Evidence map›Paper›PMID 38884190›Full record

ArticleJournal of veterinary internal medicine

Efficacy and safety of once daily oral administration of sodium-glucose cotransporter-2 inhibitor velagliflozin compared with twice daily insulin injection in diabetic cats.

Stijn J M Niessen, Hans S Kooistra, Yaiza Forcada, Charlotte R Bjørnvad, Balazs Albrecht, Franziska Roessner, Esther Herberich, Carla Kroh

Abstract readRandomized Controlled Trial, Veterinary
In one paragraph

Article in Journal of veterinary internal medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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  7. Spectrum of veterinary care in feline diabetes mellitus.Journal of feline medicine and surgery · 2026
    Review
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  11. JFMS open reports
    Article
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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.

Stijn J M NiessenVeterinary Specialist Consultations & VIN Europe, Hilversum, The Netherlands.ORCID https://orcid.org/0009-0000-9667-6678
Hans S KooistraDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Yaiza ForcadaVeterinary Specialist Consultations & VIN Europe, Hilversum, The Netherlands.
Charlotte R BjørnvadBjørnvad Consultancy, Vedbæk, Denmark.ORCID https://orcid.org/0000-0002-2876-1667
Balazs AlbrechtBoehringer Ingelheim Vetmedica GmbH, Ingelheim am Rhein, Germany.ORCID https://orcid.org/0000-0001-7687-4749
Franziska RoessnerBoehringer Ingelheim Vetmedica GmbH, Ingelheim am Rhein, Germany.
Esther HerberichBoehringer Ingelheim Vetmedica GmbH, Ingelheim am Rhein, Germany.
Carla KrohBoehringer Ingelheim Vetmedica GmbH, Ingelheim am Rhein, Germany.

Funding

Boehringer Ingelheim Animal Health
6 · The paper itself

Abstract

backgroundOptions for treatment of diabetes mellitus in cats are limited to insulin injections and monitoring for hypoglycemia. HYPOTHESIS: Once daily sodium-glucose cotransporter-2 inhibitor velagliflozin PO is noninferior to insulin injections. ANIMALS: Client-owned diabetic cats (127 safety; 116 efficacy assessment).

methodsProspective, randomized (1 mg/kg velagliflozin), positive controlled (titrated Caninsulin), open label, noninferiority field trial, comparing number of cats with treatment success in ≥1 clinical variable and ≥1 glycemic variable (margin Δ: 15%) on Day 45; secondary endpoints included glycemic and clinical assessments during 91 days.

resultsOn Day 45, 29/54 (54%) velagliflozin-treated cats and 26/62 (42%) Caninsulin-treated cats showed treatment success, demonstrating noninferiority (difference -11.8%; upper 1-sided 97.5% confidence interval, -∞ to 6.3%). By Day 91, quality of life (QoL), polyuria, and polydipsia had improved in 81%, 54% and 61% (velagliflozin); on blood glucose (BG) curves, mean BG was <252 mg/dL in 42/54 (78%; velagliflozin) and 37/62 (60%; Caninsulin); minimum BG was <162 mg/dL in 41/54 (76%; velagliflozin) and 41/62 (66%; Caninsulin); serum fructosamine was <450 μmol/L in 41/54 (76%; velagliflozin) and 38/62 (61%; Caninsulin). Velagliflozin's most frequent adverse events were loose feces/diarrhea (n = 23/61, 38%), positive urine culture (n = 19/61, 31%), and nonclinical hypoglycemia (BG <63 mg/dL; n = 8/61, 13%); Caninsulin's: clinical and nonclinical hypoglycemia (n = 35/66, 53%), positive urine culture (n = 18/66, 27%), and loose feces/diarrhea (n = 10/66, 15%). Diabetic ketoacidosis occurred in 4/61 (7%; velagliflozin) and 0/66 (Caninsulin). CONCLUSIONS AND CLINICAL IMPORTANCE: Once daily oral administration of velagliflozin was noninferior to insulin injections, showed good QoL and glycemia without clinical hypoglycemia.

Indexed as

Cat DiseasesHypoglycemic AgentsInsulinSodium-Glucose Transporter 2 InhibitorsAdministration, OralAnimalsBlood GlucoseCatsDiabetes MellitusDrug Administration ScheduleFemaleMaleProspective StudiesBlood GlucoseHypoglycemic AgentsInsulinSodium-Glucose Transporter 2 Inhibitorsantidiabeticbeta‐cellcompliancefeline diabetes mellitusglucosuriaglucotoxicityglycemic controlprospective clinical trialsodium‐glucose cotransporter‐2 (SGLT2) inhibitor

Identifiers

PMID38884190
PMCPMC11256146

What OpenQuestion holds

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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.