Evidence map›Paper›PMID 15249997›Full record

ArticleDiabetologia2004

Loss of beta cell function as fasting glucose increases in the non-diabetic range.

I F Godsland, J A R Jeffs, D G Johnston

2 registry-linked trialsOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.2field-weighted citation impact, top 4% 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.

NCT00775684 nacompletednot on this mapstarted 2008, after this paper: background citation

A Randomized, Controlled Trial Comparing the Effect of Exenatide, Sitagliptin or Glimepiride on Functional ß -Cell Mass in Patients With Impaired Fasting Glucose or Early Type 2 Diabetes

TypeinterventionalSponsorUniversity of PennsylvaniaRan2008 to 2012Enrolled47ConditionsPre-diabetes, Type 2 DiabetesArmsExenatide, Sitagliptin, Glimepiride
NCT01123122 nawithdrawnnot on this mapstarted 2011, after this paper: background citation

A Comparison of Strict Glucose Control With Usual Care at the Time of Islet Cell Transplantation

TypeinterventionalSponsorVancouver Coastal HealthRan2011 to 2015Enrolled0ConditionsDiabetes Mellitus, Type 1, Islet TransplantationArmsStrict glucose control
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 130 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Postprandial Reactive Hypoglycemia.Sisli Etfal Hastanesi tip bulteni · 2019
    Review
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

I F GodslandDepartment of Endocrinology and Metabolic Medicine, Division of Medicine, Faculty of Medicine, Imperial College London, St. Mary's Hospital, Mint Wing 2nd Floor, London, W2 1PG, UK. i.godsland@imperial.ac.uk.
J A R JeffsDepartment of Endocrinology and Metabolic Medicine, Division of Medicine, Faculty of Medicine, Imperial College London, St. Mary's Hospital, Mint Wing 2nd Floor, London, W2 1PG, UK.
D G JohnstonDepartment of Endocrinology and Metabolic Medicine, Division of Medicine, Faculty of Medicine, Imperial College London, St. Mary's Hospital, Mint Wing 2nd Floor, London, W2 1PG, UK.
Imperial College London · GBSt Mary's Hospital · GBSt. Mary’s Hospital · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisOur aim was to define the level of glycaemia at which pancreatic insulin secretion, particularly first-phase insulin release, begins to decline.

methodsPlasma glucose and insulin concentrations were measured during an IVGTT in 553 men with non-diabetic fasting plasma glucose concentrations. In 466 of the men C-peptide was also estimated. IVGTT insulin secretion in first and late phases was assessed by: (i) the circulating insulin response; (ii) population parameter deconvolution analysis of plasma C-peptide concentrations; and (iii) a combined model utilising both insulin and C-peptide concentrations. Measurements of insulin sensitivity and elimination were also derived by modelling analysis.

resultsAs fasting plasma glucose (FPG) increased, IVGTT first-phase insulin secretion declined by 73%, 71% and 68% for the three methods respectively. The FPG values at which this decline began, determined by change point regression, were 4.97, 5.16 and 5.42 mmol/l respectively. The sensitivity of late-phase insulin secretion to glucose declined at FPG concentrations above 6.0 mmol/l. Insulin elimination, but not insulin sensitivity, varied with FPG. CONCLUSIONS/

interpretationThe range of FPG over which progressive loss of the first-phase response begins may be as low as 5.0 to 5.4 mmol/l, with late-phase insulin responses declining at FPG concentrations above 6.0 mmol/l.

Indexed as

AdultAgedBlood GlucoseBlood PressureBody Mass IndexCohort StudiesC-PeptideFastingGlucose Tolerance TestHumansInsulinInsulin SecretionIslets of LangerhansMaleModels, BiologicalReference ValuesBlood GlucoseC-PeptideInsulin

Identifiers

PMID15249997
OpenAlexW1992505070

What OpenQuestion 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 OpenQuestion graph.