青春期和成年期普通人群消极症状的潜在结构》(The Latent Structure of Negative Symptoms in General Population in Adolescence and Emerging Adulthood)。

Schizophrenia Bulletin Open Pub Date : 2022-01-12 eCollection Date: 2022-01-01 DOI:10.1093/schizbullopen/sgac009
Laura Havers, Alastair Cardno, Daniel Freeman, Angelica Ronald
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引用次数: 0

摘要

消极症状可预测精神病患者、精神病高危人群和社区青少年的不良后果。人们对临床样本中消极症状的维度结构颇感兴趣,不断积累的证据表明消极症状具有五因素结构。尽管青少年的成长阶段对心理健康非常重要,但人们对其负面症状的基本结构却知之甚少。我们在社区样本中使用了确认性因子分析来测试父母报告的平均年龄为 16.32(标准差为 0.68,样本数为 4974)、17.06(标准差为 0.88,样本数为 1469)和 22.30(标准差为 0.93,样本数为 5179)的青少年消极症状的结构。鉴于之前有报道称青少年时期的总阴性症状与重度抑郁障碍(MDD)和精神分裂症的全基因组多基因评分(GPS)之间存在关联,我们评估了各个子域与这些GPS之间的关联。在每个年龄段,由平淡情绪、焦虑、逃避、失乐症和非社会性组成的 5 因子模型的拟合度最高,并且随着时间的推移而不变。我们的线性回归分析结果表明,多发性抑郁症的全球定位系统与逃避、平淡情感、失乐症和非社会性之间存在关联,而精神分裂症的全球定位系统与逃避和平淡情感之间也存在关联。我们的研究表明,在社区中,16 至 22 岁人群的阴性症状存在一个 5 因子结构。逃避与多发性精神障碍和精神分裂症的多基因易感性关系最为一致,而情感淡漠与多发性精神障碍和精神分裂症的多基因易感性关系最小。这些发现凸显了将阴性症状分解为心理测量学衍生子域的价值,并可能为早期表现出的 MDD 和精神分裂症遗传风险提供启示。
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The Latent Structure of Negative Symptoms in the General Population in Adolescence and Emerging Adulthood.

Negative symptoms predict adverse outcomes within psychotic disorders, in individuals at high-risk for psychosis, and in young people in the community. There is considerable interest in the dimensional structure of negative symptoms in clinical samples, and accumulating evidence suggests a 5-factor structure. Little is known about the underlying structure of negative symptoms in young people despite the importance of this developmental stage for mental health. We used confirmatory factor analysis to test the structure of parent-reported negative symptoms at mean ages 16.32 (SD 0.68, N = 4974), 17.06 (SD 0.88, N = 1469) and 22.30 (SD 0.93, N = 5179) in a community sample. Given previously reported associations between total negative symptoms and genome-wide polygenic scores (GPS) for major depressive disorder (MDD) and schizophrenia in adolescence, we assessed associations between individual subdomains and these GPSs. A 5-factor model of flat affect, alogia, avolition, anhedonia, and asociality provided the best fit at each age and was invariant over time. The results of our linear regression analyses showed associations between MDD GPS with avolition, flat affect, anhedonia, and asociality, and between schizophrenia GPS with avolition and flat affect. We showed that a 5-factor structure of negative symptoms is present from ages 16 to 22 in the community. Avolition was most consistently associated with polygenic liability to MDD and schizophrenia, and alogia was least associated. These findings highlight the value of dissecting negative symptoms into psychometrically derived subdomains and may offer insights into early manifestation of genetic risk for MDD and schizophrenia.

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