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 (ρ = –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.
UMIN Clinical Trials Registry UMIN000006264
Citation: Kurita M, Nishino S, Kato M, Numata Y, Sato T (2012) Plasma Brain-Derived Neurotrophic Factor Levels Predict the Clinical Outcome of Depression Treatment in a Naturalistic Study. PLoS ONE 7(6): e39212. https://doi.org/10.1371/journal.pone.0039212
Editor: Shilpa J. Buch, University of Nebraska Medical Center, United States of America
Received: March 16, 2012; Accepted: May 21, 2012; Published: June 27, 2012
Copyright: © 2012 Kurita et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by funding from Koutokukai Organisation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This study did not receive funding from pharmaceutical corporations.
Competing interests: The authors have declared that no competing interests exist.
Remission is defined in The Diagnostic and Statistical Manual (DSM-IV) as the absence of significant signs or symptoms, and is the primary goal of treatment for major depressive disorder (MDD). At present, the category of depression (e.g., severe, moderate, mild or remission) is primarily evaluated by the patient using various subjective indices; however, there is currently no biomarker that could serve as an objective index for evaluating the severity or progression of MDD.
Brain-derived neurotrophic factor (BDNF) has increasingly attracted attention among researchers investigating MDD, as numerous reports have indicated that it plays an important role in the illness . BDNF is a member of the neurotrophin family and plays a critical role in the survival, differentiation and outgrowth of peripheral and central neurons during development and in adulthood , .
Serum and plasma levels of BDNF are decreased in patients suffering from MDD , , , , . In addition, serum BDNF levels are correlated with the severity of depression , and serum BDNF levels in patients treated with antidepressants increase to levels found in healthy subjects , , . Moreover, BDNF levels in the hippocampus and prefrontal cortex are significantly reduced in suicide victims compared with non-suicide controls . Although most studies to date have shown that serum BDNF levels increase with antidepressant treatment, the usefulness of serum BDNF as a biomarker for MDD is not yet clear.
Among MDD patients, there exist two distinct groups: a group that responds to treatment (the responder group) and a group that is refractory to treatment (the non-responder group). To our knowledge, no study to date has examined plasma BDNF levels in non-responder MDD patients.
The majority of studies that have examined depression have been prospective studies. Our report describes the first naturalistic study examining BDNF levels in remission and non-responder groups. To better understand the role of BDNF in MDD, we compared the changes in plasma BDNF levels in remission and non-responder groups of patients with depressive syndrome.
The Montgomery-Åsberg Depression Rating Scale (MADRS)  is increasingly employed in clinical research since results from earlier studies had suggested that the scale could be superior to the traditional HAMD17 with respect to sensitivity to change , ,  and other psychometric properties . The severity of depression was assessed using the MADRS every two weeks by independent experienced raters. The raters were objective and were not concerned with treatment outcome. We used a MADRS score ≤18 points to separate symptoms more than moderate from symptoms mild depression . We used MADRS scores to identify patients with depressive syndrome (defined as MADRS of at least 18 points), and to differentiate between non-responders (defined as those showing a <50% reduction in MADRS score from the depressive symptom stage) and patients in remission (defined as those with a MADRS score ≤8 after treatment ). The period from the depressive syndrome stage to the response stage was 7.2±8.6 weeks, and the period from the depressive syndrome stage to the remission stage was 12.3±12.6 weeks. To investigate differences between the remission and the non-responder groups, we examined different time periods during the course of treatment. The treatment period selected for the non-responder group was closely matched with that of the remission group and was determined to be an 8-week period. Furthermore, the period-matched depressive symptom-remission time frame was determined to be 12 weeks in the non-responder group.
