Blood pressure, heart rate, and mortality in chronic obstructive pulmonary disease: the SUMMIT trial

Author:

Byrd James Brian1,Newby David E2,Anderson Julie A3,Calverley Peter M A4,Celli Bartolome R5,Cowans Nicholas J6,Crim Courtney3,Martinez Fernando J7,Vestbo Jørgen8,Yates Julie3,Brook Robert D1,

Affiliation:

1. University of Michigan Health System, 1500 E Medical Center Dr, Ann Arbor, MI 48109, USA

2. British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

3. Research & Development, GlaxoSmithKilne, Stockley Park, Iron Bridge Rd N, West Drayton, Uxbridge UB11 1BT, Middlesex, UK

4. Department of Medicine, Clinical Sciences Centre, University Hospital Aintree, University of Liverpool, Cedar House, Ashton Street, Liverpool L69 3GE, Liverpool, UK

5. Pulmonary and Critical Care Division, Brigham and Women’s Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA

6. Veramed Ltd., 5th Floor Regal House, 70 London Road, Twickenham TW1 3QS, UK

7. Division of Pulmonary and Critical Care Medicine, Weill Cornell Medicine, 525 East 68th Street, Box 130, New York, NY 10065, USA

8. Division of Infection, Immunity and Respiratory Medicine, Manchester Academic Health Sciences Centre, The University of Manchester and South Manchester, 2nd Floor Education and Research Centre, University Hospital of South Manchester NHS Foundation Trust, Manchester M23 9LT, Manchester, UK

Abstract

Abstract Aims To characterize the relationship between blood pressure (BP) or heart rate and mortality and morbidity in chronic obstructive pulmonary disease (COPD). Methods and results We performedpost hoc analysis of baseline BP or heart rate and all-cause mortality and cardiovascular events in the SUMMIT trial. SUMMIT was a randomized double-blind outcome trial of 16 485 participants (65 ± 8 years, 75% male, and 47% active smokers) enrolled at 1368 sites in 43 countries. Participants with moderate COPD with or at risk for cardiovascular disease (CVD) were randomized to placebo, long-acting beta agonist, inhaled corticosteroid, or their combination. All-cause mortality increased in relation to high systolic [≥140 mmHg; hazard ratio (HR) 1.27, 95% confidence interval (CI) 1.12–1.45] or diastolic (≥90 mmHg; HR 1.35, 95% CI 1.14–1.59) BP and low systolic (<120 mmHg; HR 1.36, 95% CI 1.13–1.63) or diastolic (<80 mmHg; HR 1.15, 95% CI 1.00–1.32) BP. Higher heart rates (≥80 per minute; HR 1.39, 95% CI 1.21–1.60) and pulse pressures (≥80 mmHg; HR 1.39, 95% CI 1.07–1.80) were more linearly related to increases in all-cause mortality. The risks of cardiovascular events followed similar patterns to all-cause mortality. Similar findings were observed in subgroups of patients without established CVD. Conclusion A ‘U-shaped’ relationship between BP and all-cause mortality and cardiovascular events exists in patients with COPD and heightened cardiovascular risk. A linear relationship exists between heart rate and all-cause mortality and cardiovascular events in this population. These findings extend the prognostic importance of BP to this growing group of patients and raise concerns that both high and low BP may pose health risks.

Funder

NIH

GlaxoSmithKline

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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