Genetic and psychosocial influence on the association between early childhood infections and later psychiatric disorders.
case-cohort study
early childhood infection
major psychiatric disorders
polygenic risk scores
sibling comparison
Journal
Acta psychiatrica Scandinavica
ISSN: 1600-0447
Titre abrégé: Acta Psychiatr Scand
Pays: United States
ID NLM: 0370364
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
revised:
12
08
2022
received:
07
04
2022
accepted:
13
08
2022
pubmed:
24
8
2022
medline:
19
10
2022
entrez:
23
8
2022
Statut:
ppublish
Résumé
To evaluate the influence of extensive genetic and psychosocial confounding on the association between early childhood infection and five major psychiatric disorders METHODS: A case-cohort study including participants from the Danish iPSYCH2012 sample, a case-cohort sample where all cases born between May 1, 1981, and December 31, 2005, diagnosed with attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar affective disorder (BIP), Major Depressive Disorder (MDD) or schizophrenia (SCZ), were identified and pooled with a representative sample (subcohort) of the Danish population. We used Cox proportional hazards regression customized to the case-cohort setup to calculate hazard ratios of outcome with 95% confidence intervals (CIs), following exposure to early childhood infection before the age of 5 years for ADHD and ASD, and before the age of 10 years for BIP, MDD, and SCZ. To evaluate psychosocial confounding we included sex, calendar period, sibling infections, urbanicity, parental socio-economic status, parental mental health information, and polygenic risk scores for all five disorders, as covariates. To estimate how liability for psychiatric disorders measured through the PRS influenced the risk of early childhood infection, we calculated odds ratios (ORs) with 95% CIs, using logistic regression RESULTS: Early childhood infection was associated with ADHD, ASD, MDD, and SCZ with number of childhood infections increasing the hazard. The HR was still significant in the model with full adjustments after 1 infection for ADHD (HR 1.29, 95% CI: 1.19-1.41), ASD (HR 1.28, 95% CI: 1.18-1.40), MDD (HR 1.23, 95% CI: 1.14-1.33), and SCZ (HR 1.21, 95% CI: 1.07-1.36), but not for BIP (HR1.17, 95% CI: 0.96-1.42). Probands exposed to sibling infections, but not own infection had an absolute risk of ADHD, BIP, MDD, and SCZ that closely approached the absolute risk for individuals exposed to own infections. We found evidence of gene-environment correlation with higher PRS of MDD and to some extent SCZ increasing the risk of infections and higher PRS of BIP associated with significantly decreased risk CONCLUSION: Early childhood infection is significantly associated with ADHD, ASD, MDD, and SCZ and not explained by genetic or psychosocial confounding. Although we found evidence of gene-environment correlation, it had minor impact on the results.
Identifiants
pubmed: 35999619
doi: 10.1111/acps.13491
pmc: PMC9826256
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
406-419Informations de copyright
© 2022 The Authors. Acta Psychiatrica Scandinavica published by John Wiley & Sons Ltd.
Références
Am J Hum Genet. 2021 Jun 3;108(6):1001-1011
pubmed: 33964208
Nat Neurosci. 2019 Mar;22(3):353-361
pubmed: 30692689
Paediatr Perinat Epidemiol. 2012 Jul;26(4):373-85
pubmed: 22686389
Nature. 2016 Feb 11;530(7589):177-83
pubmed: 26814963
Brain Behav Immun. 2020 Nov;90:364-380
pubmed: 32890697
Scand J Public Health. 2011 Jul;39(7 Suppl):54-7
pubmed: 21775352
Brain Behav Immun. 2019 Oct;81:341-347
pubmed: 31247291
Pediatrics. 2012 Dec;130(6):e1447-54
pubmed: 23147969
Stat Med. 2003 Aug 30;22(16):2591-602
pubmed: 12898546
Nat Genet. 2015 Mar;47(3):284-90
pubmed: 25642633
Acta Psychiatr Scand. 2022 Nov;146(5):406-419
pubmed: 35999619
J Inherit Metab Dis. 2007 Aug;30(4):530-6
pubmed: 17632694
Nat Genet. 2019 Mar;51(3):431-444
pubmed: 30804558
Biol Psychiatry. 2019 Feb 15;85(4):317-325
pubmed: 30446204
J Clin Epidemiol. 1999 Dec;52(12):1165-72
pubmed: 10580779
Acta Psychiatr Scand. 2019 May;139(5):404-419
pubmed: 30834514
Schizophr Bull. 2015 Mar;41(2):513-21
pubmed: 25062960
Arch Pediatr Adolesc Med. 2010 May;164(5):470-7
pubmed: 20439799
Nat Genet. 2018 May;50(5):668-681
pubmed: 29700475
N Engl J Med. 1999 Feb 25;340(8):603-8
pubmed: 10029644
Nat Genet. 2019 Jan;51(1):63-75
pubmed: 30478444
Epidemiology. 2010 May;21(3):383-8
pubmed: 20335814
Nature. 2014 Jul 24;511(7510):421-7
pubmed: 25056061
JAMA Psychiatry. 2019 Mar 1;76(3):271-279
pubmed: 30516814
Mol Psychiatry. 2019 Jun;24(6):869-887
pubmed: 30116031
Dan Med J. 2013 Feb;60(2):A4578
pubmed: 23461991
JAMA Psychiatry. 2020 Jun 1;77(6):637-644
pubmed: 31825494
JAMA Psychiatry. 2013 Aug;70(8):812-20
pubmed: 23760347
Schizophr Bull. 2014 Nov;40(6):1526-32
pubmed: 24379444
Nat Genet. 2019 May;51(5):793-803
pubmed: 31043756
Am J Psychiatry. 2011 Dec;168(12):1303-10
pubmed: 22193673
Scand J Public Health. 2011 Jul;39(7 Suppl):22-5
pubmed: 21775345
Biol Psychiatry. 2016 Oct 15;80(8):609-16
pubmed: 27364036
Scand J Public Health. 2011 Jul;39(7 Suppl):30-3
pubmed: 21775347
Am J Hum Genet. 2015 Oct 1;97(4):576-92
pubmed: 26430803
Mol Psychiatry. 2018 Jan;23(1):6-14
pubmed: 28924187
Schizophr Bull. 2017 Jan;43(1):171-179
pubmed: 27343007
Diabetologia. 2007 Mar;50(3):549-54
pubmed: 17187246
PLoS One. 2021 Apr 28;16(4):e0250181
pubmed: 33909680
Hum Hered. 2011;72(2):133-41
pubmed: 21996708
Nat Genet. 2019 Dec;51(12):1670-1678
pubmed: 31740837
Schizophr Bull. 2013 Jan;39(1):230-7
pubmed: 22021661
JAMA Psychiatry. 2015 Jul;72(7):635-41
pubmed: 25830477
J Affect Disord. 2020 Feb 15;263:555-557
pubmed: 31989991
Transl Psychiatry. 2019 Nov 11;9(1):283
pubmed: 31712607