A detailed flow chart of patient selection and grouping during the study is shown in Fig. 1. The subjects were recruited from a total of 110 MDD patients admitted to the in- and out-patient clinics of Sato Hospital, Koutokukai, between June 2006 and March 2009. All patients were suffering from a current major depressive episode–single episode [DSM-IV-TR codes: 296.2] or recurrent episodes [DSM-IV-TR codes: 296.3]–diagnosed according to the Diagnostic and Statistical Manual for Mental Disorders, fourth edition, text version (DSM-IV-TR, American Psychiatric Association, 2000). Subjects with any other diagnosed mental or severe physical illness were excluded from the study. After the procedures were fully explained, all participants gave informed consent. Written informed consent was obtained from all patients participating in the study and the study protocols were approved by the Ethics Committee of Sato Hospital, Koutokukai and the Ethics Committee of Graduate School of Pharmaceutical Sciences, Tohoku University, and was standard procedure in clinical trials involving vulnerable participants in the Japan. This study was performed according to the ethical standards of the Declaration of Helsinki. Also, written informed consent was obtained from the participants, and their parents (guardians) if the participants were children. All participants who declined to participate or otherwise did not participate were eligible for treatment and were not disadvantaged in any other way by not participating in the study.
As a criterion for inclusion of patients in this study, we chose a MADRS score ≥18 points (symptoms more than moderate). Thus, from a total of 110 patients, 79 were selected for inclusion in the study. We then categorized these patients into two groups: a remission group (patients experiencing an improvement of symptoms; MADRS scores ≤8 after treatment) and a non-responder group (patients refractory to treatment, showing a <50% reduction in MADRS score). The final analysis included 48 patients, with 38 subjects in the remission group (19 men and 19 women; average age 44.3±18.6 years, range 17–87 years), and 10 subjects in the non-responder group (three men and seven women; average age 50.4±15.2 years, range 18–71 years). Subjects were divided into two groups based on either sex or median age (43.9 years) to investigate whether these factors affected plasma BDNF. Thirty-one patients were excluded because they either ceased treatment within three months (n = 24), received intermittent treatment (n = 5), or showed response with incomplete remission (n = 2).
None of the subjects was taking hormone therapies (including oral contraceptives). Most patients (47/48 patients) had been prescribed antidepressants by psychiatrists. Psychiatrists treated patients with homogeneous psychotherapy. The following antidepressant drugs were administered to the remission group in the depressive syndrome stage: amitriptyline (50–150 mg/day; n = 2), clomipramine (30–150 mg/day; n = 4), fluvoxamine (25–150 mg/day; n = 11), imipramine (75 mg/day; n = 1), maprotiline (75 mg/day; n = 1), milnacipran (50–200 mg/day; n = 8), paroxetine (10 mg/day; n = 3), sertraline (25–100 mg/day; n = 8), sulpiride (150–300 mg/day; n = 6) and trazodone (25–100 mg/day; n = 4). The non-responder group received the following antidepressant drugs in the depressive syndrome stage: amoxapine (125 mg/day; n = 1), aripiprazole (3 mg/day; n = 1), fluvoxamine (125 mg/day; n = 1), maprotiline (25 mg/day; n = 2), milnacipran (150 mg/day; n = 1), paroxetine (10–40 mg/day; n = 5), sertraline (25–100 mg/day; n = 2), sulpiride (300 mg/day; n = 1) and trazodone (50 mg/day; n = 1). The following antidepressant drugs were administered to the remission group in the response stage: amitriptyline (50–150 mg/day; n = 3), aripiprazole (3 mg/day; n = 1), clomipramine (50–75 mg/day; n = 5), fluvoxamine (50–150 mg/day; n = 9), imipramine (150 mg/day; n = 1), maprotiline (50–75 mg/day; n = 3), milnacipran (50–150 mg/day; n = 