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      Initial responsiveness to darbepoetin alfa and its contributing factors in non-dialysis chronic kidney disease patients in Japan

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          Abstract

          Background

          Hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is associated with cardiovascular events and poor renal outcome in patients with chronic kidney disease (CKD). This study aimed to investigate the initial responsiveness to darbepoetin alfa (DA) and its contributing factors using the data from the BRIGHTEN.

          Methods

          Of 1980 patients enrolled at 168 facilities, 1695 were included in this analysis [285 patients were excluded mainly due to lack of hemoglobin (Hb) values]. The initial ESA response index (iEResI) was defined as a ratio of Hb changes over 12 weeks after DA administration per weight-adjusted total DA dose and contributing factors to iEResI were analyzed.

          Results

          The mean age was 70 ± 12 years (male 58.8%; diabetic nephropathy 27.6%). The median creatinine and mean Hb levels at DA initiation were 2.62 mg/dL and 9.8 g/dL, respectively. The most frequent number of DA administration during 12 weeks was 3 times (41.1%), followed by 4 (15.6%) times with a wide distribution of the total DA dose (15–900 μg). Remarkably, 225 patients (13.3%) did not respond to DA. Multivariate analysis showed that male gender, hypoglycemic agent use, iron supplementation, high eGFR, low Hb, low CRP, low NT-proBNP, and low urinary protein–creatinine ratio were independently associated with better initial response to DA ( P =  < 0.0001, 0.0108, < 0.0001, 0.0476, < 0.0001, 0.0004, 0.0435, and 0.0009, respectively).

          Conclusions

          Non-responder to DA accounted for 13.3% of patients with non-dialysis CKD. Iron supplementation, low CRP, low NT-proBNP, and less proteinuria were predictive and modifiable factors associated with better initial response to DA.

          Electronic supplementary material

          The online version of this article (10.1007/s10157-020-01969-7) contains supplementary material, which is available to authorized users.

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          Most cited references36

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          Revised equations for estimated GFR from serum creatinine in Japan.

          Estimation of glomerular filtration rate (GFR) is limited by differences in creatinine generation among ethnicities. Our previously reported GFR-estimating equations for Japanese had limitations because all participants had a GFR less than 90 mL/min/1.73 m2 and serum creatinine was assayed in different laboratories. Diagnostic test study using a prospective cross-sectional design. New equations were developed in 413 participants and validated in 350 participants. All samples were assayed in a central laboratory. Hospitalized Japanese patients in 80 medical centers. Patients had not participated in the previous study. Measured GFR (mGFR) computed from inulin clearance. Estimated GFR (eGFR) by using the modified isotope dilution mass spectrometry (IDMS)-traceable 4-variable Modification of Diet in Renal Disease (MDRD) Study equation using the previous Japanese Society of Nephrology Chronic Kidney Disease Initiative (JSN-CKDI) coefficient of 0.741 (equation 1), the previous JSN-CKDI equation (equation 2), and new equations derived in the development data set: modified MDRD Study using a new Japanese coefficient (equation 3), and a 3-variable Japanese equation (equation 4). Performance of equations was assessed by means of bias (eGFR - mGFR), accuracy (percentage of estimates within 15% or 30% of mGFR), root mean squared error, and correlation coefficient. In the development data set, the new Japanese coefficient was 0.808 (95% confidence interval, 0.728 to 0.829) for the IDMS-MDRD Study equation (equation 3), and the 3-variable Japanese equation (equation 4) was eGFR (mL/min/1.73 m2) = 194 x Serum creatinine(-1.094) x Age(-0.287) x 0.739 (if female). In the validation data set, bias was -1.3 +/- 19.4 versus -5.9 +/- 19.0 mL/min/1.73 m2 (P = 0.002), and accuracy within 30% of mGFR was 73% versus 72% (P = 0.6) for equation 3 versus equation 1 and -2.1 +/- 19.0 versus -7.9 +/- 18.7 mL/min/1.73 m(2) (P < 0.001) and 75% versus 73% (P = 0.06) for equation 4 versus equation 2 (P = 0.06), respectively. Most study participants had chronic kidney disease, and some may have had changing GFRs. The new Japanese coefficient for the modified IDMS-MDRD Study equation and the new Japanese equation are more accurate for the Japanese population than the previously reported equations.
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            Correction of anemia with epoetin alfa in chronic kidney disease.

