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Depression in suicidal males : Genetic risk variants in the CRHR1 gene. / Wasserman, D.; Wasserman, J.; Rozanov, V.; Sokolowski, M.

In: Genes, Brain and Behavior, Vol. 8, No. 1, 01.02.2009, p. 72-79.

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Harvard

Wasserman, D, Wasserman, J, Rozanov, V & Sokolowski, M 2009, 'Depression in suicidal males: Genetic risk variants in the CRHR1 gene', Genes, Brain and Behavior, vol. 8, no. 1, pp. 72-79. https://doi.org/10.1111/j.1601-183X.2008.00446.x

APA

Wasserman, D., Wasserman, J., Rozanov, V., & Sokolowski, M. (2009). Depression in suicidal males: Genetic risk variants in the CRHR1 gene. Genes, Brain and Behavior, 8(1), 72-79. https://doi.org/10.1111/j.1601-183X.2008.00446.x

Vancouver

Wasserman D, Wasserman J, Rozanov V, Sokolowski M. Depression in suicidal males: Genetic risk variants in the CRHR1 gene. Genes, Brain and Behavior. 2009 Feb 1;8(1):72-79. https://doi.org/10.1111/j.1601-183X.2008.00446.x

Author

Wasserman, D. ; Wasserman, J. ; Rozanov, V. ; Sokolowski, M. / Depression in suicidal males : Genetic risk variants in the CRHR1 gene. In: Genes, Brain and Behavior. 2009 ; Vol. 8, No. 1. pp. 72-79.

BibTeX

@article{8d8c5dd9ceb440f6a55ce8e3212fbeee,
title = "Depression in suicidal males: Genetic risk variants in the CRHR1 gene",
abstract = "Dysregulation in the stress response of the hypothalamic-pituitary-adrenal axis, involving the corticotrophin-releasing hormone and its main receptor (CRHR1), is considered to play a major role in depression and suicidal behavior. To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. The minor T-allele of exonic SNP rs12936511, not previously studied in the context of psychiatric disorders and suicidal behaviors, was significantly transmitted to suicidal males with increased Beck Depression Inventory (BDI) scores (n = 347; P = 0.0028). We found additional evidence of association and linkage with increased BDI scores among suicidal males with an additional SNP, located proximally to the index SNP rs4792887, as well as with two distal SNPs, which were correlated with index SNP rs4792887. Analysis of haplotypes showed that each of the risk alleles segregated onto three separate haplotypes, whereas a fourth 'nonrisk' haplotype ('CGC') contained none of the risk alleles and was preferentially transmitted to suicidal males with lowered BDI scores (P = 0.0007). The BDI scores among all suicidal males, who carried a homozygous combination of any of the three risk haplotypes (non-CGC/non-CGC; n = 160), were significantly increased (P = 0.000089) compared with suicidal male CGC carriers (n = 181). Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes.",
keywords = "CRHR1, Depression, Haplotype, Male, SNP, Stress, Suicidality",
author = "D. Wasserman and J. Wasserman and V. Rozanov and M. Sokolowski",
year = "2009",
month = feb,
day = "1",
doi = "10.1111/j.1601-183X.2008.00446.x",
language = "English",
volume = "8",
pages = "72--79",
journal = "Genes, Brain and Behavior",
issn = "1601-1848",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Depression in suicidal males

T2 - Genetic risk variants in the CRHR1 gene

AU - Wasserman, D.

AU - Wasserman, J.

AU - Rozanov, V.

AU - Sokolowski, M.

PY - 2009/2/1

Y1 - 2009/2/1

N2 - Dysregulation in the stress response of the hypothalamic-pituitary-adrenal axis, involving the corticotrophin-releasing hormone and its main receptor (CRHR1), is considered to play a major role in depression and suicidal behavior. To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. The minor T-allele of exonic SNP rs12936511, not previously studied in the context of psychiatric disorders and suicidal behaviors, was significantly transmitted to suicidal males with increased Beck Depression Inventory (BDI) scores (n = 347; P = 0.0028). We found additional evidence of association and linkage with increased BDI scores among suicidal males with an additional SNP, located proximally to the index SNP rs4792887, as well as with two distal SNPs, which were correlated with index SNP rs4792887. Analysis of haplotypes showed that each of the risk alleles segregated onto three separate haplotypes, whereas a fourth 'nonrisk' haplotype ('CGC') contained none of the risk alleles and was preferentially transmitted to suicidal males with lowered BDI scores (P = 0.0007). The BDI scores among all suicidal males, who carried a homozygous combination of any of the three risk haplotypes (non-CGC/non-CGC; n = 160), were significantly increased (P = 0.000089) compared with suicidal male CGC carriers (n = 181). Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes.

AB - Dysregulation in the stress response of the hypothalamic-pituitary-adrenal axis, involving the corticotrophin-releasing hormone and its main receptor (CRHR1), is considered to play a major role in depression and suicidal behavior. To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. The minor T-allele of exonic SNP rs12936511, not previously studied in the context of psychiatric disorders and suicidal behaviors, was significantly transmitted to suicidal males with increased Beck Depression Inventory (BDI) scores (n = 347; P = 0.0028). We found additional evidence of association and linkage with increased BDI scores among suicidal males with an additional SNP, located proximally to the index SNP rs4792887, as well as with two distal SNPs, which were correlated with index SNP rs4792887. Analysis of haplotypes showed that each of the risk alleles segregated onto three separate haplotypes, whereas a fourth 'nonrisk' haplotype ('CGC') contained none of the risk alleles and was preferentially transmitted to suicidal males with lowered BDI scores (P = 0.0007). The BDI scores among all suicidal males, who carried a homozygous combination of any of the three risk haplotypes (non-CGC/non-CGC; n = 160), were significantly increased (P = 0.000089) compared with suicidal male CGC carriers (n = 181). Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes.

KW - CRHR1

KW - Depression

KW - Haplotype

KW - Male

KW - SNP

KW - Stress

KW - Suicidality

UR - http://www.scopus.com/inward/record.url?scp=59149104755&partnerID=8YFLogxK

U2 - 10.1111/j.1601-183X.2008.00446.x

DO - 10.1111/j.1601-183X.2008.00446.x

M3 - Article

C2 - 19220485

AN - SCOPUS:59149104755

VL - 8

SP - 72

EP - 79

JO - Genes, Brain and Behavior

JF - Genes, Brain and Behavior

SN - 1601-1848

IS - 1

ER -

ID: 42217305