UKPDS 25: Autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes
UKPDS 25: Autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes
Background. Autoantibodies to islet-cell cytoplasm (ICA) and glutamic acid decarboxylase (GADA) can occur in apparently typical, non-insulin dependent diabetes mellitus (type 2). We investigated whether the presence of either or both antibodies characterises a subtype of diabetes and provides better prediction of requirement for insulin therapy by 6 years' follow-up than clinical variables. Methods. We measured ICA and GADA at diagnosis of diabetes in a representative population of 3672 white patients with type 2 diabetes, aged between 25 and 65 years. The phenotype was assessed by age of onset, body-mass index, percentage haemoglobin A(1c) (HbA(1c)), and islet β-cell function. We investigated the need for insulin therapy among 1538 patients not assigned insulin and followed up for 6 years from diagnosis. Findings. The proportion of patients with ICA and GADA decreased with increasing age at diagnosis (from 33 [21%] of 157 patients aged 25-65 to 66 [4%] of 1769 aged 55-65 for ICA; from 53 [34%] to 122 [7%] for GADA). Among patients younger than 35 at diagnosis, those with ICA or GADA had lower body-mass index than those without (mean 24.9 [SD 6.0] vs 31.7 [7.3] kg/m2; p < 0.0001 and had higher percentage of HbA(1c) (9.7 vs 8.7%, p < 0.05). 94% of patients with ICA and 84% of those with GADA required insulin therapy by 6 years, compared with 14% of those without the antibodies (p < 0.0001). Among patients older than 55 at diagnosis, the difference between those with and without antibodies in body-mass index was smaller (27.2 [5.4] vs 28.6 [4.8] kg/m2, p < 0.001); 44% of those with ICA, 34% of those with GADA, acid 5% with neither antibody required insulin therapy by 6 years (p < 0.0001). Among patients older than 45 years, body-mass index and HbA(1c) provided little predictive information for insulin requirement, whereas the positive predictive values of GADA (≤ 60 U/L) alone, or both GADA (≤ 20 U/L) and ICA (> 5 U/L), for insulin therapy were 52% and 68%. Interpretation. Among young adults with type 2 diabetes, the phenotype of those with ICA or GADA antibodies was similar to that of classic juvenile-onset insulin-dependent diabetes, and either phenotype or antibodies predicted insulin requirement. In older adults, the phenotype was closer to that of patients without antibodies and only the presence of antibodies predicted an increased likelihood of insulin requirement.
1288-1293
Turner, Robert
23da1843-122b-4241-ad8b-7c07886b3a51
Stratton, Irene
772f25b9-23c0-4240-a3f6-1e76b03b172f
Horton, Virginia
c95139b0-d5f0-4565-8641-b77f8442975e
Manley, Sue
46bacfff-cf40-4894-86d8-4aa07e302e70
Zimmet, Paul
838c5b57-2af6-45f0-9f14-168fafaaad4c
Mackay, Ian R.
a58d52bb-761d-4663-b7b5-5367da612f70
Shattock, Marion
d014a1e0-e585-4034-8fef-37afa04db3e4
Bottazzo, Gian Franco
6d33f51a-1266-439b-88e9-c68a47e9dc2d
Holman, Runy
336fb2f7-edb5-4d65-a7b0-465111cbd047
1 November 1997
Turner, Robert
23da1843-122b-4241-ad8b-7c07886b3a51
Stratton, Irene
772f25b9-23c0-4240-a3f6-1e76b03b172f
Horton, Virginia
c95139b0-d5f0-4565-8641-b77f8442975e
Manley, Sue
46bacfff-cf40-4894-86d8-4aa07e302e70
Zimmet, Paul
838c5b57-2af6-45f0-9f14-168fafaaad4c
Mackay, Ian R.
a58d52bb-761d-4663-b7b5-5367da612f70
Shattock, Marion
d014a1e0-e585-4034-8fef-37afa04db3e4
Bottazzo, Gian Franco
6d33f51a-1266-439b-88e9-c68a47e9dc2d
Holman, Runy
336fb2f7-edb5-4d65-a7b0-465111cbd047
Turner, Robert, Stratton, Irene, Horton, Virginia, Manley, Sue, Zimmet, Paul, Mackay, Ian R., Shattock, Marion, Bottazzo, Gian Franco and Holman, Runy
(1997)
UKPDS 25: Autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes.
