Interaction Between PNPLA3 and SIRT5 Genetic Variants in Association with Liver Fibrosis Severity in Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease

• Published in: Genes Vol. 15; no. 11; p. 1370
• Main Authors: Moonlisarn, Kamonchanok, Somnark, Pornjira, Boonkaew, Bootsakorn, Bunchorntavakul, Chalermarat, Tangkijvanich, Pisit
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.11.2024; MDPI
• Subjects: 17-Hydroxysteroid Dehydrogenases - genetics; Acyltransferases; Adult; Aged; Care and treatment; Development and progression; Diagnostic imaging; Fatty liver; Fatty Liver - genetics; Fatty Liver - pathology; Female; Females; Fibrosis; Gene polymorphism; Genes; Genetic aspects; Genetic diversity; Genetic polymorphisms; Genetic Predisposition to Disease; Genotype; Genotype & phenotype; Hepatitis; Humans; Hypertension; Lipase - genetics; Liver cancer; Liver cirrhosis; Liver Cirrhosis - genetics; Liver Cirrhosis - pathology; Liver diseases; Magnetic resonance imaging; Male; Membrane Proteins - genetics; Metabolic disorders; Middle Aged; Multivariate analysis; Phospholipases A2, Calcium-Independent; Polymorphism, Single Nucleotide; Population genetics; Severity of Illness Index; Sirtuins - genetics; Steatosis; Type 2 diabetes; Thailand; United States > US; metabolic dysfunction-associated steatotic liver disease (MASLD); SIRT5 rs12216101; fibrosis; HSD17B13 rs6834314; PNPLA3 rs738409; polymorphisms; steatosis
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes15111370

Background/Objectives: This study evaluated the association between polymorphisms in the PNPLA3, TM6SF2, HSD17B13, and SIRT5 genes and the severity of fibrosis and steatosis in metabolic dysfunction-associated steatotic liver disease (MASLD). Methods: Fibrosis and steatosis were assessed by MRE and MRI-PDFF, respectively. The polymorphisms were determined by allelic discrimination in blood samples. Results: 204 patients aged 57.0 ± 13.5 years were included. Sixty-two (30.4%) patients had significant fibrosis (≥F2). Among F2–F4 fibrosis, the PNPLA3 rs738409 GG genotype was significantly higher than the CC + CG genotypes (44.9% vs. 21.4%, p = 0.001). The SIRT5 rs12216101 GG vs. TT + TG genotypes also exhibited a similar trend (64.3% vs. 27.9%, p = 0.012). In multivariate analysis, the PNPLA3 GG genotype (OR = 3.48, 95%CI: 1.50–8.06; p = 0.004) and SIRT5 rs12216101 GG genotype (OR = 5.43, 95%CI: 1.32–22.33; p = 0.019) were independently associated with F2–F4 fibrosis. Additionally, the proportion of patients with F2–F4 fibrosis significantly increased with the number of combined risk genotypes. Among S2–S3 steatosis, the prevalence of HSD17B13 AG + GG genotypes was higher than that of the AA genotype (37.5% vs. 23.9%, p = 0.048) and independently associated with moderate/severe steatosis in multivariate analysis (OR = 2.26, 95%CI: 1.14–4.49; p = 0.020). Conclusions: Our data indicate that the PNPLA3 and SIRT5 polymorphisms were independently and additively linked to significant fibrosis, while the HSD17B13 polymorphism was associated with increased steatosis in Thai populations. These data might emphasize the importance of genetic variants in progressive MASLD.