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A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting

BACKGROUND: Thyroid nodules are highly prevalent, but a robust, feasible method for malignancy differentiation has not yet been well documented. This study aimed to establish a practical model for thyroid nodule discrimination. METHODS: Records for 2984 patients who underwent thyroidectomy were anal...

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Autores principales: Liu, Jia, Zheng, Dongmei, Li, Qiang, Tang, Xulei, Luo, Zuojie, Yuan, Zhongshang, Gao, Ling, Zhao, Jiajun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842594/
https://www.ncbi.nlm.nih.gov/pubmed/29514621
http://dx.doi.org/10.1186/s12902-018-0241-7
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author Liu, Jia
Zheng, Dongmei
Li, Qiang
Tang, Xulei
Luo, Zuojie
Yuan, Zhongshang
Gao, Ling
Zhao, Jiajun
author_facet Liu, Jia
Zheng, Dongmei
Li, Qiang
Tang, Xulei
Luo, Zuojie
Yuan, Zhongshang
Gao, Ling
Zhao, Jiajun
author_sort Liu, Jia
collection PubMed
description BACKGROUND: Thyroid nodules are highly prevalent, but a robust, feasible method for malignancy differentiation has not yet been well documented. This study aimed to establish a practical model for thyroid nodule discrimination. METHODS: Records for 2984 patients who underwent thyroidectomy were analyzed. Clinical, laboratory, and US variables were assessed retrospectively. Multivariate logistic regression analysis was performed and a mathematical model was established for malignancy prediction. RESULTS: The results showed that the malignant group was younger and had smaller nodules than the benign group (43.5 ± 11.6 vs. 48.5 ± 11.5 y, p < 0.001; 1.96 ± 1.16 vs. 2.75 ± 1.70 cm, p < 0.001, respectively). The serum thyrotropin (TSH) level (median = 1.63 mIU/L, IQR (0.89–2.66) vs. 1.19 (0.59–2.10), p < 0.001) was higher in the malignant group than in the benign group. Patients with malignancies tested positive for anti-thyroglobulin antibody (TGAb) and anti-thyroid peroxidase antibody (TPOAb) more frequently than those with benign nodules (TGAb, 30.3% vs. 15.0%, p < 0.001; TPOAb, 25.6% vs. 18.0%, p = 0.028). The prevalence of ultrasound (US) features (irregular shape, ill-defined margin, solid structure, hypoechogenicity, microcalcifications, macrocalcifications and central intranodular flow) was significantly higher in the malignant group. Multivariate logistic regression analysis confirmed that age (OR = 0.963, 95% CI = 0.934–0.993, p = 0.017), TGAb (OR = 4.435, 95% CI = 1.902–10.345, p = 0.001), hypoechogenicity (OR = 2.830, 95% CI = 1.113–7.195, p = 0.029), microcalcifications (OR = 4.624, 95% CI = 2.008–10.646, p < 0.001), and central intranodular flow (OR = 2.155, 95% CI = 1.011–4.594, p < 0.05) were independent predictors of thyroid malignancy. A predictive model including four variables (age, TGAb, hypoechogenicity and microcalcification) showed an optimal discriminatory accuracy (area under the curve, AUC) of 0.808 (95% CI = 0.761–0.855). The best cut-off value for prediction was 0.52, achieving sensitivity and specificity of 84.6% and 76.3%, respectively. CONCLUSION: A predictive model of malignancy that combines clinical, laboratory and sonographic characteristics would aid clinicians in avoiding unnecessary procedures and making better clinical decisions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12902-018-0241-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-58425942018-03-14 A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting Liu, Jia Zheng, Dongmei Li, Qiang Tang, Xulei Luo, Zuojie Yuan, Zhongshang Gao, Ling Zhao, Jiajun BMC Endocr Disord Research Article BACKGROUND: Thyroid nodules are highly prevalent, but a robust, feasible method for malignancy differentiation has not yet been well documented. This study aimed to establish a practical model for thyroid nodule discrimination. METHODS: Records for 2984 patients who underwent thyroidectomy were analyzed. Clinical, laboratory, and US variables were assessed retrospectively. Multivariate logistic regression analysis was performed and a mathematical model was established for malignancy prediction. RESULTS: The results showed that the malignant group was younger and had smaller nodules than the benign group (43.5 ± 11.6 vs. 48.5 ± 11.5 y, p < 0.001; 1.96 ± 1.16 vs. 2.75 ± 1.70 cm, p < 0.001, respectively). The serum thyrotropin (TSH) level (median = 1.63 mIU/L, IQR (0.89–2.66) vs. 1.19 (0.59–2.10), p < 0.001) was higher in the malignant group than in the benign group. Patients with malignancies tested positive for anti-thyroglobulin antibody (TGAb) and anti-thyroid peroxidase antibody (TPOAb) more frequently than those with benign nodules (TGAb, 30.3% vs. 15.0%, p < 0.001; TPOAb, 25.6% vs. 18.0%, p = 0.028). The prevalence of ultrasound (US) features (irregular shape, ill-defined margin, solid structure, hypoechogenicity, microcalcifications, macrocalcifications and central intranodular flow) was significantly higher in the malignant group. Multivariate logistic regression analysis confirmed that age (OR = 0.963, 95% CI = 0.934–0.993, p = 0.017), TGAb (OR = 4.435, 95% CI = 1.902–10.345, p = 0.001), hypoechogenicity (OR = 2.830, 95% CI = 1.113–7.195, p = 0.029), microcalcifications (OR = 4.624, 95% CI = 2.008–10.646, p < 0.001), and central intranodular flow (OR = 2.155, 95% CI = 1.011–4.594, p < 0.05) were independent predictors of thyroid malignancy. A predictive model including four variables (age, TGAb, hypoechogenicity and microcalcification) showed an optimal discriminatory accuracy (area under the curve, AUC) of 0.808 (95% CI = 0.761–0.855). The best cut-off value for prediction was 0.52, achieving sensitivity and specificity of 84.6% and 76.3%, respectively. CONCLUSION: A predictive model of malignancy that combines clinical, laboratory and sonographic characteristics would aid clinicians in avoiding unnecessary procedures and making better clinical decisions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12902-018-0241-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-07 /pmc/articles/PMC5842594/ /pubmed/29514621 http://dx.doi.org/10.1186/s12902-018-0241-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Liu, Jia
Zheng, Dongmei
Li, Qiang
Tang, Xulei
Luo, Zuojie
Yuan, Zhongshang
Gao, Ling
Zhao, Jiajun
A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title_full A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title_fullStr A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title_full_unstemmed A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title_short A predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
title_sort predictive model of thyroid malignancy using clinical, biochemical and sonographic parameters for patients in a multi-center setting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842594/
https://www.ncbi.nlm.nih.gov/pubmed/29514621
http://dx.doi.org/10.1186/s12902-018-0241-7
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