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dc.creatorKakouri A., Kanti G., Kapantais E., Kokkinos A., Lanaras L., Farajian P., Galanakis C., Georgantopoulos G., Vlahos N.F., Mastorakos G., Bargiota A., Valsamakis G.en
dc.date.accessioned2023-01-31T08:29:15Z
dc.date.available2023-01-31T08:29:15Z
dc.date.issued2021
dc.identifier10.3390/PH14090869
dc.identifier.issn14248247
dc.identifier.urihttp://hdl.handle.net/11615/74151
dc.description.abstractThe worldwide upward trend in obesity in adults and the increased incidence of overweight children suggests that the future risk of obesity-related illnesses will be increased. The existing anti-obesity drugs act either in the central nervous system (CNS) or in the peripheral tissues, controlling the appetite and metabolism. However, weight regain is a common homeostatic response; current anti-obesity medications show limited effectiveness in achieving long-term weight loss maintenance; in addition to being linked to various side effects. Combined anti-obesity medications (per os or injectable) target more than one of the molecular pathways involved in weight regulation, as well as structures in the CNS. In this systematic review, we conducted a search of PubMed and The ClinicalTrials.gov up to February 2021. We summarized the Food and Drug Administration (FDA)-approved medications, and we focused on the combined pharmacological treatments, related to the incretin hormones, currently in a clinical trial phase. We also assessed the mechanism of action and therapeutic utility of these novel hybrid peptides and potential interactions with other regulatory hormones that may have beneficial effects on obesity. As we improve our understanding of the pathophysiology of obesity, we hope to identify more novel treatment strategies. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.en
dc.language.isoenen
dc.sourcePharmaceuticalsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85115200656&doi=10.3390%2fPH14090869&partnerID=40&md5=4758d7261803f5f2f57200a172c9f4a0
dc.subjectamylinen
dc.subjectcagrilintideen
dc.subjectdapagliflozinen
dc.subjectexendin 4en
dc.subjectgastric inhibitory polypeptideen
dc.subjectglucagon like peptide 1en
dc.subjectglucoseen
dc.subjecthemoglobin A1cen
dc.subjectlicogliflozinen
dc.subjectoxyntomodulinen
dc.subjectpeptide YYen
dc.subjecttirzepatideen
dc.subjectantiobesity activityen
dc.subjectbody weighten
dc.subjectbody weight lossen
dc.subjectenergy expenditureen
dc.subjectfat massen
dc.subjectglucose blood levelen
dc.subjectglycemic controlen
dc.subjecthumanen
dc.subjectlifestyle modificationen
dc.subjectmetabolismen
dc.subjectnonhumanen
dc.subjectobesityen
dc.subjectpancreas islet beta cellen
dc.subjectpathophysiologyen
dc.subjectprotein expressionen
dc.subjectReviewen
dc.subjectsystematic reviewen
dc.subjectMDPIen
dc.titleNew incretin combination treatments under investigation in obesity and metabolism: A systematic reviewen
dc.typeotheren


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