Cardiometabolic Risk of Second-Generation Antipsychotic Medications During First-Time Use in Children and Adolescents
Open accessAbstract
CONTEXT: Cardiometabolic effects of second-generation antipsychotic medications are concerning but have not been sufficiently studied in pediatric and adolescent patients naive to antipsychotic medication. OBJECTIVE: To study the association of second-generation antipsychotic medications with body composition and metabolic parameters in patients without prior antipsychotic medication exposure. DESIGN, SETTING, AND PATIENTS: Nonrandomized Second-Generation Antipsychotic Treatment Indications, Effectiveness and Tolerability in Youth (SATIETY) cohort study, conducted between December 2001 and September 2007 at semi-urban, tertiary care, academic inpatient and outpatient clinics in Queens, New York, with a catchment area of 4.5-million individuals. Of 505 youth aged 4 to 19 years with 1 week or less of antipsychotic medication exposure, 338 were enrolled (66.9%). Of these patients, 272 had at least 1 postbaseline assessment (80.5%), and 205 patients [corrected] completed the study (60.7%). Patients had mood spectrum (n = 130; 47.8%), schizophrenia spectrum (n = 82; 30.1%), and disruptive or aggressive behavior spectrum (n = 60; 22.1%) disorders. Fifteen patients who refused participation or were nonadherent served as a comparison group. INTERVENTION: Treatment with aripiprazole, olanzapine, quetiapine, or risperidone for 12 weeks. MAIN OUTCOME MEASURES: Weight gain and changes in lipid and metabolic parameters. RESULTS: After a median of 10.8 weeks (interquartile range, 10.5-11.2 weeks) of treatment, weight increased by 8.5 kg (95% confidence interval [CI], 7.4 to 9.7 kg) with olanzapine (n = 45), by 6.1 kg (95% CI, 4.9 to 7.2 kg) with quetiapine (n = 36), by 5.3 kg (95% CI, 4.8 to 5.9 kg) with risperidone (n = 135), and by 4.4 kg (95% CI, 3.7 to 5.2 kg) with aripiprazole (n = 41) compared with the minimal weight change of 0.2 kg (95% CI, -1.0 to 1.4 kg) in the untreated comparison group (n = 15). With olanzapine and quetiapine, respectively, mean levels increased significantly for total cholesterol (15.6 mg/dL [95% CI, 6.9 to 24.3 mg/dL] P < .001 and 9.1 mg/dL [95% CI, 0.4 to 17.7 mg/dL] P = .046), triglycerides (24.3 mg/dL [95% CI, 9.8 to 38.9 mg/dL] P = .002 and 37.0 mg/dL [95% CI, 10.1 to 63.8 mg/dL] P = .01), non-high-density lipoprotein (HDL) cholesterol (16.8 mg/dL [95% CI, 9.3 to 24.3 mg/dL] P < .001 and 9.9 mg/dL [95% CI, 1.4 to 18.4 mg/dL] P = .03), and ratio of triglycerides to HDL cholesterol (0.6 [95% CI, 0.2 to 0.9] P = .002 and (1.2 [95% CI, 0.4 to 2.0] P = .004). With risperidone, triglycerides increased significantly (mean level, 9.7 mg/dL [95% CI, 0.5 to 19.0 mg/dL]; P = .04). Metabolic baseline-to-end-point changes were not significant with aripiprazole or in the untreated comparison group. CONCLUSIONS: First-time second-generation antipsychotic medication use was associated with significant weight gain with each medication. Metabolic changes varied among the 4 antipsychotic medications.
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The period of success of pediatric psychopharmacology was followed by challenges including growing awareness of long-term adverse effects of medications and inadequacy of long-term drug surveillance.
“This period of success was followed by a series of challenges, including a growing awareness of the long-term adverse effects of medications and of the inadequacy of long-term drug surveillance.”
From Pediatric psychopharmacology: Too much or too little? (2013) · cites this paper as [45]
The Discussion (page unavailable) reports rapid cardiometabolic changes in antipsychotic-naïve youth and calls for more frequent monitoring, citing suboptimal metabolic monitoring. It does not describe a historical period of success followed by challenges, establish long-term medication adverse effects, or assess the adequacy of long-term drug surveillance. (LLM, conf=0.82)
Experimental — accuracy not yet measuredAtypical antipsychotics, originally thought safer because of decreased risk of tardive dyskinesia, are now known to be at increased risk for cardiometabolic syndrome, particularly in adolescents.
“Originally thought safer because of decreased risk of tardive dyskinesia, these drugs are now known to be at increased risk for cardiometabolic syndrome, particularly in adolescents (45).”
From Pediatric psychopharmacology: Too much or too little? (2013) · cites this paper as [45]
The Introduction and Discussion report cardiometabolic risks of second-generation antipsychotics in children and adolescents, including substantial weight gain and metabolic changes. But the Results say metabolic syndrome developed in only 1.6% during the short study, and the paper does not establish that adolescents are at greater risk than other age groups. Our copy also does not address the claimed historical rationale about reduced tardive dyskinesia. (LLM, conf=0.87)
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References 41 · Cited by 1,050
Research works printed but not linked: 1
- [10]Correll CU Assessing and maximizing the safety and tolerability of antipsychotics used in the treatment of children and adolescents J Clin Psychiatry 2008 69 suppl 4 26 36 18533766
- Authors
- Correll, C. U.
- Affiliations
- Northwell Health (US)
- Corresponding author
- Correll, Christoph U.
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 2009-10-28
- Volume
- 302
- Issue
- 16
- Pages
- 1765
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- PMC
- PMC3055794
- OpenAlex
- W2119763231
- Cited by
- 1,050
- References
- 41
- Citations by year
- 2026: 44 · 2025: 31 · 2024: 37 · 2023: 48 · 2022: 41 · 2021: 44 · 2020: 48 · 2019: 46 · 2018: 49 · 2017: 69 · 2016: 71 · 2015: 72 · 2014: 80 · 2013: 91 · 2012: 102
- FWCI
- 57.52
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- JAMA (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (K23MH001760, MH 01760, P30MH074543, MH 074543-01)
- National Center for Research Resources (M01RR018535)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Keywords
- atypical antipsychotics, cardiometabolic risk, weight gain, lipid metabolism disorders, hypertriglyceridemia, hypercholesterolemia, aripiprazole, olanzapine, quetiapine, risperidone, children and adolescents, body composition, mood disorders, schizophrenia spectrum disorders, disruptive behavior disorders
- MeSH terms
- Aripiprazole, Quetiapine Fumarate, Olanzapine, Adolescent, Benzodiazepines, Body Composition, Child, Child, Preschool, Dibenzothiazepines, Female, Humans, Lipids, Male, Piperazines, Risk, Antipsychotic Agents, Cohort Studies, Quinolones, Weight Gain, Risperidone, Lipid Metabolism
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