Lipid-lowering drug targets associated with risk of respiratory disease: a Mendelian randomization study.

IF 2.6 3区 医学 Q2 RESPIRATORY SYSTEM
Zhipeng Gong, Dongsheng Wu, Yin Ku, Congyao Zou, Lin Qiu, Xiaohu Hao, Lunxu Liu
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Abstract

Background: Observational studies have identified a possible connection between lipid-lowering medications and respiratory illnesses. However, it remains unclear whether lipid-lowering drugs is causative for respiratory diseases, and we aimed to answer this question.

Methods: We performed Mendelian randomization (MR) analyses by integrating data from genome-wide association studies (GWAS). Three statistical approaches were employed for MR analysis: inverse variance weighting (IVW), MR-Egger, and weighted median. The purpose was to evaluate the causal relationships between 10 drug targets that lower lipid levels and the likelihood of developing 7 respiratory diseases. Additional sensitivity analyses were conducted to ensure the robustness and validity of the results.

Results: After adjusting for multiple testing, our MR analysis identified APOB (odd ratios [OR]: 0.86; 95% confidence interval [CI]: 0.77 to 0.97; PIVW = 0.01) and PCSK9 (OR: 0.84; 95% CI: 0.72 to 0.97; PIVW = 0.02) as significant risk targets for asthma. Additionally, LDLR was found to be a significant risk target for chronic obstructive pulmonary disease (OR: 0.81; 95% CI: 0.67 to 0.98; PIVW = 0.03). The sensitivity analysis validated no proof of heterogeneity or pleiotropy amongst the mentioned results.

Conclusions: Our findings suggest a likely causal relationship between respiratory diseases and lipid-lowering drug targets. Further mechanistic and clinical research is needed to confirm and validate these findings.

降脂药物靶点与呼吸系统疾病风险相关:一项孟德尔随机研究
背景:观察性研究已经确定了降脂药物与呼吸系统疾病之间可能存在的联系。然而,目前尚不清楚降脂药物是否会导致呼吸系统疾病,我们的目标是回答这个问题。方法:我们通过整合全基因组关联研究(GWAS)的数据进行孟德尔随机化(MR)分析。MR分析采用了三种统计方法:方差逆加权(IVW)、MR- egger和加权中位数。目的是评估降低血脂水平的10种药物靶点与7种呼吸系统疾病发生可能性之间的因果关系。另外进行敏感性分析以确保结果的稳健性和有效性。结果:经过多次检测调整后,我们的MR分析鉴定出APOB(奇比[OR]: 0.86;95%置信区间[CI]: 0.77 ~ 0.97;PIVW = 0.01)和PCSK9 (OR: 0.84;95% CI: 0.72 ~ 0.97;PIVW = 0.02)为哮喘的显著危险指标。此外,LDLR被发现是慢性阻塞性肺疾病的重要危险目标(OR: 0.81;95% CI: 0.67 ~ 0.98;pivw = 0.03)。敏感性分析证实上述结果中没有异质性或多效性的证据。结论:我们的研究结果提示呼吸系统疾病与降脂药物靶点之间可能存在因果关系。需要进一步的机制和临床研究来证实和验证这些发现。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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