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喉癌患者血管紧张素转换酶插入/缺失基因多态性。

Angiotensin-converting enzyme insertion/deletion gene polymorphism in patients with laryngeal cancer.

机构信息

Department of Otorhinolaryngology and Head & Neck Surgery, Süleyman Demirel University Faculty of Medicine, Isparta, Turkey.

Department of Medical Genetics, Süleyman Demirel University Faculty of Medicine, Isparta, Turkey.

出版信息

Acta Otorhinolaryngol Ital. 2023 Feb;43(1):26-31. doi: 10.14639/0392-100X-N2127.

Abstract

OBJECTIVES

The aim of this study was to compare the distribution of the angiotensin-converting enzyme (ACE) I/D polymorphism between patients with laryngeal cancer (LC) and a control group and to examine the distribution of this polymorphism with clinical parameters related to LC.

METHODS

We enrolled 44 LC patients and 61 healthy controls. The ACE I/D polymorphism was genotyped with the PCR-RFLP method. The distribution of ACE genotypes (II, ID, and DD) and alleles (I or D) was evaluated with Pearson's chi-square test, and logistic regression analysis was performed for statistically significant parameters.

RESULTS

There was no significant difference in ACE genotypes and alleles between LC patients and controls (p = 0.079 and p = 0.068, respectively). Among clinical parameters related to LC (extension of tumour, node metastasis, tumour stage and tumour location), only the presence of node metastasis was found to be significant in terms of ACE DD genotype (p = 0.137, p = 0.031, p = 0.147, p = 0.321 respectively). In the logistic regression analysis, the ACE DD genotype was increased 8.3 fold in nodal metastases.

CONCLUSIONS

The findings of the study suggest that ACE genotypes and alleles do not affect the prevalence of LC, but the DD genotype of ACE polymorphism may increase the risk of lymph node metastasis in LC patients.

摘要

目的

本研究旨在比较血管紧张素转换酶(ACE)I/D 多态性在喉癌(LC)患者和对照组之间的分布,并探讨该多态性与与 LC 相关的临床参数的分布。

方法

我们纳入了 44 例 LC 患者和 61 例健康对照者。采用 PCR-RFLP 法检测 ACE I/D 多态性。采用 Pearson 卡方检验评估 ACE 基因型(II、ID 和 DD)和等位基因(I 或 D)的分布,并对具有统计学意义的参数进行逻辑回归分析。

结果

LC 患者与对照组之间 ACE 基因型和等位基因无显著差异(p = 0.079 和 p = 0.068)。在与 LC 相关的临床参数(肿瘤的扩展、淋巴结转移、肿瘤分期和肿瘤位置)中,仅发现 ACE DD 基因型与淋巴结转移显著相关(p = 0.137、p = 0.031、p = 0.147、p = 0.321)。在逻辑回归分析中,ACE DD 基因型使淋巴结转移的风险增加了 8.3 倍。

结论

本研究结果表明,ACE 基因型和等位基因不影响 LC 的患病率,但 ACE 多态性的 DD 基因型可能增加 LC 患者发生淋巴结转移的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baab/9978305/e91ab5923044/aoi-2023-01-26-g001.jpg

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