MARC1 p.A165T variant is associated with decreased markers of liver injury and enhanced antioxidant capacity in autoimmune hepatitis

• Published in: Scientific reports Vol. 11; no. 1; p. 24407
• Main Authors: Janik, Maciej K., Smyk, Wiktor, Kruk, Beata, Szczepankiewicz, Benedykt, Górnicka, Barbara, Lebiedzińska-Arciszewska, Magdalena, Potes, Yaiza, Simões, Inês C. M., Weber, Susanne N., Lammert, Frank, Więckowski, Mariusz R., Milkiewicz, Piotr, Krawczyk, Marcin
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.12.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/208; 692/4020/4021; Adolescent; Adult; Aged; Antioxidants; Antioxidants - metabolism; Catalase; Child; Fatty liver; Female; Gene polymorphism; Genetic diversity; Genetic Predisposition to Disease - genetics; Genetic variance; Genome-Wide Association Study; Genotype; Genotyping; Hepatitis; Hepatitis, Autoimmune - complications; Hepatitis, Autoimmune - genetics; Hepatitis, Autoimmune - metabolism; Hepatitis, Autoimmune - prevention & control; Humanities and Social Sciences; Humans; Liver cancer; Liver Cirrhosis - etiology; Liver Cirrhosis - genetics; Liver Cirrhosis - metabolism; Liver Cirrhosis - prevention & control; Male; Middle Aged; Mitochondria; Mitochondrial Proteins - genetics; multidisciplinary; Oxidoreductases - genetics; Patients; Phenotype; Phenotypes; Polymorphism, Genetic - genetics; Polymorphism, Genetic - physiology; Science; Science (multidisciplinary); Transplantation; Young Adult
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-03521-3

The clinical picture of autoimmune hepatitis (AIH) varies markedly between patients, potentially due to genetic modifiers. The aim of this study was to evaluate genetic variants previously associated with fatty liver as potential modulators of the AIH phenotype. The study cohort comprised 313 non-transplanted adults with AIH. In all patients, the MARC1 (rs2642438), HSD17B13 (rs72613567), PNPLA3 (rs738409), TM6SF2 (rs58542926), and MBOAT7 (rs641738) variants were genotyped using TaqMan assays. Mitochondrial damage markers in serum were analyzed in relation to the MARC1 variant. Carriers of the protective MARC1 allele had lower ALT and AST (both P < 0.05). In patients treated for AIH for ≥ 6 months, MARC1 correlated with reduced AST, ALP, GGT (all P ≤ 0.01), and lower APRI (P = 0.02). Patients carrying the protective MARC1 genotype had higher total antioxidant activity (P < 0.01) and catalase levels (P = 0.02) in serum. The PNPLA3 risk variant was associated with higher MELD (P = 0.02) in treated patients, whereas MBOAT7 increased the odds for liver cancer (OR = 3.71). None of the variants modulated the risk of death or transplantation. In conclusion, the MARC1 polymorphism has protective effects in AIH. Genotyping of MARC1 , PNPLA3, and MBOAT7 polymorphisms might help to stratify patients with AIH.