Advances in alcoholic liver disease

被引:110
作者
Arteel, G [1 ]
Marsano, L [1 ]
Mendez, C [1 ]
Bentley, F [1 ]
McClain, CJ [1 ]
机构
[1] Univ Louisville, Ctr Med, Dept Internal Med, Louisville, KY 40292 USA
关键词
alcoholic liver disease; diagnosis; aetiology; treatment;
D O I
10.1016/S1521-6918(03)00053-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Alcoholic liver disease (ALD) remains a major cause of morbidity and mortality worldwide. For example, the Veterans Administration Cooperative Studies reported that patients with cirrhosis and superimposed alcoholic hepatitis had a 4-year mortality of >60%. Interactions between acetaldehyde, reactive oxygen and nitrogen species, inflammatory mediators and genetic factors appear to play prominent roles in the development of ALD. The cornerstone of therapy for ALD is lifestyle modification, including drinking and smoking cessation and losing weight, if appropriate. Nutrition intervention has been shown to play a positive role on both an inpatient and outpatient basis. Corticosteroids are effective in selected patients with alcoholic hepatitis and pentoxifylline appears to be a promising anti-inflammatory therapy. Some complementary and alternative medicine agents, such as milk thistle and S-adenosylmethionine, may be effective in alcoholic cirrhosis. Treatment of the complications of ALD can improve quality of life and, in some cases, decrease short-term mortality.
引用
收藏
页码:625 / 647
页数:23
相关论文
共 161 条
[1]   Alcoholism in hereditary hemochromatosis revisited: Prevalence and clinical consequences among homozygous siblings [J].
Adams, PC ;
Agnew, S .
HEPATOLOGY, 1996, 23 (04) :724-727
[2]   Genetic polymorphisms of alcohol metabolizing enzymes [J].
Agarwal, DP .
PATHOLOGIE BIOLOGIE, 2001, 49 (09) :703-709
[3]   Pentoxifylline improves short-term survival in severe acute alcoholic hepatitis: A double-blind, placebo-controlled trial [J].
Akriviadis, E ;
Botla, R ;
Briggs, W ;
Han, S ;
Reynolds, T ;
Shakil, O .
GASTROENTEROLOGY, 2000, 119 (06) :1637-1648
[4]   Oxidative stress and gene regulation [J].
Allen, RG ;
Tresini, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) :463-499
[5]   Reversal of type 1 hepatorenal syndrome with the administration of midodrine and octreotide [J].
Angeli, P ;
Volpin, R ;
Gerunda, G ;
Craighero, R ;
Rone, P ;
Merenda, R ;
Amodio, P ;
Sticca, A ;
Caregaro, L ;
Maffei-Faccioli, A ;
Gatta, A .
HEPATOLOGY, 1999, 29 (06) :1690-1697
[6]   Definition and diagnostic criteria of refractory ascites and hepatorenal syndrome in cirrhosis [J].
Arroyo, V ;
Gines, P ;
Gerbes, AL ;
Dudley, FJ ;
Gentilini, P ;
Laffi, G ;
Reynolds, TB ;
RingLarsen, H ;
Scholmerich, J .
HEPATOLOGY, 1996, 23 (01) :164-176
[7]   The effect of ethanol-induced cytochrome p4502E1 on the inhibition of proteasome activity by alcohol [J].
Bardag-Gorce, F ;
Yuan, QX ;
Li, J ;
French, BA ;
Fang, C ;
Ingelman-Sundberg, M ;
French, SW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 279 (01) :23-29
[8]   Prediction of risk of liver disease by alcohol intake, sex, and age: A prospective population study [J].
Becker, U ;
Deis, A ;
Sorensen, TIA ;
Gronbaek, M ;
BorchJohnsen, K ;
Muller, CF ;
Schnohr, P ;
Jensen, G .
HEPATOLOGY, 1996, 23 (05) :1025-1029
[9]  
Beckman J. S., 1996, NITRIC OXIDE PRINCIP, P1, DOI DOI 10.1016/B978-012435555-2/50002-4
[10]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624