Department of Internal Medicine, Isala Clinics, P.O. Box 10400, 8000 GK Zwolle, The Netherlands.
Int J Endocrinol. 2012;2012:456279. doi: 10.1155/2012/456279. Epub 2012 Jan 26.
Objective. We performed a systematic review of the literature to evaluate the effects of alpha lipoic acid for symptomatic peripheral neuropathy in patients with diabetes mellitus. Research design and methods. The databases MEDLINE and EMBASE were searched using the key words "lipoic acid", "thioctic acid", "diabet∗", and the MeSH-terms "thioctic acid" and "diabetes mellitus". Randomised controlled trials using the TSS score as the outcome measure were selected and assessed for their methodological quality. Study selection and quality assessment were performed independently by three observers. Results. Overall, the pooled standardized mean difference estimated from all trials revealed a reduction in TSS scores of -2.26 (CI: -3.12 to -1.41; P = 0.00001) in favour of alpha lipoic acid administration. Subgroup analyses of oral administration (-1.78 CI: -2.45 to -1.10; P = 0.00001) and intravenous administration (-2.81 CI: -4.16 to -1.46; P = 0.0001) confirmed the robustness of the overall result. Conclusions. When given intravenously at a dosage of 600 mg/day over a period of 3 weeks, alpha lipoic acid leads to a significant and clinically relevant reduction in neuropathic pain (grade of recommendation A). It is unclear if the significant improvements seen after 3-5 weeks of oral administration at a dosage of >600 mg/day are clinically relevant.
目的。我们对文献进行了系统回顾,以评估硫辛酸治疗糖尿病周围神经病变患者的症状性周围神经病变的效果。
研究设计和方法。使用关键词“lipoic acid”(硫辛酸)、“thioctic acid”(硫辛酸)、“diabet∗”(糖尿病),以及 MeSH 术语“thioctic acid”(硫辛酸)和“diabetes mellitus”(糖尿病),对 MEDLINE 和 EMBASE 数据库进行检索。选择并评估了使用 TSS 评分作为结局测量的随机对照试验,并评估了其方法学质量。研究选择和质量评估由三位观察者独立进行。
结果。总体而言,所有试验的汇总标准化均数差估计表明,TSS 评分降低了-2.26(CI:-3.12 至-1.41;P = 0.00001),这有利于硫辛酸治疗。口服给药(-1.78 CI:-2.45 至-1.10;P = 0.00001)和静脉给药(-2.81 CI:-4.16 至-1.46;P = 0.0001)的亚组分析证实了总体结果的稳健性。
结论。静脉给予 600 mg/天,持续 3 周,硫辛酸可显著减轻神经病理性疼痛(推荐等级 A)。目前尚不清楚每天口服给药 600mg 以上,治疗 3-5 周后观察到的显著改善是否具有临床意义。