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The prevalence of the 65-kilodalton isoform of glutamic acid decarboxylase autoantibodies by glucose tolerance status in elderly patients from the cardiovascular health study.

TitleThe prevalence of the 65-kilodalton isoform of glutamic acid decarboxylase autoantibodies by glucose tolerance status in elderly patients from the cardiovascular health study.
Publication TypeJournal Article
Year of Publication2006
AuthorsBarinas-Mitchell, E, Kuller, LH, Pietropaolo, S, Zhang, Y-J, Henderson, T, Pietropaolo, M
JournalJ Clin Endocrinol Metab
Volume91
Issue8
Pagination2871-7
Date Published2006 Aug
ISSN0021-972X
KeywordsAged, Aging, Autoantibodies, Blood Glucose, Blood Pressure, Cardiovascular Diseases, Cohort Studies, Diabetes Mellitus, Type 2, Fasting, Female, Glucose Intolerance, Glutamate Decarboxylase, Humans, Insulin, Isoenzymes, Lipids, Logistic Models, Male, Nutrition Surveys
Abstract<p><b>CONTEXT: </b>Autoantibodies (AA) to glutamic acid decarboxylase (GAD65), a determinant of risk for autoimmune diabetes, have been found in up to 10% of patients with type 2 diabetes. In older adults, this marker may also serve as a determinant of risk for autoimmune diabetes and enhance diabetes classification.</p><p><b>OBJECTIVE: </b>The objective of this study was to evaluate the relationship between GAD65AA and glucose tolerance status, current diabetes treatment, and clinical measures in older adults.</p><p><b>DESIGN: </b>GAD65AA were measured at baseline in 3318 participants from the Cardiovascular Health Study, a cohort study of 5888 individuals 65 or older.</p><p><b>SETTING: </b>The population-based cohort was recruited from four U.S. sites.</p><p><b>PATIENTS: </b>Patients included all Cardiovascular Health Study participants with known diabetes, newly diagnosed diabetes, impaired fasting glucose, impaired glucose tolerance, and a sample of normal glucose-tolerant participants.</p><p><b>MAIN OUTCOME MEASURES: </b>GAD65AA, body mass index, fasting glucose and insulin levels, blood pressure, lipid levels, and diabetes treatment at baseline were measured.</p><p><b>RESULTS: </b>The prevalence of GAD65AA increased with decreasing glucose tolerance in both Blacks (n = 560) and Whites (n = 2730), being more pronounced in known diabetic individuals. GAD65AA were found in 2.3, 5.8, 7.8, and 8.3% of diabetic participants, reporting use of no diabetes medication, oral hypoglycemic agents, insulin only, and both oral hypoglycemic agents and insulin, respectively (P = 0.02, linear trend). Among diabetic participants, GAD65AA positivity was associated with diabetes treatment, higher fasting glucose, and lower body mass index.</p><p><b>CONCLUSIONS: </b>Even among older individuals with diabetes, GAD65AA may be a useful marker in identifying a subgroup of autoimmune diabetes, serve as a marker of insulin requirement, and remain stable over years.</p>
DOI10.1210/jc.2005-2667
Alternate JournalJ Clin Endocrinol Metab
PubMed ID16720660
Grant ListN01 HC 15103 / HC / NHLBI NIH HHS / United States
N01 HC 35129 / HC / NHLBI NIH HHS / United States
N01 HC 85079 / HC / NHLBI NIH HHS / United States
N01 HC 85080 / HC / NHLBI NIH HHS / United States
N01 HC 85081 / HC / NHLBI NIH HHS / United States
N01 HC 85082 / HC / NHLBI NIH HHS / United States
N01 HC 85083 / HC / NHLBI NIH HHS / United States
N01 HC 85084 / HC / NHLBI NIH HHS / United States
N01 HC 85085 / HC / NHLBI NIH HHS / United States
N01 HC 85086 / HC / NHLBI NIH HHS / United States
P30 DK 046204 / DK / NIDDK NIH HHS / United States
R01 DK 056200 / DK / NIDDK NIH HHS / United States