Evidence map›Paper›PMID 33856475›Full record

ArticleJAMA network open2021

Association of Race/Ethnicity, Gender, and Socioeconomic Status With Sodium-Glucose Cotransporter 2 Inhibitor Use Among Patients With Diabetes in the US.

Lauren A Eberly, Lin Yang, Nwamaka D Eneanya, Utibe Essien, Howard Julien, Ashwin S Nathan, Sameed Ahmed M Khatana, Elias J Dayoub, Alexander C Fanaroff, Jay Giri and 2 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 182 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
182citing papers in PubMed, 9 pooled it
36.7field-weighted citation impact, top 1% 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

182 citing papers in PubMed, 9 syntheses or guidelines pooled it, 327 citations in OpenAlex.

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122 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 1 country.

Lauren A EberlyCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Lin YangCenter for Cardiovascular Outcomes, Quality, and Evaluative Research, University of Pennsylvania, Philadelphia.
Nwamaka D EneanyaLeonard Davis Institute of Health Economics at the University of Pennsylvania, Philadelphia.
Utibe EssienDivision of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Howard JulienCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Ashwin S NathanCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Sameed Ahmed M KhatanaCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Elias J DayoubCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Alexander C FanaroffCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Jay GiriCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Peter W GroeneveldCenter for Cardiovascular Outcomes, Quality, and Evaluative Research, University of Pennsylvania, Philadelphia.
Srinath AdusumalliCardiovascular Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
University of Pennsylvania · USPenn Center for AIDS Research · USPhiladelphia VA Medical Center · USVA Pittsburgh Healthcare System · US

Funding

Access, Quality and Equity of Anticoagulants in Veterans with Atrial FibrillationIK2HX003176 · VA · VETERANS HEALTH ADMINISTRATION · PI Utibe R. Essien · 2021 to 2026
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HSRD VA IK2 HX003176
6 · The paper itself

Abstract

Importance: Sodium-glucose cotransporter 2 (SGLT2) inhibitors significantly reduce deaths from cardiovascular conditions, hospitalizations for heart failure, and progression of kidney disease among patients with type 2 diabetes. Black individuals have a disproportionate burden of cardiovascular and chronic kidney disease (CKD). Adoption of novel therapeutics has been slower among Black and female patients and among patients with low socioeconomic status than among White or male patients or patients with higher socioeconomic status. Objective: To assess whether inequities based on race/ethnicity, gender, and socioeconomic status exist in SGLT2 inhibitor use among patients with type 2 diabetes in the US. Design, Setting, and Participants: This retrospective cohort study of commercially insured patients in the US was performed from October 1, 2015, to June 30, 2019, using the Optum Clinformatics Data Mart. Adult patients with a diagnosis of type 2 diabetes, including those with heart failure with reduced ejection fraction (HFrEF), atherosclerotic cardiovascular disease (ASCVD), or CKD, were evaluated in the analysis. Main Outcomes and Measures: Prescription of an SGLT2 inhibitor. Multivariable logistic regression models were used to assess the association of race/ethnicity, gender, and socioeconomic status with SGLT2 inhibitor use. Results: Of 934 737 patients with type 2 diabetes (mean [SD] age, 65.4 [12.9] years; 50.7% female; 57.6% White), 81 007 (8.7%) were treated with an SGLT2 inhibitor during the study period. Between 2015 and 2019, the percentage of patients with type 2 diabetes treated with an SGLT2 inhibitor increased from 3.8% to 11.9%. Among patients with type 2 diabetes and cardiovascular or kidney disease, the rate of SGLT2 inhibitor use increased but was lower than that among all patients with type 2 diabetes (HFrEF: 1.9% to 7.6%; ASCVD: 3.0% to 9.8%; CKD: 2.1% to 7.5%). In multivariable analyses, Black race (adjusted odds ratio [aOR], 0.83; 95% CI, 0.81-0.85), Asian race (aOR, 0.94; 95% CI, 0.90-0.98), and female gender (aOR, 0.84; 95% CI, 0.82-0.85) were associated with lower rates of SGLT2 inhibitor use, whereas higher median household income (≥$100 000: aOR, 1.08 [95% CI, 1.05-1.10]; $50 000-$99 999: aOR, 1.05 [95% CI, 1.03-1.07] vs <$50 000) was associated with a higher rate of SGLT2 inhibitor use. These results were similar among patients with HFrEF, ASCVD, and CKD. Conclusions and Relevance: In this cohort study, use of an SGLT2 inhibitor treatment increased among patients with type 2 diabetes from 2015 to 2019 but remained low, particularly among patients with HFrEF, CKD, and ASCVD. Black and female patients and patients with low socioeconomic status were less likely to receive an SGLT2 inhibitor, suggesting that interventions to ensure more equitable use are essential to prevent worsening of well-documented disparities in cardiovascular and kidney outcomes in the US.

Indexed as

AgedBlack or African AmericanDatabases, FactualDiabetes Mellitus, Type 2FemaleHealthcare DisparitiesHumansMaleMiddle AgedRetrospective StudiesSex DistributionSocial ClassSodium-Glucose Transporter 2 InhibitorsSodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID33856475
PMCPMC8050743
OpenAlexW3153561131

What OpenQuestion holds

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LicenceCC BY
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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.