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Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for Psychosis
Biological Psychiatry ( IF 9.6 ) Pub Date : 2024-08-23 , DOI: 10.1016/j.biopsych.2024.08.010
Charles H Schleifer 1 , Sarah E Chang 1 , Carolyn M Amir 1 , Kathleen P O'Hora 1 , Hoki Fung 1 , Jee Won D Kang 2 , Leila Kushan-Wells 1 , Eileen Daly 3 , Fabio Di Fabio 4 , Marianna Frascarelli 4 , Maria Gudbrandsen 5 , Wendy R Kates 6 , Declan Murphy 3 , Jean Addington 7 , Alan Anticevic 8 , Kristin S Cadenhead 9 , Tyrone D Cannon 8 , Barbara A Cornblatt 10 , Matcheri Keshavan 11 , Daniel H Mathalon 12 , Diana O Perkins 13 , William Stone 11 , Elaine Walker 14 , Scott W Woods 8 , Lucina Q Uddin 1 , Kuldeep Kumar 15 , Gil D Hoftman 1 , Carrie E Bearden 16
Affiliation  

22q11.2 deletion syndrome (22qDel) is a copy number variant that is associated with psychosis and other neurodevelopmental disorders. Adolescents who are at clinical high risk for psychosis (CHR) are identified based on the presence of subthreshold psychosis symptoms. Whether common neural substrates underlie these distinct high-risk populations is unknown. We compared functional brain measures in 22qDel and CHR cohorts and mapped the results to biological pathways.

中文翻译:


遗传与临床精神病高风险的独特功能神经影像学特征



22q11.2 缺失综合征 (22qDel) 是一种与精神病和其他神经发育障碍相关的拷贝数变体。临床上精神病 (CHR) 高风险的青少年根据是否存在阈下精神病症状来识别。这些不同的高危人群是否具有共同的神经底物尚不清楚。我们比较了 22qDel 和 CHR 队列中的大脑功能测量,并将结果映射到生物通路。
更新日期:2024-08-23
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