Association of the COMT val158met variant with antidepressant treatment response in major depression

被引:112
作者
Baune, Bernhard T. [1 ]
Hohoff, Christa
Berger, Klaus
Neumann, Anna
Mortense, Sunke
Roehrs, Tilmann
Deckert, Jurgen
Arolt, Volker
Domschke, Katharina
机构
[1] James Cook Univ, Sch Med, Dept Psychiat, Townsville, Qld 4811, Australia
[2] Univ Munster, Dept Psychiat, Munster, Germany
[3] Univ Munster, Inst Epidemiol Social Med, Munster, Germany
[4] Univ Wurzburg, Dept Psychiat, Wurzburg, Germany
关键词
major depression; catechol-O-methyltransferase; COMT val158met; polymorphism; antidepressants; treatment response;
D O I
10.1038/sj.npp.1301462
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In several previous biochemical, pharmacological, and genetic studies, the catechol-O-methyltransferase (COMT) has been suggested to be involved in the pathogenesis as well as the pharmacological treatment of affective disorders. In the present study, 256 patients with major depression (DSM-IV) of Caucasian descent were genotyped for the functional COMT val158met polymorphism and characterized for clinical response to antidepressive pharmacological treatment as measured by intra-individual changes of Hamilton Depression (HAM-D-21) scores over 6 weeks. The COMT 158val/val genotype conferred a significant risk of worse response after 4-6 weeks of antidepressant treatment in patients with major depression (week 4: p = 0.003; week 5: p<0.0001; week 6: p<0.0001) after Bonferroni correction for multiple comparisons. The present results strongly point toward a negative influence of the higher activity COMT 158val/val genotype on antidepressant treatment response during the first 6 weeks of pharmacological treatment in major depression, possibly conferred by consecutively decreased dopamine availability. This finding suggests a potentially beneficial effect of an antidepressive add-on therapy with substances increasing dopamine availability individually tailored according to COMT val158met genotype.
引用
收藏
页码:924 / 932
页数:9
相关论文
共 43 条
[1]   Association between the COMT locus and obsessive-compulsive disorder in females but not males [J].
Alsobrook, JP ;
Zohar, AH ;
Leboyer, M ;
Chabane, N ;
Ebstein, RP ;
Pauls, DL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (01) :116-120
[2]   Analysis of COMT gene (Val 158 Met polymorphism) in the clinical response to SSRIs in depressive patients of European origin [J].
Arias, B ;
Serretti, A ;
Lorenzi, C ;
Gastó, C ;
Catalán, R ;
Fañanás, L .
JOURNAL OF AFFECTIVE DISORDERS, 2006, 90 (2-3) :251-256
[3]   Pramipexole versus sertraline in the treatment of depression in Parkinson's disease - A national multicenter parallel-group randomized study [J].
Barone, Paolo ;
Scarzella, Leonardo ;
Marconi, Roberto ;
Antonini, Angelo ;
Morgante, Letterio ;
Bracco, Fulvio ;
Zappia, Mario ;
Musch, Bruno .
JOURNAL OF NEUROLOGY, 2006, 253 (05) :601-607
[4]   HUMAN LIVER CATECHOL-O-METHYLTRANSFERASE PHARMACOGENETICS [J].
BOUDIKOVA, B ;
SZUMLANSKI, C ;
MAIDAK, B ;
WEINSHILBOUM, R .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1990, 48 (04) :381-389
[5]   A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain [J].
Bray, NJ ;
Buckland, PR ;
Williams, NM ;
Williams, HJ ;
Norton, N ;
Owen, MJ ;
O'Donovan, MC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (01) :152-161
[6]   Ropinirole in treatment-resistant depression: A 16-week pilot study [J].
Cassano, P ;
Lattanzi, L ;
Fava, MI ;
Navari, S ;
Battistini, G ;
Abelli, M ;
Cassano, GB .
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 2005, 50 (06) :357-360
[7]   Pramipexole in treatment-resistant depression: An extended follow-up [J].
Cassano, P ;
Lattanzi, L ;
Soldani, F ;
Navari, S ;
Battistini, G ;
Gemignani, A ;
Cassano, GB .
DEPRESSION AND ANXIETY, 2004, 20 (03) :131-138
[8]   Functional analysis of genetic variation in catechol-o-methyltransferase (COMT):: Effects on mRNA, protein, and enzyme activity in postmortem human brain [J].
Chen, JS ;
Lipska, BK ;
Halim, N ;
Ma, QD ;
Matsumoto, M ;
Melhem, S ;
Kolachana, BS ;
Hyde, TM ;
Herman, MM ;
Apud, J ;
Egan, MF ;
Kleinman, JE ;
Weinberger, DR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (05) :807-821
[9]   Association study of MAO-A, COMT, 5-HT2A, DRD2, and DRD4 Polymorphisms with illness time course in mood disorders [J].
Cusin, C ;
Serretti, A ;
Lattuada, E ;
Lilli, R ;
Lorenzi, C ;
Smeraldi, E .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (04) :380-390
[10]   Dopamine, depression and antidepressants [J].
Dailly, E ;
Chenu, F ;
Renard, CE ;
Bourin, M .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 (06) :601-607