endothelin-1 and Depressive-Disorder

endothelin-1 has been researched along with Depressive-Disorder* in 2 studies

Trials

1 trial(s) available for endothelin-1 and Depressive-Disorder

ArticleYear
Endothelin-1 plasma concentrations in depressed patients and healthy controls.
    Neuropsychobiology, 1999, Volume: 40, Issue:3

    Depression and cardiovascular morbidity are known to be associated. So far, however, the pathophysiological link between these conditions is unclear. We tested the hypothesis that in depressed hypercortisolemic patients endothelin-1 (ET-1) plasma concentrations are increased and contribute to the cardiovascular risk. Diurnal plasma concentrations of cortisol and ET-1 were measured in 29 healthy controls and 22 depressed patients. ANCOVA did not reveal a significant effect of diagnosis or age upon ET-1 concentrations. However, only in depressed patients, cortisol plasma concentrations tended to be positively related to ET-1 concentrations. We conclude that ET-1 is not increased in depressed patients, but within this group, hypercortisolemia may be associated with increased ET-1 concentrations.

    Topics: Aging; Blood Pressure; Depressive Disorder; Endothelin-1; Female; Humans; Hydrocortisone; Male; Middle Aged; Psychiatric Status Rating Scales

1999

Other Studies

1 other study(ies) available for endothelin-1 and Depressive-Disorder

ArticleYear
Depression predicts elevated endothelin-1 in patients with coronary artery disease.
    Psychosomatic medicine, 2011, Volume: 73, Issue:1

    To examine the relationship of depression severity to circulating endothelin-1 (ET-1), which has previously been linked to plaque rupture and postacute coronary syndrome (ACS) survival. Depression carries an independent two- to four-fold increased risk of early morbidity and mortality after ACS. The pathway(s) linking depression to event-free survival remains to be determined.. Patients with documented history of coronary artery disease (n = 101) provided a resting morning blood sample that was assayed for ET-1, and they completed the Beck Depression Inventory (BDI). ET-1 was treated as a log-transformed continuous variable (logET-1), and as a dichotomous variable using a post-ACS risk threshold previously reported (≥1.16 fmol/mL).. BDI score was related to logET-1 in both unadjusted and adjusted models. In addition, unadjusted and adjusted logistic regression models with dichotomous ET-1 revealed that, for each point increase in BDI score, there was approximately a 14% increased likelihood of being at or above ET-1 risk threshold. Secondary logistic regression models demonstrated a >3.5-fold likelihood of being at or above this risk threshold in association with a BDI score of ≥10.. Depression symptom severity predicts ET-1 elevation that has previously been linked to post-ACS survival, with the greatest risk of elevation among those patients with worse depression symptoms. This link may identify a vulnerability to triggered ACS and poorer survival associated with depression. Future research should establish whether the observed relationship of depressive symptoms to ET-1 level mediates the link between depression and survival.

    Topics: Acute Coronary Syndrome; Aged; Depressive Disorder; Endothelin-1; Female; Humans; Logistic Models; Male; Personality Inventory; Prognosis; Risk Factors; Self Report; Severity of Illness Index; Survival Analysis; Tumor Necrosis Factor-alpha

2011