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Association between age, IL-10, IFN gamma, stimulated C-peptide and disease progression in children with newly diagnosed Type 1 diabetes

Kaas, A. (författare)
Department of Paediatrics, Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark
Pfleger, C. (författare)
Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research, Heinrich-Heine University, Düsseldorf, Germany
Kharagjitsingh, A. V. (författare)
Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
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Schloot, N .C. (författare)
Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research, Heinrich-Heine University, Düsseldorf, Germany; Medical Faculty, Department of Metabolic Diseases, University of Düsseldorf, Düsseldorf, Germany
Hansen, L. (författare)
Department of Paediatrics, Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark
Buschard, K. (författare)
Bartholin Institute, Rigshospitalet, Copenhagen, Denmark
Koeleman, B. P. C. (författare)
Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Roep, B. O. (författare)
Department of Immunohaematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands
Mortensen, H. B. (författare)
Department of Paediatrics, Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark
Alizadeh, B. Z. (författare)
Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Åman, Jan, 1948- (författare)
Region Örebro län,Hvidøre Study Group on Childhood Diabetes, Copenhagen, Denmark
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 (creator_code:org_t)
2012-05-16
2012
Engelska.
Ingår i: Diabetic Medicine. - : Wiley-Blackwell. - 0742-3071 .- 1464-5491. ; 29:6, s. 734-741
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • AIMS: The relation of disease progression and age, serum interleukin 10 (IL-10) and interferon gamma (IFNγ) and their genetic correlates were studied in paediatric patients with newly diagnosed Type 1 diabetes.METHODS: Two hundred and twenty-seven patients from the Hvidoere Study Group were classified in four different progression groups as assessed by change in stimulated C-peptide from 1 to 6 months. CA repeat variants of the IL-10 and IFNγ gene were genotyped and serum levels of IL-10 and IFNγ were measured at 1, 6 and 12 months.RESULTS: IL-10 decreased (P < 0.001) by 7.7% (1 month), 10.4% (6 months) and 8.6% (12 months) per year increase in age of child, while a twofold higher C-peptide concentration at 1 month (p = 0.06), 6 months (P = 0.0003) and 12 months (P = 0.02) was associated with 9.7%, 18.6% and 9.7% lower IL-10 levels, independent of each other. IL-10 concentrations did not associate with the disease progression groups. By contrast, IFNγ concentrations differed between the four progression groups at 6 and 12 months (P = 0.02 and P = 0.01, respectively); patients with rapid progressing disease had the highest levels at both time points. Distribution of IL-10 and IFNγ genotypes was equal among patients from the progression groups.CONCLUSION: IL-10 serum levels associate inversely with age and C-peptide. As age and C-peptide also associate, a triangular association is proposed. Genetic influence on IL-10 production seems to be masked by distinct disease mechanisms. Increased serum IFNγ concentrations associate with rapid disease progression. Functional genetic variants do not associate with a single progression pattern group, implying that disease processes override genetically predisposed cytokine production.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Nyckelord

disease progression; interferon gamma; interleukin 10; Type 1 diabetes

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