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一项针对自闭症谱系障碍患者的低剂量二甲基甘氨酸的双盲、安慰剂对照、交叉试点试验。

A double-blind, placebo-controlled, crossover pilot trial of low dose dimethylglycine in patients with autistic disorder.

作者信息

Bolman W M, Richmond J A

出版信息

J Autism Dev Disord. 1999 Jun;29(3):191-4. doi: 10.1023/a:1023023820671.

Abstract

As the treatability of the syndrome of autism becomes more possible there is a great deal more interest in the effectiveness of various therapies. Although the very influential nonmedical literature cited in the Autism Research Review International Newsletter finds that dimethylglycine (DMG) is regarded as more effective than the usual psychopharmacologic drugs, there have been no studies of DMG using the currently accepted research methodology. We report a double-blind, placebo-controlled, crossover pilot study of low dose DMG and placebo in a sample of eight autistic males ranging in age from 4 years 5 months to 30 years 8 months, who completed the full 3 1/2-month study consisting of drug-free baseline periods at the beginning, end, and in-between two, 1-month double-blind trials in which DMG or placebo was given. Measures included the Campbell-NIMH rating scale, an experimental rating scale, and an individualized scale created for each child. Analysis of all three scales revealed no statistically significant differences, and parent reports were equally distributed. The major methodologic weaknesses of the study are thought to be the low dosage of DMG and the small sample size.

摘要

随着自闭症综合征的可治疗性变得更有可能实现,人们对各种疗法的有效性产生了更大的兴趣。尽管《国际自闭症研究评论通讯》中引用的极具影响力的非医学文献发现,二甲基甘氨酸(DMG)被认为比常用的精神药物更有效,但尚未有使用当前公认研究方法对DMG进行的研究。我们报告了一项针对8名年龄在4岁5个月至30岁8个月之间的自闭症男性样本的低剂量DMG和安慰剂的双盲、安慰剂对照、交叉试点研究,这些男性完成了为期3个半月的完整研究,该研究在开始、结束时以及两次为期1个月的双盲试验(期间给予DMG或安慰剂)之间设有无药物基线期。测量指标包括坎贝尔-美国国立精神卫生研究所评定量表、一个实验性评定量表以及为每个孩子创建的个性化量表。对所有三个量表的分析均未发现统计学上的显著差异,家长报告也均匀分布。该研究的主要方法学弱点被认为是DMG的低剂量和小样本量。

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