Department of Medicine, University of California, San Francisco.
Kidney Health Research Collaborative, University of California, San Francisco.
JAMA. 2022 Sep 6;328(9):861-871. doi: 10.1001/jama.2022.13885.
Novel therapies for type 2 diabetes can reduce the risk of cardiovascular disease and chronic kidney disease progression. The equitability of these agents' prescription across racial and ethnic groups has not been well-evaluated.
To investigate differences in the prescription of sodium-glucose cotransporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1 RA) among adult patients with type 2 diabetes by racial and ethnic groups.
DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional analysis of data from the US Veterans Health Administration's Corporate Data Warehouse. The sample included adult patients with type 2 diabetes and at least 2 primary care clinic visits from January 1, 2019, to December 31, 2020.
Self-identified race and self-identified ethnicity.
The primary outcomes were prevalent SGLT2i or GLP-1 RA prescription, defined as any active prescription during the study period.
Among 1 197 914 patients (mean age, 68 years; 96% men; 1% American Indian or Alaska Native, 2% Asian, Native Hawaiian, or Other Pacific Islander, 20% Black or African American, 71% White, and 7% of Hispanic or Latino ethnicity), 10.7% and 7.7% were prescribed an SGLT2i or a GLP-1 RA, respectively. Prescription rates for SGLT2i and GLP-1 RA, respectively, were 11% and 8.4% among American Indian or Alaska Native patients; 11.8% and 8% among Asian, Native Hawaiian, or Other Pacific Islander patients; 8.8% and 6.1% among Black or African American patients; and 11.3% and 8.2% among White patients, respectively. Prescription rates for SGLT2i and GLP-1 RA, respectively, were 11% and 7.1% among Hispanic or Latino patients and 10.7% and 7.8% among non-Hispanic or Latino patients. After accounting for patient- and system-level factors, all racial groups had significantly lower odds of SGLT2i and GLP-1 RA prescription compared with White patients. Black patients had the lowest odds of prescription compared with White patients (adjusted odds ratio, 0.72 [95% CI, 0.71-0.74] for SGLT2i and 0.64 [95% CI, 0.63-0.66] for GLP-1 RA). Patients of Hispanic or Latino ethnicity had significantly lower odds of prescription (0.90 [95% CI, 0.88-0.93] for SGLT2i and 0.88 [95% CI, 0.85-0.91] for GLP-1 RA) compared with non-Hispanic or Latino patients.
Among patients with type 2 diabetes in the Veterans Health Administration system during 2019 and 2020, prescription rates of SGLT2i and GLP-1 RA medications were low, and individuals of several different racial groups and those of Hispanic ethnicity had statistically significantly lower odds of receiving prescriptions for these medications compared with individuals of White race and non-Hispanic ethnicity. Further research is needed to understand the mechanisms underlying these differences in rates of prescribing and the potential relationship with differences in clinical outcomes.
重要性:新型 2 型糖尿病治疗方法可以降低心血管疾病和慢性肾脏疾病进展的风险。这些药物在不同种族和族裔群体中的处方公平性尚未得到充分评估。
目的:调查美国退伍军人健康管理局企业数据仓库中,2 型糖尿病成年患者按种族和族裔群体使用钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)和胰高血糖素样肽-1 受体激动剂(GLP-1 RA)的差异。
设计、设置和参与者:对 2019 年 1 月 1 日至 2020 年 12 月 31 日期间至少有 2 次初级保健诊所就诊的美国退伍军人健康管理局企业数据仓库数据进行的横断面分析。样本包括 2 型糖尿病成年患者。
暴露:自我认定的种族和自我认定的族裔。
主要结果和措施:主要结局是普遍存在的 SGLT2i 或 GLP-1 RA 处方,定义为研究期间的任何活性处方。
结果:在 1197914 名患者(平均年龄 68 岁;96%为男性;1%为美洲印第安人或阿拉斯加原住民,2%为亚洲人、夏威夷原住民或其他太平洋岛民,20%为黑人或非裔美国人,71%为白人,7%为西班牙裔或拉丁裔)中,分别有 10.7%和 7.7%被处方了 SGLT2i 或 GLP-1 RA。美洲印第安人或阿拉斯加原住民患者的 SGLT2i 和 GLP-1 RA 处方率分别为 11%和 8.4%;亚洲人、夏威夷原住民或其他太平洋岛民患者分别为 11.8%和 8%;黑人或非裔美国人患者分别为 8.8%和 6.1%;白种人患者分别为 11.3%和 8.2%。西班牙裔或拉丁裔患者的 SGLT2i 和 GLP-1 RA 处方率分别为 11%和 7.1%,非西班牙裔或拉丁裔患者分别为 10.7%和 7.8%。在考虑了患者和系统层面的因素后,与白人患者相比,所有种族群体的 SGLT2i 和 GLP-1 RA 处方率均显著降低。与白人患者相比,黑人患者的处方率最低(SGLT2i 的调整后优势比为 0.72 [95%CI,0.71-0.74];GLP-1 RA 为 0.64 [95%CI,0.63-0.66])。与非西班牙裔或拉丁裔患者相比,西班牙裔或拉丁裔患者的处方率显著降低(SGLT2i 的调整后优势比为 0.90 [95%CI,0.88-0.93];GLP-1 RA 为 0.88 [95%CI,0.85-0.91])。
结论和相关性:在 2019 年至 2020 年期间,退伍军人健康管理局系统中 2 型糖尿病患者的 SGLT2i 和 GLP-1 RA 药物处方率较低,与白人种族和非西班牙裔或拉丁裔相比,几个不同种族群体和西班牙裔的个体接受这些药物处方的几率统计学上显著降低。需要进一步研究以了解这些处方率差异的背后机制以及与临床结果差异的潜在关系。