AI Article Synopsis

  • PTSD is linked to glucocorticoid hypersensitivity, but previous studies found no strong genetic links between specific SNPs in the glucocorticoid receptor gene and PTSD risk.
  • A study on Portuguese male war veterans identified the 9β SNP (rs6198) as being significantly associated with both lifetime PTSD and the severity of its symptoms.
  • Carriers of the 9β risk allele showed lower hair cortisol concentrations, suggesting a possible link between this genetic variant and stress response in both veterans and their offspring.

Article Abstract

Posttraumatic stress disorder (PTSD) has been associated with glucocorticoid (GC) hypersensitivity. Although genetic factors account for 30-46% of the variance in PTSD, no associations have been found between single nucleotide polymorphisms (SNPs) of the GC receptor (GR) gene () and risk for this disorder. We studied the association of five SNPs in the GR gene (rs10052957, rs6189/rs6190, rs6195, rs41423247, and rs6198) and haplotypes with PTSD, in a group of Portuguese male war veterans (33 with lifetime PTSD, 28 without). To determine whether the 9β SNP (rs6198) was associated with chronically altered cortisol levels, we evaluated hair cortisol concentrations (HCC) in a sample of 69 veterans' offspring. The 9β variant (G allele) was significantly associated with lifetime PTSD under a dominant model of inheritance. The 9β variant was also significantly associated with severity of current PTSD symptoms. The haplotype analysis revealed an association between a common haplotype comprising the 9β risk allele and lifetime PTSD. Carriers of the 9β risk allele had significantly lower HCC than non-carriers. We found the 9β risk allele and a haplotype comprising the 9β risk allele of the GR gene to be associated with PTSD in veterans. This 9β risk allele was also associated with lower HCC in their offspring.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915937PMC
http://dx.doi.org/10.3390/healthcare9020173DOI Listing

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