The efficacy and safety of SGLT2 inhibitors in patients with non-diabetic chronic kidney disease: a systematic review and meta-analysis

被引:9
作者
Ma, Congyuan [1 ]
Li, Xuanwei [1 ]
Li, Wenlai [1 ]
Li, Yue [2 ]
Shui, Fangfang [2 ]
Zhu, Ping [1 ]
机构
[1] China Three Gorges Univ, Inst Nephrol, Coll Clin Med Sci 1, Yichang 443003, Hubei, Peoples R China
[2] Three Gorges Univ, Renhe Hosp, Dept endocrinol, Yichang 443003, Hubei, Peoples R China
关键词
sodium-glucose cotransporter2 (SGLT2) inhibitors; Type 2 diabetes mellitus (T2DM); Diabetic kidney disease (DKD); Non-diabetic nephropathy; Estimated glomerular filtration rate(eGFR); Meta-analysis; COTRANSPORTER; 2; INHIBITORS; DAPAGLIFLOZIN;
D O I
10.1007/s11255-023-03586-1
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
PurposeIn recent years, increasing evidence has shown that sodium-glucose cotransporter 2 inhibitors (SGLT2i) drugs have potential renoprotective effects in patients with diabetes mellitus (DM). However, the renal protective effect of SGLT2i in non-diabetic nephropathy patients has not been extensively demonstrated. In this systematic review and meta-analysis, we aimed to evaluate the renal protective effect and safety of SGLT2i in non-diabetic nephropathy patients.Methodswe searched for relevant clinically randomised controlled trials and analyzed the effects of SGLT2i on estimated glomerular filtration rate (eGFR), urinary albumin/creatinine ratio (UACR), and systolic blood pressure (SBP) and the incidence of adverse events in patients with non-diabetic nephropathy.ResultsWe collated and analysed clinical data from six groups of patients with nondiabetic nephropathy. It was found that the SGLT2i significantly delayed the decline in eGFR [MD = 1.35 ml/min/1.73 m(2), 95% CI 0.84, 1.86), P < 0.0001]. Furthermore, the SGLT2i significantly reduced UACR [MD = - 24.47% l, 95% CI (- 38.9, -10.04), P = 0.0009], and showed a greater decrease in SBP [MD = - 4.13 mmHg, 95% CI (- 7.49, - 0.77), P = 0.02]. There was no significant difference in the incidence of adverse reactions between dapagliflozin/empagliflozin and the control group [OR = 1.14, 95% CI (0.88, 1.47), P = 0.33].ConclusionThis study shows that SGLT2i help to delay the progression of non-diabetic kidney disease. Therefore, SGLT2i may contribute to the general treatment of nondiabetic nephropathy.
引用
收藏
页码:3167 / 3174
页数:8
相关论文
共 25 条
[1]   Combined sodium glucose co-transporter-2 inhibitor and angiotensin-converting enzyme inhibition upregulates the renin-angiotensin system in chronic kidney disease with type 2 diabetes: Results of a randomized, double-blind, placebo-controlled exploratory trial [J].
Antlanger, Marlies ;
Domenig, Oliver ;
Kaltenecker, Christopher C. ;
Kovarik, Johannes J. ;
Rathkolb, Vincent ;
Mueller, Martin M. ;
Schwaiger, Elisabeth ;
Hecking, Manfred ;
Poglitsch, Marko ;
Saeemann, Marcus D. ;
Kopecky, Chantal .
DIABETES OBESITY & METABOLISM, 2022, 24 (05) :816-826
[2]   Sodium-Glucose Cotransporter 2 Inhibition for the Prevention of Cardiovascular Events in Patients With Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis [J].
Arnott, Clare ;
Li, Qiang ;
Kang, Amy ;
Neuen, Brendon L. ;
Bompoint, Severine ;
Lam, Carolyn S. P. ;
Rodgers, Anthony ;
Mahaffey, Kenneth W. ;
Cannon, Christopher P. ;
Perkovic, Vlado ;
Jardine, Meg J. ;
Neal, Bruce .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2020, 9 (03)
[3]  
Cherney DZI, 2020, LANCET DIABETES ENDO, V8, P582, DOI 10.1016/S2213-8587(20)30162-5
[4]   Glucose Control and the Effect of Empagliflozin on Kidney Outcomes in Type 2 Diabetes: An Analysis From the EMPA-REG OUTCOME Trial [J].
