Sociodemographic disparities in GLP-1RA and SGLT2i use among US adults with type 2 diabetes: NHANES 2005-March 2020

被引:4
作者
Mittman, Benjamin G. [1 ,2 ,5 ]
Le, Phuc [1 ]
Payne, Julia Y. [1 ,2 ]
Ayers, Gina [3 ,4 ]
Rothberg, Michael B. [1 ]
机构
[1] Cleveland Clin, Ctr Value Based Care Res, Cleveland, OH USA
[2] Case Western Reserve Univ, Sch Med, Dept Populat & Quantitat Hlth Sci, Cleveland, OH USA
[3] Cleveland Clin, Dept Pharm, Cleveland, OH USA
[4] Cleveland Clin, Ctr Geriatr Med, Cleveland, OH USA
[5] Cleveland Clin, Ctr Value Based Care Res, 9500 Euclid Ave,Mail Code G10, Cleveland, OH 44195 USA
关键词
Disparities; GLP-1RA; SGLT2i; diabetes; NHANES; RECEPTOR AGONISTS; INHIBITORS; ASSOCIATION; MEDICATIONS;
D O I
10.1080/03007995.2024.2303413
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Type 2 Diabetes (T2D) is a major cause of morbidity and mortality. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 inhibitors (SGLT2i) are highly effective but underutilized. Our objective was to assess racial/ethnic and other sociodemographic disparities in GLP-1RA/SGLT2i use among US adults with T2D.Methods: We conducted a retrospective analysis using the National Health and Nutrition Examination Survey from 2005-March 2020. Participants were adults with T2D taking >= 1 anti-diabetic medication, excluding pregnant women and adults with probable T1D. We performed univariate analyses to examine the characteristics of patients using GLP-1RA/SGLT2i and multivariable logistic regression to assess disparities in GLP-1RA/SGLT2i use after adjusting for other patient factors.Results: Among 4777 people with T2D (representing >18 million US adults) taking >= 1 medication, GLP-1RA/SGLT2i usage increased from 1.4% in 2005-2006 to 13.3% in 2017-2020. In univariate analyses, patients using GLP-1RA/SGLT2i vs. other T2D drugs were more likely to be White than nonwhite (72% vs. 60%, p = .001), but in multivariable analysis there was no significant difference in GLP-1RA/SGLT2i use for nonwhite vs. White patients (aOR = 0.84, 95% CI [0.61, 1.16]). GLP-1RA/SGLT2i use was higher for patients who completed some college (aOR = 1.83, 95% CI [1.06, 3.15]) or above (aOR = 2.06, 95% CI [1.28, 3.32]) vs. high school or less, and for those with an income-poverty ratio >= 4 vs. <2 (aOR = 2.11, 95% CI [1.30, 3.42]).Conclusions: The use of GLP-1RA/SGLT2i drugs increased over time but remained low in March 2020. Higher education and income, but not race/ethnicity, were associated with GLP-1RA/SGLT2i use.
引用
收藏
页码:377 / 383
页数:7
相关论文
共 35 条
  • [31] Recommended and Prevalent Use of Glucagon-like Peptide-1 Receptor Agonists and Sodium-Glucose Cotransporter-2 Inhibitors in a National Population-Based Sample
    Tang, Shichao
    Shao, Hui
    Ali, Mohammed K.
    Zhang, Ping
    [J]. ANNALS OF INTERNAL MEDICINE, 2023, 176 (04) : 582 - 583
  • [32] The High Cost of Diabetes Drugs: Disparate Impact on the Most Vulnerable Patients
    Taylor, Simeon I.
    [J]. DIABETES CARE, 2020, 43 (10) : 2330 - 2332
  • [33] The prevalence of cardiovascular disease and antidiabetes treatment characteristics among a large type 2 diabetes population in the United States
    Weng, Wayne
    Tian, Ye
    Kong, Sheldon X.
    Ganguly, Rahul
    Hersloev, Malene
    Brett, Jason
    Hobbs, Todd
    [J]. ENDOCRINOLOGY DIABETES & METABOLISM, 2019, 2 (03)
  • [34] Disparities in SGLT2 Inhibitor or Glucagon-Like Peptide 1 Receptor Agonist Initiation Among Medicare-Insured Adults With CKD in the United States
    Zhao, Julie Z.
    Weinhandl, Eric D.
    Carlson, Angeline M.
    Peter, Wendy L. St.
    [J]. KIDNEY MEDICINE, 2023, 5 (01)
  • [35] Association Between Use of Sodium-Glucose Cotransporter 2 Inhibitors, Glucagon-like Peptide 1 Agonists, and Dipeptidyl Peptidase 4 Inhibitors With All-Cause Mortality in Patients With Type 2 Diabetes A Systematic Review and Meta-analysis
    Zheng, Sean L.
    Roddick, Alistair J.
    Aghar-Jaffar, Rochan
    Shun-Shin, Matthew J.
    Francis, Darrel
    Oliver, Nick
    Meeran, Karim
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2018, 319 (15): : 1580 - 1591