Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial
Objective This ancillary study examined the impact of depressive symptoms on the effectiveness of a urate‐lowering therapy in the context of a clinical trial. Methods Participants included 67 adults (ages 18–40) with elevated blood pressure who were enrolled in a double‐blind, randomized, crossover...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
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Wiley
2020-12-01
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Series: | ACR Open Rheumatology |
Online Access: | https://doi.org/10.1002/acr2.11192 |
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author | Sylvie Mrug Catheryn Orihuela Elizabeth Rahn Amy Mudano Jeffrey Foster Kenneth Saag Angelo Gaffo |
author_facet | Sylvie Mrug Catheryn Orihuela Elizabeth Rahn Amy Mudano Jeffrey Foster Kenneth Saag Angelo Gaffo |
author_sort | Sylvie Mrug |
collection | DOAJ |
description | Objective This ancillary study examined the impact of depressive symptoms on the effectiveness of a urate‐lowering therapy in the context of a clinical trial. Methods Participants included 67 adults (ages 18–40) with elevated blood pressure who were enrolled in a double‐blind, randomized, crossover clinical trial evaluating the effectiveness of allopurinol (300 mg/d) versus placebo to decrease blood pressure. Depressive symptoms were measured at the beginning of each 4‐week phase with the Center for Epidemiological Studies Depression scale (CESD‐10). Serum urate (sUA) was assessed at the beginning and end of each treatment phase. Compliance to treatment was measured by having detectable oxypurinol levels. Linear regressions tested associations between depressive symptoms and change in sUA in each phase, adjusting for sex and race. Logistic regression predicted compliance from depressive symptoms. Results Participants had a mean age of 27 years and were 64% male and 39% African American. sUA levels decreased during the allopurinol treatment period but did not change during the placebo period. Higher depressive symptoms at pretreatment were associated with an attenuated urate‐lowering response during the allopurinol phase (β = 0.24, p < 0.05), but had no effect on sUA changes during the placebo phase. Depressive symptoms were not associated with treatment compliance assessed by oxypurinol levels. Conclusion Depressive symptoms were associated with reduced efficacy of allopurinol treatment for hyperuricemia in a clinical trial targeting hypertension. Studies evaluating the efficacy of urate‐lowering therapies may benefit from screening for depressive symptoms. |
first_indexed | 2024-04-09T14:15:36Z |
format | Article |
id | doaj.art-cd351b7e16ff4f49b5aa355fe6d1adcf |
institution | Directory Open Access Journal |
issn | 2578-5745 |
language | English |
last_indexed | 2024-04-09T14:15:36Z |
publishDate | 2020-12-01 |
publisher | Wiley |
record_format | Article |
series | ACR Open Rheumatology |
spelling | doaj.art-cd351b7e16ff4f49b5aa355fe6d1adcf2023-05-05T13:06:03ZengWileyACR Open Rheumatology2578-57452020-12-0121271071410.1002/acr2.11192Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical TrialSylvie Mrug0Catheryn Orihuela1Elizabeth Rahn2Amy Mudano3Jeffrey Foster4Kenneth Saag5Angelo Gaffo6University of Alabama at BirminghamUniversity of Alabama at BirminghamUniversity of Alabama at BirminghamUniversity of Alabama at BirminghamUniversity of Alabama at BirminghamUniversity of Alabama at BirminghamUniversity of Alabama at Birmingham and Birmingham VA Medical Center Birmingham AlabamaObjective This ancillary study examined the impact of depressive symptoms on the effectiveness of a urate‐lowering therapy in the context of a clinical trial. Methods Participants included 67 adults (ages 18–40) with elevated blood pressure who were enrolled in a double‐blind, randomized, crossover clinical trial evaluating the effectiveness of allopurinol (300 mg/d) versus placebo to decrease blood pressure. Depressive symptoms were measured at the beginning of each 4‐week phase with the Center for Epidemiological Studies Depression scale (CESD‐10). Serum urate (sUA) was assessed at the beginning and end of each treatment phase. Compliance to treatment was measured by having detectable oxypurinol levels. Linear regressions tested associations between depressive symptoms and change in sUA in each phase, adjusting for sex and race. Logistic regression predicted compliance from depressive symptoms. Results Participants had a mean age of 27 years and were 64% male and 39% African American. sUA levels decreased during the allopurinol treatment period but did not change during the placebo period. Higher depressive symptoms at pretreatment were associated with an attenuated urate‐lowering response during the allopurinol phase (β = 0.24, p < 0.05), but had no effect on sUA changes during the placebo phase. Depressive symptoms were not associated with treatment compliance assessed by oxypurinol levels. Conclusion Depressive symptoms were associated with reduced efficacy of allopurinol treatment for hyperuricemia in a clinical trial targeting hypertension. Studies evaluating the efficacy of urate‐lowering therapies may benefit from screening for depressive symptoms.https://doi.org/10.1002/acr2.11192 |
spellingShingle | Sylvie Mrug Catheryn Orihuela Elizabeth Rahn Amy Mudano Jeffrey Foster Kenneth Saag Angelo Gaffo Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial ACR Open Rheumatology |
title | Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial |
title_full | Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial |
title_fullStr | Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial |
title_full_unstemmed | Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial |
title_short | Depressive Symptoms and the Effectiveness of a Urate‐Lowering Therapy in a Clinical Trial |
title_sort | depressive symptoms and the effectiveness of a urate lowering therapy in a clinical trial |
url | https://doi.org/10.1002/acr2.11192 |
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