- Research article
- Open Access
- Open Peer Review
C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery
- Tjörvi E Perry1Email author,
- Jochen D Muehlschlegel1,
- Kuang-Yu Liu1,
- Amanda A Fox1,
- Charles D Collard2,
- Simon C Body†1,
- Stanton K Shernan†1 and
- the CABG Genomics Investigators
© Perry et al; licensee BioMed Central Ltd. 2009
- Received: 07 August 2008
- Accepted: 08 May 2009
- Published: 08 May 2009
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).
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.
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 × 10-4) and lower CRP levels across all postoperative time points (P = 4.8 × 10-5). rs1800947 remained highly significant after Bonferroni adjustment for multiple comparisons.
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.
- Candidate Gene Association Study
- Postoperative Time Point
- Survive Bonferroni Correction
- Ambulatory Population
- Preoperative White Blood Cell Count
Human CRP is a highly conserved protein belonging to the pentraxin family of acute phase reactants. Normal baseline plasma CRP levels are ≤1 mg/L in healthy individuals. However, as an acute-phase reactant synthesized in the liver, plasma CRP levels can rise 1000-fold in response to tissue injury or inflammation[2, 3], thereby triggering activation of the classical complement pathway[4, 5], endothelial cell surface adhesion molecule expression, leukocyte and macrophage activation, as well as platelet adhesion[1, 7]. The pro-inflammatory effects of CRP may explain the increased risk of developing cardiovascular disease (CVD) associated with persistently elevated baseline CRP levels [8–12].
Environmental factors such as age, gender, smoking, lipid levels, hypertension and body mass index (BMI) have been shown to influence baseline plasma CRP levels in the absence of overt inflammatory stimuli[8, 13]. Recent family and population-based cohort studies have found moderate heritability of baseline CRP levels [14–16]. There is now convincing evidence to support the association between CRP gene variants and baseline plasma CRP levels, and CVD in ambulatory populations [17–19]. Furthermore, two recently published genome wide association studies have identified several genes, including the CRP gene, that influence basal CRP levels[20, 21]. However, little is known about the influence of CRP gene variants on the acute-phase response of plasma CRP levels. We therefore examined the association between candidate CRP gene variants and postoperative plasma CRP levels following primary, elective coronary artery bypass graft (CABG) surgery with cardiopulmonary bypass (CPB).
Study design and population
A candidate gene association study was undertaken to examine the association between CRP gene variants and postoperative plasma CRP levels following CABG surgery with CPB. One thousand eighty-two patients scheduled for primary, elective CABG surgery at the Brigham and Women's Hospital, Boston, MA and the Texas Heart Institute, St Luke's Episcopal Hospital, Houston, TX between August 2001 and June 2007 were eligible for analysis. Following Institutional Review Boards approval, informed consent was obtained from each patient prior to enrollment. Exclusion criteria were defined prior to statistical analysis in order to exclude patients with ongoing preoperative myocardial injury or other acute inflammatory processes that may have confounded the relationship between CRP variants and postoperative CRP level. Exclusion criteria included age <20 years (n = 0), recent (<2 weeks) myocardial infarction (MI) by patient history (n = 207), preoperative white blood cell count >10.0/mm3 (n = 255), preoperative cardiac troponin I (cTnI) level >0.17 ng/mL (n = 220), and recipients of leukocyte-rich blood products within 30 days prior to surgery (n = 15). We excluded eight patients with a preoperative acute inflammatory process and elevated CRP levels (> 60 mg/L).
Preoperative demographic data, environmental risk factors and perioperative surgical and anesthetic management were recorded for all patients. Genomic DNA was isolated from whole blood samples using standard techniques. Plasma CRP concentrations were measured with a competitive format immunoassay, using a monoclonal antibody and labeled CRP, configured on Biosite's Triage device platform (Biosite Inc., San Diego, CA), from plasma drawn at six time points: preoperatively, immediately after termination of CPB, and on the mornings of postoperative days (POD) 1–4. CRP concentrations were calculated using a set of spiked plasma samples as the calibration reference. The analytical sensitivity of the CRP assay is 0.33 μg/mL with precision of 17% over the measurable range of the assay (0.33 – 300 μg/mL).
Candidate SNP identification and genotyping
In an effort to characterize the CRP gene and the surrounding region, we genotyped CRP single nucleotide polymorphisms (SNPs) previously described in the literature. In addition, we genotyped tagging SNPs for the region encompassing the CRP gene including 3000 bp upstream of the transcription start site and 1000 bp downstream of the 3' untranslated region (UTR). Tagging SNPs with minor allele frequencies (MAF) >1% were identified using Tagger based on a pairwise r2 tagging threshold of 0.8 (rs3316653, rs3316654, rs2794517, rs3122012, rs3093058, rs2808630, rs3093077, rs2794520, rs876538, rs876537, rs1572970). Genotyping was carried out using the iPLEX genotyping platform (Sequenom, San Diego, CA). SNPs that were not in Hardy-Weinberg equilibrium (P = 0.001) or with a MAF <1% were excluded from analysis. Patients with greater than 10% missing genotypes were also excluded. For haplotype association analysis, PHASE version 2.1.1[25, 26] was used to infer common CRP haplotypes (frequency >5%) for every individual.
