File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.rmed.2019.04.002
- Scopus: eid_2-s2.0-85063966300
- PMID: 31047120
- WOS: WOS:000466149200011
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: All-cause and cause-specific mortality from restrictive and obstructive spirometric patterns in Chinese adults with and without dyspnea: Guangzhou Biobank Cohort Study
Title | All-cause and cause-specific mortality from restrictive and obstructive spirometric patterns in Chinese adults with and without dyspnea: Guangzhou Biobank Cohort Study |
---|---|
Authors | |
Keywords | Restriction on spirometry Airflow obstruction Dyspnea Mortality |
Issue Date | 2019 |
Publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed |
Citation | Respiratory Medicine, 2019, v. 151, p. 66-80 How to Cite? |
Abstract | Objective: To study whether abnormal spirometric patterns were associated with differential mortality in Chinese adults with and without dyspnea.
Methods; Guangzhou Biobank Cohort Study (GBCS) participants were classified by spirometric patterns and presence of dyspnea into 6 groups: normal spirometry (NS), restriction on spirometry (ROS) and airflow obstruction (AO), each with and without dyspnea. Adjusted hazard ratios (aHRs) were calculated for mortality using Cox models.
Results: Among 16777 subjects, 1595 (9.5%) had ROS, 1036 (6.2%) had AO and 1009 (6.0%) had dyspnea. A total of 1993 deaths (11.9%) occurred during 11-year follow-up. Using NS without dyspnea as reference, NS with dyspnea was significantly associated with increased cardiovascular mortality risk (aHRs 1.61 (95% confidence interval (CI) 1.18–2.19); ROS with and without dyspnea were associated with increased risks of all-cause (aHRs 1.46 (95% CI 1.28–1.66) and 1.81 (95% CI 1.33–2.47)) and cardiovascular mortality (aHRs 1.89 (95% CI 1.55–2.31) and 1.85 (95% CI 1.12–3.03)), but not of lung cancer mortality (aHRs 1.33 (95% CI 0.91–1.94) and 1.35 (95% CI 0.49–3.70)); AO with and without dyspnea were associated with increased risks of all-cause (aHRs 1.59 (95% CI 1.36–1.86) and 2.36 (95% CI 1.77–3.15)), cardiovascular (aHRs 1.43 (95% CI 1.08–1.90) and 1.61 (95% CI 0.91–2.82)) and lung cancer mortality (aHRs 1.91 (95% CI 1.29–2.84) and 3.01 (95% CI 1.46–6.23)). These associations did not vary by sex or smoking status (all P-values for interaction >0.05).
Conclusion: Both ROS and AO, with and without dyspnea, were associated with increased all-cause and cardiovascular disease mortality. The increased risk of all-cause was greater and that of cardiovascular mortality was lower for AO than ROS. AO showed significantly increased risk of lung cancer but ROS did not. (272 words). |
Persistent Identifier | http://hdl.handle.net/10722/271168 |
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.180 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pan, J | - |
dc.contributor.author | Adab, P | - |
dc.contributor.author | Jiang, CQ | - |
dc.contributor.author | Zhang, WS | - |
dc.contributor.author | Zhu, F | - |
dc.contributor.author | Jin, YL | - |
dc.contributor.author | Thomas, GN | - |
dc.contributor.author | Lam, TH | - |
dc.date.accessioned | 2019-06-24T01:04:39Z | - |
dc.date.available | 2019-06-24T01:04:39Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Respiratory Medicine, 2019, v. 151, p. 66-80 | - |
dc.identifier.issn | 0954-6111 | - |
dc.identifier.uri | http://hdl.handle.net/10722/271168 | - |
dc.description.abstract | Objective: To study whether abnormal spirometric patterns were associated with differential mortality in Chinese adults with and without dyspnea. Methods; Guangzhou Biobank Cohort Study (GBCS) participants were classified by spirometric patterns and presence of dyspnea into 6 groups: normal spirometry (NS), restriction on spirometry (ROS) and airflow obstruction (AO), each with and without dyspnea. Adjusted hazard ratios (aHRs) were calculated for mortality using Cox models. Results: Among 16777 subjects, 1595 (9.5%) had ROS, 1036 (6.2%) had AO and 1009 (6.0%) had dyspnea. A total of 1993 deaths (11.9%) occurred during 11-year follow-up. Using NS without dyspnea as reference, NS with dyspnea was significantly associated with increased cardiovascular mortality risk (aHRs 1.61 (95% confidence interval (CI) 1.18–2.19); ROS with and without dyspnea were associated with increased risks of all-cause (aHRs 1.46 (95% CI 1.28–1.66) and 1.81 (95% CI 1.33–2.47)) and cardiovascular mortality (aHRs 1.89 (95% CI 1.55–2.31) and 1.85 (95% CI 1.12–3.03)), but not of lung cancer mortality (aHRs 1.33 (95% CI 0.91–1.94) and 1.35 (95% CI 0.49–3.70)); AO with and without dyspnea were associated with increased risks of all-cause (aHRs 1.59 (95% CI 1.36–1.86) and 2.36 (95% CI 1.77–3.15)), cardiovascular (aHRs 1.43 (95% CI 1.08–1.90) and 1.61 (95% CI 0.91–2.82)) and lung cancer mortality (aHRs 1.91 (95% CI 1.29–2.84) and 3.01 (95% CI 1.46–6.23)). These associations did not vary by sex or smoking status (all P-values for interaction >0.05). Conclusion: Both ROS and AO, with and without dyspnea, were associated with increased all-cause and cardiovascular disease mortality. The increased risk of all-cause was greater and that of cardiovascular mortality was lower for AO than ROS. AO showed significantly increased risk of lung cancer but ROS did not. (272 words). | - |
dc.language | eng | - |
dc.publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed | - |
dc.relation.ispartof | Respiratory Medicine | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Restriction on spirometry | - |
dc.subject | Airflow obstruction | - |
dc.subject | Dyspnea | - |
dc.subject | Mortality | - |
dc.title | All-cause and cause-specific mortality from restrictive and obstructive spirometric patterns in Chinese adults with and without dyspnea: Guangzhou Biobank Cohort Study | - |
dc.type | Article | - |
dc.identifier.email | Jiang, CQ: cqjiang@hkucc.hku.hk | - |
dc.identifier.email | Zhang, WS: zhangws9@hku.hk | - |
dc.identifier.email | Thomas, GN: neilt@hkucc.hku.hk | - |
dc.identifier.email | Lam, TH: hrmrlth@hkucc.hku.hk | - |
dc.identifier.authority | Lam, TH=rp00326 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/j.rmed.2019.04.002 | - |
dc.identifier.pmid | 31047120 | - |
dc.identifier.scopus | eid_2-s2.0-85063966300 | - |
dc.identifier.hkuros | 297886 | - |
dc.identifier.volume | 151 | - |
dc.identifier.spage | 66 | - |
dc.identifier.epage | 80 | - |
dc.identifier.isi | WOS:000466149200011 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0954-6111 | - |