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A comparison of DP-TOF Mass Spectroscopy (MS) and Next Generation Sequencing (NGS) methods for detecting molecular mutations in thyroid nodules fine needle aspiration biopsies.
Qian, Xiao-Qin; Agyekum, Enock Adjei; Zhao, Ling-Ling; Yu, Run-Liu; Li, Xiu-Ying; Gu, De-Jian; Yan, Na; Xu, Ming; Yuan, Yuan; Wang, Yu-Guo; Xin-Ping, Wu; Xu, Fei-Ju.
Afiliación
  • Qian XQ; Department of Ultrasound, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Agyekum EA; Department of Ultrasound, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Zhao LL; School of Medicine, Jiangsu University, Zhenjiang, China.
  • Yu RL; Research and Development Center, Hangzhou D.A. Medical Laboratory, Hangzhou, China.
  • Li XY; Research and Development Center, Hangzhou D.A. Medical Laboratory, Hangzhou, China.
  • Gu DJ; Nanjing D.A. Medical Laboratory, Nanjing, China.
  • Yan N; Nanjing D.A. Medical Laboratory, Nanjing, China.
  • Xu M; Key Laboratory of Digital Technology in Medical Diagnostics of Zhejiang Province, Dian Diagnostics Group Co., Ltd., Hangzhou, China.
  • Yuan Y; Department of Medicine, Zhejiang Digena Diagnosis Technology CO., LTD, Zhejiang, China.
  • Wang YG; Department of Ultrasound, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Xin-Ping W; Department of Ultrasound, Jiangsu Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing, China.
  • Xu FJ; Department of Ultrasound, Jiangsu Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing, China.
Front Endocrinol (Lausanne) ; 13: 928788, 2022.
Article en En | MEDLINE | ID: mdl-35992139
Mutations in the B-Raf proto-oncogene, serine/threonine kinase (BRAF), have been linked to a variety of solid tumors such as papillary thyroid carcinoma. The purpose of this study was to compare the DP-TOF, a DNA mass spectroscopy (MS) platform, and next-generation sequencing (NGS) methods for detecting multiple-gene mutations (including BRAFV600E) in thyroid nodule fine-needle aspiration fluid. In this study, we collected samples from 93 patients who had previously undergone NGS detection and had sufficient DNA samples remaining. The MS method was used to detect multiple-gene mutations (including BRAFV600E) in DNA remaining samples. NGS detection method was used as the standard. The MS method's overall sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were 95.8%, 100%, 100%, and 88%, respectively in BRAFV600E gene mutation detection. With a kappa-value of 0.92 (95%CI 0.82-0.99), the level of agreement between these methods was incredibly high. Furthermore, when compared to NGS in multiple-gene detection, the MS method demonstrated higher sensitivity and specificity, 82.9% and 100%, respectively. In addition, we collected the postoperative pathological findings of 50 patients. When the postoperative pathological findings were used as the standard, the MS method demonstrated higher sensitivity and specificity, at 80% and 80%, respectively. Our findings show that the MS method can be used as an inexpensive, accurate, and dependable initial screening method to detect genes mutations and as an adjunct to clinical diagnosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Tiroides / Nódulo Tiroideo Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Tiroides / Nódulo Tiroideo Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza