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Sponsored by: |
University of Iowa |
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Information provided by: | University of Iowa |
ClinicalTrials.gov Identifier: | NCT00585273 |
Over the last decade, second generation antipsychotics have been increasingly utilized. Since their introduction, however, atypical antipsychotics have been increasingly associated with significant metabolic complications including hyperlipidemia, insulin resistance/diabetes mellitus, and obesity. These metabolic complications increase the risk for cardiovascular disease in populations with an already elevated risk.
The initial goal of the proposed study is to identify early signs of endothelial dysfunction and vascular disease in those treated with atypical antipsychotics. The identification of early signs of vascular disease may further link metabolic complications with any cardiovascular risk.
Demonstration of changes in vascular function associated with atypical antipsychotics represents an important identifiable intermediate of more long-term cardiovascular risk.
The second goal of the proposed study is to identify genetic factors that may be associated with the development of cardiovascular disease, which can later serve as a guide to predict risk. Accurate prediction of risk may facilitate the future development of an empirical, risk-based, individualized selection process for antipsychotic medications.
Aim 1: To quantify the role of antipsychotic-induced metabolic complications on the development of vascular disease using measures of endothelial function.
Hypothesis 1: Atypical antipsychotics will lead to greater impairments in endothelial function, evidenced by decreased flow-mediated dilation from baseline measures and compared with changes over time in controls. Medication-induced metabolic complications will be temporally associated with these impairments in endothelial function.
Aim 2: To investigate the role of candidate pharmacogenetic polymorphisms with cardiovascular and metabolic complications of atypical antipsychotics.
Hypothesis 2: Profiles of polymorphisms at receptors targeted by atypical antipsychotics will be associated with impaired cardiovascular function and metabolic complications.
Condition |
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Bipolar Disorder Schizophrenia |
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | Cardiovascular Complications of First-Line, Second-Generation Antipsychotics |
Estimated Enrollment: | 50 |
Study Start Date: | September 2007 |
Estimated Study Completion Date: | December 2012 |
Groups/Cohorts |
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1
Incident users of risperidone, quetiapine, or olanzapine.
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2
Non-users of second generation antipsychotics
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Ages Eligible for Study: | 18 Years to 50 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Thirty patients, 18 - 50 years of age, who are being started on a first-line, second-generation, antipsychotic associated with weight gain (risperidone, olanzapine, or quetiapine) for the treatment of an affective or psychotic disorder, will be invited to participate. Participants must not have taken any of these antipsychotics or clozapine in the preceding three months. Another twenty psychiatric controls not taking antipsychotic medications will also be enrolled. Statistically, controls will serve primarily to compare changes in flow-mediated dilation over time rather than for direct comparison of variables between groups. Participation will be voluntary and initiated upon clinician or self-referral.
Inclusion Criteria:
Exclusion Criteria:
Contact: Lois Warren, B.S.W. | (319) 353-4523 | lois-warren@uiowa.edu |
Contact: Jess G Fiedorowicz, M.D., M.S. | (319) 353-4333 | jess-fiedorowicz@uiowa.edu |
United States, Iowa | |
University of Iowa Hospitals and Clinics | Recruiting |
Iowa City, Iowa, United States, 52242 | |
Principal Investigator: Jess G Fiedorowicz, M.D., M.S. |
Principal Investigator: | Jess G Fiedorowicz, M.D., M.S. | University of Iowa |
Responsible Party: | University of Iowa ( Jess G. Fiedorowicz ) |
Study ID Numbers: | 200703764, University of Iowa GCRC #0740 |
Study First Received: | December 19, 2007 |
Last Updated: | December 29, 2007 |
ClinicalTrials.gov Identifier: | NCT00585273 History of Changes |
Health Authority: | United States: Institutional Review Board |
Schizophrenia Affective Disorders, Psychotic Tranquilizing Agents Mental Disorders Bipolar Disorder Psychotropic Drugs |
Mood Disorders Central Nervous System Depressants Psychotic Disorders Antipsychotic Agents Schizophrenia and Disorders with Psychotic Features |
Tranquilizing Agents Bipolar Disorder Physiological Effects of Drugs Psychotropic Drugs Central Nervous System Depressants Antipsychotic Agents Pharmacologic Actions |
Schizophrenia Affective Disorders, Psychotic Mental Disorders Therapeutic Uses Mood Disorders Central Nervous System Agents Schizophrenia and Disorders with Psychotic Features |