The objective of this study is to understand the metabolic and immunologic basis of diabetes in adult blacks with diabetic ketoacidosis (DKA). Twenty-one black adults presenting with DKA ([mean ± SD] blood pH = 7.18 ± 0.09, plasma glucose = 693 ± 208 mg/dl, and positive serum ketones) had a subsequent clinical course of non-insulin-dependent diabetes mellitus (NIDDM). Human leukocyte antigens (HLAs) DR and DQ and antibodies to glutamic acid decarboxylase (GAD) and islet cell cytoplasmic proteins (ICP) were measured to assess autoimmunity. Insulin action was evaluated by the euglycemic insulin clamp, and insulin secretion was measured by C-peptide responses to oral glucose. Ketoacidosis was treated with insulin. Two subjects had a precipitating illness; four had a history of NIDDM. At the time of study, subjects' glycemic control was good (HbA1c = 5.7 ± 1.6%). Nine subjects were treated with insulin, and 12 were on either sulfonylurea treatment or diet alone. Men (n = 12) were younger than women (n = 9) (40.8 ± 9.8 and 51.1 ± 6.3 years of age, respectively, P < 0.05) but similar in body mass index (27.8 ± 2.7 and 29.98 ± 4.1 kg/m2, respectively). Antibodies to GAD and ICP were absent. All but one subject was insulin resistant compared with normal subjects (glucose disposal 3.56 ± 0.04 vs. 6.86 ± 0.02 mg.kg−1 · min−1), and insulin secretion was lower. HLA DR3 and DR4 frequency was higher than in nondiabetic black control subjects (65 vs. 30%, P < 0.012).(ABSTRACT TRUNCATED AT 250 WORDS)
Original Articles|
June 01 1994
GAD Antibody Negative NIDDM in Adult Black Subjects with Diabetic Ketoacidosis and Increased Frequency of Human Leukocyte Antigen DR3 and DR4: Flatbush Diabetes
Mary Ann Banerji;
Mary Ann Banerji
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Rochelle L Chaiken;
Rochelle L Chaiken
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Howard Huey;
Howard Huey
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Tiinamaija Tuomi;
Tiinamaija Tuomi
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Allen J Norin;
Allen J Norin
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Ian R Mackay;
Ian R Mackay
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Merrill J Rowley;
Merrill J Rowley
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Paul Z Zimmet;
Paul Z Zimmet
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Harold E Lebovitz
Harold E Lebovitz
Department of Medicine, Division of Endocrinology and Metabolism and Division of Pulmonary, and the Department of Anatomy and Cell Biology, SUNY Health Science Center at Brooklyn
New York
Centre for Molecular Biology and Medicine, Monash University
Clayton, Victoria, Australia
International Diabetes Institute
Melbourne, Victoria, Australia
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Address correspondence and reprint requests to Dr. Mary Ann Banerji, SUNY Health Science Center at Brooklyn, 450 Clarkson Avenue, Box 1205, Brooklyn, NY 11203.
Diabetes 1994;43(6):741–745
Article history
Received:
October 11 1993
Revision Received:
January 13 1994
Accepted:
January 13 1994
PubMed:
8194658
Citation
Mary Ann Banerji, Rochelle L Chaiken, Howard Huey, Tiinamaija Tuomi, Allen J Norin, Ian R Mackay, Merrill J Rowley, Paul Z Zimmet, Harold E Lebovitz; GAD Antibody Negative NIDDM in Adult Black Subjects with Diabetic Ketoacidosis and Increased Frequency of Human Leukocyte Antigen DR3 and DR4: Flatbush Diabetes. Diabetes 1 June 1994; 43 (6): 741–745. https://doi.org/10.2337/diab.43.6.741
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