2.8-8.3 年)回顾性队列研究。Cox 分析用于比较非脂肪性肝病(FLD)无代谢失调(MD;参考)、非 FLD 伴 MD、MAFLD 仅、NAFLD 仅或 FLD 两者均有的各组中发生 CKD 的风险。非 FLD 伴 MD 组(危险比 [HR]1.23,95%置信区间 [CI]1.00-1.53)、FLD 两者均有组(HR1.50,95%CI1.19-1.89)和 MAFLD 仅组(HR1.97,95%CI1.49-2.60),但不是 NAFLD 仅组(HR1.06,95%CI0.63-1.79),显示 CKD 风险增加。在超重/肥胖(HR2.94,95%CI1.91-4.55)、糖尿病(HR2.20,95%CI1.67-2.90)、MD 仅(HR1.50,95%CI1.19-1.89)、过度饮酒(HR2.71,95%CI2.11-3.47)和病毒性肝炎(HR2.38,95%CI1.48-3.84)的 MAFLD 亚组中,这种 CKD 风险增加具有统计学意义。从 NAFLD 向 MAFLD 标准的转变可能会识别出更多处于 CKD 风险中的个体。这种关联在 MAFLD 患者中也具有统计学意义,这些患者存在过度饮酒或病毒性肝炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6615/9889784/77051c6b0c86/41598_2023_27762_Fig1_HTML.jpg

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