SGLT2 Inhibitors, GLP-1 Agonists, and DPP-4 Inhibitors in Diabetes and Microvascular Complications: A Review

dc.contributor.authorEl-Mouhayyar, Christopher
dc.contributor.authorRiachy, Ruba
dc.contributor.authorKhalil, Abir Bou
dc.contributor.authorEid, Assaad A.
dc.contributor.authorAzar, Sami T.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentInternal Medicine
dc.contributor.departmentEndocrinology, Diabetes and Metabolism
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:55Z
dc.date.available2025-01-24T11:36:55Z
dc.date.issued2020
dc.description.abstractThe prevalence of diabetes and its associated complications is increasing throughout the decades. Promising diabetes medications were introduced to the market including GLP-1 agonists, DPP-4 inhibitors, and SGLT2 inhibitors aiming to target these complications. The literature lacks sufficient data regarding these new medications and their influence on nephropathy, retinopathy, and neuropathy. This review expands on the major results of effects of the 3 drug classes on microvascular complications. In our review, both SGLT2 inhibitors and GLP-1 agonists appear to have promising nephroprotective outcomes at this stage, with less promising outcomes seen with DPP-4 inhibitors. Moreover, the retinoprotective outcomes of both SGLT2 inhibitors and DPP-4 inhibitors were only tested on mice, while those of GLP-1 agonists were assessed in few trials. In addition, the results of both GLP-1 agonists and DPP-4 inhibitors showed discrepancies in these studies. On the contrary, conclusions regarding the effect of these medications on neuroprotective outcomes cannot be drawn at the time due to the lack of clinical trials targeting these complications. Hence, a clearer picture of the microvascular outcomes will manifest over time with the release of multiple upcoming clinical trials. © 2020 Christopher El Mouhayyar et al.
dc.identifier.doihttps://doi.org/10.1155/2020/1762164
dc.identifier.eid2-s2.0-85081266721
dc.identifier.urihttp://hdl.handle.net/10938/28757
dc.language.isoen
dc.publisherHindawi Limited
dc.relation.ispartofInternational Journal of Endocrinology
dc.sourceScopus
dc.subjectAlogliptin
dc.subjectCanagliflozin
dc.subjectDapagliflozin
dc.subjectDipeptidyl peptidase iv inhibitor
dc.subjectEmpagliflozin
dc.subjectExendin 4
dc.subjectGlibenclamide
dc.subjectGlucagon like peptide 1 receptor agonist
dc.subjectLinagliptin
dc.subjectLixisenatide
dc.subjectMetformin
dc.subjectSaxagliptin
dc.subjectSemaglutide
dc.subjectSodium glucose cotransporter 2 inhibitor
dc.subjectVildagliptin
dc.subjectDiabetes mellitus
dc.subjectDiabetic neuropathy
dc.subjectDiabetic retinopathy
dc.subjectDrug effect
dc.subjectHuman
dc.subjectKidney disease
dc.subjectMicroangiopathy
dc.subjectNeuroprotection
dc.subjectNon insulin dependent diabetes mellitus
dc.subjectNonhuman
dc.subjectRenal protection
dc.subjectReview
dc.subjectTreatment outcome
dc.titleSGLT2 Inhibitors, GLP-1 Agonists, and DPP-4 Inhibitors in Diabetes and Microvascular Complications: A Review
dc.typeReview

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