The Association of Peroxisome Proliferator-Activated Receptor <i>δ</i> and Additional Gene-Gene Interaction with C-Reactive Protein in Chinese Population

Ding, Xiao-Ying; Yuan, Hao-Zheng; Gu, Ru; Gao, Yan-Feng; Liu, Xiao-Gang; Gao, Ya

doi:https://doi.org/10.1155/2016/8597085

International Journal of Endocrinology

On this page

Abstract Introduction Materials and Methods Results Discussion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2016 | Article ID 8597085 | https://doi.org/10.1155/2016/8597085

The Association of Peroxisome Proliferator-Activated Receptor δ and Additional Gene-Gene Interaction with C-Reactive Protein in Chinese Population

Xiao-Ying Ding,¹Hao-Zheng Yuan,¹Ru Gu,¹Yan-Feng Gao,²Xiao-Gang Liu,³and Ya Gao⁴

Academic Editor: Francesco Perticone

Received24 Sept 2015

Accepted08 Dec 2015

Published13 Jan 2016

Abstract

Aims. To examine the association between 4 single nucleotide polymorphisms (SNPs) of peroxisome proliferator-activated receptors δ (PPARδ) polymorphisms and C-reactive protein (CRP) level and additional gene-gene interaction. Methods. Line regression analysis was performed to verify polymorphism association between SNP and CRP levels. Generalized multifactor dimensionality reduction (GMDR) was employed to analyze the interaction. Results. A total of 1028 subjects (538 men, 490 women) were selected. The carriers of the C allele (TC or CC) of rs2016520 were associated with a significant decreased level of CRP, regression coefficients was −0.338, and standard error was 0.104 (). The carriers of the G allele (CG or GG) of rs9794 were also significantly associated with decreased level of CRP, regression coefficients was −0.219, and standard error was 0.114 (). We also found a potential gene-gene interaction between rs2016520 and rs9794. Subjects with rs2016520-TC or CC, rs9794-CG or GG genotypes have lowest CRP level, difference (95% CI) = −0.50 (−0.69 to −0.21) (), compared to subjects with rs2016520-TT and rs9794-CC genotypes. Conclusions. rs2016520 and rs9794 minor allele of PPARδ and combined effect between the two SNP were associated with decreased CRP level.

1. Introduction

Inflammation is receiving an increasing amount of attention for its potential role in the pathogenesis of a variety of disorders, from insulin resistance and type 2 diabetes mellitus (T2DM) to fatty liver and cardiovascular disease (CVD) [1]. Current evidence shows that C-reactive protein (CRP) level is a plasma protein and a sensitive and dynamic systemic marker of inflammation [2] could be influenced by both clinical and genetic factors [3].

PPARs are orphan nuclear receptors belonging to the steroid, retinoid, and thyroid hormone receptor superfamily of ligand-activated transcription factors [4, 5]. Three distinct receptor types have been cloned and characterized: PPARα, PPARβ/δ, and PPARγ [6]. PPARδ was less studied in previous study, compared with PPARα and PPARγ. Several evidences suggested biological roles for PPARδ in many genotypes [7]. Deletion of PPARδ from foam cells increased the availability of inflammatory suppressors, which in turn reduced atherosclerotic lesions [8]. On the other hand, activation of PPARδ stimulates β-oxidation and triglyceride utilization in adipocytes and myocytes. PPARδ agonists could promote cholesterol accumulation in human macrophages and increase serum high density lipoprotein (HDL) while lowering triglyceride levels in obese animal models [9, 10]. These data collectively implicate PPARδ as being involved in lipid homeostasis and atherogenesis. However, the associations between variants of the PPARδ, corresponding gene-gene interactions with CRP level, were rarely studied. So in this study, we sought to examine the association between 4 PPARδ polymorphisms with CRP level and the additional interaction among the 4 single nucleotide polymorphisms (SNPs).

2. Materials and Methods

2.1. Subjects

This was a cross-sectional study. Chinese participants were consecutively recruited between January 2011 and September 2013. A total of 1096 subjects were included in investigated population, excluded subjects with abnormal increasing of CRP level (≥10 mg/L) because of any reasons, such as infection (), trauma (), and any others factor (), and CRP were missing (), a total of 1028 subjects (538 men, 490 women), with a mean age of years, were included in the study, including the genotyping of polymorphisms. The selected subjects were similar to those who were not selected in terms of age, sex, smoking status, and alcohol consumption. Informed consent was obtained from all participants.

