Evidence map›Paper›PMID 23761102›Full record

Trial reportDiabetes2013

Haptoglobin genotype and the rate of renal function decline in the diabetes control and complications trial/epidemiology of diabetes interventions and complications study.

Trevor J Orchard, Wanjie Sun, Patricia A Cleary, Saul M Genuth, John M Lachin, Paula McGee, Andrew D Paterson, Philip Raskin, Yefim Anbinder, Andrew P Levy and 1 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 39 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

11 authors at 6 institutions in 3 countries.

Trevor J OrchardGraduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. tjo@pitt.edu
Wanjie Sun
Patricia A Cleary
Saul M Genuth
John M Lachin
Paula McGee
Andrew D Paterson
Philip Raskin
Yefim Anbinder
Andrew P Levy
DCCT/EDIC Research Group
George Washington University · USTechnion – Israel Institute of Technology · ILCase Western Reserve University · USHospital for Sick Children · CASouthwestern Medical CenterUniversity of Pittsburgh · US

Funding

UNM HSC Clinical and Translational Science CenterUL1TR001449 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CAMPEN, MATTHEW J, PANDHI, NANCY · 2015 to 2024
$36.9M
University of New Mexico Clinical and Translational Science CenterUL1TR000041 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LARSON, RICHARD S · 2012 to 2014
$9.8M
The Oxidation Hypothesis Revisited:Haptoglobin Genotype and Diabetic AtheroscleroR01DK085226 · NIDDK · TECHNION-ISRAEL INSTITUTE OF TECHNOLOGY · PI LEVY, ANDREW PETER · 2009 to 2013
$664k
NCATS NIH HHS UL1 TR000041NCATS NIH HHS UL1 TR001449NIDDK NIH HHS R01 DK085226NIDDK NIH HHS R01-DK-085226-03PHS HHS U01
6 · The paper itself

Abstract

Many patients with type 1 diabetes develop renal disease despite moderately good metabolic control, suggesting other risk factors may play a role. Recent evidence suggests that the haptoglobin (HP) 2-2 genotype, which codes for a protein with reduced antioxidant activity, may predict renal function decline in type 1 diabetes. We examined this hypothesis in 1,303 Caucasian participants in the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) study. HP genotype was determined by polyacrylamide gel electrophoresis. Glomerular filtration rate was estimated by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation and albumin excretion based on timed urine samples. Participants were followed up for a mean of 22 years. HP genotype was significantly associated with the development of sustained estimated glomerular filtration rate (GFR) <60 mL/min/1.73 m(2) and with end-stage renal disease (ESRD), with HP 2-2 having greater risk than HP 2-1 and 1-1. No association was seen with albuminuria. Although there was no treatment group interaction, the associations were only significant in the conventional treatment group, where events rates were much higher. We conclude that the HP genotype is significantly associated with the development of reduced GFR and ESRD in the DCCT/EDIC study.

Indexed as

AdolescentAdultDiabetes ComplicationsDiabetes Mellitus, Type 1FemaleGenotypeGlomerular Filtration RateHaptoglobinsHumansKidney Failure, ChronicMaleYoung AdultHaptoglobins

Identifiers

PMID23761102
PMCPMC3749329
OpenAlexW2099304449

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.