Literature DB >> 22535158

Erythropoietin resistance and survival in non-dialysis patients with stage 4-5 chronic kidney disease and heart disease.

M Ángeles Guerrero-Riscos1, Rafael Montes-Delgado, María Seda-Guzmán, Juan M Praena-Fernández.   

Abstract

INTRODUCTION: Patients with chronic kidney disease (CKD) frequently suffer from heart disease as well. The combination of the two processes can exacerbate inflammation, resulting in increases in both resistance to erythropoietin (EPO) and mortality.
OBJECTIVES: The aim of this study was to determine the prevalence of heart disease in a representative group of non-dialysis patients with stage 4-5 CKD, and the influence of that entity on EPO requirements and on mortality during a period of 36 months.
METHODS: 134 patients (68% on EPO at the beginning, increasing to 72.3% during follow-up) were monitored for 36 months. To evaluate the dose-response effect of EPO therapy, we used the erythropoietin resistance index (ERI) calculated as the weekly weight-adjusted dose of EPO divided by the haemoglobin level. The ERI was determined both initially and during the last six months before the end of the study.
RESULTS: 39 patients (29.1%) had history of heart disease; 22 (16.4%) had suffered from heart failure (HF). The ERI was higher in patients with a history of heart disease or HF and those treated with drugs acting on the renin-angiotensin system (ACE inhibitors or ARBs). Using ERI as the dependent variable in the multivariate analysis, the variables that composed the final model were ferritin, haemoglobin, glomerular filtration rate and history of HF. The 36 month mortality rate (n=39 patients) was higher in the group having ERI above the median (2.6IU/week/kg/gram of haemoglobin in 100ml) (P=.002), and in the groups with heart disease (P=.001) or HF (P=.001) according to the Kaplan-Meier survival analysis.
CONCLUSIONS: Patients with history of heart disease or HF have a higher ERI, and all of these characteristics are associated with lower survival. ERI can be considered a marker for risk of death in the short to-medium term.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22535158     DOI: 10.3265/Nefrologia.pre2012.Jan.11111

Source DB:  PubMed          Journal:  Nefrologia        ISSN: 0211-6995            Impact factor:   2.033


  4 in total

1.  Renal prognoses by different target hemoglobin levels achieved by epoetin beta pegol dosing to chronic kidney disease patients with hyporesponsive anemia to erythropoiesis-stimulating agent: a multicenter open-label randomized controlled study.

Authors:  Kazuhiko Tsuruya; Terumasa Hayashi; Hiroyasu Yamamoto; Hiroki Hase; Shinichi Nishi; Kunihiro Yamagata; Masaomi Nangaku; Takashi Wada; Yukari Uemura; Yasuo Ohashi; Hideki Hirakata
Journal:  Clin Exp Nephrol       Date:  2021-01-07       Impact factor: 2.801

2.  Baseline Soluble Anti-erythropoietin Antibody Level Is an Independent Associated Factor for Follow-Up Erythropoietin Demand in Maintenance Dialysis Patients With End-Stage Renal Disease: A Prospective Cohort Study.

Authors:  Ying Zhang; Shi-Zhu Bian; Kun Yang; Yiqing Wang; Sha Tang; Weili Wang; Daihong Wang; Ling Nie; Jinghong Zhao
Journal:  Front Med (Lausanne)       Date:  2020-04-07

3.  An emerging need for developing new models for myocardial infarction as a chronic complex disease: lessons learnt from animal vs. human studies on cardioprotective effects of Erythropoietin in reperfused myocardium.

Authors:  Soroush Seifirad
Journal:  Front Physiol       Date:  2014-02-11       Impact factor: 4.566

4.  In search of potential predictors of erythropoiesis-stimulating agents (ESAs) hyporesponsiveness: a population-based study.

Authors:  Ylenia Ingrasciotta; Viviana Lacava; Ilaria Marcianò; Francesco Giorgianni; Giovanni Tripepi; Graziella D' Arrigo; Alessandro Chinellato; Daniele Ugo Tari; Domenico Santoro; Gianluca Trifirò
Journal:  BMC Nephrol       Date:  2019-09-14       Impact factor: 2.388

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.