自闭症缺锌:一项对照研究

D. Goyal, Neil, Simmons Sd, F. Mansab, S. Benjamin, Pitfield, S. Boulet, Jaleel A. Miyan
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引用次数: 7

摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是社交障碍和限制和重复的行为模式。此前已有ASD患者缺锌的报道。一项回顾性对照试验对ASD患者和非ASD患者的血清锌水平进行了研究,以探讨ASD人群中锌缺乏的潜在存在。72例ASD患者与234例非ASD对照。比较各组血清锌水平,并分析年龄、性别、补充剂使用和饮食的相关性。还比较了ASD组和对照组之间的血清铬和锰水平,以评估一般微量营养素状况。在ASD组进行了进一步的分析,调查血清锌水平与免疫功能之间的潜在相关性。86%的ASD患者缺锌,而非ASD对照组缺锌的比例为24%。ASD组与非ASD组血清锌水平平均差异为1.75 μmol/l (P< 0.001, CI为1.2 ~ 1.2)。在ASD组和对照组中,年龄和性别对血清锌水平没有影响。在ASD患者和对照组之间,铬和锰的含量没有显著差异。这些结果表明,锌缺乏症可能在ASD患者中很常见,并且是与该疾病相关的潜在可改变的环境因素。本文讨论了锌在自闭症发病机制和疾病演变中的潜在作用,并强调了考虑ASD患者锌水平的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zinc Deficiency in Autism: A Controlled Study
Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder characterised by impaired socialisation and restricted and repetitive patterns of behaviour. Zinc deficiency has previously been reported in patients with ASD. A retrospective controlled trial of serum zinc levels in patients with ASD vs. non-ASD controls was undertaken to explore the potential presence of zinc deficiency in the ASD population. 72 patients with ASD were compared with 234 non-ASD controls. Serum zinc levels were compared between groups and correlations analysed for age, sex, supplement use and diet. Serum chromium and manganese levels were also compared between ASD and control groups to assess general micronutrient status. Further analysis was undertaken in the ASD group investigating potential correlations between serum zinc levels and immune function. 86% of patients with ASD were found to be zinc deficient versus 24% of the non-ASD control group. There was a mean difference of serum zinc levels between the ASD and non-ASD groups of 1·75 μmol/l (P<0·001, CI 1·2-2·1). There was no effect of age or sex on serum zinc levels in either the ASD or control groups. There was no significant difference in chromium or manganese levels between the ASD and control group. These results suggest zinc deficiency is likely to be common in ASD patients and is a potentially modifiable environmental factor associated with the condition. Zinc’s potential role in the aetio-pathogenesis and disease evolution is discussed, and the need to consider zinc status in patients with ASD is highlighted.
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