            Anemia, a common complication of chronic kidney disease, usually develops as a consequence of erythropoietin deficiency. Recombinant human erythropoietin (epoetin alfa) is indicated for the correction of anemia associated with this condition. However, the optimal level of hemoglobin correction is not defined. In this open-label trial, we studied 1432 patients with chronic kidney disease, 715 of whom were randomly assigned to receive a dose of epoetin alfa targeted to achieve a hemoglobin level of 13.5 g per deciliter and 717 of whom were assigned to receive a dose targeted to achieve a level of 11.3 g per deciliter. The median study duration was 16 months. The primary end point was a composite of death, myocardial infarction, hospitalization for congestive heart failure (without renal replacement therapy), and stroke. A total of 222 composite events occurred: 125 events in the high-hemoglobin group, as compared with 97 events in the low-hemoglobin group (hazard ratio, 1.34; 95% confidence interval, 1.03 to 1.74; P=0.03). There were 65 deaths (29.3%), 101 hospitalizations for congestive heart failure (45.5%), 25 myocardial infarctions (11.3%), and 23 strokes (10.4%). Seven patients (3.2%) were hospitalized for congestive heart failure and myocardial infarction combined, and one patient (0.5%) died after having a stroke. Improvements in the quality of life were similar in the two groups. More patients in the high-hemoglobin group had at least one serious adverse event. The use of a target hemoglobin level of 13.5 g per deciliter (as compared with 11.3 g per deciliter) was associated with increased risk and no incremental improvement in the quality of life. (ClinicalTrials.gov number, NCT00211120 [ClinicalTrials.gov].). Copyright 2006 Massachusetts Medical Society.
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              A trial of darbepoetin alfa in type 2 diabetes and chronic kidney disease.

              Anemia is associated with an increased risk of cardiovascular and renal events among patients with type 2 diabetes and chronic kidney disease. Although darbepoetin alfa can effectively increase hemoglobin levels, its effect on clinical outcomes in these patients has not been adequately tested. In this study involving 4038 patients with diabetes, chronic kidney disease, and anemia, we randomly assigned 2012 patients to darbepoetin alfa to achieve a hemoglobin level of approximately 13 g per deciliter and 2026 patients to placebo, with rescue darbepoetin alfa when the hemoglobin level was less than 9.0 g per deciliter. The primary end points were the composite outcomes of death or a cardiovascular event (nonfatal myocardial infarction, congestive heart failure, stroke, or hospitalization for myocardial ischemia) and of death or end-stage renal disease. Death or a cardiovascular event occurred in 632 patients assigned to darbepoetin alfa and 602 patients assigned to placebo (hazard ratio for darbepoetin alfa vs. placebo, 1.05; 95% confidence interval [CI], 0.94 to 1.17; P=0.41). Death or end-stage renal disease occurred in 652 patients assigned to darbepoetin alfa and 618 patients assigned to placebo (hazard ratio, 1.06; 95% CI, 0.95 to 1.19; P=0.29). Fatal or nonfatal stroke occurred in 101 patients assigned to darbepoetin alfa and 53 patients assigned to placebo (hazard ratio, 1.92; 95% CI, 1.38 to 2.68; P<0.001). Red-cell transfusions were administered to 297 patients assigned to darbepoetin alfa and 496 patients assigned to placebo (P<0.001). There was only a modest improvement in patient-reported fatigue in the darbepoetin alfa group as compared with the placebo group. The use of darbepoetin alfa in patients with diabetes, chronic kidney disease, and moderate anemia who were not undergoing dialysis did not reduce the risk of either of the two primary composite outcomes (either death or a cardiovascular event or death or a renal event) and was associated with an increased risk of stroke. For many persons involved in clinical decision making, this risk will outweigh the potential benefits. (ClinicalTrials.gov number, NCT00093015.) 2009 Massachusetts Medical Society
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                Author and article information

