Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings. / Sildorf, Stine Møller; Eising, Stefanie; Hougaard, David M; Mortensen, Henrik Bindesbøl; Skogstrand, Kristin; Pociot, Flemming; Johannesen, Jesper; Svensson, Jannet.

I: Molecular Immunology, Bind 62, Nr. 1, 11.2014, s. 71-76.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Sildorf, SM, Eising, S, Hougaard, DM, Mortensen, HB, Skogstrand, K, Pociot, F, Johannesen, J & Svensson, J 2014, 'Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings', Molecular Immunology, bind 62, nr. 1, s. 71-76. https://doi.org/10.1016/j.molimm.2014.06.001

APA

Sildorf, S. M., Eising, S., Hougaard, D. M., Mortensen, H. B., Skogstrand, K., Pociot, F., Johannesen, J., & Svensson, J. (2014). Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings. Molecular Immunology, 62(1), 71-76. https://doi.org/10.1016/j.molimm.2014.06.001

Vancouver

Sildorf SM, Eising S, Hougaard DM, Mortensen HB, Skogstrand K, Pociot F o.a. Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings. Molecular Immunology. 2014 nov.;62(1):71-76. https://doi.org/10.1016/j.molimm.2014.06.001

Author

Sildorf, Stine Møller ; Eising, Stefanie ; Hougaard, David M ; Mortensen, Henrik Bindesbøl ; Skogstrand, Kristin ; Pociot, Flemming ; Johannesen, Jesper ; Svensson, Jannet. / Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings. I: Molecular Immunology. 2014 ; Bind 62, Nr. 1. s. 71-76.

Bibtex

@article{c399340026d3451daeef26678d2ff2b0,
title = "Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings",
abstract = "The incidence of type 1 diabetes (T1D) has during the last few decades been increasing in children and juveniles. Multi-factorial courses combining genetic disposition and environmental factors might be in play, and through the years, there has been a mounting interest in the innate immune system's role in the development of T1D. The aim of this study was to determine mannose binding lectin (MBL) levels in newly diagnosed children with T1D (n=481) over a period of 10 years (1997-2005) and to compare these levels with corresponding levels in their healthy siblings (n=479). Furthermore, the aims were to evaluate if MBL-levels in patients and siblings were influenced by season, age autoimmunity and/or changed over time. The study found that MBL levels differed between patients and their healthy siblings when adjusted for age, gender, season and period. More patients than siblings had MBL levels above 0.8 μg/ml, associated with high producing MBL genotypes, and the elevated MBL levels were associated with high levels of four T1D related cytokines (IL-1β, IL-12, IL-18 and TNF-α). MBL levels increased during the study period and siblings had seasonal variance in concentrations with the lowest level during wintertime (Dec-Feb). In conclusion, more patients than siblings had a high MBL level, and high levels of MBL were related to high levels of T1D specific cytokines, supporting a role of the innate immune system and MBL on the risk of developing T1D.",
keywords = "Adolescent, Autoantibodies, Child, Child, Preschool, Cytokines, Diabetes Mellitus, Type 1, Female, Humans, Infant, Longitudinal Studies, Male, Mannose-Binding Lectin, Seasons, Siblings, Time Factors",
author = "Sildorf, {Stine M{\o}ller} and Stefanie Eising and Hougaard, {David M} and Mortensen, {Henrik Bindesb{\o}l} and Kristin Skogstrand and Flemming Pociot and Jesper Johannesen and Jannet Svensson",
note = "Copyright {\textcopyright} 2014 Elsevier Ltd. All rights reserved.",
year = "2014",
month = nov,
doi = "10.1016/j.molimm.2014.06.001",
language = "English",
volume = "62",
pages = "71--76",
journal = "Molecular Immunology",
issn = "0161-5890",
publisher = "Pergamon Press",
number = "1",

}

RIS

TY - JOUR

T1 - Differences in MBL levels between juvenile patients newly diagnosed with type 1 diabetes and their healthy siblings

AU - Sildorf, Stine Møller

AU - Eising, Stefanie

AU - Hougaard, David M

AU - Mortensen, Henrik Bindesbøl

AU - Skogstrand, Kristin

AU - Pociot, Flemming

AU - Johannesen, Jesper

AU - Svensson, Jannet

N1 - Copyright © 2014 Elsevier Ltd. All rights reserved.

PY - 2014/11

Y1 - 2014/11

N2 - The incidence of type 1 diabetes (T1D) has during the last few decades been increasing in children and juveniles. Multi-factorial courses combining genetic disposition and environmental factors might be in play, and through the years, there has been a mounting interest in the innate immune system's role in the development of T1D. The aim of this study was to determine mannose binding lectin (MBL) levels in newly diagnosed children with T1D (n=481) over a period of 10 years (1997-2005) and to compare these levels with corresponding levels in their healthy siblings (n=479). Furthermore, the aims were to evaluate if MBL-levels in patients and siblings were influenced by season, age autoimmunity and/or changed over time. The study found that MBL levels differed between patients and their healthy siblings when adjusted for age, gender, season and period. More patients than siblings had MBL levels above 0.8 μg/ml, associated with high producing MBL genotypes, and the elevated MBL levels were associated with high levels of four T1D related cytokines (IL-1β, IL-12, IL-18 and TNF-α). MBL levels increased during the study period and siblings had seasonal variance in concentrations with the lowest level during wintertime (Dec-Feb). In conclusion, more patients than siblings had a high MBL level, and high levels of MBL were related to high levels of T1D specific cytokines, supporting a role of the innate immune system and MBL on the risk of developing T1D.

AB - The incidence of type 1 diabetes (T1D) has during the last few decades been increasing in children and juveniles. Multi-factorial courses combining genetic disposition and environmental factors might be in play, and through the years, there has been a mounting interest in the innate immune system's role in the development of T1D. The aim of this study was to determine mannose binding lectin (MBL) levels in newly diagnosed children with T1D (n=481) over a period of 10 years (1997-2005) and to compare these levels with corresponding levels in their healthy siblings (n=479). Furthermore, the aims were to evaluate if MBL-levels in patients and siblings were influenced by season, age autoimmunity and/or changed over time. The study found that MBL levels differed between patients and their healthy siblings when adjusted for age, gender, season and period. More patients than siblings had MBL levels above 0.8 μg/ml, associated with high producing MBL genotypes, and the elevated MBL levels were associated with high levels of four T1D related cytokines (IL-1β, IL-12, IL-18 and TNF-α). MBL levels increased during the study period and siblings had seasonal variance in concentrations with the lowest level during wintertime (Dec-Feb). In conclusion, more patients than siblings had a high MBL level, and high levels of MBL were related to high levels of T1D specific cytokines, supporting a role of the innate immune system and MBL on the risk of developing T1D.

KW - Adolescent

KW - Autoantibodies

KW - Child

KW - Child, Preschool

KW - Cytokines

KW - Diabetes Mellitus, Type 1

KW - Female

KW - Humans

KW - Infant

KW - Longitudinal Studies

KW - Male

KW - Mannose-Binding Lectin

KW - Seasons

KW - Siblings

KW - Time Factors

U2 - 10.1016/j.molimm.2014.06.001

DO - 10.1016/j.molimm.2014.06.001

M3 - Journal article

C2 - 24972325

VL - 62

SP - 71

EP - 76

JO - Molecular Immunology

JF - Molecular Immunology

SN - 0161-5890

IS - 1

ER -

ID: 138145805