Familial aggregation of Parkinson's disease and coaggregation with neuropsychiatric diseases: a population-based cohort study
- PMID: 29881310
- PMCID: PMC5985793
- DOI: 10.2147/CLEP.S164330
Familial aggregation of Parkinson's disease and coaggregation with neuropsychiatric diseases: a population-based cohort study
Abstract
Background: Individuals with a family history of Parkinson's disease (PD) appear to have a higher risk of developing PD and other neuropsychiatric diseases. However, estimates of the relative risks (RRs) of PD and the roles of genetic and environmental factors in PD susceptibility are unclear. The aim of this study was to examine familial aggregation and genetic contributions to PD and the RRs of other neuropsychiatric diseases in relatives of PD patients.
Methods: In this population-based family cohort study, the records of all individuals actively registered in the Taiwan National Health Insurance Research Database in 2015 were queried (N=24,349,599). In total, 149,187 individuals with a PD-affected parent, 3,698 with an affected offspring, 3,495 with an affected sibling, and 15 with an affected twin were identified. Diagnoses of PD were ascertained between January 1, 1999, and December 31, 2015. The prevalence and RRs of PD and other neuropsychiatric diseases in individuals with first-degree relatives with PD, as well as the contributions of heritability and environmental factors to PD susceptibility were investigated.
Results: The prevalence of PD was 0.46% in the general population and 0.52% in individuals with first-degree relatives with PD. The RR (95% CI) for PD was 2.20 (1.41-3.45) for siblings, 1.59 (1.47-1.73) for parents, 1.86 (1.63-2.11) for offspring, 63.12 (16.45-242.16) for twins, and 1.46 (1.41-1.52) for spouses. The RR (95% CI) in individuals with first-degree relatives with PD was 1.66 (1.57-1.76) for essential tremor, 1.68 (1.61-1.75) for schizophrenia, and 1.20 (1.12-1.28) for Alzheimer's disease. The estimated contribution to the phenotypic variance of PD was 11.0% for heritability, 9.1% for shared environmental factors, and 79.9% for non-shared environmental factors.
Conclusion: First-degree relatives of PD patients are more likely to develop PD and other neuropsychiatric diseases. Environmental factors account for a high proportion of the phenotypic variance of PD.
Keywords: Parkinson’s disease; familial risk; population-based family study.
Conflict of interest statement
Disclosure The authors report no conflicts of interest in this work.
Figures


Similar articles
-
Familial Aggregation of Systemic Lupus Erythematosus and Coaggregation of Autoimmune Diseases in Affected Families.JAMA Intern Med. 2015 Sep;175(9):1518-26. doi: 10.1001/jamainternmed.2015.3528. JAMA Intern Med. 2015. PMID: 26193127
-
Familial aggregation of myasthenia gravis in affected families: a population-based study.Clin Epidemiol. 2017 Nov 2;9:527-535. doi: 10.2147/CLEP.S146617. eCollection 2017. Clin Epidemiol. 2017. PMID: 29138598 Free PMC article.
-
Familial Aggregation and Heritability of Schizophrenia and Co-aggregation of Psychiatric Illnesses in Affected Families.Schizophr Bull. 2017 Sep 1;43(5):1070-1078. doi: 10.1093/schbul/sbw159. Schizophr Bull. 2017. PMID: 27872260 Free PMC article.
-
Familial aggregation of myocardial infarction and coaggregation of myocardial infarction and autoimmune disease: a nationwide population-based cross-sectional study in Taiwan.BMJ Open. 2019 Mar 20;9(3):e023614. doi: 10.1136/bmjopen-2018-023614. BMJ Open. 2019. PMID: 30898803 Free PMC article.
-
[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):241-62. Rinsho Shinkeigaku. 2004. PMID: 15287506 Review. Japanese.
Cited by
-
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci.Biol Psychiatry. 2021 Feb 1;89(3):227-235. doi: 10.1016/j.biopsych.2020.01.026. Epub 2020 Feb 8. Biol Psychiatry. 2021. PMID: 32201043 Free PMC article.
-
Genome- and Exome-Wide Association Studies Revealed Candidate Genes Associated with DaTscan Imaging Features.Parkinsons Dis. 2023 Aug 23;2023:2893662. doi: 10.1155/2023/2893662. eCollection 2023. Parkinsons Dis. 2023. PMID: 37664790 Free PMC article.
-
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease.NPJ Parkinsons Dis. 2024 Oct 17;10(1):188. doi: 10.1038/s41531-024-00778-z. NPJ Parkinsons Dis. 2024. PMID: 39420034 Free PMC article.
-
Subsequent Development of Epithelial Ovarian Cancer After Ovarian Surgery for Benign Ovarian Tumor: A Population-Based Cohort Study.Clin Epidemiol. 2020 Jun 18;12:637-649. doi: 10.2147/CLEP.S199349. eCollection 2020. Clin Epidemiol. 2020. PMID: 32606989 Free PMC article.
References
-
- Wirdefeldt K, Adami HO, Cole P, Trichopoulos D, Mandel J. Epidemiology and etiology of Parkinson’s disease: a review of the evidence. Eur J Epidemiol. 2011;26(Suppl 1):S1–S58. - PubMed
-
- Schrag A, Schott JM. Epidemiological, clinical, and genetic characteristics of early-onset Parkinsonism. Lancet Neurol. 2006;5(4):355–363. - PubMed
-
- Wickremaratchi MM, Perera D, O’Loghlen C, et al. Prevalence and age of onset of Parkinson’s disease in cardiff: a community based cross sectional study and meta-analysis. J Neurol Neurosurg Psychiatry. 2009;80(7):805–807. - PubMed
-
- Kowal SL, Dall TM, Chakrabarti R, Storm MV, Jain A. The current and projected economic burden of Parkinson’s disease in the United States. Mov Disord. 2013;28(3):311–318. - PubMed
-
- Sveinbjörnsdottir S, Hicks AA, Jonsson T, et al. Familial aggregation of Parkinson’s disease in Iceland. N Engl J Med. 2000;343(24):1765–1770. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources