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Identification of a distinct phenotype of elderly latent autoimmune diabetes in adults: LADA China Study 8.

Authors :
Niu X
Luo S
Li X
Xie Z
Xiang Y
Huang G
Lin J
Yang L
Liu Z
Wang X
Leslie RD
Zhou Z
Source :
Diabetes/metabolism research and reviews [Diabetes Metab Res Rev] 2019 Jan; Vol. 35 (1), pp. e3068. Date of Electronic Publication: 2018 Sep 27.
Publication Year :
2019

Abstract

Background: 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.<br />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.<br />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.<br />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.<br /> (© 2018 John Wiley & Sons, Ltd.)

Details

Language :
English
ISSN :
1520-7560
Volume :
35
Issue :
1
Database :
MEDLINE
Journal :
Diabetes/metabolism research and reviews
Publication Type :
Academic Journal
Accession number :
30160000
Full Text :
https://doi.org/10.1002/dmrr.3068