Polymorphisms in the TLR3 gene are associated with risk for type 1 diabetes mellitus

被引:41
作者
Assmann, Tais Silveira [1 ,2 ]
Brondani, Leticia de Almeida [1 ,2 ]
Bauer, Andrea Carla [1 ]
Canani, Luis Henrique [2 ]
Crispim, Daisy [1 ,2 ]
机构
[1] Hosp Clin Porto Alegre, Lab Biol Human Pancreat Islet, Div Endocrine, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Postgrad Program Med Sci Endocrinol, Porto Alegre, RS, Brazil
关键词
TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; POLYINOSINIC-POLYCYTIDYLIC ACID; PATTERN-RECOGNITION RECEPTORS; EXPRESSION; SUSCEPTIBILITY; EPIDEMIOLOGY; PATHOGENESIS; ACTIVATION; APOPTOSIS;
D O I
10.1530/EJE-13-0963
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction: Viral pathogens seem to play a role in triggering the autoimmune destruction that leads to the development of type 1 diabetes mellitus (T1DM). Toll-like receptor 3 (TLR3) has been shown to recognize double-stranded RNA, a molecular signature of most viruses. It is expressed at high levels in pancreatic beta-cells and immune cells, suggesting a role for it in the pathogenesis of T1DM. Therefore, the aim of this study was to investigate whether TLR3 polymorphisms are associated with T1DM. Methods: Frequencies of the TLR3 rs11721827, rs13126816, rs5743313, rs7668666, and rs3775291 polymorphisms were analyzed in 449 T1DM patients and in 507 nondiabetic subjects. Haplotypes constructed from the combination of these polymorphisms were inferred using a Bayesian statistical method. Results: The rs3775291 and rs13126816 polymorphisms were associated with T1DM, and the strongest association was observed for the additive model (odds ratio (OR) =2.3, 95% CI 1.3-4.2 and OR=2.1, 95% CI 1.3-3.1 respectively). In the same way, the frequency of T1DM was higher as more risk alleles of the five polymorphisms were present (P-trend=0.001). Moreover, in T1DM patients, the minor alleles of the rs5743313 and rs117221827 polymorphisms were associated with an early age at diagnosis and worse glycemic control. Conclusion: The TLR3 rs3775291 and rs13126816 polymorphisms are associated with risk for T1DM, while the rs5743313 and rs11721827 polymorphisms are associated with age at T1DM diagnosis and poor glycemic control. The number of risk alleles of the five TLR3 polymorphisms in the haplotypes seems to influence the risk for T1DM, suggesting that these polymorphisms might interact in the susceptibility for the disease.
引用
收藏
页码:519 / 527
页数:9
相关论文
共 46 条
[1]
Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[2]
Dysregulated Toll-Like Receptor-Induced Interleukin-1β and Interleukin-6 Responses in Subjects at Risk for the Development of Type 1 Diabetes [J].
Alkanani, Aimon K. ;
Rewers, Marian ;
Dong, Fran ;
Waugh, Kathleen ;
Gottlieb, Peter A. ;
Zipris, Danny .
DIABETES, 2012, 61 (10) :2525-2533
[3]
Amer Diabet Assoc, 2011, DIABETES CARE, V34, pS11, DOI [10.2337/dc10-S062, 10.2337/dc14-S081, 10.2337/dc11-S011, 10.2337/dc13-S011, 10.2337/dc13-S067, 10.2337/dc12-s064, 10.2337/dc11-S062, 10.2337/dc10-S011, 10.2337/dc12-s011]
[4]
[Anonymous], 2012, CSH PERSPECT MED, DOI [10.1101/cshperspect.a007682, DOI 10.1101/cshperspect.a007682]
[5]
Arancibia SA, 2007, BIOL RES, V40, P97, DOI 10.4067/S0716-97602007000200001
[6]
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes [J].
Barrett, Jeffrey C. ;
Clayton, David G. ;
Concannon, Patrick ;
Akolkar, Beena ;
Cooper, Jason D. ;
Erlich, Henry A. ;
Julier, Cecile ;
Morahan, Grant ;
Nerup, Jorn ;
Nierras, Concepcion ;
Plagnol, Vincent ;
Pociot, Flemming ;
Schuilenburg, Helen ;
Smyth, Deborah J. ;
Stevens, Helen ;
Todd, John A. ;
Walker, Neil M. ;
Rich, Stephen S. .
NATURE GENETICS, 2009, 41 (06) :703-707
[7]
The Toll-like receptor 3:dsRNA signaling complex [J].
Botos, Istvan ;
Liu, Lin ;
Wang, Yan ;
Segal, David M. ;
Davies, David R. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2009, 1789 (9-10) :667-674
[8]
Accuracy of conversion formulae for estimation of glycohaemoglobin [J].
Camargo, JL ;
Zelmanovitz, T ;
Paggi, A ;
Friedman, R ;
Gross, JL .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1998, 58 (06) :521-528
[9]
Choe J, 2005, SCIENCE, V309, P581, DOI 10.1126/science.1115253
[10]
Interferon-α as a mediator of polyinosinic:polycytidylic acid-induced type 1 diabetes [J].
Devendra, D ;
Jasinski, J ;
Melanitou, E ;
Nakayama, M ;
Li, M ;
Hensley, B ;
Paronen, J ;
Moriyama, H ;
Miao, DM ;
Eisenbarth, GS ;
Liu, E .
DIABETES, 2005, 54 (09) :2549-2556