ALCOHOL-CONSUMPTION AND ALCOHOLIC LIVER-DISEASE - EVIDENCE OF A THRESHOLD LEVEL OF EFFECTS OF ETHANOL

被引:127
作者
SAVOLAINEN, VT
LIESTO, K
MANNIKKO, A
PENTTILA, A
KARHUNEN, PJ
机构
[1] UNIV TAMPERE,DEPT PUBL HLTH,FORENS MED SECT,TAMPERE,FINLAND
[2] UNIV KUOPIO,DEPT CLIN PATHOL & FORENS MED,KUOPIO,FINLAND
关键词
ALCOHOL CONSUMPTION; LIVER CIRRHOSIS; ALCOHOLIC LIVER DISEASE; AUTOPSY;
D O I
10.1111/j.1530-0277.1993.tb05673.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
The effects of long-term moderate or ''social'' alcohol consumption (10-80 g daily intake) on the incidence of features of alcoholic liver disease (ALD) were delineated in a consecutive autopsy series of 210 males. The subjects' daily intake, as well 83 duration of alcohol consumption, was determined by an interview with the spouse or a close acquaintance and compared with semiquantitative histological scores for stage of ALD. No significant increase in the incidence of features of ALD could be related to all-year daily intake of ethanol below 40 g (40 g equals 1.1 liter of beer, 0.44 liter of wine, and 0.11 liter of spirits). However, daily intake between 40-80 g increased relative liver weight on average 3.1 g/kg of body weight (p < 0.02), the frequency of fatty liver from 11.7 to 47.2% [relative risk (RR) = 4.4], and the frequency of mainly slight alcoholic hepatitis up to 16.7% (RR = 7.5). The incidence of both bridging fibrosis and liver cirrhosis increased significantly (RR = 8.8) only when daily intake exceeded 80 g. Amounts of ethanol exceeding 80 g did not relate to further increases in incidence of bridging fibrosis or liver cirrhosis. These findings suggest that, in males, daily ingestion of ethanol below 40 g for a period of 25 years does not increase the risk of alcohol-related liver disease. In contrast, similar duration of daily intake between 40 and 80 g (mean 61.6 g) increased the risk of all but fibrotic liver lesions of ALD significantly and may thus represent a potential threshold level that significantly increases the risk of alcohol-related liver damage. Moreover, our results may suggest that, on an individual level, the risk function for liver fibrosis may not be directly dose-related, but rather, when a permissive threshold level is attained, further consumption is of no or little importance to the progression of ALD.
引用
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页码:1112 / 1117
页数:6
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