Evidence map›Paper›PMID 29308539›Full record

Trial reportDiabetologia2018

Haemoglobin glycation index and risk for diabetes-related complications in the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation (ADVANCE) trial.

Sigrid C van Steen, Mark Woodward, John Chalmers, Qiang Li, Michel Marre, Mark E Cooper, Pavel Hamet, Giuseppe Mancia, Stephen Colagiuri, Bryan Williams and 3 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetologia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 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 7 institutions in 7 countries.

Sigrid C van SteenDepartment of Endocrinology, Academic Medical Centre, University of Amsterdam, Postbus 22660, 1100 DD, Amsterdam, the Netherlands. s.c.vansteen@amc.uva.nl.
Mark WoodwardThe George Institute for Global Health, University of Sydney, Sydney, NSW, Australia.
John ChalmersThe George Institute for Global Health, University of Sydney, Sydney, NSW, Australia.
Qiang LiThe George Institute for Global Health, University of Sydney, Sydney, NSW, Australia.
Michel MarreDepartment of Endocrinology, Hôpital Bichat-Claude Bernard, Université Paris, Paris, France.
Mark E CooperDiabetes Domain, Baker IDI Heart and Diabetes Institute, Melbourne, VIC, Australia.
Pavel HametCentre de Rechercher, Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Québec, Canada.
Giuseppe ManciaDepartment of Medicine and Surgery, University of Milan-Bicocca, Milan, Italy.
Stephen ColagiuriBoden Institute of Obesity, Nutrition and Exercise, University of Sydney, Sydney, NSW, Australia.
Bryan WilliamsNational Institute of Health Research UCL Hospitals Biomedical Research Centre, London, UK.
Diederick E GrobbeeJulius Clinical, Zeist, the Netherlands.
J Hans DeVriesDepartment of Endocrinology, Academic Medical Centre, University of Amsterdam, Postbus 22660, 1100 DD, Amsterdam, the Netherlands.
ADVANCE Collaborative Group
The University of Sydney · AUUniversité Claude Bernard Lyon 1 · FRUniversity of Amsterdam · NLBaker Heart and Diabetes Institute · AUCentre Hospitalier de l’Université de Montréal · CANational Institute for Health Research · GBUniversity Medical Center Utrecht · NL

Funding

Medical Research Council MC_PC_13090
6 · The paper itself

Abstract

aims/hypothesisPrevious studies have suggested that the haemoglobin glycation index (HGI) can be used as a predictor of diabetes-related complications in individuals with type 1 and type 2 diabetes. We investigated whether HGI was a predictor of adverse outcomes of intensive glucose lowering and of diabetes-related complications in general, using data from the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation (ADVANCE) trial.

methodsWe studied participants in the ADVANCE trial with data available for baseline HbA

resultsIntensive glucose control lowered mortality risk in individuals with high HGI only (HR 0.74 [95% CI 0.61, 0.91]; p = 0.003), while there was no difference in the effect of intensive treatment on mortality in those with high HbA CONCLUSIONS/

interpretationHGI predicts risk for complications in ADVANCE participants, irrespective of treatment allocation, but no better than HbA

Indexed as

AgedAntihypertensive AgentsDiabetes ComplicationsDiabetes Mellitus, Type 2Drug CombinationsFemaleGliclazideGlycosylationHemoglobinsHumansHypoglycemic AgentsIndapamideMaleMicrocirculationMiddle AgedPerindoprilAntihypertensive AgentsDrug CombinationsGliclazideHemoglobinsHypoglycemic AgentsIndapamideindapamide, perindopril drug combinationPerindopril(Blood) glucoseCardiovascular complicationsDiabetes mellitus, type 2HbA1cHypoglycaemiaMortality

Identifiers

PMID29308539
PMCPMC6448976
OpenAlexW2782307991

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.