Miyashita Mitsuhiro, Yamasaki Syudo, Ando Shuntaro, Suzuki Kazuhiro, Toriumi Kazuya, Horiuchi Yasue, Yoshikawa Akane, Imai Atsushi, Nagase Yukihiro, Miyano Yasuhiro, Inoue Tomoko, Endo Kaori, Morimoto Yuko, Morita Masaya, Kiyono Tomoki, Usami Satoshi, Okazaki Yuji, Furukawa Toshiaki A, Hiraiwa-Hasegawa Mariko, Itokawa Masanari, Kasai Kiyoto, Nishida Atsushi, Arai Makoto
Schizophrenia Research Project, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Department of Psychiatry, Tokyo Metropolitan Matsuzawa Hospital, Tokyo, Japan.
NPJ Schizophr. 2021 Aug 12;7(1):37. doi: 10.1038/s41537-021-00167-y.
Case control studies have suggested that advanced glycation end products play a key role in the pathophysiology of chronic schizophrenia. However, the longitudinal association between advanced glycation end products and psychotic symptoms among drug-naïve adolescents remains unclear. This study examined whether advanced glycation end products could predict the trajectory of psychotic symptoms in drug-naive adolescents using data from prospective population-based biomarker subsample study of the Tokyo Teen Cohort. A total of 277 community-dwelling adolescents aged 13 years without antipsychotic medication were analyzed. Fingertip advanced glycation end products were measured in adolescents using noninvasive technology that can be used quickly. The trajectory of psychotic symptoms in a 12-month follow-up was assessed by experienced psychiatrists using a semi-structured interview. Of the 277 participants, 13 (4.7%) experienced persistent psychotic symptoms (psychotic symptoms at baseline and follow-up), 65 (23.5%) experienced transient psychotic symptoms (psychotic symptoms at baseline or follow-up), and 199 (71.8%) did not have psychotic symptoms. Multinomial logistic regression analysis adjusted for age and sex revealed that baseline fingertip advanced glycation end products might predict the risk of persistent psychotic symptoms (odds ratio = 1.68; 95% confidence interval, 1.05-2.69; P = 0.03). Altogether, fingertip advanced glycation end products potentially predicted the trajectory of psychotic symptoms among drug-naive adolescents, which indicated its involvement in the pathophysiology of early psychosis. Further studies are required to identify strategies to reduce adolescent advanced glycation end products, which may contribute to preventing the onset of psychosis.
病例对照研究表明,晚期糖基化终产物在慢性精神分裂症的病理生理学中起关键作用。然而,在未使用药物的青少年中,晚期糖基化终产物与精神病症状之间的纵向关联仍不明确。本研究利用东京青少年队列基于人群的前瞻性生物标志物子样本研究数据,检验了晚期糖基化终产物是否能预测未使用药物的青少年精神病症状的发展轨迹。共分析了277名年龄为13岁、未服用抗精神病药物的社区青少年。采用可快速使用的非侵入性技术测量青少年指尖的晚期糖基化终产物。经验丰富的精神科医生通过半结构化访谈评估了12个月随访期间精神病症状的发展轨迹。在277名参与者中,13名(4.7%)经历了持续性精神病症状(基线和随访时均有精神病症状),65名(23.5%)经历了短暂性精神病症状(基线或随访时有精神病症状),199名(71.8%)没有精神病症状。经年龄和性别调整的多项逻辑回归分析显示,基线指尖晚期糖基化终产物可能预测持续性精神病症状的风险(比值比=1.68;95%置信区间,1.05 - 2.69;P = 0.03)。总之,指尖晚期糖基化终产物可能预测未使用药物的青少年精神病症状的发展轨迹,这表明其参与了早期精神病的病理生理学过程。需要进一步研究以确定降低青少年晚期糖基化终产物的策略,这可能有助于预防精神病的发作。