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Glucose-lowering drugs with cardiovascular benefits as modifiers of critical elements of the human life history.
- Source :
-
The lancet. Diabetes & endocrinology [Lancet Diabetes Endocrinol] 2022 Dec; Vol. 10 (12), pp. 882-889. Date of Electronic Publication: 2022 Sep 28. - Publication Year :
- 2022
-
Abstract
- The life history theory assumes that all organisms are under selective pressure to harvest external resources and allocate them to maximise fitness: only organisms making the best use of energy obtain the greatest fitness benefits. The trade-off of energy spans four functions: maintenance, growth, reproduction, and defence against pathogens. The innovative antihyperglycaemic agents glucagon-like peptide 1 (GLP-1) receptor agonists and sodium-glucose cotransporter 2 (SGLT2) inhibitors decrease bodyweight and have the potential to counter low-grade inflammation. These key activities could rewire two components of the life history theory operative in adulthood-ie, maintenance and defence. In this Personal View, we postulate that the benefits of these medications on the cardiovascular system, beyond their glucose-lowering effects, could be mediated by the reduction of the maintenance cost driven by obesity and efforts spent on blunting low-grade inflammation.<br />Competing Interests: Declaration of interests AA received research grants, lecture, and advisory board fees from Mundipharma, Merck Sharp & Dome, AstraZeneca, Novartis, Boehringer Ingelheim, Sanofi, Mediolanum, Novo Nordisk, Eli Lilly, Servier, and Takeda. MLM received lecture fees, advisory fees, and grant support from Mylan, SLA Pharma, Servier Laboratories, Eli Lilly, MSD, and Novo Nordisk. GPF received lecture fees, consultancy fees, grant support, and advisory board fees from Abbott, AstraZeneca, Boehringer Ingelheim, Daiichi Sankyo, Eli Lilly, Novo Nordisk, Sanofi, and Takeda. SDP consulted for Applied Therapeutics, AstraZeneca, Boehringer Ingelheim, Eli Lilly, MSD, Novartis, Novo Nordisk, and Sanofi, and received funding for these consulting services; received grant support from AstraZeneca and Boehringer Ingelheim; and received speaker fees from AstraZeneca, Boehringer Ingelheim, Eli Lilly, MSD, Novartis, Novo Nordisk, and Sanofi. SVdK declares no competing interests.<br /> (Copyright © 2022 Elsevier Ltd. All rights reserved.)
- Subjects :
- Humans
Adult
Glucagon-Like Peptide-1 Receptor agonists
Glucose
Hypoglycemic Agents therapeutic use
Hypoglycemic Agents pharmacology
Inflammation drug therapy
Sodium-Glucose Transporter 2 Inhibitors pharmacology
Sodium-Glucose Transporter 2 Inhibitors therapeutic use
Diabetes Mellitus, Type 2 drug therapy
Cardiovascular System
Cardiovascular Diseases drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 2213-8595
- Volume :
- 10
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- The lancet. Diabetes & endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 36182702
- Full Text :
- https://doi.org/10.1016/S2213-8587(22)00247-9