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 (NR3C1) 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.

Highlights

  • Posttraumatic stress disorder (PTSD) has been associated with altered regulation of the hypothalamic pituitary adrenal (HPA) axis, with increased glucocorticoid (GC) sensitivity [1,2]

  • Since we found associations between the single nucleotide polymorphisms (SNPs) 9β and lifetime and current PTSD, we performed an analysis aimed at determining whether carrying 9β risk allele was associated with HPA axis function measuring hair cortisol concentrations (HCC)

  • We found an association between the GC receptor (GR) gene 9β SNP risk allele and lifetime and current PTSD, and current PTSD symptoms in the sample of veterans from

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Summary

Introduction

Posttraumatic stress disorder (PTSD) has been associated with altered regulation of the hypothalamic pituitary adrenal (HPA) axis, with increased glucocorticoid (GC) sensitivity [1,2]. This has been shown by means of dexamethasone suppression tests and an increased glucocorticoid receptor (GR) number [2,3]. Lower levels of cortisol have mainly been found in specific populations and at specific moments of the day [4]. HCC represent cumulative cortisol levels over prolonged periods of time providing insight into chronic HPA axis dysregulation [6]. HCC have been influenced by time since trauma, type of trauma, childhood adversities, and hair manipulations [9,10]

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