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Published on: January 28, 2020
C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery
Tjörvi E Perry1, Jochen D Muehlschlegel, Kuang-Yu Liu
1Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. tjorviperry@gmail.com
Insights
A specific C-reactive protein (CRP) gene variant, rs1800947, is linked to lower CRP levels after coronary artery bypass graft (CABG) surgery. This finding may impact understanding of cardiovascular disease risk and surgical inflammation.
Area of Science:
- Genetics and Molecular Biology
- Cardiovascular Disease Research
- Surgical Inflammation
Background:
- Elevated C-reactive protein (CRP) is a known cardiovascular disease risk factor.
- CRP gene variants influence baseline CRP levels, but their role in surgical inflammation is unclear.
- Investigating CRP gene variants in the context of coronary artery bypass graft (CABG) surgery is crucial.
Purpose of the Study:
- To examine the association between candidate CRP gene variants and postoperative plasma CRP levels.
- To understand the impact of CRP gene variants on CRP levels during the acute inflammatory response to CABG surgery with cardiopulmonary bypass (CPB).
Main Methods:
- A multicenter candidate gene association study design was employed.
- Seventeen candidate CRP single nucleotide polymorphisms (SNPs) and haplotypes were analyzed in 604 patients undergoing CABG surgery.
- Perioperative CRP levels were measured at multiple time points: pre-surgery, post-CPB, and on postoperative days 1-4.
Main Results:
- Postoperative CRP levels were significantly elevated compared to preoperative levels (P < 0.0001).
- The minor allele of the synonymous coding SNP, rs1800947, was significantly associated with lower peak postoperative CRP levels (P = 2.4 x 10(-4)) and overall lower postoperative CRP levels (P = 4.8 x 10(-5)).
- The association of rs1800947 with lower CRP levels remained significant after Bonferroni adjustment.
Conclusions:
- A specific CRP gene SNP (rs1800947) is associated with reduced postoperative CRP levels in patients undergoing CABG surgery.
- Further research is needed to elucidate the clinical significance of this CRP gene variant association.
- Understanding this relationship may offer insights into adverse postoperative outcomes related to acute-phase CRP response.
Background:
Elevated baseline C-reactive protein (CRP) levels are associated with increased risk for developing cardiovascular disease. Several CRP gene variants have been associated with altered baseline CRP levels in ambulatory populations. However, the influence of CRP gene variants on CRP levels during inflammatory states, such as surgery, is largely unexplored. We describe the association between candidate CRP gene variants and postoperative plasma CRP levels in patients undergoing primary, elective coronary artery bypass graft (CABG) surgery with cardiopulmonary bypass (CPB).
Methods:
Using a multicenter candidate gene association study design, we examined the association between seventeen candidate CRP single nucleotide polymorphisms (SNPs) and inferred haplotypes, and altered postoperative CRP levels in 604 patients undergoing CABG surgery with CPB. Perioperative CRP levels were measured immediately prior to surgery, post-CPB and on postoperative days (POD) 1-4.
Results:
CRP levels were significantly elevated at all postoperative time points when compared with preoperative levels (P < 0.0001). After adjusting for clinical covariates, the minor allele of the synonymous coding SNP, rs1800947 was associated with lower peak postoperative CRP levels (P = 2.4 x 10(-4)) and lower CRP levels across all postoperative time points (P = 4.8 x 10(-5)). rs1800947 remained highly significant after Bonferroni adjustment for multiple comparisons.
Conclusion:
We identified a CRP gene SNP associated with lower postoperative CRP levels in patients undergoing CABG surgery with CPB. Further investigation is needed to clarify the significance of this association between CRP gene variants and the acute-phase rise in postoperative CRP levels with regard to the risk of adverse postoperative outcomes.
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