Gender-specific association of alexithymia and norepinephrine/cortisol ratios. A preliminary report

Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found...

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Published inJournal of psychosomatic research Vol. 59; no. 2; pp. 73 - 76
Main Authors Spitzer, Carsten, Brandl, Stephan, Rose, Hans-Joachim, Nauck, Matthias, Freyberger, Harald J.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.08.2005
New York, NY Elsevier
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Abstract Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations. Twenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients and 23 healthy controls (HC) and tested for N and free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) and the Symptom Check List (SCL). Controlling for depression, the neuroendocrine parameters did not differ between the MDD and HC participants nor between women and men. The TAS was not associated with N, C or the N/C ratio in the MDD and HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS ( r=.80). Our preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity and a decreased basal activity of the hypothalamic–pituitary–adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men and women.
AbstractList Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations.OBJECTIVEAlexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations.Twenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients and 23 healthy controls (HC) and tested for N and free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) and the Symptom Check List (SCL).METHODSTwenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients and 23 healthy controls (HC) and tested for N and free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) and the Symptom Check List (SCL).Controlling for depression, the neuroendocrine parameters did not differ between the MDD and HC participants nor between women and men. The TAS was not associated with N, C or the N/C ratio in the MDD and HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS (r = .80).RESULTSControlling for depression, the neuroendocrine parameters did not differ between the MDD and HC participants nor between women and men. The TAS was not associated with N, C or the N/C ratio in the MDD and HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS (r = .80).Our preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity and a decreased basal activity of the hypothalamic-pituitary-adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men and women.CONCLUSIONSOur preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity and a decreased basal activity of the hypothalamic-pituitary-adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men and women.
Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations. Twenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients and 23 healthy controls (HC) and tested for N and free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) and the Symptom Check List (SCL). Controlling for depression, the neuroendocrine parameters did not differ between the MDD and HC participants nor between women and men. The TAS was not associated with N, C or the N/C ratio in the MDD and HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS ( r=.80). Our preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity and a decreased basal activity of the hypothalamic–pituitary–adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men and women.
Objective: Alexithymia & posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) & decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations. Methods: Twenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients & 23 healthy controls (HC) & tested for N & free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) & the Symptom Check List (SCL). Results: Controlling for depression, the neuroendocrine parameters did not differ between the MDD & HC participants nor between women & men. The TAS was not associated with N, C or the N/C ratio in the MDD & HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS (r=.80). Conclusions: Our preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity & a decreased basal activity of the hypothalamic-pituitary-adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men & women. 2 Tables, 29 References. [Copyright 2005 Elsevier Inc.]
Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased cortisol (C) levels, resulting in a high N/C ratio, at least among male alcoholics. We aimed to explore if this association can also be found in other populations. Twenty-four-hour urine samples were obtained from 12 major depressive disorder (MDD) patients and 23 healthy controls (HC) and tested for N and free C. Participants completed the 20-item Toronto Alexithymia Scale (TAS) and the Symptom Check List (SCL). Controlling for depression, the neuroendocrine parameters did not differ between the MDD and HC participants nor between women and men. The TAS was not associated with N, C or the N/C ratio in the MDD and HC participants nor in females alone. However, in men, the N/C ratio correlated significantly with the TAS (r = .80). Our preliminary findings indicate that alexithymia is associated with an increased noradrenergic activity and a decreased basal activity of the hypothalamic-pituitary-adrenal (HPA) axis among men. This gender difference may reflect divergent underlying neurobiological processes of alexithymia in men and women.
Author Nauck, Matthias
Brandl, Stephan
Rose, Hans-Joachim
Freyberger, Harald J.
Spitzer, Carsten
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Issue 2
Keywords Urinary norepinephrine and cortisol
Posttraumatic stress disorder
N/C ratio
Alexithymia
Mood disorder
Human
Hypothalamohypophysoadrenal axis
Steroid hormone
Sex
Neuroendocrine regulation
Depression
Daily variation
Personality
Catecholamine
Hydrocortisone
Glucocorticoid
Sociodemographic factor
Adrenal hormone
Norepinephrine
Comparative study
Language English
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Snippet Alexithymia and posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) and decreased...
Objective: Alexithymia & posttraumatic stress disorder (PTSD) might share a neuroendocrine pattern characterized by increased urinary norepinephrine (N) &...
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SubjectTerms Adult
Adult and adolescent clinical studies
Affective Symptoms - epidemiology
Affective Symptoms - physiopathology
Affective Symptoms - urine
Alexithymia
Biological and medical sciences
Chromatography, High Pressure Liquid - methods
Cortisol
Depression
Depressive Disorder, Major - epidemiology
Depressive Disorder, Major - physiopathology
Depressive Disorder, Major - urine
Diagnostic and Statistical Manual of Mental Disorders
Female
Fundamental and applied biological sciences. Psychology
Humans
Hydrocortisone - urine
Hypothalamo-Hypophyseal System - physiopathology
Male
Medical sciences
Middle Aged
Mood disorders
N/C ratio
Norepinephrine - urine
Personality traits
Personality. Affectivity
Pituitary-Adrenal System - physiopathology
Posttraumatic Stress Disorder
Psychology. Psychoanalysis. Psychiatry
Psychology. Psychophysiology
Psychopathology. Psychiatry
Sex Factors
Stress Disorders, Post-Traumatic - epidemiology
Stress Disorders, Post-Traumatic - physiopathology
Stress Disorders, Post-Traumatic - urine
Urinary norepinephrine and cortisol
Title Gender-specific association of alexithymia and norepinephrine/cortisol ratios. A preliminary report
URI https://www.clinicalkey.com/#!/content/1-s2.0-S002239990400546X
https://dx.doi.org/10.1016/j.jpsychores.2004.07.006
https://www.ncbi.nlm.nih.gov/pubmed/16186001
https://www.proquest.com/docview/57140332
https://www.proquest.com/docview/68630414
Volume 59
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