Gentric A, Fouilhoux A, Caroff M, Mottier D, Jouquan J
Clinique Médicale Harvier, CHU A. Morvan, Brest.
J Am Geriatr Soc. 1993 May;41(5):550-1. doi: 10.1111/j.1532-5415.1993.tb01894.x.
We report the case of an elderly woman with severe dysautonomic orthostatic hypotension in whom a deficit in dopamine B hydroxylase has been established. In the literature, such a deficit has been described in six young adults with long standing symptoms of postural hypotension. This enzyme catalyses the conversion of dopamine to noradrenaline. In our elderly patient, noradrenaline and adrenaline were undetectable in the plasma, but plasma dopamine was detectable. Treatment with the synthetic amino acid, DL-threo-dihydroxyphenylserine, which is converted to noradrenaline by dopa-decarboxylase, resulted in a significant increase in blood pressure. The mechanism of this acquired deficit is not elucidated.
我们报告了一例患有严重自主神经功能障碍性直立性低血压的老年女性病例,该病例已确诊存在多巴胺β羟化酶缺乏。在文献中,这种缺乏在六名有长期体位性低血压症状的年轻成年人中有所描述。这种酶催化多巴胺转化为去甲肾上腺素。在我们的老年患者中,血浆中未检测到去甲肾上腺素和肾上腺素,但可检测到血浆多巴胺。用合成氨基酸DL-苏式二羟基苯丝氨酸治疗,该氨基酸通过多巴脱羧酶转化为去甲肾上腺素,导致血压显著升高。这种后天性缺乏的机制尚不清楚。