8), paroxetine (10–30 mg/day; n = 3), sertraline (25–100 mg/day; n = 9), sulpiride (50–300 mg/day; n = 7) and trazodone (25–100 mg/day; n = 3). The non-responder group received the following antidepressant drugs at the 8-week period: amitriptyline (25 mg/day; n = 1), amoxapine (175 mg/day; n = 1), aripiprazole (18 mg/day; n = 1), clomipramine (105 mg/day; n = 1), hange-kobuku-to (a Chinese herbal medicine; 7.5 g/day; n = 1), imipramine (30 mg/day; n = 1), maprotiline (75 mg/day; n = 1), milnacipran (50–60 mg/day; n = 3), paroxetine (20–40 mg/day; n = 4), sertraline (25 mg/day; n = 1), sulpiride (300 mg/day; n = 1) and trazodone (50 mg/day; n = 1). The following antidepressant drugs were administered to the remission group in the remission stage: amitriptyline (50–150 mg/day; n = 3), aripiprazole (6 mg/day; n = 1), clomipramine (50–100 mg/day; n = 7), fluvoxamine (50–150 mg/day; n = 7), imipramine (250 mg/day; n = 1), maprotiline (75–100 mg/day; n = 2), milnacipran (50–200 mg/day; n = 8), paroxetine (10–30 mg/day; n = 4), sertraline (25–100 mg/day; n = 9), sulpiride (150–300 mg/day; n = 5) and trazodone (25–100 mg/day; n = 3). Meanwhile, the non-responder group received the following antidepressant drugs during the 12-week period: amitriptyline (25 mg/day; n = 1), amoxapine (100–175 mg/day; n = 3), aripiprazole (15 mg/day; n = 1), clomipramine (25–225 mg/day; n = 2), hange-kobuku-to (7.5 g/day; n = 1), maprotiline (75 mg/day; n = 1), milnacipran (50–180 mg/day; n = 3), paroxetine (20–40 mg/day; n = 2), sertraline (25 mg/day; n = 1) and trazodone (50 mg/day; n = 1). Although one subject underwent modified electroconvulsive therapy (weeks 36–41), the patient did not achieve a response. In one patient, the side effects of the antidepressants were considered too adverse; therefore, the patient asked to receive Chinese medicine rather than antidepressants. There was no bias in treatments with SSRIs, SNRIs, TCA and tetracyclic antidepressants between the remission and non-responder groups within the depressive syndrome stage and at the end point (Chi-square test, p>0.05).
Blood was withdrawn from each subject by venipuncture into a blood collection tube containing EDTA as an anticoagulant between 10∶00 and 17∶00. The tubes were immediately cooled to 4°C and then centrifuged at 2000×g for 20 min. Plasma was kept frozen at –80°C until assayed.
Plasma BDNF levels were measured using an ELISA kit (BDNF Emax Immunoassay System, Promega, Madison, WI, USA) after appropriate dilution of samples (1∶10 to 1∶50) in blocking and sample buffer according to the manufacturer’s instructions. The BDNF standard provided with this system was used to generate a standard curve that was linear between 3.9 and 500 pg/ml. Beyond these limits, BDNF concentrations could not be accurately extrapolated from the standard curve. Therefore, to determine BDNF concentrations in the diluted samples, we used only values that were within the linear range of this standard curve. Briefly, 96-well flat-bottom immunoplates were coated with anti-BDNF monoclonal antibody (mAb) and incubated at 4°C for 18 h. Plates were washed with Tris-buffered saline containing 0.1% Tween 20, pH 7.6 (TBS-T). After blocking non-specific binding with blocking and sample buffer for 1 h at room temperature (RT), standards and samples were added to the plates, incubated on a shaker for 2 h at RT, and then washed with TBS-T. The plates were subsequently incubated with anti-human BDNF polyclonal antibody at RT for 2 hours, washed, and incubated with anti-IgY antibody conjugated to horseradish peroxidase for 1 hour at RT, followed by washing with TBS-T. Tetramethyl-benzidine was then added to produce the color reaction. After stopping the reaction with 1 N HCl, the absorbance was read at 450 nm on a Sunrise Classic microplate reader (Tecan, Mannedolf, Switzerland) and BDNF concentrations were determined automatically according to the BDNF standard curve (ranging from 7.8 to 500 pg/ml of BDNF). Measurements were performed in duplicate.
