Evidence map›Paper›PMID 27367910›Full record

ReviewCurrent opinion in nephrology and hypertension2016

Therapeutic angiogenesis by vascular endothelial growth factor supplementation for treatment of renal disease.

Omar C Logue, Jeremy W D McGowan, Eric M George, Gene L Bidwell

Abstract readReview
In one paragraph

Review in Current opinion in nephrology and hypertension, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. The endothelium response to kidney injury.Nature reviews. Nephrology · 2026
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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 2 countries.

Omar C LogueaDepartment of Neurology bDepartment of Physiology and Biophysics cDepartment of Biochemistry, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Jeremy W D McGowan
Eric M George
Gene L Bidwell
Institute of Molecular Biology and Biophysics · RUUniversity of Mississippi Medical Center · US

Funding

Hypertension and Cardiorenal Research Training ProgramT32HL105324 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI Joey P. Granger · 2010 to 2026
$7.8M
A Novel Protein Delivery System for Therapy of PreeclampsiaR01HL121527 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI BIDWELL, GENE LEFLORE · 2014 to 2023
$4.1M
Microcirculation in Renovascular HypertensionR01HL095638 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHADE, ALEJANDRO ROBERTO · 2010 to 2021
$3.9M
Hypertensive Mechanisms in PreeclampsiaR00HL116774 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI GEORGE, ERIC MATTHEW · 2014 to 2016
$746k
NHLBI NIH HHS R00 HL116774NHLBI NIH HHS R01 HL095638NHLBI NIH HHS R01 HL121527NHLBI NIH HHS T32 HL105324
6 · The paper itself

Abstract

purpose of reviewVascular endothelial growth factors (VEGFs) influence renal function through angiogenesis, with VEGF-A being the most potent inducer of vascular formation. In the normal glomerulus, tight homeostatic balance is maintained between the levels of VEGF-A isoforms produced by podocyte cells, and the VEGF receptors (VEGFRs) expressed by glomerular endothelial, mesangial, and podocyte cells. Renal disease occurs when this homeostatic balance is lost, manifesting in the abnormal autocrine and paracrine VEGF-A/VEGFR signaling, ultrastructural glomerular and tubular damage, and impaired filtration. RECENT

findingsPreclinical disease models of ischemic renal injury, including acute ischemia/reperfusion, thrombotic microangiopathy, and chronic renovascular disease, treated with exogenous VEGF supplementation demonstrated therapeutic efficacy. These results suggest a therapeutic VEGF-A paracrine effect on endothelial cells in the context of acute or chronic obstructive ischemia. Conversely, renal dysfunction in diabetic nephropathy appears to occur through an upregulated VEGF autocrine effect on podocyte cells, which is exacerbated by hyperglycemia. Therefore, VEGF supplementation therapy may be contraindicated for treatment of diabetic nephropathy, but specific results will depend on dose and on the specific site of VEGF delivery. A drug delivery system that demonstrates cell specificity for glomerular or peritubular capillaries could be employed to restore balance to VEGF-A/VEGFR2 signaling, and by doing so, prevent the progression to end-stage renal disease. SUMMARY: The review discusses the preclinical data available for VEGF supplementation therapy in models of renal disease.

Indexed as

Acute Kidney InjuryAnimalsDiabetic NephropathiesEndothelial CellsHumansIschemiaKidney GlomerulusNeovascularization, PhysiologicSignal TransductionVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth FactorsFLT1 protein, humanVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factors

Identifiers

PMID27367910
PMCPMC4974125
OpenAlexW2466230370

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.