Department of Epidemiology, University Medical Centre Groningen, University of Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.
Department of Psychiatry, University Medical Centre Groningen, University Centre for Psychiatry, Rob Giel Research Centre, University of Groningen, Groningen, The Netherlands.
Soc Psychiatry Psychiatr Epidemiol. 2024 Oct;59(10):1733-1750. doi: 10.1007/s00127-024-02630-4. Epub 2024 Mar 8.
We aimed to explore the multidimensional nature of social inclusion (mSI) among patients diagnosed with schizophrenia spectrum disorder (SSD), and to identify the predictors of 3-year mSI and the mSI prediction using traditional and data-driven approaches.
We used the baseline and 3-year follow-up data of 1119 patients from the Genetic Risk and Outcome in Psychosis (GROUP) cohort in the Netherlands. The outcome mSI was defined as clusters derived from combined analyses of thirteen subscales from the Social Functioning Scale and the brief version of World Health Organization Quality of Life questionnaires through K-means clustering. Prediction models were built through multinomial logistic regression (Model) and random forest (Model), internally validated via bootstrapping and compared by accuracy and the discriminability of mSI subgroups.
We identified five mSI subgroups: "very low (social functioning)/very low (quality of life)" (8.58%), "low/low" (12.87%), "high/low" (49.24%), "medium/high" (18.05%), and "high/high" (11.26%). The mSI was robustly predicted by a genetic predisposition for SSD, premorbid adjustment, positive, negative, and depressive symptoms, number of met needs, and baseline satisfaction with the environment and social life. The Model (61.61% [54.90%, 68.01%]; P =0.013) was cautiously considered outperform the Model (59.16% [55.75%, 62.58%]; P =0.994).
We introduced and distinguished meaningful subgroups of mSI, which were modestly predictable from baseline clinical characteristics. A possibility for early prediction of mSI at the clinical stage may unlock the potential for faster and more impactful social support that is specifically tailored to the unique characteristics of the mSI subgroup to which a given patient belongs.
本研究旨在探讨精神分裂症谱系障碍(SSD)患者的社会包容的多维性(mSI),并确定 3 年 mSI 的预测因子以及传统和数据驱动方法的 mSI 预测。
我们使用了荷兰精神分裂症遗传风险和结局(GROUP)队列的 1119 名患者的基线和 3 年随访数据。mSI 的结局定义为通过 K-均值聚类对社会功能量表和世界卫生组织生活质量问卷简短版的 13 个分量表的综合分析得出的聚类。通过多项逻辑回归(模型)和随机森林(模型)构建预测模型,通过自举法进行内部验证,并通过准确性和 mSI 亚组的可区分性进行比较。
我们确定了五个 mSI 亚组:“非常低(社会功能)/非常低(生活质量)”(8.58%)、“低/低”(12.87%)、“高/低”(49.24%)、“中/高”(18.05%)和“高/高”(11.26%)。mSI 可由 SSD 的遗传易感性、病前适应、阳性、阴性和抑郁症状、需要满足的数量以及对环境和社会生活的基线满意度等因素稳健地预测。模型(61.61%[54.90%,68.01%];P=0.013)被谨慎认为优于模型(59.16%[55.75%,62.58%];P=0.994)。
我们介绍并区分了 mSI 的有意义的亚组,这些亚组可以从基线临床特征中适度预测。在临床阶段对 mSI 进行早期预测的可能性可能会释放出潜力,从而更快地提供更具影响力的社会支持,这些支持是根据特定患者所属的 mSI 亚组的独特特征量身定制的。