LADA and CARDS: A Prospective Study of Clinical Outcome in Established Adult-Onset Autoimmune Diabetes

被引:68
作者
Hawa, Mohammed Iqbal [1 ]
Buchan, Ana Paula [1 ]
Ola, Thomas [1 ]
Wun, Chuan Chuan [2 ]
DeMicco, David A. [2 ]
Bao, Weihang [2 ]
Betteridge, D. John [3 ]
Durrington, Paul N. [4 ]
Fuller, John H. [5 ]
Neil, H. Andrew W. [6 ]
Colhoun, Helen [7 ]
Leslie, Richard David [1 ]
Hitman, Graham A. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Ctr Diabet, London, England
[2] Pfizer Inc, New York, NY USA
[3] UCL, Dept Diabet, London, England
[4] Univ Manchester, Dept Med, Manchester M13 9PL, Lancs, England
[5] UCL, Dept Epidemiol & Publ Hlth, London, England
[6] Univ Oxford, Ctr Diabet Endocrinol & Metab, Oxford, England
[7] Univ Dundee, Med Res Inst, Dundee, Scotland
关键词
ANTIBODY STANDARDIZATION PROGRAM; GLUTAMIC-ACID DECARBOXYLASE; CHRONIC COMPLICATIONS; METABOLIC SYNDROME; AUTOANTIBODIES; TYPE-1; TIME; ATORVASTATIN; MULTICENTER; PHENOTYPE;
D O I
10.2337/dc13-2383
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE Diabetes-associated autoantibodies can be detected in adult-onset diabetes, even when initially non insulin requiring, i.e., with latent autoimmune diabetes. We aimed to identify adult-onset autoimmune diabetes in patients with established "type 2 diabetes" participating in the Collaborative Atorvastatin Diabetes Study (CARDS) to characterize their phenotype and clinical outcome. RESEARCH DESIGN AND METHODS We prospectively studied 2,425 European patients with presumed type 2 diabetes (mean age 62 years, diabetes duration 7.9 years) for outcomes at 3.9 years after randomization to either atorvastatin or placebo. Subjects were screened for autoantibodies to GAD (GADA), insulinoma-associated antigen-2 (IA-2A), and zinc-transporter 8 (ZnT8A). RESULTS A total of 173 patients (7.1%) had GADA, of whom 11 (0.5%) and 5(0.2%) were also positive for IA-2A and ZnT8A, respectively. At baseline, 44% of GADA-positive patients were not on insulin. Fewer autoantibody-positive than autoantibody-negative patients had metabolic syndrome (64 vs. 80%), and more were on insulin (56 vs. 17%) (P < 0.0001 for each) without lower HbA(1c), (69 mmol/mol [8.5%] vs. 62 mmol/mol [7.8%]). The frequency of microvascular and macrovascular events was similar in both cohorts, independent of atorvastatin. CONCLUSIONS Adult-onset autoimmune diabetes was prevalent, even in patients with established diabetes presumed to have type 2 diabetes. After 11.8 years' diabetes duration, nearly half the patients with autoimmune diabetes were not on insulin treatment and almost two-thirds had metabolic syndrome. The type of diabetes, whether autoimmune diabetes or type 2 diabetes, did not impact the risk of microvascular disease.
引用
收藏
页码:1643 / 1649
页数:7
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