Parkinson's disease determinants, prediction and gene-environment interactions in the UK Biobank.
Adult
Aged
Alcohol Drinking
/ epidemiology
Biological Specimen Banks
Depression
/ epidemiology
Diabetes Mellitus
/ epidemiology
Disorders of Excessive Somnolence
/ epidemiology
Epilepsy
/ epidemiology
Female
Gene-Environment Interaction
Genetic Predisposition to Disease
Humans
Logistic Models
Male
Menarche
Middle Aged
Parkinson Disease
/ epidemiology
Protective Factors
Risk Factors
Smoking
/ epidemiology
United Kingdom
/ epidemiology
Journal
Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
26
04
2020
revised:
30
06
2020
accepted:
02
07
2020
entrez:
16
9
2020
pubmed:
17
9
2020
medline:
23
3
2021
Statut:
ppublish
Résumé
To systematically investigate the association of environmental risk factors and prodromal features with incident Parkinson's disease (PD) diagnosis and the interaction of genetic risk with these factors. To evaluate whether existing risk prediction algorithms are improved by the inclusion of genetic risk scores. We identified individuals with an incident diagnosis of PD (n=1276) and controls (n=500 406) in UK Biobank. We determined the association of risk factors with incident PD using adjusted logistic regression models. We constructed polygenic risk scores (PRSs) using external weights and selected the best PRS from a subset of the cohort (30%). The PRS was used in a separate testing set (70%) to examine gene-environment interactions and compare predictive models for PD. Strong evidence of association (false discovery rate <0.05) was found between PD and a positive family history of PD, a positive family history of dementia, non-smoking, low alcohol consumption, depression, daytime somnolence, epilepsy and earlier menarche. Individuals with the highest 10% of PRSs had increased risk of PD (OR 3.37, 95% CI 2.41 to 4.70) compared with the lowest risk decile. A higher PRS was associated with earlier age at PD diagnosis and inclusion of the PRS in the PREDICT-PD algorithm led to a modest improvement in model performance. We found evidence of an interaction between the PRS and diabetes. Here, we used UK Biobank data to reproduce several well-known associations with PD, to demonstrate the validity of a PRS and to demonstrate a novel gene-environment interaction, whereby the effect of diabetes on PD risk appears to depend on background genetic risk for PD.
Identifiants
pubmed: 32934108
pii: jnnp-2020-323646
doi: 10.1136/jnnp-2020-323646
pmc: PMC7509524
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1046-1054Subventions
Organisme : Parkinson's UK
ID : F-1201
Pays : United Kingdom
Organisme : Parkinson's UK
ID : G-1606
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N026004/1
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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