Kidney outcomes of SGLT2 inhibitors among older patients with diabetic kidney disease in real-world clinical practice: the Japan Chronic Kidney Disease Database Ex

被引:2
作者
Kitaoka, Kaori [1 ]
Yano, Yuichiro [1 ,2 ]
Nagasu, Hajime [3 ]
Kanegae, Hiroshi [4 ]
Chishima, Noriharu [5 ]
Akiyama, Hiroki [5 ]
Tamura, Kouichi [6 ]
Kashihara, Naoki [7 ]
机构
[1] Shiga Univ Med Sci, Noncommunicable Dis NCD Epidemiol Res Ctr, Otsu, Japan
[2] Juntendo Univ, Fac Med, Dept Gen Med, Tokyo, Japan
[3] Kawasaki Med Sch, Dept Nephrol & Hypertens, Kurashiki, Japan
[4] Genki Plaza Med Ctr Hlth Care, Off Res & Anal, Tokyo, Japan
[5] Cardiovasc Renal & Metab, BioPharmaceut Med, AstraZeneca, Osaka, Japan
[6] Yokohama City Univ, Sch Med, Grad Sch Med, Dept Med Sci & Cardiorenal Med, Yokohama, Japan
[7] Kawasaki Geriatr Med Ctr, Okayama, Japan
关键词
Diabetes Mellitus; Type; 2; PROPENSITY SCORE; GFR DECLINE; END-POINT; TRIALS; LIFE; V2.5;
D O I
10.1136/bmjdrc-2024-004115
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction We compared the kidney outcomes between patients with diabetic kidney disease (DKD) aged >= 75 years initiating sodium-glucose cotransporter 2 (SGLT2) inhibitors versus other glucose-lowering drugs, additionally presenting with or without proteinuria. Research design and methods Using the Japan Chronic Kidney Disease Database, we developed propensity scores, implementing a 1:1 matching protocol. The primary outcome included the decline rate in estimated glomerular filtration rate (eGFR), and secondary outcomes incorporated a composite of a 40% reduction in eGFR or progression to end-stage kidney disease. Results At baseline, the mean age at initiation of SGLT2 inhibitors (n=348) or other glucose-lowering medications (n=348) was 77.7 years. The mean eGFR was 59.3 mL/min/1.73m(2 )and proteinuria was 230 (33.0%) patients. Throughout the follow-up period, the mean annual rate of eGFR change was -0.80 mL/min/1.73 m2/year (95% CI -1.05 to -0.54) among SGLT2 inhibitors group and -1.78 mL/min/1.73 m(2)/year (95% CI -2.08 to -1.49) in other glucose-lowering drugs group (difference in the rate of eGFR decline between the groups was 0.99 mL/min/1.73 m2/year (95% CI 0.5 to 1.38)), favoring SGLT2 inhibitors (p<0.001). Composite renal outcomes were observed 38 in the SGLT2 inhibitors group and 57 in the other glucose-lowering medications group (HR 0.64, 95% CI 0.42 to 0.97). There was no evidence of an interaction between SGLT2 inhibitors initiation and proteinuria. Conclusions The benefits of SGLT2 inhibitors on renal outcomes are also applicable to older patients with DKD aged >= 75 years.
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