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Peripheral Blood Telomere Attrition in Persons at Risk for Familial Pulmonary Fibrosis.

作者信息

Salisbury Margaret L, Markin Cheryl R, Wu Pingsheng, Cogan Joy D, Mitchell Daphne B, Liu Qi, Loyd James E, Lancaster Lisa H, Kropski Jonathan A, Blackwell Timothy S

机构信息

Vanderbilt University Medical Center Nashville, Tennessee.

Vanderbilt University Nashville, Tennessee.

出版信息

Am J Respir Crit Care Med. 2023 Jan 15;207(2):208-211. doi: 10.1164/rccm.202204-0766LE.

DOI:10.1164/rccm.202204-0766LE
PMID:36036734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9893319/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd8/9893319/9b7f2b123c9c/rccm.202204-0766LEf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd8/9893319/9b7f2b123c9c/rccm.202204-0766LEf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd8/9893319/9b7f2b123c9c/rccm.202204-0766LEf1.jpg

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本文引用的文献

1
Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations.家族性短端粒综合征基因突变非携带者的肺纤维化。
Respirology. 2021 Dec;26(12):1160-1170. doi: 10.1111/resp.14145. Epub 2021 Sep 27.
2
Measurement of Telomere Length for Longitudinal Analysis: Implications of Assay Precision.端粒长度的纵向分析测量：检测精度的影响。
Am J Epidemiol. 2021 Jul 1;190(7):1406-1413. doi: 10.1093/aje/kwab025.
3
Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society.
肺纤维化的遗传学和基因组学：描绘分子图谱，塑造精准医学。
Am J Respir Crit Care Med. 2024 Aug 15;210(4):401-423. doi: 10.1164/rccm.202401-0238SO.
偶然在 CT 上发现的肺间质异常：弗勒施纳学会的立场文件。
Lancet Respir Med. 2020 Jul;8(7):726-737. doi: 10.1016/S2213-2600(20)30168-5.
4
Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial Interstitial Lung Disease.家族性间质性肺疾病风险个体的放射学异常的发展和进展。
Am J Respir Crit Care Med. 2020 May 15;201(10):1230-1239. doi: 10.1164/rccm.201909-1834OC.
5
A role for telomere length and chromosomal damage in idiopathic pulmonary fibrosis.端粒长度和染色体损伤在特发性肺纤维化中的作用。
Respir Res. 2018 Jul 9;19(1):132. doi: 10.1186/s12931-018-0838-4.
6
Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.端粒酶基因中蛋白改变变异的分析及其与特发性肺纤维化患者 MUC5B 常见变异体状态的关系：候选基因测序研究。
Lancet Respir Med. 2018 Aug;6(8):603-614. doi: 10.1016/S2213-2600(18)30135-8. Epub 2018 Jun 18.
7
Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in Families.PARN基因中的罕见遗传变异与家族性肺纤维化相关。
Am J Respir Crit Care Med. 2017 Dec 1;196(11):1481-1484. doi: 10.1164/rccm.201703-0635LE.
8
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.序列变异解读的标准与指南：美国医学遗传学与基因组学学会和分子病理学协会的联合共识推荐
Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.
9
Rare variants in RTEL1 are associated with familial interstitial pneumonia.RTEL1基因中的罕见变异与家族性间质性肺炎相关。
Am J Respir Crit Care Med. 2015 Mar 15;191(6):646-55. doi: 10.1164/rccm.201408-1510OC.
10
Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease.对家族性间质性肺炎高危个体进行广泛的表型分析揭示了间质性肺疾病发病机制的线索。
Am J Respir Crit Care Med. 2015 Feb 15;191(4):417-26. doi: 10.1164/rccm.201406-1162OC.