Evidence map›Paper›PMID 31434620›Full record

ArticleJournal of diabetes and its complications2019

Serum pigment epithelium-derived factor: Relationships with cardiovascular events, renal dysfunction, and mortality in the Veterans Affairs Diabetes Trial (VADT) cohort.

Kelly J Hunt, Alicia J Jenkins, Dongxu Fu, Danielle Stevens, Jian-Xing Ma, Richard L Klein, Madona Azar, Sarah X Zhang, Maria F Lopes-Virella, Timothy J Lyons and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of diabetes and its complications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Glucose Variability is Independently Correlated with Serum Level of Pigment Epithelium-Derived Factor in Type 2 Diabetes.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2021
    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

11 authors at 4 institutions in 1 country.

Kelly J HuntDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, United States of America; Research Service, Ralph H. Johnson VA Medical Center, Charleston, SC, United States of America. Electronic address: huntke@musc.edu.
Alicia J JenkinsDivision of Endocrinology, Department of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Dongxu FuSection of Endocrinology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.
Danielle StevensDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, United States of America.
Jian-Xing MaDepartment of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.
Richard L KleinResearch Service, Ralph H. Johnson VA Medical Center, Charleston, SC, United States of America; Division of Endocrinology, Department of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Madona AzarSection of Endocrinology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States of America.
Sarah X ZhangDepartment of Ophthalmology and Ross Eye Institute, University at Buffalo & SUNY Eye Institute, State University of New York, Buffalo, NY, United States of America.
Maria F Lopes-VirellaResearch Service, Ralph H. Johnson VA Medical Center, Charleston, SC, United States of America; Division of Endocrinology, Department of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Timothy J LyonsDivision of Endocrinology, Department of Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
VADT Investigators
Medical University of South Carolina · USUniversity of Oklahoma Health Sciences Center · USRalph H. Johnson VA Medical Center · USUniversity at Buffalo, State University of New York · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
ZINC AND COPPER METABOLISM IN COLLAGEN DISORDERSM01RR001070 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI REVES, JOSEPH G · 1985 to 2009
$16.3M
Trt. of Primary Hyperaldosteronism w/ACE Inhibitors &Angiotension Rec. BlockersM01RR014467 · NCRR · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LYONS, TIMOTHY J · 2001 to 2007
$10.4M
SECRETED ADIPOCYTE PROTEINS, INSULIN RESISTANCE VASCULARP01HL055782 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LOPES-VIRELLA, MARIA F · 1996 to 2005
$8.9M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Lipoproteins and PEDF in the Vascular Complications of DiabetesR01DK080043 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LYONS, TIMOTHY J · 2009 to 2010
$1.4M
Apolipoproteins and the complications of Type 1 diabetesR21HL080921 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LYONS, TIMOTHY J · 2004 to 2005
$535k
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NCRR NIH HHS M01 RR001070NCRR NIH HHS M01 RR014467NHLBI NIH HHS P01 HL055782NHLBI NIH HHS R21 HL080921NIDDK NIH HHS R01 DK080043
6 · The paper itself

Abstract

backgroundTo determine if serum pigment epithelium-derived factor (PEDF) levels predict cardiovascular events, renal dysfunction and mortality in the Veterans Affairs Diabetes Study (VADT).

methodsPEDF was evaluated in relation to subsequent cardiovascular outcomes, mortality, and renal dysfunction (defined as urinary albumin creatinine ratio (ACR) ≥300 mg/g), or chronic kidney disease (CKD) stages 3 (eGFR<60 ml/min) or 4 (eGFR<60 and <30 ml/min respectively). PEDF was measured by ELISA on sera from 881 participants collected a median (range) of 1.7 (0-5.0) years post-baseline, and later, from 832 participants 4.0 (1.5-6.9) years post-baseline.

resultsIn 743 participants, PEDF was measured at both time-points. PEDF increased over time from (mean ± SD) 10.5 ± 4.03 to 11.0 ± 4.86 ng/ml (paired t-test p = 0.0092). Lower eGFR (p < 0.01), higher serum creatinine (p < 0.01) and urinary ACR (p < 0.01) were associated with increasing PEDF. Multivariate event time models included either one or two follow-up windows (i.e., between first and second PEDF measures; and, when available, from second PEDF measure until study-end). PEDF tertiles were not associated with cardiovascular events, but were significantly associated with all-cause mortality [HR = 2.00 (1.03, 3.89) comparing first to third tertile] in models adjusted for age, minority status, VADT treatment arm and prior cardiovascular event status. Higher PEDF levels also associated with development of kidney dysfunction with adjusted HRs (95% CI comparing third to first PEDF tertiles: 2.74 (1.71, 4.39) for stage 3 CKD; and 3.84 (95% CI: 1.17, 12.5) for stage 4 CKD.

conclusionsOver 2-years, higher serum PEDF levels predicted advanced nephropathy in patients with type 2 diabetes.

Indexed as

AlbuminuriaBiomarkersCardiovascular DiseasesDiabetes Mellitus, Type 2Diabetic AngiopathiesDiabetic NephropathiesEye ProteinsFemaleGlomerular Filtration RateHumansMaleMiddle AgedNerve Growth FactorsPigment Epithelium-Derived FactorRenal Insufficiency, ChronicSerpinsBiomarkersEye ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorSerpinsCardiovascularCohortPEDFRenalRisk factor

Identifiers

PMID31434620
PMCPMC6786884
OpenAlexW2965958465

What Socratic 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 Socratic graph.