DNA Diagnostics for Minimizing Metabolic Side-Effects of Antipsychotics
NCT ID: NCT00752960
Last Updated: 2008-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
1000 participants
OBSERVATIONAL
2007-01-31
2009-12-31
Brief Summary
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Detailed Description
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The long-term goal of this collaborative study is to identify, for each individual atypical antipsychotic (AAP) medication, the gene variations associated with elevated risk of diabetic metabolic symptoms (DiMS). If such genes are identified, in the future genetic testing may help mental health care professionals choose treatment while minimizing the risk of undesirable side effects of antipsychotics. We propose to develop a novel product termed "Physiotype" to deliver personalized information for each patient on the drug specific risks among aripiprazole, olanzapine, quetiapine, risperidone, and ziprasidone. The Physiotype consists of a multi-gene ensemble of single nucleotide polymorphisms (SNPs) that, interpreted with a biomathematical algorithm, may explain most of the inter-individual differences in DiMS among the 5 AAPs. If this study does identify related genes, genetic tests will be developed to provide patients and health care professionals with tools to identify those patients who are at risk of developing adverse metabolic side effects to antipsychotics.
Conditions
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Keywords
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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A
Patients receiving olanzapine
No interventions assigned to this group
B
patients receiving risperidone
No interventions assigned to this group
C
Patients receiving quetiapine
No interventions assigned to this group
D
Patients receiving aripiprazole
No interventions assigned to this group
E
patients receiving ziprasidone
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* who have taken \>50% of the prescribed dose for the last month.
Exclusion Criteria
18 Years
59 Years
ALL
No
Sponsors
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Hartford Hospital
OTHER
University of Kentucky
OTHER
Genomas, Inc
INDUSTRY
Responsible Party
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Genomas, Inc.
Principal Investigators
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Gualberto Ruano, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Genomas, Inc
Locations
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Hartford Hospital Institute of Living
Hartford, Connecticut, United States
University of Kentucky
Lexington, Kentucky, United States
Countries
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Central Contacts
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Facility Contacts
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Steven Woolley, PhD
Role: primary
John D. Goethe, MD
Role: backup
Jose de Leon, MD
Role: primary
References
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Ruano G, Blair CL, Bower B, Windemuth A, Kocherla M, Aleman Y, Pearlson G, Goethe JW, Schwartz HI. Somatic complications of psychotropic medications in a patient with multiple CYP2 drug metabolism deficiencies. Conn Med. 2007 Apr;71(4):197-200.
de Leon J, Susce MT, Johnson M, Hardin M, Pointer L, Ruano G, Windemuth A, Diaz FJ. A clinical study of the association of antipsychotics with hyperlipidemia. Schizophr Res. 2007 May;92(1-3):95-102. doi: 10.1016/j.schres.2007.01.015. Epub 2007 Mar 8.
Ruano G, Goethe JW, Caley C, Woolley S, Holford TR, Kocherla M, Windemuth A, de Leon J. Physiogenomic comparison of weight profiles of olanzapine- and risperidone-treated patients. Mol Psychiatry. 2007 May;12(5):474-82. doi: 10.1038/sj.mp.4001944. Epub 2007 Jan 2.
Windemuth A, de Leon J, Goethe JW, Schwartz HI, Woolley S, Susce M, Kocherla M, Bogaard K, Holford TR, Seip RL, Ruano G. Validation of candidate genes associated with cardiovascular risk factors in psychiatric patients. Prog Neuropsychopharmacol Biol Psychiatry. 2012 Mar 30;36(2):213-9. doi: 10.1016/j.pnpbp.2011.08.001. Epub 2011 Aug 6.
Related Links
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Institute of Living, Hartford Hospital, Hartford, CT
Other Identifiers
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50R44 MH073291-03
Identifier Type: -
Identifier Source: secondary_id