Effects of Sodium-Glucose Cotransporter-2 Inhibitors on Kidney Outcomes across Baseline Cardiovascular-Kidney-Metabolic Conditions: A Systematic Review and Meta-Analyses

被引:3
|
作者
Siddiqi, Tariq Jamal [1 ]
Cherney, David [2 ]
Siddiqui, Hasan Fareed [3 ]
Jafar, Tazeen H. [4 ]
Januzzi, James L. [5 ,6 ]
Khan, Muhammad Shahzeb [7 ]
Levin, Adeera [8 ]
Marx, Nikolaus [9 ]
Rangaswami, Janani [10 ]
Testani, Jeffrey [11 ,12 ]
Usman, Muhammad Shariq [13 ]
Wanner, Christoph [14 ]
Zannad, Faiez [15 ,16 ]
Butler, Javed [17 ,18 ]
机构
[1] Baylor Univ, Dept Med, Med Ctr, Dallas, TX USA
[2] Univ Toronto, Univ Hlth Network, Div Nephrol, Toronto, ON, Canada
[3] Dow Univ Hlth Sci, Dept Med, Karachi, Pakistan
[4] Duke NUS Med Sch, Program Hlth Serv & Syst Res, Singapore, Singapore
[5] Massachusetts Gen Hosp, Boston, MA USA
[6] Baim Inst Clin Res, Boston, MA USA
[7] Duke Univ, Div Cardiol, Sch Med, Durham, NC USA
[8] Univ British Columbia, St Pauls Hosp, Div Nephrol, Vancouver, BC, Canada
[9] Rhein Westfal TH Aachen, Univ Hosp Aachen, Dept Internal Med 1, Aachen, Germany
[10] Washington DV VA Med Ctr, Div Nephrol, Washington, DC USA
[11] Smidt Heart Inst, Dept Cardiol, Los Angeles, CA USA
[12] Yale Univ, Dept Internal Med, Sect Cardiovasc Med, Sch Med, New Haven, CT USA
[13] UT Southwestern Med Ctr, Dept Med, Dallas, TX USA
[14] Univ Wurzburg, Renal Res Unit, Dept Clin Res & Epidemiol, Comprehens Heart Failure Ctr, Wurzburg, Germany
[15] Univ Lorraine, INSERM, Ctr Invest Clin, Plurithemat 1433, Nancy, France
[16] CHRU, INSERM, U1116, F CRIN INI CRCT Cardiovasc & Renal Clin Trialists, Nancy, France
[17] Univ Mississippi, Med Ctr, Dept Med, Jackson, MS 39216 USA
[18] Baylor Scott & White Hlth, Baylor Scott & White Res Inst, Dallas, TX 75246 USA
来源
关键词
CKD; diabetes mellitus; heart failure;
D O I
10.1681/ASN.0000000000000491
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 effects of sodium-glucose cotransporter-2 inhibitors (SGLT2is) on kidney outcomes in patients with varying combinations of heart failure, CKD, and type 2 diabetes mellitus have not been quantified. Methods PubMed and Scopus were queried up to December 2023 for primary and secondary analyses of placebo-controlled trials of SGLT2is in patients with heart failure, CKD, or type 2 diabetes mellitus. Outcomes of interest were composite kidney end point (combination of eGFR <15 ml/min per 1.73 m(2), sustained doubling of serum creatinine, varying percent change in eGFR, and need for KRT), rate of eGFR slope decline, and albuminuria progression. Hazard ratios (HRs) and mean differences with their 95% confidence intervals (CIs) were extracted onto an Excel sheet, and the results were then pooled using a random-effect model through Review Manager (version 5.3, Cochrane Collaboration). Results Eleven trials (n=80,928 patients) were included. Compared with the placebo, SGLT2is reduced the risk of the composite kidney end point by 41% (HR, 0.59; 95% CI, 0.42 to 0.83) in heart failure with reduced ejection fraction, 36% (HR, 0.64; 95% CI, 0.55 to 0.73) in CKD, and 38% (HR, 0.62; 95% CI, 0.56 to 0.69) in type 2 diabetes mellitus. A similar pattern of benefit was observed in combinations of these comorbidities and in patients without baseline heart failure, CKD, or type 2 diabetes mellitus. SGLT2is slowed the rate of eGFR slope decline and reduced the risk of sustained doubling of serum creatinine by 36% (HR, 0.64; 95% CI, 0.56 to 0.72) in the overall population, and a consistent effect on kidney outcomes was observed in most subpopulations with available data. Conclusions SGLT2i improved kidney outcomes in cohorts with heart failure, CKD, and type 2 diabetes mellitus, and these effects were consistent across patients with different combinations of these comorbidities.
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收藏
页码:242 / 255
页数:14
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