Association between high-sensitivity C-reactive protein and coronary atherosclerosis in a general middle-aged population

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作者
Sofia Cederström
Pia Lundman
Joakim Alfredsson
Emil Hagström
Annica Ravn-Fischer
Stefan Söderberg
Troels Yndigegn
Per Tornvall
Tomas Jernberg
机构
[1] Danderyd Hospital,Department of Clinical Sciences
[2] Karolinska Institutet,Department of Health, Medicine and Caring Sciences and Department of Cardiology
[3] Linköping University,Department of Medical Sciences, Cardiology
[4] Uppsala University,Department of Cardiology, Sahlgrenska University Hospital, Institute of Medicine, Department of Molecular and Clinical Medicine
[5] Sahlgrenska Academy at University of Gothenburg,Department of Public Health and Clinical Medicine, Heart Centre
[6] Umeå University,Department of Cardiology, Clinical Sciences
[7] Skåne University Hospital,Department of Clinical Science and Education
[8] Lund University,undefined
[9] Södersjukhuset,undefined
[10] Karolinska Institutet,undefined
来源
Scientific Reports | / 13卷
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摘要
Despite abundant knowledge about the relationship between inflammation and coronary atherosclerosis, it is still unknown whether systemic inflammation measured as high-sensitivity C-reactive protein (hsCRP) is associated with coronary atherosclerosis in a general population. This study aimed to examine the association between hsCRP and coronary computed tomography angiography (CCTA)-detected coronary atherosclerosis in a population-based cohort. Out of 30,154 randomly invited men and women aged 50 to 64 years in the Swedish Cardiopulmonary Bioimage Study (SCAPIS), 25,408 had a technically acceptable CCTA and analysed hsCRP. Coronary atherosclerosis was defined as presence of plaque of any degree in any of 18 coronary segments. HsCRP values were categorised in four groups. Compared with hsCRP below the detection limit, elevated hsCRP (≥ 2.3 mg/L) was weakly associated with any coronary atherosclerosis (OR 1.15, 95% CI 1.07–1.24), coronary diameter stenosis ≥ 50% (OR 1.27, 95% CI 1.09–1.47), ≥ 4 segments involved (OR 1.13, 95% CI 1.01–1.26 ) and severe atherosclerosis (OR 1.33, 95% CI 1.05–1.69) after adjustment for age, sex and traditional risk factors. The associations were attenuated after further adjustment for body mass index (BMI), although elevated hsCRP still associated with noncalcified plaques (OR 1.16, 95% CI 1.02–1.32), proposed to be more vulnerable. In conclusion, the additional value of hsCRP to traditional risk factors in detection of coronary atherosclerosis is low. The association to high-risk noncalcified plaques, although unlikely through a causal pathway, could explain the relationship between hsCRP and clinical coronary events in numerous studies.
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