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Quantifying between‐cohort and between‐sex genetic heterogeneity in major depressive disorder

Authors :
Trzaskowski, Maciej
Mehta, Divya
Peyrot, Wouter J.
Hawkes, David
Davies, Daniel
Howard, David M.
Kemper, Kathryn E.
Sidorenko, Julia
Maier, Robert
Ripke, Stephan
Mattheisen, Manuel
Baune, Bernhard T.
Grabe, Hans J.
Heath, Andrew C.
Jones, Lisa
Jones, Ian
Madden, Pamela A.F.
McIntosh, Andrew M.
Breen, Gerome
Lewis, Cathryn M.
Børglum, Anders D.
Sullivan, Patrick F.
Martin, Nicholas G.
Kendler, Kenneth S.
Levinson, Douglas F.
Wray, Naomi R.
Source :
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics; September 2019, Vol. 180 Issue: 6 p439-447, 9p
Publication Year :
2019

Abstract

Major depressive disorder (MDD) is clinically heterogeneous with prevalence rates twice as high in women as in men. There are many possible sources of heterogeneity in MDD most of which are not measured in a sufficiently comparable way across study samples. Here, we assess genetic heterogeneity based on two fundamental measures, between‐cohort and between‐sex heterogeneity. First, we used genome‐wide association study (GWAS) summary statistics to investigate between‐cohort genetic heterogeneity using the 29 research cohorts of the Psychiatric Genomics Consortium (PGC; Ncases = 16,823, Ncontrols = 25,632) and found that some of the cohort heterogeneity can be attributed to ascertainment differences (such as recruitment of cases from hospital vs. community sources). Second, we evaluated between‐sex genetic heterogeneity using GWAS summary statistics from the PGC, Kaiser Permanente GERA, UK Biobank, and the Danish iPSYCH studies but did not find convincing evidence for genetic differences between the sexes. We conclude that there is no evidence that the heterogeneity between MDD data sets and between sexes reflects genetic heterogeneity. Larger sample sizes with detailed phenotypic records and genomic data remain the key to overcome heterogeneity inherent in assessment of MDD.

Details

Language :
English
ISSN :
15524841 and 1552485X
Volume :
180
Issue :
6
Database :
Supplemental Index
Journal :
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics
Publication Type :
Periodical
Accession number :
ejs50705471
Full Text :
https://doi.org/10.1002/ajmg.b.32713