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Effects of glucagon-like peptide 1 receptor agonists on comorbidities in older patients with diabetes mellitus.

Ther Adv Chronic Dis · 2019

Last updated 2026-05-28

A review of studies found that GLP-1 receptor agonists—such as liraglutide, semaglutide, and dulaglutide—may help older adults with diabetes by addressing multiple health issues at once. These drugs are used for diabetes and some are also approved for obesity, and they may improve conditions like high blood pressure, high cholesterol, fatty liver disease, osteoporosis, and sleep apnea. Using one medication to treat several conditions could reduce the number of drugs needed, lower costs, and decrease side effects or missed doses.

AI summary of the abstract below.

JournalTher Adv Chronic Dis, 2019
Citations44
Relative citation ratio2.09
NIH percentile75
Molecules
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction, Chronic Kidney Disease, Obesity, Heart Failure

Abstract

Elderly patients with diabetes are at high risk of polypharmacy because of multiple coexisting diseases and syndromes. Polypharmacy increases the risk of drug-drug and drug-disease interactions in these patients, who may already have age-related sensory and cognitive deficits; such deficits may delay timely communication of early symptoms of adverse drug events. Several glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have been approved for diabetes: liraglutide, exenatide, lixisenatide, dulagluatide, semaglutide, and albiglutide. Some are also approved for treatment of obesity. The current review of literature along with clinical case discussion provides evidence supporting GLP-1 RAs as diabetes medications for polypharmacy reduction in older diabetes patients because of their multiple pleiotropic effects on comorbidities (e.g. hyperlipidemia, hypertension, and fatty liver) and syndromes (e.g. osteoporosis and sleep apnea) that commonly co-occur with diabetes. Using one medication (in this case, GLP-1 RAs) to address multiple conditions may help reduce costs, medication burden, adverse drug events, and medication nonadherence.

Verbatim abstract via PubMed 31321014 ↗