Cooper, Mark E. ;
Inzucchi, Silvio E. ;
Zinman, Bernard ;
Hantel, Stefan ;
von Eynatten, Maximilian ;
Wanner, Christoph ;
Koitka-Weber, Audrey .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2019, 74 (05) :713-715
[5]   Nephroprotection by SGLT2 Inhibition: Back to the Future? [J].
De Nicola, Luca ;
Gabbai, Francis B. ;
Garofalo, Carlo ;
Conte, Giuseppe ;
Minutolo, Roberto .
JOURNAL OF CLINICAL MEDICINE, 2020, 9 (07) :1-14
[6]   Sodium-Glucose Co-transporters and Their Inhibition: Clinical Physiology [J].
Ferrannini, Ele .
CELL METABOLISM, 2017, 26 (01) :27-38
[7]   Effect of dapagliflozin on the rate of decline in kidney function in patients with chronic kidney disease with and without type 2 diabetes: a prespecified analysis from the DAPA-CKD trial [J].
Heerspink, Hiddo J. L. ;
Jongs, Niels ;
Chertow, Glenn M. ;
Langkilde, Anna Maria ;
McMurray, John J., V ;
Correa-Rotter, Ricardo ;
Rossing, Peter ;
Sjostrom, C. David ;
Stefansson, Bergur, V ;
Toto, Robert D. ;
Wheeler, David C. ;
Greene, Tom .
LANCET DIABETES & ENDOCRINOLOGY, 2021, 9 (11) :743-754
[8]   Rationale and protocol of the Dapagliflozin And Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) randomized controlled trial [J].
Heerspink, Hiddo J. L. ;
Stefansson, Bergur, V ;
Chertow, Glenn M. ;
Correa-Rotter, Ricardo ;
Greene, Tom ;
Hou, Fan-Fan ;
Lindberg, Magnus ;
McMurray, John ;
Rossing, Peter ;
Toto, Roberto ;
Langkilde, Anna Maria ;
Wheeler, David C. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2020, 35 (02) :274-282
[9]   Renoprotective effects of sodium-glucose cotransporter-2 inhibitors [J].
Heerspink, Hiddo J. L. ;
Kosiborod, Mikhail ;
Inzucchi, Silvio E. ;
Cherney, David Z. I. .
KIDNEY INTERNATIONAL, 2018, 94 (01) :26-39
[10]   Empagliflozin in Patients with Chronic Kidney Disease [J].
Herrington, William G. ;
Staplin, Natalie ;
Wanner, Christoph ;
Green, Jennifer B. ;
Hauske, Sibylle J. ;
Emberson, Jonathan R. ;
Preiss, David ;
Judge, Parminder ;
Mayne, Kaitlin J. ;
Ng, Sarah Y. A. ;
Sammons, Emily ;
Zhu, Doreen ;
Hill, Michael ;
Stevens, Will ;
Wallendszus, Karl ;
Brenner, Susanne ;
Cheung, Alfred K. ;
Liu, Zhi-Hong ;
Li, Jing ;
Hooi, Lai Seong ;
Liu, Wen ;
Kadowaki, Takashi ;
Nangaku, Masaomi ;
Levin, Adeera ;
Cherney, David ;
Maggioni, Aldo P. ;
Pontremoli, Roberto ;
Deo, Rajat ;
Goto, Shinya ;
Rossello, Xavier ;
Tuttle, Katherine R. ;
Steubl, Dominik ;
Petrini, Michaela ;
Massey, Dan ;
Eilbracht, Jens ;
Brueckmann, Martina ;
Landray, Martin J. ;
Baigent, Colin ;
Haynes, Richard .
NEW ENGLAND JOURNAL OF MEDICINE, 2023, 388 (02) :117-127