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一种 COPD 发病年龄的多基因风险评分。

A polygenic risk score and age of diagnosis of COPD.

机构信息

Channing Division of Network Medicine, Dept of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

The Pulmonary Center, Section of Pulmonary, Allergy, Sleep, and Critical Care Medicine, Dept of Medicine, Boston University School of Medicine, Boston, MA, USA.

出版信息

Eur Respir J. 2022 Sep 15;60(3). doi: 10.1183/13993003.01954-2021. Print 2022 Sep.

Abstract

BACKGROUND

Genetic susceptibility may be associated with earlier onset of chronic obstructive pulmonary disease (COPD). We hypothesised that a polygenic risk score (PRS) for COPD would be associated with earlier age of diagnosis of COPD.

METHODS

In 6647 non-Hispanic White (NHW) and 2464 African American (AA) participants from COPDGene, and 6812 participants from the Framingham Heart Study (FHS), we tested the relationship of the PRS and age of COPD diagnosis. Age at diagnosis was determined by: 1) self-reported age at COPD diagnosis or 2) age at visits when moderate-to-severe airflow limitation (Global Initiative for Chronic Obstructive Lung Disease (GOLD) grade 2-4) was observed on spirometry. We used Cox regression to examine the overall and time-dependent effects of the PRS on incident COPD. In the COPDGene study, we also examined the PRS's predictive value for COPD at age <50 years (COPD50) using logistic regression and area under the curve (AUC) analyses, with and without the addition of other risk factors present at early life ( childhood asthma).

RESULTS

In Cox models, the PRS demonstrated age-dependent associations with incident COPD, with larger effects at younger ages in both cohorts. The PRS was associated with COPD50 (OR 1.55 (95% CI 1.41-1.71) for NHW, OR 1.23 (95% CI 1.05-1.43) for AA and OR 2.47 (95% CI 2.12-2.88) for FHS participants). In COPDGene, adding the PRS to known early-life risk factors improved prediction of COPD50 in NHW (AUC 0.69 0.74; p<0.0001) and AA (AUC 0.61 0.64; p=0.04) participants.

CONCLUSIONS

A COPD PRS is associated with earlier age of diagnosis of COPD and retains predictive value when added to known early-life risk factors.

摘要

背景

遗传易感性可能与慢性阻塞性肺疾病(COPD)的发病年龄较早有关。我们假设 COPD 的多基因风险评分(PRS)与 COPD 的诊断年龄较早有关。

方法

在 COPDGene 中的 6647 名非西班牙裔白人(NHW)和 2464 名非裔美国人(AA)参与者,以及 Framingham 心脏研究(FHS)中的 6812 名参与者中,我们测试了 PRS 与 COPD 诊断年龄的关系。诊断年龄通过以下方式确定:1)自我报告的 COPD 诊断年龄,或 2)在肺量计上观察到中度至重度气流受限(慢性阻塞性肺疾病全球倡议(GOLD)2-4 级)时的就诊年龄。我们使用 Cox 回归检验 PRS 对 COPD 发病的总体和时变影响。在 COPDGene 研究中,我们还使用逻辑回归和曲线下面积(AUC)分析,在不添加或添加早期生命中存在的其他危险因素(儿童哮喘)的情况下,检验 PRS 对 COPD50 的预测价值。

结果

在 Cox 模型中,PRS 显示与 COPD 发病呈年龄依赖性相关,在两个队列中,年轻患者的影响更大。PRS 与 COPD50 相关(NHW 的 OR 为 1.55(95%CI 为 1.41-1.71),AA 的 OR 为 1.23(95%CI 为 1.05-1.43),FHS 的 OR 为 2.47(95%CI 为 2.12-2.88))。在 COPDGene 中,将 PRS 添加到已知的早期生命危险因素中,提高了 NHW(AUC 为 0.69 0.74;p<0.0001)和 AA(AUC 为 0.61 0.64;p=0.04)参与者中 COPD50 的预测能力。

结论

COPD 的 PRS 与 COPD 的诊断年龄较早有关,并且在添加已知的早期生命危险因素后仍具有预测价值。

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A polygenic risk score and age of diagnosis of COPD.一种 COPD 发病年龄的多基因风险评分。
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