PMID- 34585897 OWN - NLM STAT- MEDLINE DCOM- 20211001 LR - 20211001 IS - 0004-5772 (Print) IS - 0004-5772 (Linking) VI - 69 IP - 9 DP - 2021 Sep TI - Current Role of Dapagliflozin in Clinical Practice. PG - 11-12 AB - Dapagliflozin is the first in a novel class of glucose-lowering agents known as sodium-glucose co-transporter-2 (SGLT2) inhibitors which was approved by USFDA in management of type 2 diabetes mellitus (T2DM) as an adjunct to diet and exercise to improve glycemic control in adults initially, followed by to reduce the risk of hospitalization for heart failure (HHF) in adults with T2DM and established cardiovascular disease or multiple cardiovascular risk factors. Most recently, it is approved to reduce the risk of cardiovascular death and in adults with heart failure (HF) with reduced ejection fraction (NYHA class II-IV). Dapagliflozin has been studied in a wide range of patients with diabetes and plethora of evidence has confirmed its efficacy as a monotherapy as well as an add-on to the oral therapies and insulin, when compared to placebo. Additional advantages include weight reduction which has been consistently demonstrated in Phase III studies and good tolerability. Also there is a demonstrable reduction in systolic blood pressure in patients treated with SGLT2 inhibitors. DECLARE TIMI 58 study clearly demonstrated that Dapagliflozin was non inferior in reducing major adverse cardiovascular events (MACE) in patients with T2DM and high CV risk compared with placebo. 27% risk reduction in heart failure hospitalisation was noted along without increased risk of amputation. DAPA HF evaluated the efficacy and safety of the dapagliflozin in patients with HF and reduced ejection fraction, irrespective of the presence or absence of diabetes. Patients with symptomatic HF due to reduced ejection fraction treated with dapagliflozin had positive outcomes with reduction in cardiovascular deaths and HF events. The DAPA-CKD trial which was conducted to assess the efficacy and safety of dapagliflozin in patients with chronic kidney disease (CKD), with or without type 2 diabetes found that it significantly lowered the risk of a sustained decline in the estimated GFR of at least 50%, end-stage kidney disease, or death from renal or cardiovascular causes in patients with CKD, regardless of the presence or absence of diabetes. Ongoing trials like DELIVER, DAPA ACT HF-TIMI 68, DICTATE-AHF, HF readmission study, DAPA MI Study, Effectiveness of Dapagliflozin for Weight Loss, will throw more light on the precise effects of dapagliflozin in several clinical scenarios. To conclude - Dapagliflozin was well studied not only in T2DM but also in HF and CKD patients with positive results and good safety profile. CI - (c) Journal of the Association of Physicians of India 2011. FAU - Zargar, Abdul Hamid AU - Zargar AH AD - Medical Director, Centre for Diabetes and Endocrine Care, Srinagar, Jammu Kashmir. FAU - Trailokya, Abhijit Anil AU - Trailokya AA AD - Pharmaceutical Geriatric Medicine, DGM Medical Affairs, Medical Affairs Team, Alkem Labs., Mumbai, Maharashtra. FAU - Ghag, Suraj AU - Ghag S AD - Senior Medical Advisor, Medical Affairs Team, Alkem Labs., Mumbai, Maharashtra. FAU - Pawar, Roshan AU - Pawar R AD - Senior Medical Advisor, Medical Affairs Team, Alkem Labs., Mumbai, Maharashtra. FAU - Aiwale, Amol AU - Aiwale A AD - Senior Medical Advisor, Medical Affairs Team, Alkem Labs., Mumbai, Maharashtra. FAU - Zalke, Ashish AU - Zalke A AD - Medical Advisor, Medical Affairs Team, Alkem Labs., Mumbai, Maharashtra. LA - eng PT - Journal Article PL - India TA - J Assoc Physicians India JT - The Journal of the Association of Physicians of India JID - 7505585 RN - 0 (Benzhydryl Compounds) RN - 0 (Glucosides) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) RN - 1ULL0QJ8UC (dapagliflozin) SB - IM MH - Benzhydryl Compounds/therapeutic use MH - *Diabetes Mellitus, Type 2/complications/drug therapy MH - Glucosides/therapeutic use MH - *Heart Failure/drug therapy MH - Humans MH - *Sodium-Glucose Transporter 2 Inhibitors/therapeutic use EDAT- 2021/09/30 06:00 MHDA- 2021/10/02 06:00 CRDT- 2021/09/29 10:57 PHST- 2021/09/29 10:57 [entrez] PHST- 2021/09/30 06:00 [pubmed] PHST- 2021/10/02 06:00 [medline] PST - ppublish SO - J Assoc Physicians India. 2021 Sep;69(9):11-12.