Wolfson Centre for Young People's Mental Health, Section of Child and Adolescent Psychiatry, MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Lancet Psychiatry. 2021 Dec;8(12):1053-1061. doi: 10.1016/S2215-0366(21)00281-9. Epub 2021 Oct 18.
Depression often first emerges in adolescence and, for many, is a lifelong disorder. The long-term clinical course of depression is highly variable. We aimed to examine the adult outcomes of adolescent-onset trajectories of clinically significant depressive symptoms and to identify factors differentiating trajectories that persist and desist in adulthood.
We included participants from the English population-based Avon Longitudinal Study of Parents and Children with data on depressive symptoms. Self-reported depression symptoms were assessed on ten occasions when participants were age 10·5-25 years using the short Mood and Feelings Questionnaire, and major depressive disorder episodes were assessed at age 13·0 years, 15·0 years, 17·5 years, and 25·0 years. We characterised trajectories of depression symptoms using latent class growth analysis, for which we required depression data at least once from each of three key phases: ages 10·5-13·5 years; 16·5-18·5 years; and 21-25 years. We examined adult outcomes by assessing lifetime suicidal self-harm and functional impairment at age 24·0 years, and employment, education, and the self-reported Strengths and Difficulties Questionnaire at age 25·0 years.
We studied 4234 participants: 2651 (63%) female, 1582 (37%) male, and one individual with missing sex data. The mean age was 10·6 years (SD 0·2) at baseline and 25·8 years (SD 0·5) at the final timepoint. Data on ethnicity were not available in our data set. We identified four depression trajectory classes: adolescent-persistent depression with onset early in adolescence (7%, n≈279), adolescent-limited depression with onset later in adolescence and remittance by adult life (14%, n≈592), adult-increasing depression (25%, n≈1056), and stable-low levels of depression (54%, n≈2307). The adolescent-persistent class was associated with poor adult outcomes for functional impairment (62%), suicidal self-harm (27%), mental health difficulties (25%), and not being in education, employment, or training (16%). Adolescent-limited depression was associated with transient adolescent stress, but by early adulthood functional impairment and mental health difficulties were similar to the stable-low group. Major depressive disorder polygenic score (odds ratio [OR] 1·36, 95% CI 1·04-1·79), adolescent educational attainment (OR 0·47, 0·30-0·74), and any early childhood adversity (OR 2·60, 1·42-4·78), that persisted into adulthood (OR 1·60, 1·38-1·87) distinguished the adolescent-persistent and adolescent-limited groups.
The future course of adolescent depression can be differentiated by age at onset during adolescence, adolescent academic attainment, early and persistent adversity, and genetic loading. A detailed social and educational history could be helpful in making clinical decisions about the intensity of interventions for young people with clinically elevated depressive symptoms who seek help.
Medical Research Council, Wolfson Centre for Young People's Mental Health, Wolfson Foundation.
抑郁症通常在青少年时期首次出现,对于许多人来说,这是一种终身疾病。抑郁症的长期临床病程变化很大。我们旨在研究具有临床意义的抑郁症状的青少年发病轨迹的成年结局,并确定区分持续和停止成年的轨迹的因素。
我们纳入了来自英国人群的 Avon Longitudinal Study of Parents and Children 的参与者,该研究的数据包括抑郁症状。使用短情绪和感觉问卷,在参与者年龄为 10.5-25 岁时,共进行了 10 次自我报告的抑郁症状评估,在 13.0 岁、15.0 岁、17.5 岁和 25.0 岁时评估了主要抑郁障碍发作。我们使用潜在类别增长分析来描述抑郁症状的轨迹,其中我们要求在三个关键阶段中的每个阶段至少有一次抑郁数据:10.5-13.5 岁;16.5-18.5 岁;21-25 岁。我们通过评估 24.0 岁时的终生自杀自残和功能障碍,以及 25.0 岁时的就业、教育和自我报告的困难问卷,来检查成年结局。
我们研究了 4234 名参与者:2651 名(63%)女性,1582 名(37%)男性,1 名个体的性别数据缺失。基线时的平均年龄为 10.6 岁(标准差 0.2),最后一次随访时的平均年龄为 25.8 岁(标准差 0.5)。我们的数据集中没有种族数据。我们确定了四个抑郁轨迹类别:青春期持续抑郁,发病于青春期早期(7%,n≈279),青春期后期发病且成年期缓解的青春期有限抑郁(14%,n≈592),成年期逐渐增加的抑郁(25%,n≈1056),以及稳定的低水平抑郁(54%,n≈2307)。青少年持续抑郁与成年后功能障碍(62%)、自杀自残(27%)、心理健康问题(25%)和未接受教育、就业或培训(16%)等不良结局有关。青春期有限抑郁与青春期短暂压力有关,但在成年早期,功能障碍和心理健康问题与稳定的低水平组相似。主要抑郁障碍多基因评分(比值比 [OR] 1.36,95%置信区间 [CI] 1.04-1.79)、青春期教育程度(OR 0.47,0.30-0.74)和任何早期童年逆境(OR 2.60,1.42-4.78),这些因素在成年期持续存在(OR 1.60,1.38-1.87),将青少年持续和青少年有限的两组区分开来。
青少年抑郁症的未来病程可以通过青春期发病时的年龄、青春期学业成绩、早期和持续的逆境以及遗传负荷来区分。详细的社会和教育史有助于在临床决策中帮助年轻人,对寻求帮助的具有临床显著抑郁症状的年轻人,可根据干预的强度做出决策。
医学研究委员会、青年心理健康沃尔夫森中心、沃尔夫森基金会。