Sodium-Glucose Cotransporter-2 Inhibitors versus Glucagon-Like Peptide 1 Receptor Agonists Effects on Kidney and Clinical Outcomes in Veterans with Type 2 Diabetes

被引:2
|
作者
Morello, Candis M. [1 ,2 ]
Awdishu, Linda [1 ]
Lam, Stepfanie [3 ]
Heman, Amy [4 ]
Bounthavong, Mark [1 ,5 ]
机构
[1] Univ Calif La Jolla, San Diego Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92037 USA
[2] Vet Affairs San Diego Healthcare Syst, San Diego, CA USA
[3] Stanford Hlth Care, Palo Alto, CA USA
[4] Sharp Grossmont Hosp, San Diego, CA USA
[5] US Dept Vet Affairs, Hlth Econ Resource Ctr, Menlo Pk, CA USA
来源
KIDNEY360 | 2024年 / 5卷 / 11期
关键词
CKD; diabetes; GFR; renal function; SGLT2; MULTIPLE IMPUTATION; PROPENSITY SCORE;
D O I
10.34067/KID.0000000597
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background The primary aim of this study was to compare kidney end points between patients with type 2 diabetes (T2D) 36 months after initiation on a sodium-glucose cotransporter-2 inhibitor (SGLT2i) or a glucagon-like peptide 1 receptor agonist (GLP-1RA). Secondary aims compared eGFR, hemoglobin A1c (HbA1c), weight, and urine albumin-creatinine ratio (UACR) changes. Methods We conducted a retrospective cohort study of propensity score-matched veterans with T2D, baseline eGFR >20 ml/min per 1.73 m(2), and initiated on a SGLT2i versus GLP-1RA between April 1, 2009 and September 1, 2020. Cox proportional hazard models were constructed to evaluate effectiveness between both groups on composite endpoint (decline of >= 40% in eGFR from baseline, ESKD event, and all-cause mortality) and its components, adjusting for baseline characteristics. Spline models were constructed to evaluate eGFR change, and linear mixed effects models were constructed to evaluate changes in HbA1c, weight, and UACR. We used an intent-to-treat (ITT) approach as our main analysis followed by a per-protocol (PP) approach excluding veterans who discontinued or switched therapy during the study period. Results A total of 29,146 propensity score-matched veterans were included in SGLT2i and GLP-1RA groups (14,573 per group). In the ITT and PP analyses, veterans initiated on SGLT2i had a 35% (hazard ratio, 0.65; 95% confidence interval [CI], 0.62 to 0.68) and 34% (hazard ratio, 0.66; 95% CI, 0.62 to 0.69) reduction in the hazard of experiencing the composite endpoint compared with veterans initiated on GLP-1RA adjusting for baseline characteristics, respectively. Between 6 and 36 months, we found an improved chronic eGFR slope with SGLT2i compared with GLP-1RA in both ITT and PP analyses; +1.19 ml/min per 1.73 m(2) (95% CI, 0.93 to 1.45) and +1.29 ml/min per 1.73 m(2) (95% CI, 1.01 to 1.57), respectively. The annual difference in chronic eGFR slope in both ITT and PP analyses were +0.97 ml/min per 1.73 m(2) per year (95% CI, 0.82 to 1.11) and +1.08 ml/min per 1.73 m(2) per year (95% CI, 0.92 to 1.25). Improved HbA1c, weight loss, and UACR were reported for both groups. Conclusions In this real-world study, veterans with T2D initiated on SGLT2i were associated with reduced hazard of experiencing mortality, worsening eGFR, or developing ESKD and improved glycemic, metabolic, and renal end points compared with GLP-1RA use.
引用
收藏
页码:1633 / 1643
页数:11
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