Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population.
Bipolar and Related Disorders
Genetics/Genomics
Neurodevelopmental Disorders
Schizophrenia Spectrum and Other Psychotic Disorders
Journal
The American journal of psychiatry
ISSN: 1535-7228
Titre abrégé: Am J Psychiatry
Pays: United States
ID NLM: 0370512
Informations de publication
Date de publication:
01 01 2023
01 01 2023
Historique:
pmc-release:
01
01
2024
pubmed:
8
12
2022
medline:
4
1
2023
entrez:
7
12
2022
Statut:
ppublish
Résumé
Autism, schizophrenia, and other clinically distinct neurodevelopmental psychiatric disorders (NPDs) have shared genetic etiologies, including single-gene and multigenic copy number variants (CNVs). Because rare variants are primarily investigated in clinical cohorts, population-based estimates of their prevalence and penetrance are lacking. The authors determined the prevalence, penetrance, and NPD risk of pathogenic single-gene variants in a large health care system population. The authors analyzed linked genomic and electronic health record (EHR) data in a subset of 90,595 participants from Geisinger's MyCode Community Health Initiative, known as the DiscovEHR cohort. Loss-of-function pathogenic variants in 94 high-confidence NPD genes were identified through exome sequencing, and NPD penetrance was calculated using preselected EHR diagnosis codes. NPD risk was estimated using a case-control comparison of DiscovEHR participants with and without NPD diagnoses. Results from single-gene variant analyses were also compared with those from 31 previously reported pathogenic NPD CNVs. Pathogenic variants were identified in 0.34% of the DiscovEHR cohort and demonstrated a 34.3% penetrance for NPDs. Similar to CNVs, sequence variants collectively conferred a substantial risk for several NPD diagnoses, including autism, schizophrenia, and bipolar disorder. Significant NPD risk remained after participants with intellectual disability were excluded from the analysis, confirming the association with major psychiatric disorders in individuals without severe cognitive deficits. Collectively, rare single-gene variants and CNVs were found in >1% of individuals in a large health care system population and play an important contributory role in mental health disorders. Diagnostic genetic testing for pathogenic variants among symptomatic individuals with NPDs could improve clinical outcomes through early intervention and anticipatory therapeutic support.
Identifiants
pubmed: 36475376
doi: 10.1176/appi.ajp.22010062
pmc: PMC10017070
mid: NIHMS1872917
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
65-72Subventions
Organisme : NIMH NIH HHS
ID : R01 MH074090
Pays : United States
Organisme : NIMH NIH HHS
ID : U01 MH119705
Pays : United States
Commentaires et corrections
Type : CommentIn
Références
Am J Hum Genet. 2019 Aug 1;105(2):267-282
pubmed: 31327507
Genet Med. 2020 Feb;22(2):245-257
pubmed: 31690835
Mol Psychiatry. 2016 Jul;21(7):885-93
pubmed: 27217147
Hum Mutat. 2018 Nov;39(11):1517-1524
pubmed: 30192042
Genome Med. 2017 May 30;9(1):43
pubmed: 28554332
Genet Med. 2022 Mar;24(3):703-711
pubmed: 34906480
J Med Genet. 2019 Mar;56(3):131-138
pubmed: 30343275
Nature. 2018 Oct;562(7726):203-209
pubmed: 30305743
Lancet. 2015 Apr 4;385(9975):1305-14
pubmed: 25529582
Nature. 2014 Nov 13;515(7526):216-21
pubmed: 25363768
Genet Med. 2016 Sep;18(9):906-13
pubmed: 26866580
PLoS Genet. 2017 Nov 29;13(11):e1007104
pubmed: 29186148
JAMA Netw Open. 2020 May 1;3(5):e203382
pubmed: 32383744
Nat Genet. 2017 Aug;49(8):1167-1173
pubmed: 28650482
Nat Genet. 2019 Jan;51(1):106-116
pubmed: 30559488
Cell. 2014 Jul 17;158(2):263-276
pubmed: 24998929
J Pers Med. 2021 May 01;11(5):
pubmed: 34062946
Nature. 2020 May;581(7809):434-443
pubmed: 32461654
JAMA Psychiatry. 2020 Dec 1;77(12):1276-1285
pubmed: 32697297
Genet Med. 2019 Jul;21(7):1611-1620
pubmed: 30504930
Am J Hum Genet. 2018 Jun 7;102(6):1204-1211
pubmed: 29861106
Autism Res. 2019 Dec;12(12):1728-1736
pubmed: 31705629
Front Genet. 2019 Apr 03;10:258
pubmed: 31001316
Am J Hum Genet. 2019 Feb 7;104(2):275-286
pubmed: 30665703
Nature. 2014 Jan 16;505(7483):361-6
pubmed: 24352232
JAMA Psychiatry. 2016 Mar;73(3):275-83
pubmed: 26817790
Cell. 2019 Aug 8;178(4):850-866.e26
pubmed: 31398340
JAMA. 2015 May 26;313(20):2044-54
pubmed: 26010633
Science. 2016 Dec 23;354(6319):
pubmed: 28008009
Nature. 2017 Feb 23;542(7642):433-438
pubmed: 28135719
Genet Med. 2015 May;17(5):405-24
pubmed: 25741868
Mol Autism. 2013 Oct 03;4(1):36
pubmed: 24090431
MMWR Morb Mortal Wkly Rep. 2018 Aug 17;67(32):882-887
pubmed: 30114005
Curr Opin Genet Dev. 2021 Jun;68:1-8
pubmed: 33434711
Lancet Neurol. 2013 Apr;12(4):406-14
pubmed: 23518333
Genet Med. 2016 Apr;18(4):302-4
pubmed: 26158229
Nat Neurosci. 2020 Feb;23(2):185-193
pubmed: 31932770
Pediatrics. 2019 Oct;144(4):
pubmed: 31558576
Genome Med. 2017 Dec 20;9(1):114
pubmed: 29262854
Nat Neurosci. 2016 Sep;19(9):1194-6
pubmed: 27479843
Am J Hum Genet. 2018 May 3;102(5):874-889
pubmed: 29727688
JAMA Psychiatry. 2015 Feb;72(2):119-26
pubmed: 25493922