Evidence map›Paper›PMID 24918153›Full record

ArticleKidney international2015

Markers of endothelial dysfunction and inflammation predict progression of diabetic nephropathy in African Americans with type 1 diabetes.

Monique S Roy, Malvin N Janal, Juan Crosby, Robert Donnelly

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. A Five-Plasma Protein-Based Algorithm for Predicting Incident CKD in Type 2 Diabetes.Journal of the American Society of Nephrology : JASN · 2026
    Article
  3. Assessment of Eotaxin Concentration in Children with Chronic Kidney Disease.International journal of molecular sciences · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Accelerated Kidney Aging in Diabetes Mellitus.Oxidative medicine and cellular longevity · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Sirtuin 1: A Target for Kidney Diseases.Molecular medicine (Cambridge, Mass.) · 2015
    Review
  16. 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

4 authors at 2 institutions in 1 country.

Monique S RoyInstitute of Ophthalmology and Visual Science, UMDNJ, Rutgers University, Newark, New Jersey, USA.
Malvin N JanalDepartment of Epidemiology and Health Promotion, NYU College of Dentistry, New York, New York, USA.
Juan CrosbyDepartment of Pathology and Laboratory Medicine and NJMS Molecular Resource Facility, Rutgers University, Newark, New Jersey, USA.
Robert DonnellyDepartment of Pathology and Laboratory Medicine and NJMS Molecular Resource Facility, Rutgers University, Newark, New Jersey, USA.
Rutgers, The State University of New Jersey · USYork University · US

Funding

RISK FACTORS FOR DIABETIC RETINOPATHY IN BLACK AMERICANSR01EY009860 · NEI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ROY, MONIQUE S · 1993 to 2003
$1.9M
Inflammatory Biomarkers and Progression of Diabetic RetinopathyR21EY019750 · NEI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ROY, MONIQUE S · 2009 to 2010
$432k
NEI NIH HHS R01 EY009860NEI NIH HHS R01 EY 09860NEI NIH HHS R21 EY019750NEI NIH HHS R21EY019750
6 · The paper itself

Abstract

African Americans with early-onset type 1 diabetes mellitus are at a high risk for severe diabetic nephropathy and end-stage renal disease. In order to determine whether baseline plasma levels of inflammatory markers predict incidence of overt proteinuria or renal failure in African Americans with type 1 diabetes mellitus, we re-examined data of 356 participants in our observational follow-up study of 725 New Jersey African Americans with type 1 diabetes. At baseline and 6-year follow-up, a detailed structured clinical interview was conducted to document medical history including kidney dialysis or transplant, other diabetic complications, and renal-specific mortality. Plasma levels of 28 inflammatory biomarkers were measured using a multiplex bead analysis system. After adjusting for baseline age, glycohemoglobin, and other confounders, the baseline plasma levels of soluble intercellular adhesion molecule-1 (sICAM-1) in the upper two quartiles were, respectively, associated with a three- to fivefold increase in the risk of progression from no albuminuria or microalbuminuria to overt proteinuria. Baseline plasma levels of the chemokine eotaxin in the upper quartile were significantly associated with a sevenfold increase in risk of incident renal failure. These associations were independent of traditional risk factors for progression of diabetic nephropathy. Thus, in type 1 diabetic African Americans, sICAM-1 predicted progression to overt proteinuria and eotaxin-predicted progression to renal failure.

Indexed as

AdolescentAdultBiomarkersBlack or African AmericanCohort StudiesCytokinesDiabetes Mellitus, Type 1Diabetic NephropathiesDisease ProgressionFemaleFollow-Up StudiesHumansInflammation MediatorsIntercellular Adhesion Molecule-1MaleMiddle AgedBiomarkersCytokinesInflammation MediatorsIntercellular Adhesion Molecule-1

Identifiers

PMID24918153
PMCPMC4263810
OpenAlexW2071623074

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.