Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/172353
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dc.creatorBelo, L.
dc.creatorRocha, Susana
dc.creatorCoimbra, Susana
dc.creatorCatarino, Cristina
dc.creatorBronze-da-Rocha, E.
dc.creatorRocha-Pereira, Petronila
dc.creatorFaria, Maria do Sameiro
dc.creatorOliveira, José Gerardo
dc.creatorFernandes, João Carlos Esteves
dc.creatorMiranda, Vasco M. P.
dc.creatorSantos-Silva, Alice
dc.date.accessioned2026-02-04T00:20:30Z-
dc.date.available2026-02-04T00:20:30Z-
dc.date.issued2025
dc.identifier.issn0931-0509
dc.identifier.othersigarra:756273
dc.identifier.urihttps://hdl.handle.net/10216/172353-
dc.description.abstract<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background and Aims</jats:title> <jats:p>Anemia is common in patients under regular hemodialysis therapy. Despite treatment with erythropoiesis-stimulating agents (ESA), hypo-responsiveness to this therapy can occur (refractory cases). We studied the association between ESA resistance in hemodialysis patients and potential causes of ineffective treatment, including nutritional, iron metabolism, and inflammatory variables, and dialysis related parameters.</jats:p> </jats:sec> <jats:sec> <jats:title>Method</jats:title> <jats:p>We performed a cross-sectional study involving 289 hemodialysis patients. Ultrafiltration rate adjusted to weight (UFR/W), urea reduction ratio (URR) and Kt/V were obtained for the session where blood samples were collected. Blood analyses were performed by using automated technology or by enzyme-linked commercialized immunoassays, as previously described [1]. Erythropoietin (EPO) resistance index (ERI) was calculated by the formula: EPOdoseperweek (IU)/bodyweight (kg)/hemoglobin (g/dL).</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>The mean age of patients was 68.7 years (±13.6), 240 patients (83%) were under ESA prescription and 186 (64.4%) were receiving intravenous iron. The median (interquartile range) for ERI was 7.1 (3.711.7) IU/kg/g/dL, and for median transferrin saturation (TSAT) was 21.9 (16.828.5) %. ERI was positively correlated with levels of soluble transferrin receptor (sTfR, r = 0.556, P = 7.8×1021; Fig. 1), interleukin (IL)-6 (r = 0.196, P = 0.002), pentraxin 3 (r = 0.192, P = 0.003), C-reactive protein (r = 0.130, P = 0.043) and UFR/W values (r = 0.135, P = 0.037) and inversely correlated with body mass index (r = 0.179, P = 0.005) and levels of iron (r = 0.382, P = 9.2×1010), TSAT (r = 0.340, P = 6.8×108), hepcidin (r = 0.197, P = 0.002) and albumin (r = 0.166, P = 0.010). By performing multivariate linear regression analysis (after normalization of non-normally distributed data), levels of sTfR (ß = 0.487, P &lt; 0.001), iron (ß = 0.176, P = 0.003), and IL-6 (ß = 0.111, P = 0.035), and UFR/W values (ß = 0.168, P = 0.001) were independent predictors of ERI. When iron repleted patients (ferritin 100 µg/L and TSAT 20%) receiving EPO therapy were analyzed separately (n = 138), sTfR and UFR/W were kept in the regression model as predictors of ERI (ß = 0.504, P &lt; 0.001 and ß = 0.207, P = 0.006, respectively); within these patients, those with UFR/W &gt; 10 ml/h/kg presented higher ERI than those below 10 ml/h/kg (Fig. 2).</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Besides lower iron, raised UFR/W and IL-6 are independently associated with hypo-responsiveness to ESA. sTFR seems to be a valuable tool to access ESA-driven erythropoiesis in hemodialysis patients, particularly in iron repleted patients. Our results support the idea that the modulation of inflammation and UFR prescription can improve anemia management.</jats:p> </jats:sec>
dc.language.isoeng
dc.rightsopenAccess
dc.subjectCiências da Saúde
dc.subjectHealth sciences
dc.titleUltrafiltration rate and interleukin-6 levels are independent predictors of erythropoietin resistance in chronic hemodialysis patients
dc.typeOutras Publicações
dc.contributor.uportoFaculdade de Farmácia
dc.identifier.doi10.1093/ndt/gfaf116.0757
dc.identifier.authenticusP-01A-CNM
Appears in Collections:FFUP - Outras Publicações

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