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Published on: January 28, 2020
Association between high-sensitivity C-reactive protein and coronary atherosclerosis in a general middle-aged
Sofia Cederström1, Pia Lundman2, Joakim Alfredsson3
1Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden. sofia.cederstrom@ki.se.
Insights
Systemic inflammation, measured by high-sensitivity C-reactive protein (hsCRP), shows a weak association with coronary atherosclerosis in the general population. Elevated hsCRP is linked to noncalcified plaques, but its additional value beyond traditional risk factors for detecting coronary atherosclerosis is low.
Area of Science:
- Cardiovascular Medicine
- Inflammation Research
- Biomarker Analysis
Background:
- The link between inflammation and coronary atherosclerosis is established, but the role of systemic inflammation markers like hsCRP in the general population remains unclear.
- High-sensitivity C-reactive protein (hsCRP) is a marker of systemic inflammation.
- Coronary atherosclerosis is a significant public health concern.
Purpose of the Study:
- To investigate the association between hsCRP levels and coronary atherosclerosis detected by coronary computed tomography angiography (CCTA).
- To evaluate the added value of hsCRP to traditional risk factors in identifying coronary atherosclerosis.
Main Methods:
- A population-based cohort study (SCAPIS) involving 25,408 individuals aged 50-64 years.
- Coronary atherosclerosis was assessed using CCTA, defined by plaque presence in coronary segments.
- hsCRP levels were measured and categorized, with statistical adjustments for age, sex, traditional risk factors, and BMI.
Main Results:
- Elevated hsCRP (≥2.3 mg/L) showed a weak association with any coronary atherosclerosis, significant stenosis (≥50%), and involvement of ≥4 segments.
- Associations were attenuated after adjusting for BMI, but elevated hsCRP remained linked to noncalcified plaques.
- The predictive value of hsCRP for coronary atherosclerosis, beyond traditional risk factors, was found to be low.
Conclusions:
- hsCRP has limited additional value in detecting coronary atherosclerosis when traditional risk factors are considered.
- The association between hsCRP and noncalcified plaques may partially explain its link to clinical coronary events, though a direct causal pathway is unlikely.
- Further research may clarify the role of hsCRP in specific plaque types and clinical outcomes.
Abstract:
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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