No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)

ISSN:
1432-0428
Keywords:
Keywords Type I diabetes ; oral insulin ; insulin antibodies ; prevention.
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
Type of Medium:
Electronic Resource
URL:
_version_ 1798295382430580737
autor Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
autorsonst Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
book_url http://dx.doi.org/10.1007/s001250051482
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM199949921
issn 1432-0428
journal_name Diabetologia
materialart 1
notes Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
package_name Springer
publikationsjahr_anzeige 2000
publikationsjahr_facette 2000
publikationsjahr_intervall 7999:2000-2004
publikationsjahr_sort 2000
publisher Springer
reference 43 (2000), S. 1000-1004
schlagwort Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
search_space articles
shingle_author_1 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
shingle_author_2 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
shingle_author_3 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
shingle_author_4 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
shingle_catch_all_1 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
1432-0428
14320428
Springer
shingle_catch_all_2 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
1432-0428
14320428
Springer
shingle_catch_all_3 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
1432-0428
14320428
Springer
shingle_catch_all_4 Pozzilli, P.
Pitocco, D.
Visalli, N.
Cavallo, M. G.
Buzzetti, R.
Crinò, A.
Spera, S.
Suraci, C.
Multari, G.
Cervoni, M.
Manca Bitti, M. L.
Matteoli, M. C.
Marietti, G.
Ferrazzoli, F.
Cassone Faldetta, M. R.
Giordano, C.
Sbriglia, M.
Sarugeri, E.
Ghirlanda, G.
No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Keywords Type I diabetes
oral insulin
insulin antibodies
prevention.
Abstract Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Type I diabetes (DPT-1), oral insulin is given with the aim of preventing disease insurgence. We investigated whether if given at diagnosis of Type I diabetes in humans, oral insulin can still act as a tolerogen and therefore preserve residual beta-cell function, which is known to be substantial at diagnosis. Methods. A double-blind trial was carried out in patients (mean age ± SD: 14 ± 8 years) with recent-onset Type I diabetes to whom oral insulin (5 mg daily) or placebo was given for 12 months in addition to intensive subcutaneous insulin therapy. A total of 82 patients with clinical Type I diabetes ( 〈 4 weeks duration) were studied. Basal C peptide and glycated haemoglobin were measured and the insulin requirement monitored every 3 months up to 1 year. Insulin antibodies were also measured in 27 patients treated with oral insulin and in 18 patients receiving placebo at the beginning of the trial and after 3, 6 and 12 months of treatment. Results. The trial was completed by 80 patients. Overall and without distinction between age at diagnosis, at 3, 6, 9 and 12 months baseline mean C-peptide secretion in patients treated with oral insulin did not differ from that of those patients treated with placebo. In patients younger than 15 years a tendency for lower C-peptide values at 9 and 12 months was observed in the oral insulin group. Insulin requirement at 1 year was similar between the two groups as well as the percentage of glycated haemoglobin. Finally, IgG insulin antibodies were similar in the two groups at each time point. Conclusion/interpretation. The results of this study indicate that the addition of 5 mg of oral insulin does not modify the course of the disease in the first year after diagnosis and probably does not statistically affect the humoral immune response against insulin. [Diabetologia (2000) 43: 1000–1004]
1432-0428
14320428
Springer
shingle_title_1 No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
shingle_title_2 No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
shingle_title_3 No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
shingle_title_4 No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
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timestamp 2024-05-06T09:35:19.224Z
titel No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
titel_suche No effect of oral insulin on residual beta-cell function in recent-onset Type I diabetes (the IMDIAB VII)
topic WW-YZ
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