Prevalence of Metabolic Dysfunction–Associated Fatty Liver Disease Among Patients With Diabetic Kidney Disease: A Systematic Review and Meta-Analysis Publisher



Rahmanian M¹ ; Deravi N¹ ; Poudineh M² ; Poopak A³ ; Mirmohammadali SN⁴ ; Fekrvand S⁶ ; Tadbir K⁶ ; Ebrahimian S⁷ ; Zargarzadeh N⁶ ; Pirzadeh M⁷ ; Abdi A⁸ ; Firouzabadi FD⁹ ; Mechanick JI¹⁰
Source: Egyptian Liver Journal Published:2024

Abstract

Background: Mechanistic relationships between metabolic dysfunction–associated fatty liver disease (MAFLD) and chronic kidney disease are well characterized. Specifically, in type 2 diabetes (T2D), insulin resistance leads to MAFLD, and hyperglycemia leads to microvascular complications such as diabetic kidney disease (DKD). This systematic review and meta-analysis aims to describe the specific association between MAFLD and DKD for the first time. Methods: PubMed, Web of Science, Google Scholar, and Scopus databases were searched up to February 2023 to identify relevant published articles. After screening the titles, abstracts, and full texts of the retrieved articles, cross-sectional studies and cohorts reporting on MAFLD in patients with DKD were identified and then analyzed. Results: A total of 2615 articles were identified, of which 5 had sufficient data and fulfilled the eligibility criteria for meta-analysis. A total of 2345 patients with DKD were in the included studies. The prevalence rates of radiologically diagnosed MAFLD among patients with DKD ranged from 25 to 96%. The pooled prevalence rate of radiologically diagnosed MAFLD among patients with DKD was 0.55 (95% CI = 0.21–0.89, I2 = 99.79%, P-value < 0.01). Conclusion: MAFLD is prevalent in patients with DKD. This finding emphasizes the need for aggressive case finding and then guideline-directed medical therapy of MAFLD, especially in patients with T2D and DKD to prevent further complications. Future studies should investigate mechanisms underpinning MAFLD and DKD in patients with T2D, especially in the context of cardiometabolic risk. © The Author(s) 2024.