Heterogeneity of Psychosis Risk Within Individuals at Clinical High Risk: A Meta-analytical Stratification
Autor: | Jun Soo Kwon, Masafumi Mizuno, Jimmy Lee, Tae Young Lee, Anita Riecher-Rössler, Alison R. Yung, Jean Addington, Wolfram Kawohl, Stefan Borgwardt, Dorien H. Nieman, Suk Kyoon An, Cheryl Corcoran, Grazia Rutigliano, Barnaby Nelson, Patrick D. McGorry, Szabolcs Kéri, Amel Braham, Scott W. Woods, Philip McGuire, Wulf Rössler, Paul Amminger, Paolo Fusar-Poli, Sibylle Metzler, Tim Ziermans, Chen-Chung Liu, Marco Cappucciati, Andor E. Simon, Daniel Stahl, May M.L. Lam, Kristen A. Woodberry, Jesus Perez, Javier Labad |
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Přispěvatelé: | University of Zurich, Fusar-Poli, Paolo, ANS - Mood, Anxiety, Psychosis, Stress & Sleep, Adult Psychiatry, APH - Amsterdam Public Health |
Rok vydání: | 2016 |
Předmět: |
Risk
Psychosis medicine.medical_specialty Funnel plot Psychosis risk MEDLINE 610 Medicine & health 2738 Psychiatry and Mental Health 03 medical and health sciences symbols.namesake 0302 clinical medicine Internal medicine medicine Humans Genetic risk Psychiatry Psychotic Disorders medicine.disease 030227 psychiatry Psychiatry and Mental health Increased risk Bonferroni correction Data extraction 10054 Clinic for Psychiatry Psychotherapy and Psychosomatics symbols Psychology 030217 neurology & neurosurgery |
Zdroj: | Fusar-Poli, P, Cappucciati, M, Borgwardt, S, Woods, S W, Addington, J, Nelson, B, Nieman, D H, Stahl, D R, Rutigliano, G, Riecher-Rössler, A, Simon, A E, Mizuno, M, Lee, T Y, Kwon, J S, Lam, M M L, Perez, J, Keri, S, Amminger, P, Metzler, S, Kawohl, W, Rössler, W, Lee, J, Labad, J, Ziermans, T, An, S K, Liu, C C, Woodberry, K A, Braham, A, Corcoran, C, McGorry, P, Yung, A R & McGuire, P K 2016, ' Heterogeneity of psychosis risk within individuals at clinical high risk : A meta-analytical stratification ', JAMA Psychiatry, vol. 73, no. 2, pp. 113-120 . https://doi.org/10.1001/jamapsychiatry.2015.2324 JAMA psychiatry, 73(2), 113-120. American Medical Association |
ISSN: | 2168-6238 |
Popis: | IMPORTANCE Individuals can be classified as being at clinical high risk (CHR) for psychosis if they meet at least one of the ultra-high-risk (UHR) inclusion criteria (brief limited intermittent psychotic symptoms [BLIPS] and/or attenuated psychotic symptoms [APS] and/or genetic risk and deterioration syndrome [GRD]) and/or basic symptoms [BS]. Themeta-analytical risk of psychosis of these different subgroups is still unknown. OBJECTIVE To compare the risk of psychosis in CHR individuals who met at least one of the major inclusion criteria and in individuals not at CHR for psychosis (CHR-). DATA SOURCES Electronic databases (Web of Science, MEDLINE, Scopus) were searched until June 18, 2015, along with investigation of citations of previous publications and a manual search of the reference lists of retrieved articles. STUDY SELECTION We included original follow-up studies of CHR individuals who reported the risk of psychosis classified according to the presence of any BLIPS, APS and GRD, APS alone, GRD alone, BS, and CHR-. DATA EXTRACTION AND SYNTHESIS Independent extraction by multiple observers and random-effects meta-analysis of proportions. Moderators were tested with meta-regression analyses (Bonferroni corrected). Heterogeneity was assessed with the I2 index. Sensitivity analyses tested robustness of results. Publication biases were assessed with funnel plots and the Egger test. MAIN OUTCOMES AND MEASURES The proportion of each subgroup with any psychotic disorder at 6, 12, 24, 36, and 48 or more months of follow-up. RESULTS Thirty-three independent studies comprising up to 4227 individualswere included. The meta-analytical proportion of individuals meeting each UHR subgroup at intakewas: 0.85 APS (95%CI, 0.79-0.90), 0.1 BLIPS (95%CI, 0.06-0.14), and 0.05 GRD (95%CI, 0.03-0.07). There were no significant differences in psychosis risk at any time point between the APS and GRD and the APS-alone subgroups. Therewas a higher risk of psychosis in the any BLIPS greater than APS greater than GRD-alone subgroups at 24, 36, and 48 or more months of follow-up. Therewas no evidence that the GRD subgroup has a higher risk of psychosis than the CHR- subgroup. There were too fewBS or BS and UHR studies to allowrobust conclusions. CONCLUSIONS AND RELEVANCE There is meta-analytical evidence that BLIPS represents separate risk subgroup compared with the APS. The GRD subgroup is infrequent and not associated with an increased risk of psychosis. Future studies are advised to stratify their findings across these different subgroups. The CHR guidelines should be updated to reflect these differences. |
Databáze: | OpenAIRE |
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