Plasma Brain-Derived Neurotrophic Factor Levels Predict the Clinical Outcome of Depression Treatment in a Naturalistic Study

被引:59
作者
Kurita, Masatake [1 ,2 ]
Nishino, Satoshi [1 ,2 ]
Kato, Maiko [1 ]
Numata, Yukio [1 ]
Sato, Tadahiro [1 ]
机构
[1] Sato Hosp, Yamagata, Japan
[2] Tohoku Univ, Dept Cellular Signaling, Grad Sch Pharmaceut Sci, Sendai, Miyagi 980, Japan
关键词
BDNF LEVELS; MAJOR DEPRESSION; SERUM; ANTIDEPRESSANTS; MONTGOMERY; DISORDER; WOMEN;
D O I
10.1371/journal.pone.0039212
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Remission is the primary goal of treatment for major depressive disorder (MDD). However, some patients do not respond to treatment. The main purpose of this study was to determine whether brain-derived neurotrophic factor (BDNF) levels are correlated with treatment outcomes. In a naturalistic study, we assessed whether plasma BDNF levels were correlated with clinical outcomes by measuring plasma BDNF in patients with depressive syndrome (MADRS score >= 18), and subsequently comparing levels between the subgroup of patients who underwent remission (MADRS score <= 8) and the subgroup who were refractory to treatment (non-responders). Patients with depressive syndrome who underwent remission had significantly higher plasma BDNF levels (p < 0.001), regardless of age or sex. We also found a significant negative correlation between MADRS scores and plasma BDNF levels within this group (rho = -0.287, p = 0.003). In contrast, non-responders had significantly lower plasma BDNF levels (p = 0.029). Interestingly, plasma BDNF levels in the non-responder group were significantly higher than those in the remission group in the initial stage of depressive syndrome (p = 0.002). Our results show that plasma BDNF levels are associated with clinical outcomes during the treatment of depression. We suggest that plasma BDNF could potentially serve as a prognostic biomarker for depression, predicting clinical outcome.
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相关论文
共 30 条
[1]
Increased Concentrations of Nerve Growth Factor and Brain-Derived Neurotrophic Factor in the Rat Cerebellum After Exposure to Environmental Enrichment [J].
Angelucci, Francesco ;
De Bartolo, Paola ;
Gelfo, Francesca ;
Foti, Francesca ;
Cutuli, Debora ;
Bossu, Paola ;
Caltagirone, Carlo ;
Petrosini, Laura .
CEREBELLUM, 2009, 8 (04) :499-506
[2]
Brain-derived neurotrophic factor (BDNF) changes in the serum of depressed women [J].
Aydemir, Cigdem ;
Yalcin, Esra Suer ;
Aksaray, Sabahat ;
Kisa, Cebrail ;
Yildirim, Sema Gulen ;
Uzbay, Tayfun ;
Goka, Erol .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2006, 30 (07) :1256-1260
[3]
The effect of chronic antidepressant treatment on serum brain-derived neurotrophic factor levels in depressed patients: a preliminary study [J].
Aydemir, O ;
Deveci, A ;
Taneli, F .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2005, 29 (02) :261-265
[4]
Current trends in the assessment and somatic treatment of resistant/refractory major depression: An overview [J].
Berlim, Marcelo T. ;
Fleck, Marcelo P. ;
Turecki, Gustavo .
ANNALS OF MEDICINE, 2008, 40 (02) :149-159
[5]
Antidepressants increase neural progenitor cells in the human hippocampus [J].
Boldrini, Maura ;
Underwood, Mark D. ;
Hen, Rene ;
Rosoklija, Gorazd B. ;
Dwork, Andrew J. ;
Mann, J. John ;
Arango, Victoria .
NEUROPSYCHOPHARMACOLOGY, 2009, 34 (11) :2376-2389
[6]
Dreimuller N, 2011, NEUROPHARMACOLOGY
[7]
Duman RS, 1997, ARCH GEN PSYCHIAT, V54, P597
[8]
Inverse correlation of brain and blood BDNF levels in a genetic rat model of depression [J].
Elfving, Betina ;
Plougmann, Pia Hogh ;
Muller, Heidi Kaastrup ;
Mathe, Aleksander A. ;
Rosenberg, Raben ;
Wegener, Gregers .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2010, 13 (05) :563-572
[9]
Fujimura H, 2002, THROMB HAEMOSTASIS, V87, P728
[10]
Effect of treatment on serum brain-derived neurotrophic factor levels in depressed patients [J].
Gonul, AS ;
Akdeniz, F ;
Taneli, F ;
Donat, O ;
Eker, Ç ;
Vahip, S .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2005, 255 (06) :381-386