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探索终生酒精摄入量与慢性嗜肝病毒感染对有症状肝硬化风险的联合作用。意大利肝病研究协作组。

Exploring the combined action of lifetime alcohol intake and chronic hepatotropic virus infections on the risk of symptomatic liver cirrhosis. Collaborative Groups for the Study of Liver Diseases in Italy.

作者信息

Corrao G, Torchio P, Zambon A, Ferrari P, Aricò S, di Orio F

机构信息

Department of Statistics, University of Milan, Italy.

出版信息

Eur J Epidemiol. 1998 Jul;14(5):447-56. doi: 10.1023/a:1007411423766.

Abstract

Although alcohol intake and hepatitis B and C virus (HBV and HCV) infections are the major determinants of liver cirrhosis (LC) in western countries, the joint effect of these factors on LC risk has not yet been adequately studied. Data from three case-control studies performed in Italy were used. Cases were 462 cirrhotic patients admitted to Hospitals for liver decompensation. Controls were 651 inpatients admitted for acute diseases unrelated to alcohol. Alcohol consumption was expressed as lifetime daily alcohol intake (LDAI). Three approaches were used to explore the interaction structure. The Breslow and Storer parametric family of relative risk functions showed that an intermediate structure of interaction from additive to multiplicative was the most adequate one. The Rothman synergism index showed that the interaction structure between LDAI and viral status differed significantly from the additive model in particular for high levels of alcohol intake. When multiple regression additive and multiplicative models were compared after adjustment for the known confounding variables. a trend of the interaction structure towards the multiplicative model was observed at increasing levels of consumption. Better methods are needed for assessing mixed interaction structures in conditions characterized by multifactorial etiologies like cirrhosis of the liver.

摘要

尽管在西方国家,酒精摄入以及乙型和丙型肝炎病毒(HBV和HCV)感染是肝硬化(LC)的主要决定因素,但这些因素对LC风险的联合影响尚未得到充分研究。我们使用了在意大利进行的三项病例对照研究的数据。病例为462名因肝失代偿而入院的肝硬化患者。对照为651名因与酒精无关的急性疾病入院的住院患者。酒精消费量以终生每日酒精摄入量(LDAI)表示。采用了三种方法来探索相互作用结构。Breslow和Storer相对风险函数的参数族表明,从相加到相乘的中间相互作用结构是最合适的。Rothman协同指数表明,LDAI与病毒状态之间的相互作用结构与相加模型有显著差异,特别是对于高酒精摄入量而言。在对已知混杂变量进行调整后比较多元回归相加模型和相乘模型时,随着消费水平的增加,观察到相互作用结构有向相乘模型发展的趋势。在像肝硬化这样具有多因素病因的情况下,需要更好的方法来评估混合相互作用结构。

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