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丙酮酸脱氢酶磷酸酶缺乏症:罕见病还是诊断不足的病症?

Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?

作者信息

Maj M C, Cameron J M, Robinson B H

机构信息

Metabolism Research Programme, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, Ont., Canada M5G 1X8.

出版信息

Mol Cell Endocrinol. 2006 Apr 25;249(1-2):1-9. doi: 10.1016/j.mce.2006.02.003. Epub 2006 Mar 29.

Abstract

Pyruvate dehydrogenase phosphatase (PDP) is an enzyme which regulates the activity of the pyruvate dehydrogenase complex (PDHc). In the past, PDHc deficiency has been attributed to mutations in the complex itself and the regulatory enzymes have not been considered. We have recently reported the first mutation in PDP1, one of the two isoforms of PDP, which results in severe exercise intolerance and mild developmental delay in patients. This novel process of aberrant pyruvate metabolism opens up a new avenue for investigation into PDHc deficiency, that has hitherto been underappreciated.

摘要

丙酮酸脱氢酶磷酸酶(PDP)是一种调节丙酮酸脱氢酶复合体(PDHc)活性的酶。过去,PDHc缺乏症被认为是由于该复合体自身的突变所致,而调节酶未被纳入考虑。我们最近报道了PDP的两种同工型之一PDP1中的首个突变,该突变导致患者出现严重的运动不耐受和轻度发育迟缓。这种丙酮酸代谢异常的新机制为研究PDHc缺乏症开辟了一条新途径,而这一点迄今为止一直未得到充分认识。

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