From the Department of Psychology, University of Haifa, Haifa, Israel.
Syneos Health Inc, Raleigh, NC.
J Clin Psychopharmacol. 2021;41(5):579-584. doi: 10.1097/JCP.0000000000001435.
PURPOSE/BACKGROUND: Heterogeneity has been documented in trajectories of symptom change during antidepressant treatment for major depressive disorder (MDD). It is unclear whether distinct trajectories of change exist for functioning during antidepressant treatment.
METHODS/PROCEDURES: This analysis explored distinct trajectories of functioning in MDD and tested whether they corresponded to trajectories of symptom change. Data were from 4317 patients and were pooled from 9 randomized placebo-controlled trials. Growth mixture modeling was used to identify trajectories of Hamilton Rating Scale for Depression (HRSD) and Sheehan Disability Scale (SDS) for placebo- and desvenlafaxine-treated patients.
FINDINGS/RESULTS: Three trajectories were identified for symptoms (HRSD) in patients receiving placebo (mean reduction baseline to week 8, -18.4 [most favorable] to -2.6 points [least favorable]). Four HRSD trajectories were identified for patients receiving desvenlafaxine (mean reduction from baseline to week 8, -17.2 [most favorable] to -2.6 points [least favorable]). Four trajectories were identified for functioning (SDS) in patients receiving placebo (mean reduction baseline to week 8, -13.6 [most favorable] to -0.8 points [least favorable]), and 3 for desvenlafaxine (-12.8 to -1.4 points, respectively). Percentages of agreement between most favorable HRSD and SDS trajectories were 75% (placebo) and 85% (desvenlafaxine), and for least favorable trajectories were 88% (placebo) and 80% (desvenlafaxine).
IMPLICATIONS/CONCLUSIONS: Distinct trajectories of change based on symptoms and functioning were identified among patients with MDD receiving desvenlafaxine and among patients with MDD receiving placebo. Differentiating subpopulations of patients has the potential to provide a more personalized treatment of patients with MDD.ClinicalTrials.govIdentifiers: NCT00072774; NCT00277823; NCT00300378; NCT00384033; NCT00798707; NCT00863798; NCT01121484; NCT00824291; NCT01432457.
目的/背景:在抗抑郁治疗期间,重度抑郁症(MDD)的症状变化轨迹存在异质性。目前尚不清楚抗抑郁治疗期间功能的变化是否存在不同的轨迹。
方法/过程:本分析探讨了 MDD 中功能的不同轨迹,并检验了它们是否与症状变化轨迹相对应。数据来自 4317 名患者,来自 9 项随机安慰剂对照试验的汇总。使用增长混合模型来识别接受安慰剂和去甲文拉法辛治疗的患者的汉密尔顿抑郁量表(HRSD)和 Sheehan 残疾量表(SDS)的轨迹。
结果/发现:接受安慰剂的患者的症状(HRSD)确定了三个轨迹(从基线到第 8 周的平均减少,-18.4 [最有利]至-2.6 分 [最不利])。接受去甲文拉法辛的患者确定了四个 HRSD 轨迹(从基线到第 8 周的平均减少,-17.2 [最有利]至-2.6 分 [最不利])。接受安慰剂的患者确定了四个功能(SDS)轨迹(从基线到第 8 周的平均减少,-13.6 [最有利]至-0.8 分 [最不利]),而接受去甲文拉法辛的患者则确定了 3 个轨迹(-12.8 至-1.4 分)。最有利的 HRSD 和 SDS 轨迹之间的一致性百分比为 75%(安慰剂)和 85%(去甲文拉法辛),而最不利的轨迹为 88%(安慰剂)和 80%(去甲文拉法辛)。
结论/意义:在接受去甲文拉法辛的 MDD 患者和接受安慰剂的 MDD 患者中,基于症状和功能的变化确定了不同的变化轨迹。区分患者亚群有可能为 MDD 患者提供更个性化的治疗。
临床试验.gov 标识符:NCT00072774;NCT00277823;NCT00300378;NCT00384033;NCT00798707;NCT00863798;NCT01121484;NCT00824291;NCT01432457。