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External validity of type 2 diabetes clinical trials on cardiovascular outcomes for a multimorbid population

dc.contributor.authorLazar Neto, Felippe
dc.contributor.authorMendes, Thiago Bosco [UNESP]
dc.contributor.authorMatos, Paulo Marcelo Pontes Gomes
dc.contributor.authorde Oliveira, Julio César
dc.contributor.authorFavarato, Maria Helena Sampaio
dc.contributor.authorLin, Chin An
dc.contributor.authorMartins, Milton Arruda
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T10:20:20Z
dc.date.available2021-06-25T10:20:20Z
dc.date.issued2021-04-01
dc.description.abstractAim: To investigate the external validity of recent antihyperglycaemic trials evaluating cardiovascular outcomes in a multimorbid population. Materials and Methods: Selection criteria of 15 randomized controlled trials from the 2020 American Diabetes Association Standard of Care statement were applied in a stepwise manner to tertiary care patients with type 2 diabetes. Primary outcomes were the number of patients eligible per individual trial and for the aggregate of trials. Secondary outcomes included patient predictors of trial eligibility. Results: Of 1059 patients, the mean (SD) age was 66 (10.74) years, the median (IQR) Charlson index was 2 (2, 3) and 458 (43%) had documented cardiovascular disease. The median (IQR) number of patients included in individual trials was 263 (174.25–308.75) and 795 (75.1%) of them were eligible for at least one trial. Among those 264 ineligible, 127 (48.1%) had an HbA1c level of 7% or less and no cardiovascular disease; 53.5% and 34.4% of the patients were eligible for two and three different classes of drugs, respectively. The strongest predictor of trial eligibility was cardiovascular disease (risk ratio 2.17, 95% CI 2.01–2.35). Conclusions: A considerable proportion of multimorbid patients would be eligible for recent antihyperglycaemic trials. This positive finding can be attributed to development guidance in diabetes trials and the different approach we took, in which we evaluated inclusion by trials as an aggregate.en
dc.description.affiliationDepartment of Internal Medicin Faculdade de Medicina da Universidade de São Paulo (FMUSP)
dc.description.affiliationDepartment of Internal Medicine Faculdade de Medicina da Universidade Estadual de São Paulo (UNESP)
dc.description.affiliationUnespDepartment of Internal Medicine Faculdade de Medicina da Universidade Estadual de São Paulo (UNESP)
dc.format.extent971-979
dc.identifierhttp://dx.doi.org/10.1111/dom.14303
dc.identifier.citationDiabetes, Obesity and Metabolism, v. 23, n. 4, p. 971-979, 2021.
dc.identifier.doi10.1111/dom.14303
dc.identifier.issn1463-1326
dc.identifier.issn1462-8902
dc.identifier.scopus2-s2.0-85099335542
dc.identifier.urihttp://hdl.handle.net/11449/205735
dc.language.isoeng
dc.relation.ispartofDiabetes, Obesity and Metabolism
dc.sourceScopus
dc.subjectantidiabetic drug
dc.subjectcanagliflozin
dc.subjectcardiovascular disease
dc.subjectDPP-4 inhibitor
dc.subjectGLP-1
dc.subjectinsulin analogues
dc.titleExternal validity of type 2 diabetes clinical trials on cardiovascular outcomes for a multimorbid populationen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.author.orcid0000-0002-0051-9537[1]
unesp.author.orcid0000-0001-8349-3303[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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