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激惹及其在重性抑郁障碍中的临床应用:使用激惹和抑郁严重程度的早期变化预测个体急性期结局。

Irritability and Its Clinical Utility in Major Depressive Disorder: Prediction of Individual-Level Acute-Phase Outcomes Using Early Changes in Irritability and Depression Severity.

机构信息

From the Center for Depression Research and Clinical Care, UT Southwestern Medical Center, Dallas (Jha, Minhajuddin, South, Trivedi); the Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York (Jha); Duke-National University of Singapore (Rush); the Department of Psychiatry, Duke Medical School, Durham, N.C. (Rush); and Texas Tech University-Health Sciences Center, Permian Basin, Midland-Odessa (Rush).

出版信息

Am J Psychiatry. 2019 May 1;176(5):358-366. doi: 10.1176/appi.ajp.2018.18030355. Epub 2019 Mar 29.

Abstract

OBJECTIVE

The authors evaluated improvement in irritability with antidepressant treatment and its prognostic utility in treatment-seeking adult outpatients with major depressive disorder.

METHODS

Mixed-model analyses were used to assess changes in irritability (as measured with the five-item irritability domain of the Concise Associated Symptom Tracking [CAST-IRR] scale) from baseline to week 4 after controlling for depression severity (as measured with the 16-item Quick Inventory of Depressive Symptomatology-Clinician Rated [QIDS-C]) in the Combining Medications to Enhance Depression Outcomes (CO-MED) trial (N=664). An interactive calculator for remission (QIDS-C score ≤5) and no meaningful benefit (<30% reduction in QIDS-C score from baseline) at week 8 was developed with logistic regression analyses in the CO-MED trial using participants with complete data (N=431) and independently replicated in the Suicide Assessment and Methodology Study (SAMS) (N=163).

RESULTS

In the CO-MED trial, irritability was significantly reduced (effect size=1.06) from baseline to week 4, and this reduction remained significant after adjusting for QIDS-C change (adjusted effect size=0.36). A one-standard-deviation greater reduction in CAST-IRR score from baseline to week 4 predicted a 1.73 times higher likelihood of remission and a 0.72 times lower likelihood of no meaningful benefit at week 8, independent of baseline QIDS-C and CAST-IRR scores and reduction in QIDS-C score from baseline to week 4. The model estimates for remission (area under the curve [AUC]=0.79) and no meaningful benefit (AUC=0.76) in the CO-MED trial were used to predict remission (AUC=0.80) and no meaningful benefit (AUC=0.84) in SAMS and to develop an interactive calculator.

CONCLUSIONS

Irritability is an important symptom domain of major depressive disorder that is not fully reflected in depressive symptom severity measures. Early reductions in irritability, when combined with changes in depressive symptom severity, provide a robust estimate of likelihood of remission or no meaningful benefit in outpatients with major depression.

摘要

目的

作者评估了抗抑郁治疗对成人门诊重度抑郁症患者激惹的改善作用,及其预后预测价值。

方法

混合模型分析用于评估 CO-MED 试验中(N=664),从基线到第 4 周时激惹(使用简明相关症状跟踪量表[CAST-IRR]的五分量表评估)的变化,同时控制抑郁严重程度(使用 16 项贝克抑郁自评量表-临床医生评定[QIDS-C])。CO-MED 试验中,使用具有完整数据的 431 名参与者(N=431)进行逻辑回归分析开发了第 8 周时缓解(QIDS-C 评分≤5)和无明显获益(QIDS-C 评分较基线降低<30%)的交互计算器,并在 Suicide Assessment and Methodology Study(SAMS)(N=163)中独立复制。

结果

CO-MED 试验中,从基线到第 4 周激惹显著降低(效应量=1.06),且调整 QIDS-C 变化后仍保持显著(调整效应量=0.36)。从基线到第 4 周时 CAST-IRR 评分每降低一个标准差,预示着第 8 周时缓解的可能性增加 1.73 倍,无明显获益的可能性降低 0.72 倍,与基线 QIDS-C 和 CAST-IRR 评分以及从基线到第 4 周时 QIDS-C 评分的降低无关。CO-MED 试验中,缓解(曲线下面积[AUC]=0.79)和无明显获益(AUC=0.76)的模型估计用于预测 SAMS 中的缓解(AUC=0.80)和无明显获益(AUC=0.84),并开发了一个交互计算器。

结论

激惹是重度抑郁症的一个重要症状领域,在抑郁严重程度测量中并未完全反映。激惹的早期减少,与抑郁症状严重程度的变化相结合,为门诊重度抑郁症患者的缓解或无明显获益的可能性提供了强有力的估计。

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