Litcius/Paper detail

Skeletal muscle mass is associated with erythropoietin response in hemodialysis patients

Tomoaki Takata, Yukari Mae, Kentaro Yamada, Sosuke Taniguchi, Shintaro Hamada, Marie Yamamoto, Takuji Iyama, Hajime Isomoto

2021BMC Nephrology18 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Hyporesponsiveness to erythropoietin stimulating agent (ESA) is associated with poor outcomes in patients with chronic kidney disease. Although ESA hyporesponsiveness and sarcopenia have a common pathophysiological background, clinical evidence linking them is scarce. The purpose of the study was to investigate the relationship between ESA responsiveness and skeletal muscle mass in hemodialysis patients. METHODS: This cross-sectional study analyzed 70 patients on maintenance hemodialysis who were treated with ESA. ESA responsiveness was evaluated by erythropoietin resistance index (ERI), calculated as a weekly dose of ESA divided by body weight and hemoglobin (IU/kg/week/dL), and a weekly dose of ESA/hemoglobin (IU/week/dL). A dose of ESA is equivalated to epoetin β. Correlations between ESA responsiveness and clinical parameters including skeletal muscle mass were analyzed. RESULTS: Among the 70 patients, ERI was positively correlated to age (p < 0.002) and negatively correlated to height (p < 0.001), body weight (p < 0.001), BMI (p < 0.001), skeletal muscle mass (p < 0.001), transferrin saturation (TSAT) (p = 0.049), and zinc (p = 0.006). In the multiple linear regression analysis, TSAT, zinc, and skeletal muscle mass were associated with ERI and weekly ESA dose/hemoglobin. CONCLUSIONS: Skeletal muscle mass was the independent predictor for ESA responsiveness as well as TSAT and zinc. Sarcopenia is another target for the management of anemia in patients with hemodialysis.

Topics & Concepts

MedicineInternal medicineSarcopeniaAnemiaHemodialysisErythropoietinTransferrin saturationNephrologyKidney diseaseBody mass indexHemoglobinGastroenterologySkeletal muscleEndocrinologyIron deficiencyErythropoietin and Anemia TreatmentDialysis and Renal Disease ManagementIron Metabolism and Disorders