Boelaert K, Horacek J, Holder R L, Watkinson J C, Sheppard M C, Franklyn J A
Division of Medical Sciences, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, Birmingham B15 2TH, United Kingdom.
J Clin Endocrinol Metab. 2006 Nov;91(11):4295-301. doi: 10.1210/jc.2006-0527. Epub 2006 Jul 25.
Thyroid nodules and goiter are common, and fine-needle aspiration biopsy (FNAB) is the first investigation of choice in distinguishing benign from malignant disease.
The objective of the study was to assess whether simple clinical and biochemical parameters can predict the likelihood of thyroid malignancy in subjects undergoing FNAB.
The design was a prospective cohort.
The study was conducted at a single secondary/tertiary care clinic.
One thousand five hundred consecutive patients without overt thyroid dysfunction (1304 females and 196 males, mean age 47.8 yr) presenting with palpable thyroid enlargement between 1984 and 2002 were evaluated by FNAB of the thyroid.
INTERVENTION(S): There were no interventions.
Goiter type was assessed clinically and classified as diffuse in 183, multinodular in 456, or solitary nodule in 861 cases. Serum TSH concentration at presentation was measured in a sensitive assay in patients presenting after 1988 (n = 1183). The final cytological or histological diagnosis was determined after surgery (n = 553) or a minimum 2-yr clinical follow-up period (mean 9.5 yr, range 2-18 yr).
The overall sensitivity and specificity of FNAB in predicting malignancy were 88 and 84%, respectively. The risk of diagnosis of malignancy rose in parallel with the serum TSH at presentation, with significant increases evident in patients with serum TSH greater than 0.9 mU/liter, compared with those with lower TSH. Binary logistic regression analysis revealed significantly increased adjusted odds ratios (AORs) for the diagnosis of malignancy in subjects with serum TSH 1.0-1.7 mU/liter, compared with TSH less than 0.4 mU/liter [AOR 2.72, 95% confidence interval (CI) 1.02-7.27, P = 0.046], with further increases evident in those with TSH 1.8-5.5 mU/liter (AOR 3.88, 95% CI 1.48-10.19, P = 0.006, compared with TSH < 0.4 mU/liter) and greater than 5.5 mU/liter (AOR 11.18, 95% CI 3.23-8.63, P < 0.001, compared with TSH < 0.4 mU/liter). Males (AOR 1.8, 95% CI 1.04-3.1, P = 0.04), younger patients (AOR 1.1, 95% CI 1.01-1.15, P = 0.025), and those with clinically solitary nodules (AOR 2.53, 95% CI 1.5-4.28, P = 0.001) were also at increased risk. Based on these findings, a formula to predict the risk of the diagnosis of thyroid malignancy in individual patients, taking into account their gender, age, goiter type determined clinically, and serum TSH, was calculated.
The risk of malignancy in a thyroid nodule increases with serum TSH concentrations within the normal range. In addition to patient's gender, age, and goiter type, the serum TSH concentration at presentation is an independent predictor of the presence of thyroid malignancy. We propose that these simple clinical and biochemical factors can serve as an adjunct to FNAB in predicting risk of malignancy.
甲状腺结节和甲状腺肿很常见,细针穿刺活检(FNAB)是区分良性和恶性疾病的首选初步检查方法。
本研究的目的是评估简单的临床和生化参数是否能预测接受FNAB检查的患者患甲状腺恶性肿瘤的可能性。
前瞻性队列研究。
研究在一家二级/三级医疗诊所进行。
1984年至2002年间连续1500例无明显甲状腺功能障碍的患者(1304例女性和196例男性,平均年龄47.8岁)因可触及甲状腺肿大而接受甲状腺FNAB检查。
无干预措施。
临床评估甲状腺肿类型,183例为弥漫性,456例为多结节性,861例为单结节性。1988年后就诊的患者(n = 1183)采用敏感检测方法测定就诊时血清促甲状腺激素(TSH)浓度。术后(n = 553)或至少2年的临床随访期(平均9.5年,范围2 - 18年)后确定最终的细胞学或组织学诊断。
FNAB预测恶性肿瘤的总体敏感性和特异性分别为88%和84%。诊断为恶性肿瘤的风险与就诊时的血清TSH水平平行上升,血清TSH大于0.9 mU/L的患者与TSH较低的患者相比,明显增加。二元逻辑回归分析显示,血清TSH为1.0 - 1.7 mU/L的患者与TSH小于0.4 mU/L的患者相比,诊断为恶性肿瘤的调整优势比(AOR)显著增加[AOR = 2.72,95%置信区间(CI)1.02 - 7.27,P = 0.046],TSH为1.8 - 5.5 mU/L的患者进一步增加(AOR = 3.88,95% CI 1.48 - 10.19,与TSH < 0.4 mU/L相比,P = 0.006),TSH大于5.5 mU/L的患者增加更明显(AOR = 11.18,95% CI 3.23 - 8.63,与TSH < 0.4 mU/L相比,P < 0.001)。男性(AOR = 1.8,95% CI 1.04 - 3.1,P = 0.04)、年轻患者(AOR = 1.1,95% CI 1.01 - 1.15,P = 0.025)以及临床诊断为单结节的患者(AOR = 2.53,95% CI 1.5 - 4.28,P = 0.001)风险也增加。基于这些发现,计算了一个考虑患者性别、年龄、临床确定的甲状腺肿类型和血清TSH来预测个体患者甲状腺恶性肿瘤诊断风险的公式。
甲状腺结节的恶性风险在正常范围内随血清TSH浓度升高而增加。除患者性别、年龄和甲状腺肿类型外,就诊时的血清TSH浓度是甲状腺恶性肿瘤存在的独立预测因素。我们建议这些简单的临床和生化因素可作为FNAB预测恶性风险的辅助手段。