2.2. Body Measurements

Data on demographic information and lifestyle risk factors for all participants were obtained using a standard questionnaire administered by trained staffs. Body weight and height were measured, and body mass index (BMI) was calculated as weight in kilograms divided by the square of the height in meters. Cigarette smokers were those who self-reported smoking cigarettes at least once a day for 1 year or more [11]. Alcohol consumption was expressed as the sum of milliliters of alcohol per week from wine, beer, and spirits [12]. Physical activity was divided into three levels, including light, moderate, and heavy [13]. Blood samples were collected in the morning after at least 8 hours of fasting. All plasma and serum samples were frozen at –80°C until laboratory testing. Plasma glucose was measured using an oxidase enzymatic method. Particle enhanced immune latex agglutination high sensitive assay was used to detect CRP level. All analysis was performed by the same lab.

2.3. Genomic DNA Extraction and Genotyping

We selected SNPs within the PPARδ gene using the following methods: (1) previously reported associations with metabolic abnormalities, (2) known heterozygosity and a minor allele frequency (MAF) greater than 1%. 4 SNPs of PPARδ were selected for genotyping in the study: rs2016520, rs9794, rs1053046, and rs1053049. Genomic DNA from participants was extracted from EDTA-treated whole blood, using the DNA Blood Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. All SNPs were detected by Taqman fluorescence probe. Probe sequences of all SNPs were shown in Table 1. ABI Prism7000 software and allelic discrimination procedure were used for genotyping of aforementioned 4 SNPs. A 25 μL reaction mixture including 1.25 μL SNP Genotyping Assays (20x), 12.5 μL Genotyping Master Mix (2x), and 20 ng DNA and the conditions were as follows: initial denaturation for 10 min and 95°C, denaturation for 15 s and 92°C, annealing and extension for 90 s and 60°C, and 50 cycles.

2.4. Statistical Analysis

The mean and standard deviation (SD) for normally distributed continuous variables and percentages for categorical variable were calculated and compared. The genotype and allele frequencies were obtained by direct count. The categorical data were analyzed using test or the Fisher exact test if necessary. Further, continuous variables were analyzed using Student’s -test or one-way analysis of variance, followed by the least significant difference multiple-range tests for comparison between groups. Hardy-Weinberg equilibrium (HWE) was performed by using SNPStats (available online at http://bioinfo.iconcologia.net/SNPstats). Line regression analysis was performed to verify polymorphism association between SNP with CRP levels using gender, age, smoking and alcohol status, and physical activity as covariates in the model.

Generalized multifactor dimensionality reduction (GMDR) [14] was employed to analyze the interaction among 4 SNPs; some parameters was calculated, including cross-validation consistency, the testing balanced accuracy, and the sign test, to assess each selected interaction. The cross-validation consistency score is a measure of the degree of consistency with which the selected interaction is identified as the best model among all possibilities considered. The testing balanced accuracy is a measure of the degree to which the interaction accurately predicts case-control status with scores between 0.50 (indicating that the model predicts no better than chance) and 1.00 (indicating perfect prediction). Finally, a sign test or a permutation test (providing empirical values) for prediction accuracy can be used to measure the significance of an identified model.

3. Results

A total of 1028 subjects (538 men, 490 women), with a mean age of years, were selected. Minor allele frequencies of rs2016520, rs9794, rs1053046, and rs1053049 were shown in Table 2. All genotypes were distributed according to Hardy-Weinberg equilibrium (all values more than 0.05).

Line regression analysis on association between 4 SNPs and CRP level was conducted (Table 3). We found that the CRP level was lower in the subjects with minor alleles of rs2016520 and rs9794, compared to subjects with wild genotype. Compared to the carriers of the common genotype (rs2016520-TT), the carriers of the C allele (TC + CC) of rs2016520 were associated with a significant decreased level of CRP, regression coefficients were −0.338, and standard error was 0.104 (). Compared to the carriers of the common genotype (rs9794-CC), the carriers of the G allele (CG + GG) of rs9794 were also significantly associated with decreased level of CRP, regression coefficients were −0.219, and standard error was 0.114 (). However, the other 2 SNPs in PPARδ were not significantly associated with CRP level after covariate adjustment.

