Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphism in Chronic Rhinosinusitis with Nasal Polyps.

IF 0.6 Q4 OTORHINOLARYNGOLOGY Turkish Archives of Otorhinolaryngology Pub Date : 2025-01-10 DOI:10.4274/tao.2024.2024-4-4
Mehmet Emre Sivrice, Vural Akın, Hasan Yasan, Kuyaş Hekimler Öztürk, Yusuf Çağdaş Kumbul
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Abstract

Objective: Inflammatory processes play a role in the etiopathogenesis of chronic rhinosinusitis. Many gene polymorphisms have been associated with inflammation. In this study, we aimed to examine the relationship between angiotensin-converting enzyme insertion/deletion gene polymorphism and chronic rhinosinusitis.

Methods: Fifty-two cases with nasal polyps and 139 control patients were included in the study. Angiotensin-converting enzyme insertion/deletion gene polymorphisms, genotype, and allele distributions were determined. Results were statistically compared between groups.

Results: Statistically significant differences were found between the chronic rhinosinusitis with nasal polyps group and the control group in terms of genotype and allele distribution (p=0.015, 0.003, respectively). There were no significant differences in genotype distribution in the chronic rhinosinusitis with nasal polyps group in terms of non-steroidal anti-inflammatory drug (NSAID) allergy, asthma, and NSAID-exacerbated respiratory disease (p=0.645, 0.660, 0.095, respectively).

Conclusion: We observed that the risk of chronic rhinosinusitis is higher in individuals with the deletion-deletion genotype and D allele of the angiotensin-converting enzyme insertion/deletion gene polymorphism. We believe that these results could be related to the high angiotensin-converting enzyme levels in these patients.

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慢性鼻窦炎伴鼻息肉患者血管紧张素转换酶插入/缺失基因多态性研究
目的:炎症过程在慢性鼻窦炎的发病机制中发挥作用。许多基因多态性与炎症有关。在这项研究中,我们旨在研究血管紧张素转换酶插入/缺失基因多态性与慢性鼻窦炎的关系。方法:选取52例鼻息肉患者和139例对照患者作为研究对象。测定血管紧张素转换酶插入/缺失基因多态性、基因型和等位基因分布。结果组间比较有统计学意义。结果:慢性鼻窦炎伴鼻息肉组与对照组在基因型和等位基因分布上差异有统计学意义(p=0.015, 0.003)。慢性鼻窦炎伴鼻息肉组在非甾体抗炎药(NSAID)过敏、哮喘、非甾体抗炎药加重呼吸系统疾病的基因型分布差异无统计学意义(p分别为0.645、0.660、0.095)。结论:我们观察到血管紧张素转换酶插入/缺失基因多态性的缺失-缺失基因型和D等位基因的个体患慢性鼻窦炎的风险更高。我们认为这些结果可能与这些患者的高血管紧张素转换酶水平有关。
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