Cullen Alexis E, Roberts Ruth E, Fisher Helen L, Laurens Kristin R
Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Division of Insurance Medicine, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Schizophrenia (Heidelb). 2024 Sep 30;10(1):83. doi: 10.1038/s41537-024-00507-8.
Identification of youth presenting early risk factors for psychosis may facilitate preventive intervention. Through school-based screening, we recruited 112 children aged 9-12 years who presented multiple putative antecedents of schizophrenia (ASz), a family history of schizophrenia (FHx), or neither of these risk factors (typically-developing; TD). Clinical and functional outcomes were assessed at age 17-21 years (N = 93). Compared to the TD group, the ASz group had higher total Prodromal Questionnaire (PQ) scores (β = 10.59, 95% CI = 3.76, 17.42) and total psychopathology scores (β = 6.13, 95% CI: 1.03, 11.23), were more likely to score above-threshold on the PQ positive symptoms scale (OR = 4.00, 95% CI = 1.08, 14.83), and had lower scores on the Social and Occupational Functioning Scale (β = -9.43, 95% CI = -15.08, -3.77) at follow-up. The FHx and TD groups did not differ on any outcome. Findings suggest that population screening for putative antecedents of schizophrenia may identify children who would benefit from preventative intervention.
识别出现精神病早期风险因素的青少年可能有助于预防性干预。通过基于学校的筛查,我们招募了112名9至12岁的儿童,他们呈现出多种精神分裂症假定前驱症状(ASz)、精神分裂症家族史(FHx),或两者都没有这些风险因素(发育正常;TD)。在17至21岁时评估临床和功能结局(N = 93)。与TD组相比,ASz组在前驱症状问卷(PQ)总分(β = 10.59,95%CI = 3.76,17.42)和精神病理学总分(β = 6.13,95%CI:1.03,11.23)上更高,在PQ阳性症状量表上得分高于阈值的可能性更大(OR = 4.00,95%CI = 1.08,14.83),并且在随访时社会和职业功能量表上得分更低(β = -9.43,95%CI = -15.08,-3.77)。FHx组和TD组在任何结局上均无差异。研究结果表明,对精神分裂症假定前驱症状进行人群筛查可能会识别出将从预防性干预中受益的儿童。