The hierarchical taxonomy of psychopathology in clinical high risk for psychosis: Validation and extension.

IF 3.1 Q2 PSYCHIATRY
Journal of psychopathology and clinical science Pub Date : 2024-04-01 Epub Date: 2024-03-28 DOI:10.1037/abn0000893
Trevor F Williams, Alexander L Williams, Henry R Cowan, Elaine F Walker, Tyrone D Cannon, Carrie E Bearden, Matcheri Keshavan, Barbara A Cornblatt, Jean Addington, Scott W Woods, Diana O Perkins, Daniel H Mathalon, Kristin S Cadenhead, William S Stone, Vijay A Mittal
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Abstract

The Hierarchical Taxonomy of Psychopathology (HiTOP) consortium's transdiagnostic dimensional model of psychopathology has considerable support; however, this model has been underresearched in individuals at clinical high risk for psychosis (CHR-P), a population that may advance the model. CHR-P individuals not only have attenuated psychotic symptoms that vary in severity, but also have many comorbid diagnoses and varied clinical outcomes, including disorders with uncertain relations to HiTOP (e.g., obsessive-compulsive disorder). The present study used self-report and interview data from North American Prodrome Longitudinal Study-3 (710 CHR, 96 controls) to replicate the HiTOP model and test specific hypotheses regarding disorders with uncertain relations to its dimensions. Additionally, the present study examined the HiTOP model in relation to childhood trauma, declines in social functioning, and development of full psychosis. Confirmatory factor analysis indicated that the HiTOP model's fit was nearly adequate (e.g., comparative fit index = .89), though several theory-relevant modifications were indicated. Additionally, specific tests were conducted to gain a more fine-grained perspective on how disorders with less clear prior evidence were related to the HiTOP model. Notable findings from these analyses include bipolar spectrum disorders relating to the psychosis super spectrum (i.e., .39 loading), and obsessive-compulsive disorder showing a complex pattern of loadings (e.g., internalizing and psychosis). The final model parsimoniously accounted for childhood trauma (e.g., super spectra rs = .22-.32), associations with current functioning, and predicted future conversion to a psychotic disorder (e.g., super spectra R² = .13). Overall, these results inform the HiTOP model and suggest its promise for CHR-P research. (PsycInfo Database Record (c) 2024 APA, all rights reserved).

精神病临床高危人群精神病理学分层分类法:验证与扩展。
精神病理学层次分类法(HiTOP)联盟提出的精神病理学跨诊断维度模型得到了相当多的支持;然而,该模型在精神病临床高危人群(CHR-P)中的研究却不足,而这一人群可能会推动该模型的发展。CHR-P人群不仅有严重程度不同的减轻的精神病症状,而且有许多合并诊断和不同的临床结果,包括与HiTOP关系不确定的疾病(如强迫症)。本研究利用北美前驱症纵向研究-3(710 名 CHR,96 名对照组)的自我报告和访谈数据,复制了 HiTOP 模型,并检验了与该模型各维度关系不确定的疾病的具体假设。此外,本研究还检验了 HiTOP 模型与童年创伤、社会功能下降和完全精神病的发展之间的关系。确认性因素分析表明,HiTOP 模型的拟合度几乎是适当的(例如,比较拟合指数 = 0.89),但也指出了几处与理论相关的修改。此外,我们还进行了一些特定的测试,以便从更精细的角度了解先前证据不太明确的失调症与 HiTOP 模型的关系。这些分析的显著发现包括躁狂症谱系障碍与精神病超级谱系的关系(即 0.39 负载),以及强迫症显示出复杂的负载模式(如内化和精神病)。最终模型合理地考虑了童年创伤(如超谱 Rs = 0.22-0.32)、与当前功能的关联以及未来向精神病性障碍转化的预测(如超谱 R² = 0.13)。总之,这些结果为HiTOP模型提供了参考,并表明其在CHR-P研究中大有可为。(PsycInfo Database Record (c) 2024 APA,保留所有权利)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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