Evidence map›Paper›PMID 32185544›Full record

Observational studyClinical and experimental nephrology2020

Early responsiveness to continuous erythropoietin receptor activator predicts renal prognosis and is determined by a novel antioxidative marker in non-dialysis chronic kidney disease: a prospective, observational, single-center study.

Jun Ino, Eri Kasama, Mio Kodama, Takako Harada, Keitaro Sato, Hitoshi Eizumi, Youichiro Kawashima, Kosaku Nitta

Abstract readObservational Study
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In one paragraph

Observational study in Clinical and experimental nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Jun InoDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan. pikkun46@hotmail.com.
Eri KasamaDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Mio KodamaDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Takako HaradaDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Keitaro SatoDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Hitoshi EizumiDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Youichiro KawashimaDepartment of Nephrology, Toda Central General Hospital, 1-19-3 Hon-cho, Toda city, Saitama, 335-0023, Japan.
Kosaku NittaDepartment of Internal Medicine IV, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjyuku-ku, Tokyo, 162-0054, Japan.
Tokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResponsiveness to erythropoietin-stimulating agents (ESAs) is important for anemia management in chronic kidney disease (CKD). We assessed the effects of a continuous erythropoietin receptor activator (CERA) on renoprotection beyond anemia management and the correlation between the responsiveness to ESAs and oxidative stress markers in CKD.

methodsThis single-center, prospective, observational study was conducted over 24 months. We administered CERA to 35 non-dialysis patients with hemoglobin (Hb) < 11 g/dL and examined the results of the serum diacron-reactive oxygen metabolite (dROMs) test for oxidative stress markers and biological antioxidant potential (BAP) test for antioxidant markers. We then examined the renoprotective effects of CERA and the responsiveness to CERA.

resultsEighteen patients experienced renal events (doubling of serum creatinine levels, decreased estimated glomerular filtration rate to < 6.0 mL/min/1.73 m

conclusionResponsiveness to CERA during the first 3 months was an important indicator of CKD progression. Moreover, BAP test results determined responsiveness to CERA. This is the first report to show how antioxidant levels can be a potential marker of CERA's ability to control anemia in CKD patients.

Indexed as

AgedAged, 80 and overAnemiaAntioxidantsBiomarkersCreatinineDisease ProgressionErythropoietinFemaleGlomerular Filtration RateHematinicsHemoglobinsHumansMaleMiddle AgedOxidative StressAntioxidantsBiomarkerscontinuous erythropoietin receptor activatorCreatinineErythropoietinHematinicsHemoglobinsPolyethylene GlycolsReactive Oxygen SpeciesChronic kidney diseaseContinuous erythropoietin receptor activatorOxidative stressRenal anemia

Identifiers

PMID32185544
OpenAlexW3011500780

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.