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...

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Main Authors: Sylvie Mrug, Catheryn Orihuela, Elizabeth Rahn, Amy Mudano, Jeffrey Foster, Kenneth Saag, Angelo Gaffo
Format: Article
Language:English
Published: Wiley 2020-12-01
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.
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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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