Evidence map›Paper›PMID 25785731›Full record

ArticlePloS one2015

Impaired glucose metabolism among those with and without diagnosed diabetes and mortality: a cohort study using Health Survey for England data.

Vanessa L Z Gordon-Dseagu, Jennifer S Mindell, Andrew Steptoe, Alison Moody, Jane Wardle, Panayotes Demakakos, Nicola J Shelton

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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  9. Review
  10. Determinants of mortality in patients with type 2 diabetes: a review.Reviews in endocrine & metabolic disorders · 2016
    Review
  11. Article
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

7 authors.

Vanessa L Z Gordon-DseaguDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Jennifer S MindellDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Andrew SteptoeDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Alison MoodyDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Jane WardleDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Panayotes DemakakosDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.
Nicola J SheltonDepartment of Epidemiology and Public Health, UCL (University College London), 1-19 Torrington Place, London, WC1E 6BT, United Kingdom.

Funding

Cancer Research UK 14133Medical Research Council
6 · The paper itself

Abstract

backgroundThe extent that controlled diabetes impacts upon mortality, compared with uncontrolled diabetes, and how pre-diabetes alters mortality risk remain issues requiring clarification.

methodsWe carried out a cohort study of 22,106 Health Survey for England participants with a HbA1C measurement linked with UK mortality records. We estimated hazard ratios (HRs) of all-cause, cancer and cardiovascular disease (CVD) mortality and 95% confidence intervals (CI) using Cox regression.

resultsAverage follow-up time was seven years and there were 1,509 deaths within the sample. Compared with the non-diabetic and normoglycaemic group (HbA1C <5.7% [<39 mmol/mol] and did not indicate diabetes), undiagnosed diabetes (HbA1C ≥6.5% [≥48 mmol/mol] and did not indicate diabetes) inferred an increased risk of mortality for all-causes (HR 1.40, 1.09-1.80) and CVD (1.99, 1.35-2.94), as did uncontrolled diabetes (diagnosed diabetes and HbA1C ≥6.5% [≥48 mmol/mol]) and diabetes with moderately raised HbA1C (diagnosed diabetes and HbA1C 5.7-<6.5% [39-<48 mmol/mol]). Those with controlled diabetes (diagnosed diabetes and HbA<5.7% [<39 mmol/mol]) had an increased HR in relation to mortality from CVD only. Pre-diabetes (those who did not indicate diagnosed diabetes and HbA1C 5.7-<6.5% [39-<48 mmol/mol]) was not associated with increased mortality, and raised HbA1C did not appear to have a statistically significant impact upon cancer mortality. Adjustment for BMI and socioeconomic status had a limited impact upon our results. We also found women had a higher all-cause and CVD mortality risk compared with men.

conclusionsWe found higher rates of all-cause and CVD mortality among those with raised HbA1C, but not for those with pre-diabetes, compared with those without diabetes. This excess differed by sex and diabetes status. The large number of deaths from cancer and CVD globally suggests that controlling blood glucose levels and policies to prevent hyperglycaemia should be considered public health priorities.

Indexed as

AdultAgedBiomarkersBody Mass IndexCardiovascular DiseasesDiabetes ComplicationsDiabetes MellitusFemaleGlycated HemoglobinHealth SurveysHumansHyperglycemiaIncidenceMaleMiddle AgedNeoplasmsBiomarkersGlycated Hemoglobinhemoglobin A1c protein, human

Identifiers

PMID25785731
PMCPMC4365017

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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.