Delisi L E, Jeste D V, Phelps B H, Wyatt R J
J Clin Psychopharmacol. 1982 Oct;2(5):315-7.
Two peripheral enzymes, dopamine-beta-hydroxylase (DBH) and monoamine oxidase (MAO), have previously been found to be altered in patients with tardive dyskinesia (TD). In order to examine whether these changes relate to the inherited component of enzyme activity or environmental factors, we assayed DBH and MAO activities in families of six TD probands and six matched non-TD probands. Five of six TD probands had DBH activity at least 50% greater than that of the family mean, whereas two of six non-TD probands had the same trend. No deviation from family means was suggested for MAO activity in the TD group. A study of chronic schizophrenic quadruplets with a history of prolonged neuroleptic treatment showed that only one quadruplet had TD. This quadruplet had plasma DBH activity four standard deviations above the means for her three siblings and three other family members. Our data do not support inheritance of predisposition to develop TD. The enzymatic alterations in TD patients do not seem to have been determined genetically, but they are probably a result of abnormal biochemical effects of prolonged neuroleptic treatment in those patients.
此前已发现,迟发性运动障碍(TD)患者体内的两种外周酶——多巴胺-β-羟化酶(DBH)和单胺氧化酶(MAO)发生了改变。为了研究这些变化是与酶活性的遗传成分有关,还是与环境因素有关,我们对6名TD先证者和6名匹配的非TD先证者的家族成员进行了DBH和MAO活性检测。6名TD先证者中有5名的DBH活性至少比家族平均值高50%,而6名非TD先证者中有2名也有同样的趋势。TD组的MAO活性未显示出与家族平均值有偏差。一项对有长期抗精神病药物治疗史的慢性精神分裂症四胞胎的研究表明,只有一个四胞胎患有TD。这个四胞胎的血浆DBH活性比她的三个兄弟姐妹和其他三名家庭成员的平均值高出四个标准差。我们的数据不支持TD易感性的遗传。TD患者的酶改变似乎并非由基因决定,而可能是这些患者长期抗精神病药物治疗产生异常生化效应的结果。