Evidence map›Paper›PMID 40853201›Full record

ArticleJournal of veterinary internal medicine

Effects of Velagliflozin in 8 Cats With Diabetes Mellitus and Hypersomatotropism.

Francesca Del Baldo, Andrea Corsini, Francesca Bresciani, Valeria Pergolese, Isabella Tirelli, Antonio Maria Tardo, Federico Fracassi

Abstract readMulticenter Study
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 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Guideline
  2. Spectrum of veterinary care in feline diabetes mellitus.Journal of feline medicine and surgery · 2026
    Review
  3. 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

7 authors.

Francesca Del BaldoDepartment of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-5577-0657
Andrea CorsiniDepartment of Veterinary Science, University of Parma, Parma, Italy.ORCID https://orcid.org/0000-0003-1673-8715
Francesca BrescianiVet Hospital H24, VetPartners Italia, Florence, Italy.
Valeria PergoleseDepartment of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
Isabella TirelliDepartment of Veterinary Science, University of Parma, Parma, Italy.ORCID https://orcid.org/0009-0008-0044-7220
Antonio Maria TardoDepartment of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.ORCID https://orcid.org/0009-0009-3636-0415
Federico FracassiDepartment of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-3121-2199

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVelagliflozin is a sodium-glucose cotransporter 2 inhibitor licensed for the treatment of diabetes mellitus (DM) in cats, but its use in cats with hypersomatotropism is not described. HYPOTHESIS/

objectivesTo describe the use of velagliflozin in cats with DM and hypersomatotropism. ANIMALS: Eight client-owned cats with DM and hypersomatotropism treated with velagliflozin.

methodsRetrospective multicentric case series. Clinical data, including diabetic clinical score, insulin dose, and continuous glucose monitoring-derived metrics were compared between the last follow-up before velagliflozin introduction (T0) and the first (T1) and last (T2) follow-ups after velagliflozin introduction.

resultsDiabetic clinical score improved in 6/8 cats after velagliflozin initiation. Median daily insulin dose decreased from 1.9 U/kg (range 0.8-7.1) at T0 to 0.5 U/kg (0-2.3) at T1 (median difference [MD] = -1.2 U/kg; 95% CI: -5.2 to 0.5; p = 0.02). Mean glucose was lower both at T1 (207 mg/dL, 96-326) and T2 (273 mg/dL, 155-350) than at T0 (435 mg/dL, 298-477; MD = -177 mg/dL, 95% CI: -238 to -92, p = 0.008 and MD = -113 mg/dL, 95% CI: -280 to -18, p = 0.03, respectively). Percentage of time in range was higher at T1 (71%, 21-98) and T2 (41%, 14-100) than at T0 (3%, 0-32; MD = 61%, 95% CI: 21 to 80, p = 0.008 and MD = 34%, 95% CI: 2 to 98, p = 0.03, respectively). Velagliflozin allowed for insulin discontinuation in two cats. One cat developed diabetic ketoacidosis on day 143, and one cat had acute kidney injury. CONCLUSIONS AND CLINICAL IMPORTANCE: Velagliflozin improved diabetic control in cats with DM and hypersomatotropism, either in combination with insulin or as monotherapy.

Indexed as

Bridged Bicyclo Compounds, HeterocyclicCat DiseasesDiabetes MellitusGlucosidesHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsAnimalsBlood GlucoseCatsFemaleInsulinMaleRetrospective StudiesBlood GlucoseBridged Bicyclo Compounds, HeterocyclicGlucosidesHypoglycemic AgentsInsulinSodium-Glucose Transporter 2 Inhibitorscontinuous glucose monitoringdiabetic ketoacidosisinsulin‐resistancemean glucoseSGLT2 inhibitors acromegaly

Identifiers

PMID40853201
PMCPMC12376337

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.