Evidence mapPaperPMID 28303626Full record

SynthesisDiabetes/metabolism research and reviews2017

Lixisenatide as add-on treatment among patients with different β-cell function levels as assessed by HOMA-β index.

Riccardo C Bonadonna, Lawrence Blonde, Mikhail Antsiferov, Rachele Berria, Pierre Gourdy, Mensud Hatunic, Viswanathan Mohan, Michael Horowitz

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in Diabetes/metabolism research and reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Observational
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Fixed-Ratio Combination of Insulin and GLP-1 RA in Patients with Longstanding Type 2 Diabetes: A Subanalysis of LixiLan-L.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2020
    Article
  14. Article
  15. Review
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

8 authors at 8 institutions in 7 countries.

Riccardo C BonadonnaUniversity of Parma and Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.ORCID 0000-0002-9809-1005
Lawrence BlondeFrank Riddick Diabetes Institute, Department of Endocrinology, Ochsner Medical Center, New Orleans, LA, USA.
Mikhail AntsiferovMoscow Department of Health Care, Moscow, Russian Federation.
Rachele BerriaSanofi, Bridgewater, NJ, USA.
Pierre GourdyDiabetology Department, Toulouse University Hospital, Toulouse, France.
Mensud HatunicDepartment of Endocrinology, Mater Misericordiae University Hospital, Dublin, Ireland.
Viswanathan MohanMadras Diabetes Research Foundation & Dr Mohan's Diabetes Specialities Centre, Chennai, India.
Michael HorowitzRoyal Adelaide Hospital, Adelaide, Australia.
Madras Diabetes Research Foundation · INMater Misericordiae University Hospital · IEOchsner Medical Center · USRoyal Adelaide Hospital · AUSanofi (United States) · USScientific Center of Children's Health · RUUniversité Fédérale de Toulouse Midi-Pyrénées · FRUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe effect of lixisenatide-a prandial once-daily glucagon-like peptide-1 receptor agonist-on glycaemic control in patients with inadequately controlled type 2 diabetes mellitus (T2DM), stratified by baseline β-cell function, was assessed.

methodsThe 24-week GetGoal-M, -P and -S trials evaluated the efficacy and safety of lixisenatide in combination with oral antidiabetic agents. This post hoc analysis used data from patients receiving lixisenatide in these trials, divided into matched cohorts by propensity scoring, and stratified according to baseline homeostasis model assessment of β-cell function (HOMA-β) index levels, high HOMA-β: > median HOMA-β (28.49%); low HOMA-β: ≤ median.

resultsThe matched "low" and "high" HOMA-β index cohorts (N = 546 patients) had comparable baseline parameters. Mean change from baseline in glycated haemoglobin (HbA

conclusionsIn patients with T2DM, lixisenatide was associated with reduction in HbA

Indexed as

AdultAgedDiabetes Mellitus, Type 2Double-Blind MethodDrug Therapy, CombinationFemaleGlucagon-Like Peptide-2 ReceptorHumansHypoglycemic AgentsInsulin ResistanceInsulin-Secreting CellsMaleMiddle AgedMulticenter Studies as TopicPeptidesPlacebosGlucagon-Like Peptide-2 ReceptorHypoglycemic AgentslixisenatidePeptidesPlacebosHOMA-β indexlixisenatidetype 2 diabetes mellitusβ-cell function

Identifiers

PMID28303626
PMCPMC5600123
OpenAlexW2595991351

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.