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Am J Psychiatry DOI:10.1176/appi.ajp.2009.08111633

A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder.

Publication TypeJournal Article
Year of Publication2009
AuthorsPerlis, RH, Smoller, JW, Ferreira, MAR, McQuillin, A, Bass, N, Lawrence, J, Sachs, GS, Nimgaonkar, V, Scolnick, EM, Gurling, H, Sklar, P, Purcell, S
JournalAm J Psychiatry
Volume166
Issue6
Pages718-25
Date Published2009 Jun
ISSN1535-7228
KeywordsAdult, Alleles, Antipsychotic Agents, Bipolar Disorder, Chromosomes, Human, Pair 4, Diagnostic and Statistical Manual of Mental Disorders, Female, Genome, Genotype, Humans, Lithium Carbonate, Male, Polymorphism, Single Nucleotide, Receptors, AMPA, Secondary Prevention
Abstract

OBJECTIVE: Lithium remains a first-line treatment for bipolar disorder, but the mechanisms by which it prevents the recurrence of mood episodes are not known. The authors utilized data from a genomewide association study to examine associations between single nucleotide polymorphisms (SNPs) and the outcome of lithium treatment in two cohorts of patients with bipolar I disorder or bipolar II disorder.

METHOD: The hazard for mood episode recurrence was examined among 1,177 patients with bipolar I disorder or bipolar II disorder, including 458 individuals treated with lithium carbonate or citrate, who were participants in the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD) cohort. SNPs showing the greatest evidence of association in Cox regression models were then examined for association with positive lithium response among 359 bipolar I or II disorder patients treated with lithium carbonate or citrate in a second cohort from the University College London.

RESULTS: The strongest association in the STEP-BD cohort (minimum p=5.5 x 10(-7)) was identified for a region on chromosome 10p15 (rs10795189). Of the regions showing suggestive evidence (p<5 x 10(-4)) of association with lithium response, five were further associated with positive lithium response in the University College London cohort, including SNPs in a region on chromosome 4q32 spanning a gene coding for the glutamate/alpha-amino-3-hydroxy-5-methyl-4-isoxazolpropionate (AMPA) receptor GRIA2.

CONCLUSIONS: Multiple novel loci merit further examination for association with lithium response in bipolar disorder patients, including one region that spans the GRIA2 gene, for which expression has been shown to be regulated by lithium treatment.

DOI10.1176/appi.ajp.2009.08111633
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/19448189?dopt=Abstract

Alternate JournalAm J Psychiatry
PubMed ID19448189
PubMed Central IDPMC3908470
Grant ListMH-062137 / MH / NIMH NIH HHS / United States
R01 MH062137 / MH / NIMH NIH HHS / United States
N01 MH080001 / MH / NIMH NIH HHS / United States
MH-067288 / MH / NIMH NIH HHS / United States
MH63420 / MH / NIMH NIH HHS / United States
R01 MH067288 / MH / NIMH NIH HHS / United States
G0500791 / / Medical Research Council / United Kingdom
G9623693N / / Medical Research Council / United Kingdom
MH-063445 / MH / NIMH NIH HHS / United States
R01 MH063420 / MH / NIMH NIH HHS / United States
N01MH80001 / MH / NIMH NIH HHS / United States
R01 MH063445 / MH / NIMH NIH HHS / United States