Characterizing Covariant Trajectories of Individuals at Clinical High Risk for Psychosis Across Symptomatic and Functional Domains

被引:45
作者
Allswede, Dana M. [1 ]
Addington, Jean [3 ]
Bearden, Carrie E. [4 ]
Cadenhead, Kristin S. [5 ]
Cornblatt, Barbara A. [7 ,8 ]
Mathalon, Daniel H. [9 ,10 ]
McGlashan, Thomas [2 ]
Perkins, Diana O. [11 ]
Seidman, Larry J. [12 ]
Tsuang, Ming T. [5 ,6 ]
Walker, Elaine F. [13 ]
Woods, Scott W. [2 ]
Cannon, Tyrone D. [1 ,2 ]
机构
[1] Yale Univ, Dept Psychol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Psychiat, New Haven, CT 06520 USA
[3] Univ Calgary, Dept Psychiat, Calgary, AB, Canada
[4] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA
[5] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Ctr Behav Genom, La Jolla, CA 92093 USA
[7] Donald & Barbara Zucker Sch Med Hofstra Northwell, Dept Psychiat, Hempstead, NY USA
[8] Donald & Barbara Zucker Sch Med Hofstra Northwell, Dept Mol Med, Hempstead, NY USA
[9] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA
[10] San Francisco VA Med Ctr, San Francisco, CA USA
[11] Univ N Carolina, Sch Med, Dept Psychiat, Chapel Hill, NC 27515 USA
[12] Harvard Med Sch, Dept Psychiat, Boston, MA 02115 USA
[13] Emory Univ, Dept Psychol, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
ULTRA-HIGH RISK; REMISSION; OUTCOMES; METAANALYSIS;
D O I
10.1176/appi.ajp.2019.18111290
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The authors sought to characterize differences in outcomes among help-seeking individuals at clinical high risk for psychosis by identifying covariant longitudinal patterns of symptoms and functioning. Methods: Group-basedmultitrajectorymodeling was applied to longitudinal ratings of four symptom domains (positive, negative, disorganized, general) and general functioning among clinical high-risk individuals in an initial discovery sample (N=422). An independent sample (N=133) was used to test replicability. Results: Three trajectory groups were identified among clinical high-risk individuals in the discovery sample: group 1 (30%) exhibited substantial improvement across all domains, with half reaching positive outcomes for both functioning and positive symptoms; group 2 (49%) exhibited moderate impairments across domains, with approximately one-quarter meeting criteria for positive outcomes; the remaining participants (group 3; 22%) exhibited consistent levels of severe impairment across domains and did not experience positive outcomes. These trajectory groups and remission patterns were replicated in an independent sample. Conclusions: Replicable subgroups of help-seeking clinical high-risk cases can be ascertained based on distinctive profiles of change over time in symptoms and functioning. Within each of the three identified subgroups, similar patterns of change (i.e., rapid, moderate, or no improvement) were observed across the four symptom domains and functioning. This consistency of change over time across domains within each subgroup is a novel observation supporting the syndrome consistency of clinical high-risk symptoms and signs. The observed trajectory subgroups are suggestive of different degrees of need for clinical interventions, ranging from minimal or supportive for about one-third of cases to increasingly intensive among the remainder.
引用
收藏
页码:164 / 171
页数:8
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