Lung function, forced expiratory volume in 1 s decline and COPD hospitalisations over 44 years of follow-up
The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based “Men Born in 1914” cohort. Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had...
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Published in | The European respiratory journal Vol. 47; no. 3; pp. 742 - 750 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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England
01.03.2016
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Abstract | The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based “Men Born in 1914” cohort.
Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had spirometry reassessed at age 68 years. The cohort was divided into three groups using fixed ratio (FR) and lower limit of normal (LLN) criterion: forced expiratory volume in 1 s (FEV 1 )/vital capacity (VC) ≥70%, FEV 1 /VC <70% but ≥LLN (FR + LLN − ), and FEV 1 /VC <70% and <LLN (FR + LLN + ).
Over 44 years of follow-up, 88 men were hospitalised due to COPD and 686 died. Hazard ratios (95% CI) for incident COPD hospitalisation were 4.15 (2.24–7.69) for FR + LLN − and 7.88 (4.82–12.87) for FR + LLN + (reference FEV 1 /VC ≥70%). Hazard ratios for death were 1.30 (0.98–1.72) for FR + LLN − and 1.58 (1.25–2.00) for FR + LLN + . The adjusted FEV 1 decline between 55 and 68 years of age was higher for FR + LLN − and FR + LLN + relative to the reference. Of those with FR + LLN − at 55 years, 53% had progressed to the FR + LLN + group at 68 years.
Airflow obstruction at age 55 years is a powerful risk factor for future COPD hospitalisations. The FR + LLN − group should be carefully evaluated in clinical practice in relation to future risks and potential benefit from early intervention. This is reinforced by the increased FEV 1 decline in this group. |
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AbstractList | The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based "Men Born in 1914" cohort.Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had spirometry reassessed at age 68 years. The cohort was divided into three groups using fixed ratio (FR) and lower limit of normal (LLN) criterion: forced expiratory volume in 1 s (FEV1)/vital capacity (VC) ≥70%, FEV1/VC <70% but ≥LLN (FR(+)LLN(-)), and FEV1/VC <70% and <LLN (FR(+)LLN(+)).Over 44 years of follow-up, 88 men were hospitalised due to COPD and 686 died. Hazard ratios (95% CI) for incident COPD hospitalisation were 4.15 (2.24-7.69) for FR(+)LLN(-) and 7.88 (4.82-12.87) for FR(+)LLN(+) (reference FEV1/VC ≥70%). Hazard ratios for death were 1.30 (0.98-1.72) for FR(+)LLN(-) and 1.58 (1.25-2.00) for FR(+)LLN(+). The adjusted FEV1 decline between 55 and 68 years of age was higher for FR(+)LLN(-) and FR(+)LLN(+) relative to the reference. Of those with FR(+)LLN(-) at 55 years, 53% had progressed to the FR(+)LLN(+) group at 68 years.Airflow obstruction at age 55 years is a powerful risk factor for future COPD hospitalisations. The FR(+)LLN(-) group should be carefully evaluated in clinical practice in relation to future risks and potential benefit from early intervention. This is reinforced by the increased FEV1 decline in this group. The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based “Men Born in 1914” cohort. Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had spirometry reassessed at age 68 years. The cohort was divided into three groups using fixed ratio (FR) and lower limit of normal (LLN) criterion: forced expiratory volume in 1 s (FEV 1 )/vital capacity (VC) ≥70%, FEV 1 /VC <70% but ≥LLN (FR + LLN − ), and FEV 1 /VC <70% and <LLN (FR + LLN + ). Over 44 years of follow-up, 88 men were hospitalised due to COPD and 686 died. Hazard ratios (95% CI) for incident COPD hospitalisation were 4.15 (2.24–7.69) for FR + LLN − and 7.88 (4.82–12.87) for FR + LLN + (reference FEV 1 /VC ≥70%). Hazard ratios for death were 1.30 (0.98–1.72) for FR + LLN − and 1.58 (1.25–2.00) for FR + LLN + . The adjusted FEV 1 decline between 55 and 68 years of age was higher for FR + LLN − and FR + LLN + relative to the reference. Of those with FR + LLN − at 55 years, 53% had progressed to the FR + LLN + group at 68 years. Airflow obstruction at age 55 years is a powerful risk factor for future COPD hospitalisations. The FR + LLN − group should be carefully evaluated in clinical practice in relation to future risks and potential benefit from early intervention. This is reinforced by the increased FEV 1 decline in this group. The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based "Men Born in 1914" cohort.Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had spirometry reassessed at age 68 years. The cohort was divided into three groups using fixed ratio (FR) and lower limit of normal (LLN) criterion: forced expiratory volume in 1 s (FEV1)/vital capacity (VC) ≥70%, FEV1/VC <70% but ≥LLN (FR(+)LLN(-)), and FEV1/VC <70% and <LLN (FR(+)LLN(+)).Over 44 years of follow-up, 88 men were hospitalised due to COPD and 686 died. Hazard ratios (95% CI) for incident COPD hospitalisation were 4.15 (2.24-7.69) for FR(+)LLN(-) and 7.88 (4.82-12.87) for FR(+)LLN(+) (reference FEV1/VC ≥70%). Hazard ratios for death were 1.30 (0.98-1.72) for FR(+)LLN(-) and 1.58 (1.25-2.00) for FR(+)LLN(+). The adjusted FEV1 decline between 55 and 68 years of age was higher for FR(+)LLN(-) and FR(+)LLN(+) relative to the reference. Of those with FR(+)LLN(-) at 55 years, 53% had progressed to the FR(+)LLN(+) group at 68 years.Airflow obstruction at age 55 years is a powerful risk factor for future COPD hospitalisations. The FR(+)LLN(-) group should be carefully evaluated in clinical practice in relation to future risks and potential benefit from early intervention. This is reinforced by the increased FEV1 decline in this group.The use of baseline lung function in the prediction of chronic obstructive pulmonary disease (COPD) hospitalisations, all-cause mortality and lung function decline was assessed in the population-based "Men Born in 1914" cohort.Spirometry was assessed at age 55 years in 689 subjects, of whom 392 had spirometry reassessed at age 68 years. The cohort was divided into three groups using fixed ratio (FR) and lower limit of normal (LLN) criterion: forced expiratory volume in 1 s (FEV1)/vital capacity (VC) ≥70%, FEV1/VC <70% but ≥LLN (FR(+)LLN(-)), and FEV1/VC <70% and <LLN (FR(+)LLN(+)).Over 44 years of follow-up, 88 men were hospitalised due to COPD and 686 died. Hazard ratios (95% CI) for incident COPD hospitalisation were 4.15 (2.24-7.69) for FR(+)LLN(-) and 7.88 (4.82-12.87) for FR(+)LLN(+) (reference FEV1/VC ≥70%). Hazard ratios for death were 1.30 (0.98-1.72) for FR(+)LLN(-) and 1.58 (1.25-2.00) for FR(+)LLN(+). The adjusted FEV1 decline between 55 and 68 years of age was higher for FR(+)LLN(-) and FR(+)LLN(+) relative to the reference. Of those with FR(+)LLN(-) at 55 years, 53% had progressed to the FR(+)LLN(+) group at 68 years.Airflow obstruction at age 55 years is a powerful risk factor for future COPD hospitalisations. The FR(+)LLN(-) group should be carefully evaluated in clinical practice in relation to future risks and potential benefit from early intervention. This is reinforced by the increased FEV1 decline in this group. |
Author | Engström, Gunnar Wollmer, Per Zaigham, Suneela |
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Cites_doi | 10.1016/j.rmed.2011.01.008 10.1016/j.rmed.2013.06.016 10.1164/rccm.201501-0044ST 10.1186/1465-9921-14-103 10.1183/09041950.005s1693 10.3109/15412555.2012.667851 10.1136/bmjopen-2014-005685 10.3346/jkms.2009.24.4.621 10.1378/chest.06-1349 10.1186/1465-9921-12-136 10.1378/chest.10-0189 10.1136/thx.2008.095554 10.1183/09031936.00021707 10.1136/thx.2008.098483 10.1370/afm.1714 10.1183/09031936.00164608 10.1378/chest.11-2837 10.1371/journal.pone.0109732 10.1097/00004872-200107000-00004 10.1378/chest.11-0797 10.1378/chest.07-1434 10.1164/rccm.201202-0223OC 10.3109/15412555.2013.773303 10.3132/pcrj.2007.00012 10.1378/chest.130.1.200 10.1016/j.hrtlng.2013.07.002 10.1183/13993003.00635-2015 10.1136/thx.2006.068379 10.1016/j.rmed.2005.03.035 10.1177/1403494812463172 10.1016/j.rmed.2009.10.030 10.1186/1465-9921-13-13 10.1007/s10654-012-9750-2 10.1183/09031936.00158212 10.2337/diacare.27.12.2966 10.1159/000282171 10.1080/15412550600651552 10.1155/2011/780215 10.1186/1471-2466-12-12 10.1016/j.amjmed.2009.07.037 |
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CorporateAuthor | Kardiovaskulär forskning - epidemiologi Institutionen för translationell medicin Department of Translational Medicine Lunds universitet Profile areas and other strong research environments Department of Clinical Sciences, Malmö Lund University Strategiska forskningsområden (SFO) EpiHealth: Epidemiology for Health Faculty of Medicine Klinisk fysiologi och nuklearmedicin, Malmö Clinical Physiology and Nuclear Medicine, Malmö Strategic research areas (SRA) Medicinska fakulteten Cardiovascular Research - Epidemiology Profilområden och andra starka forskningsmiljöer Institutionen för kliniska vetenskaper, Malmö |
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SubjectTerms | Aged Clinical Medicine Follow-Up Studies Forced Expiratory Volume Hospitalization - statistics & numerical data Humans Kaplan-Meier Estimate Klinisk medicin Linear Models Lungmedicin och allergi Male Medical and Health Sciences Medicin och hälsovetenskap Middle Aged Proportional Hazards Models Pulmonary Disease, Chronic Obstructive - mortality Pulmonary Disease, Chronic Obstructive - physiopathology Respiratory Medicine and Allergy Risk Factors Smoking Spirometry - methods Sweden Tidal Volume |
Title | Lung function, forced expiratory volume in 1 s decline and COPD hospitalisations over 44 years of follow-up |
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