National Heart and Lung Institute, Imperial College London, London, UK
Institute for Biomedicine, Eurac Research, Bolzano, Italy.
Eur Respir J. 2023 May 25;61(5). doi: 10.1183/13993003.01585-2022. Print 2023 May.
Gastro-oesophageal reflux disease (GORD) is associated with idiopathic pulmonary fibrosis (IPF) in observational studies. It is not known if this association arises because GORD causes IPF or because IPF causes GORD, or because of confounding by factors, such as smoking, associated with both GORD and IPF. We used bidirectional Mendelian randomisation (MR), where genetic variants are used as instrumental variables to address issues of confounding and reverse causation, to examine how, if at all, GORD and IPF are causally related.
A bidirectional two-sample MR was performed to estimate the causal effect of GORD on IPF risk and of IPF on GORD risk, using genetic data from the largest GORD (78 707 cases and 288 734 controls) and IPF (4125 cases and 20 464 controls) genome-wide association meta-analyses currently available.
GORD increased the risk of IPF, with an OR of 1.6 (95% CI 1.04-2.49; p=0.032). There was no evidence of a causal effect of IPF on the risk of GORD, with an OR of 0.999 (95% CI 0.997-1.000; p=0.245).
We found that GORD increases the risk of IPF, but found no evidence that IPF increases the risk of GORD. GORD should be considered in future studies of IPF risk and interest in it as a potential therapeutic target should be renewed. The mechanisms underlying the effect of GORD on IPF should also be investigated.
在观察性研究中,胃食管反流病(GORD)与特发性肺纤维化(IPF)有关。目前尚不清楚这种关联是由于 GORD 导致 IPF,还是由于 IPF 导致 GORD,还是由于与 GORD 和 IPF 都相关的吸烟等混杂因素所致。我们使用双向孟德尔随机化(MR),其中遗传变异被用作工具变量来解决混杂和反向因果关系的问题,以检查 GORD 和 IPF 是否存在因果关系。
进行双向两样本 MR,使用来自最大 GORD(78707 例和 288734 例对照)和 IPF(4125 例和 20464 例对照)全基因组关联荟萃分析的遗传数据,估计 GORD 对 IPF 风险的因果效应以及 IPF 对 GORD 风险的因果效应。
GORD 增加了 IPF 的风险,OR 为 1.6(95%CI 1.04-2.49;p=0.032)。没有证据表明 IPF 对 GORD 风险有因果影响,OR 为 0.999(95%CI 0.997-1.000;p=0.245)。
我们发现 GORD 增加了 IPF 的风险,但没有证据表明 IPF 增加了 GORD 的风险。在未来的 IPF 风险研究中应考虑 GORD,重新关注其作为潜在治疗靶点的可能性。还应研究 GORD 对 IPF 影响的机制。