Mützell S
Department of Family Medicine, University Hospital of Uppsala, Sweden.
Ups J Med Sci. 1992;97(2):183-94. doi: 10.3109/03009739209179295.
Computed tomography (CT) of the brain was performed in a random sample of a total of 195 men and 211 male alcoholic patients admitted for the first time during a period of two years from the same geographically limited area of Greater Stockholm as the sample. The same medical, social and neuroradiological methods were used for examination of the alcoholic inpatients as for the random controls. Laboratory tests were performed, including liver and pancreatic tests. Toxicological screening was performed and the consumption of hepatotoxic drugs was also investigated and the following were the types of drugs used: antiarrhythmics, antiepileptics, antiphlogistics, mixed analgesics, barbiturates, sulphonamides, benzodiazepines, clomethiazole and phenothiazine derivatives, all of which are metabolised by the liver. The group of male alcoholic inpatients and the random sample were then subdivided with respect to alcohol consumption and use of hepatotoxic drugs: Group IA, men from the random sample with low or moderate alcohol consumption and no use of hepatotoxic drugs; IB, men from the random sample with low or moderate alcohol consumption with use of hepatotoxic drugs; IIA, alcoholic inpatients with use of alcohol and no drugs; and IIB, alcoholic inpatients with use of alcohol and drugs. Group IIB was found to have a higher incidence of cortical and subcortical changes than group IA. Group IB had a higher incidence of subcortical changes than group IA, and they differed only in drug use. Groups IIB and IIA only differed in drug use, and IIB had a higher incidence of brain damage except for anterior horn index and wide cerebellar sulci indicating vermian atrophy. Significantly higher serum (S) levels of bilirubin, gamma-glutamyl transpeptidase (GGT), aspartate aminotransferase (ASAT), alanine amino-transferase (ALAT), creatine kinase (CK), lactate dehydrogenase (LD) and amylase were found in IIB. The results indicate that drug use influences the incidence of cortical and subcortical aberrations, except anterior horn index. It is concluded that the groups with alcohol abuse who used hepatotoxic drugs showed a picture of cortical changes (wide transport sulci and clear-cut or high-grade cortical changes) and also of subcortical aberrations, expressed as an increased widening of the third ventricle.
在两年时间里,从大斯德哥尔摩地区同一地理范围内首次入院的195名男性和211名男性酒精性患者中随机抽取样本,对其进行脑部计算机断层扫描(CT)。对酒精性住院患者和随机对照者采用相同的医学、社会和神经放射学检查方法。进行了实验室检查,包括肝脏和胰腺检查。进行了毒理学筛查,并调查了肝毒性药物的使用情况,所用药物类型如下:抗心律失常药、抗癫痫药、消炎药、复合镇痛药、巴比妥类药物、磺胺类药物、苯二氮䓬类药物、氯美噻唑和吩噻嗪衍生物,所有这些药物均由肝脏代谢。然后,根据酒精摄入量和肝毒性药物的使用情况,将男性酒精性住院患者组和随机样本进行细分:IA组,来自随机样本且酒精摄入量低或中等且未使用肝毒性药物的男性;IB组,来自随机样本且酒精摄入量低或中等且使用肝毒性药物的男性;IIA组,使用酒精但未使用药物的酒精性住院患者;IIB组,使用酒精且使用药物的酒精性住院患者。发现IIB组皮质和皮质下改变的发生率高于IA组。IB组皮质下改变的发生率高于IA组,且两组仅在药物使用方面存在差异。IIB组和IIA组仅在药物使用方面存在差异,除了提示蚓部萎缩的前角指数和小脑沟增宽外,IIB组脑损伤的发生率更高。IIB组的胆红素、γ-谷氨酰转肽酶(GGT)、天冬氨酸转氨酶(ASAT)、丙氨酸转氨酶(ALAT)、肌酸激酶(CK)、乳酸脱氢酶(LD)和淀粉酶的血清(S)水平显著更高。结果表明,药物使用会影响皮质和皮质下异常的发生率,但前角指数除外。得出的结论是,滥用酒精且使用肝毒性药物的组表现出皮质改变(交通沟增宽以及明确的或高级别的皮质改变)以及皮质下异常,表现为第三脑室增宽增加。