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The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients

BACKGROUND: Uremic pruritus or chronic kidney disease-associated pruritus (CKD-aP) is a frequent compromising symptom in end-stage renal disease. Despite the little attention paid to drugs used among hemodialysis (HD) patients, investigating medications used in this population of patients and examin...

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Autores principales: Azimi, Seyyede Zeinab, Alizadeh, Narges, Ramezanzadeh, Elham, Monfared, Ali, Leili, Ehsan Kazemnejad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854926/
https://www.ncbi.nlm.nih.gov/pubmed/36685022
http://dx.doi.org/10.4103/jrms.jrms_633_21
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author Azimi, Seyyede Zeinab
Alizadeh, Narges
Ramezanzadeh, Elham
Monfared, Ali
Leili, Ehsan Kazemnejad
author_facet Azimi, Seyyede Zeinab
Alizadeh, Narges
Ramezanzadeh, Elham
Monfared, Ali
Leili, Ehsan Kazemnejad
author_sort Azimi, Seyyede Zeinab
collection PubMed
description BACKGROUND: Uremic pruritus or chronic kidney disease-associated pruritus (CKD-aP) is a frequent compromising symptom in end-stage renal disease. Despite the little attention paid to drugs used among hemodialysis (HD) patients, investigating medications used in this population of patients and examining the status of CKD-aP may lead to the identification of medications that improve or worsen the pruritus condition. We aimed to assess the role of underlying diseases-related drugs on CKD-aP in HD patients. MATERIALS AND METHODS: We performed a case − control study on HD patients aged over 18 years old. The demographic data and clinical parameters including HD parameters, drug history, dermatologic assessments, and laboratory examination were assessed. RESULTS: We compared 128 patients with CKD-aP as cases and 109 patients without CKD-aP as controls. Cases were on the longer course of dialysis (44.69 ± 43.24 months for cases vs. 38.87 ± 50.73 months for controls; P = 0.02). In multiple analyses of variables related to CKD-aP, backward LR logistic regression revealed that only atorvastatin (P = 0.036) was considered to be a predictive factor associated with CKD-aP. Thus, the use of atorvastatin reduced the index of CKD-aP (95% confidence interval: 0.256–0.954, odd's Ratio = 0.494). CONCLUSION: Atorvastatin was associated with decreased frequencies of CKD-aP among HD patients in our study. This knowledge may guide further clinical trials to evaluate atorvastatin's immunomodulatory and anti-inflammatory effects on the CKD-aP in HD populations.
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spelling pubmed-98549262023-01-21 The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients Azimi, Seyyede Zeinab Alizadeh, Narges Ramezanzadeh, Elham Monfared, Ali Leili, Ehsan Kazemnejad J Res Med Sci Original Article BACKGROUND: Uremic pruritus or chronic kidney disease-associated pruritus (CKD-aP) is a frequent compromising symptom in end-stage renal disease. Despite the little attention paid to drugs used among hemodialysis (HD) patients, investigating medications used in this population of patients and examining the status of CKD-aP may lead to the identification of medications that improve or worsen the pruritus condition. We aimed to assess the role of underlying diseases-related drugs on CKD-aP in HD patients. MATERIALS AND METHODS: We performed a case − control study on HD patients aged over 18 years old. The demographic data and clinical parameters including HD parameters, drug history, dermatologic assessments, and laboratory examination were assessed. RESULTS: We compared 128 patients with CKD-aP as cases and 109 patients without CKD-aP as controls. Cases were on the longer course of dialysis (44.69 ± 43.24 months for cases vs. 38.87 ± 50.73 months for controls; P = 0.02). In multiple analyses of variables related to CKD-aP, backward LR logistic regression revealed that only atorvastatin (P = 0.036) was considered to be a predictive factor associated with CKD-aP. Thus, the use of atorvastatin reduced the index of CKD-aP (95% confidence interval: 0.256–0.954, odd's Ratio = 0.494). CONCLUSION: Atorvastatin was associated with decreased frequencies of CKD-aP among HD patients in our study. This knowledge may guide further clinical trials to evaluate atorvastatin's immunomodulatory and anti-inflammatory effects on the CKD-aP in HD populations. Wolters Kluwer - Medknow 2022-11-25 /pmc/articles/PMC9854926/ /pubmed/36685022 http://dx.doi.org/10.4103/jrms.jrms_633_21 Text en Copyright: © 2022 Journal of Research in Medical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Azimi, Seyyede Zeinab
Alizadeh, Narges
Ramezanzadeh, Elham
Monfared, Ali
Leili, Ehsan Kazemnejad
The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title_full The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title_fullStr The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title_full_unstemmed The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title_short The impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
title_sort impact of underlying diseases-related drugs on the chronic kidney disease-associated pruritus in hemodialysis patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854926/
https://www.ncbi.nlm.nih.gov/pubmed/36685022
http://dx.doi.org/10.4103/jrms.jrms_633_21
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