Relationship of liver fat content with systemic metabolism and chronic complications in patients with type 2 diabetes mellitus
- PMID: 36694216
- PMCID: PMC9872378
- DOI: 10.1186/s12944-023-01775-6
Relationship of liver fat content with systemic metabolism and chronic complications in patients with type 2 diabetes mellitus
Abstract
Objective: This study investigated the correlation of liver fat content (LFC) with metabolic characteristics and its association with chronic complications in type 2 diabetes mellitus (T2DM) patients.
Methods: Eighty-one prospectively enrolled T2DM patients were divided into non-alcoholic fatty liver disease (NAFLD) group and the non-NAFLD group according to the presence of NAFL complications. LFC was determined by MRI IDEAL-IQ Sequence, and patients were divided into 4 groups according to LFC by quartile method. Basic information, metabolic indexes, and occurrence of chronic complications in different groups were analyzed and compared.
Results: BMI, SBP, DBP, TG, ALT, AST, GGT, UA, HbA1c, FCP, 2 h CP, HOMA-IR, and HOMA-IS in the NAFLD group were significantly higher than the non-NAFLD group (P < 0.05). The incidences of chronic complications in the NAFLD group were higher than in the non-NAFLD group but not statistically significant (P > 0.05). BMI, SBP, DBP, TC, TG, ALT, AST, FCP, 2 h CP, HOMA-IR, and HOMA-IS showed significant differences between the patients with different LFC, and these indexes were significantly higher in patients with higher LFC than those with lower LFC (P < 0.05). Moreover, diabetes duration, TC, HOMA-IR, and LFC were the risk factors for ASCVD complications, while diabetes duration, TG, and LDL-C were risk factors for DN complications. Also, diabetes duration and SBP were risk factors for both DR and DPN complications in T2DM patients (P < 0.05).
Conclusion: LFC is positively correlated with the severity of the systemic metabolic disorder and chronic complications in T2DM patients.
Keywords: Chronic complications; IDEAL-IQ; Liver fat content; Metabolic disorder; Type 2 diabetes mellitus.
© 2023. The Author(s).
Conflict of interest statement
All authors declare that there are no conflicts of interest.
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