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DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia.

Authors :
Hannon E
Dempster EL
Mansell G
Burrage J
Bass N
Bohlken MM
Corvin A
Curtis CJ
Dempster D
Di Forti M
Dinan TG
Donohoe G
Gaughran F
Gill M
Gillespie A
Gunasinghe C
Hulshoff HE
Hultman CM
Johansson V
Kahn RS
Kaprio J
Kenis G
Kowalec K
MacCabe J
McDonald C
McQuillin A
Morris DW
Murphy KC
Mustard CJ
Nenadic I
O'Donovan MC
Quattrone D
Richards AL
Rutten BP
St Clair D
Therman S
Toulopoulou T
Van Os J
Waddington JL
Sullivan P
Vassos E
Breen G
Collier DA
Murray RM
Schalkwyk LS
Mill J
Source :
ELife [Elife] 2021 Feb 26; Vol. 10. Date of Electronic Publication: 2021 Feb 26.
Publication Year :
2021

Abstract

We performed a systematic analysis of blood DNA methylation profiles from 4483 participants from seven independent cohorts identifying differentially methylated positions (DMPs) associated with psychosis, schizophrenia, and treatment-resistant schizophrenia. Psychosis cases were characterized by significant differences in measures of blood cell proportions and elevated smoking exposure derived from the DNA methylation data, with the largest differences seen in treatment-resistant schizophrenia patients. We implemented a stringent pipeline to meta-analyze epigenome-wide association study (EWAS) results across datasets, identifying 95 DMPs associated with psychosis and 1048 DMPs associated with schizophrenia, with evidence of colocalization to regions nominated by genetic association studies of disease. Many schizophrenia-associated DNA methylation differences were only present in patients with treatment-resistant schizophrenia, potentially reflecting exposure to the atypical antipsychotic clozapine. Our results highlight how DNA methylation data can be leveraged to identify physiological (e.g., differential cell counts) and environmental (e.g., smoking) factors associated with psychosis and molecular biomarkers of treatment-resistant schizophrenia.<br />Competing Interests: EH, ED, GM, JB, NB, MB, AC, CC, DD, TD, GD, MG, AG, CG, HH, CH, VJ, RK, JK, GK, CM, AM, DM, KM, CM, IN, DQ, AR, BR, DS, ST, TT, JV, JW, EV, GB, LS, JM No competing interests declared, MD M Di Forti reports personal fees from Janssen, outside the submitted work. FG Fiona Gaughran has received honoraria from Lundbeck, Otsuka, and Sunovion. She has a family member with professional links to Lilly and GSK, including shares. KK Kaarina Kowalec has consulted with Emerald Lake Safety Ltd. (2017-2018) and has received speaker honoraria from Biogen/Fraser Health Multiple Sclerosis Clinic (2018). Both are unrelated to the work published here. JM James MacCabe has received research funding from H Lundbeck. MO Michael C O'Donovan is supported by a collaborative research grant from Takeda Pharmaceuticals. Takeda played no part in the conception, design, implementation, or interpretation of this study. PS PF Sullivan reports the following potentially competing financial interests. Current: Lundbeck (advisory committee, grant recipient). Past three years: Pfizer (scientific advisory board). DC David A Collier is a full time employee and stockholder of Eli Lilly and Company. RM Robin M Murray reports personal fees from Janssen, Lundbeck, Sunovion, Recordati and Otsuka<br /> (© 2021, Hannon et al.)

Details

Language :
English
ISSN :
2050-084X
Volume :
10
Database :
MEDLINE
Journal :
ELife
Publication Type :
Academic Journal
Accession number :
33646943
Full Text :
https://doi.org/10.7554/eLife.58430