Department of Internal Medicine, Bassett Medical Center, Cooperstown, New York, USA.
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Mayo Clinic, Jacksonville, Florida, USA.
J Gastroenterol Hepatol. 2020 Oct;35(10):1789-1794. doi: 10.1111/jgh.15045. Epub 2020 Apr 12.
The association between palatin-like phospholipase domain-containing 3 (PNPLA3) I148M (rs738409) polymorphism and mortality is not well understood. We investigated the impact of PNPLA3 I148M (rs738409) polymorphism on overall and cardiovascular mortality based on the presence of nonalcoholic fatty liver disease (NAFLD).
The third National Health and Nutrition Examination Survey (NHANES) from 1991 to 1994 and National Health and Nutrition Examination Survey III-linked mortality data through 31 December 2015 were utilized in this study.
Of 4814 participants, 50.7% were homozygous for the C-allele and 12.6% were homozygous for the G-allele. During a follow up of 20 years, there were a total of 1255 deaths, 422 attributed to cardiovascular disease. There was a significant association with overall mortality among those with the PNPLA3 I148M (rs738409) GG genotype (hazard ratio [HR] 1.34, 95% confidence interval [CI] 1.02-1.77) or G-allele (HR 1.22, 95% CI 1.09-1.36) in the general population. NAFLD with homozygous PNPLA3 I148M (rs738409) GG genotype had higher overall mortality after adjusting for multiple metabolic risk factors (HR 1.45, 95% CI 1.01-2.08). The PNPLA3 I148M (rs738409) G-allele had a tendency of increased cardiovascular mortality in the total population. This association was not noted in those with NAFLD.
The homozygous PNPLA3 I148M (rs738409) GG genotype showed an increase in overall mortality in the general population and NAFLD independent of multiple metabolic risk factors.
PNPLA3 I148M(rs738409)多态性与死亡率之间的关联尚不清楚。我们基于非酒精性脂肪性肝病(NAFLD)的存在,研究了 PNPLA3 I148M(rs738409)多态性对总死亡率和心血管死亡率的影响。
本研究利用了 1991 年至 1994 年的第三次全国健康和营养调查(NHANES)以及截至 2015 年 12 月 31 日的与全国健康和营养调查 III 相关的死亡率数据。
在 4814 名参与者中,50.7%为 C-等位基因纯合子,12.6%为 G-等位基因纯合子。在 20 年的随访期间,共有 1255 人死亡,其中 422 人归因于心血管疾病。在一般人群中,PNPLA3 I148M(rs738409)GG 基因型(风险比 [HR] 1.34,95%置信区间 [CI] 1.02-1.77)或 G 等位基因(HR 1.22,95% CI 1.09-1.36)与总死亡率之间存在显著关联。在调整了多种代谢风险因素后,NAFLD 伴纯合子 PNPLA3 I148M(rs738409)GG 基因型的总死亡率更高(HR 1.45,95% CI 1.01-2.08)。PNPLA3 I148M(rs738409)G 等位基因在总人群中存在心血管死亡率增加的趋势,但在 NAFLD 患者中未见此关联。
在一般人群和独立于多种代谢风险因素的 NAFLD 中,PNPLA3 I148M(rs738409)GG 基因型纯合子显示出总死亡率增加。