Evidence map›Paper›PMID 34190365›Full record

ArticleJournal of veterinary internal medicine2021

An ultra-long-acting recombinant insulin for the treatment of diabetes mellitus in cats.

Chen Gilor, Sean E Hulsebosch, Jully Pires, Michael J Bannasch, Thomas Lancaster, Andrea Delpero, Ramya Ragupathy, Sylaja Murikipudi, Todd Zion

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of veterinary internal medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Research Advances in Fusion Protein-Based Drugs for Diabetes Treatment.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Chen GilorDepartment of Veterinary Medicine and Epidemiology, University of California, Davis, Davis, California, USA.ORCID https://orcid.org/0000-0003-0393-4135
Sean E HulseboschDepartment of Veterinary Medicine and Epidemiology, University of California, Davis, Davis, California, USA.
Jully PiresDepartment of Veterinary Medicine and Epidemiology, University of California, Davis, Davis, California, USA.
Michael J BannaschDepartment of Veterinary Medicine and Epidemiology, University of California, Davis, Davis, California, USA.
Thomas LancasterAkston Biosciences, Beverly, Massachusetts, USA.
Andrea DelperoAkston Biosciences, Beverly, Massachusetts, USA.
Ramya RagupathyAkston Biosciences, Beverly, Massachusetts, USA.
Sylaja MurikipudiAkston Biosciences, Beverly, Massachusetts, USA.
Todd ZionAkston Biosciences, Beverly, Massachusetts, USA.
Akston Biosciences (United States) · USUniversity of California, Davis · USUniversity of Florida · US

Funding

VCCT/Center for Companion Animal Health 2017-75-F
6 · The paper itself

Abstract

backgroundTreatment of diabetes mellitus (DM) in cats typically requires insulin injections q12h-q24h, posing a major compliance barrier for caregivers. Novel treatments enabling decreased injection frequency while maintaining safety are highly desirable. Insulin fused with feline immunoglobulin fragment crystallizable (Fc) has an ultra-long plasma half-life because it recycles through cells where it is protected from proteolysis. HYPOTHESIS: Glycemic control can be achieved in diabetic cats with a recombinant fusion protein of a synthetic insulin and feline Fc (AKS-267c) administered SC weekly. ANIMALS: Five cats with spontaneous DM.

methodsCats previously controlled using insulin glargine q12h were transitioned to once-weekly injection of AKS-267c. The dose of AKS-267c was titrated weekly for 7 weeks based on continuous glucose monitoring. Clinical signs, body weight, fructosamine concentrations, and mean interstitial glucose concentrations (IG) were compared between baseline (week 0, on insulin glargine) and the last week of treatment. Data were assessed for normality and compared using parametric or nonparametric paired tests (as appropriate).

resultsAfter 7 weeks of once-weekly injections, compared to baseline, there were no significant changes in clinical signs, body weight (median [range] gain, 0.1 kg [-0.1 to +0.7]; P = .5), fructosamine (-60 mmol/L [-338 to +206]; P = .6), and mean IG concentrations (change = -153 mmol/L [-179 to +29]; P = .3), and no adverse reactions were reported.

conclusionSuccessful control of clinical signs and maintenance of glycemia was achieved with this once-weekly novel insulin treatment. The efficacy and safety of this novel formulation should be further assessed in a large clinical trial.

Indexed as

Cat DiseasesDiabetes Mellitus, Type 2AnimalsBlood GlucoseBlood Glucose Self-MonitoringCatsHypoglycemic AgentsInsulin GlargineBlood GlucoseHypoglycemic AgentsInsulin Glargineadherencecompliancecontinuous glucose monitoringFcRnIgG

Identifiers

PMID34190365
PMCPMC8478034
OpenAlexW3173484286

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.