Serum Thyroid Hormone Autoantibodies in Type 1 Diabetes Mellitus

被引:25
作者
Benvenga, Salvatore [2 ,3 ,4 ]
Pintaudi, Basilio [5 ]
Vita, Roberto [1 ]
Di Vieste, Giacoma [6 ]
Di Benedetto, Antonino [6 ]
机构
[1] Univ Messina, Sch Med, Dept Clin & Expt Med, I-98125 Messina, Italy
[2] Univ Messina, Sch Med, Master Program Childhood Adolescent & Womens Endo, I-98125 Messina, Italy
[3] Univ Messina, Univ Hosp, Interdept Program Mol & Clin Endocrinol, I-98125 Messina, Italy
[4] Univ Messina, Univ Hosp, Womens Endocrine Hlth, I-98125 Messina, Italy
[5] Fdn Mario Negri Sud, Dept Clin Pharmacol & Epidemiol, I-66030 Santa Maria Imbaro, CH, Italy
[6] Univ Messina, Dept Clin & Expt Med, I-98125 Messina, Italy
关键词
HASHIMOTOS-THYROIDITIS; THYROXINE; BINDING; TRANSIENT; DISEASE;
D O I
10.1210/jc.2014-3950
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Context: Autoimmune thyroid diseases (AITDs) can be associated with type 1 diabetes (DM1). The prevalence of serum antibodies against thyroid hormones (THAb) in subjects with autoimmune diseases other than DM1 is increasing. No data are available for DM1. Objective: The objectives were evaluate the rate of associated AITD; the rate of positiveness for serum THAb; the panel of THAb based on thyroid hormone interaction and on Ig class; and the association of AITD alone, THAb alone, or AITD plus THAb with diabetes-related complications. Design: This was an observational, prospective study with 6-year (2005-2011) follow-up. Setting: The setting was an outpatient diabetes clinic. Patients: Fifty-two consecutive subjects (53.8% males; mean age, 37.4 +/- 7.4 y; diabetes duration, 19.9 +/- 8.2 y) with DM1. All participants completed the study. Main Outcome Measures: Main outcome measures were AITD rate; THAb positivity according to hormone interaction and Ig class; association of AITD and THAb with diabetes-related complications. Results: AITD rate increased from baseline (34.6%) to follow-up (38.5%). Subjects with DM1 had a high prevalence of THAb (92.3%). The presence of AITD at baseline was associated with subsequent development of macroangiopathy (0 vs 33% at baseline and follow-up, respectively; P = .029). Some THAb patterns, the majority having T-3 binding in common, were associated with the progression and development of diabetes-related complications. Conclusions: THAb synthesis in DM1 might be driven by increased glycosylation of thyroglobulin. Anti T-3-THAb may cause a relative "tissue hypothyroidism" by sequestering thyroid hormone, this at least partially contributing to worsening diabetes-related vascular complications. In a clinical setting THAb positivity could identify subjects more likely to develop diabetes complications.
引用
收藏
页码:1870 / 1878
页数:9
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