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Cardiometabolic Risk in Patients With First-Episode Schizophrenia Spectrum Disorders: Baseline Results From the RAISE-ETP Study
Abstract
IMPORTANCE: The fact that individuals with schizophrenia have high cardiovascular morbidity and mortality is well established. However, risk status and moderators or mediators in the earliest stages of illness are less clear. OBJECTIVE: To assess cardiometabolic risk in first-episode schizophrenia spectrum disorders (FES) and its relationship to illness duration, antipsychotic treatment duration and type, sex, and race/ethnicity. DESIGN, SETTING, AND PARTICIPANTS: Baseline results of the Recovery After an Initial Schizophrenia Episode (RAISE) study, collected between July 22, 2010, and July 5, 2012, from 34 community mental health facilities without major research, teaching, or clinical FES programs. Patients were aged 15 to 40 years, had research-confirmed diagnoses of FES, and had less than 6 months of lifetime antipsychotic treatment. EXPOSURE: Prebaseline antipsychotic treatment was based on the community clinician's and/or patient's decision. MAIN OUTCOMES AND MEASURES: Body composition and fasting lipid, glucose, and insulin parameters. RESULTS: In 394 of 404 patients with cardiometabolic data (mean [SD] age, 23.6 [5.0] years; mean [SD] lifetime antipsychotic treatment, 47.3 [46.1] days), 48.3% were obese or overweight, 50.8% smoked, 56.5% had dyslipidemia, 39.9% had prehypertension, 10.0% had hypertension, and 13.2% had metabolic syndrome. Prediabetes (glucose based, 4.0%; hemoglobin A1c based, 15.4%) and diabetes (glucose based, 3.0%; hemoglobin A1c based, 2.9%) were less frequent. Total psychiatric illness duration correlated significantly with higher body mass index, fat mass, fat percentage, and waist circumference (all P<.01) but not elevated metabolic parameters (except triglycerides to HDL-C ratio [P=.04]). Conversely, antipsychotic treatment duration correlated significantly with higher non-HDL-C, triglycerides, and triglycerides to HDL-C ratio and lower HDL-C and systolic blood pressure (all P≤.01). In multivariable analyses, olanzapine was significantly associated with higher triglycerides, insulin, and insulin resistance, whereas quetiapine fumarate was associated with significantly higher triglycerides to HDL-C ratio (all P≤.02). CONCLUSIONS AND RELEVANCE: In patients with FES, cardiometabolic risk factors and abnormalities are present early in the illness and likely related to the underlying illness, unhealthy lifestyle, and antipsychotic medications, which interact with each other. Prevention of and early interventions for psychiatric illness and treatment with lower-risk agents, routine antipsychotic adverse effect monitoring, and smoking cessation interventions are needed from the earliest illness phases.
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“In patients with first-episode schizophrenia spectrum disorders, cardiometabolic risk factors were present early in the illness; this was related to the underlying disorder, unhealthy lifestyle and antipsychotic medications, which interact with each other.437”
From 2016 ESC/EAS Guidelines for the Management of Dyslipidaemias (2016) · cites this paper as [437]
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Is autonomous motivation the key to maintaining an active lifestyle in first‐episode psychosis?
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Physical Health and Drug Safety in Individuals with Schizophrenia
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Elevated allostatic load early in the course of schizophrenia
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Specialised early intervention teams for recent-onset psychosis
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Crosstalk between Schizophrenia and Metabolic Syndrome: The Role of Oxytocinergic Dysfunction
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Clinical management of comorbid diabetes and psychotic disorders
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Treatment following myocardial infarction in patients with schizophrenia
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Second to none: rationale, timing, and clinical management of clozapine use in schizophrenia
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Metadata
- Authors
- Correll, C. U., Robinson, D. G., Schooler, N. R., Brunette, M. F., Mueser, K. T., Rosenheck, R. A., Marcy, P., Addington, J., Estroff, S. E., Robinson, J., Penn, D. L., Azrin, S., Goldstein, A., Severe, J., Heinssen, R., & Kane, J. M.
- Affiliations
- Northwell Health (US)
- Geisel School of Medicine at Dartmouth, Dartmouth, New Hampshire7Bureau of Behavioral Health, Department of Health and Human Services, Dartmouth, New Hampshire
- Boston University (US)
- Yale University (US)
- University of Calgary (CA)
- University of North Carolina at Chapel Hill (US)
- Nathan Kline Institute for Psychiatric Research (US)
- National Institute of Mental Health (US)
- ORCID
- Venue
- JAMA Psychiatry
- Publisher
- American Medical Association (AMA)
- Published
- 2014-12-01
- Volume
- 71
- Issue
- 12
- Pages
- 1350
- ISSN
- 2168-622X (ISSN-L)
- OpenAlex
- W2134164029
- Cited by
- 384
- References
- 88
- Citations by year
- 2026: 11 · 2025: 18 · 2024: 27 · 2023: 22 · 2022: 33 · 2021: 35 · 2020: 40 · 2019: 31 · 2018: 39 · 2017: 45 · 2016: 39 · 2015: 39 · 2014: 2
- FWCI
- 31.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- JAMA Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (HHSN271200900019C)
- National Institute of Mental Health (R03MH112053)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Infectious Diseases › HIV-related health complications and treatments
- Keywords
- cardiometabolic risk, first-episode schizophrenia, schizophrenia spectrum disorders, antipsychotic treatment duration, olanzapine, metabolic syndrome, dyslipidemia, insulin resistance, prediabetes, obesity, smoking, hypertension, body composition, HDL cholesterol
- MeSH terms
- Adolescent, Adult, Blood Glucose, Body Composition, Cardiovascular Diseases, Ethnicity, Female, Humans, Insulin, Lipids, Male, Middle Aged, Obesity, Prospective Studies, Psychotic Disorders, Risk Factors, Schizophrenia, Sex Factors, Time Factors, Antipsychotic Agents, Metabolic Syndrome, Overweight, Young Adult
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