Åpne denne publikasjonen i ny fane eller vindu >>Department of Clinical Science, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Science, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Science and Education, Division of Cardiology, Karolinska Institutet, Stockholm, Sweden.
Department of Cardiology, Clinical Sciences, Lund University, Skåne University Hospital, Lund, Sweden.
Department of Cardiology, Clinical Sciences, Lund University, Skåne University Hospital, Lund, Sweden.
Department of Medical Sciences, Uppsala University, Uppsala, Sweden; Uppsala Clinical Research Centre, Uppsala University, Uppsala, Sweden.
Clinical Department of Cardiology, Region Östergötland, Linköping, Sweden; Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Global Project, Respiratory and Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Uppsala Clinical Research Centre, Uppsala University, Uppsala, Sweden.
Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Örebro universitet, Institutionen för medicinska vetenskaper. Region Örebro län. Department of Cardiology.
Cardiovascular Research Unit, Division of Clinical Medicine, University of Sheffield, Sheffield, UK; NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Cardiovascular Research Unit, Division of Clinical Medicine, University of Sheffield, Sheffield, UK; NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Cardiovascular Research Unit, Division of Clinical Medicine, University of Sheffield, Sheffield, UK; NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Clinical Development, Respiratory and Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Global Medical Affairs, Global Medical Affairs, Cardiovascular, Renal & Metabolic Disease, BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
Global Clinical Operations, Respiratory and Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
Department of Medical Sciences, Uppsala University, Uppsala, Sweden; Uppsala Clinical Research Centre, Uppsala University, Uppsala, Sweden.
Cardiovascular Research Unit, Division of Clinical Medicine, University of Sheffield, Sheffield, UK; NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
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2026 (engelsk)Inngår i: The International Journal of Chronic Obstructive Pulmonary Disease, ISSN 1176-9106, E-ISSN 1178-2005, Vol. 21, artikkel-id 580301Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]
PURPOSE: The study aimed to investigate the associations between impaired spirometry such as obstructive pattern and preserved ratio impaired spirometry (PRISm) and occurrent cardiovascular events and deaths in patients with acute myocardial infarction.
PATIENTS AND METHODS: Cohort study of 517 patients with age ≥40 years and ≥10 pack-years of smoking, hospitalized for myocardial infarction at eight sites in Sweden and the United Kingdom. The Vitalograph® COPD-6 device was used to assess the ratio of forced expiratory volume in 1 and 6 seconds (FEV1/FEV6) and FEV1 as a percentage of the predicted value (FEV1%pred). Obstructive pattern was defined as FEV1/FEV6 <0.7, PRISm as FEV1/FEV6 >0.7 and FEV1%pred <80, and normal findings as FEV1/FEV6 ≥0.7 and FEV1%pred ≥80. Follow-up data were obtained from national registers or follow-up visits. Multivariable Cox regression was used to analyze the associations of obstructive pattern and PRISm with the incidence of acute ischemic cardiovascular events or major adverse cardiovascular events (MACE), respectively, within one year.
RESULTS: Obstructive pattern was found in 95 (18%), PRISm in 192 (37%) and normal spirometry in 230 (45%) patients. A cardiovascular event occurred in 21 (4%) and MACE in 28 (5%). Compared with normal spirometry, PRISm was independently associated with both new cardiovascular events (HR (95% CI) 3.44 (1.07-11.0)) and MACE (4.94 (1.63 to 15.0)), and obstructive pattern with MACE (3.87 (1.08-13.8)). Further adjustment for cardiac or COPD treatment did not substantially change the results.
CONCLUSION: About half of patients with acute myocardial infarction and a ≥10 pack-year smoking history have abnormal spirometry findings. Both obstructive pattern and PRISm are independently associated with increased risk for MACE within one year. We suggest that spirometry should be considered as a routine assessment in patients with smoking history and recent myocardial infarction.
sted, utgiver, år, opplag, sider
Dove Medical Press, 2026
Emneord
COPD, MACE, PRISm, acute ischemic cardiovascular events, chronic obstructive pulmonary disease, major adverse cardiovascular events, obstructive pattern, preserved ratio impaired spirometry
HSV kategori
Identifikatorer
urn:nbn:se:oru:diva-128317 (URN)10.2147/COPD.S580301 (DOI)001735594200001 ()41947782 (PubMedID)
Forskningsfinansiär
AstraZeneca
2026-04-152026-04-152026-04-15bibliografisk kontrollert