Abstract
Purpose: We assessed the temporal pattern of 29 immune and inflammatory proteins in post-acute coronary syndrome (ACS) patients, prior to the development of recurrent ACS. Methods: High-frequency blood sampling was performed in 844 patients admitted for ACS during one-year follow-up. We conducted a case-control study on the 45 patients who experienced reACS (cases) and two matched event-free patients (controls) per case. Olink Proteomics’ immunoassay was used to obtain serum levels of the 29 proteins, expressed in an arbitrary unit on the log2-scale (Normalized Protein eXpression, NPX). Linear mixed-effects models were applied to examine the temporal pattern of the proteins, and to illustrate differences between cases and controls. Results: Mean age was 66 ± 12 years and 80% were men. Cases and controls had similar baseline clinical characteristics. During the first 30 days, and after multiple testing correction, cases had significantly higher serum levels of CXCL1 (difference of 1.00 NPX, p = 0.002), CD84 (difference of 0.64 NPX, p = 0.002) and TNFRSF10A (difference of 0.41 NPX, p < 0.001) than controls. After 30 days, serum levels of all 29 proteins were similar in cases and controls. In particular, no increase was observed prior to reACS. Conclusions: Among 29 immune and inflammatory proteins, CXCL1, CD84 and TNFRSF10A were associated with early reACS after initial ACS-admission.
| Original language | English |
|---|---|
| Pages (from-to) | 199-205 |
| Number of pages | 7 |
| Journal | Biomarkers |
| Volume | 24 |
| Issue number | 2 |
| Early online date | 4 Dec 2018 |
| DOIs | |
| Publication status | Published - Mar 2019 |
Keywords
- Acute coronary syndrome
- biomarkers
- immune and inflammatory system
- proteins
- proteomics
- temporal pattern
- Humans
- Middle Aged
- Male
- Immunity, Innate/genetics
- Inflammation/blood
- Receptors, TNF-Related Apoptosis-Inducing Ligand/genetics
- Acute Coronary Syndrome/blood
- Proteomics
- Biomarkers/blood
- Female
- Aged
- Chemokine CXCL1/genetics
- Signaling Lymphocytic Activation Molecule Family/genetics