This article is part of the supplement: International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour .

Oral presentation

Role of stress in neuropsychiatric and neurocognitive disorders in older adults, specifically on late life depression and cognition

Ruth O'Hara

Stanford University School of Medicine, USA

corresponding author email

from International Society on Brain and Behaviour: 2nd International Congress on Brain and Behaviour
Thessaloniki, Greece. 17–20 November 2005

Annals of General Psychiatry 2006, 5(Suppl 1):S16doi:10.1186/1744-859X-5-S1-S16

Published:	28 February 2006

First paragraph (this article has no abstract)

Recent investigations suggest the Hypothalamic-Pituitary-Adrenal Axis (HPA) plays an important role in neuropsychiatric and neurocognitive disorders in older adults. Effects of HPA activity on cognition and depression are well documented. It is unclear, however, if this relationship is mediated by psychosocial stress. Here we report on the current status of the literature in this field and also present our findings from a large, longitudinal investigation of the interaction of psychosocial stress and HPA activity on neurocognitive and neuropsychiatric function. In a sample of 162 community-dwelling older adults, aged 60–102 years, we investigated the relationship of waking cortisol, slope of diurnal cortisol and psychosocial stress to cognition, mood and brain function. Older adults with increased waking cortisol exhibited poorer memory performance (p < 0.01). This effect was strongest in individuals with the Apolipoprotein ε4 allele, who are at increased risk for the development of cognitive decline and dementia. Additionally, older adults with higher waking cortisol had reduced hippocampal volumes (p < 0.01). There was no effect of slope of diurnal cortisol on any of the cognitive or brain measures, in either ε4 or non-ε4 carriers. Although we observed no impact of cortisol on mood, individuals with the short allele of the 5HTT gene promoter polymorphism region (5HTTLPR), which is associated with lower levels of serotonin uptake, had poorer cognitive function and higher levels of cortisol. Strikingly, none of these observed effects were impacted by psychosocial stress. Implications of our findings for the role of neuroendocrine function in age-related neurocognitive and neuropsychiatric disorders will be discussed.