Nielsen J B, Bach F W, Buchholt J, Lou H
Department of Neuropaediatrics, John F. Kennedy Institute, Glostrup, Denmark.
Dev Med Child Neurol. 1991 May;33(5):406-11. doi: 10.1111/j.1469-8749.1991.tb14900.x.
An hypothesis of increased endorphinergic activity has been proposed to account for the characteristic symptoms of Rett syndrome. Cerebrospinal fluid samples from eight girls with Rett syndrome were analysed for beta-endorphin (beta-EP) immunoactivity and compared with samples from a control group of 15 children with acute leukaemia in remission. Severity of symptoms was not found to be related to beta-EP level. A group of early-treated adolescents with phenylketonuria had beta-EP levels similar to the Rett syndrome patients, but no symptoms resembling theirs. Therefore it is unlikely that increased levels of beta-EP are of primary pathogenetic significance. The conflicting findings of many earlier reports may be a result of differences between control groups.
有人提出内啡肽能活性增加的假说,以解释雷特综合征的特征性症状。对8名雷特综合征女孩的脑脊液样本进行了β-内啡肽(β-EP)免疫活性分析,并与15名急性白血病缓解期儿童的对照组样本进行了比较。未发现症状严重程度与β-EP水平相关。一组早期接受治疗的苯丙酮尿症青少年的β-EP水平与雷特综合征患者相似,但没有类似他们的症状。因此,β-EP水平升高不太可能具有主要的致病意义。许多早期报告相互矛盾的结果可能是由于对照组之间的差异所致。