Evidence map›Paper›PMID 27198863›Full record

ArticleScientific reports2016

Proteinuria as a Therapeutic Target in Advanced Chronic Kidney Disease: a Retrospective Multicenter Cohort Study.

Chang-Hsu Chen, Hon-Yen Wu, Chieh-Li Wang, Feng-Jung Yang, Pei-Chen Wu, Szu-Chun Hung, Wei-Chih Kan, Chung-Wei Yang, Chih-Kang Chiang, Jenq-Wen Huang and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Observational
  10. Proteinuria in COVID-19.Clinical kidney journal · 2021
    Review
  11. Article
  12. Article
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

11 authors.

Chang-Hsu ChenDivision of Nephrology, Tungs' Taichung MetroHarbor Hospital, Taichung City, Taiwan.
Hon-Yen WuDivision of Nephrology, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
Chieh-Li WangDivision of Nephrology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.
Feng-Jung YangDivision of Nephrology, National Taiwan University Hospital Yun-Lin Branch, Yunlin County, Taiwan.
Pei-Chen WuDivision of Nephrology, Da Chien General Hospital, Miaoli County, Taiwan.
Szu-Chun HungDivision of Nephrology, Buddhist Tzu Chi Hospital Taipei Branch, New Taipei City, Taiwan.
Wei-Chih KanDepartment of Nephrology, Chi Mei Medical Center, Tainan City, Taiwan.
Chung-Wei YangDivision of Nephrology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu City, Taiwan.
Chih-Kang ChiangDivision of Nephrology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.
Jenq-Wen HuangDivision of Nephrology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.
Kuan-Yu HungDivision of Nephrology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current evidence of proteinuria reduction as a surrogate target in advanced chronic kidney disease (CKD) is incomplete due to lack of patient-pooled database. We retrospectively studied a multicenter cohort of 1891 patients who were enrolled in the nationwide multidisciplinary pre-end stage renal disease care program with a baseline glomerular filtration rate (GFR) <45 mL/min/1.73 m(2) and followed longitudinally to investigate the effect of the change in proteinuria on renal death (defined as composite of dialysis and death occurring before initiation of dialysis). The group with a change in proteinuria ≤0.30 g/g (n = 1261) had lower cumulative probabilities of renal death (p < 0.001). In a linear regression model, a higher baseline proteinuria and a greater increase in proteinuria were associated with faster annual GFR decline. Cox's analysis showed that every 1 unit increase in natural log(baseline proteinuria, 10 g/g) and every 0.1 g/g increase in the change in proteinuria resulted in 67% (HR = 1.67, 95% CI: 1.46-1.91) and 1% (HR = 1.01, 95% CI: 1.01-1.01) greater risk of renal death respectively after adjusting for the effects of the other covariates. Our study provided a patient-based evidence to support proteinuria as a therapeutic target in advanced CKD.

Indexed as

AgedAged, 80 and overCreatinineDisease ProgressionEvidence-Based MedicineFemaleGlomerular Filtration RateHumansLinear ModelsLongitudinal StudiesMaleMiddle AgedProteinuriaRenal Insufficiency, ChronicRetrospective StudiesRisk FactorsCreatinine

Identifiers

PMID27198863
PMCPMC4873744

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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.