Antipsychotic effects on estimated 10-year coronary heart disease risk in the CATIE schizophrenia study
- PMID: 18775645
- PMCID: PMC2614656
- DOI: 10.1016/j.schres.2008.07.006
Antipsychotic effects on estimated 10-year coronary heart disease risk in the CATIE schizophrenia study
Abstract
Objective: Persons with schizophrenia die earlier than the general population, in large part due to cardiovascular disease. The study objective was to examine effects of different antipsychotic treatments on estimates of 10-year coronary heart disease (CHD) risk calculated by the Framingham Heart Study formula.
Method: Change in 10-year risk for CHD was compared between treatment groups in 1125 patients followed for 18 months or until treatment discontinuation in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Schizophrenia Trial.
Results: The covariate-adjusted mean change in 10-year CHD risk differed significantly between treatments. Olanzapine was associated with a 0.5% (SE 0.3) increase and quetiapine, a 0.3% (SE 0.3) increase; whereas risk decreased in patients treated with perphenazine, -0.5% (SE 0.3), risperidone, -0.6% (SE 0.3), and ziprasidone -0.6% (SE 0.4). The difference in 10-year CHD risk between olanzapine and risperidone was statistically significant (p=0.004). Differences in estimated 10-year CHD risk between drugs were most marked in the tertile of subjects with a baseline CHD risk of at least 10%. Among individual CHD risk factors used in the Framingham formula, only total and HDL cholesterol levels differed between treatments.
Conclusions: These results indicate that the impact on 10-year CHD risk differs significantly between antipsychotic agents, with olanzapine producing the largest elevation in CHD risk of the agents studied in CATIE.
Figures
| Sample sizes by visit and treatment group are: | |||||
| visit | olanzapine | perphenazine | quetiapine | risperidone | ziprasidone |
| 3 | 269 | 208 | 257 | 261 | 140 |
| 6 | 200 | 130 | 163 | 175 | 74 |
| 12 | 157 | 85 | 109 | 126 | 55 |
| 18 | 129 | 66 | 64 | 97 | 37 |
| Sample sizes by visit and treatment group are: | |||||
| visit | olanzapine | perphenazine | quetiapine | risperidone | ziprasidone |
| 3 | 161 | 122 | 179 | 157 | 89 |
| 6 | 117 | 82 | 108 | 108 | 43 |
| 12 | 96 | 49 | 72 | 79 | 35 |
| 18 | 79 | 41 | 45 | 63 | 24 |
| Sample sizes by visit and treatment group are: | |||||
| visit | olanzapine | perphenazine | quetiapine | risperidone | ziprasidone |
| 3 | 108 | 86 | 78 | 104 | 49 |
| 6 | 83 | 48 | 55 | 67 | 30 |
| 12 | 61 | 36 | 37 | 47 | 20 |
| 18 | 50 | 25 | 19 | 34 | 13 |
References
-
- Allison DB, Fontaine KR, et al. The distribution of body mass index among individuals with and without schizophrenia. J Clin Psychiatry. 1999;60(4):215–220. - PubMed
-
- Allison DB, Mentore JL, et al. Antipsychotic-induced weight gain: a comprehensive research synthesis. Am J Psychiatry. 1999;156(11):1686–1696. - PubMed
-
- American Diabetes Association and American Psychiatric Association. Consensus Development Conference on Antipsychotic Drugs and Obesity and Diabetes. Diabetes Care. 2004;27(2):596–558. - PubMed
-
- Atmaca M, Kuloglu M, et al. Weight gain, serum leptin and triglyceride levels in patients with schizophrenia on antipsychotic treatment with quetiapine, olanzapine and haloperidol. Schizophrenia Research. 2003;60(1):99–100. - PubMed
-
- Brown C, Goetz J, et al. A psychiatric rehabilitation approach to weight loss. Psychiatr Rehabil J. 2006;29(4):267–273. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
