TY - JOUR
T1 - Trajectories of individual symptoms in remitters versus non-remitters with depression
AU - Sakurai, Hitoshi
AU - Uchida, Hiroyuki
AU - Abe, Takayuki
AU - Nakajima, Shinichiro
AU - Suzuki, Takefumi
AU - Pollock, Bruce G.
AU - Sato, Yuji
AU - Mimura, Masaru
N1 - Funding Information:
Data used in the preparation of this article were obtained from the limited access datasets distributed from the NIH -supported “Sequenced Treatment Alternatives to Relieve Depression” (STAR⁎D). STAR⁎D focused on non-psychotic major depressive disorder in adults seen in outpatient settings. The primary purpose of this research study was to determine which treatments work best if the first treatment with medication does not produce an acceptable response. The study was supported by NIMH Contract # N01MH90003 to the University of Texas Southwestern Medical Center . The ClinicalTrials.gov identifier is NCT00021528 . The version of the dataset used was 2. This analysis was partially funded by Eli Lily.
Funding Information:
Financial disclosures : Dr. Uchida has received grants from Pfizer and Dainippon-Sumitomo Pharma, and speaker’s honoraria from Otsuka Pharmaceutical, Eli Lilly, Novartis Pharma, Shionogi, GlaxoSmithKline, Yoshitomi Yakuhin, Dainippon-Sumitomo Pharma, and Janssen Pharma within the past 3 years. Dr. Nakajima has received grants from Japan Society for the Promotion of Science and Inokashira Hospital Research Fund, and speaker’s honoraria from GlaxoSmithKline, Janssen Pharmaceutical, Pfizer and Yoshitomi Yakuhin within the past 3 years. Dr. Suzuki has received manuscript fees or speaker’s honoraria from Dainippon Sumitomo Phama, Eli Lilly, Astellas Pharma, Novartis Pharma, and Meiji Sekia Pharma within the past 3 years. Dr. Pollock has received research support from the National Institutes of Health, Canadian Institutes of Health Research, American Psychiatric Association and the Foundation of the Centre for Addiction and Mental Health. Within the past three years, he has been a faculty member of the Lundbeck International Neuroscience Foundation. Dr. Sato has served as a consultant, given lectures and presentations, and thereby received honoraria from Astra Zeneca, Pfizer, Sanofi-Aventis, GlaxoSmithKline, Eli Lilly, Abbott, Novartis, MSD, Asahi-kasei, Takeda, Daiichi-Sankyo, Japan Chemical Research, EPS, Taisho, Ajinomoto, Tasly, Parexel, and Icon. Dr. Mimura has received grants, consultant fees and/or speaker’s honoraria from Asahi Kasei, Astellas, Daiichi Sankyo, Dainippon Sumitomo, Eisai, Eli Lilly, GlaxoSmithKline, Janssen, Meiji, Mochida, Novartis, Otsuka, Pfizer, Shionogi, and Yoshitomi within the past 3 years. Dr. Sakurai and Dr. Abe have nothing to disclose.
PY - 2013/11
Y1 - 2013/11
N2 - Background It remains unclear regarding the contribution of each individual symptom in predicting the outcome in major depressive disorder (MDD). The objective of this analysis was to evaluate trajectories of individual symptoms over time to identify which specific depressive item(s) could predict subsequent clinical response. Methods The data of 2874 outpatients with nonpsychotic MDD who received citalopram for up to 14 weeks in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial were analyzed. Average trajectories of individual symptoms over time were estimated for remitters and non-remitters. Moreover, specific symptoms whose improvement at week 2 predicted remission were identified, using binary logistic regression analysis. Results Trajectories were significantly different between remitters and non-remitters in all depressive symptoms. All depressive symptoms in the 16-item Quick Inventory of Depressive Symptomatology, Self-Report (QIDS-SR16) in the two groups, except for hypersomnia and weight change in non-remitters, substantially improved within 2 weeks and gradually continued to improve thereafter throughout the 14 weeks. Early improvements in the following five symptoms, in order of magnitude, in the QIDS-SR16 were significantly associated with remission: sad mood, negative self-view, feeling slowed down, low energy, and restlessness (P<0.001, P<0.001, P=0.001, P=0.004, P=0.021). Limitations The participants were limited to the nonpsychotic MDD outpatients who received citalopram. Further, symptomatology was not evaluated at the very beginning of treatment. Conclusions While the data pertain to citalopram and replication is necessary for other antidepressants, early improvements in certain core depressive symptoms may serve as a predictor of subsequent remission.
AB - Background It remains unclear regarding the contribution of each individual symptom in predicting the outcome in major depressive disorder (MDD). The objective of this analysis was to evaluate trajectories of individual symptoms over time to identify which specific depressive item(s) could predict subsequent clinical response. Methods The data of 2874 outpatients with nonpsychotic MDD who received citalopram for up to 14 weeks in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial were analyzed. Average trajectories of individual symptoms over time were estimated for remitters and non-remitters. Moreover, specific symptoms whose improvement at week 2 predicted remission were identified, using binary logistic regression analysis. Results Trajectories were significantly different between remitters and non-remitters in all depressive symptoms. All depressive symptoms in the 16-item Quick Inventory of Depressive Symptomatology, Self-Report (QIDS-SR16) in the two groups, except for hypersomnia and weight change in non-remitters, substantially improved within 2 weeks and gradually continued to improve thereafter throughout the 14 weeks. Early improvements in the following five symptoms, in order of magnitude, in the QIDS-SR16 were significantly associated with remission: sad mood, negative self-view, feeling slowed down, low energy, and restlessness (P<0.001, P<0.001, P=0.001, P=0.004, P=0.021). Limitations The participants were limited to the nonpsychotic MDD outpatients who received citalopram. Further, symptomatology was not evaluated at the very beginning of treatment. Conclusions While the data pertain to citalopram and replication is necessary for other antidepressants, early improvements in certain core depressive symptoms may serve as a predictor of subsequent remission.
KW - Depression
KW - Major depressive disorder
KW - Prediction
KW - Remission
UR - http://www.scopus.com/inward/record.url?scp=84885474874&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84885474874&partnerID=8YFLogxK
U2 - 10.1016/j.jad.2013.06.035
DO - 10.1016/j.jad.2013.06.035
M3 - Article
C2 - 23886402
AN - SCOPUS:84885474874
SN - 0165-0327
VL - 151
SP - 506
EP - 513
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
IS - 2
ER -