                Contributors
                naritai@med.niigata-u.ac.jp
                Journal
                Clin Exp Nephrol
                Clin Exp Nephrol
                Clinical and Experimental Nephrology
                Springer Singapore (Singapore )
                1342-1751
                1437-7799
                19 September 2020
                19 September 2020
                2021
                : 25
                : 2
                : 110-119
                Affiliations
                [1 ]Department of Kidney Disease and Hypertension, Osaka General Medical Center, Osaka, Japan
                [2 ]GRID grid.26999.3d, ISNI 0000 0001 2151 536X, Division of Nephrology and Endocrinology, , The University of Tokyo Graduate School of Medicine, ; Tokyo, Japan
                [3 ]Translational Research Center for Medical Innovation, Kobe, Japan
                [4 ]Fukuoka Renal Clinic, Fukuoka, Japan
                [5 ]GRID grid.9707.9, ISNI 0000 0001 2308 3329, Department of Nephrology and Laboratory Medicine, Faculty of Medicine, , Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, ; Kanazawa, Japan
                [6 ]GRID grid.69566.3a, ISNI 0000 0001 2248 6943, Division of Clinical Pharmacology and Therapeutics, , Tohoku University Graduate School of Pharmaceutical Sciences and Faculty of Pharmaceutical Sciences, ; Sendai, Japan
                [7 ]GRID grid.414811.9, ISNI 0000 0004 1763 8123, Department of Nephrology and Rheumatology, , Kagawa Prefectural Central Hospital, ; Takamatsu, Japan
                [8 ]GRID grid.470097.d, ISNI 0000 0004 0618 7953, Department of Nephrology, , Hiroshima University Hospital, ; Hiroshima, Japan
                [9 ]GRID grid.411898.d, ISNI 0000 0001 0661 2073, Division of Nephrology and Hypertension, Department of Internal Medicine, , The Jikei University School of Medicine, ; Tokyo, Japan
                [10 ]GRID grid.470115.6, Division of Nephrology, , Toho University Ohashi Medical Center, ; Tokyo, Japan
                [11 ]GRID grid.177174.3, ISNI 0000 0001 2242 4849, Department of Health Care Administration and Management, , Graduate School of Medical Sciences, Kyushu University, ; Fukuoka, Japan
                [12 ]Nakayamadera Imai Clinic, Takarazuka, Japan
                [13 ]GRID grid.490945.5, Mitsukoshi Health and Welfare Foundation, ; Tokyo, Japan
                [14 ]GRID grid.268441.d, ISNI 0000 0001 1033 6139, School of Data Science, , Yokohama City University, ; Yokohama, Japan
                [15 ]GRID grid.410714.7, ISNI 0000 0000 8864 3422, Division of Nephrology, Department of Medicine, , Showa University School of Medicine, ; Tokyo, Japan
                [16 ]GRID grid.458430.e, Course of Safety Management in Health Care Sciences, , Graduate School of Health Care Sciences, Jikei Institute, ; Osaka, Japan
                [17 ]GRID grid.27476.30, ISNI 0000 0001 0943 978X, Department of Nephrology, , Nagoya University Graduate School of Medicine, ; Nagoya, Japan
                [18 ]GRID grid.260975.f, ISNI 0000 0001 0671 5144, Division of Clinical Nephrology and Rheumatology, , Niigata University Graduate School of Medical and Dental Sciences, ; 757 Ichibancho Asahimachidori Chuo-ku, Niigata, 951-8510 Japan
                Author information
                http://orcid.org/0000-0001-7692-3096
                Article
                1969
                10.1007/s10157-020-01969-7
                7880978
                32949295
                fc063d7d-770d-4754-9b10-a7c67f7fdf8b
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 9 January 2020
                : 4 August 2020
                Categories
                Original Article
                Custom metadata
                © Japanese Society of Nephrology 2021

                Nephrology
                erythropoiesis-stimulating agents,hyporesponsiveness,darbepoetin alfa,chronic kidney disease,pre-dialysis

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