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Correlation of antidepressant target dose optimization and achievement of glycemic control

INTRODUCTION: Depression is a recognized cause of disability globally with a propensity to be comorbid in patients with diabetes, leading to poorer health-related outcomes. Although a number of studies have investigated the correlation between improvement in depression and chronic disease, none have...

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Autores principales: Grisham-Takac, Catlin, Lai, Phillip, Srinivasa, Maaya, Vasquez, Lindsay, Rascati, Karen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: College of Psychiatric & Neurologic Pharmacists 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322821/
https://www.ncbi.nlm.nih.gov/pubmed/30627498
http://dx.doi.org/10.9740/mhc.2019.01.012
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author Grisham-Takac, Catlin
Lai, Phillip
Srinivasa, Maaya
Vasquez, Lindsay
Rascati, Karen L.
author_facet Grisham-Takac, Catlin
Lai, Phillip
Srinivasa, Maaya
Vasquez, Lindsay
Rascati, Karen L.
author_sort Grisham-Takac, Catlin
collection PubMed
description INTRODUCTION: Depression is a recognized cause of disability globally with a propensity to be comorbid in patients with diabetes, leading to poorer health-related outcomes. Although a number of studies have investigated the correlation between improvement in depression and chronic disease, none have reported on achievement of target doses of antidepressant therapies and diabetes control. The objective of this study is to determine the influence of antidepressant dosing optimization on reducing hemoglobin A1c (HbA1c). METHODS: This was a retrospective cohort study of patients seen at CommUnityCare Health Centers who were initiated on an antidepressant and had uncontrolled diabetes (HbA1c > 7%). Eligible patients were followed for 12 months after initiation and separated into those who achieved target dose and those who did not. Patient health questionnaire scores were collected when available in an attempt to quantify change in depressive symptoms. RESULTS: A total of 178 patients met inclusion criteria with 76 achieving an optimal dose (target group) and 102 patients below optimal dose (control group) at the end of the study period. Patients in both groups were similar at baseline with an HbA1c of 9.29% compared to 9.24% in the target and control groups, respectively. At the end of the study period, more patients in the target group achieved an HbA1c < 7% (22.9%, n = 48 vs 4.3%, n = 23, respectively; P < .05). DISCUSSION: These results suggest that optimization of antidepressant dosing in patients with diabetes may lead to an increased likelihood of reaching goal HbA1c < 7% although correlation to improvement of depression remains unknown.
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spelling pubmed-63228212019-01-09 Correlation of antidepressant target dose optimization and achievement of glycemic control Grisham-Takac, Catlin Lai, Phillip Srinivasa, Maaya Vasquez, Lindsay Rascati, Karen L. Ment Health Clin Original Research INTRODUCTION: Depression is a recognized cause of disability globally with a propensity to be comorbid in patients with diabetes, leading to poorer health-related outcomes. Although a number of studies have investigated the correlation between improvement in depression and chronic disease, none have reported on achievement of target doses of antidepressant therapies and diabetes control. The objective of this study is to determine the influence of antidepressant dosing optimization on reducing hemoglobin A1c (HbA1c). METHODS: This was a retrospective cohort study of patients seen at CommUnityCare Health Centers who were initiated on an antidepressant and had uncontrolled diabetes (HbA1c > 7%). Eligible patients were followed for 12 months after initiation and separated into those who achieved target dose and those who did not. Patient health questionnaire scores were collected when available in an attempt to quantify change in depressive symptoms. RESULTS: A total of 178 patients met inclusion criteria with 76 achieving an optimal dose (target group) and 102 patients below optimal dose (control group) at the end of the study period. Patients in both groups were similar at baseline with an HbA1c of 9.29% compared to 9.24% in the target and control groups, respectively. At the end of the study period, more patients in the target group achieved an HbA1c < 7% (22.9%, n = 48 vs 4.3%, n = 23, respectively; P < .05). DISCUSSION: These results suggest that optimization of antidepressant dosing in patients with diabetes may lead to an increased likelihood of reaching goal HbA1c < 7% although correlation to improvement of depression remains unknown. College of Psychiatric & Neurologic Pharmacists 2019-01-04 /pmc/articles/PMC6322821/ /pubmed/30627498 http://dx.doi.org/10.9740/mhc.2019.01.012 Text en © 2019 CPNP. The Mental Health Clinician is a publication of the College of Psychiatric and Neurologic Pharmacists. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Grisham-Takac, Catlin
Lai, Phillip
Srinivasa, Maaya
Vasquez, Lindsay
Rascati, Karen L.
Correlation of antidepressant target dose optimization and achievement of glycemic control
title Correlation of antidepressant target dose optimization and achievement of glycemic control
title_full Correlation of antidepressant target dose optimization and achievement of glycemic control
title_fullStr Correlation of antidepressant target dose optimization and achievement of glycemic control
title_full_unstemmed Correlation of antidepressant target dose optimization and achievement of glycemic control
title_short Correlation of antidepressant target dose optimization and achievement of glycemic control
title_sort correlation of antidepressant target dose optimization and achievement of glycemic control
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322821/
https://www.ncbi.nlm.nih.gov/pubmed/30627498
http://dx.doi.org/10.9740/mhc.2019.01.012
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