Impact of Vitamin D Receptor Genotypes on Taiwan Asthma Risk.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-07-01 DOI:10.21873/invivo.13985
Shou-Cheng Wang, Hou-Yu Shih, Jie-Long He, Jaw-Chyun Chen, Yun-Chi Wang, Chia-Wen Tsai, Wen-Shin Chang, Te-Chun Hsia, DA-Tian Bau
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引用次数: 0

Abstract

Background/aim: Vitamin D plays a critical role in regulating immune function. In literature, several studies have indicated that variations in the vitamin D receptor gene (VDR) may be associated with the risk of asthma risk. However, the findings remain inconsistent. The current study aimed to assess the influence of VDR polymorphisms on both asthma risk and severity.

Patients and methods: A cohort comprising 453 non-asthmatic healthy controls and 198 asthmatic cases was assembled, and the VDR rs731236, rs1544410, rs2228570, and rs7975232 genotypes were determined utilizing polymerase chain reaction-restriction fragment length polymorphism methodology.

Results: Our findings indicated that people carrying the variant AG and AA genotypes of VDR rs2228570 demonstrated an elevated risk of asthma compared to wild-type GG carriers (odds ratio=1.55 and 2.19, 95% confidence interval=1.02-2.35 and 1.37-3.49; p=0.0507 and 0.0014, respectively). Furthermore, individuals carrying the variant A allele at VDR rs2228570 exhibited a higher risk of asthma than those carrying the wild-type G allele (odds ratio=1.51, 95% confidence interval=1.19-1.92; p=0.0008). Moreover, a significant association was observed between VDR rs2228570 A-carrying genotypes and increased the severity of asthma symptoms among asthmatic patients (p for trend=0.0024).

Conclusion: The variant A allele at VDR rs2228570 was associated with higher asthma susceptibility, and may serve as a predictor for asthma symptom severity. Our findings encouraged further validation in larger and diverse populations to further elucidate the significance of VDR genotype in asthma development.

维生素D受体基因型对台湾哮喘风险的影响
背景/目的:维生素D在调节免疫功能中起关键作用。在文献中,一些研究表明,维生素D受体基因(VDR)的变异可能与哮喘风险有关。然而,调查结果仍然不一致。目前的研究旨在评估VDR多态性对哮喘风险和严重程度的影响。患者和方法:选取453例非哮喘健康对照和198例哮喘患者,采用聚合酶链反应-限制性片段长度多态性方法测定VDR rs731236、rs1544410、rs2228570和rs7975232基因型。结果:我们的研究结果表明,携带VDR rs2228570变异AG和AA基因型的人与野生型GG携带者相比,患哮喘的风险更高(优势比=1.55和2.19,95%置信区间=1.02-2.35和1.37-3.49;P分别=0.0507和0.0014)。此外,携带VDR rs2228570变异等位基因A的个体比携带野生型G等位基因的个体患哮喘的风险更高(优势比=1.51,95%置信区间=1.19-1.92;p = 0.0008)。此外,携带VDR rs2228570 a基因型与哮喘患者哮喘症状严重程度增加之间存在显著相关性(p =0.0024)。结论:VDR位点rs2228570变异等位基因A与哮喘易感性增高相关,并可能作为哮喘症状严重程度的预测因子。我们的研究结果鼓励在更大和更多样化的人群中进一步验证,以进一步阐明VDR基因型在哮喘发展中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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