Extending the ambit of SGLT2 inhibitors beyond diabetes: a review of clinical and preclinical studies on non-diabetic kidney disease

被引:4
作者
Nayak, Saurabh [1 ]
Rathore, Vinay [1 ]
Bharati, Joyita [2 ]
Sahu, Kamal Kant [3 ]
机构
[1] All India Inst Med Sci, Dept Nephrol, Raipur, Madhya Pradesh, India
[2] Postgrad Inst Med Educ & Res, Dept Nephrol, Chandigarh, India
[3] Univ Utah, Huntsman Canc Inst, Dept Internal Med, Div Hematol & Med Oncol, Salt Lake City, UT 84112 USA
关键词
SGLT2i; non-diabetic CKD; diabetic kidney disease; NHE3; AMPK-SIRT1; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; DAPAGLIFLOZIN REDUCES ALBUMINURIA; COTRANSPORTER; INHIBITION; POST-HOC ANALYSIS; SERUM URIC-ACID; GLOMERULAR HYPERFILTRATION; ATUBULAR GLOMERULI; PROXIMAL TUBULE; CARDIOVASCULAR OUTCOMES; POTENTIAL MECHANISM;
D O I
10.1080/17512433.2021.2028620
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are novel antidiabetic agents with overwhelming cardiorenal protection. Recent trials focusing on the nephroprotective role of SGLT2i have underscored its success as a phenomenal agent in halting the progression of kidney disease in patients with and without Type 2 diabetes mellitus. Multitudes of pleiotropic effects on tubules have raised hopes for reasonable nephroprotection beyond the purview of the hyperglycemic milieu. Area covered This review summarizes various animal and human data as evidence for the utility of SGLT2i in non-diabetic chronic kidney disease (CKD). Web-based medical database entries were searched. On the premise of existing evidence, we have discussed mechanisms likely contributing to nephroprotection by SGLT2i in patients with non-diabetic CKD. Expert opinion Further elucidation of mechanisms of nephroprotection offered by SGLT2i is required to extend its use as a nephroprotective agent. The use of non-traditional markers of kidney damage in future studies would improve the evaluation of their role in attenuating CKD progression. Emerging animal data support the early use of SGLT2i in states of modest proteinuria for superior outcomes. Future long-term trials in patients should aim to address the time of intervention with SGLT2i during the natural disease course of CKD for best outcomes.
引用
收藏
页码:1513 / 1526
页数:14
相关论文
共 126 条
[51]   How Does Empagliflozin Reduce Cardiovascular Mortality? Insights From a Mediation Analysis of the EMPA-REG OUTCOME Trial [J].
Inzucchi, Silvio E. ;
Zinman, Bernard ;
Fitchett, David ;
Wanner, Christoph ;
Ferrannini, Ele ;
Schumacher, Martin ;
Schmoor, Claudia ;
Ohneberg, Kristin ;
Johansen, Odd Erik ;
George, Jyothis T. ;
Hantel, Stefan ;
Bluhmki, Erich ;
Lachin, John M. .
DIABETES CARE, 2018, 41 (02) :356-363
[52]   Residual proteinuria and eGFR predict progression of renal impairment within 2 years in type 2 diabetic patients with nephropathy who are receiving optimal treatment with angiotensin receptor blockers [J].
Ivory, Sara E. ;
Packham, David K. ;
Reutens, Anne T. ;
Wolfe, Rory ;
Rohde, Richard D. ;
Lewis, Julia ;
Atkins, Robert C. .
NEPHROLOGY, 2013, 18 (07) :516-524
[53]   Effect of dapagliflozin on urinary albumin excretion in patients with chronic kidney disease with and without type 2 diabetes: a prespecified analysis from the DAPA-CKD trial [J].
Jongs, Niels ;
Greene, Tom ;
Chertow, Glenn M. ;
McMurray, John J., V ;
Langkilde, Anna Maria ;
Correa-Rotter, Ricardo ;
Rossing, Peter ;
Sjostrom, C. David ;
Stefansson, Bergur, V ;
Toto, Robert D. ;
Wheeler, David C. ;
Heerspink, Hiddo J. L. .
LANCET DIABETES & ENDOCRINOLOGY, 2021, 9 (11) :755-766
[54]   Sodium-glucose cotransporter 2 inhibitors regulate ketone body metabolism via inter-organ crosstalk [J].
Kim, Jin Hee ;
Lee, Minyoung ;
Kim, Soo Hyun ;
Kim, So Ra ;
Lee, Byung-Wan ;
Kang, Eun Seok ;
Cha, Bong-Soo ;
Cho, Jin Won ;
Lee, Yong-ho .
DIABETES OBESITY & METABOLISM, 2019, 21 (04) :801-811
[55]   Empagliflozin alleviates podocytopathy and enhances glomerular nephrin expression in db/db diabetic mice [J].
Klimontov, Vadim V. ;
Korbut, Anton, I ;
Taskaeva, Iuliia S. ;
Bgatova, Nataliya P. ;
Dashkin, Maksim, V ;
Orlov, Nikolai B. ;
Khotskina, Anna S. ;
Zavyalov, Evgenii L. ;
Klein, Thomas .
WORLD JOURNAL OF DIABETES, 2020, 11 (12) :596-610
[56]   SGLT2 inhibition in a kidney with reduced nephron number: modeling and analysis of solute transport and metabolism [J].
Layton, Anita T. ;
Vallon, Volker .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2018, 314 (05) :F969-F984
[57]   The effects of canagliflozin on gout in type 2 diabetes: a post-hoc analysis of the CANVAS Program [J].
Li, JingWei ;
Badve, Sunit, V ;
Zhou, Zien ;
Rodgers, Anthony ;
Day, Richard ;
Oh, Richard ;
Lee, Mary ;
Perkovic, Vlado ;
de Zeeuw, Dick ;
Mahaffey, Kenneth W. ;
Futcher, Greg ;
Matthews, David R. ;
Neal, Bruce .
LANCET RHEUMATOLOGY, 2019, 1 (04) :E220-E228
[58]   Renal protective effects of empagliflozin via inhibition of EMT and aberrant glycolysis in proximal tubules [J].
Li, Jinpeng ;
Liu, Haijie ;
Takagi, Susumu ;
Nitta, Kyoko ;
Kitada, Munehiro ;
Srivastava, Swayam Prakash ;
Takagaki, Yuta ;
Kanasaki, Keizo ;
Koya, Daisuke .
JCI INSIGHT, 2020, 5 (06)
[59]   Effect of a SGLT2 inhibitor on the systemic and intrarenal renin-angiotensin system in subtotally nephrectomized rats [J].
Li, Lei ;
Konishi, Yoshio ;
Morikawa, Takashi ;
Zhang, Yifan ;
Kitabayashi, Chizuko ;
Kobara, Hideki ;
Masaki, Tsutomu ;
Nakano, Daisuke ;
Hitomi, Hirofumi ;
Kobori, Hiroyuki ;
Nishiyama, Akira .
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2018, 137 (02) :220-223
[60]   Proximal Tubule-Specific Deletion of the NHE3 (Na+/H+ Exchanger 3) in the Kidney Attenuates Ang II (Angiotensin II)-Induced Hypertension in Mice [J].
Li, Xiao C. ;
Zhu, Dongmin ;
Chen, Xu ;
Zheng, Xiaowen ;
Zhao, Chunling ;
Zhang, Jianfeng ;
Soleimani, Manoocher ;
Rubera, Isabelle ;
Tauc, Michel ;
Zhou, Xinchun ;
Zhuo, Jia L. .
HYPERTENSION, 2019, 74 (03) :526-535