Sakurai Hitoshi, Suzuki Takefumi, Yoshimura Kimio, Mimura Masaru, Uchida Hiroyuki
Department of Neuropsychiatry, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Department of Health Policy and Management, Keio University School of Medicine, Tokyo, Japan.
Psychopharmacology (Berl). 2017 Aug;234(16):2453-2461. doi: 10.1007/s00213-017-4634-5. Epub 2017 May 3.
Residual symptoms are detrimental to prognosis in major depressive disorder (MDD); however, little is known about the contribution of each residual symptom in predicting outcomes. The objective of this analysis was to identify which individual symptoms, based on self-report and clinician interview, could predict subsequent relapse.
The data of 1133 outpatients with nonpsychotic MDD who entered a 12-month naturalistic follow-up phase after achieving remission with level 1 treatment (i.e., citalopram for up to 14 weeks) and had at least one post-baseline contact in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial were analyzed. Specific residual symptoms in the 16-item Quick Inventory of Depressive Symptomatology, self-report (QIDS-SR) and clinician rating (QIDS-C), at the follow-up entry that predicted relapse were identified, using a Cox proportional hazards model.
The following three QIDS-SR symptoms were significantly associated with subsequent relapse: restlessness (HR = 1.197, p = 0.018), hypersomnia (HR = 1.190, p = 0.009), and weight change (HR = 1.127, p = 0.041). On the other hand, the following three symptoms in the QIDS-C at the follow-up entry were significantly associated with relapse in the follow-up phase: restlessness (HR = 1.328, p = 0.001), sleep onset insomnia (HR = 1.129, p = 0.047), and weight change (HR = 1.125, p = 0.045).
The original trial was not designed to evaluate the issue addressed herein. Individual symptoms may be associated with each other and functional status was not addressed.
Some residual symptoms, including restlessness, insomnia, and weight change, may help better identify patients with MDD vulnerable to relapse. Contribution of individual residual symptoms to subsequent relapse was similar between self-report and clinician-rated symptoms.
残留症状对重度抑郁症(MDD)的预后有害;然而,对于每种残留症状在预测结局方面的作用知之甚少。本分析的目的是确定基于自我报告和临床医生访谈的哪些个体症状可以预测随后的复发。
对1133例非精神病性MDD门诊患者的数据进行分析,这些患者在接受1级治疗(即西酞普兰治疗长达14周)后进入为期12个月的自然随访阶段,并在缓解抑郁症状的序贯治疗替代方案(STAR*D)试验中有至少一次基线后接触。使用Cox比例风险模型确定随访开始时16项抑郁症状快速自评量表(QIDS-SR)和临床医生评定量表(QIDS-C)中预测复发的特定残留症状。
以下三个QIDS-SR症状与随后的复发显著相关:坐立不安(HR = 1.197,p = 0.018)、嗜睡(HR = 1.190,p = 0.009)和体重变化(HR = 1.127,p = 0.041)。另一方面,随访开始时QIDS-C中的以下三个症状与随访阶段的复发显著相关:坐立不安(HR = 1.328,p = 0.001)、入睡困难(HR = 1.129,p = 0.047)和体重变化(HR = 1.125,p = 0.045)。
原试验并非旨在评估本文所探讨的问题。个体症状可能相互关联,且未涉及功能状态。
一些残留症状,包括坐立不安、失眠和体重变化,可能有助于更好地识别易复发的MDD患者。自我报告症状和临床医生评定症状中个体残留症状对随后复发的作用相似。