Both thyroid autoimmunity and increased serum TSH are independent risk factors for malignancy in patients with thyroid nodules

被引:74
作者
Boi, F. [1 ]
Minerba, L. [2 ]
Lai, M. L. [3 ]
Marziani, B. [1 ]
Figus, B. [1 ]
Spanu, F. [1 ]
Borghero, A. [1 ]
Mariotti, S. [1 ]
机构
[1] Univ Cagliari, Endocrinol Unit, Dept Med Sci M Aresu, I-09042 Cagliari, Italy
[2] Univ Cagliari, Dept Publ Hlth, I-09042 Cagliari, Italy
[3] Univ Cagliari, Dept Cytomorphol, San Giovanni di Dio Hosp, I-09042 Cagliari, Italy
关键词
Thyroid autoantibodies; thyroid carcinoma; thyroid cytology; thyroid nodules; TSH; FINE-NEEDLE-ASPIRATION; CHRONIC LYMPHOCYTIC THYROIDITIS; HASHIMOTOS-THYROIDITIS; PAPILLARY CARCINOMA; FOLLICULAR CELLS; IMMUNE-RESPONSE; HIGH PREVALENCE; L-THYROXINE; CANCER; EXPRESSION;
D O I
10.3275/8579
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: To assess the relevance of thyroid autoimmunity and TSH as risk factors for malignancy in thyroid nodules (TN). Subjects and methods: Retrospective analysis on 2053 patients with single/prevalent TN submitted to fine needle aspiration cytology (FNAC). Anti-thyroid autoantibodies (ATA) [anti-thyroperoxidase (TPOAb), anti-thyroglobulin (TgAb)] and TSH were measured. Cytology was classified as benign (class II), indeterminate (class III), and suspicious or malignant (class IV). Histology was available in 301 patients. Associations of malignancy with independent variables were determined by multivariate logistic regression analysis. Results: Higher prevalence of class IV (14.2% vs 6.8%: p<0.001) and class III (23.5% vs 17.1%: p<0.001) were found in ATA+ vs ATA- TN. Histology confirmed increased prevalence of cancer in ATA+ (p<0.05) TN and in those with diffuse lymphocytic thyroid infiltration (p<0.05). Interestingly, the prevalence of malignancies observed in operated class III nodules was strikingly lower in ATM- (1/20, 5%), than in ATA- patients (34/67, 50.7%; p<0.001). Increased independent odds ratio (OR) for malignancy was conferred by any ATA [OR 2.21; 95% confidence interval (CI)=1.49-3.29, p<0.0001]; TPOAb (OR 2.15; CI=1.42-3.25, p<0.0001) and TgAb (OR 1.67; CI=1.05-2.67, p<0.05), by serum TSH>1.0 mu UI/ml (OR 1.95; CI=1.01-3.76, p<0.05), and by young age (10-29 yr: OR 2.09; CI=1.02-4.26, p<0.05). A formula was calculated to assess the relative contribution of ATA, TSH, and age to the risk of TN malignancy. Conclusions: Both thyroid autoimmunity and increased TSH represent independent risk factors for TN malignancy. (C) 2013, Editrice Kurtis
引用
收藏
页码:313 / 320
页数:8
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