Next Article in Journal
Molecular Docking Studies of a Cyclic Octapeptide-Cyclosaplin from Sandalwood
Next Article in Special Issue
The Steroidogenesis Inhibitor Finasteride Reduces the Response to Both Stressful and Rewarding Stimuli
Previous Article in Journal
Therapeutic Potential of α- and β-Pinene: A Miracle Gift of Nature
Previous Article in Special Issue
ACSL1 Regulates TNFα-Induced GM-CSF Production by Breast Cancer MDA-MB-231 Cells
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association of RS708272 (CETP Gene Variant) with Lipid Profile Parameters and the Risk of Myocardial Infarction in the White Population of Western Siberia

1
Institute of Internal and Preventive Medicine – branch of Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (SB RAS), 630089 Novosibirsk, Russia
2
Federal research center Institute of Cytology and Genetics, SB RAS, 630090 Novosibirsk, Russia
*
Author to whom correspondence should be addressed.
Biomolecules 2019, 9(11), 739; https://doi.org/10.3390/biom9110739
Submission received: 11 October 2019 / Revised: 7 November 2019 / Accepted: 12 November 2019 / Published: 14 November 2019
(This article belongs to the Special Issue Bioactive Lipids in Health and Disease)

Abstract

:
The TaqI B (rs708272) single-nucleotide variant, i.e., the +279 G/A substitution in intron 1 of the CETP gene, is actively investigated as a risk factor of lipid metabolism disorders. The aim of this study was to analyze the association of rs708272 with lipid parameters and the risk of myocardial infarction in the population of Western Siberia (Russia). The study population was selected from a sample surveyed within the framework of the Health, Alcohol and Psychosocial Factors In Eastern Europe (HAPIEE) study (9360 participants, >90% white, aged 45–69 years, males: 50%). In total, 3132 randomly selected patients were included. Plasma lipid levels were determined by standard enzymatic assays. Rs708272 was analyzed by RT-PCR via TaqMan single-nucleotide polymorphism (SNP) Genotyping Assays (Thermo Fisher Scientific, USA). The frequencies of rs708272 genotypes AA (homozygote), AG (heterozygote), and GG were 0.21, 0.49, and 0.30, respectively, in this population. Allele A frequency was 0.46. We found an association of allele G with low levels of high-density lipoprotein cholesterol and a high index of atherogenicity in this population (p < 0.001 and p < 0.001, respectively). Allele G was significantly associated with the risk of myocardial infarction among the male participants (odds ratio 1.96, 95% confidence interval 1.208–3.178, p = 0.008) and in the study population (odds ratio 1.465, 95% confidence interval 1.028–2.087, p = 0.036). Thus, rs708272 is associated with myocardial infarction in the white population of Western Siberia (Russia).

1. Introduction

Cardiovascular diseases (CVDs) are the leading cause of death in developed countries [1]. The lipid metabolism disorder that underlies the atherosclerotic process is one of the main risk factors of CVDs [2]. Genetic markers of predisposition to lipid metabolism disorders can be used for the early diagnosis and for the development of programs for primary prevention of CVD.
There is a correlation between the level of high-density lipoprotein cholesterol (HDL-C) and the risk of CVD; this correlation is in part explainable by the participation of HDL in reverse cholesterol transport [3]. The latter is a process of transfer of cholesterol esters via HDL particles into the liver, with subsequent cholesterol oxidation to bile acids. One of the key proteins taking part in this phenomenon is cholesterol ester transport protein (CETP). This is a hydrophobic glycoprotein regulating the reverse cholesterol transport from peripheral tissues to the liver and participating in the exchange of cholesterol esters and triacylglycerides between various classes of lipoproteins. A change in the activity and concentration of CETP causes disturbances in reverse cholesterol transport as well as transformation of atherosclerosis manifestations [4].
The CETP gene is located in the chromosomal region 16q21, consists of 16 exons, and produces a hydrophobic glycoprotein 476-amino acids long (https://www.ncbi.nlm.nih.gov/gene/1071). Several polymorphisms of CETP are known, including rs5883, rs247616, rs247617, rs1532624, rs1800775, rs3764261, and rs9989419, which lead to changes in the amino acid sequence and/or function of the protein [5,6,7].
TaqI B (rs708272) is the best-studied polymorphism of this gene and is a G > A substitution at position +279 of intron 1, thereby giving rise to alleles B1 and B2. Allele B1 affects the size of the CETP protein, its function, and the HDL-C level. Allele B2 results in a lower molecular weight CETP and in higher HDL-C concentration and—according to some studies—correlates with a lower risk of ischemic heart disease [8,9,10,11]. Other research indicates sex-specific dependence of the associations of the TaqI B polymorphism as well as dependence on the body mass index (BMI), alcohol consumption, and insulin level [12,13]. These effects may be caused by other polymorphisms linked to TaqI B.
Our aim was to analyze the association of rs708272 with lipid profile parameters and with the risk of myocardial infarction in the population of Western Siberia (Russia).