We employed the GMDR analysis to assess the impact of the interaction among 4 SNPs, after adjustment for covariates including gender, age, smoke and alcohol status, and physical activity. Table 4 summarizes the results obtained from GMDR analysis for two- to four-locus models with covariates adjustment. There was a significant two-locus model () involving rs2016520 and rs9794, indicating a potential gene-gene interaction between rs2016520 and rs9794. Overall, the two-locus models had a cross-validation consistency of 10 and had the testing accuracy of 62.17%.

To obtain ORS and 95% CIs for the joint effects of candidate SNPs (rs2016520 and rs9794) on CRP, we conducted interaction analysis among SNPs in the 2-locus models. Subjects with rs2016520-TC or CC and rs9794-CG or GG genotypes have lowest CRP level, difference (95% CI) = −0.50 (−0.69 to −0.21) (), compared to subjects with rs2016520-TT and rs9794-CC genotypes, after adjustment for gender, age, smoke and alcohol status, and physical activity (Table 5).

4. Discussion

The frequency of the C allele was 24.9% in the present population, which is lower than the proportion in the Han population of Dalian reported by Yu et al. [15], similar to that in Korean populations [16], Swedish populations [17], and Scotland populations [18]. C-reactive protein (CRP) is a well-established biochemical marker of inflammation and has been used to predict future cardiovascular disease, metabolic syndrome, and future development of type 2 diabetes mellitus [3, 19–21]. Current evidence shows that CRP level is a complex trait, influenced by both clinical and genetic factors [3]. Family and twin studies have found that additive genetic factors account for 27–40% of the variance in CRP level [22], suggesting a role for genetic variation in determining serum levels. So it is meaningful to investigate mutation risk factors for level. The results of this study indicated that minor alleles of rs2016520 and rs9794 were associated with lower CRP level, compared to subjects with wild genotype. Compared to the carriers of the common genotype (rs2016520-TT), the carriers of the C allele (TC + CC) of rs2016520 were associated with a significant decreased level of CRP. Compared to the carriers of the common genotype (rs9794-CC), the carriers of the G allele (CG + GG) of rs9794 were also significantly associated with decreased level of CRP. However, the other 2 SNPs in PPARδ were not significantly associated with CRP level after covariate adjustment. In contrast to PPARγ and PPARα, the role of PPARδ in CRP level is less well defined. Gu et al. [23] indicated that rs2016520 in PPARδ was not associated with CRP level both in normal weight and obese subjects in a Chinese population. Liang et al. [24] suggested that PPARδ attenuated CRP-induced proinflammatory effects through CD32 and NF-κB pathway. PPARδ may serve as a more potent therapeutic target than PPARγ in atherosclerosis or inflammatory therapy, and the potency of 1 μM PPARδ is similar to that of 10 μM PPARγ in anti-inflammatory effect.

As we have known that a multiple genotype was influenced by both genetic and environment factors and the genetic factors including many gene mutations, so it is necessary to investigate the synergistic effect of multiple SNP on CRP level. We employed the GMDR analysis to assess the impact of the interaction among the 4 SNPs on CRP level with covariates adjustment. The results indicated a potential gene-gene interaction between rs2016520 and rs9794. Subjects with rs2016520-TC or CC and rs9794-CG or GG genotypes have lowest CRP level, difference (95% CI) = −0.50 (−0.69 to −0.21) (), compared to subjects with rs2016520-TT and rs9794-CC genotypes. In addition, rs9794 was not associated with CRP, but it can significantly affect level when accompanied with rs2016520. These findings indicate that a minor gene (even when its main effects are close to nil) can have a strong effect on level, due to the presence of gene-gene interaction.

Several mechanisms of association between activation of PPARδ and decreased CRP level have been suggested. Liang et al. [24] indicated that untreated endothelial cells express a basal level of PPARδ and PPARδ agonist exerts an anti-inflammatory effect in CRP-treated endothelial cells. We also demonstrated that less concentration of PPARδ than PPARγ agonist is needed to attenuate both CRP-induced adhesion molecules and the ability of monocyte to attach to endothelial cells. PPARδ could attenuate CRP-induced NF-κB activation and VCAM-1 and MCP-1 expression in endothelial cells. Moreover, it was found that the decreased adhesion molecule expression would result in significant fewer monocytes attaching on the CRP-treated endothelial cells [25]. Similar to one of the mechanisms in endothelial cells, activation of PPARδ has been shown to promote the binding of inflammatory suppressor BCL-6 to the promoter of group IIA secretory phospholipase A2, an inflammatory marker for atherosclerosis, and therefore inhibit the inflammation induced by IL-1b in VSMCs [25].

