Weight-centric pharmacological management of type 2 diabetes mellitus - An essential component of cardiovascular disease prevention
- PMID: 32499116
- DOI: 10.1016/j.jdiacomp.2020.107619
Weight-centric pharmacological management of type 2 diabetes mellitus - An essential component of cardiovascular disease prevention
Abstract
Obesity and overweight are contributing factors for diseases such as type 2 diabetes mellitus (T2DM), hypertension, hyperlipidemia, and ultimately, cardiovascular (CV) disease. Obesity is imposing an increasing health burden in rich and poor nations, with almost 30% of people globally now either obese or overweight - a staggering 2.1 billion. The link between obesity and T2DM is widely held to involve two adverse effects: obesity-induced insulin resistance and β-cell failure. This "unified field theory" raises questions about whether defects favoring progressive weight gain and metabolic impairment also contribute to β-cell decompensation. The concept of weight-centric management of T2DM is considered justified because of the strong negative impact of obesity on the effects of treatment of diabetes. Two pharmacotherapy options are considered: drugs developed primarily for blood glucose control that also exert a favorable effect on body weight and drugs developed primarily to induce weight loss that also have a favorable effect on glycemia. Treating hunger counter-regulatory mechanisms will have an additional effect on glucose control in T2DM. This narrative review addresses advances in pharmacotherapy for the management of obesity and obesity-related co-morbidities, with a focus on T2DM. It is also important to identify the correct balance between weight-centric and glucose-centric management of T2DM.
Keywords: Cardiovascular risk; Obesity; Pharmacotherapy; Type 2 diabetes mellitus; Weight loss; Weight-centric management.
Copyright © 2020 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest EM has given talks or attended conferences sponsored by Novo Nordisk, SANOFI, AstraZeneca, SERVIER, MSD and Amgen. DPM has given talks, acted as a consultant or attended conferences sponsored by Amgen, Novo Nordisk and Libytec. The other author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
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