Lancet, 350 (9087), .
(doi:10.1016/S0140-6736(97)03062-6).
Abstract
Background. Autoantibodies to islet-cell cytoplasm (ICA) and glutamic acid decarboxylase (GADA) can occur in apparently typical, non-insulin dependent diabetes mellitus (type 2). We investigated whether the presence of either or both antibodies characterises a subtype of diabetes and provides better prediction of requirement for insulin therapy by 6 years' follow-up than clinical variables. Methods. We measured ICA and GADA at diagnosis of diabetes in a representative population of 3672 white patients with type 2 diabetes, aged between 25 and 65 years. The phenotype was assessed by age of onset, body-mass index, percentage haemoglobin A(1c) (HbA(1c)), and islet β-cell function. We investigated the need for insulin therapy among 1538 patients not assigned insulin and followed up for 6 years from diagnosis. Findings. The proportion of patients with ICA and GADA decreased with increasing age at diagnosis (from 33 [21%] of 157 patients aged 25-65 to 66 [4%] of 1769 aged 55-65 for ICA; from 53 [34%] to 122 [7%] for GADA). Among patients younger than 35 at diagnosis, those with ICA or GADA had lower body-mass index than those without (mean 24.9 [SD 6.0] vs 31.7 [7.3] kg/m2; p < 0.0001 and had higher percentage of HbA(1c) (9.7 vs 8.7%, p < 0.05). 94% of patients with ICA and 84% of those with GADA required insulin therapy by 6 years, compared with 14% of those without the antibodies (p < 0.0001). Among patients older than 55 at diagnosis, the difference between those with and without antibodies in body-mass index was smaller (27.2 [5.4] vs 28.6 [4.8] kg/m2, p < 0.001); 44% of those with ICA, 34% of those with GADA, acid 5% with neither antibody required insulin therapy by 6 years (p < 0.0001). Among patients older than 45 years, body-mass index and HbA(1c) provided little predictive information for insulin requirement, whereas the positive predictive values of GADA (≤ 60 U/L) alone, or both GADA (≤ 20 U/L) and ICA (> 5 U/L), for insulin therapy were 52% and 68%. Interpretation. Among young adults with type 2 diabetes, the phenotype of those with ICA or GADA antibodies was similar to that of classic juvenile-onset insulin-dependent diabetes, and either phenotype or antibodies predicted insulin requirement. In older adults, the phenotype was closer to that of patients without antibodies and only the presence of antibodies predicted an increased likelihood of insulin requirement.
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Published date: 1 November 1997
Additional Information:
Funding Information:
We thank the patients and staff at the centres for their cooperation. We also thank Wellcome Trust for a grant for the ICA and GADA assays; Merrill Rowley for his cooperation; Ray Spark for doing the GADA assays; Ivy Samuel and Caroline Wood for typing the manuscript; and E M Kingsley and Jennifer Griffiths for typing the tables. The study was funded by the Medical Research Council, British Diabetic Association, the UK Department of Health, the National Eye Institute and the National Institute of Digestive, Diabetes, and Kidney Disease in the National Institutes of Health, USA, the British Heart Foundation, the Health Promotion Research Trust, Charles Wolfson Charitable Trust, the Alan and Babette Sainsbury Trust, the Clothworkers' Foundation, the Oxford University Medical Research Fund Committee and by pharmaceutical companies, including Bayer, Novo-Nordisk, Bristol Myers Squibb, Hoechst, Lilly, Lipha, and Farmitalia Carlo Erba.
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Local EPrints ID: 487203
URI: http://eprints.soton.ac.uk/id/eprint/487203
ISSN: 0140-6736
PURE UUID: 6f0d086f-d300-40bf-a09a-3b7e8c84110a
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Date deposited: 16 Feb 2024 10:30
Last modified: 16 Aug 2024 02:03
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Contributors
Author:
Robert Turner
Author:
Irene Stratton
Author:
Virginia Horton
Author:
Sue Manley
Author:
Paul Zimmet
Author:
Ian R. Mackay
Author:
Marion Shattock
Author:
Gian Franco Bottazzo
Author:
Runy Holman
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