Early reactions of brain-derived neurotrophic factor in plasma (pBDNF) and outcome to acute antidepressant treatment in patients with Major Depression

被引:51
作者
Dreimueller, Nadine [1 ]
Schlicht, Konrad Friedrich [1 ]
Wagner, Stefanie [1 ]
Peetz, Dirk [2 ,3 ]
Borysenko, Liudmyla [1 ]
Hiemke, Christoph [1 ]
Lieb, Klaus [1 ]
Tadic, Andre [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Psychiat & Psychotherapy, Mainz, Germany
[2] Berlin Buch, Helios Clin, Inst Lab Med, D-13125 Berlin, Germany
[3] Univ Med Ctr Mainz, Inst Clin Chem & Lab Med, Mainz, Germany
关键词
Biomarker; Brain-derived neurotrophic factor; Major Depressive Disorder; Plasma; Treatment outcome; Early improvement; EARLY IMPROVEMENT; HUMAN PLATELETS; RATING-SCALE; BLOOD-BRAIN; BDNF LEVELS; METAANALYSIS; HIPPOCAMPUS; EXPRESSION; REMISSION; MECHANISM;
D O I
10.1016/j.neuropharm.2011.07.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In Major Depressive Disorder, a growing data base suggests that the onset of antidepressants' action can be detected by improvement of depressive symptoms in the first 10-14 days of treatment. Previous studies showed that the mean concentration of the brain-derived neurotrophic factor (BDNF) in blood increases during antidepressant treatment and positively correlates with amelioration of MOD symptoms. We previously showed an association between very early changes of the serum BDNF concentration and treatment outcome (Tadic et al., 2011. Prog Neuropsychopharmacol Bid l Psychiatry 35, 415 -420). However, no study has yet investigated whether BDNF concentration in plasma increases in the early course of treatment and enables the prediction of final treatment outcome. The goal of this study was to investigate in MDD patients, whether the change of pBDNF in the early course of treatment is a specific and sensitive marker for final treatment outcome. For this purpose, we performed a naturalistic pilot study with 39 inpatients with MDD according to DSM-IV. Depression severity and pBDNF were measured in weekly intervals from baseline (EP) to endpoint (EP, max. week six) with the 21-item Hamilton Depression Rating Scale (HAMD-21) and enzyme-linked immunosorbent assay (ELISA), respectively. According to ROC-analysis, the best cut-off value for the prediction of response at EP is an increase of 338 pg/ml or 126%, respectively, of pBDNF between BL and day 7. The single markers pBDNF change and HAMD-21 improvement from BL-d7 predicted later treatment outcome with moderate to high sensitivity and specificity (pBDNF: 42% and 96%, resp.; HAMD improvement: 83% and 65%, resp.). The combined marker early pBDNF change plus HAMD-21 improvement at day 7 increased the specificity for response to 100%. Our data provide first preliminary evidence that an early change of pBDNF in conjunction with early improvement might be a peripheral marker predictive for treatment outcome in patients with MDD. This has to be confirmed in further investigations. This article is part of a Special Issue entitled 'Anxiety and Depression'. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:264 / 269
页数:6
相关论文
共 53 条
[1]  
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[2]   The AGNP-TDM expert group consensus guidelines:: Therapeutic Drug Monitoring in psychiatry [J].
Baumann, P ;
Hiemke, C ;
Ulrich, S ;
Eckermann, G ;
Gaertner, I ;
Gerlach, M ;
Kuss, HJ ;
Laux, G ;
Müller-Oerlinghausen, B ;
Rao, ML ;
Riederer, P ;
Zernig, G .
PHARMACOPSYCHIATRY, 2004, 37 (06) :243-265
[3]   Serum and plasma BDNF levels in major depression: A replication study and meta-analyses [J].
Bocchio-Chiavetto, Luisella ;
Bagnardi, Vincenzo ;
Zanardini, Roberta ;
Molteni, Raffaella ;
Nielsen, Maria Gabriela ;
Placentino, Anna ;
Giovannini, Caterina ;
Rillosi, Luciana ;
Ventriglia, Mariacarla ;
Riva, Marco A. ;
Gennarelli, Massimo .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2010, 11 (06) :763-773
[4]   Cellular sources of enhanced brain-derived neurotrophic factor production in a mouse model of allergic inflammation [J].
Braun, A ;
Lommatzsch, M ;
Mannsfeldt, A ;
Neuhaus-Steinmetz, U ;
Fischer, A ;
Schnoy, N ;
Lewin, GR ;
Renz, H .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 21 (04) :537-546
[5]   A systematic review and meta-analysis of clinical studies on major depression and BDNF levels: implications for the role of neuroplasticity in depression [J].
Brunoni, Andre Russowsky ;
Lopes, Mariana ;
Fregni, Felipe .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2008, 11 (08) :1169-1180
[6]   Serum brain-derived neurotrophic factor: Determinants and relationship with depressive symptoms in a community population of middle-aged and elderly people [J].
Bus, Boudewijn A. A. ;
Tendolkar, Indira ;
Franke, Barbara ;
de Graaf, Jacqueline ;
Den Heijer, Martin ;
Buitelaar, Jan K. ;
Voshaar, Richard C. Oude .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2012, 13 (01) :39-47
[7]   Associations between Brain-Derived Neurotrophic Factor Plasma Levels and Severity of the Illness, Recurrence and Symptoms in Depressed Patients [J].
Dell'Osso, Liliana ;
Del Debbio, Alessandro ;
Veltri, Antonello ;
Bianchi, Carolina ;
Roncaglia, Isabella ;
Carlini, Marina ;
Massimetti, Gabriele ;
Dell'Osso, Mario Catena ;
Vizzaccaro, Chiara ;
Marazziti, Donatella ;
Piccinni, Armando .
NEUROPSYCHOBIOLOGY, 2010, 62 (04) :207-212
[8]  
DONOVAN MJ, 1995, AM J PATHOL, V147, P309
[9]   A neurotrophic model for stress-related mood disorders [J].
Duman, Ronald S. ;
Monteggia, Lisa M. .
BIOLOGICAL PSYCHIATRY, 2006, 59 (12) :1116-1127
[10]   CONCEPTUALIZATION AND RATIONALE FOR CONSENSUS DEFINITIONS OF TERMS IN MAJOR DEPRESSIVE DISORDER - REMISSION, RECOVERY, RELAPSE, AND RECURRENCE [J].
FRANK, E ;
PRIEN, RF ;
JARRETT, RB ;
KELLER, MB ;
KUPFER, DJ ;
LAVORI, PW ;
RUSH, AJ ;
WEISSMAN, MM .
ARCHIVES OF GENERAL PSYCHIATRY, 1991, 48 (09) :851-855