Evidence map›Paper›PMID 26873651›Full record

Observational studyLupus2016

Predicting decline of kidney function in lupus nephritis using urine biomarkers.

K M Abulaban, H Song, X Zhang, P L Kimmel, J W Kusek, R G Nelson, H I Feldman, R S Vasan, J Ying, M Mauer and 4 more

Abstract readObservational Study
In one paragraph

Observational study in Lupus, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
6.9field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. Ferroptosis and secondary nephrosis.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Urinary biomarkers in lupus nephritis.Journal of translational autoimmunity · 2020
    Review
  13. Article
  14. Utilization of Biomarkers in Lupus Nephritis.Advances in chronic kidney disease · 2019
    Review
  15. Article
  16. Article
  17. Precision medicine in lupus nephritis: can biomarkers get us there?Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  18. Observational
  19. Article
  20. 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

14 authors at 8 institutions in 1 country.

K M AbulabanDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, USA Department of Pediatrics, Helen DeVos Childrens Hospital, Michigan State University, Grand Rapids, USA.
H SongDepartment of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, USA.
X ZhangDepartment of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, USA.
P L KimmelNational Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD.
J W KusekNational Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD.
R G NelsonNational Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, USA.
H I FeldmanDepartment of Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, USA.
R S VasanPreventive Medicine and Cardiology Sections, and Department of Medicine, Boston University School of Medicine, Boston, USA.
J YingDepartment of Environmental Health, University of Cincinnati, Cincinnati, USA.
M MauerDepartment of Pediatrics, University of Minnesota, Minneapolis, USA.
G L NelsestuenDepartment of Pediatrics, University of Minnesota, Minneapolis, USA.
M BennettDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, USA.
H I BrunnerDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, USA.
B H RovinDepartment of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, USA Brad.Rovin@osumc.edu.
National Institute of Diabetes and Digestive and Kidney Diseases · USThe Ohio State University Wexner Medical Center · USCincinnati Children's Hospital Medical Center · USUniversity of Minnesota · USBoston University · USHelen DeVos Children's Hospital · USUniversity of Cincinnati · USUniversity of Pennsylvania · US

Funding

Epidemiology, Pathophysiology and Treatment of Diabetic NephropathyZIADK069062 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NELSON, ROBERT G · 2009 to 2023
$10.1M
Proteomics CoreP50DK096418 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI DEVARAJAN, PRASAD · 2012 to 2021
$8.4M
Discovery & Validation of Biomarkers of Kidney PathologyU01DK096927 · NIDDK · OHIO STATE UNIVERSITY · PI ROVIN, BRAD H · 2013 to 2017
$2.0M
Forecasters of futute and progressive CDK in patients with microvascular glomerulU01DK085673 · NIDDK · OHIO STATE UNIVERSITY · PI KLEIN, JON, ROVIN, BRAD H · 2009 to 2013
$2.0M
NIDDK NIH HHS P50 DK096418NIDDK NIH HHS U01 DK085673NIDDK NIH HHS U01 DK096927
6 · The paper itself

Abstract

objectiveTo evaluate candidate biomarkers to predict future renal function decline (RFD) in children and adults with lupus nephritis (LN).

methodsAt the time of enrollment into prospective observational LN cohort studies liver-type fatty acid binding protein (LFABP), albumin, monocyte chemoattractant protein-1 (MCP-1), uromodulin, transferrin, and hepcidin were measured in urine samples of two cohorts of patients with LN, one followed at a pediatric (cohort-1; n = 28) and one at an adult institution (cohort-2; n = 69). The primary outcome was RFD, defined in cohort-1 as a decrease in estimated glomerular filtration rate (eGFR) of ≥20% and in cohort-2 as a sustained increase of ≥25% in serum creatinine concentration (SCr), both from baseline.

resultsAll patients (n = 97) had normal eGFR or SCr at the time of urine collection at baseline. RFD occurred in 29% (8/28) of patients in cohort-1 during a mean follow-up of 6.1 months, and in 30% (21/69) of those in cohort-2 during a mean follow-up of 60 months. Individually, in cohort-1, levels of MCP-1, transferrin, LFABP, and albumin were higher in the RFD group than those who maintained renal function, with statistical significance for LFABP and albumin. In cohort-2 the RFD group also had higher levels of urine MCP-1 and albumin than others. The combination of LFABP, MCP-1, albumin, and transferrin had good predictive accuracy for RFD in both cohorts (area under the ROC curve = 0.77-0.82).

conclusionThe combinatorial urine biomarker LFABP, MCP-1, albumin, and transferrin shows promise as a predictor of renal functional decline in LN, and warrants further investigation.

Indexed as

AdolescentAdultBiomarkersChemokine CCL2ChildCreatinineFemaleGlomerular Filtration RateHepcidinsHumansKidney Function TestsLupus NephritisMaleMiddle AgedProspective StudiesTransferrinBiomarkersCCL2 protein, humanChemokine CCL2CreatinineHepcidinsTransferrinUMOD protein, humanUromodulinbiomarkerkidney injurylupus nephritisrenal function declineSLE

Identifiers

PMID26873651
PMCPMC4945408
OpenAlexW2295569311

What OpenQuestion holds

Textmetadata
LicenceTDM
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.