期刊
EXPERT OPINION ON DRUG SAFETY
卷 14, 期 2, 页码 219-241出版社
TAYLOR & FRANCIS LTD
DOI: 10.1517/14740338.2015.979150
关键词
adolescents; antipsychotics; children; diabetes; glucose; hemoglobin A1c; healthy controls; incidence; insulin; psychiatric controls
资金
- National Institute of Mental Health Advanced Center for Services and Intervention Research
- Zucker Hillside Hospital [P30MH090590]
- American Academy of Child and Adolescent Psychiatry BMS
- Janssen/JJ
- National Institute of Mental Health
- Novo Nirdisk A/S
- Ostuka
- Takeda
- Thrasher Foundation
Introduction: Glucose dysregulation and type 2 diabetes mellitus (T2DM) are feared antipsychotic drug adverse effects. Despite increasing utilization, data about antipsychotic risk of T2DM in youth are scarce. Areas covered: We conducted a systematic PubMed/MEDLINE search until 15 May 2014 focusing on studies with >= 20 youths aged <= 24 years, reporting quantitative data on: i) change in fasting glucose, hemoglobin A1c, insulin or insulin resistance after antipsychotic initiation (studies = 19, n = 2123, age = 13.3 years, follow up = 28.8 weeks); or ii) prevalence (studies = 4) or incidence (studies = 8, follow up = 1.57 years) of T2DM in antipsychotic-exposed youth (studies = 10, n = 65,486, age = 14.2 years) versus healthy controls (studies = 4, n = 246,828), psychiatric controls (studies = 5, n = 61,784) or without control groups (studies = 2). Expert opinion: Antipsychotics are associated with early adverse changes in glucose metabolism that are greater with all analyzable antipsychotics compared to controls, being highest with olanzapine, followed by quetiapine, aripiprazole and risperidone; but data were scarce. Although T2DM is fortunately rare in antipsychotic-treated youth, its prevalence (odds ratio [OR] = 8.176, 95% CI = 7.139-9.362) and incidence (OR = 1.450, 95% CI = 1.101-1.911, p = 0.006) were higher than in healthy controls. Similarly, T2DM prevalence (OR = 3.475, 95% CI = 3.019-4.001, p < 0.0001) and incidence (OR = 5.376, 95% CI = 4.004-7.233, p < 0.0001, excluding one outlying study) were higher than in psychiatric controls. Antipsychotics should only be used after lower-risk interventions failed, and inappropriately low clinical metabolic monitoring must be remedied.
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