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Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers.
Sugier, Pierre-Emmanuel; Lucotte, Elise A; Domenighetti, Cloé; Law, Matthew H; Iles, Mark M; Brown, Kevin; Amos, Christopher; McKay, James D; Hung, Rayjean J; Karimi, Mojgan; Bacq-Daian, Delphine; Boland-Augé, Anne; Olaso, Robert; Deleuze, Jean-François; Lesueur, Fabienne; Ostroumova, Evgenia; Kesminiene, Ausrele; de Vathaire, Florent; Guénel, Pascal; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Grover, Sandeep; May, Patrick; Bobbili, Dheeraj R; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B; Hernandez, Dena G; Edsall, Connor; Mellick, George D; Zimprich, Alexander; Pirker, Walter; Rogaeva, Ekaterina; Lang, Anthony E; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugénie; Brockmann, Kathrin; Deutschländer, Angela B; Hadjigeorgiou, Georges M; Dardiotis, Efthimios; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Straniero, Letizia.
Affiliation
  • Sugier PE; Université Paris-Saclay, UVSQ, Inserm, Gustave Roussy, Team "Exposome, Heredity, Cancer and Health", CESP, Villejuif, France.
  • Lucotte EA; Laboratoire de Mathématiques et de leurs Applications de Pau, E2S UPPA, CNRS, Pau, France.
  • Domenighetti C; Université Paris-Saclay, UVSQ, Inserm, Gustave Roussy, Team "Exposome, Heredity, Cancer and Health", CESP, Villejuif, France.
  • Law MH; Université Paris-Saclay, UVSQ, Inserm, Gustave Roussy, Team "Exposome, Heredity, Cancer and Health", CESP, Villejuif, France.
  • Iles MM; Statistical Genetics, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
  • Brown K; Faculty of Health, Queensland University of Technology, Brisbane, Australia.
  • Amos C; Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
  • McKay JD; Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Hung RJ; Institute for Clinical and Translational Research, Baylor Medical College of Medecine, Houston, Texas, USA.
  • Karimi M; International Agency for Research on Cancer, Lyon, France.
  • Bacq-Daian D; Lunenfeld-Tanenbuaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
  • Boland-Augé A; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Olaso R; Université Paris-Saclay, UVSQ, Inserm, Gustave Roussy, Team "Exposome, Heredity, Cancer and Health", CESP, Villejuif, France.
  • Deleuze JF; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, Evry, France.
  • Lesueur F; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, Evry, France.
  • Ostroumova E; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, Evry, France.
  • Kesminiene A; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, Evry, France.
  • de Vathaire F; Inserm, U900, Institut Curie, PSL University, Mines ParisTech, Paris, France.
  • Guénel P; International Agency for Research on Cancer, Lyon, France.
  • Sreelatha AAK; Université Paris-Saclay, UVSQ, Gustave Roussy, Inserm, Team "Epidemiology of radiations," CESP, Villejuif, France.
  • Schulte C; Université Paris-Saclay, UVSQ, Inserm, Gustave Roussy, Team "Exposome, Heredity, Cancer and Health", CESP, Villejuif, France.
  • May P; Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tubingen, Tübingen, Germany.
  • Bobbili DR; Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tubingen, Tübingen, Germany.
  • Radivojkov-Blagojevic M; German Center for Neurodegenerative Diseases, Tübingen, Germany.
  • Lichtner P; Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tubingen, Tübingen, Germany.
  • Singleton AB; Translational Neuroscience, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Belval, Luxembourg.
  • Hernandez DG; Translational Neuroscience, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-Belval, Luxembourg.
  • Edsall C; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Mellick GD; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Zimprich A; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.
  • Pirker W; Center For Alzheimer's and Related Dementias, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.
  • Rogaeva E; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.
  • Lang AE; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.
  • Koks S; Griffith Institute for Drug Discovery, Griffith University, Nathan, Australia.
  • Taba P; Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Lesage S; Department of Neurology, Klinik Ottakring, Vienna, Austria.
  • Brice A; Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada.
  • Corvol JC; Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN, Toronto, Ontario, Canada.
  • Chartier-Harlin MC; Division of Neurology, University of Toronto, Toronto, Ontario, Canada.
  • Mutez E; Krembil Brain Institute, Toronto, Ontario, Canada.
  • Brockmann K; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Murdoch, Australia.
  • Deutschländer AB; Perron Institute for Neurological and Translational Science, Nedlands, Australia.
  • Hadjigeorgiou GM; Department of Neurology and Neurosurgery, University of Tartu, Tartu, Estonia.
  • Dardiotis E; Neurology Clinic, Tartu University Hospital, Tartu, Estonia.
  • Stefanis L; Department of Neurology, Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Simitsi AM; Department of Neurology, Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Valente EM; Department of Neurology, Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Petrucci S; Assistance Publique Hôpitaux de Paris, Department of Neurology, CIC Neurosciences, Paris, France.
  • Straniero L; Université de Lille, Inserm, CHU Lille, UMR-S 1172, LilNCog, Centre de Recherche Lille Neurosciences & Cognition, Lille, France.
Mov Disord ; 38(4): 604-615, 2023 04.
Article in En | MEDLINE | ID: mdl-36788297
ABSTRACT

BACKGROUND:

Epidemiological studies that examined the association between Parkinson's disease (PD) and cancers led to inconsistent results, but they face a number of methodological difficulties.

OBJECTIVE:

We used results from genome-wide association studies (GWASs) to study the genetic correlation between PD and different cancers to identify common genetic risk factors.

METHODS:

We used individual data for participants of European ancestry from the Courage-PD (Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease; PD, N = 16,519) and EPITHYR (differentiated thyroid cancer, N = 3527) consortia and summary statistics of GWASs from iPDGC (International Parkinson Disease Genomics Consortium; PD, N = 482,730), Melanoma Meta-Analysis Consortium (MMAC), Breast Cancer Association Consortium (breast cancer), the Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (prostate cancer), International Lung Cancer Consortium (lung cancer), and Ovarian Cancer Association Consortium (ovarian cancer) (N comprised between 36,017 and 228,951 for cancer GWASs). We estimated the genetic correlation between PD and cancers using linkage disequilibrium score regression. We studied the association between PD and polymorphisms associated with cancers, and vice versa, using cross-phenotypes polygenic risk score (PRS) analyses.

RESULTS:

We confirmed a previously reported positive genetic correlation of PD with melanoma (Gcorr = 0.16 [0.04; 0.28]) and reported an additional significant positive correlation of PD with prostate cancer (Gcorr = 0.11 [0.03; 0.19]). There was a significant inverse association between the PRS for ovarian cancer and PD (odds ratio [OR] = 0.89 [0.84; 0.94]). Conversely, the PRS of PD was positively associated with breast cancer (OR = 1.08 [1.06; 1.10]) and inversely associated with ovarian cancer (OR = 0.95 [0.91; 0.99]). The association between PD and ovarian cancer was mostly driven by rs183211 located in an intron of the NSF gene (17q21.31).

CONCLUSIONS:

We show evidence in favor of a contribution of pleiotropic genes to the association between PD and specific cancers. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Parkinson Disease / Prostatic Neoplasms / Lung Neoplasms / Melanoma Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Parkinson Disease / Prostatic Neoplasms / Lung Neoplasms / Melanoma Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2023 Document type: Article Affiliation country:
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