Evidence map›Paper›PMID 29119713›Full record

ArticleDiabetes, obesity & metabolism2018

Impact of differing glucose-lowering regimens on the pattern of association between glucose control and survival.

Craig J Currie, Sarah E Holden, Sara Jenkins-Jones, Christopher Ll Morgan, Bernd Voss, Swapnil N Rajpathak, Berhanu Alemayehu, John R Peters, Samuel S Engel

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
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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

9 authors at 5 institutions in 4 countries.

Craig J CurrieInstitute of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-6154-818X
Sarah E HoldenGlobal Epidemiology, Pharmatelligence, Cardiff, UK.ORCID 0000-0002-4315-5681
Sara Jenkins-JonesGlobal Epidemiology, Pharmatelligence, Cardiff, UK.ORCID 0000-0003-3836-8102
Christopher Ll MorganGlobal Epidemiology, Pharmatelligence, Cardiff, UK.ORCID 0000-0001-8796-7406
Bernd VossMSD RBSC GmbH, Germany.
Swapnil N RajpathakMerck & Co. Inc, Kenilworth, New Jersey.
Berhanu AlemayehuMerck & Co. Inc, Kenilworth, New Jersey.
John R PetersDiabetes and Endocrinology, University Hospital of Wales, Cardiff, UK.
Samuel S EngelMerck & Co. Inc, Kenilworth, New Jersey.ORCID 0000-0002-4439-6356
Cardiff University · GBMerck & Co., Inc., Rahway, NJ, USA (United States) · USMSD (Germany) · DEUniversity Hospital of Wales · GBUniversity of Wales Institute Cardiff · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo characterize survival in relation to achieved glycated haemoglobin (HbA1c) level within alternative glucose-lowering regimens with differing risks of hypoglycaemia.

methodsData were extracted from the UK Clinical Practice Research Datalink and the corresponding Hospital Episode Statistics. Patients with type 2 diabetes prescribed glucose-lowering therapy in monotherapy or dual therapy with metformin between 2004 and 2013 were identified. Risk of all-cause mortality within treatment cohorts was evaluated using the Cox proportional hazards model, introducing mean HbA1c as a quarterly updated, time-dependent covariable.

resultsThere were 6646 deaths in a total follow-up period of 374 591 years. Survival for lower (<7%) vs moderate HbA1c levels (≥7%, <8.5%) differed by cohort: metformin, adjusted hazard ratio (aHR) 1.03 (95% confidence interval [CI] 0.95-1.12); sulphonylurea, aHR 1.11 (95% CI 0.99-1.25); insulin, aHR 1.47 (95% CI 1.25-1.72); combined regimens with low hypoglycaemia risk, aHR 1.02 (95% CI 0.94-1.10); and combined regimens with higher hypoglycaemia risk excluding insulin, aHR 1.24 (95% CI 1.13-1.35) and including insulin, aHR 1.28 (95% CI 1.18-1.37). Higher HbA1c levels were associated with increased mortality in regimens with low hypoglycaemia risk. Post hoc analysis by HbA1c deciles revealed an elevated risk of all-cause mortality for the lowest deciles across all cohorts, but particularly in those regimens associated with hypoglycaemia. High HbA1c was associated with no difference, or a small increase in mortality risk in regimens with increased risk of hypoglycaemia.

conclusionsThe pattern of mortality risk across the range of HbA1c differed by glucose-lowering regimen. Lower HbA1c was associated with increased mortality risk compared with moderate control, especially in those regimens associated with hypoglycaemia. High levels of HbA1c were associated with the expected elevated mortality risk in regimens with low hypoglycaemia risk.

Indexed as

AgedAged, 80 and overBlood GlucoseCardiovascular DiseasesDiabetes Mellitus, Type 2Diabetic AngiopathiesFemaleHumansHypoglycemic AgentsMaleMiddle AgedRetrospective StudiesRisk FactorsSurvival AnalysisUnited KingdomBlood GlucoseHypoglycemic Agentsdiabetesglucosehypoglycaemiamortalitysurvival

Identifiers

PMID29119713
PMCPMC5888185
OpenAlexW2767771078

What OpenQuestion holds

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LicenceCC BY-NC
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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.