GAD autoantibodies and epitope reactivities persist after diagnosis in latent autoimmune diabetes in adults but do not predict disease progression: UKPDS 77
Version 2 2024-03-25, 16:36Version 2 2024-03-25, 16:36
Version 1 2023-10-18, 09:59Version 1 2023-10-18, 09:59
journal contribution
posted on 2024-03-25, 16:36 authored by MAa Desai, CAAAb Cull, VAAAa Horton, MARAc Christie, EAd Bonifacio, VAd Lampasona, PAJAe Bingley, JACAa Levy, IARAf Mackay, PAg Zimmet, RARAb Holman, AAa h Clark<p>Aims/hypothesis: Latent autoimmune diabetes in adults (LADA) is a slowly progressive form of autoimmune diabetes, with autoantibodies to islet proteins developing in older patients who have no immediate requirement for insulin therapy. Markers of its clinical course are uncharacterised. The aim of this study was to determine whether persistence of, or changes in, GAD65 autoantibodies (GADAs) in the LADA patients who participated in the United Kingdom Prospective Diabetes Study (UKPDS) were associated with disease progression or insulin requirement. Methods: GADA levels and their relative epitope reactivities to N-terminal, middle and C-terminal regions of human GAD65 were determined in 242 UKPDS patients who were GADA-positive at diagnosis; samples taken after 0.5, 3 and 6 years of follow-up were tested using a radiobinding assay. Comparisons were made of GADA status with clinical details and disease progression assessed by the requirement for intensified glucose-lowering therapy. Results: GADA levels fluctuated between 0.5 and 6 years but persisted in 225 of 242 patients. No association of GADA levels with disease progression or insulin requirement was observed. Antibody reactivity was directed to C-terminal and middle epitopes of GAD65 in >70 patients, and the N-terminal in <9. There were no changes in epitope reactivity pattern over the 6 year follow-up period, nor any association between epitope reactivity and insulin requirement. Conclusions/interpretation: GADAs persist for 6 years after diagnosis of LADA, but levels and reactivity to different GAD65 epitopes are not associated with disease progression. © 2007 Springer-Verlag.</p>
History
School affiliated with
- Department of Life Sciences (Research Outputs)
Publication Title
DiabetologiaVolume
50Issue
10Pages/Article Number
2052-2060External DOI
ISSN
0012186XDate Submitted
2015-07-31Date Accepted
2015-07-31Date of First Publication
2015-07-31Date of Final Publication
2015-07-31ePrints ID
18120Usage metrics
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Keywords
adultAge of Onsetagedamino terminal sequenceantigen antibody reactionarticleAutoantibodiesBody Mass Indexcarboxy terminal sequenceclinical trialcontrolled clinical trialcontrolled studyDiabetes Mellitusdisease associationdisease courseDisease Progressionenzyme activityepitopeEpitopesfemalefollow upFollow-Up StudiesGlutamate Decarboxylaseglutamate decarboxylase 65 antibodyGlycosylatedHemoglobin AhumanHumansimpaired glucose toleranceinsulininsulin treatmentmajor clinical studymaleMiddle AgedPeptide FragmentsPredictive Value of Testspriority journalrandomized controlled trialTime Factorstreatment failureType 1United Kingdom
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