2. Materials and Methods

A cross-sectional epidemiological study of the adult population was conducted in Novosibirsk (Western Siberia, Russia). From the Novosibirsk residents surveyed during 2007–2008 within the framework of the Health, Alcohol and Psychosocial Factors In Eastern Europe (HAPIEE) study [14], we compiled the main representative sample (9360 subjects, 45–69 years old [mean ± standard error: 53.8 ± 7.0 years], >90% whites) by means of a table of random numbers. The study protocol was approved by the Ethics Committee of the Institute of Internal and Preventive Medicine—a branch of the Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences (approval #7 of 22 June 2008). Each participant provided informed consent to be examined and to collection of a blood sample for the study.
The clinical examination program included collection of sociodemographic data, clinical examination, a standard questionnaire on tobacco smoking, anthropometric measurements (height, body weight, and waist circumference), measurement of arterial blood pressure (BP), and assays of biochemical indicators in blood serum (total cholesterol [TC], HDL-C, triglycerides [TGs], and fasting glucose). Blood collection from the median cubital vein was performed in the morning after a 12 h overnight fast. Parameters of the blood lipid profile (TC, TGs, HDL-C, and low-density lipoprotein cholesterol [LDL-C]) were measured by enzymatic assays using standard kits (Biocon Fluitest; Lichtenfels, Germany) on a Labsystem FP-901 biochemical analyzer (Helsinki, Finland). An index of atherogenicity (IA) was calculated via the following formula: IA = (TC − HDL-C)/HDL-C.
For molecular genetic analysis, from the main representative sample, we selected 3132 subjects (hereafter: study population or study subjects) by the random-number method. To isolate DNA from the blood, phenol–chloroform extraction was performed [15]. Genotyping of rs708272 was conducted by means of TaqMan single-nucleotide polymorphism (SNP) Genotyping Assays (Thermo Fisher Scientific, Foster City, CA, USA) and the BioMaster HS-qPCR HI-ROX Kit (Biolabmix, Novosibirsk, Russia) on a StepOnePlus real-time PCR System (Thermo Fisher Scientific). The laboratory personnel performing the genotyping were blinded to the physical and clinical examination data.
Significance of the differences in allele frequencies among the subgroups under study and conformance to the Hardy–Weinberg equilibrium were determined by the χ2 test. Evaluation of differences in mean continuous variables among various genotypes was carried out after adjustment for sex, age, and BMI via the generalized linear model (GLM) in the SPSS software for Windows.

3. Results

The characteristics of the examined subjects are presented in Table 1. Males constituted 48% and females 52% of the study population. The prevalence of arterial hypertension (>140/90 mmHg) was 42.3%, that of type 2 diabetes mellitus 7.9%, and that of dyslipidemia (TC > 200 mg/dL or 5.2 mM) 82.8%.
For rs708272 in the study population, the distribution of genotype frequencies complied with the Hardy–Weinberg equilibrium (χ2 = 1.36). The frequency of allele A of CETP rs708272 in the white population of Western Siberia (Table 2) was consistent with its frequency in the white populations of Eastern and Western Europe (according to gnomAD Genomes European data: G frequency = 0.5541, A frequency = 0.4459 (http://www.ncbi.nlm.nih.gov).
After the analysis of associations of rs708272 with parameters of the blood lipid profile (TC, HDL-C, LDL-C, TGs, and the index of atherogenicity), the differences in mean HDL-C levels among the genotypes were found to be statistically significant in the study population (p < 0.001), among males (p = 0.006) and among females (p < 0.001). The lowest concentrations of HDL-C were registered in allele G carriers (Table 3). In all subgroups, the highest mean index of atherogenicity was noted in genotype GG carriers, and this difference was statistically significant both among females and in the study population (p < 0.001 and p < 0.001, respectively).
In the generalized linear model of the subgroups being studied, we did not detect statistically significant associations of rs708272 with TC, LDL-C, TGs, fasting glucose, BMI, systolic BP, diastolic BP, or heart rate (Table 3).
Thus, we uncovered statistically significant associations of rs708272 genotypes with HDL-C and with the index of atherogenicity in the white population of Western Siberia.
During a 10-year period (2007–2017), in the main representative sample (N = 9360), investigators collected data on new cases of myocardial infarction at the Novosibirsk City Registry of Myocardial Infarctions [16]. During this observation period, 509 new cases of myocardial infraction were registered. In the study population (n = 3132), which was genotyped for rs708272, there were 137 cases of myocardial infarction during the 2007–2017 period. In the white population of Western Siberia, a significant association of rs708272 with myocardial infarction was confirmed among males (Table 4). The carriage of allele G was found to be a risk factor of myocardial infarction.
It should be noted that the presence of allele G in various populations has been linked with changes in the activity of the CETP protein, thus leading to lower HDL-C levels, which can raise the risk of CVDs [6,8,9].