A linear regression model of clinical predictors of postoperative plasma CRP levels was constructed. Clinically relevant variables and those with a P = 0.20 on univariate analysis were entered into the model using stepwise regression. Variables included in the final model were age, gender, race, institution, preoperative CRP level, body mass index (BMI), history of chronic inflammatory disease of the bowel, joints or skin, current smoker, corticosteroid use in the month prior to surgery, HMG-CoA reductase inhibitor use within 24 hours of surgery and administration of a homologous blood product during the perioperative period.
Subsequently, the association between CRP gene variants and rank-ordered peak postoperative CRP levels was tested for dominant, additive and recessive genetic models while adjusting for the variables in the clinical model. To gain additional insight as to how CRP gene variants influence the temporal profile of CRP levels on POD 1–4, CRP measurements were first logit-transformed to approximate a normal distribution – logit-transformation is applied over other forms of transformation to map a bounded variable to the entire real line as is the case with our CRP measurements. Subsequently a repeated-measure Tobit regression model, adjusted for the above-mentioned clinical predictors, was applied to estimate the censored normal distribution of the transformed CRP levels while accounting for the correlated observations on different postoperative days for all patients. The repeated-measure Tobit regression model included a random effect to account for the correlation between repeated measures. Finally, robust standard errors were computed based on Huber sandwich estimators to reduce the leverage exerted by any remaining outlier observation in the parameter estimation. Taking into account the posterior probabilities of each possible haplotypic pair, inferred CRP haplotypes were tested for association with CRP levels using the repeated-measure Tobit regression model with the most frequent haplotype (H1) as the reference haplotype. A bootstrapping procedure was applied to estimate the effect of each minor allele or haplotype on postoperative plasma CRP levels, and to mitigate the potential for overfitting[28, 29]. CRP concentrations are presented as medians with inter-quartile ranges. A P < 0.05 after Bonferroni correction was considered statistically significant. SAS version 9.1.3 (SAS Institute, Cary, NC) was used to build the clinical model, R Statistical Software was used for repeated-measure Tobit regression model , and PLINK was used for the peak CRP gene association analysis .
Baseline demographic and clinical characteristics of the study population (n = 604)*.
Age at enrollment (Yrs)
65 ± 10
Gender (Male %)
Race (Caucasian vs. Other %)
Institution A, (%)
Body mass index (kg/m2)
28.8 ± 4.9
History of diabetes (Types I and II) (%)
aHistory of peripheral vascular disease (%)
bHistory of chronic inflammation (%)
Current smoker (%)
cPreoperative CRP level (mg/L)
Preoperative creatinine (mg/dL)
1.09 ± 0.30
dPreoperative steroid use (%)
Duration of statin use prior to CABG (%)
No statin use
≥ 6 months
Last statin dose administered prior to CABG (%)
≥ 72 hours
Preoperative aspirin use (%)
eBlood product transfusion (%)
Aortic cross clamp time (min)
73 ± 34
Cardiopulmonary bypass time (min)
98 ± 43
Number of coronary grafts (%)
Candidate CRP gene single nucleotide polymorphisms.
CRP gene single nucleotide polymorphisms association results for postoperative plasma CRP levels following coronary artery bypass graft surgery.
9.0 × 10-3
2.4 × 10-4*
4.8 × 10-5*
2.1 × 10-3
2.0 × 10-3
Common CRP haplotypes and association results for altered postoperative CRP levels adjusted for clinical covariates following coronary artery bypass graft surgery.
4.64 × 10-3
We investigated the association between 17 candidate CRP SNPs and perioperative plasma CRP levels in patients undergoing primary, elective CABG surgery with CPB. After adjusting for clinical covariates, the minor allele of the synonymous coding SNP, rs1800947 was associated with lower peak postoperative CRP levels, and lower CRP levels across all postoperative time points. Although the rs3091244 T allele did not survive Bonferroni correction for multiple comparisons, this CRP SNP was strongly associated with elevated postoperative plasma CRP levels following CABG surgery. Furthermore, these associations were not influenced by race. In the largest cardiac surgical cohort study to date to look at CRP polymorphisms, we provide novel evidence that two CRP gene SNPs independently predict postoperative plasma CRP levels following CABG surgery.
The minor allele for the rs1800947 polymorphism has consistently been associated with lower baseline plasma CRP levels[16, 19, 32–36] and decreased prevalence of CVD-related mortality in ambulatory populations[18, 37]. However, the association between CRP gene variants and postoperative plasma CRP levels is largely unexplored. Brull et al. sought to test the hypothesis that common CRP gene variants influence both baseline and postoperative plasma CRP levels in patients undergoing CABG surgery. Possibly limited by low statistical power, these authors failed to demonstrate an association between rs1800947 and increased postoperative CRP levels.
