Evidence map›Paper›PMID 39925502›Full record

ArticleCureus2025

Breaking Barriers: Tackling Racial and Socioeconomic Disparities in the Prescription of Life-Saving SGLT2 Inhibitors for Proteinuria.

Shay Taylor, Samrawit W Zinabu, Elijah McMillan, Emmanuel Ocampo, Alexis Edmonds, Sierra Lyles, John Pempeh, Kira Yates, Miriam Micheal

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

9 authors.

Shay TaylorInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
Samrawit W ZinabuInternal Medicine, Howard University Hospital, Washington, DC, USA.
Elijah McMillanInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
Emmanuel OcampoInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
Alexis EdmondsInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
Sierra LylesInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
John PempehInternal Medicine, Howard University Hospital, Washington, DC, USA.
Kira YatesInternal Medicine, Howard University College of Medicine, Washington, DC, USA.
Miriam MichealInternal Medicine, Howard University College of Medicine, Washington, DC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe underutilization of sodium-glucose co-transporter type 2 inhibitors (SGLT2i), despite their proven cardiovascular and renal benefits, raises concerns about healthcare equity. SGLT2i effectively reduces proteinuria, a key indicator of kidney disease, making them an essential treatment for individuals with or without diabetes, particularly those at higher risk, such as the Black American population, who have a higher prevalence of proteinuria. However, studies show disparities in SGLT2i prescriptions with race, ethnicity, and socioeconomic status contributing to lower utilization rates among vulnerable populations. This study aims to explore SGLT2i prescription patterns in Maryland, focusing on patients with proteinuria to address these disparities and improve access to care.

objectiveThe objective of the study was to identify racial and socioeconomic disparities in access to SGLT2i.

methodsThis retrospective cohort study utilized de-identified electronic health records (EHR) sourced from the Epic database across the University of Maryland Medical System (UMMS), spanning a 10-year period from January 1, 2014, to December 31, 2023, and evaluated SGLT2i prescription patterns among patients with proteinuria.

resultOf the 5,866,616 patients in the UMMS system, 28,136 were diagnosed with proteinuria, of whom 4,360 (15.5%) were prescribed SGLT2i medications. Among those receiving prescriptions, 37.9% self-identified as Black American, while 54.7% identified as White American. Notable geographical disparities were observed in prescription rates. In affluent areas such as Fulton, MD (zip code 20759), only 0.046% of patients with proteinuria received SGLT2i prescriptions, compared to 1.4% in the lower-income area of West Baltimore, MD (zip code 21223). Bivariate analysis revealed significant disparities in SGLT2i prescription rates, with Black American patients having lower odds of receiving prescriptions compared to White American patients (OR = 0.68,

conclusionThis study reveals significant disparities in the prescription of SGLT2i among patients with proteinuria in Maryland, United States, highlighting the influence of socioeconomic factors on access to these vital treatments. Despite the established benefits of SGLT2i in managing proteinuria and reducing the risk of kidney and cardiovascular disease, systemic inequities persist, potentially leaving high-risk populations underserved. These findings call for a deeper examination of the structural and systemic barriers contributing to these disparities, as well as the development of strategies to promote equitable access to care. Ensuring that all patients, regardless of their background or socioeconomic status, have access to evidence-based therapies is essential for improving outcomes and reducing healthcare inequities.

Indexed as

prescription patternproteinuriasglt-2 inhibitorsocioeconomic disparitiestreatment barriers

Identifiers

PMID39925502
PMCPMC11805696

What OpenQuestion holds

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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.