Newer Oral Antidiabetics & SGLT2 Inhibitors
Gliflozins, incretin-based agents and the shift from glucose-lowering to cardiorenal-outcome modification
Past RGUHS + DNB + MPMSU + MUHS · 16
MPMSUMay '25
MPMSUJan '25
MPMSUMay '25
MPMSUAug '21
MPMSU2019
MUHSSummer '19
MUHSWinter '19
RGUHSNov '17
MPMSUJun '17
DNBDec '16
DNBDec '15
DNBDec '13
RGUHSMay '11
MPMSU2011
RGUHSOct '09
MPMSU2009
Introduction
- Definition — The newer antidiabetics are the post-sulfonylurea/post-biguanide classes that exploit three previously untapped targets — the incretin axis (GLP-1 receptor agonists, the dual GIP/GLP-1 agonist tirzepatide, DPP-4 inhibitors), renal tubular glucose reabsorption (SGLT2 inhibitors), and PPARγ (glitazones).
- Paradigm shift — Their defining contribution is the move from "HbA1c-lowering alone" to cardiorenal-outcome modification — SGLT2 inhibitors and several GLP-1 RAs reduce MACE, heart-failure hospitalisation and kidney-disease progression independently of, and beyond, glucose lowering.
- Flagship class — SGLT2 inhibitors ("gliflozins") and GLP-1 RAs are now placed early in type 2 DM for ASCVD, heart failure or CKD — chosen independently of baseline HbA1c — and extend to HF/CKD irrespective of diabetes status.
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Newer Antidiabetics Sglt2i
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