Evidence map›Paper›PMID 40580026›Full record

ArticleTherapeutic advances in respiratory disease

Effects of sodium-glucose cotransport-2 inhibitors treatment in patients with pulmonary hypertension.

Mohammed Obeidat, Aravinthan Vignarajah, Rashid Abdel-Razeq, Ala'eddien Nathir, Nishanthi A Vigneswaramoorthy, Adriano R Tonelli

Abstract readMulticenter Study
In one paragraph

Article in Therapeutic advances in respiratory disease. 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
–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

2 citing papers in PubMed.

  1. Review
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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

6 authors.

Mohammed ObeidatDepartment of Internal Medicine, Cleveland Clinic, Fairview Hospital, Cleveland, OH, USA.ORCID 0009-0008-7331-1586
Aravinthan VignarajahDepartment of Internal Medicine, Cleveland Clinic, Fairview Hospital, Cleveland, OH, USA.
Rashid Abdel-RazeqDepartment of Internal Medicine, Cleveland Clinic, Fairview Hospital, Cleveland, OH, USA.
Ala'eddien NathirSchool of Medicine, University of Jordan, Amman, Jordan.
Nishanthi A VigneswaramoorthyDepartment of Internal Medicine, Sunny Upstate Medical University, Syracuse, NY, USA.
Adriano R TonelliRespiratory Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.ORCID 0000-0002-2321-9545

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary hypertension (PH) is a complex disorder associated with various underlying conditions, including cardiac and respiratory diseases. PH is classified into five groups based on etiology, disease mechanisms, hemodynamic data, and treatment options. Preliminary data suggest that sodium-glucose cotransport-2 inhibitors (SGLT2-I), known for their benefits in chronic kidney disease, heart failure, and type-2 diabetes mellitus, may have therapeutic implications in PH through their metabolic effects, which include reducing aerobic glycolysis, improving mitochondrial function, and enhancing fatty acid oxidation.

objectiveThis study aimed to evaluate the clinical effects of SGLT2-I in PH by analyzing a large multicenter database of medical records from the TriNetX Network.

designThe cohort included adult patients with PH diagnosed between January 1, 2012, and January 1, 2023, classified by PH group and treatment with SGLT2-I. Propensity score matching (PSM) was used to balance baseline characteristics between the SGLT2-I and non-SGLT2-I groups.

methodsThe primary endpoint was a composite of all-cause mortality, RHF, and hospital admissions over 365 days. Secondary endpoints included the individual components of the primary endpoint, intubations, RHF incidence, IV diuretic use, and NT-Pro-BNP levels. PSM was used to adjust for baseline differences between cohorts.

resultsA total of 771,490 patients with PH were identified, with 58,303 treated with SGLT2-I. After PSM, each cohort of treated and untreated patients included 58,302 patients. Patients treated with SGLT inhibitors had a significant reduction in the primary composite endpoint (HR 0.71, 95% CI: 0.707-0.729). Secondary outcomes, including all-cause mortality, hospitalization, and the number of intubations, were also significantly lower in patients treated with SGLT-2 inhibitors. Beneficial effects of SGLT2-I were observed across all PH groups.

conclusionThis study demonstrates that SGLT2-I may be clinically beneficial in patients with PH by reducing all-cause mortality, RHF, and hospital admissions. Our findings support the role of SGLT2-I as a therapeutic option in PH and provide support for future randomized controlled trials using this treatment.

Indexed as

Hypertension, PulmonarySodium-Glucose Transporter 2 InhibitorsAdultAgedDatabases, FactualFemaleHospitalizationHumansMaleMiddle AgedRetrospective StudiesTime FactorsTreatment OutcomeSodium-Glucose Transporter 2 InhibitorsPulmonary HypertensionSGLT2- I

Identifiers

PMID40580026
PMCPMC12206267

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LicenceCC BY-NC-ND
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Registered trials

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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.