Reduced hedonic capacity in euthymic bipolar subjects: A trait-like feature?

被引:49
作者
Di Nicola, Marco [1 ,4 ]
De Risio, Luisa [1 ]
Battaglia, Claudia [1 ]
Camardese, Giovanni [1 ]
Tedeschi, Daniela [1 ]
Mazza, Marianna [1 ]
Martinotti, Giovanni [3 ]
Pozzi, Gino [1 ]
Niolu, Cinzia [2 ]
Di Giannantonio, Massimo [3 ]
Siracusano, Alberto [2 ]
Janiri, Luigi [1 ,4 ]
机构
[1] Catholic Univ, Sch Med, Inst Psychiat & Psychol, I-00168 Rome, Italy
[2] Univ Tor Vergata, Inst Psychiat, Dept Neurosci, Rome, Italy
[3] G dAnnunzio Univ Chieti Pescara, Inst Psychiat, Dept Neurosci & Imaging, Chieti, Italy
[4] Univ Consortium Humanitas, Rome, Italy
关键词
Anhedonia; Affective disorders; Dopaminergic system; Reward circuit; PHYSICAL ANHEDONIA; MAJOR DEPRESSION; RATING-SCALE; DISORDER; DOPAMINE; PATHOPHYSIOLOGY; SCHIZOPHRENIA; SYMPTOM; TASK;
D O I
10.1016/j.jad.2012.10.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The aim of our study was to assess hedonic capacity in euthymic bipolar subjects, identifying possible differences compared to remitted unipolar depressed patients and healthy controls. Methods: 107 subjects with bipolar disorders, 86 with major depressive disorder and 106 healthy controls, homogeneous with respect to demographic characteristics, were enrolled. The following scales were administered: the Snaith-Hamilton pleasure scale (SHAPS), the subscale for 'anhedonia/asociality' of the scale for the assessment of negative symptoms (SANS) and the visual analogue scale (VAS) for hedonic capacity. Results: Scores on SHAPS total, interests and social interactions, SANS 'anhedonia/asociality' and VAS were all significantly higher in affective disorder patients compared to healthy controls. No difference was found between clinical groups. 20.5% (n=22) of bipolar disorder subjects and 24.5% (n=21) of major depressed subjects showed a significant reduction in hedonic capacity (SHAPS total score >= 3), compared to 7.5% (n=8) of healthy controls (chi(2)=12.03; p=.002). Limitations: Limitations include heterogeneity with respect to pharmacological status and longitudinal course (i.e., 'single' vs. 'recurrent' affective episodes). Conclusions: The major finding of our study is that euthymic bipolar patients and remitted major depressed patients display residual anhedonic symptoms. This suggests that, in affective disorder patients, altered hedonic capacity could represent an enduring trait and that, possibly, dysfunctions in the neurobiological mechanisms underlying hedonic response and reward processing persist, irrespective of mood state. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:446 / 450
页数:5
相关论文
共 38 条
[1]   MEASUREMENT OF FEELINGS USING VISUAL ANALOGUE SCALES [J].
AITKEN, RCB .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1969, 62 (10) :989-+
[2]  
Andreasen N.C., 1989, BR J PSYCHIAT S, P49
[3]  
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[4]   Dopamine modulates neural networks involved in effort-based decision-making [J].
Assadi, Seyed M. ;
Yucel, Murat ;
Pantelis, Christos .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2009, 33 (03) :383-393
[5]   Dopamine dysregulation syndrome: implications for a dopamine hypothesis of bipolar disorder [J].
Berk, M. ;
Dodd, S. ;
Kauer-Sant'Anna, M. ;
Malhi, G. S. ;
Bourin, M. ;
Kapczinski, F. ;
Norman, T. .
ACTA PSYCHIATRICA SCANDINAVICA, 2007, 116 :41-49
[6]   A functional magnetic resonance imaging study of bipolar disorder - State- and trait-related dysfunction in ventral prefrontal cortices [J].
Blumberg, HP ;
Leung, HC ;
Skudlarski, P ;
Lacadie, CM ;
Fredericks, CA ;
Harris, BC ;
Charney, DS ;
Gore, JC ;
Krystal, JH ;
Peterson, BS .
ARCHIVES OF GENERAL PSYCHIATRY, 2003, 60 (06) :601-609
[7]  
Cooper JR., 2003, The biochemical basis of neuropharmacology, V8th
[8]   Anhedonia as a Phenotype for the Val158Met COMT Polymorphism in Relatives of Patients With Schizophrenia [J].
Docherty, Anna R. ;
Sponheim, Scott R. .
JOURNAL OF ABNORMAL PSYCHOLOGY, 2008, 117 (04) :788-798
[9]   Neuroimaging abnormalities in the subgenual prefrontal cortex: implications for the pathophysiology of familial mood disorders [J].
Drevets, WC ;
Ongur, D ;
Price, JL .
MOLECULAR PSYCHIATRY, 1998, 3 (03) :220-226
[10]   The role of dopamine in the pathophysiology of depression [J].
Dunlop, Boadie W. ;
Nemeroff, Charles B. .
ARCHIVES OF GENERAL PSYCHIATRY, 2007, 64 (03) :327-337