情感症状的生命历程轨迹及其早期生活预测因子。

Pub Date : 2022-05-01 DOI:10.1332/175795921X16487298020502
Ellen J Thompson, George B Ploubidis, Marcus Richards, Darya Gaysina
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引用次数: 0

摘要

背景:情感症状(抑郁和焦虑)的生命历程轨迹是异质性的。然而,很少有研究调查了早期生活风险因素在这些轨迹发展中的作用。本研究旨在:(1)推导超过50年(13-69岁)的情感症状的潜在轨迹,(2)检查早期生活风险因素与情感症状的特定生命历程轨迹的关联。方法:参与者来自MRC全国健康与发展调查(NSHD) (n = 5362)。情感症状在13岁、15岁、36岁、43岁、53岁、60-64岁和69岁时进行前瞻性测量。采用潜在变量建模框架对情感症状的纵向分布进行建模。使用多项逻辑回归测试了24项前瞻性的早期生活预测因子与不同症状的相关性。结果:确定了情感性症状的四种生命历程特征:(1)无症状(占样本的66.6%);(2)青少年症状,成人预后良好(15.2%);(3)只有成人症状(青春期和晚年无症状)(12.9%);(4)青春期和成年中期的症状(5.2%)。在观察到的24个早期生活预测因素中,只有4个与生命历程轨迹有关,观察到的效应很小。结论:人们在焦虑和抑郁症状的生命历程轨迹上存在差异,这些差异在很大程度上受本研究中测试的早期生活因素的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Life course trajectories of affective symptoms and their early life predictors.

Background: Life course trajectories of affective symptoms (depression and anxiety) are heterogenous. However, few studies have investigated the role of early life risk factors in the development of these trajectories. The present study aimed to: (1) derive latent trajectories of affective symptoms over a period of more than 50 years (ages 13-69), and (2) examine early life risk factors for associations with specific life course trajectories of affective symptoms.

Method: Participants are from the MRC National Survey of Health and Development (NSHD) (n = 5,362). Affective symptoms were measured prospectively at ages 13, 15, 36, 43, 53, 60-64 and 69. A latent variable modelling framework was implemented to model longitudinal profiles of affective symptoms. Twenty-four prospectively measured early life predictors were tested for associations with different symptom profiles using multinomial logistic regression.

Results: Four life course profiles of affective symptoms were identified: (1) absence of symptoms (66.6% of the sample); (2) adolescent symptoms with good adult outcome (15.2%); (3) adult symptoms only (with no symptoms in adolescence and late life) (12.9%); (4) symptoms in adolescence and mid adulthood (5.2%). Of the 24 early life predictors observed, only four were associated with life course trajectories, with small effect sizes observed.

Conclusions: People differ in their life course trajectories of anxiety and depression symptoms and that these differences are not largely influenced by early life factors tested in this study.

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