Sodium-Glucose Cotransporter-2 Inhibitor and Glucagon-Like Peptide-1 Receptor Agonist Combination Therapy in Type 2 Diabetes: Protocol for a Kidney End Points Real-world Study (COMBi-KID Study)

被引:0
作者
Feher, Michael [1 ]
Hinton, William [1 ]
Forbes, Anna [1 ]
Munro, Neil [2 ]
Joy, Mark [1 ]
Wheeler, David [3 ]
de Lusignan, Simon [1 ]
机构
[1] Univ Oxford, Nuffield Dept Primary Care Hlth Sci, Clin Informat & Hlth Outcomes Res Grp, Eagle House,Walton Well Rd, Oxford OX2 6ED, England
[2] Univ Surrey, Clin Informat, Guildford, Surrey, England
[3] UCL, Dept Renal Med, London, England
关键词
type; 2; diabetes; sodium-glucose cotransporter-2 inhibitor; glucagon-like peptide-1 receptor agonist; renal; kidney; electronic health records; CARDIOVASCULAR OUTCOMES; EMPAGLIFLOZIN;
D O I
10.2196/34206
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Sodium-glucose cotransporter-2 inhibitors (SGLT2is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) are both considered to be part of standard care in the management of glycemia in type 2 diabetes. Recent trial evidence has indicated benefits on primary kidney end points for individual drugs within each medication class. Despite the potential benefits of combining SGLT2is and GLP-1RAs for glycemia management, according to national and international guideline recommendations, there is currently limited data on kidney end points for this drug combination. Objective: The aims of the study are to assess the real-world effects of combination SGLT2i and GLP-1RA therapies for diabetes management on kidney end points, glycemic control, and weight in people with type 2 diabetes who are being treated with renin-angiotensin system blockade medication. Methods: This retrospective cohort study will use the electronic health records of people with type 2 diabetes that are registered with general practices covering over 15 million people in England and Wales and are included in the Oxford-Royal College of General Practitioners Research and Surveillance Centre network. A propensity score-matched cohort of prevalent new users of SGLT2is and GLP-1RAs and those who have been prescribed SGLT2is and GLP-1RAs in combination will be identified. They will be matched based on drug histories, comorbidities, and demographics. A repeated-measures, multilevel, linear regression analysis will be performed to compare the mean change (from baseline) in estimated glomerular filtration rate at 12 and 24 months between those who switched to combined therapy and those continuing monotherapy with an SGLT2i or GLP-IRA. The secondary end points will be albuminuria, serum creatinine level, glycated hemoglobin level, and BMI. These will also be assessed for change at the 12- and 24-month follow-ups. Results: The study is due to commence in March 2022 and is expected to be complete by September 2022. Conclusions: Our study will be the first to assess the impact of combination SGLT2i and GLP-1RA therapy in type 2 diabetes on primary kidney end points from a real-world perspective.
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