Meta-analysis of longitudinal neurocognitive performance in people at clinical high-risk for psychosis

被引:20
作者
Hedges, Emily P. [1 ]
See, Cheryl [1 ]
Si, Shuqing [1 ]
McGuire, Philip [1 ]
Dickson, Hannah [2 ]
Kempton, Matthew J. [1 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, London SE5 8AF, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Forens & Neurodev Sci, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
CHR; cognition; processing speed; psychosis; UHR; CONSENSUS COGNITIVE BATTERY; INDIVIDUALS; ONSET; SCHIZOPHRENIA; VULNERABILITY; PRODROME; DEFICITS; EPISODE; BIAS;
D O I
10.1017/S0033291722001830
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Persons at clinical high-risk for psychosis (CHR) are characterised by specific neurocognitive deficits. However, the course of neurocognitive performance during the prodromal period and over the onset of psychosis remains unclear. The aim of this meta-analysis was to synthesise results from follow-up studies of CHR individuals to examine longitudinal changes in neurocognitive performance. Three electronic databases were systematically searched to identify articles published up to 31 December 2021. Thirteen studies met inclusion criteria. Study effect sizes (Hedges' g) were calculated and pooled for each neurocognitive task using random-effects meta-analyses. We examined whether changes in performance between baseline and follow-up assessments differed between: (1) CHR and healthy control (HC) individuals, and (2) CHR who did (CHR-T) and did not transition to psychosis (CHR-NT). Meta-analyses found that HC individuals had greater improvements in performance over time compared to CHR for letter fluency (g = -0.32, p = 0.029) and digit span (g = -0.30, p = 0.011) tasks. Second, there were differences in longitudinal performance of CHR-T and CHR-NT in trail making test A (TMT-A) (g = 0.24, p = 0.014) and symbol coding (g = -0.51, p = 0.011). Whilst CHR-NT improved in performance on both tasks, CHR-T improved to a lesser extent in TMT-A and had worsened performance in symbol coding over time. Together, neurocognitive performance generally improved in all groups at follow-up. Yet, evidence suggested that improvements were less pronounced for an overall CHR group, and specifically for CHR-T, in processing speed tasks which may be a relevant domain for interventions aimed to enhance neurocognition in CHR populations.
引用
收藏
页码:2009 / 2016
页数:8
相关论文
共 59 条
[1]   Clinical and functional characteristics of youth at clinical high-risk for psychosis who do not transition to psychosis [J].
Addington, Jean ;
Stowkowy, Jacqueline ;
Liu, Lu ;
Cadenhead, Kristin S. ;
Cannon, Tyrone D. ;
Cornblatt, Barbara A. ;
McGlashan, Thomas H. ;
Perkins, Diana O. ;
Seidman, Larry J. ;
Tsuang, Ming T. ;
Walker, Elaine F. ;
Bearden, Carrie E. ;
Mathalon, Daniel H. ;
Santesteban-Echarri, Olga ;
Woods, Scott W. .
PSYCHOLOGICAL MEDICINE, 2019, 49 (10) :1670-1677
[2]   Longitudinal Cognitive Performance in Individuals at Ultrahigh Risk for Psychosis: A 10-year Follow-up [J].
Allott, Kelly ;
Wood, Stephen J. ;
Yuen, Hok Pan ;
Yung, Alison R. ;
Nelson, Barnaby ;
Brewer, Warrick J. ;
Spiliotacopoulos, Daniela ;
Bruxner, Annie ;
Simmons, Magenta ;
Broussard, Christina ;
Mallawaarachchi, Sumudu ;
Pantelis, Christos ;
McGorry, Patrick D. ;
Lin, Ashleigh .
SCHIZOPHRENIA BULLETIN, 2019, 45 (05) :1101-1111
[3]   The course of cognitive functioning over six months in individuals at clinical high risk for psychosis [J].
Barbato, Mariapaola ;
Colijn, Mark A. ;
Keefe, Richard S. E. ;
Perkins, Diana O. ;
Woods, Scott W. ;
Hawkins, Keith A. ;
Christensen, Bruce K. ;
Addington, Jean .
PSYCHIATRY RESEARCH, 2013, 206 (2-3) :195-199
[4]   Properties of sufficiency and statistical tests [J].
Bartlett, MS .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1937, 160 (A901) :0268-0282
[5]   Neurocognitive functioning before and after the first psychotic episode: does psychosis result in cognitive deterioration? [J].
Becker, H. E. ;
Nieman, D. H. ;
Wiltink, S. ;
Dingemans, P. M. ;
de Fliert, J. R. van ;
Velthorst, E. ;
de Haan, L. ;
van Amelsvoort, T. A. ;
Linszen, D. H. .
PSYCHOLOGICAL MEDICINE, 2010, 40 (10) :1599-1606
[6]   Meta-analysis of Cognitive Deficits in Ultra-high Risk to Psychosis and First-Episode Psychosis: Do the Cognitive Deficits Progress Over, or After, the Onset of Psychosis? [J].
Bora, Emre ;
Murray, Robin M. .
SCHIZOPHRENIA BULLETIN, 2014, 40 (04) :744-755
[7]  
Borenstein M., 2009, Introduction to Meta-Analysis, P225, DOI [DOI 10.1002/9780470743386, https://doi.org/10.1002/9780470743386.ch16, DOI 10.1002/9780470743386.CH16, 10.1002/9780470743386.ch13, DOI 10.1002/9780470743386.CH13, 10.1002/9780470743386.ch24, DOI 10.1002/9780470743386.CH24]
[8]   Generalized and specific cognitive performance in clinical high-risk cohorts: A review highlighting potential vulnerability markers for psychosis [J].
Brewer, Warrick J. ;
Wood, Stephen J. ;
Phillips, Lisa J. ;
Francey, Shona M. ;
Pantelis, Christos ;
Yung, Alison R. ;
Cornblatt, Barbara ;
McGorry, Patrick D. .
SCHIZOPHRENIA BULLETIN, 2006, 32 (03) :538-555
[9]   Meta-Analysis of 89 Structural MRI Studies in Posttraumatic Stress Disorder and Comparison With Major Depressive Disorder [J].
Bromis, Konstantinos ;
Calem, Maria ;
Reinders, Antje A. T. S. ;
Williams, Steven C. R. ;
Kempton, Matthew J. .
AMERICAN JOURNAL OF PSYCHIATRY, 2018, 175 (10) :989-998
[10]   Scoring Higher the Second Time Around: Meta-Analyses of Practice Effects in Neuropsychological Assessment [J].
Calamia, Matthew ;
Markon, Kristian ;
Tranel, Daniel .
CLINICAL NEUROPSYCHOLOGIST, 2012, 26 (04) :543-570