Evidence map›Paper›PMID 28340079›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2017

Measured glomerular filtration rate does not improve prediction of mortality by cystatin C and creatinine.

Per-Ola Sundin, Per Sjöström, Ian Jones, Lovisa A Olsson, Ruzan Udumyan, Anders Grubb, Veronica Lindström, Scott Montgomery

Abstract read
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. GFR estimated with creatinine rather than cystatin C is more reflective of the true risk of adverse outcomes with low GFR in kidney transplant recipients.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Optimally predicting mortality with kidney function markers is not the same as optimally determining how kidney function predicts mortality.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    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

8 authors.

Per-Ola SundinSchool of Medical Sciences, Örebro University, SE 701 82 Örebro, Sweden.
Per SjöströmSchool of Medical Sciences, Örebro University, SE 701 82 Örebro, Sweden.
Ian JonesSchool of Medical Sciences, Örebro University, SE 701 82 Örebro, Sweden.
Lovisa A OlssonSchool of Medical Sciences, Örebro University, SE 701 82 Örebro, Sweden.
Ruzan UdumyanClinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden.
Anders GrubbDepartment of Clinical Chemistry, Laboratory Medicine, University Hospital, Lund, Sweden.
Veronica LindströmDepartment of Clinical Chemistry, Laboratory Medicine, University Hospital, Lund, Sweden.
Scott MontgomeryClinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCystatin C may add explanatory power for associations with mortality in combination with other filtration markers, possibly indicating pathways other than glomerular filtration rate (GFR). However, this has not been firmly established since interpretation of associations independent of measured GFR (mGFR) is limited by potential multicollinearity between markers of GFR. The primary aim of this study was to assess associations between cystatin C and mortality, independent of mGFR. A secondary aim was to evaluate the utility of combining cystatin C and creatinine to predict mortality risk.

methodsCox regression was used to assess the associations of cystatin C and creatinine with mortality in 1157 individuals referred for assessment of plasma clearance of iohexol.

resultsSince cystatin C and creatinine are inversely related to mGFR, cystatin C - 1 and creatinine - 1 were used. After adjustment for mGFR, lower cystatin C - 1 (higher cystatin C concentration) and higher creatinine - 1 (lower creatinine concentration) were independently associated with increased mortality. When nested models were compared, avoiding the potential influence of multicollinearity, the independence of the associations was supported. Among models combining the markers of GFR, adjusted for demographic factors and comorbidity, cystatin C - 1 and creatinine - 1 combined explained the largest proportion of variance in associations with mortality risk ( R 2  = 0.61). Addition of mGFR did not improve the model.

conclusionsOur results suggest that both creatinine and cystatin C have independent associations with mortality not explained entirely by mGFR and that mGFR does not offer a more precise mortality risk assessment than these endogenous filtration markers combined.

Indexed as

Glomerular Filtration RateModels, StatisticalAdolescentAdultAgedAged, 80 and overBiomarkersComorbidityCreatinineCystatin CFemaleHumansIohexolKidney DiseasesMaleMiddle AgedBiomarkersCreatinineCystatin CIohexolcreatininecystatin CepidemiologyGFRprognosis

Identifiers

PMID28340079
PMCPMC6433429

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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.