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尿黑酸尿症中帕金森病患病率增加。

Increased prevalence of Parkinson's disease in alkaptonuria.

作者信息

Ranganath Lakshminarayan, Khedr Milad, Milan Anna M, Davison Andrew S, Norman Brendan P, Janssen Mirian C H, Lock Edward, Bou-Gharios George, Gallagher James A

机构信息

Department of Clinical Biochemistry and Metabolic Medicine Royal Liverpool University Hospital Liverpool UK.

Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences University of Liverpool Liverpool UK.

出版信息

JIMD Rep. 2023 May 11;64(4):282-292. doi: 10.1002/jmd2.12367. eCollection 2023 Jul.

Abstract

Amongst a cohort of 88 alkaptonuria (AKU) patients attending the United Kingdom National Alkaptonuria Centre (NAC), four unrelated patients had co-existing Parkinson's disease (PD). Two of the NAC patients developed PD before receiving nitisinone (NIT) while the other two developed overt PD during NIT therapy. NIT lowers redox-active homogentisic acid (HGA) and profoundly increases tyrosine (TYR). A further unpublished case of a Dutch patient with AKU and PD on deep brain stimulation is included in this report. A Pubmed search revealed a further five AKU patients with PD, all without NIT usage. The prevalence of PD in AKU in the NAC appears to be nearly 20-times higher than in the non-AKU population ( < 0.001) even when adjusted for age. We propose that life-long exposure to redox-active HGA may account for the higher prevalence of PD in AKU. Furthermore, the appearance of PD in AKU patients during NIT therapy may be due to unmasking dopamine deficiency in susceptible individuals, as a result of the tyrosinaemia during NIT therapy inhibiting the rate-limiting brain tyrosine hydroxylase.

摘要

在英国国家黑尿症中心(NAC)就诊的88名黑尿症(AKU)患者队列中,有4名无亲缘关系的患者同时患有帕金森病(PD)。其中两名NAC患者在接受尼替西农(NIT)治疗前就已患上帕金森病,另外两名在接受NIT治疗期间出现了明显的帕金森病症状。NIT可降低具有氧化还原活性的尿黑酸(HGA)水平,并显著提高酪氨酸(TYR)水平。本报告还纳入了另一例未发表的荷兰患者病例,该患者患有AKU和帕金森病,正在接受深部脑刺激治疗。通过PubMed搜索又发现了另外5名患有帕金森病的AKU患者,他们均未使用过NIT。即使在对年龄进行调整后,NAC中AKU患者的帕金森病患病率似乎也比非AKU人群高出近20倍(<0.001)。我们认为,终生暴露于具有氧化还原活性的HGA可能是AKU患者中帕金森病患病率较高的原因。此外,AKU患者在NIT治疗期间出现帕金森病,可能是由于NIT治疗期间的酪氨酸血症抑制了大脑中限速酶酪氨酸羟化酶,从而使易感个体的多巴胺缺乏症状显现出来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0b8/10315388/3665776a390c/JMD2-64-282-g002.jpg

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