Evidence map›Paper›PMID 22745274›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2012

Serum β-trace protein and risk of mortality in incident hemodialysis patients.

Tariq Shafi, Rulan S Parekh, Bernard G Jaar, Laura C Plantinga, Pooja C Oberai, John H Eckfeldt, Andrew S Levey, Neil R Powe, Josef Coresh

Open access · greenAbstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Large uremic toxins: an unsolved problem in end-stage kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2018
    Review
  8. Exploring the Clinical Relevance of Providing Increased Removal of Large Middle Molecules.Clinical journal of the American Society of Nephrology : CJASN · 2018
    Review
  9. Observational
  10. Article
  11. Filtration markers as predictors of ESRD and mortality in Southwestern American Indians with type 2 diabetes.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2015
    Article
  12. Novel filtration markers as predictors of all-cause and cardiovascular mortality in US adults.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2013
    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

9 authors at 1 institution in 1 country.

Tariq ShafiDivision of Nephrology, Johns Hopkins University School of Medicine, 301 Mason Lord Drive, Suite 2500, Baltimore, MD 21224-2780, USA. tshafi@jhmi.edu
Rulan S Parekh
Bernard G Jaar
Laura C Plantinga
Pooja C Oberai
John H Eckfeldt
Andrew S Levey
Neil R Powe
Josef Coresh
Johns Hopkins Medicine · US

Funding

Longitudinal Study of DialysisR01DK072367 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PAREKH, RULAN S · 2007 to 2011
$3.7M
Retained Organic Solutes and Clinical Outcomes in HemodialysisR01DK080123 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI POWE, NEIL R. · 2008 to 2012
$3.2M
PROCESS, OUTCOME AND QUALITY OF CARE IN ESRDR01DK059616 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI POWE, NEIL R. · 2000 to 2004
$3.1M
RISK FACTORS FOR CV DISEASE IN A DIALYSIS COHORTR01HL062985 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CORESH, JOSEF · 2000 to 2003
$2.4M
PATIENT ORIENTED RESEARCH IN KIDNEY DISEASEK24DK002643 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI POWE, NEIL R. · 1999 to 2009
$1.4M
Residual Kidney Function in ESRD: Measurements, Serum Markers and OutcomesK23DK083514 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SHAFI, TARIQ · 2010 to 2014
$904k
DIALYSIS CARE: CHOICES, OUTCOMES, COSTS AND TRADEOFFSR01HS008365 · AHRQ · JOHNS HOPKINS UNIVERSITY · PI POWE, NEIL R. · 1994 to 1998
–
AHRQ HHS R01 HS008365AHRQ HHS R01-HS-008365NHLBI NIH HHS R01 HL062985NHLBI NIH HHS R01-HL-62985NIDDK NIH HHS K23 DK083514NIDDK NIH HHS K23-DK-083514NIDDK NIH HHS K24 DK002643NIDDK NIH HHS K24-DK-02643NIDDK NIH HHS R01 DK059616NIDDK NIH HHS R01-DK-059616NIDDK NIH HHS R01 DK072367NIDDK NIH HHS R01-DK-072367NIDDK NIH HHS R01 DK080123NIDDK NIH HHS R01-DK-080123
6 · The paper itself

Abstract

BACKGROUND AND

objectivesResidual kidney function in dialysis patients is associated with better survival, but there are no simple methods for its assessment. β-Trace protein is a novel endogenous filtration marker of kidney function that is not removed during hemodialysis and may serve as a marker for residual kidney function similar to serum creatinine in patients not on dialysis. The objective of this study was to determine the association of serum β-trace protein with mortality in incident hemodialysis patients. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Serum β-trace protein was measured in baseline samples from 503 participants of a national prospective cohort study of incident dialysis patients with enrollment during 1995-1998 and follow-up until 2004. Outcomes were all-cause and cardiovascular disease mortality analyzed using Cox regression adjusted for demographic, clinical, and treatment factors.

resultsSerum β-trace protein levels were higher in individuals with no urine output compared with individuals with urine output (9.0±3.5 versus 7.6±3.1 mg/L; P<0.001). There were 321 deaths (159 deaths from cardiovascular disease) during follow-up (median=3.3 years). Higher β-trace protein levels were associated with higher risk of mortality. The adjusted hazard ratio and 95% confidence interval for all-cause mortality per doubling of serum β-trace protein was 1.36 (1.09-1.69). The adjusted hazard ratios (95% confidence intervals) for all-cause mortality in the middle and highest tertiles compared with the lowest tertile were 0.95 (0.69-1.32) and 1.72 (1.25-2.37). Similar results were noted for cardiovascular disease mortality.

conclusionsThe serum level of β-trace protein is an independent predictor of death and cardiovascular disease mortality in incident hemodialysis patients.

Indexed as

AdultAgedBiomarkersCardiovascular DiseasesCause of DeathChi-Square DistributionFemaleHumansIncidenceIntramolecular OxidoreductasesKidneyKidney Failure, ChronicLinear ModelsLipocalinsMaleMiddle AgedBiomarkersIntramolecular OxidoreductasesLipocalinsprostaglandin R2 D-isomerase

Identifiers

PMID22745274
PMCPMC3430954
OpenAlexW2118281781

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.