小儿和青少年甲状腺结节中的 DICER1 变异

IF 5.8 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Thyroid Pub Date : 2024-10-01 Epub Date: 2024-09-27 DOI:10.1089/thy.2024.0188
Karolina Mastnikova, Barbora Bulanova Pekova, Vlasta Kuklikova, Eliska Vaclavikova, Jitka Carkova, Rami Katra, Lucie Fialova, Petr Vlcek, Daniela Kodetova, Martin Chovanec, Jana Drozenova, Radoslav Matej, Petra Pacesova, Zdenek Novak, Kristyna Procykova, Josef Vcelak, Bela Bendlova
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引用次数: 0

摘要

背景 最近的研究表明,DICER1基因的致病变异可能是一些小儿甲状腺结节发生改变的驱动因素,但相关数据仍然有限。本研究旨在检测一大批小儿甲状腺结节患者的 DICER1 基因变异,并将其与临床病理数据相关联,重点关注甲状腺癌患者的疾病预后。方法 这项回顾性队列研究包括350名患有甲状腺结节的儿童和年轻成人患者(2-21岁),其中收集了275份新鲜冷冻甲状腺结节样本和92份细针穿刺活检(FNAB)样本。在对甲状腺肿瘤主要基因变异进行分析后,采用新一代测序和多重连接依赖性探针扩增方法确定了DICER1基因的变异。对DICER1阳性肿瘤患者的外周血进行了分析。然后将基因分析结果与临床病理数据进行关联。结果 在 24/350 例(6.9%;95%CI [4.4;10.0])儿童和年轻成人患者中,分别有 10/119 例(8.4%;[4.1;14.9])的良性鲜冻组织患者、8/141 (5.7%; [1.9;9.5])的甲状腺乳头状癌(PTC)患者和6/86 (7.0%; [4.1;14.6])的FNAB患者。在DICER1阳性样本中未发现其他基因改变。在 11/24 例(45.8%;[25.6;67.2])患者中发现了种系 DICER1 变异。在 9/24 例(37.5%;[18.8;59.4])甲状腺结节患者中发现了 DICER1 基因的两个体细胞(双拷贝)变异。2/24(8.3%;[1.0;27.0])个病例中发现了至少 3 Mbp 长的体细胞缺失。与DICER1阴性的PTC相比,DICER1阳性的PTC与PTC的滤泡亚型(p = 0.001)、包裹性(p = 0.006)和体积较大(p = 0.035)有显著相关性,但没有甲状腺外扩展(p = 0.039),淋巴结转移也较少(p = 0.003)。75%的 DICER1 阳性 PTC 患者对治疗反应良好。结论 DICER1基因变异常出现在儿童和年轻成人患者的甲状腺结节中。在我们的患者中,DICER1阳性PTC的侵袭性很低。我们的研究结果支持考虑对 DICER1 阳性的低风险 PTC 采取更保守的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DICER1 Variants in Pediatric and Young Adult Thyroid Nodules.

Background: Recent studies have suggested that pathogenic variants of the DICER1 gene could be a driver of alterations in some pediatric thyroid nodules, but data are still limited. The aim of this study was to detect variants in the DICER1 gene in a large cohort of pediatric thyroid nodules and then correlate them with clinicopathological data, with a focus on the disease prognosis in patients with thyroid carcinoma. Methods: This retrospective cohort study consisted of 350 pediatric and young adult patients (aged 2-21 years) with thyroid nodules, from whom 275 fresh-frozen thyroid nodule samples and 92 fine-needle aspiration biopsy (FNAB) samples were collected. After an analysis of variants in major genetic alterations of thyroid tumors, variants in the DICER1 gene were identified using next-generation sequencing and multiplex ligation-dependent probe amplification methods. Peripheral blood was analyzed from patients with DICER1-positive tumors. The results of genetic analysis were then correlated with clinicopathological data. Results: Variants in the DICER1 gene were detected in a total of 24/350 (6.9%; 95%CI [4.4;10.0]) pediatric and young adult patients, respectively, in 10/119 (8.4%; [4.1;14.9]) patients with benign fresh-frozen tissue, in 8/141 (5.7%; [1.9;9.5]) with papillary thyroid carcinoma (PTC) and in 6/86 (7.0%; [4.1;14.6]) patients with FNAB. No other gene alteration was found in DICER1-positive samples. Germline DICER1 variants were identified in 11/24 (45.8%; [25.6;67.2]) patients. Two somatic (biallelic) variants in the DICER1 gene were found in 9/24 (37.5%; [18.8;59.4]) thyroid nodules. Somatic deletions of at least 3 Mbp long were revealed in 2/24 (8.3%; [1.0;27.0]) cases. DICER1-positive PTCs were significantly associated with the follicular subtype of PTC (p = 0.001), encapsulation (p = 0.006) and were larger in size (p = 0.035), but with no extrathyroidal extension (p = 0.039), and less frequent lymph node metastases (p = 0.003) compared with DICER1-negative PTCs. Patients with DICER1-positive PTC had an excellent response to treatment in 75% of cases. Conclusions: Variants of the DICER1 gene are frequently found in the thyroid nodules of pediatric and young adult patients. In our patients, DICER1-positive PTCs showed low invasiveness. Our findings support considering more conservative management for DICER1-positive low-risk PTCs.

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来源期刊
Thyroid
Thyroid 医学-内分泌学与代谢
CiteScore
12.30
自引率
6.10%
发文量
195
审稿时长
6 months
期刊介绍: This authoritative journal program, including the monthly flagship journal Thyroid, Clinical Thyroidology® (monthly), and VideoEndocrinology™ (quarterly), delivers in-depth coverage on topics from clinical application and primary care, to the latest advances in diagnostic imaging and surgical techniques and technologies, designed to optimize patient care and outcomes. Thyroid is the leading, peer-reviewed resource for original articles, patient-focused reports, and translational research on thyroid cancer and all thyroid related diseases. The Journal delivers the latest findings on topics from primary care to clinical application, and is the exclusive source for the authoritative and updated American Thyroid Association (ATA) Guidelines for Managing Thyroid Disease.
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