Validation of a Hamilton subscale for endogenomorphic depression

Thase, Michael E.; Hersen, Michel; Bellack, Alan S.; Himmelhoch, Jonathan M.; Kupfer, David J.

doi:10.1016/0165-0327(83)90050-2

Cited by 107 publications

(51 citation statements)

References 31 publications

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“…Secondly the unipolar major depressives were dichotomized into ENDO and NENDO using the endogenomorphic subscale of the HDRS [22]. The depressives with a score higher than 9 were included in the ENDO group and those with a score lower than 7 were included in the NENDO group.…”

Section: Discussionmentioning

confidence: 99%

Anhedonia, Alexithymia and Locus of Control in Unipolar Major Depressive Disorders

Loas

Dhee-Perot²,

Chaperot³

et al. 1998

Psychopathology

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The relationship between anhedonia, alexithymia and locus of control was studied in a group of healthy subjects (n = 56) and in a group of unipolar major depressives (n = 59). These dimensions were rated using the Physical Anhedonia Scale (PAS), the Toronto Alexithymia Scale (TAS) and the Internal Powerful others and Chance Scale. The unipolar major depressives were divided into two subgroups using the endogenomorphic subscale of the Hamilton Depression Rating Scale. There are respectively 25 and 17 depressives in the nonendogenomorphic (NENDO) and endogenomorphic (ENDO) subgroups. The unipolar major depressives were significantly more anhedonic, alexithymic and externalized than the controls. In the ENDO group the PAS and TAS Feelings scores were positively correlated suggesting that a third variable of emotional deficit could characterize endogenomorphic depression. In the NENDO group the PAS, TAS Daydreaming, Powerful others and Chance scores were positively correlated. In nonendogenomorphic depression anhedonia could be related to a poverty of imagery and could be interpreted as a consequence of external causes.

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Section: Discussionmentioning

confidence: 99%

Anhedonia, Alexithymia and Locus of Control in Unipolar Major Depressive Disorders

Loas

Dhee-Perot²,

Chaperot³

et al. 1998

Psychopathology

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show abstract

“…Patients met the following inclusion criteria: diagnosis of major depression, a baseline total score of 20 or higher on the 21-item Hamilton Depression Rating Scale, and a score of at least 7 on the Core Endogenomorphic Scale (18), which uses eight items of the 21-item Hamilton depression scale. The latter two criteria were designed to ensure inclusion of patients with psychotic major depression and patients with nonpsychotic major depression with similar minimum levels of endogenous-type symptoms.…”

Section: Methodsmentioning

confidence: 99%

Neuropsychological Deficits in Psychotic Versus Nonpsychotic Major Depression and No Mental Illness

Schatzberg

Posener²,

DeBattista³

et al. 2000

AJP

182

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“…Depressed patients with (11 subjects) and without (17 subjects) psychosis were included. All depressed subjects were required to have a minimum score of 21 on the HDRS and a minimum score of 7 on the Thase Core Endogenomorphic Scale (Thase et al 1983) modified for the 21-item HDRS (Posener et al 2000). These latter two criteria were designed to ensure inclusion of participants with similar minimum levels of severity of endogenous-type symptoms.…”

Section: Subjectsmentioning

confidence: 99%

Resting-State Functional Connectivity in Major Depression: Abnormally Increased Contributions from Subgenual Cingulate Cortex and Thalamus

Greicius

Flores

Menon

et al. 2007

Biological Psychiatry

2,008

120

1,486

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Background: Positron emission tomography (PET) studies of major depression have revealed resting-state abnormalities in the prefrontal and cingulate cortices. Recently, fMRI has been adapted to examine connectivity within a specific resting-state neural network-the default-mode network -that includes the medial prefrontal and anterior cingulate cortices. The goal of this study was to examine resting-state, default-mode network functional connectivity in subjects with major depression and in healthy comparison subjects.

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Validation of a Hamilton subscale for endogenomorphic depression

Cited by 107 publications

References 31 publications

Anhedonia, Alexithymia and Locus of Control in Unipolar Major Depressive Disorders

Anhedonia, Alexithymia and Locus of Control in Unipolar Major Depressive Disorders

Neuropsychological Deficits in Psychotic Versus Nonpsychotic Major Depression and No Mental Illness

Resting-State Functional Connectivity in Major Depression: Abnormally Increased Contributions from Subgenual Cingulate Cortex and Thalamus

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