Evidence mapPaperPMID 36053820Full record

ArticleDiabetes, obesity & metabolism2022

Improved patient-reported outcomes with iGlarLixi versus premix BIAsp 30 in people with type 2 diabetes in the SoliMix trial.

William H Polonsky, Francesco Giorgino, Julio Rosenstock, Katherine Whitmire, Elisheva Lew, Mathieu Coudert, Agustina Alvarez, Charlie Nicholls, Rory J McCrimmon

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Use of Fixed Ratio Combinations to Improve Glycemic Control in Individuals with Type 2 Diabetes: Experts' Opinion from the Gulf Region.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2026
    Review
  5. Observational
  6. Observational
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. 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 6 countries.

William H PolonskyBehavioral Diabetes Institute, San Diego, California.ORCID 0000-0001-9064-6144
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
Julio RosenstockDallas Diabetes Research Center at Medical City, Dallas, Texas.ORCID 0000-0001-8324-3275
Katherine WhitmireSouthwest Medical Associates, Las Vegas, Nevada.
Elisheva LewSanofi, Chilly-Mazarin, France.ORCID 0000-0001-5097-0169
Mathieu CoudertBiostatistics and Programming Department, Sanofi, Chilly-Mazarin, France.
Agustina AlvarezSanofi, Buenos Aires, Argentina.
Charlie NichollsSanofi, Reading, UK.ORCID 0000-0003-4856-4369
Rory J McCrimmonDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-3957-1981
Sanofi (France) · FRDallas Diabetes Research Center · USInstitute of Behavioral Sciences · JPLongenecker and Associates (United States) · USSanofi (Argentina) · ARSanofi (United Kingdom) · GBUniversity of Bari Aldo Moro · ITUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo assess patient-reported outcomes (PROs) in the SoliMix trial, which compared the efficacy and safety of iGlarLixi versus BIAsp 30 in people with type 2 diabetes (T2D). MATERIALS AND

methodsSoliMix (EudraCT: 2017-003370-13), a 26-week, open-label study, randomized (1:1) 887 adults with T2D and HbA1c ≥7.5%-≤10.0% (≥58-≤86 mmol/mol) on basal insulin plus oral antihyperglycaemic drugs (OADs) to once-daily iGlarLixi or twice-daily premix insulin, BIAsp 30. PROs were assessed using the Treatment-Related Impact Measure Diabetes (TRIM-D) and Global Treatment Effectiveness Evaluation (GTEE) questionnaires.

resultsOver 26 weeks, iGlarLixi showed greater improvement from baseline versus BIAsp 30 in total TRIM-D score (least squares mean difference [95% confidence interval]: 5.08 [3.69, 6.47]; effect size: 0.32) and in each TRIM-D domain, with the greatest differences seen in diabetes management (8.47 [6.11, 10.84]) and treatment burden (6.95 [4.83, 9.07]). GTEE scores showed a greater proportion of participants and physicians rated a complete or marked improvement of diabetes control with iGlarLixi (80.5%, 82.8%) versus BIAsp 30 (63.3%, 65.1%) at week 26. Post hoc analyses showed that after adjusting for HbA1c, body weight and hypoglycaemia outcomes, iGlarLixi continued to show greater improvements in TRIM-D total scores versus BIAsp 30.

conclusionsIn addition to better glycaemic control, weight benefit and less hypoglycaemia, once-daily iGlarLixi provided improved diabetes management, treatment burden and perceived effectiveness versus twice-daily premix BIAsp 30, further supporting iGlarLixi as an advanced treatment option in people with suboptimally controlled T2D on basal insulin plus OADs.

Indexed as

Diabetes Mellitus, Type 2HypoglycemiaAdultBiphasic InsulinsBlood GlucoseGlycated HemoglobinHumansHypoglycemic AgentsInsulin AspartInsulin GlargineInsulin, IsophanePatient Reported Outcome MeasuresTreatment OutcomeBiphasic InsulinsBlood GlucoseGlycated HemoglobinHypoglycemic AgentsInsulin Aspartinsulin aspart, insulin aspart protamine drug combination 30:70Insulin GlargineInsulin, Isophanebasal insulinGLP-1 analogueglycaemic controliGlarLixipatient-reported outcomestype 2 diabetes

Identifiers

PMID36053820
PMCPMC9805099
OpenAlexW4292708036

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.