Robertson D, Haile V, Perry S E, Robertson R M, Phillips J A, Biaggioni I
Department of Pharmacology, Vanderbilt University, Nashville, Tenn. 37232-2195.
Hypertension. 1991 Jul;18(1):1-8. doi: 10.1161/01.hyp.18.1.1.
Dopamine beta-hydroxylase (DBH) deficiency is a genetic disorder in which affected patients cannot synthesize norepinephrine, epinephrine, and octopamine in either the central nervous system or the peripheral autonomic neurons. Dopamine acts as a false neurotransmitter in their noradrenergic neurons. Neonates with DBH deficiency have had episodic hypothermia, hypoglycemia, and hypotension, but survivors sometimes cope relatively well until late childhood when overwhelming orthostatic hypotension profoundly limits their activities. The hypotension may be so severe that clonic seizures supervene. Most currently recognized patients are young or middle-aged adults. The diagnosis is established by the observation of severe orthostatic hypotension in a patient whose plasma norepinephrine/dopamine ratio is much less than one.
多巴胺β-羟化酶(DBH)缺乏症是一种遗传性疾病,患病患者在中枢神经系统或外周自主神经元中均无法合成去甲肾上腺素、肾上腺素和章鱼胺。多巴胺在其去甲肾上腺素能神经元中充当假性神经递质。患有DBH缺乏症的新生儿会出现间歇性体温过低、低血糖和低血压,但幸存者有时在童年晚期之前应对相对良好,直到严重的直立性低血压严重限制他们的活动。低血压可能非常严重,以至于会出现阵挛性惊厥。目前大多数已确诊的患者为青年或中年成年人。通过观察血浆去甲肾上腺素/多巴胺比值远低于1的患者出现严重直立性低血压来确诊。