Located on exon 2 of the CRP gene, rs1800947 is a synonymous coding polymorphism. Until recently, it has been thought that synonymous coding polymorphisms, such as rs1800947 (CTG [Leu]→CTC [Leu]), do not affect gene function or phenotype. However, recent evidence suggests that allele-specific differences in codons can result in altered post-translational protein folding and function[39, 40]. Nonetheless, without supporting mRNA expression analyses to further elucidate the functional effects of the rs1800947 SNP on plasma CRP levels, we can only speculate as to the functionality of rs1800947. Alternatively, rs1800947 may be in linkage disequilibrium (LD) with a true functional polymorphism; the closest polymorphisms in LD with rs1800947 are rs11265263 (r2 = 0.88) and rs11588887 (r2 = 0.58), 27 kbp and 33.7 kbp in the 5' direction, respectively. Although we were unable to demonstrate significant LD between rs1800947 and other candidate CRP SNPs in this study, more extensive genotyping would be necessary to fully exclude LD with surrounding polymorphisms.
rs3091244 is a tri-allelic SNP located in the promotor region of the CRP gene that has been associated with elevated baseline CRP levels[19, 41–44], and increased risk of coronary artery disease (CAD) in ambulatory patients. However, no study to date has examined the association between rs3091244 and postoperative plasma CRP levels. Located in the second of four identified promotor elements (E-box2) in the CRP gene promotor region, Szalai et al. recently demonstrated that rs3091244 affects promotor activity in vitro by altering transcription factor binding sites. Alternatively, rs3091244 may be a marker allele for a true functional CRP gene variant as it is highly correlated with rs3116653, rs3122012, rs1417938 and rs1130864 (r2 ≥ 0.93). Of note, rs3091244 is in strong LD with rs1130864 (r2 ≥ 0.94), the CRP polymorphism described by Brull et al. as having a similar effect on postoperative plasma CRP levels in patients undergoing CABG surgery. Further investigation is warranted to determine the importance of rs3091244 in regulating baseline and possibly the postoperative acute-phase rise plasma CRP levels.
The results of our CRP haplotype analysis are consistent with our SNP analysis findings. Our result suggests that compared with the GC haplotype (H1), the CC haplotype (H4) was significantly associated with decreased postoperative plasma CRP levels and the GT haplotype (H2) with increased CRP levels. Furthermore, the effect size of the CC haplotype (H4) appeared larger than that of the GT haplotype (H2). This would correspond to two independent modifying effects of the rs1800947C (decrease) and rs3091244T (increase) alleles, consistent with the SNP association findings from Table 3 as H4 was tagged by rs1800947C allele and, H2 tagged by the rs3091244T allele. As such, the results of our haplotype analysis add little additional information to our SNP association findings.
Several limitations in this study warrant consideration. Based on a similar study design, we truncated our plasma CRP measurement at 300 mg/L . In an effort to approximate normal distribution, we logit-transformed the left-skewed postoperative CRP distribution, and applied a Tobit regression to recover the truncated CRP levels. Despite estimated median postoperative CRP levels below 300 mg/L in both groups, the effects of CRP gene variants on postoperative plasma CRP levels were large enough to be statistically significant. If we assume that many of the patients with truncated postoperative plasma CRP levels of 300 mg/L in fact had levels greater than 300 mg/L, then our results may in fact underestimate the significance of the association between CRP gene variants and postoperative CRP levels after CABG surgery. Genetic association testing of multiple SNPs to CRP levels at many time points in a large sample population also introduces the potential for false positive findings as a result of multiple testing and over-fitting. After applying the Bonferroni correction to address multiple tests of statistical significance, the rs1800947 remained significantly correlated with altered postoperative plasma CRP levels. While rs3091244 did not survive Bonferroni correction, based on prior studies, we believe its biological significance deserves consideration in future investigations. Inherent bias within the sample population can lead to overfitting and false positive results. Bootstrapping is a statistical re-sampling procedure that alleviates the potential for model overfitting by eliminating bias. Our results show that after applying the bootstrapping procedure, the effect of the genetic variants on postoperative plasma CRP levels remained significantly different, therefore making overfitting unlikely. Finally, recently published results from genome-wide association studies suggest that additional proinflammatory genes (GCKR, HNF1A, LEPR, IL6R, APOE) influence baseline plasma CRP levels in ambulatory populations[20, 21]. It is likely therefore, that a number of genes or a combination thereof, may also influence the acute-phase rise in CRP levels.
Emerging evidence that CRP gene variants associated with elevated baseline plasma CRP levels[16, 32, 36, 41] are heritable [14–16]. We submit that the acute-phase rise in postoperative plasma CRP levels after CABG surgery is influenced by CRP gene variants. Further investigation is needed to clarify the significance of the association between CRP gene variants and the acute-phase rise in postoperative CRP levels with regard to the risk of adverse perioperative outcomes.
TEP was supported in part by the Scholars in Clinical Science Program, Harvard Medical School K30 RR022292. JDM was supported in part by a Bayer Fellowship in Blood Conservation. SCB was supported in part by a K23 HL68774. We acknowledge the outstanding contributory efforts of the CABG Genomics research staff: James Gosnell, RN; Kujtim Bodinaku, MD; Jai Madan, MD, MPH; Svetlana Gorbatov, MPH; Juliette Dean, RN; James Chen, RN; Jacques Estephan, RN and Isabella Canderlaria, BS.
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