与体重指数相关的遗传因素和慢性阻塞性肺病成像表型

Jingzhou Zhang, Matthew Moll, Catherine L. Debban, Brian D. Hobbs, Heena Rijhwani, George R. Washko, Bartolome Celli, Edwin K. Silverman, Per Bakke, Elizabeth C Oelsner, R Graham Barr, Alvar Agusti, Rosa Faner, Guy Brusselle, Stephen M Humphries, David A Lynch, Josee Dupuis, Ani W. Manichaikul, George T. O'Connor, Michael H. Cho
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引用次数: 0

摘要

背景:虽然低体重指数(BMI)与肺气肿有关,肥胖与慢性阻塞性肺疾病(COPD)的气道疾病有关,但其潜在机制尚不清楚。研究方法我们汇总了基于人群的全基因组关联研究中的遗传变异,生成了 BMI 的多基因评分(PGSBMI)。我们计算了慢性阻塞性肺病富集队列和社区队列中参与者的这一分数,并研究了其与计算机断层扫描肺气肿和气道壁厚度(AWT)的自动量化和视觉解读之间的关联。我们采用荟萃分析法对结果进行了总结:结果:在综合所有队列(n=16,349)结果的随机效应荟萃分析中,PGSBMI 标准差的增加与低衰减区域对数变换百分比≤ 950 Hounsfield 单位(β= -0.062,p<0.0001)和肺密度直方图第15百分位值(β=2.27,p<0.0001),以及以10毫米腔周气道壁面积平方根(β=0.016,p=0.0006)和平均节段支气管壁面积百分比(β=0.26,p=0.0013)量化的AWT增加。对于通过肉眼判读评估的成像特征,在慢性阻塞性肺病富集队列(严重程度分级较高的OR=0.89,p=0.0080)和基于社区的弗雷明汉心脏研究(存在肺气肿的OR=0.82,p=0.0034)中,较高的PGSBMI与较低的肺气肿相关,而在COPDGene研究中,气道壁增厚的风险较高(OR=1.17,p=0.0023)。结论在患有或未患有慢性阻塞性肺病的个体中,较高的体重指数多基因风险与肺气肿的定量和视觉减少以及气道壁增厚的增加有关,这表明体重指数的遗传决定因素对肺气肿和气道壁增厚都有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BMI-related Genetic Factors and COPD Imaging Phenotypes
Background: While low body mass index (BMI) is associated with emphysema and obesity is associated with airway disease in chronic obstructive pulmonary disease (COPD), the underlying mechanisms are unclear. Methods: We aggregated genetic variants from population-based genome-wide association studies to generate a polygenic score of BMI (PGSBMI). We calculated this score for participants from COPD-enriched and community-based cohorts and examined associations with automated quantification and visual interpretation of computed tomographic emphysema and airway wall thickness (AWT). We summarized the results using meta-analysis. Results: In the random-effects meta-analyses combining results of all cohorts (n=16,349), a standard deviation increase of the PGSBMI was associated with less emphysema as quantified by log-transformed percent of low attenuation areas ≤ 950 Hounsfield units (β= -0.062, p<0.0001) and 15th percentile value of lung density histogram (β=2.27, p<0.0001), and increased AWT as quantified by the square root of wall area of a 10-mm lumen perimeter airway (β=0.016, p=0.0006) and mean segmental bronchial wall area percent (β=0.26, p=0.0013). For imaging characteristics assessed by visual interpretation, a higher PGSBMI was associated with reduced emphysema in both COPD-enriched cohorts (OR for a higher severity grade=0.89, p=0.0080) and in the community-based Framingham Heart Study (OR for the presence of emphysema=0.82, p=0.0034), and a higher risk of airway wall thickening in the COPDGene study (OR=1.17, p=0.0023). Conclusions: In individuals with and without COPD, a higher body mass index polygenic risk is associated with both quantitative and visual decreased emphysema and increased AWT, suggesting genetic determinants of BMI affect both emphysema and airway wall thickening.
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