Statistical analyses of MADRS scores and plasma BDNF levels were performed using one-way repeated measures analysis of variance (rep-ANOVA) with three levels of symptoms or periods. Post-hoc tests were performed on ANOVA results using the Bonferroni correction for multiple comparisons. Between-group comparisons were performed using unpaired, two-tailed Student’s t-tests. Data are shown as the means ± standard deviation (mean ± S.D.). Correlation analysis was performed using Spearman’s correlation. Statistical significance was defined as p<0.05. Normality testing was performed using the Shapiro-Wilk test. Possible violations of the sphericity assumption were assessed by Mauchly’s test. Analyses were performed using SPSS software version 16.0.
Characteristics of MDD Patients
The subjects’ characteristics are summarized in Table 1. No significant differences were found between the remission and non-responder groups in terms of gender, age or MADRS score in the depressive syndrome stage.
Remission group patients were defined as those with a MADRS score ≤8, reducing from a score of at least 18 points, after treatment. The MADRS scores before treatment and at the time of response and remission after treatment were 33.7±8.9, 10.9±5.9, and 5.0±2.4, respectively. Patients in the remission group had significantly reduced MADRS scores during the treatment (repeated-measures ANOVA; F1, 37 = 344.017, p<0.001). There were significant differences in MADRS scores among stages within the remission group (depressive symptoms vs response (p<0.001), depressive symptoms vs remission (p<0.001), and response vs remission (p<0.001); Bonferroni’s multiple comparison).
The period-matched symptom-response and symptom-remission outcomes were examined at 8 and 12 weeks, respectively, in the non-responder group. Plasma BDNF levels were measured by immunoassay. Each point represents the mean. The statistical significance of differences was calculated using repeated-measures ANOVA with post-hoc Bonferroni testing (*p<0.05). The statistical significance of differences in plasma BDNF levels between remission (▪) and non-responder (□) groups at the depressive syndrome stage were calculated using the Students’ t-test (#p<0.05).
The period from the depressive syndrome stage to the response stage was 7.2±8.6 weeks, and the period from the depressive syndrome stage to the remission stage was 12.3±12.6 weeks. Plasma BDNF levels in the depressive syndrome, response and remission stages in the remission group were 1 827±1 340, 2 402±1 610, and 3 158±2 033 pg/ml, respectively. Patients in the remission group had significantly higher plasma BDNF levels at remission than in the depressive syndrome and response stages (repeated-measures ANOVA; F1, 37 = 25.083, p<0.001) (Fig.2). Plasma BDNF levels differed significantly among stages within the remission group (depressive symptoms vs response (p = 0.004); depressive symptoms vs remission (p<0.001); and response vs remission (p = 0.003); post hoc ANOVA Bonferroni’s Multiple Comparison).
Treatment of the remission group led to an expected decrease in MADRS scores, and this was accompanied by a significant increase in plasma BDNF levels. Correspondingly, we found a significant negative correlation between MADRS scores and plasma BDNF levels within the remission group (ρ = –0.287, p = 0.003, n = 114) (Fig.3).
To investigate differences between the remission and the non-responder groups, we examined different time periods during the course of treatment.
The MADRS scores in the non-responder group at the depressive syndrome stage, and at 8 and 12 weeks after the commencement of treatment were 35.1±6.5, 25.8±7.7, and 35.2±11.4, respectively. Patients in the non-responder group exhibited no significant change in MADRS score between 8 and 12 weeks (repeated-measures ANOVA; F1, 9 = 0.001, p = 0.982).
Plasma BDNF levels in the non-responder group at the depressive syndrome stage, and at 8 and 12 weeks after the commencement of treatment were 2 932±2 373, 2 117±2 042, and 1 619±1 698 pg/ml, respectively. Interestingly, patients in the non-responder group showed significantly reduced plasma BDNF levels between weeks 8 and 12 (repeated-measures ANOVA; F1, 9 = 6.743, p = 0.029) (Fig.2). Surprisingly, treatment of the non-responder group produced no change in MADRS score by 12 weeks, although these patients did show a significant decrease in plasma BDNF levels. We found no significant correlation between MADRS scores and plasma BDNF levels (ρ = –0.112, p = 0.554, n = 30) in the non-responder group.
