Affiliations 

  • 1 National University of Singapore, Singapore, Singapore
  • 2 Rajavithi Hospital, College of Medicine, Rangsit University, Bangkok, Thailand
  • 3 Department of Medicine, University of Malaya Medical Center, Kuala Lumpur, Malaysia
  • 4 Department of Medicine, Section of Endocrinology, Diabetes and Metabolism, University of Santo Tomas Hospital, Manila, Philippines
  • 5 Division of Endocrinology and Metabolism, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan
  • 6 Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity and Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong
  • 7 The Medicity, Gurgaon, India
  • 8 Faculty of Medicine, Udayana University, Sanglah General Hospital, Bali, Indonesia
  • 9 Department of Endocrinology & Metabolism, Seoul St Mary's Hospital, The Catholic University of Korea, Seoul, South Korea
  • 10 Peking University People's Hospital, Peking, China
  • 11 FV Hospital, Ho Chi Minh City, Vietnam
  • 12 The University of Sydney School of Medicine, Sydney, New South Wales, Australia
Diabetes Obes Metab, 2021 Feb;23(2):299-317.
PMID: 33155749 DOI: 10.1111/dom.14251

Abstract

Early onset of type 2 diabetes and a high prevalence of co-morbidities predispose the Asian population to a high risk for, and rapid progression of, diabetic kidney disease (DKD). Apart from renin-angiotensin system inhibitors, sodium-glucose co-transporter-2 (SGLT-2) inhibitors have been shown to delay renal disease progression in patients with DKD. In this review article, we consolidate the existing literature on SGLT-2 inhibitor use in Asian patients with DKD to establish contemporary guidance for clinicians. We extensively reviewed recommendations from international and regional guidelines, data from studies on Asian patients with DKD, global trials (DAPA-CKD, CREDENCE and DELIGHT) and cardiovascular outcomes trials. In patients with DKD, SGLT-2 inhibitor therapy significantly reduced albuminuria and the risk of hard renal outcomes (defined as the onset of end-stage kidney disease, substantial decline in renal function from baseline and renal death), cardiovascular outcomes and hospitalization for heart failure. In all the cardiovascular and renal outcomes trials, there was an initial decline in the estimated glomerular filtration rate (eGFR), which was followed by a slowing in the decline of renal function compared with that seen with placebo. Despite an attenuation in glucose-lowering efficacy in patients with low eGFR, there were sustained reductions in body weight and blood pressure, and an increase in haematocrit. Based on the available evidence, we conclude that SGLT-2 inhibitors represent an evidence-based therapeutic option for delaying the progression of renal disease in Asian patients with DKD and preserving renal function in patients at high risk of kidney disease.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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