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X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease.

Thiago Peixoto LealJennifer N French-KwawuMateus H GouveiaVíctor BordaMiguel Inca-MartinezEmily A MasonAndrea R V R HorimotoDouglas P LoeschElif I SarihanMario R Cornejo-OlivasLuis E TorresPilar E Mazzetti-SolerCarlos CosentinoElison H Sarapura-CastroAndrea Rivera-ValdiviaAngel C MedinaElena M DieguezVíctor E RaggioAndrés LescanoVitor TumasVanderci BorgesHenrique Ballalai FerrazCarlos Roberto de Mello RiederArtur Francisco Schumacher-SchuhBruno Lopes Dos Santos-LobatoCarlos Velez-PardoMarlene Jimenez-Del-RioFrancisco LoperaSonia MorenoPedro Chaná-CuevasWilliam FernandezGonzalo ArboledaHumberto ArboledaCarlos E Arboleda BustosDora YearoutMaria F Lima-CostaEduardo TarazonaCyrus P ZabetianTimothy A ThorntonTimothy D O'ConnorIgnacio Fernandez Mata
Published in: medRxiv : the preprint server for health sciences (2023)
Sex differences in Parkinson Disease (PD) risk are well-known. However, it is still unclear the role of sex chromosomes in the development and progression of PD. We performed the first X-chromosome Wide Association Study (XWAS) for PD risk in Latin American individuals. We used data from three admixed cohorts: (i) Latin American Research consortium on the GEnetics of Parkinson's Disease (n=1,504) as discover cohort and (ii) Latino cohort from International Parkinson Disease Genomics Consortium (n = 155) and (iii) Bambui Aging cohort (n= 1,442) as replication cohorts. After developing a X-chromosome framework specifically designed for admixed populations, we identified eight linkage disequilibrium regions associated with PD. We fully replicated one of these regions (top variant rs525496; discovery OR [95%CI]: 0.60 [0.478 - 0.77], p = 3.13 × 10 -5 ; replication OR: 0.60 [0.37-0.98], p = 0.04). rs525496 is an expression quantitative trait loci for several genes expressed in brain tissues, including RAB9B, H2BFM, TSMB15B and GLRA4 . We also replicated a previous XWAS finding (rs28602900), showing that this variant is associated with PD in non-European populations. Our results reinforce the importance of including X-chromosome and diverse populations in genetic studies.
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