Poikolainen Kari, Alho Hannu
Finnish Foundation for Alcohol Studies, Helsinki, Finland.
Subst Abuse Treat Prev Policy. 2008 Jan 25;3:1. doi: 10.1186/1747-597X-3-1.
Magnesium (Mg) deficiency is common among alcoholics. Earlier research suggests that Mg treatment may help to normalize elevated enzyme activities and some other clinically relevant parameters among alcoholics but the evidence is weak.
The effect of Mg was studied in a randomized, parallel group, double-blind trial. The patients were first treated for alcohol withdrawal symptoms and then received for 8 weeks either 500 mg of Mg divided into two tablets or matching placebo. Measurements were made at the beginning and in the end of the Mg treatment period. The primary outcome was serum gamma-glutamyltransferase (S-GGT) activity; secondary outcomes included aspartate-aminotransferase (S-AST) and alanine-aminotransferase (S-ALT) activity.
The number of randomized patients (completers) was 64 (27) in the treatment and 54 (31) in the control group. In intention-to-treat-analyses and in most analyses of study completers, there were no significant differences between the Mg-treated and placebo groups in the outcome variables. When baseline serum Mg level, coffee intake, and the number of unused Mg tablets were controlled for in a multivariate regression model, after-treatment serum Mg levels were found to be higher among the Mg-treated group than in the placebo group (t-test 3.334, df = 53, p = 0.002). After controlling for age, body weight, baseline alcohol intake, subsequent change in alcohol intake and baseline S-AST, the after-treatment S-AST levels were found to be lower among the Mg-treated group than in the placebo group (t-test 2.061, df = 49, p = 0.045).
Mg treatment may speed up the S-AST decrease in compliant patients. This might decrease the risk of death from alcoholic liver disease.
ClinicalTrials.gov ID NCT00325299.
镁(Mg)缺乏在酗酒者中很常见。早期研究表明,镁治疗可能有助于使酗酒者升高的酶活性和其他一些临床相关参数恢复正常,但证据不足。
在一项随机、平行组、双盲试验中研究了镁的作用。患者首先接受戒酒症状治疗,然后接受为期8周的治疗,即每天服用两片共500毫克镁或匹配的安慰剂。在镁治疗期开始和结束时进行测量。主要结局是血清γ-谷氨酰转移酶(S-GGT)活性;次要结局包括天冬氨酸转氨酶(S-AST)和丙氨酸转氨酶(S-ALT)活性。
治疗组随机分组患者(完成者)人数为64(27),对照组为54(31)。在意向性分析和大多数研究完成者分析中,镁治疗组和安慰剂组在结局变量上无显著差异。在多变量回归模型中控制基线血清镁水平、咖啡摄入量和未使用镁片数量后,发现镁治疗组治疗后血清镁水平高于安慰剂组(t检验3.334,自由度=53,p=0.002)。在控制年龄、体重、基线酒精摄入量、随后酒精摄入量变化和基线S-AST后,发现镁治疗组治疗后S-AST水平低于安慰剂组(t检验2.061,自由度=49,p=0.045)。
镁治疗可能会加速依从性患者S-AST的下降。这可能会降低酒精性肝病导致的死亡风险。
ClinicalTrials.gov标识符NCT00325299。