Determinants of Lung Fissure Completeness.
van der Molen, MC
Hartman, JE
Vermeulen, CJ
van den Berge, M
Faiz, A
Kerstjens, HAM
Charbonnier, J-P
Vanfleteren, LEGW
Slebos, D-J
- Publisher:
- AMER THORACIC SOC
- Publication Type:
- Journal Article
- Citation:
- Am J Respir Crit Care Med, 2021, 204, (7), pp. 807-816
- Issue Date:
- 2021-10-01
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Determinants of Lung Fissure Completeness.pdf | Published version | 1.38 MB | Adobe PDF |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | van der Molen, MC | |
dc.contributor.author | Hartman, JE | |
dc.contributor.author | Vermeulen, CJ | |
dc.contributor.author | van den Berge, M | |
dc.contributor.author |
Faiz, A https://orcid.org/0000-0003-1740-3538 |
|
dc.contributor.author | Kerstjens, HAM | |
dc.contributor.author | Charbonnier, J-P | |
dc.contributor.author | Vanfleteren, LEGW | |
dc.contributor.author | Slebos, D-J | |
dc.date.accessioned | 2022-01-29T19:34:52Z | |
dc.date.available | 2022-01-29T19:34:52Z | |
dc.date.issued | 2021-10-01 | |
dc.identifier.citation | Am J Respir Crit Care Med, 2021, 204, (7), pp. 807-816 | |
dc.identifier.issn | 1073-449X | |
dc.identifier.issn | 1535-4970 | |
dc.identifier.uri | http://hdl.handle.net/10453/153809 | |
dc.description.abstract | Rationale: New advanced bronchoscopic treatment options for patients with severe chronic obstructive pulmonary disease (COPD) have led to increased interest for COPD phenotyping, including fissure completeness. Objectives: We investigated clinical, environmental, and genetic factors contributing to fissure completeness in patients with and without COPD. Methods: We used data from 9,926 participants of the COPDGene study who underwent chest computed tomographic (CT) scans. Fissure completeness was calculated from CT scans after quantitative CT analysis at baseline and 5-year follow-up. Clinical and environmental factors, including sex, race, smoking, COPD, emphysema, maternal smoking during pregnancy and maternal COPD, were tested for impact on fissure completeness. Genome-wide association analyses were performed separately in non-Hispanic White subjects and African American subjects. Measurements and Main Results: African American subjects had significantly higher fissure completeness than non-Hispanic White subjects for all three fissures (P < 0.001). There was no change in fissure completeness between baseline and 5-year follow-up. For all fissures, no clinically relevant differences in fissure completeness were found for other clinical or environmental factors, including COPD severity. Rs2173623, rs264866, rs2407284, rs7310342, rs4904145, rs6504172, and rs7209556 showed genome-wide significant associations with fissure completeness in non-Hispanic White subjects. In African American subjects, rs264866, rs4904145 and rs6504172 were identified as significant associations. Rs2173623, rs6504172, and rs7209556 lead to WNT5A and HOXB antisense RNA expression, which play an important role during embryogenesis. Conclusions: Fissure completeness is genetically determined and not dependent on age, sex, smoking status, the presence and severity of COPD (including exacerbation frequency), maternal smoking during pregnancy, or maternal COPD. | |
dc.format | ||
dc.language | eng | |
dc.publisher | AMER THORACIC SOC | |
dc.relation.ispartof | Am J Respir Crit Care Med | |
dc.relation.isbasedon | 10.1164/rccm.202102-0260OC | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 11 Medical and Health Sciences | |
dc.subject.classification | Respiratory System | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Case-Control Studies | |
dc.subject.mesh | Ethnicity | |
dc.subject.mesh | Female | |
dc.subject.mesh | Follow-Up Studies | |
dc.subject.mesh | Genetic Markers | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Genome-Wide Association Study | |
dc.subject.mesh | Genotyping Techniques | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Linear Models | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Polymorphism, Single Nucleotide | |
dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
dc.subject.mesh | Tomography, X-Ray Computed | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Genetic Markers | |
dc.subject.mesh | Tomography, X-Ray Computed | |
dc.subject.mesh | Linear Models | |
dc.subject.mesh | Case-Control Studies | |
dc.subject.mesh | Follow-Up Studies | |
dc.subject.mesh | Polymorphism, Single Nucleotide | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Ethnic Groups | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Genome-Wide Association Study | |
dc.subject.mesh | Genotyping Techniques | |
dc.title | Determinants of Lung Fissure Completeness. | |
dc.type | Journal Article | |
utslib.citation.volume | 204 | |
utslib.location.activity | United States | |
utslib.for | 11 Medical and Health Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
utslib.copyright.status | closed_access | * |
dc.date.updated | 2022-01-29T19:34:47Z | |
pubs.issue | 7 | |
pubs.publication-status | Published | |
pubs.volume | 204 | |
utslib.citation.issue | 7 |
Abstract:
Rationale: New advanced bronchoscopic treatment options for patients with severe chronic obstructive pulmonary disease (COPD) have led to increased interest for COPD phenotyping, including fissure completeness. Objectives: We investigated clinical, environmental, and genetic factors contributing to fissure completeness in patients with and without COPD. Methods: We used data from 9,926 participants of the COPDGene study who underwent chest computed tomographic (CT) scans. Fissure completeness was calculated from CT scans after quantitative CT analysis at baseline and 5-year follow-up. Clinical and environmental factors, including sex, race, smoking, COPD, emphysema, maternal smoking during pregnancy and maternal COPD, were tested for impact on fissure completeness. Genome-wide association analyses were performed separately in non-Hispanic White subjects and African American subjects. Measurements and Main Results: African American subjects had significantly higher fissure completeness than non-Hispanic White subjects for all three fissures (P < 0.001). There was no change in fissure completeness between baseline and 5-year follow-up. For all fissures, no clinically relevant differences in fissure completeness were found for other clinical or environmental factors, including COPD severity. Rs2173623, rs264866, rs2407284, rs7310342, rs4904145, rs6504172, and rs7209556 showed genome-wide significant associations with fissure completeness in non-Hispanic White subjects. In African American subjects, rs264866, rs4904145 and rs6504172 were identified as significant associations. Rs2173623, rs6504172, and rs7209556 lead to WNT5A and HOXB antisense RNA expression, which play an important role during embryogenesis. Conclusions: Fissure completeness is genetically determined and not dependent on age, sex, smoking status, the presence and severity of COPD (including exacerbation frequency), maternal smoking during pregnancy, or maternal COPD.
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