دورية أكاديمية

Therapeutic Reference Range for Aripiprazole in Schizophrenia Revised: a Systematic Review and Metaanalysis.

التفاصيل البيبلوغرافية
العنوان: Therapeutic Reference Range for Aripiprazole in Schizophrenia Revised: a Systematic Review and Metaanalysis.
المؤلفون: Hart, Xenia M., Hiemke, Christoph, Eichentopf, Luzie, Lense, Xenija M., Clement, Hans Willi, Conca, Andreas, Faltraco, Frank, Florio, Vincenzo, Grüner, Jessica, Havemann-Reinecke, Ursula, Molden, Espen, Paulzen, Michael, Schoretsanitis, Georgios, Riemer, Thomas G., Gründer, Gerhard
المصدر: Psychopharmacology; Nov2022, Vol. 239 Issue 11, p3377-3391, 15p, 1 Diagram, 4 Charts, 3 Graphs
مصطلحات موضوعية: ARIPIPRAZOLE, SCHIZOPHRENIA, PHARMACOLOGY, DRUG side effects, DOPAMINE receptors
مستخلص: Rationale: While one of the basic axioms of pharmacology postulates that there is a relationship between the concentration and effects of a drug, the value of measuring blood levels is questioned by many clinicians. This is due to the often-missing validation of therapeutic reference ranges. Objectives: Here, we present a prototypical meta-analysis of the relationships between blood levels of aripiprazole, its target engagement in the human brain, and clinical effects and side effects in patients with schizophrenia and related disorders. Methods: The relevant literature was systematically searched and reviewed for aripiprazole oral and injectable formulations. Population-based concentration ranges were computed (N = 3,373) and pharmacokinetic influences investigated. Results: Fifty-three study cohorts met the eligibility criteria. Twenty-nine studies report blood level after oral, 15 after injectable formulations, and nine were positron emission tomography studies. Conflicting evidence for a relationship between concentration, efficacy, and side effects exists (assigned level of evidence low, C; and absent, D). Population-based reference ranges are well in-line with findings from neuroimaging data and individual efficacy studies. We suggest a therapeutic reference range of 120–270 ng/ml and 180–380 ng/ml, respectively, for aripiprazole and its active moiety for the treatment of schizophrenia and related disorders. Conclusions: High interindividual variability and the influence of CYP2D6 genotypes gives a special indication for Therapeutic Drug Monitoring of oral and long-acting aripiprazole. A starting dose of 10 mg will in most patients result in effective concentrations in blood and brain. 5 mg will be sufficient for known poor metabolizers. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00333158
DOI:10.1007/s00213-022-06233-2