Association between metabolic abnormalities and HBV related hepatocelluar carcinoma in Chinese: A cross-sectional study

被引:31
作者
Zhao, Jinyan [1 ]
Zhao, Yunpeng [1 ]
Wang, Hao [2 ]
Gu, Xing [1 ]
Ji, Jun [1 ]
Gao, Chunfang [1 ]
机构
[1] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Lab Med, Shanghai, Peoples R China
[2] Second Mil Med Univ, Changzheng Hosp, Dept Lab Med, Shanghai, Peoples R China
关键词
FATTY LIVER-DISEASE; CHRONIC HEPATITIS-C; INSULIN-RESISTANCE; DIABETES INCREASES; TRANSGENIC MICE; RISK; OBESITY; EPIDEMIOLOGY; CHOLESTEROL; CELL;
D O I
10.1186/1475-2891-10-49
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Previous studies suggested that the abnormality of metabolism is a newly identified risk factor in HBV-related hepatocellular carcinoma (HCC). The association between metabolic factors and hepatocellular carcinoma (HCC) has not been clarified up to now. This study was conducted to investigate the prevalence of metabolic abnormalities in HCC and to probe the association between metabolic parameters and liver function as well, so as to evaluate the interactions between metabolism and the development of HBV-related HCC. Methods: Totally 179 cases of HBV-related HCC, who were surgically treated and pathologically confirmed were enrolled. HBV carriers (n = 100) and healthy controls (n = 150) were recruited from routine physical examination during the same period. Body mass index (BMI) was obtained from medical documentation. All the metabolic-related parameters and liver function tests were determined with routine biochemical or immunological analytic methods. Malondialdehyde (MDA) and total antioxidant capacity(TAOC) were detected by chemical analytic methods. A stratified analysis was conducted according to BMI, glycated albumin (GA), free fatty acids (FFA), and the relationships between the metabolic-related parameters and liver functions were analyzed in HCC and control subjects. Results: HCC group showed significantly high levels of mean BMI, serum glucose, low serum lipids levels than controls (P < 0.05). Acquired by stratified analysis, the higher the BMI, the higher level of insulin and homeostasis model assessment for insulin resistance (HOMA-IR) (P < 0.01) were found in HCC patients. Elevated level of MDA and g-glutamyltransferase (GGT) were revealed in those with high serum FFA level for the first time. Strong associations between metabolic factors and liver function were shown in HCC (P < 0.05). Higher GA level was strongly associated with increased risk of cancer compared to healthy controls (OR = 9.87, 95% confidence interval: 1.86 similar to 52.29). Serum triglycerides (TG) and low-density lipoprotein cholesterol (LDL-C) levels were negative contributory factors for HCC (OR = 0.05, 95% confidence interval: 0.01 similar to 0.27 and OR = 0.32, 95% confidence interval, 0.11 similar to 0.95: respectively). Conclusions: Metabolic abnormalities are closely associated with the occurrence and development of HBV-related HCC. Oxidative stress and/or lipid peroxidation might be involved in the pathogenesis and acceleration of liver function impairments in HCC.
引用
收藏
页数:8
相关论文
共 50 条
[11]   Non-alcoholic fatty liver disease progresses to hepatocellular carcinoma in the absence of apparent cirrhosis [J].
Ertle, Judith ;
Dechene, Alexander ;
Sowa, Jan-Peter ;
Penndorf, Volker ;
Herzer, Kerstin ;
Kaiser, Gernot ;
Schlaak, Joerg F. ;
Gerken, Guido ;
Syn, Wing-Kin ;
Canbay, Ali .
INTERNATIONAL JOURNAL OF CANCER, 2011, 128 (10) :2436-2443
[12]   Metabolic Syndrome and Insulin Resistance Significantly Correlate with Body Mass Index [J].
Esteghamati, Alireza ;
Khalilzadeh, Omid ;
Anvari, Mehdi ;
Ahadi, Maral Seyed ;
Abbasi, Mehrshad ;
Rashidi, Armin .
ARCHIVES OF MEDICAL RESEARCH, 2008, 39 (08) :803-808
[13]   Epidemiology of non-alcoholic fatty liver disease in China [J].
Fan, Jian-Gao ;
Farrell, Geoffrey C. .
JOURNAL OF HEPATOLOGY, 2009, 50 (01) :204-210
[14]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[15]   Hepatocellular carcinoma: Epidemiology, risk factors and pathogenesis [J].
Gomaa, Asmaa Ibrahim ;
Khan, Shahid A. ;
Toledano, Mireille B. ;
Waked, Imam ;
Taylor-Robinson, Simon D. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (27) :4300-4308
[16]  
Grundy SM, 2004, CIRCULATION, V109, P433, DOI [10.1161/01.CIR.0000111245.75752.C6, 10.1161/01.CIR.0000112379.88385.67]
[17]   EXTENSIVE OXIDATIVE DNA-DAMAGE IN HEPATOCYTES OF TRANSGENIC MICE WITH CHRONIC ACTIVE HEPATITIS DESTINED TO DEVELOP HEPATOCELLULAR-CARCINOMA [J].
HAGEN, TM ;
HUANG, S ;
CURNUTTE, J ;
FOWLER, P ;
MARTINEZ, V ;
WEHR, CM ;
AMES, BN ;
CHISARI, FV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12808-12812
[18]   Insulin resistance is associated with hepatocellular carcinoma in chronic hepatitis C infection [J].
Hung, Chao-Hung ;
Wang, Jing-Houng ;
Hu, Tsung-Hui ;
Chen, Chien-Hung ;
Chang, Kuo-Chin ;
Yen, Yi-Hao ;
Kuo, Yuan-Hung ;
Tsai, Ming-Chao ;
Lu, Sheng-Nan ;
Lee, Chuan-Mo .
WORLD JOURNAL OF GASTROENTEROLOGY, 2010, 16 (18) :2265-2271
[19]   Metabolic factors and subsequent risk of hepatocellular carcinoma by hepatitis virus infection status: a large-scale population-based cohort study of Japanese men and women (JPHC Study Cohort II) [J].
Inoue, Manami ;
Kurahashi, Norie ;
Iwasaki, Motoki ;
Tanaka, Yasuhito ;
Mizokami, Masashi ;
Noda, Mitsuhiko ;
Tsugane, Shoichiro .
CANCER CAUSES & CONTROL, 2009, 20 (05) :741-750
[20]  
JAN CF, 2006, INT J OBESITY, P1