HLA 与鼻息肉病易感性:全球研究的 Meta 分析。

IF 1.3 4区 医学 Q3 OTORHINOLARYNGOLOGY Annals of Otology Rhinology and Laryngology Pub Date : 2024-11-01 Epub Date: 2024-08-22 DOI:10.1177/00034894241275476
Ryan Witcher, Sugosh M Anur, Dylan Thibaut, Luciano Venturino, Jordon G Grube
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引用次数: 0

摘要

研究目的鼻息肉病(NP)是一种常见的鼻窦腔复发性疾病,对患者的生活质量有很大影响。鼻息肉的病理生理学涉及遗传、环境和免疫因素的复杂相互作用。有几项研究探讨了人类白细胞抗原(HLA)II 类等位基因与鼻咽癌之间的关系,但结果并不一致。本荟萃分析旨在研究 HLA II 类等位基因,特别是 HLA-DQA1、HLA-DQB1 和 HLA-DRB1 与 NP 风险之间的关联:使用电子数据库(包括 PubMed、Google Scholar 和 Cochrane Library)进行了系统综述,以确定调查 HLA II 类等位基因与 NP 之间关系的研究。通过特定的纳入和排除标准确定了符合条件的研究。评估 HLA II 类等位基因与 NP 风险之间的相关性时,采用了带有 95% 置信区间 (CI) 的几率比 (OR)。采用随机效应模型计算汇总 OR 和相应的 95% CI,一项研究需要一个异质性评估值 I2 研究设计:元分析:本荟萃分析共纳入四项研究,涉及 258 个 NP 等位基因和 802 个对照等位基因。分析表明,DQA1*0201(OR = 3.08,95% CI [1.70,5.59])和 DRB1*7(OR = 2.04,95% CI [1.14,3.66])与 NP 风险增加显著相关。对 NP 风险等位基因 DQA1*0201 和 DRB1*7 的分析具有 I2 结论:这项荟萃分析提供了证据,证明 HLA-DQA1*0201 和 HLA-DRB1*7 等位基因是 NP 发病的风险因素。这些发现有助于更好地了解 NP 的遗传易感性,并可能对开发预防和治疗 NP 的新方法产生影响。
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HLA and Nasal Polyposis Susceptibility: A Meta-analysis of Worldwide Studies.

Objectives: Nasal polyposis (NP) is a common and recurrent condition of the sinonasal cavity which has significant impact on patients' quality of life. NP pathophysiology involves a complex interplay of genetic, environmental, and immunological factors. Several studies have explored the association between human leukocyte antigen (HLA) class II alleles and NP, but the results have been conflicting. The aim of this meta-analysis is to investigate the association between HLA class II alleles, specifically HLA-DQA1, HLA-DQB1, and HLA-DRB1and NP risk.

Methods: A systematic review was conducted using electronic databases, including PubMed, Google Scholar, and Cochrane Library, to identify studies investigating the association between HLA class II alleles and NP. Eligible studies were identified by specific inclusion and exclusion criteria. The odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the association between HLA class II alleles and NP risk. A random-effects model was used to calculate the pooled OR and corresponding 95% CI, and a study required a heterogeneity assessment value I2 < 25% to be considered for analysis.

Study design: Meta-analysis.

Results: A total of four studies were included in this meta-analysis, involving a total of 258 NP alleles and 802 control alleles. The analysis indicated that DQA1*0201 (OR = 3.08, 95% CI [1.70, 5.59]) and DRB1*7 (OR = 2.04, 95% CI [1.14, 3.66]) were significantly associated with increased risk of NP. The analysis of the NP risk alleles DQA1*0201 and DRB1*7 had an I2 < 0% representing low heterogeneity. Sensitivity analysis with LFK indices showed minor asymmetry in either allele.

Conclusions: This meta-analysis provides evidence that the HLA-DQA1*0201 and HLA-DRB1*7 alleles are risk factors for the development of NP. These findings could contribute to a better understanding of the genetic predisposition of NP and may have implications for the development of novel approaches for the prevention and treatment of this condition.

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来源期刊
CiteScore
3.10
自引率
7.10%
发文量
171
审稿时长
4-8 weeks
期刊介绍: The Annals of Otology, Rhinology & Laryngology publishes original manuscripts of clinical and research importance in otolaryngology–head and neck medicine and surgery, otology, neurotology, bronchoesophagology, laryngology, rhinology, head and neck oncology and surgery, plastic and reconstructive surgery, pediatric otolaryngology, audiology, and speech pathology. In-depth studies (supplements), papers of historical interest, and reviews of computer software and applications in otolaryngology are also published, as well as imaging, pathology, and clinicopathology studies, book reviews, and letters to the editor. AOR is the official journal of the American Broncho-Esophagological Association.
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