The impact of denosumab and calcitriol on asthma risk and lung function: a drug target mendelian randomization study.

IF 2.7 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Zehua Jiang, Maosen Zhang, Maolan Wu, Shuanglinzi Deng, Boyu Zhang, Ting Lei, Wenjun Du, Wuliang Diao, Xiangrong Zheng
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引用次数: 0

Abstract

Background: Osteoporosis and asthma are prevalent chronic conditions that significantly impact public health. Inflammatory cell merging, leading to reduced bone density, increases the risk of fractures, while asthma is a chronic respiratory disease characterized by airway inflammation and bronchoconstriction. More and more emerging research suggests a potential connection through shared pathways and biological mechanisms. In this study, we aim to investigate the causal effect of anti-osteoporosis drug treatment on chronic disease asthma through the Mendelian randomization (MR) analysis method.

Method: In our study, we employed a two-stage study design, utilizing observational data from the National Health and Nutrition Examination Survey (NHANES) and summary statistics data from genome-wide association studies (GWAS) with a large sample of European adults. Section-cross research was performed using NHANES datasets and analysis of the risk of asthma with bone mineral density (BMD) through a risk proportion regression model. After that, a two-sample MR analysis was performed to investigate the causal effect of anti-osteoporosis drug therapy on asthma. Finally, sensitivity analysis was conducted to evaluate the stability of the results.

Results: Our study revealed a non-linear association between femur BMD and asthma risk, with a critical inflection point at a BMD value of 1.114 g/cm2. MR analysis indicated that denosumab did not exert a causal effect on asthma risk (OR = 1.008, 95% CI: 0.994-1.022, P = 0.285) but was associated with improved lung function (β = 0.085, 95% CI: 0.006-0.164, P = 0.035). Conversely, calcitriol exhibited a protective effect against both asthma (OR = 0.931, 95% CI: 0.894-0.969, P < 0.001) and lung function decline (β = 0.294, 95% CI: 0.062-0.525, P = 0.013). These findings suggest a pleiotropic role for these anti-osteoporosis drugs in respiratory health.

Conclusion: This study provides novel insights into the complex relationships between osteoporosis treatments, bone health, and asthma risk. The use of MR analysis enhances the reliability of our findings and highlights the potential benefits of osteoporosis treatments in reducing asthma risk and improving lung function. These results call for further research and may have implications for developing integrated treatment approaches for individuals managing osteoporosis and asthma.

denosumab和骨化三醇对哮喘风险和肺功能的影响:一项药物靶向孟德尔随机研究。
背景:骨质疏松症和哮喘是严重影响公众健康的常见慢性疾病。炎症细胞合并,导致骨密度降低,增加骨折的风险,而哮喘是一种以气道炎症和支气管收缩为特征的慢性呼吸道疾病。越来越多的新兴研究表明,通过共享的途径和生物机制,两者之间存在潜在的联系。在本研究中,我们旨在通过孟德尔随机化(MR)分析方法探讨抗骨质疏松药物治疗对慢性疾病哮喘的因果关系。方法:在我们的研究中,我们采用了两阶段的研究设计,利用了来自国家健康和营养检查调查(NHANES)的观察数据和来自全基因组关联研究(GWAS)的汇总统计数据,其中有大量的欧洲成年人样本。使用NHANES数据集进行横断面研究,并通过风险比例回归模型分析哮喘风险与骨密度(BMD)的关系。之后,进行双样本MR分析,探讨抗骨质疏松药物治疗对哮喘的因果关系。最后进行敏感性分析,评价结果的稳定性。结果:我们的研究揭示了股骨骨密度与哮喘风险之间的非线性关联,骨密度值为1.114 g/cm2时存在一个关键拐点。MR分析显示,denosumab对哮喘风险无因果影响(OR = 1.008, 95% CI: 0.994-1.022, P = 0.285),但与肺功能改善相关(β = 0.085, 95% CI: 0.006-0.164, P = 0.035)。相反,骨化三醇对两种哮喘均有保护作用(OR = 0.931, 95% CI: 0.894-0.969, P)。结论:本研究为骨质疏松治疗、骨骼健康和哮喘风险之间的复杂关系提供了新的见解。磁共振分析的使用增强了我们研究结果的可靠性,并强调了骨质疏松症治疗在降低哮喘风险和改善肺功能方面的潜在益处。这些结果需要进一步的研究,并可能对开发针对骨质疏松症和哮喘患者的综合治疗方法产生影响。
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来源期刊
CiteScore
5.40
自引率
3.40%
发文量
170
审稿时长
3-8 weeks
期刊介绍: The European Journal of Clinical Pharmacology publishes original papers on all aspects of clinical pharmacology and drug therapy in humans. Manuscripts are welcomed on the following topics: therapeutic trials, pharmacokinetics/pharmacodynamics, pharmacogenetics, drug metabolism, adverse drug reactions, drug interactions, all aspects of drug development, development relating to teaching in clinical pharmacology, pharmacoepidemiology, and matters relating to the rational prescribing and safe use of drugs. Methodological contributions relevant to these topics are also welcomed. Data from animal experiments are accepted only in the context of original data in man reported in the same paper. EJCP will only consider manuscripts describing the frequency of allelic variants in different populations if this information is linked to functional data or new interesting variants. Highly relevant differences in frequency with a major impact in drug therapy for the respective population may be submitted as a letter to the editor. Straightforward phase I pharmacokinetic or pharmacodynamic studies as parts of new drug development will only be considered for publication if the paper involves -a compound that is interesting and new in some basic or fundamental way, or -methods that are original in some basic sense, or -a highly unexpected outcome, or -conclusions that are scientifically novel in some basic or fundamental sense.
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