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Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease

Background: Mitochondrial dysfunction plays a key role in PD, but the underlying molecular mechanisms remain unresolved. We hypothesized that the disruption of mitochondrial function in PD is primed by rare, protein‐altering variation in nuclear genes controlling mitochondrial structure and function...

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Autores principales: Gaare, Johannes J., Nido, Gonzalo S., Sztromwasser, Paweł, Knappskog, Per M., Dahl, Olav, Lund‐Johansen, Morten, Maple‐Grødem, Jodi, Alves, Guido, Tysnes, Ole‐Bjørn, Johansson, Stefan, Haugarvoll, Kristoffer, Tzoulis, Charalampos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282592/
https://www.ncbi.nlm.nih.gov/pubmed/30256453
http://dx.doi.org/10.1002/mds.64
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author Gaare, Johannes J.
Nido, Gonzalo S.
Sztromwasser, Paweł
Knappskog, Per M.
Dahl, Olav
Lund‐Johansen, Morten
Maple‐Grødem, Jodi
Alves, Guido
Tysnes, Ole‐Bjørn
Johansson, Stefan
Haugarvoll, Kristoffer
Tzoulis, Charalampos
author_facet Gaare, Johannes J.
Nido, Gonzalo S.
Sztromwasser, Paweł
Knappskog, Per M.
Dahl, Olav
Lund‐Johansen, Morten
Maple‐Grødem, Jodi
Alves, Guido
Tysnes, Ole‐Bjørn
Johansson, Stefan
Haugarvoll, Kristoffer
Tzoulis, Charalampos
author_sort Gaare, Johannes J.
collection PubMed
description Background: Mitochondrial dysfunction plays a key role in PD, but the underlying molecular mechanisms remain unresolved. We hypothesized that the disruption of mitochondrial function in PD is primed by rare, protein‐altering variation in nuclear genes controlling mitochondrial structure and function. Objective: The objective of this study was to assess whether genetic variation in genes associated with mitochondrial function influences the risk of idiopathic PD. Methods: We employed whole‐exome sequencing data from 2 independent cohorts of clinically validated idiopathic PD and controls, the Norwegian ParkWest cohort (n = 411) and the North American Parkinson's Progression Markers Initiative (n = 640). We applied burden‐based and variance‐based collapsing methods to assess the enrichment of rare, nonsynonymous, and damaging genetic variants on genes, exome‐wide, and on a comprehensive set of mitochondrial pathways, defined as groups of genes controlling specific mitochondrial functions. Results: Using the sequence kernel association test, we detected a significant polygenic enrichment of rare, nonsynonymous variants in the gene‐set encoding the pathway of mitochondrial DNA maintenance. Notably, this was the strongest association in both cohorts and survived multiple testing correction (ParkWest P = 6.3 × 10(−3), Parkinson's Progression Markers Initiative P = 6.9 × 10(−5), metaanalysis P = 3.2 × 10(−6)). Conclusions: Our results show that the enrichment of rare inherited variation in the pathway controlling mitochondrial DNA replication and repair influences the risk of PD. We propose that this polygenic enrichment contributes to the impairment of mitochondrial DNA homeostasis, thought to be a key mechanism in the pathogenesis of PD, and explains part of the disorder's “missing heritability.” © 2018 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society
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spelling pubmed-62825922018-12-11 Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease Gaare, Johannes J. Nido, Gonzalo S. Sztromwasser, Paweł Knappskog, Per M. Dahl, Olav Lund‐Johansen, Morten Maple‐Grødem, Jodi Alves, Guido Tysnes, Ole‐Bjørn Johansson, Stefan Haugarvoll, Kristoffer Tzoulis, Charalampos Mov Disord Research Articles Background: Mitochondrial dysfunction plays a key role in PD, but the underlying molecular mechanisms remain unresolved. We hypothesized that the disruption of mitochondrial function in PD is primed by rare, protein‐altering variation in nuclear genes controlling mitochondrial structure and function. Objective: The objective of this study was to assess whether genetic variation in genes associated with mitochondrial function influences the risk of idiopathic PD. Methods: We employed whole‐exome sequencing data from 2 independent cohorts of clinically validated idiopathic PD and controls, the Norwegian ParkWest cohort (n = 411) and the North American Parkinson's Progression Markers Initiative (n = 640). We applied burden‐based and variance‐based collapsing methods to assess the enrichment of rare, nonsynonymous, and damaging genetic variants on genes, exome‐wide, and on a comprehensive set of mitochondrial pathways, defined as groups of genes controlling specific mitochondrial functions. Results: Using the sequence kernel association test, we detected a significant polygenic enrichment of rare, nonsynonymous variants in the gene‐set encoding the pathway of mitochondrial DNA maintenance. Notably, this was the strongest association in both cohorts and survived multiple testing correction (ParkWest P = 6.3 × 10(−3), Parkinson's Progression Markers Initiative P = 6.9 × 10(−5), metaanalysis P = 3.2 × 10(−6)). Conclusions: Our results show that the enrichment of rare inherited variation in the pathway controlling mitochondrial DNA replication and repair influences the risk of PD. We propose that this polygenic enrichment contributes to the impairment of mitochondrial DNA homeostasis, thought to be a key mechanism in the pathogenesis of PD, and explains part of the disorder's “missing heritability.” © 2018 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society John Wiley and Sons Inc. 2018-09-05 2018-10 /pmc/articles/PMC6282592/ /pubmed/30256453 http://dx.doi.org/10.1002/mds.64 Text en © 2018 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Gaare, Johannes J.
Nido, Gonzalo S.
Sztromwasser, Paweł
Knappskog, Per M.
Dahl, Olav
Lund‐Johansen, Morten
Maple‐Grødem, Jodi
Alves, Guido
Tysnes, Ole‐Bjørn
Johansson, Stefan
Haugarvoll, Kristoffer
Tzoulis, Charalampos
Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title_full Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title_fullStr Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title_full_unstemmed Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title_short Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
title_sort rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282592/
https://www.ncbi.nlm.nih.gov/pubmed/30256453
http://dx.doi.org/10.1002/mds.64
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