Evidence map›Paper›PMID 36309941›Full record

ArticleDiabetes, obesity & metabolism2023

Findings for iGlarLixi versus BIAsp 30 confirmed in groups of people with type 2 diabetes with different biomedical characteristics.

Philip D Home, Rory J McCrimmon, Julio Rosenstock, Matthias Blüher, Katrin Pegelow, Lydie Melas-Melt, Khier Djaballah, Francesco Giorgino, SoliMix trial investigators

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. 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

9 authors at 8 institutions in 5 countries.

Philip D HomeTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Rory J McCrimmonDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-3957-1981
Julio RosenstockVelocity Clinical Research at Medical City, Dallas, Texas, USA.ORCID 0000-0001-8324-3275
Matthias BlüherDepartment of Medicine, University of Leipzig, Leipzig, Germany.
Katrin PegelowSanofi, Berlin, Germany.
Lydie Melas-MeltIVIDATA Life Sciences, Levallois-Perret, France.
Khier DjaballahSanofi, Paris, France.
Francesco GiorginoDepartment of Emergency and Organ Transplantation, Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.ORCID 0000-0001-7372-2678
SoliMix trial investigators
Arysta LifeScience (France) · FRLeipzig University · DENewcastle University · GBSanofi (France) · FRSanofi (Germany) · DEUniversity of Bari Aldo Moro · ITUniversity of Dundee · GBVelocity Clinical Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo report prespecified and post hoc analyses of the SoliMix dataset exploring the impact of baseline participant characteristics on the original SoliMix study outcomes, to enable informed treatment choices for people with different biomedical characteristics.

methodsSoliMix (EudraCT 2017-003370-13) compared once-daily iGlarLixi (a fixed-ratio combination of insulin glargine 100 U/mL and the glucagon-like peptide-1 receptor agonist lixisenatide) with twice-daily BIAsp 30 (30% insulin aspart and 70% insulin aspart protamine). In this analysis, the original primary outcomes of noninferiority of iGlarLixi versus BIAsp 30 in terms of glycated haemoglobin (HbA1c) change and superiority in terms of body weight change, together with change in basal insulin dose and hypoglycaemia outcomes, were investigated by baseline age, duration of diabetes, insulin dose, HbA1c level, body mass index (BMI), and renal function.

resultsNo evidence of difference in comparative treatment effect was detected across baseline age, duration of diabetes, insulin dose, HbA1c level, BMI and renal function subgroups for any endpoint (all heterogeneity P > 0.05), except American Diabetes Association Level 2 hypoglycaemia event rate when stratified by insulin dose (P = 0.011), which may be a chance difference given multiple testing and the small numbers of Level 2 events.

conclusionsTreatment effects of iGlarLixi were consistent irrespective of baseline HbA1c, insulin dose, BMI, age, duration of diabetes and renal function, supporting the use of iGlarLixi as an efficacious and well-tolerated treatment option in people with type 2 diabetes with a wide range of biomedical characteristics.

Indexed as

Diabetes Mellitus, Type 2HypoglycemiaBiphasic InsulinsBlood GlucoseDrug CombinationsGlycated HemoglobinHumansHypoglycemic AgentsInsulin AspartInsulin GlargineInsulin, IsophaneBiphasic InsulinsBlood GlucoseDrug CombinationsGlycated HemoglobinHypoglycemic AgentsInsulin Aspartinsulin aspart, insulin aspart protamine drug combination 30:70Insulin GlargineInsulin, Isophanebasal insulinGLP-1 analogueglycaemic controlhypoglycaemiaiGlarLixiinsulin therapyrandomized trialtype 2 diabetes

Identifiers

PMID36309941
PMCPMC10099981
OpenAlexW4307623932

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.