Impact of PNPLA3 rs738409 Polymorphism on the Development of Liver-Related Events in Patients With Nonalcoholic Fatty Liver Disease

被引:25
|
作者
Rosso, Chiara [1 ]
Caviglia, Gian Paolo [1 ]
Birolo, Giovanni [1 ]
Armandi, Angelo [1 ,2 ]
Pennisi, Grazia [3 ]
Pelusi, Serena [4 ]
Younes, Ramy [5 ]
Liguori, Antonio [6 ]
Perez-Diaz-del-Campo, Nuria [1 ]
Nicolosi, Aurora [1 ]
Govaere, Olivier [7 ]
Castelnuovo, Gabriele [1 ]
Olivero, Antonella [1 ]
Abate, Maria Lorena [1 ]
Ribaldone, Davide Giuseppe [1 ]
Fariselli, Piero [1 ]
Valenti, Luca [4 ]
Miele, Luca [6 ,8 ,9 ]
Petta, Salvatore [3 ]
Romero-Gomez, Manuel [10 ,11 ]
Anstee, Quentin M. [7 ,12 ]
Bugianesi, Elisabetta [1 ,13 ]
机构
[1] Univ Turin, Dept Med Sci, Div Gastroenterol & Hepatol, Turin, Italy
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Med 1, Metab Liver Dis Res Program, Mainz, Germany
[3] Univ Palermo, Sez Gastroenterol, PROMISE, Palermo, Italy
[4] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Transfus Med, Precis Med, Milan, Italy
[5] Boehringer Ingelheim Int GmbH, Ingelheim, Germany
[6] Univ Cattolica Sacro Cuore, Dipartimento Univ Med & Chirurg Traslaz, Rome, Italy
[7] Newcastle Univ, Newcastle Liver Res Grp, Translat & Clin Res Inst, Fac Med Sci, Newcastle Upon Tyne, England
[8] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy
[9] Fdn Policlin Gemelli IRCCS, Dipartimento Sci Med & Chirurg, Rome, Italy
[10] Univ Seville, Virgen del Rocio Univ Hosp, Inst Biomed Seville, UCM Digest Dis, Seville, Spain
[11] Univ Seville, Virgen del Rocio Univ Hosp, Inst Biomed Seville, SeLiver Grp, Seville, Spain
[12] Newcastle Tyne Hosp NHS Trust, Newcastle NIHR Biomed Res Ctr, Newcastle Upon Tyne, England
[13] Univ Turin, Dept Med Sci, Div Gastroenterol & Hepatol, AO Cittadella Salute & Sci Torino, Corso Dogliotti 14, I-10126 Turin, Italy
基金
欧盟地平线“2020”;
关键词
NAFLD; NASH; PNPLA3; Liver-Related Outcomes; SCORING SYSTEM; RISK; CONFERS; SCORES;
D O I
10.1016/j.cgh.2023.04.024
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND AND AIMS: Nonalcoholic fatty liver disease (NAFLD) is a complex disease, resulting from the interplay between environmental determinants and genetic variations. Single nucleotide polymorphism rs738409 C>G in the PNPLA3 gene is associated with hepatic fibrosis and with higher risk of developing hepatocellular carcinoma. Here, we analyzed a longitudinal cohort of biopsy-proven NAFLD subjects with the aim to identify individuals in whom genetics may have a stronger impact on disease progression. METHODS: We retrospectively analyzed 756 consecutive, prospectively enrolled biopsy-proven NAFLD subjects from Italy, United Kingdom, and Spain who were followed for a median of 84 months (interquartile range, 65-109 months). We stratified the study cohort according to sex, body mass index (BMI) </>= 30 kg/m(2)) and age (</>= 50 years). Liver-related events (hepatic decompensation, hepatic encephalopathy, esophageal variceal bleeding, and hepatocellular carcinoma) were recorded during the follow-up and the log-rank test was used to compare groups. RESULTS: Overall, the median age was 48 years and most individuals were men (64.7%). The PNPLA3 rs738409 genotype was CC in 235 (31.1%), CG in 328 (43.4%), and GG in 193 (25.5%) patients. At univariate analysis, the PNPLA3 GG risk genotype was associated with female sex and inversely related to BMI (odds ratio, 1.6; 95% confidence interval, 1.1-2.2; P = .006; and odds ratio, 0.97; 95% confidence interval, 0.94-0.99; P = .043, respectively). Specifically, PNPLA3 GG risk homozygosis was more prevalent in female vs male individuals (31.5% vs 22.3%; P = .006) and in nonobese compared with obese NAFLD subjects (50.0% vs 44.2%; P = .011). Following stratification for age, sex, and BMI, we observed an increased incidence of liver-related events in the subgroup of nonobese women older than 50 years of age carrying the PNPLA3 GG risk genotype (log-rank test, P = .0047). CONCLUSIONS: Nonobese female patients with NAFLD 50 years of age and older, and carrying the PNPLA3 GG risk genotype, are at higher risk of developing liver-related events compared with those with the wild-type allele (CC/CG). This finding may have implications in clinical practice for risk stratification and personalized medicine.
引用
收藏
页码:3314 / +
页数:11
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