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dc.contributor.authorGarcía de Lucas, M.D.*
dc.contributor.authorCaballero, I.*
dc.contributor.authorFernández-García, J.C.*
dc.contributor.authorDomínguez-Rodríguez, M.*
dc.contributor.authorMoreno-Moreno, P.*
dc.contributor.authorJiménez-Millán, A.*
dc.contributor.authorBotana-López, M.*
dc.contributor.authorAvilés, B.*
dc.contributor.authorMerino-Torres, J.F.*
dc.contributor.authorSoto, A.*
dc.contributor.authorTejera Pérez, Cristina *
dc.contributor.authorMorales, C.*
dc.date.accessioned2025-09-10T08:38:31Z
dc.date.available2025-09-10T08:38:31Z
dc.date.issued2023
dc.identifier.citationGarcía de Lucas MD, Caballero I, Fernández-García JC, Domínguez-Rodríguez M, Moreno-Moreno P, Jiménez-Millán A, et al. Influence of chronic kidney disease and its severity on the efficacy of semaglutide in type 2 diabetes patients: a multicenter real-world study. Frontiers in Endocrinology. 2023;14.
dc.identifier.issn1664-2392
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/655f4e51dfaaaa2236076b37
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21663
dc.description.abstractObjectives: Semaglutide is a glucagon-like peptide 1 receptor agonist that improves glycemic control and achieves weight loss in type 2 diabetes (T2D) patients. Subcutaneous (s.c.) semaglutide at 1 mg once weekly (OW) is safe in T2D patients with chronic kidney disease (CKD). Whether or not CKD and its severity influence treatment response remains undetermined. Method: This is an observational, ambispective, multicenter, nationwide, real-world study designed to compare safety/efficacy of OW s.c. 1 mg semaglutide in T2D patients with or without CKD. The influence of CKD severity was also addressed. Patients were followed up for 12 months. Primary end-points were glycosylated hemoglobin (HbA1c), weight, and renal outcomes. Secondary end-points included insulin resistance, atherogenic and hepatic steatosis indexes, and changes in antihyperglycemic medications. Results: A total of 296 and 190 T2D patients without or with CKD, respectively, were recruited. Baseline CKD risk was moderate, high, or very high in 82, 53, and 45 patients, respectively. Treatment reduced HbA1c by 0.90%-1.20%. Relevant differences were seen neither between non-CKD and CKD patients nor among CKD subgroups. Notable weight losses were achieved in both non-CKD and CKD patients. The median reduction was higher in the former at 6 months (5.90 kg vs. 4.50 kg, P = 0.008) and at end of study (6.90 kg vs. 5.00 kg, P = 0.087). A trend toward slightly lower weight losses as CKD severity increased was observed. CKD markers improved across all CKD subgroups. Relevant differences were not observed for other variables, either between non-CKD and CKD patients, or among CKD subgroups. Safety concerns were not reported. Conclusion: The safety/efficacy of OW s.c. semaglutide to improve glycemic control and weight in T2D patients with CKD is not notably lower than that in T2D patients without renal failure. CKD severity barely influences treatment response. OW s.c. semaglutide can be useful to manage T2D patients with CKD in daily clinical practice.
dc.description.sponsorshipThis work received funding from Novo Nordisk. The funder was not involved in the study design, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshHumans *
dc.subject.meshDiabetes Mellitus, Type 2 *
dc.subject.meshGlycated Hemoglobin*
dc.subject.meshRenal Insufficiency, Chronic *
dc.subject.meshWeight Loss *
dc.titleInfluence of chronic kidney disease and its severity on the efficacy of semaglutide in type 2 diabetes patients: a multicenter real-world study
dc.typeArtigo
dc.authorsophosGarcía de Lucas, M.D.; Caballero, I.; Fernández-García, J.C.; Domínguez-Rodríguez, M.; Moreno-Moreno, P.; Jiménez-Millán, A.; Botana-López, M.; Avilés, B.; Merino-Torres, J.F.; Soto, A.; Tejera, C.; Morales, C.
dc.identifier.doi10.3389/fendo.2023.1240279
dc.identifier.sophos655f4e51dfaaaa2236076b37
dc.journal.titleFrontiers in Endocrinology*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Ferrol::Endocrinoloxía e nutrición
dc.relation.projectIDThis work received funding from Novo Nordisk. The funder was not involved in the study design, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
dc.relation.projectIDNovo Nordisk
dc.relation.publisherversionhttps://doi.org/10.3389/fendo.2023.1240279
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Ferrol
dc.subject.keywordCHUF
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number14


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)