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Mitochondrial haplogroups and cognitive progression in Parkinson's disease.

Ganqiang LiuChunming NiJiamin ZhanWeimin LiJunfeng LuoZhixiang LiaoJoseph J LocascioWenbiao XianLing ChenZhong PeiJean-Christophe CorvolJodi Maple-GrødemMeghan C CampbellAlexis ElbazSuzanne LesageAlexis BriceAlbert Y HungMichael A SchwarzschildMichael T HayesAnne-Marie WillsBernard RavinaIra ShoulsonPille TabaSulev KõksThomas G BeachFlorence Cormier-DequaireGuido AlvesOle-Bjørn TysnesJoel S PerlmutterPeter HeutinkJacobus J van HiltenRoger A BarkerCaroline H Williams-GrayClemens R Scherzernull null
Published in: Brain : a journal of neurology (2022)
Mitochondria are a culprit in the onset of Parkinson's disease, but their role during disease progression is unclear. Here we used Cox proportional hazards models to exam the effect of variation in the mitochondrial genome on longitudinal cognitive and motor progression over time in 4064 patients with Parkinson's disease. Mitochondrial macro-haplogroup was associated with reduced risk of cognitive disease progression in the discovery and replication population. In the combined analysis, patients with the super macro-haplogroup J, T, U# had a 41% lower risk of cognitive progression with P = 2.42 × 10-6 compared to those with macro-haplogroup H. Exploratory analysis indicated that the common mitochondrial DNA variant, m.2706A>G, was associated with slower cognitive decline with a hazard ratio of 0.68 (95% confidence interval 0.56-0.81) and P = 2.46 × 10-5. Mitochondrial haplogroups were not appreciably linked to motor progression. This initial genetic survival study of the mitochondrial genome suggests that mitochondrial haplogroups may be associated with the pace of cognitive progression in Parkinson's disease over time.
Keyphrases
  • mitochondrial dna
  • oxidative stress
  • copy number
  • cognitive decline
  • genome wide
  • mild cognitive impairment
  • cell death
  • small molecule