Evidence map›Paper›PMID 36601021›Full record

ReviewJournal of the Endocrine Society2022

Sodium-Glucose Cotransporter-2 Inhibition Benefits in Cardiorenal Risk in Men and Women.

Jacob E Pruett, Seth T Lirette, Damian G Romero, Licy L Yanes Cardozo

Open access · goldAbstract readReview
In one paragraph

Review in Journal of the Endocrine Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Jacob E PruettDepartment of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.ORCID https://orcid.org/0000-0002-5440-9413
Seth T LiretteDepartment of Data Science, University of Mississippi Medical Center, Jackson, MS, USA.ORCID https://orcid.org/0000-0003-2603-6071
Damian G RomeroDepartment of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.ORCID https://orcid.org/0000-0002-7268-9690
Licy L Yanes CardozoDepartment of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.ORCID https://orcid.org/0000-0002-7295-1871
Jackson Memorial Hospital · USUniversity of Mississippi Medical Center · US

Funding

Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI JONES, ALAN E · 2016 to 2025
$38.2M
Investigator Development CoreP50MD017338 · NIMHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BASKIN, MONICA L. · 2021 to 2025
$27.7M
Role of obesity in preeclamptic pregnancy.P20GM121334 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI Ashley C. Johnson, Babbette LaMarca · 2017 to 2026
$26.4M
Role of microRNA_21 in acetaminophen-induced acute liver failureR21DK113500 · NIDDK · UNIVERSITY OF MISSISSIPPI MED CTR · PI ROMERO, DAMIAN G. · 2017 to 2019
$580k
Impact of SGLT-2 Inhibition on the Cardiometabolic Profile of PCOSF30DK127527 · NIDDK · UNIVERSITY OF MISSISSIPPI MED CTR · PI PRUETT, JACOB E · 2021 to 2022
$76k
NIDDK NIH HHS F30 DK127527NIDDK NIH HHS R21 DK113500NIGMS NIH HHS P20 GM121334NIGMS NIH HHS U54 GM115428NIMHD NIH HHS P50 MD017338
6 · The paper itself

Abstract

Introduction: In addition to their antihyperglycemic action, sodium-glucose cotransporter-2 (SGLT2) inhibitors are used in patients with type 2 diabetes due to their cardioprotective effects. Meta-analyses of large clinical trials have reported mixed results when examining sex differences in their cardioprotective effects. For example, some studies reported that, compared to women, men had a greater reduction in cardiovascular risk with SGLT2 inhibition. Taking advantage of several recently completed large-scale randomized controlled clinical trials, we tested the hypothesis that women have an attenuated response in primary cardiorenal outcomes to SGLT2 inhibition compared to men. Methods: We performed a systematic search using PubMed and the Cochrane Library to find completed large-scale, prospective, randomized controlled Phase III clinical trials with primary outcomes testing cardiovascular or renal benefit. Studies had to include at least 1000 participants and report data about sex differences in their primary cardiovascular or renal outcomes. Results: The present meta-analysis confirmed that SGLT2 inhibition decreased adverse cardiorenal outcomes in a pooled sex analysis using 13 large-scale clinical trials. SGLT2 inhibition exhibited similar reduction in hazard ratios for both men (0.79, 95% CI, 0.73-0.85) and women (0.78, 95% CI, 0.72-0.84) for adverse cardiorenal outcomes. Conclusion: In contrast to previous findings, our updated meta-analysis suggests that women and men experience similar cardiorenal benefit in response to SGLT2 inhibition. These findings strongly suggest that SGLT2 inhibition therapy should be considered in patients with high risk for cardiovascular disease irrespective of the patient sex.

Indexed as

cardiorenal riskmeta-analysissex differencessodium-glucose cotransporter-2

Identifiers

PMID36601021
PMCPMC9795477
OpenAlexW4311220127

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.