Jugend & Entwicklung
Studienlage · Detail Systematische Review + Meta-Analyse · Jugend & Entwicklung · 2005

Cannabis as a risk factor for psychosis: systematic review.

Schaden GRADE Moderat 422 Zitate
Stichprobek = 7 Studien
DauerPublikationen Januar 1966 bis…
KontrolleKein Cannabiskonsum
EndpunktOdds Ratio
Verblindungunklar
DesignSystematische Review + Meta-Analyse
Kernaussage

Cannabiskonsum erhöht das Risiko für Psychose und Schizophrenie unabhängig um das etwa Dreifache (OR 2,9).

Zusammenfassung

SR + Meta-Analyse (k=7, OR=2,9; 95%-KI 2,4–3,6) zu Cannabis als Psychose-Risikofaktor; frühzeitiger Cannabiskonsum in der Adoleszenz war als eigenständige vulnerable Gruppe identifiziert — dosisabhängiger Effekt auf psychotische Symptome bei Jugendlichen und Personen mit hohem genetischem Risiko.

P
PopulationPersonen aus Kohorten- und Fall-Kontroll-Studien zu Cannabis und Psychose/Schizophrenie (gepoolte Stichprobe nicht explizit berichtet)
I
InterventionCannabiskonsum (als Expositionsfaktor)
C
KontrolleKein Cannabiskonsum
O
OutcomeOdds Ratio 2,9 (95%-KI 2,4–3,6) für Psychose/Schizophrenie bei Cannabiskonsum; kein Hinweis auf Publikationsbias oder Heterogenität; früher Cannabiskonsum erhöhte das Risiko zusätzlich
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Publikationsbias
Qualitätsprofil
Größe
Verblindung
Effektstärke Schaden
Zitate / Jahr
Autoren
Semple DM, McIntosh AM, Lawrie SM.
DOI 10.1177/0269881105049040
Design: Systematische Review + Meta-Analyse
Teilen
Abstract
Various lines of evidence suggest an association between cannabis and psychosis. Five years ago, the only significant case-control study addressing this question was the Swedish Conscript Cohort. Within the last few years, other studies have emerged, allowing the evidence for cannabis as a risk factor to be more systematically reviewed and assessed. Using specific search criteria on Embase, PsychINFO and Medline, all studies examining cannabis as an independent risk factor for schizophrenia, psychosis or psychotic symptoms, published between January 1966 and January 2004, were examined. Additional studies were also reviewed from references found in retrieved articles, reviews, and a cited reference search (ISI-Web of Science). Studies selected for meta-analysis included: (i) case-control studies where exposure to cannabis preceded the onset of schizophrenia or schizophrenia-like psychosis and (ii) cohort studies of healthy individuals recruited before the median age of illness onset, with cannabis exposure determined prospectively and blind to eventual diagnosis. Studies of psychotic symptoms were also tabulated for further discussion. Eleven studies were identified examining the relationship between cannabis use and psychosis. Seven were included in the meta-analysis, with a derived odds ratio (fixed effects) of 2-9 (95 % confidence interval = 2.4-3.6). No evidence of publication bias or heterogeneity was found. Early use of cannabis did appear to increase the risk of psychosis. For psychotic symptoms, a dose-related effect of cannabis use was seen, with vulnerable groups including individuals who used cannabis during adolescence, those who had previously experienced psychotic symptoms, and those at high genetic risk of developing schizophrenia. In conclusion, the available evidence supports the hypothesis that cannabis is an independent risk factor, both for psychosis and the development of psychotic symptoms. Addressing cannabis use, particularly in vulnerable populations, is likely to have beneficial effects on psychiatric morbidity.

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