TY - JOUR
T1 - No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes
AU - Johnson, Emma C.
AU - Border, Richard
AU - Melroy-Greif, Whitney E.
AU - de Leeuw, Christiaan A.
AU - Ehringer, Marissa A.
AU - Keller, Matthew C.
N1 - Publisher Copyright:
© 2017 Society of Biological Psychiatry
PY - 2017/11/15
Y1 - 2017/11/15
N2 - Background A recent analysis of 25 historical candidate gene polymorphisms for schizophrenia in the largest genome-wide association study conducted to date suggested that these commonly studied variants were no more associated with the disorder than would be expected by chance. However, the same study identified other variants within those candidate genes that demonstrated genome-wide significant associations with schizophrenia. As such, it is possible that variants within historic schizophrenia candidate genes are associated with schizophrenia at levels above those expected by chance, even if the most-studied specific polymorphisms are not. Methods The present study used association statistics from the largest schizophrenia genome-wide association study conducted to date as input to a gene set analysis to investigate whether variants within schizophrenia candidate genes are enriched for association with schizophrenia. Results As a group, variants in the most-studied candidate genes were no more associated with schizophrenia than were variants in control sets of noncandidate genes. While a small subset of candidate genes did appear to be significantly associated with schizophrenia, these genes were not particularly noteworthy given the large number of more strongly associated noncandidate genes. Conclusions The history of schizophrenia research should serve as a cautionary tale to candidate gene investigators examining other phenotypes: our findings indicate that the most investigated candidate gene hypotheses of schizophrenia are not well supported by genome-wide association studies, and it is likely that this will be the case for other complex traits as well.
AB - Background A recent analysis of 25 historical candidate gene polymorphisms for schizophrenia in the largest genome-wide association study conducted to date suggested that these commonly studied variants were no more associated with the disorder than would be expected by chance. However, the same study identified other variants within those candidate genes that demonstrated genome-wide significant associations with schizophrenia. As such, it is possible that variants within historic schizophrenia candidate genes are associated with schizophrenia at levels above those expected by chance, even if the most-studied specific polymorphisms are not. Methods The present study used association statistics from the largest schizophrenia genome-wide association study conducted to date as input to a gene set analysis to investigate whether variants within schizophrenia candidate genes are enriched for association with schizophrenia. Results As a group, variants in the most-studied candidate genes were no more associated with schizophrenia than were variants in control sets of noncandidate genes. While a small subset of candidate genes did appear to be significantly associated with schizophrenia, these genes were not particularly noteworthy given the large number of more strongly associated noncandidate genes. Conclusions The history of schizophrenia research should serve as a cautionary tale to candidate gene investigators examining other phenotypes: our findings indicate that the most investigated candidate gene hypotheses of schizophrenia are not well supported by genome-wide association studies, and it is likely that this will be the case for other complex traits as well.
KW - Candidate genes
KW - Complex traits
KW - GWAS
KW - Gene set analysis
KW - Genome-wide association study
KW - SNP
KW - Schizophrenia
KW - Single nucleotide polymorphism
UR - http://www.scopus.com/inward/record.url?scp=85027437069&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2017.06.033
DO - 10.1016/j.biopsych.2017.06.033
M3 - Article
C2 - 28823710
AN - SCOPUS:85027437069
SN - 0006-3223
VL - 82
SP - 702
EP - 708
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 10
ER -