Comparison of the Remission and Non-responder Groups at the Depressive Syndrome Stage
To determine whether plasma BDNF levels could predict treatment outcome, we examined plasma BDNF levels in the remission and non-responder groups at the initial depressive syndrome stage. Surprisingly, the non-responder group had higher plasma BDNF levels compared with the remission group (p = 0.002) (Fig.2).
No Effect of Sex or Age on Plasma BDNF
We next investigated whether sex and/or age affected plasma BDNF. We divided the subjects into two groups based on either sex or median age (43.9 years). The results for the remission group are summarized in Table 2. Plasma BDNF was not affected by sex or age.
To gain insight into the different outcomes during the course of treatment for depression, we examined whether plasma BDNF levels underwent a change at different stages (syndrome, response and remission) and the equivalent time points in non-responders, focusing on differences between remission and non-responder groups. In the remission group, plasma BDNF levels increased significantly with clinical improvement, independent of sex and age.
Although options for pharmacologic treatment have expanded significantly in the past 20 years, between one- and two-thirds of patients do not respond to the first antidepressant prescribed, and 15–33% do not respond to multiple interventions . In this study, the non-responder group comprised 21% (10/48) of the study population, consistent with the above report. However, the resultant difference in the numbers of patients in the remission (79% (38/48)) and non-responder groups (21% (10/48)) is a limitation of a naturalistic study such as ours.
Of note, we show for the first time that patients in the non-responder group have significantly decreased plasma BDNF levels during the syndrome’s 8–12 week period. Thus, plasma BDNF may serve as an important biomarker for the prognosis of MDD.
In this study, we focused on remission. An advantage of a naturalistic study such as ours is that we could compare plasma BDNF as a biomarker between patients achieving remission and non-responders. For the purposes of comparison, we observed scores in non-responders at the corresponding time points to those at which patients in the remission achieved a response and remission. However, the disagreement of the period of remission and the period examined in non-responders (despite each stage being matched) is a limitation of naturalistic studies. Another limitation is the potential variation in drug treatment between the two groups of depressed patients. The effects of antidepressants on peripheral BDNF levels are not uniform , . Thus, although most studies to date have shown that serum BDNF levels increase with antidepressant treatment, different classes of antidepressants-induced changes in BDNF in the peripheral blood are not always uniform. However, in the present naturalistic study, there was no major bias in drug treatment between the remission and non-responder groups. There was no bias in treatments with SSRIs, SNRIs, TCA and tetracyclic antidepressants between the remission and non-responder groups within the depressive syndrome stage and at the end point (Chi-square test, p>0.05). Also, some patients were treated with multiple antidepressants.
Individual differences in plasma BDNF levels were large, and consequently, plasma BDNF levels may have differed between groups. Therefore, although plasma BDNF may be a valuable biomarker for the treatment of depression, it may not be appropriate or feasible to establish a normal range (as is done for numerous other serum components to establish a baseline for assessing physiological status). Thus, it is necessary to measure plasma BDNF regularly in each MDD patient, and a careful examination of the BDNF profile, to examine trends or shifts, is necessary for the clinician to select an appropriate treatment.
Plasma BDNF levels decreased during the course of treatment in the non-responder group. BDNF levels are increased by not only antidepressants, but also by environmental enrichment  and modest exercise . In contrast, BDNF levels are decreased by stressful events. Plasma BDNF levels were decreased in non-responders treated with antidepressants suggesting that the ability of stress to decrease BDNF levels may be greater than the ability of antidepressants to increase BDNF levels.
