Clinical psychopathology in youth at familial high risk for psychosis

被引:7
作者
Shah, Jai L. [1 ,2 ,3 ,4 ]
Tandon, Neeraj [1 ,5 ]
Montrose, Debra M. [6 ]
Mermon, Diana [6 ]
Eack, Shaun M. [7 ]
Miewald, Jean [6 ]
Keshavan, Matcheri S. [1 ,2 ,6 ]
机构
[1] Beth Israel Deaconess Med Ctr, Massachusetts Mental Hlth Ctr, 6th Floor,75 Fenwood Rd, Boston, MA 02118 USA
[2] Harvard Med Sch, Dept Psychiat, Boston, MA 02115 USA
[3] Douglas Mental Hlth Univ Inst, PEPP Montreal, Montreal, PQ, Canada
[4] McGill Univ, Dept Psychiat, Montreal, PQ, Canada
[5] Baylor Coll Med, Houston, TX 77030 USA
[6] Univ Pittsburgh, Sch Med, Western Psychiat Inst & Clin, Pittsburgh, PA USA
[7] Univ Pittsburgh, Sch Social Work, Pittsburgh, PA 15260 USA
关键词
characteristics; diagnosis; emergence; familial high risk; psychopathology; psychosis; AGE-OF-ONSET; DIAGNOSTIC STABILITY; YOUNG RELATIVES; EARLY INTERVENTION; STAGING MODEL; 1ST EPISODE; SCHIZOPHRENIA; PREDICTION; ADOLESCENTS; DISORDERS;
D O I
10.1111/eip.12480
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Aim While the course of psychopathology has been explored from an index mental health diagnosis onwards, there are few detailed, prospective studies of the occurrence of clinical psychopathology in youth with familial risk for severe mental illnesses such as psychosis. We sought to describe the appearance of Axis I psychopathology in a unique sample of adolescents with a family history of schizophrenia (FHR). Methods One hundred and sixty two first- and second-degree relatives (mean age 15.7 +/- 3.6; range 8-25) of probands with schizophrenia or schizoaffective disorder were assessed at baseline and annual intervals for up to 3 years, focusing on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) Axis I psychopathology. Results Fourteen individuals (8.6%) developed a psychotic disorder. One hundred and five subjects (65%) met criteria for an Axis I disorder over the course of the study, the most common of which was a depressive episode (40 subjects; 25%). Of the 148 individuals who did not develop psychosis, 91 (61%) had one or more Axis I disorders compared with 10/14 converters who had a comorbid Axis I disorder (71%). Ordered by increasing age of onset, diagnoses included cognitive and externalizing disorders, anxiety disorders, affective disorders, substance use disorders and psychotic disorders. Conclusions In addition to an elevated risk of psychosis, young FHR relatives manifest a broad range of non-psychotic Axis I psychopathology in childhood and adolescence. This breadth of diagnoses has implications for the structure and function of mental health services for young people.
引用
收藏
页码:297 / 303
页数:7
相关论文
共 50 条
  • [41] Impacts of risk thresholds and age on clinical high risk for psychosis: a comparative network analysis
    Gauld, Christophe
    Fourneret, Pierre
    Alderson-Day, Ben
    Palmer-Cooper, Emma
    Donde, Clement
    EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2024, : 947 - 958
  • [42] Sensitivity of the familial high-risk approach for the prediction of future psychosis: a total population study
    Healy, Colm
    Lang, Ulla
    O'Hare, Kirstie
    Veijola, Juha
    O'Connor, Karen
    Lahti-Pulkkinen, Marius
    Kajantie, Eero
    Kelleher, Ian
    WORLD PSYCHIATRY, 2024, 23 (03) : 432 - 437
  • [43] Sources of clinical distress in young people at ultra high risk of psychosis
    Rapado-Castro, Marta
    McGorry, Patrick D.
    Yung, Alison
    Calvo, Ana
    Nelson, Barnaby
    SCHIZOPHRENIA RESEARCH, 2015, 165 (01) : 15 - 21
  • [44] Asperger Syndrome and/or Clinical High Risk of Psychosis? A Differential Diagnostic Challenge
    Schmidt, Stefanie J.
    Behar, Ayla
    Schultze-Lutter, Frauke
    PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE, 2018, 67 (03) : 274 - 293
  • [45] Attributional style among youth at clinical risk for psychosis
    DeVylder, Jordan E.
    Ben-David, Shelly
    Kimhy, David
    Corcoran, Cheryl M.
    EARLY INTERVENTION IN PSYCHIATRY, 2013, 7 (01) : 84 - 88
  • [46] Development of a Boston Treatment Program for Youth at Clinical High Risk for Psychosis: Center for Early Detection, Assessment, and Response to Risk (CEDAR)
    Friedman-Yakoobian, Michelle S.
    West, Michelle L.
    Woodberry, Kristen A.
    O'Donovan, Keira E.
    Zimmet, Suzannah V.
    Gnong-Granato, Andrea
    Giuliano, Anthony J.
    Guyer, Margaret E.
    Rodenhiser-Hill, Janine
    Keshavan, Matcheri S.
    Seidman, Larry J.
    HARVARD REVIEW OF PSYCHIATRY, 2018, 26 (05) : 274 - 286
  • [47] Social aversive conditioning in youth at clinical high risk for psychosis and with psychosis: An ERP study
    Watters, Anna J.
    Rupert, Petra E.
    Wolf, Daniel H.
    Calkins, Monica E.
    Gur, Ruben C.
    Gur, Raquel E.
    Turetsky, Bruce, I
    SCHIZOPHRENIA RESEARCH, 2018, 202 : 291 - 296
  • [48] Evaluating the impact of cannabis use on thalamic connectivity in youth at clinical high risk of psychosis
    Lisa Buchy
    Tyrone D. Cannon
    Alan Anticevic
    Kristina Lyngberg
    Kristin S. Cadenhead
    Barbara A. Cornblatt
    Thomas H. McGlashan
    Diana O. Perkins
    Larry J. Seidman
    Ming T. Tsuang
    Elaine F. Walker
    Scott W. Woods
    Carrie E. Bearden
    Daniel H. Mathalon
    Jean Addington
    BMC Psychiatry, 15
  • [49] The impact of early factors on persistent negative symptoms in youth at clinical high risk for psychosis
    Devoe, Daniel J. J.
    Lui, Lu
    Cannon, Tyrone D. D.
    Cadenhead, Kristin Suzanne
    Cornblatt, Barbara A. A.
    Keshavan, Matcheri
    McGlashan, Tom H. H.
    Perkins, Diana. O.
    Seidman, Larry J. J.
    Stone, William S. S.
    Tsuang, Ming T. T.
    Woods, Scott W. W.
    Walker, Elaine F. F.
    Mathalon, Daniel H. H.
    Bearden, Carrie E. E.
    Addington, Jean
    FRONTIERS IN PSYCHIATRY, 2023, 14
  • [50] Timing of menarche and abnormal hippocampal connectivity in youth at clinical-high risk for psychosis
    Damme, Katherine S. F.
    Ristanovic, Ivanka
    Vargas, Teresa
    Mittal, Vijay A.
    PSYCHONEUROENDOCRINOLOGY, 2020, 117