Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults

<p>Abstract</p> <p>Background</p> <p>Latent autoimmune diabetes in adults [LADA] is a type 1 diabetes that is slowly developing. This means many people are treated as having type 2 diabetes at diagnosis as they are adults who are not immediately insulin dependent. LADA...

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Main Authors: Lloyd Janet, Beaverstock Charles, Wareham Kathie, Richards Kez, Cheung Wei-yee, Stephens Jeffrey W, Bain Stephen, Davies Helen, Brophy Sinead, Page Don, Williams Meurig, Russell Ian, Williams Rhys
Format: Article
Language:English
Published: BMC 2008-07-01
Series:BMC Endocrine Disorders
Online Access:http://www.biomedcentral.com/1472-6823/8/8
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spelling doaj-8636f07eb05446b986f1dac4e7df22312020-11-25T03:13:14ZengBMCBMC Endocrine Disorders1472-68232008-07-0181810.1186/1472-6823-8-8Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adultsLloyd JanetBeaverstock CharlesWareham KathieRichards KezCheung Wei-yeeStephens Jeffrey WBain StephenDavies HelenBrophy SineadPage DonWilliams MeurigRussell IanWilliams Rhys<p>Abstract</p> <p>Background</p> <p>Latent autoimmune diabetes in adults [LADA] is a type 1 diabetes that is slowly developing. This means many people are treated as having type 2 diabetes at diagnosis as they are adults who are not immediately insulin dependent. LADA can be distinguished from type 2 diabetes by antibody tests. Patients who are antibody positive have an autoimmune reaction which is similar to that of type 1 diabetes and is not found in type 2 diabetes. We would like to examine the best way of treating LADA in the early phase of the conditions, with tablets (similar to type 2 diabetes) or with insulin (similar to type 1 diabetes).</p> <p>Methods/design</p> <p>This is an open parallel group prospective randomised trial. Participants need to have a GAD antibody test results of 101 WHO units or more and a diagnosis of diabetes not requiring insulin at diagnosis. Participants will need to have been diagnosed within 12 months and not treated with insulin at study entry. They will be randomised to receive either insulin (NovoMix 30) or tablets (diet treated followed by metformin followed by glitazone (with or without metformin) followed by insulin). Primary outcome assessment will be for change in HbA1c and change in fasting C-peptide over 24 months. Secondary outcome measures will include Quality of life, GAD antibody levels, adverse events, inflammatory markers, insulin resistance, and markers of the metabolic syndrome.</p> <p>Discussion</p> <p>This study seeks the best treatment for early LADA in terms of maintaining glycaemic control and maintaining natural insulin production.</p> <p>Trial registration</p> <p>ISRCTN63815121</p> http://www.biomedcentral.com/1472-6823/8/8
collection DOAJ
language English
format Article
sources DOAJ
author Lloyd Janet
Beaverstock Charles
Wareham Kathie
Richards Kez
Cheung Wei-yee
Stephens Jeffrey W
Bain Stephen
Davies Helen
Brophy Sinead
Page Don
Williams Meurig
Russell Ian
Williams Rhys
spellingShingle Lloyd Janet
Beaverstock Charles
Wareham Kathie
Richards Kez
Cheung Wei-yee
Stephens Jeffrey W
Bain Stephen
Davies Helen
Brophy Sinead
Page Don
Williams Meurig
Russell Ian
Williams Rhys
Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
BMC Endocrine Disorders
author_facet Lloyd Janet
Beaverstock Charles
Wareham Kathie
Richards Kez
Cheung Wei-yee
Stephens Jeffrey W
Bain Stephen
Davies Helen
Brophy Sinead
Page Don
Williams Meurig
Russell Ian
Williams Rhys
author_sort Lloyd Janet
title Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
title_short Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
title_full Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
title_fullStr Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
title_full_unstemmed Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
title_sort randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults
publisher BMC
series BMC Endocrine Disorders
issn 1472-6823
publishDate 2008-07-01
description <p>Abstract</p> <p>Background</p> <p>Latent autoimmune diabetes in adults [LADA] is a type 1 diabetes that is slowly developing. This means many people are treated as having type 2 diabetes at diagnosis as they are adults who are not immediately insulin dependent. LADA can be distinguished from type 2 diabetes by antibody tests. Patients who are antibody positive have an autoimmune reaction which is similar to that of type 1 diabetes and is not found in type 2 diabetes. We would like to examine the best way of treating LADA in the early phase of the conditions, with tablets (similar to type 2 diabetes) or with insulin (similar to type 1 diabetes).</p> <p>Methods/design</p> <p>This is an open parallel group prospective randomised trial. Participants need to have a GAD antibody test results of 101 WHO units or more and a diagnosis of diabetes not requiring insulin at diagnosis. Participants will need to have been diagnosed within 12 months and not treated with insulin at study entry. They will be randomised to receive either insulin (NovoMix 30) or tablets (diet treated followed by metformin followed by glitazone (with or without metformin) followed by insulin). Primary outcome assessment will be for change in HbA1c and change in fasting C-peptide over 24 months. Secondary outcome measures will include Quality of life, GAD antibody levels, adverse events, inflammatory markers, insulin resistance, and markers of the metabolic syndrome.</p> <p>Discussion</p> <p>This study seeks the best treatment for early LADA in terms of maintaining glycaemic control and maintaining natural insulin production.</p> <p>Trial registration</p> <p>ISRCTN63815121</p>
url http://www.biomedcentral.com/1472-6823/8/8
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