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dc.contributor.authorNiu, Xen_US
dc.contributor.authorLuo, Sen_US
dc.contributor.authorLi, Xen_US
dc.contributor.authorXie, Zen_US
dc.contributor.authorXiang, Yen_US
dc.contributor.authorHuang, Gen_US
dc.contributor.authorLin, Jen_US
dc.contributor.authorYang, Len_US
dc.contributor.authorLiu, Zen_US
dc.contributor.authorWang, Xen_US
dc.contributor.authorLeslie, RDen_US
dc.contributor.authorZhou, Zen_US
dc.date.accessioned2019-10-04T17:01:20Z
dc.date.available2018-08-09en_US
dc.date.issued2019-01en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/60010
dc.description.abstractBACKGROUND: Latent autoimmune diabetes in adults (LADA) exhibits significant clinical heterogeneity, but the underlying causes remain unclear. The aim of this study was to investigate whether age of onset of LADA contributes to the observed clinical heterogeneity by comparing the clinical, metabolic, and immunogenetic characteristics between elderly and young LADA patients. METHODS: The cross-sectional study included a total of 579 patients with LADA which was further divided into elderly LADA (E-LADA) group (n = 135, age of onset ≥60 years) and young LADA (Y-LADA) group (n = 444, age of onset <60 years). Age-matched subjects with type 2 diabetes were served as control (E-T2D group, n = 622). Clinical characteristics, serum autoantibodies, and HLA-DQ haplotypes were compared among these groups. RESULTS: Compared with patients with Y-LADA, patients with E-LADA have better residual beta-cell function and higher level of insulin resistance (both P < .01), more metabolic syndrome characteristics, similar proportion of islet autoantibody positivity, and strikingly different HLA-DQ genetic background. In comparison with E-T2D patients, E-LADA patients tend to have similar metabolic syndrome prevalence, comparable C-peptide levels, and insulin resistance levels and share similar HLA-DQ genetic characteristics. CONCLUSIONS: Elderly LADA differs phenotypically and genetically from Y-LADA but has a clinical and genetic profile more similar to that of E-T2D. These distinct phenotypes could potentially help physicians better manage patients with E-LADA.en_US
dc.format.extente3068 - ?en_US
dc.languageengen_US
dc.relation.ispartofDiabetes Metab Res Reven_US
dc.rights"This is the peer reviewed version of the following article: Niu, X, Luo, S, Li, X, et al. Identification of a distinct phenotype of elderly latent autoimmune diabetes in adults: LADA China Study 8. Diabetes Metab Res Rev. 2019; 35:e3068. https://doi.org/10.1002/dmrr.3068 which has been published in final form at https://doi.org/10.1002/dmrr.3068. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions."
dc.subjectLADAen_US
dc.subjectclass II antigensen_US
dc.subjectclinical characteristicsen_US
dc.subjectlatent autoimmune diabetes in adultsen_US
dc.subjectmetabolic syndromeen_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectAutoantibodiesen_US
dc.subjectChinaen_US
dc.subjectCross-Sectional Studiesen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectInsulin Resistanceen_US
dc.subjectLatent Autoimmune Diabetes in Adultsen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectPhenotypeen_US
dc.titleIdentification of a distinct phenotype of elderly latent autoimmune diabetes in adults: LADA China Study 8.en_US
dc.typeArticle
dc.identifier.doi10.1002/dmrr.3068en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/30160000en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume35en_US
dcterms.dateAccepted2018-08-09en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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