Notably, we found that plasma BDNF concentrations were significantly different between the remission and non-responder groups at the depressive syndrome stage. This important observation suggests that the biological backgrounds of patients with treatment-responsive MDD and patients with treatment-resistant MDD might differ, and that high plasma BDNF levels during the depressive syndrome stage may be indicative of treatment-resistant MDD patients. Thus, plasma BDNF levels may help the clinician to predict clinical outcome. In particular, if plasma BDNF levels decrease or are unchanged in an individual with regularly measured plasma BDNF, the clinician may need to reevaluate treatment strategy.
In 2002, the involvement of serum BDNF in stress and major depression was reported for the first time . Over the last 14 years, most studies have examined serum BDNF rather than plasma BDNF . However, Piccinni et al suggested that plasma BDNF may be more appropriate as a biomarker of physiological status, while serum BDNF is more likely to represent a trait marker . Very recently, plasma BDNF was associated with response in the early course of treatment for depression .
In our study, plasma BDNF levels in patients in the remission group significantly increased during the transition from syndrome to response to remission stages, suggesting that plasma BDNF may be a useful marker of physiological status and that it should be examined in patients on a regular basis.
A correlation between cortical BDNF and serum BDNF in young rats was first shown by Karege et al. . In contrast, Elfving et al. found a negative correlation between hippocampal and serum BDNF levels . In blood, BDNF is mainly stored in thrombocytes, with only a minor free fraction present in plasma . Recently, plasma BDNF levels were shown to be positively correlated with hippocampal BDNF levels . The origin of plasma BDNF is not entirely clear, although it appears that the hippocampus is the main source.
Brain imaging studies have documented a reduction in hippocampal volume in depressed subjects , which can be attenuated , or even improve  with antidepressant treatment. These observations suggest that plasma BDNF may be involved in the pathophysiology of MDD. Thus, we posit that increased plasma BDNF may have a therapeutic effect on the hippocampus.
Six of the 38 patients (16%) in the remission group exhibited a reduction in plasma BDNF levels. One possible explanation for this is that, although depression was diagnosed according to DSM-IV-TR, differences in biological backgrounds may generate different subgroups within the remission group. Another possibility is that an improvement in depressive symptoms may be directly due to an effect of increased monoamine levels produced by the antidepressant, although this hypothesis needs to be examined. These findings suggest that plasma BDNF levels are likely to be a biomarker for MDD, and that the onset and improvement of the disease might be associated with changes in plasma BDNF levels elicited by antidepressant treatment.
In summary, the present study shows that plasma BDNF levels are positively correlated with clinical improvement in patients who undergo remission, and that patients who are refractory to treatment have higher plasma BDNF levels than patients who achieve remission at the initial depressive syndrome stage. Therefore, it is very likely that plasma BDNF levels play an important role in MDD. Our naturalistic preliminary study reveals that plasma BDNF could represent a useful biomarker for predicting clinical outcome during the course of treatment for MDD.
We thank Dr. Nobuyuki Nakajima, M.D., Ph.D. who, before his death in 2011, provided thoughtful contributions on the study design and data interpretation. We are also grateful for the contributions of Dr. Norimichi Nakahata Ph.D. who, before his death in 2010, was involved in the data interpretation. We thank the study participants, without whom this study could not have been accomplished, as well as the following psychiatrists of Sato Hospital and Wakamiya Kospital, Koutokukai, for their participation in this study: Kazuo Kenmi, M.D., Ph.D.; Asao Hasegawa, M.D.; Masaaki Mitomo, M.D.; Tadanori Kumasaka, M.D., Ph.D.; Tomotaka Suzuki, M.D.; Yukihiro Takeuchi, M.D., Ph.D.; Hiroshi Yamamoto, M.D.; Daisuke Saito, M.D.; Kenji Takeyoshi, M.D.; and Kohei Koizumi, M.D.
