Evidence mapPaperPMID 21791495Full record

SynthesisBMJ (Clinical research ed.)2011

Effect of intensive glucose lowering treatment on all cause mortality, cardiovascular death, and microvascular events in type 2 diabetes: meta-analysis of randomised controlled trials.

Rémy Boussageon, Theodora Bejan-Angoulvant, Mitra Saadatian-Elahi, Sandrine Lafont, Claire Bergeonneau, Behrouz Kassaï, Sylvie Erpeldinger, James M Wright, François Gueyffier, Catherine Cornu

Registry-linked trialOpen access · hybridAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in BMJ (Clinical research ed.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02540486 (A 12 Week, Parallel, Open-label, Randomized, Multi-center Study Evaluating Use, Safety and Effectiveness of a Web Based Tool vs. Enhanced Usual Therapy of Glargine Titration in T2DM Patients With a 4 Week Safety Extension), which is not on this map. Cited by 264 papers, 17 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
264citing papers in PubMed, 17 pooled it
50.0field-weighted citation impact, top 1% 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.

NCT02540486 nacompletednot on this mapstarted 2013, after this paper: background citation

A 12 Week, Parallel, Open-label, Randomized, Multi-center Study Evaluating Use, Safety and Effectiveness of a Web Based Tool vs. Enhanced Usual Therapy of Glargine Titration in T2DM Patients With a 4 Week Safety Extension

TypeinterventionalSponsorLMC Diabetes & Endocrinology Ltd.Ran2013 to 2015Enrolled139ConditionsType 2 Diabetes MellitusArmsLong-acting insulin glargine titration web tool (LTHome), Diabetes Education
3 · Its place in the literature

Who cites it

264 citing papers in PubMed, 17 syntheses or guidelines pooled it, 804 citations in OpenAlex.

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  10. Atencion primaria · 2018
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  14. Glycemic Control for Patients With Type 2 Diabetes Mellitus: Our Evolving Faith in the Face of Evidence.Circulation. Cardiovascular quality and outcomes · 2016 · on this map
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204 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Rémy BoussageonDepartment of General Medicine, Université Claude Bernard Lyon 1, Lyon, France.
Theodora Bejan-Angoulvant
Mitra Saadatian-Elahi
Sandrine Lafont
Claire Bergeonneau
Behrouz Kassaï
Sylvie Erpeldinger
James M Wright
François Gueyffier
Catherine Cornu
Université Claude Bernard Lyon 1 · FRHospices Civils de Lyon · FRCentre National de la Recherche Scientifique · FRUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine all cause mortality and deaths from cardiovascular events related to intensive glucose lowering treatment in people with type 2 diabetes.

designMeta-analysis of randomised controlled trials. DATA SOURCES: Medline, Embase, and the Cochrane database of systematic reviews. STUDY SELECTION: Randomised controlled trials that assessed the effect of intensive glucose lowering treatment on cardiovascular events and microvascular complications in adults (≥ 18 years) with type 2 diabetes. DATA EXTRACTION: Primary end points were all cause mortality and death from cardiovascular causes. Secondary end points were severe hypoglycaemia and macrovascular and microvascular events. Synthesis of results Results are reported as risk ratios with 99% confidence intervals. Statistical heterogeneity between trials was assessed with χ(2), τ(2), and I(2) statistics. A fixed effect model was used to assess the effect on the outcomes of intensive glucose lowering versus standard treatment. The quality of clinical trials was assessed by the Jadad score.

results13 studies were included. Of 34,533 patients, 18,315 received intensive glucose lowering treatment and 16,218 standard treatment. Intensive treatment did not significantly affect all cause mortality (risk ratio 1.04, 99% confidence interval 0.91 to 1.19) or cardiovascular death (1.11, 0.86 to 1.43). Intensive therapy was, however, associated with reductions in the risk of non-fatal myocardial infarction (0.85, 0.74 to 0.96, P<0.001), and microalbuminuria (0.90, 0.85 to 0.96, P<0.001) but a more than twofold increase in the risk of severe hypoglycaemia (2.33, 21.62 to 3.36, P<0.001). Over a treatment period of five years, 117 to 150 patients would need to be treated to avoid one myocardial infarction and 32 to 142 patients to avoid one episode of microalbuminuria, whereas one severe episode of hypoglycaemia would occur for every 15 to 52 patients. In analysis restricted to high quality studies (Jadad score >3), intensive treatment was not associated with any significant risk of reductions but resulted in a 47% increase in risk of congestive heart failure (P<0.001).

conclusionsThe overall results of this meta-analysis show limited benefits of intensive glucose lowering treatment on all cause mortality and deaths from cardiovascular causes. We cannot exclude a 9% reduction or a 19% increase in all cause mortality and a 14% reduction or a 43% increase in cardiovascular death. The benefit:risk ratio of intensive glucose lowering treatment in the prevention of macrovascular and microvascular events remains uncertain. The harm associated with severe hypoglycaemia might counterbalance the potential benefit of intensive glucose lowering treatment. More double blind randomised controlled trials are needed to establish the best therapeutic approach in people with type 2 diabetes.

Indexed as

AdultAgedAlbuminuriaBlood GlucoseCause of DeathDiabetes Mellitus, Type 2Diabetic AngiopathiesFemaleHumansHypoglycemiaHypoglycemic AgentsMaleMicrocirculationMiddle AgedMyocardial InfarctionRandomized Controlled Trials as TopicBlood GlucoseHypoglycemic Agents

Identifiers

PMID21791495
PMCPMC3144314
OpenAlexW2115653936

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.