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Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients.
Curr Pharm Biotechnol. 2017; 18(4):303-308.CP

Abstract

Chronic kidney disease (CKD) is an important health problem, because of unsuccessful outcomes such as CKD progression to end stage renal disease and high risk of cardiovascular disease (CVD). Anemia, associated with CKD, is considered a non-traditional risk factor for CVD which may contribute to faster CKD progression. Anemia treatment with erythropoiesis-stimulating agents (ESAs) seems to exert non-hematopoietic effects on different tissues and organs, including cardiovascular system and kidneys. On the other hand, clinical use of high doses of short-acting ESAs and higher target hemoglobin level were associated with higher risk of CVD. Literature data indicate the usefulness of long-acting ESAs in treatment of anemia in non-dialysis CKD patients. In particular, continuous erythropoietin receptor activator seems to be a good choice in these patients because of its efficiency, safety and monthly administration. Continuous but slower erythropoietin receptor activation, using methoxy polyethylene glycol-epoetin beta (MPG-EPO), administered once a month, slowly corrects anemia without exceeding the recommended hemoglobin level. An overview of the available literature may suggest nephroprotective and cardiovascular protective effects of MPG-EPO. It seems possible that anemia treatment with a novel ESAs, MPG-EPO in early stages of CKD may reduce CVD risk in these patients and delay CKD progression. This review of available literature evaluates the correlation between continuous erythropoietin receptor activation using MPG-EPO and CKD progression and CVD risk in non-dialysis CKD patients.

Authors+Show Affiliations

Department of Nephrology, Hypertension and Family Medicine, Zeromski Street 113, 90-596 Lodz. Poland.Department of Nephrology, Hypertension and Family Medicine, Medical University of Lodz, Lodz. Poland.Department of Nephrology, Hypertension and Family Medicine, Medical University of Lodz, Lodz. Poland.

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

28137221

Citation

Piotr, Bartnicki, et al. "Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent With Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients." Current Pharmaceutical Biotechnology, vol. 18, no. 4, 2017, pp. 303-308.
Piotr B, Mariusz S, Jacek R. Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients. Curr Pharm Biotechnol. 2017;18(4):303-308.
Piotr, B., Mariusz, S., & Jacek, R. (2017). Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients. Current Pharmaceutical Biotechnology, 18(4), 303-308. https://doi.org/10.2174/1389201018666170127104801
Piotr B, Mariusz S, Jacek R. Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent With Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients. Curr Pharm Biotechnol. 2017;18(4):303-308. PubMed PMID: 28137221.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients. AU - Piotr,Bartnicki, AU - Mariusz,Stepien, AU - Jacek,Rysz, PY - 2016/09/15/received PY - 2016/11/22/revised PY - 2017/01/23/accepted PY - 2017/2/1/pubmed PY - 2017/12/30/medline PY - 2017/2/1/entrez KW - Erythropoietin KW - anemia KW - chronic kidney disease KW - continuous erythropoietin receptor activator KW - methoxy polyethylene glycol-epoetin beta SP - 303 EP - 308 JF - Current pharmaceutical biotechnology JO - Curr Pharm Biotechnol VL - 18 IS - 4 N2 - Chronic kidney disease (CKD) is an important health problem, because of unsuccessful outcomes such as CKD progression to end stage renal disease and high risk of cardiovascular disease (CVD). Anemia, associated with CKD, is considered a non-traditional risk factor for CVD which may contribute to faster CKD progression. Anemia treatment with erythropoiesis-stimulating agents (ESAs) seems to exert non-hematopoietic effects on different tissues and organs, including cardiovascular system and kidneys. On the other hand, clinical use of high doses of short-acting ESAs and higher target hemoglobin level were associated with higher risk of CVD. Literature data indicate the usefulness of long-acting ESAs in treatment of anemia in non-dialysis CKD patients. In particular, continuous erythropoietin receptor activator seems to be a good choice in these patients because of its efficiency, safety and monthly administration. Continuous but slower erythropoietin receptor activation, using methoxy polyethylene glycol-epoetin beta (MPG-EPO), administered once a month, slowly corrects anemia without exceeding the recommended hemoglobin level. An overview of the available literature may suggest nephroprotective and cardiovascular protective effects of MPG-EPO. It seems possible that anemia treatment with a novel ESAs, MPG-EPO in early stages of CKD may reduce CVD risk in these patients and delay CKD progression. This review of available literature evaluates the correlation between continuous erythropoietin receptor activation using MPG-EPO and CKD progression and CVD risk in non-dialysis CKD patients. SN - 1873-4316 UR - https://www.unboundmedicine.com/medline/citation/28137221/Methoxy_Polyethylene_Glycol_Epoetin_Beta_as_a_Novel_Erythropoiesis_Stimulating_Agent_with_Possible_Nephroprotective_and_Cardiovascular_Protective_Effects_in_Non_Dialysis_Chronic_Kidney_Disease_Patients_ DB - PRIME DP - Unbound Medicine ER -