睡眠多导睡眠图作为儿童和青少年重度抑郁症复发的预测因子。

G. Emslie, G. Emslie, R. Armitage, W. Weinberg, A. Rush, T. Mayes, T. Mayes, R. Hoffmann
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引用次数: 82

摘要

患有重度抑郁症(MDD)的成年人表现出一定的睡眠多导睡眠图异常,包括睡眠连续性障碍、慢波睡眠减少、快速眼动潜伏期缩短和快速眼动密度增加。抑郁症儿童和青少年的睡眠脑电图研究结果产生了相互矛盾的结果,可能是因为研究方法的差异。然而,总的来说,研究表明,与对照组相比,抑郁的儿童和青少年表现出更少的睡眠连续性和非快速眼动睡眠差异。因此,成人睡眠多导睡眠图研究的结果不一定适用于儿童和青少年。在症状发作期间快速眼动潜伏期减少的抑郁症成年人在停止治疗后比正常快速眼动潜伏期的患者更容易复发。尚无关于抑郁症儿童和青少年睡眠多导睡眠图变量与临床病程关系的研究报道。对113名抑郁症儿童(<或= 12岁;N = 51)和青少年(>或= 13岁;N = 62)(56名住院患者和57名门诊患者),其中至少有1年的自然随访数据。研究对象来自两项针对重度抑郁症儿童和青少年的睡眠多导睡眠描记术研究。临床病程采用儿童纵向随访评估(K-LIFE)进行评估。该访谈用于定义重度抑郁症指数发作的恢复和复发,即满足重度抑郁症全部标准的新发作。临床上,在最初评估的1年内,102/113名受试者从抑郁指数发作中恢复(60天内症状轻微或无症状)。在102名恢复的受试者中,36名(35.3%)有重度抑郁症复发。大多数复发的受试者(55%)在复发时未服用药物。与没有复发的受试者相比,复发的受试者在基线时更有可能报告自杀念头或企图(67%对37%;F = 8.77;P = 0.004)。在基线睡眠多导睡眠图中,复发较晚的受试者睡眠效率下降,睡眠开始时间延迟(睡眠潜伏期> 10分钟)。12个月时的复发率为0.39,而非延迟睡眠者为0.15 (p = 0.005)。基于睡眠多导睡眠图的基线自杀意念和睡眠失调预测抑郁症儿童和青少年的复发。儿童和青少年的抑郁症通常是一种慢性、复发性疾病。能够预测临床病程的因素对于增加我们对这一年龄组抑郁症的了解非常重要。
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Sleep polysomnography as a predictor of recurrence in children and adolescents with major depressive disorder.
Adults with major depressive disorder (MDD) demonstrate certain sleep polysomnographic abnormalities, including sleep continuity disturbances, reduced slow-wave sleep, shortened rapid eye movement (REM) latency, and increased REM density. Findings of sleep EEG studies in depressed children and adolescents have yielded conflicting results, possibly because of methodological variations across the studies. Generally, however, studies have demonstrated that depressed children and adolescents exhibit less sleep continuity and non-REM sleep differences in comparison with control subjects than do adults. Thus, results from adult sleep polysomnography studies cannot necessarily be generalized to children and adolescents. Depressed adults who have reduced REM latency during the symptomatic episode appear more likely to have a relapse once treatment is discontinued than those with normal REM latency. No studies of the relationship between sleep polysomnographic variables and clinical course have been reported in depressed children and adolescents. Data for baseline clinical variables and 3 nights of sleep polysomnography were examined in 113 depressed children (< or = 12 yr; n = 51) and adolescents (> or = 13 yr; n = 62) (56 in-patients and 57 outpatients) where data was available on at least 1 yr of naturalistic follow-up. Subjects came from 2 studies of sleep polysomnography in children and adolescents with MDD. Clinical course was assessed using the Kiddie-Longitudinal Interval Follow-Up Evaluation (K-LIFE). This interview was used to define recovery from the index episode of MDD and recurrence, a new episode of meeting full criteria for MDD. Clinically, within 1 yr of initial evaluation 102/113 subjects had recovered from their index episode of depression (minimal or no symptoms for 60 d). Of the 102 subjects who recovered, 36 (35.3%) had a recurrence of MDD. The majority of subjects (55%) who had a recurrence were not on medication at the time of recurrence. Subjects who had a recurrence were more likely to report suicidal thoughts or attempts at baseline compared to those without a recurrence (67 vs. 37%; F = 8.77; p = 0.004). On baseline sleep polysomnography, subjects with a later recurrence had decreased sleep efficiency and delayed sleep onset (sleep latency > 10 min). Probability of recurrence at 12 months was 0.39 compared to 0.15 in subjects with non-delayed sleep onset (p = 0.005). Baseline suicidal ideation and sleep dysregulation on sleep polysomnography predicted recurrence in a large sample of depressed children and adolescents. Depression in children and adolescents is frequently a chronic, recurrent illness. Factors that can predict clinical course are important in increasing our understanding of depression in this age group.
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