炎性综合指标与分化型甲状腺癌临床病理特征的关系。

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.3389/fmolb.2025.1660379
Li-Yuan Yang, Li-Peng Yang
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引用次数: 0

摘要

目的:探讨分化型甲状腺癌(DTC)患者单核细胞与淋巴细胞比值(MLR)、全身炎症反应指数(SIRI)、全身免疫炎症指数(SII)等综合炎症指标与临床病理特征的关系。为改进DTC患者主动监测(AS)策略的患者选择标准提供新的见解。方法:本回顾性研究分析2021年1月至2023年2月在上海交通大学医学院附属上海第六人民医院接受治疗的231例DTC患者的术前MLR、SIRI和SII值。将这些炎症指标按临床病理特征分层进行亚组比较。随后,根据MLR、SIRI、SII的中位数将患者分为低表达组和高表达组,对比分析两组患者的临床病理特征。结果:对比分析:在肿瘤最大直径较大、Ki-67指数较高、淋巴结转移(LNM)、囊膜浸润及双侧甲状腺肿瘤患者中,SIRI水平显著升高(P < 0.05)。同样,SII水平在最大肿瘤直径较大、恶性病变、LNM和囊膜浸润的患者中显著升高(P < 0.05)。相比之下,MLR与任何临床病理亚组分析均无显著相关性(均P < 0.05)。亚组分析:与高mlr组相比,低mlr组沙瘤体患病率明显降低,多灶性肿瘤发生率明显降低(均P < 0.05)。SIRI组比较:高SIRI组肿瘤最大直径显著大于低SIRI组,淋巴血管浸润率显著高于低SIRI组(P < 0.05)。SII组比较:与低SII组相比,高SII组表现出更高的侵袭性病理变异发生率(P < 0.05)。结论:术前MLR、SIRI和SII水平升高的DTC患者术后多种不良临床病理特征的发生率明显高于基线炎症指标水平较低的患者。这些发现提示MLR、SIRI和SII可以作为DTC不良肿瘤临床病理特征的预测性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The association between composite inflammatory indicators and the clinicopathological characteristics of differentiated thyroid carcinoma.

The association between composite inflammatory indicators and the clinicopathological characteristics of differentiated thyroid carcinoma.

The association between composite inflammatory indicators and the clinicopathological characteristics of differentiated thyroid carcinoma.

Purpose: This study examined the associations between composite inflammatory indicators-including the Monocyte-to-Lymphocyte Ratio (MLR), Systemic Inflammation Response Index (SIRI), and Systemic Immune-Inflammation Index (SII)-and the clinicopathological characteristics in patients with Differentiated Thyroid Carcinoma (DTC). To provide a novel insight into refining patient selection criteria for active surveillance (AS) strategies in DTC patients.

Methods: This retrospective study analyzed preoperative MLR, SIRI, and SII values in 231 DTC patients treated at Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine between January 2021 and February 2023. Comparisons of these inflammatory indicators were performed across subgroups stratified by clinicopathological characteristics. Subsequently, patients were categorized into low-expression and high-expression groups based on the median values of MLR, SIRI, and SII, followed by comparative analyses of clinicopathological features between the two groups.

Results: Comparative Analysis: SIRI levels were significantly elevated (P < 0.05) in patients with larger maximum tumor diameter, higher Ki-67 index, lymph node metastasis (LNM), capsular invasion and bilateral thyroid tumors. Similarly, SII levels were significantly elevated (P < 0.05) in patients with larger maximum tumor diameter, aggressive pathologic variants, LNM, and capsular invasion. In contrast, the MLR showed no significant associations with any of the clinicopathological subgroups analyzed (all P > 0.05). Subgroup Analysis: Compared to the high-MLR group, the low-MLR group showed a significantly lower prevalence of psammoma bodies, and lower incidence of multifocal tumors (all P < 0.05). SIRI Group Comparisons: The high-SIRI group exhibited significantly larger maximum tumor diameter, higher rates of lymphovascular invasion compared to those in the low-SIRI group (P < 0.05). SII Group Comparisons: The high-SII group demonstrated a significantly higher prevalence of aggressive pathologic variants compared to the low-SII group (P < 0.05).

Conclusion: Patients with DTC presenting elevated preoperative levels of MLR, SIRI, and SII demonstrated a significantly higher incidence of multiple adverse clinicopathological features postoperatively compared to those with lower baseline inflammatory indicators levels. These findings suggest that MLR, SIRI, and SII may serve as predictive biomarkers for adverse tumor clinicopathological characteristics in DTC.

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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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