Effect of moderate alcohol consumption on liver enzymes increases with increasing body mass index

被引:100
作者
Alatalo, Paeivikki I. [1 ,2 ,3 ]
Koivisto, Heidi M. [1 ,2 ,3 ]
Hietala, Johanna P. [1 ,2 ,3 ]
Puukka, Katri S. [1 ,2 ,3 ]
Bloigu, Risto [4 ]
Niemelae, Onni J. [1 ,2 ,3 ]
机构
[1] Seinajoki Cent Hosp, Dept Lab Med, FIN-60220 Seinajoki, Finland
[2] Seinajoki Cent Hosp, Med Res Unit, FIN-60220 Seinajoki, Finland
[3] Univ Tampere, Seinajoki, Finland
[4] Univ Oulu, Med Informat Grp, Oulu, Finland
关键词
D O I
10.1093/ajcn/88.4.1097
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: Although both ethanol consumption and overweight alter the activities of hepatic enzymes in circulation, the differentiation of an alcohol or nonalcohol basis for such changes remains problematic. The magnitude of alterations occurring among moderate drinkers has remained obscure. Objective: We examined the links between moderate ethanol consumption, body mass index (BMI; in kg/m(2)), and liver enzymes. Design: Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyltransferase (GGT) were recorded from 2164 apparently healthy participants (1028 men, 1136 women) reporting either no alcohol (abstainers) or < 40 g ethanol consumption per day (moderate drinkers). The study population was further classified according to BMI as follows: < 19 (underweight), >= 19 and < 25 (normal weight), >= 25 and >= 30 (overweight), and >= 30 ( obese). Results: Serum ALT ( P < 0.05) and GGT ( P < 0.001) but not AST ( P = 0.805) activities in moderate drinkers were higher than those in abstainers. For all enzymes, a significant main effect was observed of increasing BMI, which was more striking in moderate drinkers than in abstainers. Tests of between- subjects effects indicated significant interactions with sex and drinking status, although not with sex and BMI. Conclusions: The effect of moderate alcohol consumption on liver enzymes increases with increasing BMI. These findings should be considered in the clinical assessment of overweight alcohol consumers and in the definition of normal ranges for liver enzymes. These results may also help to develop new approaches for examining patients with fatty liver induced by either ethanol or adiposity.
引用
收藏
页码:1097 / 1103
页数:7
相关论文
共 47 条
  • [41] ROLE OF HEPATIC GAMMA-GLUTAMYL-TRANSFERASE IN THE DEGRADATION OF CIRCULATING GLUTATHIONE - STUDIES IN THE INTACT GUINEA-PIG PERFUSED LIVER
    SPEISKY, H
    SHACKEL, N
    VARGHESE, G
    WADE, D
    ISRAEL, Y
    [J]. HEPATOLOGY, 1990, 11 (05) : 843 - 849
  • [42] Body fat distribution, relative weight, and liver enzyme levels: A population-based study
    Stranges, S
    Dorn, JM
    Muti, P
    Freudenheim, JL
    Farinaro, E
    Russell, M
    Nochajski, TH
    Trevisan, M
    [J]. HEPATOLOGY, 2004, 39 (03) : 754 - 763
  • [43] Values and limitations of serum aminotransferases in clinical trials of nonalcoholic steatohepatitis
    Suzuki, Ayako
    Lymp, James
    St. Sauver, Jenny
    Angulo, Paul
    Lindor, Keith
    [J]. LIVER INTERNATIONAL, 2006, 26 (10) : 1209 - 1216
  • [44] EXPERIMENTAL LIVER-CIRRHOSIS INDUCED BY ALCOHOL AND IRON
    TSUKAMOTO, H
    HORNE, W
    KAMIMURA, S
    NIEMELA, O
    PARKKILA, S
    YLAHERTTUALA, S
    BRITTENHAM, GM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (01) : 620 - 630
  • [45] High alanine aminotransferase is associated with decreased hepatic insulin sensitivity and predicts the development of type 2 diabetes
    Vozarova, B
    Stefan, N
    Lindsay, RS
    Saremi, A
    Pratley, RE
    Bogardus, C
    Tataranni, PA
    [J]. DIABETES, 2002, 51 (06) : 1889 - 1895
  • [46] Hepatic cytochrome p450 2E1 is increased in patients with nonalcoholic steatohepatitis
    Weltman, MD
    Farrell, GC
    Hall, P
    Ingelman-Sundberg, M
    Liddle, C
    [J]. HEPATOLOGY, 1998, 27 (01) : 128 - 133
  • [47] Sex is a major determinant of CYP3A4 expression in human liver
    Wolbold, R
    Klein, K
    Burk, O
    Nüssler, AK
    Neuhaus, P
    Eichelbaum, M
    Schwab, M
    Zanger, UM
    [J]. HEPATOLOGY, 2003, 38 (04) : 978 - 988