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DOI 10.4088/jcp.15m10314

Медицинская библиотека · The Journal of clinical psychiatry · 2017

Genetic Risk Score Analysis in Early-Onset Bipolar Disorder.

Croarkin Paul E, Luby Joan L, Cercy Kelly, Geske Jennifer R, Veldic Marin, Simonson Matthew, Joshi Paramjit T, Wagner Karen Dineen, Walkup John T, Nassan Malik M, Cuellar-Barboza Alfredo B, Casuto Leah, McElroy Susan L, Jensen Peter S, Frye Mark A, Biernacka Joanna M

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

In this study, we performed a candidate genetic risk score (GRS) analysis of early-onset bipolar disorder (BD).

METHODS

Treatment of Early Age Mania (TEAM) study enrollment and sample collection took place from 2003 to 2008. Mayo Clinic Bipolar Biobank samples were collected from 2009 to 2013. Genotyping and analyses for the present study took place from 2013 to 2014. The diagnosis of BD was based on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision criteria. Eight single-nucleotide polymorphisms (SNPs), previously reported in genome-wide association studies to be associated with BD, were chosen for GRS analysis in early-onset bipolar disease. These SNPs map to 3 genes: CACNA1C (calcium channel, voltage-dependent, L type, alpha 1C subunit), ANK3 (ankyrin-3, node of Ranvier [ankyrin G]), and ODZ4 (teneurin transmembrane protein 4 [formerly "odz, odd Oz/10-m homolog 4 {Drosophila}, ODZ4"]). The 8 candidate SNPs were genotyped in patients from the TEAM study (n = 69); adult patients with BD (n = 732), including a subset with early-onset illness (n = 192); and healthy controls (n = 776). GRS analyses were performed to compare early-onset cases with controls. In addition, associations of early-onset BD with individual SNPs and haplotypes were explored.

RESULTS

GRS analysis revealed associations of the risk score with early-onset BD (P = .01). Gene-level haplotype analysis comparing TEAM patients with controls suggested association of early-onset BD with a CACNA1C haplotype (global test, P = .01). At the level of individual SNPs, comparison of TEAM cases with healthy controls provided nominally significant evidence for association of SNP rs10848632 in CACNA1C with early-onset BD (P = .017), which did not remain significant after correction for multiple comparisons.

CONCLUSIONS

These preliminary analyses suggest that previously identified BD risk loci, especially CACNA1C, have a role in early-onset BD, possibly with stronger effects than for late-onset BD.

Для цитирования: Croarkin Paul E, Luby Joan L, Cercy Kelly, Geske Jennifer R, Veldic Marin, Simonson Matthew, Joshi Paramjit T, Wagner Karen Dineen, Walkup John T, Nassan Malik M, Cuellar-Barboza Alfredo B, Casuto Leah, McElroy Susan L, Jensen Peter S, Frye Mark A, Biernacka Joanna M. Genetic Risk Score Analysis in Early-Onset Bipolar Disorder.. The Journal of clinical psychiatry. 2017. DOI: 10.4088/jcp.15m10314.

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