Data from this study were presented at the 8th meeting of the Japanese Society of Mood Disorders, Osaka, Japan, July 1 and 2, 2011, as well as to the joint 21st meeting of the Japanese Society of Neuropsychopharmacology (JSNP) and the 41st meeting of the Japanese Society of Clinical Neuropsychopharmacology (JSCNP), Tokyo Japan, Oct 27–29, 2011.
The current study is registered in the UMIN Clinical Trials Registry (UMIN-CTR): Analysis of genome and blood components for elucidation and treatment of mood disorders; https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgifunction=brows&action=brows&recptno=R000007415&type=summary&language=E; UMIN000006264.
Conceived and designed the experiments: M. Kurita. Performed the experiments: M. Kurita SN. Analyzed the data: M. Kurita SN. Contributed reagents/materials/analysis tools: M. Kurita SN M. Kato YN TS. Wrote the paper: M. Kurita SN.
- 1. Duman RS, Heninger GR, Nestler EJ (1997) A molecular and cellular theory of depression. Arch Gen Psychiatry 54: 597–606.
- 2. Lewin GR, Barde YA (1996) Physiology of the neurotrophins. Annu Rev Neurosci 19: 289–317.
- 3. Lindsay RM, Wiegand SJ, Altar CA, DiStefano PS (1994) Neurotrophic factors: from molecule to man. Trends Neurosci 17: 182–190.
- 4. Aydemir C, Yalcin ES, Aksaray S, Kisa C, Yildirim SG, et al. (2006) Brain-derived neurotrophic factor (BDNF) changes in the serum of depressed women. Prog Neuropsychopharmacol Biol Psychiatry 30: 1256–1260.
- 5. Karege F, Perret G, Bondolfi G, Schwald M, Bertschy G, et al. (2002) Decreased serum brain-derived neurotrophic factor levels in major depressed patients. Psychiatry Res 109: 143–148.
- 6. Lee BH, Kim H, Park SH, Kim YK (2007) Decreased plasma BDNF level in depressive patients. J Affect Disord 101: 239–244.
- 7. Piccinni A, Marazziti D, Catena M, Domenici L, Del Debbio A, et al. (2008) Plasma and serum brain-derived neurotrophic factor (BDNF) in depressed patients during 1 year of antidepressant treatments. J Affect Disord 105: 279–283.
- 8. Shimizu E, Hashimoto K, Okamura N, Koike K, Komatsu N, et al. (2003) Alterations of serum levels of brain-derived neurotrophic factor (BDNF) in depressed patients with or without antidepressants. Biol Psychiatry 54: 70–75.
- 9. Karege F, Bondolfi G, Gervasoni N, Schwald M, Aubry JM, et al. (2005) Low brain-derived neurotrophic factor (BDNF) levels in serum of depressed patients probably results from lowered platelet BDNF release unrelated to platelet reactivity. Biol Psychiatry 57: 1068–1072.
- 10. Aydemir O, Deveci A, Taneli F (2005) The effect of chronic antidepressant treatment on serum brain-derived neurotrophic factor levels in depressed patients: a preliminary study. Prog Neuropsychopharmacol Biol Psychiatry 29: 261–265.
- 11. Gonul AS, Akdeniz F, Taneli F, Donat O, Eker C, et al. (2005) Effect of treatment on serum brain-derived neurotrophic factor levels in depressed patients. Eur Arch Psychiatry Clin Neurosci 255: 381–386.
- 12. Karege F, Vaudan G, Schwald M, Perroud N, La Harpe R (2005) Neurotrophin levels in postmortem brains of suicide victims and the effects of antemortem diagnosis and psychotropic drugs. Brain Res Mol Brain Res 136: 29–37.
- 13. Montgomery SA, Asberg M (1979) A new depression scale designed to be sensitive to change. Br J Psychiatry 134: 382–389.
- 14. Montgomery SA, Smeyatsky N, de Ruiter M, Montgomery DB (1985) Profiles of antidepressant activity with the Montgomery-Asberg Depression Rating Scale. Acta Psychiatr Scand. pp. 38–42.
