TY - JOUR PY - 2010// TI - Dysregulation of the sympathetic nervous system, hypothalamic-pituitary-adrenal axis and executive function in individuals at risk for suicide JO - Journal of psychiatry and neuroscience A1 - McGirr, A. A1 - Diaconu, G. A1 - Berlim, M.T. A1 - Pruessner, J.C. A1 - Sablé, R. A1 - Cabot, S. A1 - Turecki, G. SP - 399 EP - 408 VL - 35 IS - 6 N2 - BACKGROUND: Suicidal behaviour aggregates in families, and the hypothalamic-pituitary-adrenal (HPA) axis and noradrenergic dysregulation may play a role in suicide risk. It is unclear whether stress dysregulation is a heritable trait of suicide or how it might increase risk. We investigated stress reactivity of the autonomic nervous system and the HPA axis in suicide predisposition and characterized the effect of this dysregulation on neuropsychologic function.

METHODS: In this family-based study of first-degree relatives (n = 14) of suicide completers and matched controls with no family or personal history of suicidal behaviour (n = 14), participants underwent the Trier Social Stress Test (TSST). We used salivary α-amylase and cortisol levels to characterize stress reactivity and diurnal variation. We administered a series of neuropsychologic and executive function tests before and after the TSST.

RESULTS: Despite normal diurnal variation, relatives of suicide completers exhibited blunted cortisol and α-amylase TSST reactivity. Although there were no baseline differences in conceptual reasoning, sustained attention or executive function, the relatives of suicide completers did not improve on measures of inhibition upon repeated testing after TSST. Secondary analyses suggested that these effects were related to suicide vulnerability independ ent of major depression. Limitations: The sample size was small, and the design prevents us from disentangling our findings from the possible traumatic consequences of losing a relative by suicide.

CONCLUSIONS: Blunted stress response may be a trait of suicide risk, and impairment of stress-induced executive function may contribute to suicide vulnerability. © 2010 Canadian Medical Association.

Language: en

LA - en SN - 1180-4882 UR - http://dx.doi.org/10.1503/jpn.090121 ID - ref1 ER -