Evidence map›Paper›PMID 33511679›Full record

ArticleClinical transplantation2021

Podocyte density is reduced in kidney allografts with high-risk APOL1 genotypes at transplantation.

Dhruti P Chen, Ziad S Zaky, Jesse D Schold, Leal C Herlitz, Rasha El-Rifai, Paul E Drawz, Leslie A Bruggeman, Laura Barisoni, Susan L Hogan, Yichun Hu and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Dhruti P ChenDivision of Nephrology, UNC Kidney Center, University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0002-6078-8392
Ziad S ZakyGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Jesse D ScholdGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Leal C HerlitzPathology and Lab Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Rasha El-RifaiDivision of Renal Diseases and Hypertension, University of Minnesota, Minneapolis, MN, USA.
Paul E DrawzDivision of Renal Diseases and Hypertension, University of Minnesota, Minneapolis, MN, USA.
Leslie A BruggemanGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Laura BarisoniDepartments of Pathology and Medicine, Division of Nephrology, Duke University School of Medicine, Durham, NC, USA.
Susan L HoganDivision of Nephrology, UNC Kidney Center, University of North Carolina, Chapel Hill, NC, USA.
Yichun HuDivision of Nephrology, UNC Kidney Center, University of North Carolina, Chapel Hill, NC, USA.
John F O'TooleGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Emilio D PoggioGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
John R SedorGlickman Urology and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0002-6780-9168
Cleveland Clinic · USUniversity of North Carolina at Chapel Hill · USUniversity of Minnesota · USDuke University · US

Funding

RENAL EPIDEMIOLOGY TRAINING PROGRAMT32DK007750 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FALK, RONALD J · 1999 to 2022
$5.5M
CWRU NEPHROLOGY TRAINING PROGRAMT32DK007470 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI SEDOR, JOHN R. · 1986 to 2019
$2.9M
Mechanisms of APOL1-mediated kidney diseaseR01DK108329 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI BRUGGEMAN, LESLIE A, O'TOOLE, JOHN F. · 2015 to 2019
$2.0M
Kidney disease mechanisms associated with human genetic variationR01DK097836 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI BRUGGEMAN, LESLIE A, O'TOOLE, JOHN F. · 2014 to 2017
$2.0M
NIDDK NIH HHS R01 DK097836NIDDK NIH HHS R01 DK108329NIDDK NIH HHS T32 DK007470NIDDK NIH HHS T32 DK007750
6 · The paper itself

Abstract

Variants in apolipoprotein L1 (APOL1) gene are associated with nondiabetic kidney diseases in black subjects and reduced kidney transplant graft survival. Living and deceased black kidney donors (n = 107) were genotyped for APOL1 variants. To determine whether allografts from high-risk APOL1 donors have reduced podocyte densities contributing to allograft failure, we morphometrically estimated podocyte number, glomerular volume, and podocyte density. We compared allograft loss and eGFR trajectories stratified by APOL1 high-risk and low-risk genotypes. Demographic characteristics were similar in high-risk (n = 16) and low-risk (n = 91) donors. Podocyte density was significantly lower in high-risk than low-risk donors (108 ± 26 vs 127 ± 40 podocytes/10

Indexed as

Apolipoprotein L1Kidney TransplantationPodocytesAllograftsGenotypeGraft SurvivalHumansKidneyAPOL1 protein, humanApolipoprotein L1disparitieskidney donoroutcomespodometricstransplant

Identifiers

PMID33511679
PMCPMC9009375
OpenAlexW3121846817

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.