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Association of metabolic dysfunction-associated fatty liver disease, type 2 diabetes mellitus, and metabolic goal achievement with risk of chronic kidney disease

Bibliographic Data

ID22091014
AuthorsWeitao Su (0000-0002-7831-1955, Fujian Medical University), Minhui Chen (0000-0001-5684-2504), Ling Xiao (0000-0003-0199-5137, Fujian Medical University), Shanshan Du (0009-0003-2340-9394, Fujian Medical University), Lihua Xue (0000-0002-8293-6771), Ruimei Feng (0000-0001-8020-2654, Fujian Medical University), Weimin Ye (0000-0002-6859-4648, Fujian Medical University, corresponding author)
Year2022
Volume10
Pages1047794-1047794
Publication date2022-11-07
Open AccessYes
TypeARTICLE
VenueFrontiers in Public Health (JOURNAL)
Journal identifiersISSN: 2296-2565 • E-ISSN: 2296-2565
PublisherFrontiers Media SA (PUBLISHER • CH)
DOI10.3389/fpubh.2022.1047794
PMID36420005
OpenAlexW4308452510
LanguageEN
Citations received1
References cited41

Background Although type 2 diabetes mellitus (T2DM) plays a significant role in the association between metabolic dysfunction-associated fatty liver disease (MAFLD) and chronic kidney disease (CKD), how T2DM development and glycemic deterioration affect CKD and its renal function indicators, estimated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio (UACR), remains unknown. We aimed to assess the association between MAFLD, along with T2DM, and risk of CKD, and then evaluate the effect of metabolic goal achievement in MAFLD on the risk of CKD. Methods In this cross-sectional study, 5,594 participants were included. Multivariate logistic regression and linear regression were used to examine the association between MAFLD with its T2DM status and metabolic goal achievement and risk of CKD, as well as eGFR and UACR. Results The MAFLD group had a higher prevalence of CKD (16.2 vs. 7.6%, P < 0.001) than the non-MAFLD group. MAFLD was independently associated with an increased risk of CKD (odds ratio [OR]: 1.35, 95% CI: 1.09–1.67) and increased eGFR and UACR. Among the three MAFLD subtypes, only the T2DM subtype exhibited significant associations with increased risk of CKD (OR: 2.85, 95% CI: 2.24–3.63), as well as increased eGFR and UACR. Glycemic deterioration in MAFLD was dose-dependently associated with an increased risk of CKD ( P -trend < 0.001). Achieved metabolic goals in MAFLD decreased the risk of CKD, eGFR, and UACR; MAFLD with 2 or 3 achieved metabolic goals was not significantly associated with the risk of CKD (OR: 0.81, 95% CI: 0.59–1.12) and albuminuria. Conclusion MAFLD was independently associated with an increased risk of CKD, as well as increased eGFR and UACR. This association is strongly driven by T2DM status. Glycemic deterioration in MAFLD was dose-dependently associated with an increased risk of CKD. Achieved metabolic goals in MAFLD decreased the risk of CKD by reducing the risk of albuminuria

Albuminuria · Creatinine · Diabetes mellitus · Disease · Fatty liver · Glycemic · Insulin resistance · Kidney disease · Odds ratio · Renal function · Type 2 diabetes · Type 2 Diabetes Mellitus · Chronic Kidney Disease and Diabetes · Diabetes, Cardiovascular Risks, and Lipoproteins · Liver Disease Diagnosis and Treatment · Medicine · Endocrinology · Internal Medicine

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    Open Access•Emmanuel Ekpor, Samuel Akyirem et al.•PLOS Global Public Health•2024

  • Standards of Medical Care in Diabetes—2011

    Open Access•American Diabetes Association•Diabetes Care•2011

  • Prevalence of chronic kidney disease in China

    Open Access•Luxia Zhang, Fang Wang et al.•The Lancet•2012

  • Analysis of the Global Burden of Disease study highlights the global, regional, and national trends of chronic kidney disease epidemiology from 1990 to 2016

    Open Access•Yan Xie, Benjamin Bowe et al.•Kidney International•2018

  • A New Equation to Estimate Glomerular Filtration Rate

    Open Access•Andrew S Levey, Lesley A Stevens et al.•Annals of Internal Medicine•2009

Citations per year0.5
Citation span2024 - 2024 (1)
Highly citedNo

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