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Cardiovascular effects of antipsychotics
James W Michelsen1, Jonathan M Meyer
1University of California, San Diego, Department of Medicine, CA, USA. james.michelsen2@va.gov
Insights
Schizophrenia patients face high cardiovascular risks due to lifestyle and antipsychotic medications. Atypical antipsychotics significantly increase this risk through metabolic side effects like weight gain and diabetes.
Area of Science:
- Psychiatry
- Cardiology
- Pharmacology
Background:
- Schizophrenia patients exhibit high cardiovascular disease (CVD) mortality.
- CVD risk is exacerbated by lifestyle factors and comorbidities like dyslipidemia, metabolic syndrome, and Type 2 diabetes.
- Antipsychotic medications are a significant contributor to cardiovascular risk in this population.
Purpose of the Study:
- To review the cardiovascular risks associated with antipsychotic medication treatment.
- To elucidate the mechanisms underlying these risks, particularly metabolic adverse effects.
- To compare cardiovascular risks among different antipsychotic agents, focusing on atypical antipsychotics.
Main Methods:
- Literature review of antipsychotic cardiovascular effects.
- Analysis of mechanisms, including muscarinic cholinergic antagonism, alpha(1)-adrenergic antagonism, and cardiac conduction.
- Focus on metabolic adverse effects such as weight gain, dyslipidemia, and diabetes mellitus.
Main Results:
- Cardiovascular risks from antipsychotics include tachycardia, orthostatic hypotension, and sudden death.
- Since 2000, focus has shifted to metabolic adverse effects.
- Atypical antipsychotics are particularly associated with weight gain, dyslipidemia, and diabetes mellitus, increasing cardiovascular burden.
Conclusions:
- Antipsychotic treatment poses significant cardiovascular risks to schizophrenia patients.
- Metabolic adverse effects, especially from atypical antipsychotics, are a primary driver of this risk.
- Understanding these risks is crucial for managing cardiovascular health in schizophrenia.
Abstract:
There is great concern over cardiovascular disease in the schizophrenic population owing to the high incidence of cardiovascular mortality. Increased cardiovascular mortality is related to lifestyle choices (e.g., smoking and sedentary lifestyle) and a high prevalence of comorbid medical conditions, including dyslipidemia, the metabolic syndrome and Type 2 diabetes. One factor that increases cardiovascular risk is the medications used to treat the core features of schizophrenia. Adverse cardiovascular effects of antipsychotic treatment have been recognized for many decades, especially tachycardia, orthostatic hypotension and rare instances of sudden death; but, since 2000, there has been a significant shift in the focus of risk perception. The older antipsychotic literature is replete with papers primarily concerned with the physiological consequences of muscarinic cholinergic antagonism, alpha(1)-adrenergic antagonism or receptors associated with cardiac conduction, but the current literature recognizes that, for most antipsychotic-exposed patients, the more significant cardiovascular burden of treatment is mediated by metabolic adverse effects such as weight gain, dyslipidemia and diabetes mellitus. The purpose of this review is to examine the cardiovascular risks of treatment with antipsychotic medications, elucidating relevant mechanisms and differences between various agents, especially for metabolic adverse effects seen with atypical antipsychotics.
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