- 15. Peyre F, Martinez R, Calache M, Verdoux H, Bourgeois M (1989) [New validation of the Montgomery and Asberg Depression Scale (MADRS) on a sample of 147 hospitalized depressed patients]. Ann Med Psychol (Paris) 147: 762–767.
- 16. Maier W, Philipp M, Heuser I, Schlegel S, Buller R, et al. (1988) Improving depression severity assessment–I. Reliability, internal validity and sensitivity to change of three observer depression scales. J Psychiatr Res 22: 3–12.
- 17. Mittmann N, Mitter S, Borden EK, Herrmann N, Naranjo CA, et al. (1997) Montgomery-Asberg severity gradations. Am J Psychiatry 154: 1320–1321.
- 18. Berlim MT, Fleck MP, Turecki G (2008) Current trends in the assessment and somatic treatment of resistant/refractory major depression: an overview. Ann Med 40: 149–159.
- 19. Matrisciano F, Bonaccorso S, Ricciardi A, Scaccianoce S, Panaccione I, et al. (2009) Changes in BDNF serum levels in patients with major depression disorder (MDD) after 6 months treatment with sertraline, escitalopram, or venlafaxine. J Psychiatr Res 43: 247–254.
- 20. Molendijk ML, Bus BA, Spinhoven P, Penninx BW, Kenis G, et al. (2011) Serum levels of brain-derived neurotrophic factor in major depressive disorder: state-trait issues, clinical features and pharmacological treatment. Mol Psychiatry 16: 1088–1095.
- 21. Angelucci F, De Bartolo P, Gelfo F, Foti F, Cutuli D, et al. (2009) Increased concentrations of nerve growth factor and brain-derived neurotrophic factor in the rat cerebellum after exposure to environmental enrichment. Cerebellum 8: 499–506.
- 22. Laske C, Banschbach S, Stransky E, Bosch S, Straten G, et al. (2010) Exercise-induced normalization of decreased BDNF serum concentration in elderly women with remitted major depression. Int J Neuropsychopharmacol 13: 595–602.
- 23. Sen S, Duman R, Sanacora G (2008) Serum brain-derived neurotrophic factor, depression, and antidepressant medications: meta-analyses and implications. Biol Psychiatry 64: 527–532.
- 24. Dreimuller N, Schlicht KF, Wagner S, Peetz D, Borysenko L, et al. (2011) Early reactions of brain-derived neurotrophic factor in plasma (pBDNF) and outcome to acute antidepressant treatment in patients with Major Depression. Neuropharmacology.
- 25. Elfving B, Plougmann PH, Muller HK, Mathe AA, Rosenberg R, et al. (2010) Inverse correlation of brain and blood BDNF levels in a genetic rat model of depression. Int J Neuropsychopharmacol 13: 563–572.
- 26. Fujimura H, Altar CA, Chen R, Nakamura T, Nakahashi T, et al. (2002) Brain-derived neurotrophic factor is stored in human platelets and released by agonist stimulation. Thromb Haemost 87: 728–734.
- 27. Klein AB, Williamson R, Santini MA, Clemmensen C, Ettrup A, et al. (2011) Blood BDNF concentrations reflect brain-tissue BDNF levels across species. Int J Neuropsychopharmacol 14: 347–353.
- 28. Koolschijn PC, van Haren NE, Lensvelt-Mulders GJ, Hulshoff Pol HE, Kahn RS (2009) Brain volume abnormalities in major depressive disorder: a meta-analysis of magnetic resonance imaging studies. Hum Brain Mapp 30: 3719–3735.
- 29. Boldrini M, Underwood MD, Hen R, Rosoklija GB, Dwork AJ, et al. (2009) Antidepressants increase neural progenitor cells in the human hippocampus. Neuropsychopharmacology 34: 2376–2389.
- 30. MacQueen GM (2009) Magnetic resonance imaging and prediction of outcome in patients with major depressive disorder. J Psychiatry Neurosci 34: 343–349.