Limitations of this study should be considered. Firstly, only 4 SNPs of PPARδ were chosen. The selected SNPs were not sufficient to capture most genetic information of the PPARδ. Further studies should include more SNPs, even the other PPAR isoforms, such as PPARα or PPARγ. Secondly, there was a relatively small sample size in the study, though the number of study participants met the requirement for analysis; future studies should be conducted in different races. Thirdly, the interaction between gene-environment factors on level should be studied in the future papers.

In conclusion, the results of this study indicated that minor alleles of rs2016520 and rs9794 were associated with lower CRP level, compared to subjects with wild genotype, and we also found a potential gene-gene interaction between rs2016520 and rs9794 on decreased CRP level.

Conflict of Interests

There is no conflict of interests.

Acknowledgments

This work was supported by National Science Foundation of China (30900800), Science and Technology Program of Shan-Xi Province, and the Fundamental Research Funds for the Central Universities. The authors thank all the partners and staffs who help us in the process of this study.

References

S. E. Shoelson and A. B. Goldfine, “Getting away from glucose: fanning the flames of obesity-induced inflammation,” Nature Medicine, vol. 15, no. 4, pp. 373–374, 2009.
View at: Publisher Site | Google Scholar
P. M. Ridker, C. H. Hennekens, J. E. Buring, and N. Rifai, “C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women,” The New England Journal of Medicine, vol. 342, no. 12, pp. 836–843, 2000.
View at: Publisher Site | Google Scholar
T. B. Ledue and N. Rifai, “Preanalytic and analytic sources of variations in C-reactive protein measurement: implications for cardiovascular disease risk assessment,” Clinical Chemistry, vol. 49, no. 8, pp. 1258–1271, 2003.
View at: Publisher Site | Google Scholar
A. L. Bookout, Y. Jeong, M. Downes, R. T. Yu, R. M. Evans, and D. J. Mangelsdorf, “Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network,” Cell, vol. 126, no. 4, pp. 789–799, 2006.
View at: Publisher Site | Google Scholar
L. Michalik, J. Auwerx, J. P. Berger et al., “International Union of Pharmacology. LXI. Peroxisome proliferator-activated receptors,” Pharmacological Reviews, vol. 58, no. 4, pp. 726–741, 2006.
View at: Publisher Site | Google Scholar
L. Guo and R. Tabrizchi, “Peroxisome proliferator-activated receptor γ as a drug target in the pathogenesis of insulin resistance,” Pharmacology and Therapeutics, vol. 111, no. 1, pp. 145–173, 2006.
View at: Publisher Site | Google Scholar
L. Michalik, B. Desvergne, C. Dreyer, M. Gavillet, R. N. Laurini, and W. Wahli, “PPAR expression and function during vertebrate development,” International Journal of Developmental Biology, vol. 46, no. 1, pp. 105–114, 2002.
View at: Google Scholar
C.-H. Lee, A. Chawla, N. Urbiztondo, D. Liao, W. A. Boisvert, and R. M. Evans, “Transcriptional repression of atherogenic inflammation: modulation by PPARδ,” Science, vol. 302, no. 5644, pp. 453–457, 2003.
View at: Publisher Site | Google Scholar
H. Vosper, L. Patel, T. L. Graham et al., “The peroxisome proliferator-activated receptor δ promotes lipid accumulation in human macrophages,” The Journal of Biological Chemistry, vol. 276, no. 47, pp. 44258–44265, 2001.
View at: Publisher Site | Google Scholar
W. R. Oliver Jr., J. L. Shenk, M. R. Snaith et al., “A selective peroxisome proliferator-activated receptor δ agonist promotes reverse cholesterol transport,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 9, pp. 5306–5311, 2001.
View at: Publisher Site | Google Scholar
H. Iida, J. V. Kumar, D. T. Kopycka-Kedzierawski, and R. J. Billings, “Effect of tobacco smoke on the oral health of US women of childbearing age,” Journal of Public Health Dentistry, vol. 69, no. 4, pp. 231–241, 2009.
View at: Publisher Site | Google Scholar
M. S. Freiberg, H. J. Cabral, T. C. Heeren, R. S. Vasan, and R. C. Ellison, “Alcohol consumption and the prevalence of the metabolic syndrome in the US,” Diabetes Care, vol. 27, no. 12, pp. 2954–2959, 2004.
