Systematic review with meta-analysis: the I148M variant of patatin-like phospholipase domain-containing 3 gene (PNPLA3) is significantly associated with alcoholic liver cirrhosis

被引:64
|
作者
Chamorro, A-J. [1 ]
Torres, J-L. [1 ]
Miron-Canelo, J-A. [2 ]
Gonzalez-Sarmiento, R. [3 ]
Laso, F-J. [1 ]
Marcos, M. [1 ]
机构
[1] Hosp Univ Salamanca, Inst Biomed Res Salamanca IBSAL, Dept Internal Med, Alcoholism Unit, Salamanca 37007, Spain
[2] Univ Salamanca, Dept Epidemiol, IBSAL, E-37008 Salamanca, Spain
[3] Univ Salamanca, Mol Med Unit, IBSAL, SACYL,CSIC, E-37008 Salamanca, Spain
关键词
HEPATOCELLULAR-CARCINOMA; DISEASE; RISK; POLYMORPHISM; RS738409; SUSCEPTIBILITY; MODEL;
D O I
10.1111/apt.12890
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Several studies have reported an association between alcoholic liver cirrhosis (ALC) or other forms of alcoholic liver disease (ALD) and the genetic variant rs738409 (C>G) in adiponutrin/patatin-like phospholipase domain-containing 3 gene (PNPLA3). Aim To evaluate the influence of this variant on ALC and other forms of ALD. Methods We performed a systematic review of previous studies on the relationship between rs738409 of PNPLA3 and ALD and meta-analysis was conducted in a random-effects model. Calculations of the odds ratios (ORs) and their confidence intervals (CIs), tests for heterogeneity and sensitivity analyses were performed. Results Database search identified 11 previous studies available for inclusion with a total of 3495 patients with ALD (2087 with ALC) and 5038 controls (4007 healthy subjects and 1031 alcoholics without ALD). Patients with ALC compared to controls had a significantly higher prevalence of the G allele when comparing GG vs. CC (OR 4.30, 95% CI 3.25-5.69; P < 0.00001) or GC vs. CC genotypes (GC vs. CC: OR 1.91, 95% CI 1.67-2.17) or under a recessive or dominant model. Similar results were found when comparing separately patients with ALC vs. alcoholics without ALD or healthy subjects. An association of the G allele with ALD emerged when comparing ALD patients vs. alcoholics without ALD and/or healthy subjects although moderate to large heterogeneity was observed. Our data suggested an additive genetic model for this variant in ALD. Conclusion Our meta-analysis shows that the rs738409 variant of PNPLA3 is clearly associated with alcoholic liver cirrhosis.
引用
收藏
页码:571 / 581
页数:11
相关论文
共 50 条
  • [41] Patatin-like Phospholipase Domain-Containing Protein 3 and Liver Disease: Opportunities to Unravel Mechanisms Underlying Statistical Associations
    Boursier, Jerome
    Diehl, Anna Mae
    HEPATOLOGY, 2015, 61 (01) : 18 - 20
  • [42] Role of patatin-like phospholipase domain-containing 3 gene for decreasing kidney function in recently diagnosed diabetes mellitus
    Zaharia, Oana Patricia
    Strassburger, Klaus
    Knebel, Birgit
    Binsch, Christian
    Kupriyanova, Yuliya
    Moeser, Clara
    Bodis, Kalman
    Prystupa, Katsiaryna
    Yurchenko, Iryna
    Cardenas, Dania Marel Mendez
    Schoen, Martin
    Herder, Christian
    Al-Hasani, Hadi
    Schrauwen-Hinderling, Vera
    Jandeleit-Dahm, Karin
    Wagner, Robert
    Roden, Michael
    DIABETES & METABOLIC SYNDROME-CLINICAL RESEARCH & REVIEWS, 2024, 18 (10)
  • [43] PNPLA3 I148M variant in nonalcoholic fatty liver disease:Demographic and ethnic characteristics and the role of the variant in nonalcoholic fatty liver fibrosis
    Li-Zhen Chen
    Yong-Ning Xin
    Ning Geng
    Man Jiang
    Ding-Ding Zhang
    Shi-Ying Xuan
    World Journal of Gastroenterology, 2015, (03) : 794 - 802
  • [44] PNPLA3 I148M variant in nonalcoholic fatty liver disease: Demographic and ethnic characteristics and the role of the variant in nonalcoholic fatty liver fibrosis
    Chen, Li-Zhen
    Xin, Yong-Ning
    Geng, Ning
    Jiang, Man
    Zhang, Ding-Ding
    Xuan, Shi-Ying
    WORLD JOURNAL OF GASTROENTEROLOGY, 2015, 21 (03) : 794 - 802
  • [45] Patatin-Like Phospholipase Domain-Containing Protein 3 rs738409-G in Recipients of Liver Transplants Is a Risk Factor for Graft Steatosis
    Finkenstedt, Armin
    Auer, Claudia
    Glodny, Bernhard
    Posch, Ursula
    Steitzer, Hansjoerg
    Lanzer, Gerhard
    Pratschke, Johann
    Biebl, Matthias
    Steurer, Michael
    Graziadei, Ivo
    Vogel, Wolfgang
    Zoller, Heinz
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2013, 11 (12) : 1667 - 1672
  • [46] Association between the PNPLA3 I148M Polymorphism and Non-Alcoholic Fatty Liver Disease in the Uygur and Han Ethnic Groups of Northwestern China
    Zhang, Yuexin
    Cai, Wen
    Song, Jiangmei
    Miao, Lei
    Zhang, Bei
    Xu, Qin
    Zhang, Lijuan
    Yao, Hua
    PLOS ONE, 2014, 9 (10):
  • [47] I148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver disease
    Park, Jin-Ho
    Cho, BeLong
    Kwon, Hyuktae
    Prilutsky, Daria
    Yun, Jae Moon
    Choi, Ho Chun
    Hwang, Kyu-Baek
    Lee, In-Hee
    Kim, Jong-Il
    Kong, Sek Won
    LIVER INTERNATIONAL, 2015, 35 (12) : 2537 - 2546
  • [48] PNPLA3 I148M gene variant and chronic kidney disease in type 2 diabetic patients with NAFLD: Clinical and experimental findings
    Mantovani, Alessandro
    Taliento, Alice
    Zusi, Chiara
    Baselli, Guido
    Prati, Daniele
    Granata, Simona
    Zaza, Gianluigi
    Colecchia, Antonio
    Maffeis, Claudio
    Byrne, Christopher D.
    Valenti, Luca
    Targher, Giovanni
    LIVER INTERNATIONAL, 2020, 40 (05) : 1130 - 1141
  • [49] I148M Variant of PNPLA3 Confer Increased Risk for Nonalcoholic Fatty Liver Disease Not Only in European Population, but Also in Chinese Population
    Li, Xiaohua
    Zhao, Qingchuan
    Wu, Kaichun
    Fan, Daiming
    HEPATOLOGY, 2011, 54 (06) : 2275 - 2275
  • [50] Association between PNPLA3 rs738409 polymorphism and nonalcoholic fatty liver disease: a systematic review and meta-analysis
    Salari, Nader
    Darvishi, Niloufar
    Mansouri, Kamran
    Ghasemi, Hooman
    Hosseinian-Far, Melika
    Darvishi, Fateme
    Mohammadi, Masoud
    BMC ENDOCRINE DISORDERS, 2021, 21 (01)