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J Affect Disord. 2015 Nov 1;186:367-75. doi: 10.1016/j.jad.2015.07.014. Epub 2015 Jul 31.

Identification of circadian gene variants in bipolar disorder in Latino populations.

Author information

1
Department of Psychiatry and Center of Excellence for Neurosciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA. Electronic address: Robert99.Gonzalez@ttuhsc.edu.
2
Department of Psychiatry and Center of Excellence for Neurosciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA.
3
Langley Porter Psychiatric Institute, University of California at San Francisco, San Francisco, CA, USA.
4
Centro de Investigación en Biología Celular y Molecular y Escuela de Biologia, Universidad de Costa Rica, San Jose, Costa Rica.
5
Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA; South Texas Veterans Health Care System, San Antonio, TX, USA.
6
Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
7
Los Angeles Biomedical Research Center at Harbor, University of California Los Angeles Medical Center, Torrance, CA, USA.
8
Centro Internacional de Trastornos Afectivos y de la Conducta Adictiva, Guatemala, Guatemala.
9
Instituto de Información e Investigación en Salud Mental AC, Monterrey, Nuevo Leon, Mexico.
10
Grupo de Estudios Médicos y Familiares Carracci, S.C., México, D.F., Mexico.

Abstract

BACKGROUND:

Variations in circadian genes can impact biological rhythms. Given the rhythm disturbances that characterize bipolar disorder (BD), genes encoding components of molecular clocks are good candidate genes for the illness.

METHODS:

A family based association analysis of circadian gene single nucleotide polymorphisms (SNPs) and BD was conducted in Latino pedigrees. 884 individuals from 207 pedigrees (473BP phenotype and 411 unaffected family members) were genotyped. Family based single marker association testing was performed. Ancestral haplotypes (SNPs found to be in strong LD defined using confidence intervals) were also tested for association with BD.

RESULTS:

Multiple suggestive associations between circadian gene SNPs and BD were noted. These included CSNK1E (rs1534891, p=0.00689), ARNTL (rs3789327, p=0.021172), CSNK1D (rs4510078, p=0.022801), CLOCK (rs17777927, p=0.031664). Individually, none of the SNPs were significantly associated with BD after correction for multiple testing. However, a 4-locus CSNK1E haplotype encompassing the rs1534891 SNP (Z-score=2.685, permuted p=0.0076) and a 3-locus haplotype in ARNTL (Z-score=3.269, permuted p=0.0011) showed a significant association with BD.

LIMITATIONS:

Larger samples are required to confirm these findings and assess the relationship between circadian gene SNPs and BD in Latinos.

CONCLUSIONS:

The results suggest that ARNTL and CSKN1E variants may be associated with BD. Further studies are warranted to assess the relationships between these genes and BD in Latino populations.

KEYWORDS:

Aryl Hydrocarbon Receptor Nuclear Translocator-Like; Bipolar disorder; Casein Kinase 1 Epsilon; Circadian; Family-based association test; Latino

PMID:
26283580
DOI:
10.1016/j.jad.2015.07.014
[Indexed for MEDLINE]
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