کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5654853 1589416 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Neonatal levels of adiponectin, interleukin-10 and interleukin-12 are associated with the risk of developing type 1 diabetes in childhood and adolescence: A nationwide Danish case-control study
ترجمه فارسی عنوان
سطوح جدید آدیپونکتین، اینترلوکین 10 و اینترلوکین 12 با خطر ابتلا به دیابت نوع 1 در دوران کودکی و نوجوانی همراه است: یک مطالعه در مورد کشوری در دانمارک
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


- Neonatal levels of adiponectin were lower in cases compared to controls.
- Neonatal levels of IL-10 and IL-12 were increased in cases compared to controls.
- No clear patterns were found between pro- and anti-inflammatory immune mediators.

Background/aimAn in-depth understanding of the early phase of type 1 diabetes (T1D) pathogenesis is important for targeting primary prevention. We examined if 14 preselected mediators of immune responses differed in neonates that later developed T1D compared to control neonates.MethodsThe study is a case-control study with a 1:2 matching. The individuals were born between 1981 through 2002. Cases were validated using the National Patient Register and the Danish Childhood Diabetes Register. Interleukin(IL)-1β, IL-4, IL-6, IL-8, IL-10, IL-12p70, interferon gamma, tumor necrosis factor alpha, transforming growth factor beta 1 (active form), leptin, adiponectin, c-reactive protein, mannose-binding lectin and soluble triggering receptor expressed on myeloid cells-1 were measured by using a flowmetric Luminex xMAP® technology. We tested two models both including a number of possible confounders. In the first model (model 1) we also adjusted for HLA-DQB1 genotype. A total of 1930 groups of assay-matched cases and controls (4746 individuals) were included in the statistical analyses.ResultsAdiponectin was negatively associated with later risk of T1D in both models (relative change (RC), model 1: 0.95, P = 0.046 and model 2: 0.95, P = 0.006). IL-10 and IL-12 were both positively associated with T1D risk in the model 2 (RC, 1.19, P = 0.006 and 1.07, P = 0.02, respectively)-these results were borderline significant in model 1, but showed the same direction as the results from model 2.ConclusionsOur results indicate that specific immunological signatures are already present at time of birth in children developing T1D before the age of 18 years.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinical Immunology - Volume 174, January 2017, Pages 18-23
نویسندگان
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