4. Discussion

The individual risk of CVDs depends both on genetic factors and on lifestyle factors. In this study, we present the results of an examination of a white population regarding a possible association of rs708272 (in the CETP gene) with clinical and biochemical parameters. We found that some changes in genomic DNA sequence are independent risk factors of myocardial infarction, in agreement with the findings of other studies [17,18,19,20,21,22,23,24]. The severity of the prognosis depends on the presence of a certain allele or genotype, according to our results.
In our study, rs708272 allele G turned out to be statistically significantly associated with the mean levels of HDL-C in the white population of Western Siberia as well as with the index of atherogenicity among the females in the study population (p < 0.001); a similar association for the index of atherogenicity was noted among males but did not reach significance. Previously, we reported a statistically significant association between the genotypes of polymorphism TaqI B (rs708272) and HDL-C in subgroups defined by different mean TC concentrations [25]. A higher HDL-C level correlated with the B2B2 (GG) genotype in the group of patients with hypercholesterolemia in that study. This finding underscores the importance of not only population-level studies but also research on subjects with specific phenotypes of the lipid profile in order to determine the contribution of genetic factors to the predisposition to common diseases. These observations are consistent with the results of several studies [6,8,9]. For instance, Gilberto Vargas-Alarcon and coworkers demonstrated an association of allele G with a lowered HDL-C concentration and a higher risk of acute coronary syndrome (odds ratio = 1.45, p = 0.036) [8].
In 2016, Guo and colleagues conducted a meta-analysis and revealed a correlation of genotype AA with a higher HDL-C level (as compared to genotype GG carriers; p < 0.001) as well as with an elevated risk of cardiovascular events in allele G carriers (odds ratio = 1.15, p < 0.001) among subjects from Asian and white populations [9]. Previously, a similar association was found for a Chinese population in a meta-analysis by Li Y. et al. in 2013 [26].
For the Russian population, the evaluation of the usefulness of myocardial infarction genetic markers (identified in genome-wide association studies) has yielded inconsistent results [27]. Out of nine single-nucleotide variants (SNVs) associated with myocardial infarction in other white populations, only five SNVs showed an association with myocardial infarction in the white population of Russia [27]. The research on the role of SNVs in the development of pathologies in various populations indicates their clinical value and allows investigators to select the most reliable markers manifesting an association not only with the main pathological phenotype but also with its risk factors.
We uncovered an independent statistically significant contribution of the rs708272 SNV to the risk of myocardial infarction among males in the white population of Western Siberia. A sex-specific association of rs708272 with the blood lipid level but not the risk of CVD was demonstrated by Cai G. and coworkers in the Asian Han population in 2018 [28]. In our study, the absence of a statistically significant association of rs708272 with the risk of myocardial infarction in females is probably related to the development of ischemic heart disease in females at a later age as compared to males [29,30,31].
The present study has some limitations. We examined only rs708272 and traditional cardiovascular risk factors and thus could not rule out the influence of other factors, including lifestyle factors, that may affect the results of observational studies.
The research into genetic risk factors of CVDs is important for the development of primary-prevention programs, considering that it is possible to determine genetic variation before the first clinical manifestations of the disease. In addition, the information about genetic risk factors of the disease may help to optimize the clinical management of the patients.

Author Contributions

S.S.: genetic part of the work and participation in the discussion; E.S.: analysis and interpretation of the data, drafting of the manuscript, and participation in the discussion; P.O.: genetic part of the work; D.I.: data analysis and participation in the discussion; S.M.: analysis of the clinical data; V.G.: analysis of the data from the Novosibirsk City Registry of Myocardial Infarction; Y.R.: analysis of the biochemical data; M.V.: study conception and design and critical revision of the manuscript; all the coauthors have read and approved the final manuscript.

