Hodgson M, van Thiel D H, Goodman-Klein B
Department of Medicine (Occupational and Environmental Medicine Program), University of Pittsburgh School of Medicine, PA 15261.
Br J Ind Med. 1991 Oct;48(10):690-5. doi: 10.1136/oem.48.10.690.
Generally fatty liver disease (FLD) is attributed either to alcohol, diabetes mellitus, or obesity. To evaluate this commonly held clinical belief, a case-control study of FLD in Western Pennsylvania was conducted with 19 cases being identified over a two year period. Cases of FLD were significantly heavier and were significantly more likely than controls to have exposures to either agents with recognised animal hepatotoxicity (odds ratio [OR] 8, p = 0.018) or to agents with potential hepatotoxicity--that is, documented in humans, animals, or expected on the basis of structure activity relations (OR = 4.5; p = 0.18). By contrast, they had not consumed significantly more alcohol than the controls. A logistic regression model of this experience suggests that both exposure to hepatotoxins and obesity are independent risk factors for FLD, which have an additive rather than a multiplicative interaction. Based upon these data, an occupational exposure to either recognised or potential hepatotoxins should be considered as a cause of liver dysfunction in subjects with FLD, independent of obesity and a history of alcohol consumption.
一般来说,脂肪肝疾病(FLD)要么归因于酒精、糖尿病,要么归因于肥胖。为了评估这种普遍存在的临床观点,在宾夕法尼亚西部进行了一项FLD的病例对照研究,在两年期间确定了19例病例。FLD病例明显更重,并且与对照组相比,接触具有公认动物肝毒性的药物(比值比[OR]为8,p = 0.018)或具有潜在肝毒性的药物(即在人类、动物中记录或根据构效关系预期的药物,OR = 4.5;p = 0.18)的可能性显著更高。相比之下,他们摄入的酒精量并不比对照组显著更多。基于这一经验的逻辑回归模型表明,接触肝毒素和肥胖都是FLD的独立危险因素,它们具有相加而非相乘的相互作用。根据这些数据,职业接触公认的或潜在的肝毒素应被视为FLD患者肝功能障碍的一个原因,独立于肥胖和饮酒史。