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Increased prevalence of Parkinson's disease in alkaptonuria.
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.
Affiliation
  • Ranganath L; Department of Clinical Biochemistry and Metabolic Medicine Royal Liverpool University Hospital Liverpool UK.
  • Khedr M; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences University of Liverpool Liverpool UK.
  • Milan AM; Department of Clinical Biochemistry and Metabolic Medicine Royal Liverpool University Hospital Liverpool UK.
  • Davison AS; Department of Clinical Biochemistry and Metabolic Medicine Royal Liverpool University Hospital Liverpool UK.
  • Norman BP; Department of Clinical Biochemistry and Metabolic Medicine Royal Liverpool University Hospital Liverpool UK.
  • Janssen MCH; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences University of Liverpool Liverpool UK.
  • Lock E; Departments of Internal Medicine & Pediatrics Radboud University Nijmegen Medical Centre Nijmegen Netherlands.
  • Bou-Gharios G; School of Pharmacy and Biomolecular Sciences Liverpool John Moores University Liverpool UK.
  • Gallagher JA; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences University of Liverpool Liverpool UK.
JIMD Rep ; 64(4): 282-292, 2023 Jul.
Article in En | MEDLINE | ID: mdl-37404676
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 A further unpublished case of a Dutch patient with AKU and PD on deep brain stimulation is included in this report.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 (p < 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prevalence_studies / Risk_factors_studies Language: En Journal: JIMD Rep Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prevalence_studies / Risk_factors_studies Language: En Journal: JIMD Rep Year: 2023 Document type: Article