Heritability of cerebral glutamate levels and their association with schizophrenia spectrum disorders: a 1 [H]-spectroscopy twin study

C.S. Legind, B.V. Broberg, R.C.W. Mandl, R. Brouwer, S.J. Anhøj, R. Hilker, M.H. Jensen, P. McGuire, H.H. Pol, B. Fagerlund, E. Rostrup, B.Y. Glenthøj

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

© 2018, American College of Neuropsychopharmacology.Research findings implicate cerebral glutamate in the pathophysiology of schizophrenia, including genetic studies reporting associations with glutamatergic neurotransmission. The extent to which aberrant glutamate levels can be explained by genetic factors is unknown, and if glutamate can serve as a marker of genetic susceptibility for schizophrenia remains to be established. We investigated the heritability of cerebral glutamate levels and whether a potential association with schizophrenia spectrum disorders could be explained by genetic factors. Twenty-three monozygotic (MZ) and 20 dizygotic (DZ) proband pairs con- or discordant for schizophrenia spectrum disorders, along with healthy control pairs (MZ = 28, DZ = 18) were recruited via the National Danish Twin Register and the Psychiatric Central Register (17 additional twins were scanned without their siblings). Glutamate levels in the left thalamus and the anterior cingulate cortex (ACC) were measured using 1[H]-magnetic resonance spectroscopy at 3 Tesla and analyzed by structural equation modeling. Glutamate levels in the left thalamus were heritable and positively correlated with liability for schizophrenia spectrum disorders (phenotypic correlation, 0.16, [0.02–0.29]; p = 0.010). The correlation was explained by common genes influencing both the levels of glutamate and liability for schizophrenia spectrum disorders. In the ACC, glutamate and glx levels were heritable, but not correlated to disease liability. Increases in thalamic glutamate levels found in schizophrenia spectrum disorders are explained by genetic influences related to the disease, and as such the measure could be a potential marker of genetic susceptibility, useful in early detection and stratification of patients with psychosis.
Original languageEnglish
Pages (from-to)581-589
JournalNeuropsychopharmacology
Volume44
Issue number3
DOIs
Publication statusPublished - 1 Feb 2019
Externally publishedYes

Funding

The study was funded by The Lundbeck Foundation (grant no. 25-A2701 and R155-2013-16337) and C.S.L. was supported by a grant from The Mental Health Services – Capital Region of Denmark. Dr. Glenthøj is the leader of a Lundbeck Foundation Centre of Excellence for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), which is partially financed by an independent grant from the Lundbeck Foundation, based on international review and partially financed by the Mental Health Services in the Capital Region of Denmark, the University of Copenhagen, and other foundations. Her group has also received a research grant from Lundbeck A/S for another independent investigator initiated study. All grants are the property of the Mental Health Services in the Capital Region of Denmark and administrated by them. She has no other conflicts to disclose. The authors declare no competing interests.

FundersFunder number
Mental Health Services in the Capital Region of Denmark
Mental Health Services – Capital Region of Denmark
Københavns Universitet
LundbeckfondenR155-2013-16337, 25-A2701
H. Lundbeck A/S

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