Gastro Hep Advances (Jan 2024)

Polymorphisms Associated With Metabolic Dysfunction-Associated Steatotic Liver Disease Influence the Progression of End-Stage Liver Disease

  • Zehra N. Kocas-Kilicarslan,
  • Zeliha Cetin,
  • Lanuza A.P. Faccioli,
  • Takashi Motomura,
  • Sriram Amirneni,
  • Ricardo Diaz-Aragon,
  • Rodrigo M. Florentino,
  • Yiyue Sun,
  • Iris Pla-Palacin,
  • Mengying Xia,
  • Mark T. Miedel,
  • Takeshi Kurihara,
  • Zhiping Hu,
  • Alina Ostrowska,
  • Zi Wang,
  • Robert Constantine,
  • Albert Li,
  • D. Lansing Taylor,
  • Jaideep Behari,
  • Alejandro Soto-Gutierrez,
  • Edgar N. Tafaleng

Journal volume & issue
Vol. 3, no. 1
pp. 67 – 77

Abstract

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Background and Aims: Chronic liver injury that results in cirrhosis and end-stage liver disease (ESLD) causes more than 1 million deaths annually worldwide. Although the impact of genetic factors on the severity of metabolic dysfunction-associated steatotic liver disease (MASLD) and alcohol-related liver disease (ALD) has been previously studied, their contribution to the development of ESLD remains largely unexplored. Methods: We genotyped 6 MASLD-associated polymorphisms in healthy (n = 123), metabolic dysfunction-associated steatohepatitis (MASH) (n = 145), MASLD-associated ESLD (n = 72), and ALD-associated ESLD (n = 57) cohorts and performed multinomial logistic regression to determine the combined contribution of genetic, demographic, and clinical factors to the progression of ESLD. Results: Distinct sets of factors are associated with the progression to ESLD. The PNPLA3 rs738409:G and TM6SF2 rs58542926:T alleles, body mass index (BMI), age, and female sex were positively associated with progression from a healthy state to MASH. The PNPLA3 rs738409:G allele, age, male sex, and having type 2 diabetes mellitus were positively associated, while BMI was negatively associated with progression from MASH to MASLD-associated ESLD. The PNPLA3 rs738409:G and GCKR rs780094:T alleles, age, and male sex were positively associated, while BMI was negatively associated with progression from a healthy state to ALD-associated ESLD. The findings indicate that the PNPLA3 rs738409:G allele increases susceptibility to ESLD regardless of etiology, the TM6SF2 rs58542926:T allele increases susceptibility to MASH, and the GCKR rs780094:T allele increases susceptibility to ALD-associated ESLD. Conclusion: The PNPLA3, TM6SF2, and GCKR minor alleles influence the progression of MASLD-associated or ALD-associated ESLD. Genotyping for these variants in MASLD and ALD patients can enhance risk assessment, prompting early interventions to prevent ESLD.

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