Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/105887
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dc.contributor.authorFadiga, Lúcia-
dc.contributor.authorSaraiva, Joana-
dc.contributor.authorCatarino, Diana-
dc.contributor.authorFrade, João-
dc.contributor.authorMelo, Miguel-
dc.contributor.authorPaiva, Isabel-
dc.date.accessioned2023-03-14T10:45:20Z-
dc.date.available2023-03-14T10:45:20Z-
dc.date.issued2020-12-03-
dc.identifier.issn1758-5996pt
dc.identifier.urihttps://hdl.handle.net/10316/105887-
dc.description.abstractIntroduction: Adult-onset autoimmune diabetes (AID) has two different phenotypes: classic type 1 diabetes mellitus (T1DM), with insulin requirement just after diagnosis, and latent autoimmune diabetes in adults (LADA). The purpose of this study is to characterize patients with AID followed on a tertiary centre, comparing classic T1DM and LADA. Methods: We collected data from patients with diabetes and positive islet autoantibodies, aged 30 years old and over at diagnosis. Patients who started insulin in the first 6 months were classified as T1DM and patients with no insulin requirements in the first 6 months were classified as LADA. Data regarding clinical presentation, autoantibodies, A1C and C-peptide at diagnosis, pharmacologic treatment and complications were analysed. Results: We included 92 patients, 46 with classic T1DM and 46 with LADA. The percentage of females was 50% in T1DM group and 52.1% in LADA group. The median age at diagnosis was 38 years (IQR–15) for T1DM and 42 years (IQR–15) for LADA (p = 0.057). The median time between diagnosis of diabetes and diagnosis of autoimmune aetiology was 0 months in T1DM group and 60 months in LADA group (p < 0.001). The mean BMI at diagnosis was 24.1 kg/ m2 in T1DM group and 26.1 kg/m2 in LADA group (p = 0.042). In T1DM group, 67.4% of the patients had more than one positive autoantibody, comparing to 41.3% of LADA patients (p = 0.012). There was no statistical difference in what concerns to title of GAD autoantibodies, A1C and C-peptide at diagnosis of autoimmune aetiology. The presence of symptoms at diagnosis was associated with T1DM group (p < 0.001). The median daily insulin dose was 40 IU for T1DM (0.58 IU/kg) and 33.5 IU for LADA (0.57 IU/kg), with no statistical difference. LADA patients were more often under non-insulin antidiabetic drugs (p = 0.001). At 10 years follow up, 21.1% of T1DM patients and 63.3% of LADA patients had microvascular complications (p = 0.004). Diabetic nephropathy was present in 23.5% of T1DM patients and 53.3% of LADA patients (p = 0.047). At the last evaluation, 55.6% of T1DM and 82.6% of LADA patients had metabolic syndrome and this difference was independent of diabetes duration. Conclusion: Patients with classic T1DM presented more often with symptoms, lower BMI and higher number of autoantibodies, which may be related to a more aggressive autoimmune process. Patients with LADA developed more frequently microvascular complications for the same disease duration, namely diabetic nephropathy, and had more often metabolic syndrome.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectAutoimmune diseasept
dc.subjectDiabetes complicationspt
dc.subjectDiabetes mellituspt
dc.subjecttype 1pt
dc.subjectLatent autoimmune diabetes in adultspt
dc.subjectInsulin resistancept
dc.titleAdult-onset autoimmune diabetes: comparative analysis of classical and latent presentationpt
dc.typearticle-
degois.publication.firstPage107pt
degois.publication.issue1pt
degois.publication.titleDiabetology and Metabolic Syndromept
dc.peerreviewedyespt
dc.identifier.doi10.1186/s13098-020-00616-1pt
degois.publication.volume12pt
dc.date.embargo2020-12-03*
uc.date.periodoEmbargo0pt
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons