Division of Clinical Gastroenterology and Hepatology, Department of Gastroenterology, University of São Paulo School of Medicine (FMUSP), Sao Paulo, Brazil; Division of Gastroenterology (Gastrocentro), School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Institute of Tropical Medicine, LIM 07, University of Sao Paulo, Sao Paulo, Brazil.
Ann Hepatol. 2019 May-Jun;18(3):466-471. doi: 10.1016/j.aohep.2018.10.004. Epub 2019 Apr 18.
Studies have shown that two polymorphisms were associated with steatosis and progression of non-alcoholic fatty liver disease (NAFLD) in different populations: the Patatin-like Phospholipase Domain Containing 3 (PNPLA3) and Transmembrane 6 Superfamily Member 2 (TM6SF2). However, the frequency and significance of these polymorphisms in an admixed population, i.e., Brazilian, is unknown. Therefore, we aimed to evaluate them in healthy subjects in comparison to patients with NAFLD.
This was a multicenter cross-sectional study in 248 patients with biopsy-proven NAFLD and in 134 healthy controls from two tertiary centers in Brazil. PNPLA3 (rs738409 c.444C>G) and TM6SF2 (rs58542926 c.449C>T) polymorphisms were evaluated.
In controls, the frequencies of PNPLA3 CC and CG+GG were 49.25% and 50.74%, respectively; in NAFLD patients, this was 31.05% and 68.88% (p=0.0044, 95% CI 1.037-2.977). PNPLA3 GG subjects had an increased risk (3.29-fold) of having NAFLD when compared to CC subjects (p=0.0044, 95% CI 1.504-7.225). In patients with nonalcoholic steatohepatitis (NASH), PNPLA3 GG compared to CC was associated with higher AST levels [38.4±25.3 versus 36.7±40.1IU/L, p=0.0395)] and with the presence of liver fibrosis (≥F2 fibrosis, p=0.0272). TM6SF2 polymorphisms were not in Hardy-Weinberg equilibrium in our NAFLD group precluding further analysis.
We demonstrated for the first time that PNPLA3 CG+GG increase the risk of NAFLD among Brazilian subjects. Moreover, PNPLA3 GG was associated with liver enzyme elevation and fibrosis in NASH patients.
研究表明,两种多态性与不同人群的脂肪变性和非酒精性脂肪性肝病(NAFLD)的进展有关:脂肪酶磷蛋白类似物 3(PNPLA3)和跨膜 6 超家族成员 2(TM6SF2)。然而,这些多态性在混合人群(即巴西人)中的频率和意义尚不清楚。因此,我们旨在将其与 NAFLD 患者进行比较,以评估健康受试者。
这是一项在巴西两个三级中心的 248 例经活检证实的 NAFLD 患者和 134 例健康对照者中进行的多中心横断面研究。评估了 PNPLA3(rs738409 c.444C>G)和 TM6SF2(rs58542926 c.449C>T)多态性。
在对照组中,PNPLA3 CC 和 CG+GG 的频率分别为 49.25%和 50.74%;在 NAFLD 患者中,这分别为 31.05%和 68.88%(p=0.0044,95%CI 1.037-2.977)。与 CC 相比,PNPLA3 GG 患者发生 NAFLD 的风险增加(3.29 倍)(p=0.0044,95%CI 1.504-7.225)。在非酒精性脂肪性肝炎(NASH)患者中,PNPLA3 GG 与 CC 相比,AST 水平升高[38.4±25.3 与 36.7±40.1IU/L,p=0.0395)]和肝纤维化(≥F2 纤维化,p=0.0272)。我们的 NAFLD 组中 TM6SF2 多态性未处于 Hardy-Weinberg 平衡,因此无法进一步分析。
我们首次证明,PNPLA3 CG+GG 增加了巴西人群患 NAFLD 的风险。此外,PNPLA3 GG 与 NASH 患者的肝酶升高和纤维化有关。