View at: Publisher Site | Google Scholar
G. Hu, J. Tuomilehto, K. Silventoinen, N. Barengo, and P. Jousilahti, “Joint effects of physical activity, body mass index, waist circumference and waist-to-hip ratio with the risk of cardiovascular disease among middle-aged Finnish men and women,” European Heart Journal, vol. 25, no. 24, pp. 2212–2219, 2004.
View at: Publisher Site | Google Scholar
X.-Y. Lou, G.-B. Chen, L. Yan et al., “A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence,” The American Journal of Human Genetics, vol. 80, no. 6, pp. 1125–1137, 2007.
View at: Publisher Site | Google Scholar
X. J. Yu, B. L. Su, X. M. Wang, C. J. Jin, J. M. Qu, and H. J. Feng, “The relationship of some indices of glycometabolism with peroxisome proliferator-activated receptor delta polymorphism,” Chinese Journal of Diabetes, vol. 15, no. 10, pp. 596–597, 2007.
View at: Google Scholar
H. D. Shin, B. L. Park, L. H. Kim et al., “Genetic polymorphisms in peroxisome proliferator-activated receptor δ associated with obesity,” Diabetes, vol. 53, no. 3, pp. 847–851, 2004.
View at: Publisher Site | Google Scholar
J. Skogsberg, K. Kannisto, T. N. Cassel, A. Hamsten, P. Eriksson, and E. Ehrenborg, “Evidence that peroxisome proliferator-activated receptor delta influences cholesterol metabolism in men,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 23, no. 4, pp. 637–643, 2003.
View at: Publisher Site | Google Scholar
J. Skogsberg, A. D. McMahon, F. Karpe, A. Hamsten, C. J. Packard, and E. Ehrenborg, “Peroxisome proliferator activated receptor delta genotype in relation to cardiovascular risk factors and risk of coronary heart disease in hypercholesterolaemic men,” Journal of Internal Medicine, vol. 254, no. 6, pp. 597–604, 2003.
View at: Publisher Site | Google Scholar
P. M. Ridker, “C-reactive protein and the prediction of cardiovascular events among those at intermediate risk: moving an inflammatory hypothesis toward consensus,” Journal of the American College of Cardiology, vol. 49, no. 21, pp. 2129–2138, 2007.
View at: Publisher Site | Google Scholar
T. Yang, C.-H. Chu, P.-C. Hsieh et al., “C-reactive protein concentration as a significant correlate formetabolic syndrome: a Chinese population-based study,” Endocrine, vol. 43, no. 2, pp. 351–359, 2013.
View at: Publisher Site | Google Scholar
B. Gelaye, L. Revilla, T. Lopez et al., “Association between insulin resistance and C-reactive protein among Peruvian adults,” Diabetology and Metabolic Syndrome, vol. 2, no. 1, article 30, 2010.
View at: Publisher Site | Google Scholar
A. J. MacGregor, J. R. Gallimore, T. D. Spector, and M. B. Pepys, “Genetic effects on baseline values of C-reactive protein and serum amyloid a protein: a comparison of monozygotic and dizygotic twins,” Clinical Chemistry, vol. 50, no. 1, pp. 130–134, 2004.
View at: Publisher Site | Google Scholar
S.-J. Gu, D.-H. Chen, Z.-R. Guo, Z.-Y. Zhou, X.-S. Hu, and M. Wu, “Effect of obesity on the association between common variations in the PPAR gene and C-reactive protein level in Chinese Han population,” Endocrine, vol. 48, no. 1, pp. 195–202, 2015.
View at: Publisher Site | Google Scholar
Y.-J. Liang, Y.-C. Liu, C.-Y. Chen et al., “Comparison of PPARδ and PPARγ in inhibiting the pro-inflammatory effects of C-reactive protein in endothelial cells,” International Journal of Cardiology, vol. 143, no. 3, pp. 361–367, 2010.
View at: Publisher Site | Google Scholar
L. Ravaux, C. Denoyelle, C. Monne, I. Limon, M. Raymondjean, and K. El Hadri, “Inhibition of interleukin-1β-induced group IIA secretory phospholipase A2 expression by peroxisome proliferator- activated receptors (PPARs) in rat vascular smooth muscle cells: cooperation between PPAR β and the proto-oncogene BCL-6,” Molecular and Cellular Biology, vol. 27, no. 23, pp. 8374–8387, 2007.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2016 Xiao-Ying Ding et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

907

Downloads

850

Citations