Using a pharmacogenomic algorithm to guide the treatment of depression
Autor: | Joanna M. Biernacka, L L Eisterhold, Josiah D. Allen, J J Jordan, Maureen S. Drews, Joel G. Winner, David A. Mrazek, R S Nesheim, Daniel K. Hall-Flavin, Karen Snyder |
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Rok vydání: | 2012 |
Předmět: |
Adult
Male medicine.medical_specialty Genotyping Techniques Pharmacogenomic Testing Pilot Projects Ambulatory Care Facilities Cohort Studies Cellular and Molecular Neuroscience Patient satisfaction Cytochrome P-450 Enzyme System Internal medicine genomics Medicine Humans Receptor Serotonin 5-HT2A Dosing Prospective Studies Prospective cohort study Psychiatry Biological Psychiatry Depression (differential diagnoses) Aged Psychiatric Status Rating Scales Serotonin Plasma Membrane Transport Proteins pharmacogenomics Depressive Disorder Major business.industry psychiatric treatment Hamilton Rating Scale for Depression personalized medicine Middle Aged Antidepressive Agents Psychiatry and Mental health Treatment Outcome Pharmacogenetics Cohort depression Female Original Article business Algorithms Cohort study |
Zdroj: | Translational Psychiatry |
ISSN: | 2158-3188 |
Popis: | The objective of this study was to evaluate the potential benefit of utilizing a pharmacogenomic testing report to guide the selection and dosing of psychotropic medications in an outpatient psychiatric practice. The non-randomized, open label, prospective cohort study was conducted from September 2009 to July 2010. In the first cohort, depressed patients were treated without the benefit of pharmacogenomic testing (the unguided group). A DNA sample was obtained from patients in the unguided group, but the results were not shared with either the physicians or patients until the end of the 8-week study period. In the second cohort (the guided group), testing results were provided at the beginning of the 8-week treatment period. Depression ratings were collected at baseline and after 2 weeks, 4 weeks and 8 weeks of treatment using the Quick Inventory of Depressive Symptomatology, Clinician Rated (QIDS-C16) and the 17-item Hamilton Rating Scale for Depression (HAM-D17). Clinician and patient satisfaction was also assessed. The reduction in depressive symptoms achieved within the guided treatment group was greater than the reduction of depressive symptoms in the unguided treatment group using either the QIDS-C16 (P=0.002) or HAM-D17 (P=0.04). We concluded that a rapidly available pharmacogenomic interpretive report provided clinical guidance that was associated with improved clinical outcomes for depressed patients treated in an outpatient psychiatric clinic setting. |
Databáze: | OpenAIRE |
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