4.5 Article

The Associations between Erythropoietic Response with Inflammation Markers and Perfluorinated Chemicals in Hemodialysis Patients

Journal

HEALTHCARE
Volume 11, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/healthcare11030442

Keywords

continuous erythropoietin receptor activator; erythropoiesis-stimulating agents; hemodialysis; inflammation; erythropoietic response; perfluorinated chemicals

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This study investigated the impact of inflammation and environmental toxins on the erythropoietic response of hemodialysis patients receiving ESA treatment. The results suggest that age, glucose, chloride, liver function, and inflammation are associated with the frequency of fixed CERA dosage administration.
Erythropoiesis-stimulating agents (ESA) are used to treat anemia in hemodialysis (HD) patients. We investigated the role of inflammation and accumulation of environmental toxins (perfluorinated chemicals (PFCs), such as perfluorooctanoic acid and perfluorooctane sulfonate) in the erythropoietic response of HD patients who receive a fixed monthly continuous erythropoietin receptor activator (CERA) dosage. Forty-five patients underwent three successive phases of ESA treatment for two months each (phase one: 100 mu g CERA once monthly; phase two: 50 mu g CERA twice monthly; phase three: 100 mu g CERA once monthly). Patient data were collected to determine the association of various factors with erythropoietic response (change in hematocrit). Liquid chromatography-tandem mass spectrometry was used to analyze perfluorinated chemicals. Twenty-eight patients exhibited a poor erythropoietic response that was significantly associated with: age > 80 years, initial hematocrit > 36%, glucose > 200 mg/dL, alanine aminotransferase > 21 U/L, c-reactive protein > 1 mg/dL, interleukin-6 > 10 ng/mL, lactate dehydrogenase <= 190 U/L, and chloride <= 93 mEq/L. There was also a borderline significant association between inflammation and PFCs, although PFCs failed to show any impact on ESA response. Age, glucose, chloride, liver function, and inflammation may be associated with cost-effective fixed CERA dosage administered at an increased frequency.

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