Funding

The molecular genetic study was conducted within the framework of Russian Foundation for Basic Research project No. 17-06-01045 and as part of the main topic in state assignment No. 0259-2019-0009 (АААА-А19-119100990053-4). The clinical examination of patients was conducted as part of the main topic in state assignment No. 0324-2018-0001 (АААА-А17-117112850280-2).

Acknowledgments

The English language was corrected and certified by shevchuk-editing.com. The authors are grateful to Vladimir N. Maksimov (the Laboratory of Molecular Genetic Investigations of Therapeutic Diseases, the Institute of Internal and Preventive Medicine – a branch of the Institute of Cytology and Genetics, SB RAS) for the technical assistance. The authors thank the patients for participation in this study.

Conflicts of Interest

The authors declare that they have no conflicts of interest associated with publication of this article.

Abbreviations

CVDcardiovascular disease
HDL-Chigh-density lipoprotein cholesterol
LDL-Clow-density lipoprotein cholesterol
PCRpolymerase chain reaction
SNVsingle-nucleotide variant
TCtotal cholesterol
TGstriglycerides

References

  1. Nielsen, S.H.; Mouton, A.J.; DeLeon-Pennell, K.Y.; Genovese, F.; Karsdal, M.; Lindsey, M.L. Understanding cardiac extracellular matrix remodeling to develop biomarkers of myocardial infarction outcomes. Matrix Biol. 2019, 75–76, 43–47. [Google Scholar] [CrossRef] [PubMed]
  2. Lewington, S.; Whitlock, G.; Clarke, R.; Sherliker, P.; Emberson, J.; Halsey, J.; Qizilbash, N.; Peto, R.; Collins, R. Blood cholesterol and vascular mortality by age, sex, and blood pressure: A meta-analysis of individual data from 61 prospective studies with 55,000 vascular deaths. Lancet 2007, 370, 1829–1839. [Google Scholar] [CrossRef] [PubMed]
  3. Bruce, C.; Chouinard, R.A., Jr.; Tall, A.R. Plasma lipid transfer proteins, high-density lipoproteins, and reverse cholesterol transport. Annu. Rev. Nutr. 1998, 18, 297–330. [Google Scholar] [CrossRef] [PubMed]
  4. Khera, A.V.; Cuchel, M.; de la Llera-Moya, M.; Rodrigues, A.; Burke, M.F.; Jafri, K.; French, B.C.; Phillips, J.A.; Mucksavage, M.L.; Wilensky, R.L.; et al. Cholesterol Efflux Capacity, High-Density Lipoprotein Function, and Atherosclerosis. N. Engl. J. Med. 2011, 364, 127–135. [Google Scholar] [CrossRef]
  5. Paththinige, C.S.; Sirisena, N.D.; Dissanayake, V.H.W. Genetic determinants of inherited susceptibility to hypercholesterolemia—A comprehensive literature review. Lipids Health Dis. 2017, 16, 103. [Google Scholar] [CrossRef]
  6. Iwanicka, J.; Iwanicki, T.; Niemiec, P.; Balcerzyk, A.; Krauze, J.; Górczyńska-Kosiorz, S.; Ochalska-Tyka, A.; Grzeszczak, W.; Żak, I. Relationship between CETP gene polymorphisms with coronary artery disease in Polish population. Mol. Biol. Rep. 2018, 45, 1929–1935. [Google Scholar] [CrossRef]
  7. Arikan, G.D.; Isbir, S.; Yilmaz, S.G.; Isbir, T. Characteristics of coronary artery disease patients who have a polymorphism in the cholesterol ester transfer protein (CETP) gene. In Vivo 2019, 33, 787–792. [Google Scholar] [CrossRef]
  8. Vargas-Alarcon, G.; Perez-Mendez, O.; Herrera-Maya, G.; Garcia-Sanchez, C.; Martinez-Rios, M.A.; Peña-Duque, M.A.; Posadas-Sanchez, R.; Posadas-Romero, C.; Escobedo, G.; Fragoso, J.M. CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome. Lipids 2018, 53, 157–166. [Google Scholar] [CrossRef]
  9. Guo, S.X.; Yao, M.H.; Ding, Y.S.; Zhang, J.Y.; Yan, Y.Z.; Liu, J.M.; Zhang, M.; Rui, D.S.; Niu, Q.; Jia, H.; et al. Associations of Cholesteryl Ester Transfer Protein TaqIB Polymorphism with the Composite Ischemic Cardiovascular Disease Risk and HDL-C Concentrations: A Meta-Analysis. Int. J. Env. Res. Public Health 2016, 13, 882. [Google Scholar] [CrossRef]
