PNPLA3 I148M polymorphism and progressive liver disease

被引:238
作者
Dongiovanni, Paola [1 ]
Donati, Benedetta [1 ]
Fares, Roberta [1 ]
Lombardi, Rosa [1 ]
Mancina, Rosellina Margherita [2 ]
Romeo, Stefano [2 ,3 ]
Valenti, Luca [1 ]
机构
[1] Univ Milan, Fdn IRCCS Ca Granda Osped Policlin Milano, Dept Pathophysiol & Transplantat, I-20122 Milan, Italy
[2] Univ Gothenburg, Dept Mol & Clin Med, Sahlgrenska Ctr Cardiovasc & Metab Res Wallenberg, S-40530 Gothenburg, Sweden
[3] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, Clin Nutr Unit, I-88100 Catanzaro, Italy
关键词
Alcoholic liver disease; Chronic hepatitis C virus hepatitis; Fibrogenesis; Genetics; Hepatocellular carcinoma; Liver disease; Nonalcoholic fatty liver disease; Patatin-like phospholipase domain-containing 3; Single nucleotide polymorphism; Steatosis; CHRONIC HEPATITIS-C; DOMAIN-CONTAINING; 3; GENOME-WIDE ASSOCIATION; B-VIRUS INFECTION; GREATER-THAN-G; FATTY LIVER; INSULIN-RESISTANCE; HEPATOCELLULAR-CARCINOMA; NONALCOHOLIC STEATOHEPATITIS; GENETIC VARIANT;
D O I
10.3748/wjg.v19.i41.6969
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
The 148 Isoleucine to Methionine protein variant (I148M) of patatin-like phospholipase domain-containing 3 (PNPLA3), a protein is expressed in the liver and is involved in lipid metabolism, has recently been identified as a major determinant of liver fat content. Several studies confirmed that the I148M variant predisposes towards the full spectrum of liver damage associated with fatty liver: from simple steatosis to steatohepatitis and progressive fibrosis. Furthermore, the I148M variant represents a major determinant of progression of alcohol related steatohepatitis to cirrhosis, and to influence fibrogenesis and related clinical outcomes in chronic hepatitis C virus hepatitis, and possibly chronic hepatitis B virus hepatitis, hereditary hemochromatosis and primary sclerosing cholangitis. All in all, studies suggest that the I148M polymorphism may represent a general modifier of fibrogenesis in liver diseases. Remarkably, the effect of the I148M variant on fibrosis was independent of that on hepatic steatosis and inflammation, suggesting that it may affect both the quantity and quality of hepatic lipids and the biology of non-parenchymal liver cells besides hepatocytes, directly promoting fibrogenesis. Therefore, PNPLA3 is a key player in liver disease progression. Assessment of the I148M polymorphism will possibly inform clinical practice in the future, whereas the determination of the effect of the 148M variant will reveal mechanisms involved in hepatic fibrogenesis. (C) 2013 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:6969 / 6978
页数:10
相关论文
共 97 条
[1]
Steatosis accelerates the progression of liver damage of chronic hepatitis C patients and correlates with specific HCV genotype and visceral obesity [J].
Adinolfi, LE ;
Gambardella, M ;
Andreana, A ;
Tripodi, MF ;
Utili, R ;
Ruggiero, G .
HEPATOLOGY, 2001, 33 (06) :1358-1364
[2]
Efficacy of interferon monotherapy to 394 consecutive naive cases infected with hepatitis C virus genotype 2a in Japan: therapy efficacy as consequence of tripartite interaction of viral, host and interferon treatment-related factors [J].
Akuta, N ;
Suzuki, F ;
Tsubota, A ;
Suzuki, Y ;
Someya, T ;
Kobayashi, M ;
Saitoh, S ;
Arase, Y ;
Ikeda, K ;
Kumada, H .
JOURNAL OF HEPATOLOGY, 2002, 37 (06) :831-836
[3]
Pnpla3/Adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome [J].
Basantani, Mahesh K. ;
Sitnick, Mitch T. ;
Cai, Lingzhi ;
Brenner, Daniel S. ;
Gardner, Noah P. ;
Li, John Zhong ;
Schoiswohl, Gabriele ;
Yang, Kui ;
Kumari, Manju ;
Gross, Richard W. ;
Zechner, Rudolf ;
Kershaw, Erin E. .
JOURNAL OF LIPID RESEARCH, 2011, 52 (02) :318-329
[4]
HCV and the hepatic lipid pathway as a potential treatment target [J].
Bassendine, Margaret F. ;
Sheridan, David A. ;
Felmlee, Daniel J. ;
Bridge, Simon H. ;
Toms, Geoffrey L. ;
Neely, R. Dermot G. .
JOURNAL OF HEPATOLOGY, 2011, 55 (06) :1428-1440
[5]
Bathum L, 2001, CLIN CHEM, V47, P81
[6]
Prevalence of and risk factors for hepatic steatosis in northern Italy [J].
Bellentani, S ;
Saccoccio, G ;
Masutti, F ;
Crocè, LS ;
Brandi, G ;
Sasso, F ;
Cristanini, G ;
Tiribelli, C .
ANNALS OF INTERNAL MEDICINE, 2000, 132 (02) :112-117
[7]
The burden of liver disease in Europe: A review of available epidemiological data [J].
Blachier, Martin ;
Leleu, Henri ;
Peck-Radosavljevic, Markus ;
Valla, Dominique-Charles ;
Roudot-Thoraval, Francoise .
JOURNAL OF HEPATOLOGY, 2013, 58 (03) :593-608
[8]
Prevalence of hepatic steatosis in an urban population in the United States: Impact of ethnicity [J].
Browning, JD ;
Szczepaniak, LS ;
Dobbins, R ;
Nuremberg, P ;
Horton, JD ;
Cohen, JC ;
Grundy, SM ;
Hobbs, HH .
HEPATOLOGY, 2004, 40 (06) :1387-1395
[9]
Insulin resistance in non-diabetic patients with non-alcoholic fatty liver disease: sites and mechanisms [J].
Bugianesi, E ;
Gastaldelli, A ;
Vanni, E ;
Gambino, R ;
Cassader, M ;
Baldi, S ;
Ponti, V ;
Pagano, G ;
Ferrannini, E ;
Rizzetto, M .
DIABETOLOGIA, 2005, 48 (04) :634-642
[10]
Expanding the natural history from cryptogenic cirrhosis to of nonalcoholic steatohepatitis: Hepatocellular carcinoma [J].
Bugianesi, E ;
Leone, N ;
Vanni, E ;
Marchesini, G ;
Brunello, F ;
Carucci, P ;
Musso, A ;
De Paolis, P ;
Capussotti, L ;
Salizzoni, M ;
Rizzetto, M .
GASTROENTEROLOGY, 2002, 123 (01) :134-140