Evidence map›Paper›PMID 25388519›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2015

Urinary elafin and kidney injury in hematopoietic cell transplant recipients.

Sangeeta Hingorani, Laura S Finn, Emily Pao, Rick Lawler, Gary Schoch, George B McDonald, Behzad Najafian, Brenda Sandmaier, Ted Gooley

Abstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2015. 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. Review
  3. Article
  4. Review
  5. Review
  6. Acute Kidney Injury in Children after Hematopoietic Cell Transplantation Is Associated with Elevated Urine CXCL10 and CXCL9.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2020
    Observational
  7. Article
  8. Article
  9. Review
  10. Acute kidney injury in HCT: an update.Bone marrow transplantation · 2016
    Review
  11. Review
  12. NIH Consensus development project on criteria for clinical trials in chronic graft-versus-host disease: II. The 2014 Pathology Working Group Report.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
    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.

Sangeeta HingoraniDepartments of Pediatrics, Gastroenterology, and Pathology, University of Washington, Seattle, Washington; Seattle Children's Hospital, Seattle, Washington; and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington sangeeta.hingorani@seattlechildrens.org.
Laura S FinnDepartments of Pediatrics, Gastroenterology, and Pathology, University of Washington, Seattle, Washington; Seattle Children's Hospital, Seattle, Washington; and.
Emily PaoSeattle Children's Hospital, Seattle, Washington; and.
Rick LawlerClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Gary SchochClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
George B McDonaldDepartments of Pediatrics, Gastroenterology, and Pathology, University of Washington, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Behzad NajafianDepartments of Pediatrics, Gastroenterology, and Pathology, University of Washington, Seattle, Washington;
Brenda SandmaierClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Ted GooleyClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Chronic kidney disease in survivors of hematopoietic cell transplantR01DK080860 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI HINGORANI, SANGEETA · 2008 to 2012
$1.6M
NCI NIH HHS CA015704NCI NIH HHS CA018029NCI NIH HHS P01 CA018029NCI NIH HHS P30 CA015704NIDDK NIH HHS 1R01-DK080860-01NIDDK NIH HHS DK080860NIDDK NIH HHS R01 DK080860
6 · The paper itself

Abstract

BACKGROUND AND

objectivesGraft-versus-host disease (GVHD) is associated with kidney injury after hematopoietic cell transplantation (HCT). Because plasma elafin levels correlate with skin GVHD, this study examined urinary elafin as a potential marker of renal inflammation and injury. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Urine was collected prospectively on 205 patients undergoing their first HCT from 2003 to 2010. Collections were done at baseline, weekly through day 100, and monthly through year 1 to measure elafin and urine albumin-to-creatinine ratio (ACR). Associations between urinary elafin levels and microalbuminuria, macroalbuminuria, AKI and CKD, and mortality were examined using Cox proportional hazards or linear regression models. Available kidney biopsy specimens were processed for immunohistochemistry.

resultsMean urinary elafin levels to day 100 were higher in patients with micro- or macroalbuminuria (adjusted mean difference, 529 pg/ml; P=0.03) at day 100 than in those with a normal ACR (adjusted mean difference, 1295 pg/ml; P<0.001). Mean urinary elafin levels were higher in patients with AKI compared with patients without AKI (adjusted mean difference, 558 pg/ml; P<0.01). The average urinary elafin levels within the first 100 days after HCT were higher in patients who developed CKD at 1 year than in patients without CKD (adjusted mean difference, 894 pg/ml; P=0.002). Among allogeneic recipients, a higher proportion of patients with micro- or macroalbuminuria at day 100 also had grade II-IV acute GVHD (80% and 86%, respectively) compared with patients with a normal ACR (58%; global P<0.01). Each increase in elafin of 500 pg/ml resulted in a 10% increase in risk of persistent macroalbuminuria (hazard ratio, 1.10; 95% confidence interval [95% CI], 1.06 to 1.13; P<0.001) and a 7% increase in the risk of overall mortality (95% CI, 1.02 to 1.13, P<0.01). Renal biopsy specimens from a separate cohort of HCT survivors demonstrated elafin staining in distal and collecting duct tubules.

conclusionHigher urinary elafin levels are associated with an increased risk of micro- and macroalbuminuria, AKI and CKD, and death after HCT.

Indexed as

Acute Kidney InjuryAdolescentAdultAgedAlbuminuriaBiomarkersBiopsyCase-Control StudiesChildChild, PreschoolCreatinineElafinFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansBiomarkersCreatinineElafinPI3 protein, humanchronic kidney diseasehematopoietic cell transplantmicroalbuminuriaproteinuriarenal tubular epithelial cells

Identifiers

PMID25388519
PMCPMC4284403

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.