慢性阻塞性肺病肺实质和小气道改变可能的遗传影响:一项使用HRCT对双胞胎的初步研究。

D L Tarnoki, A D Tarnoki, Zs Lazar, Cs Korom, V Berczi, I Horvath, K Karlinger
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引用次数: 2

摘要

未标记:遗传效应会增加患慢性阻塞性肺疾病(COPD)的风险,已有报道。我们的目的是估计遗传对双胞胎COPD相关CT特征的可能影响。方法:对2对copd不一致和1对copd一致的同卵(MZ)双胞胎以及2对对照异卵(DZ)双胞胎进行吸气和呼气时的低剂量高分辨率计算机断层扫描(HRCT) (Philips Brilliance 16)。结果:与异卵双胞胎相比,同卵双胞胎在肺容量呼气和空气捕获评分方面更相似(分别为382 cm(3)对2303 cm(3)和17.6%对26.6%)。总的来说,MZ双胞胎表现出几乎相同的HRCT特征,与吸烟态度和COPD状态无关。与MZ双胞胎相比,异卵双胞胎在HRCT特征上的差异更大。结论:肺实质和小气道改变(肺密度、支气管壁增厚、支气管扩张和/或粘液塞形成、空气困住和肺气肿评分)似乎是与遗传相关的特征,独立于吸烟/COPD病史。未来更大样本量的研究应该会证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A possible genetic influence in parenchyma and small airway changes in COPD: a pilot study of twins using HRCT.

Unlabelled: Genetic effects that contribute to the risk of developing chronic obstructive pulmonary disease (COPD) have been reported. Our purpose was to estimate the possible genetic influence on CT features related to COPD in twins.

Methods: Two COPD-discordant and one COPD-concordant monozygotic (MZ) twin pair, in addition to 2 control dizygotic (DZ) twin pairs underwent a low-dose high resolution computer tomography (HRCT) in inspiration and expiration (Philips Brilliance 16).

Results: Monozygotic twins were more similar in lung volume expiration and in air trapping score compared to dizygotics (382 cm(3) vs. 2303 cm(3) and 17.6% vs. 26.6%, respectively). In general, MZ twin pairs showed almost identical HRCT features independently of smoking attitude and COPD status. The dizygotic twin pairs showed larger differences in HRCT features compared to MZ twins.

Conclusions: Lung parenchymal and small airway changes (lung density, presence of bronchial wall thickening, bronchiectasis and/or mucus plug formation, air trapping and emphysema score) seem to be genetically associated traits, independently of smoking/COPD history. A future study with a larger sample size should confirm our findings.

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来源期刊
Acta physiologica Hungarica
Acta physiologica Hungarica 医学-生理学
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