  10. Nagano, M.; Yamashita, S.; Hirano, K.; Takano, M.; Maruyama, T.; Ishihara, M.; Sagehashi, Y.; Kujiraoka, T.; Tanaka, K.; Hattori, H.; et al. Molecular mechanisms of cholesterol ester transfer protein deficiency in Japanese. J. Atheroscler. Thromb. 2004, 11, 110–121. [Google Scholar] [CrossRef]
  11. Kuivenhoven, J.A.; de Knijff, P.; Boer, J.M.; Smalheer, H.A.; Botma, G.J.; Seidell, J.C.; Kastelein, J.J.; Pritchard, P.H. Heterogeneity at the CETP gene locus: Influence on plasma CETP concentrations and HDL cholesterol levels. Arterioscler. Thromb. Vasc. Biol. 1997, 17, 560–568. [Google Scholar] [CrossRef] [PubMed]
  12. Anagnostopoulou, K.K.; Kolovou, G.D.; Kostakou, P.M.; Mihas, C.; Hatzigeorgiou, G.; Marvaki, C.; Degiannis, D.; Mikhailidis, D.P.; Cokkinos, D.V. Sex-associated effect of CETP and LPL polymorphisms on postprandial lipids in familial hypercholesterolaemia. Lipids Health Dis. 2009, 8, 24. [Google Scholar] [CrossRef] [PubMed]
  13. Odorvas, J.M.; Cupples, L.A.; Corella, D.; Otvos, J.D.; Osgood, D.; Martinez, A.; Lahoz, C.; Coltell, O.; Wilson, P.W.; Schaefer, E.J. Association of cholesteryl ester transfer protein—TaqI B polymorphism with variations in lipoprotein subclasses and coronary heart disease risk: The Framingham study. Arter. Thromb. Vasc. Biol. 2000, 20, 1323–1329. [Google Scholar] [CrossRef]
  14. Peasey, A.; Bobak, M.; Kubinova, R.; Malyutina, S.; Pajak, A.; Tamosiunas, A.; Pikhart, H.; Nicholson, A.; Marmot, M. Determinants of cardiovascular disease and other non-communicable diseases in Central and Eastern Europe: Rationale and Design of the HAPIEE study. BMC Public Health 2006, 6, 255–264. [Google Scholar] [CrossRef]
  15. Sambrook, J.; Russel, D.W. Purification of nucleic acids by extraction with phenol:chloroform. CSH Protoc. 2006, 1. [Google Scholar] [CrossRef]
  16. Gafarov, V.; Gafarova, A. Who programs: “register acute myocardial infarction”, “Monica”—Dynamics acute cardiovascular accident at years 1977–2009 in general population aged 25–64 years in Russia. Rus. J. Cardiol. 2016, 132, 129–134. [Google Scholar] [CrossRef]
  17. Khera, A.V.; Emdin, C.A.; Drake, I.; Natarajan, P.; Bick, A.G.; Cook, N.R.; Chasman, D.I.; Baber, U.; Mehran, R.; Rader, D.J.; et al. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N. Engl. J. Med. 2016. [Google Scholar] [CrossRef]
  18. Tada, H.; Melander, O.; Louie, J.Z.; Catanese, J.J.; Rowland, C.M.; Devlin, J.J.; Kathiresan, S.; Shiffman, D. Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history. Eur. Heart J. 2016, 37, 561–567. [Google Scholar] [CrossRef]
  19. Mega, J.L.; Stitziel, N.O.; Smith, J.G.; Chasman, D.I.; Caulfield, M.; Devlin, J.J.; Nordio, F.; Hyde, C.; Cannon, C.P.; Sacks, F.; et al. Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: An analysis of primary and secondary prevention trials. Lancet 2015, 385, 2264–2271. [Google Scholar] [CrossRef]
  20. Brautbar, A.; Pompeii, L.A.; Dehghan, A.; Ngwa, J.S.; Nambi, V.; Virani, S.S.; Rivadeneira, F.; Uitterlinden, A.G.; Hofman, A.; Witteman, J.C.; et al. A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies. Atherosclerosis 2012, 223, 421–426. [Google Scholar] [CrossRef]
  21. Thanassoulis, G.; Peloso, G.M.; Pencina, M.J.; Hoffmann, U.; Fox, C.S.; Cupples, L.A.; Levy, D.; D’Agostino, R.B.; Hwang, S.J.; O’Donnell, C.J. A genetic risk score is associated with incident cardiovascular disease and coronary artery calcium: The Framingham Heart Study. Circ. Cardiovasc. Genet. 2012, 5, 113–121. [Google Scholar] [CrossRef] [PubMed]
  22. Ripatti, S.; Tikkanen, E.; Orho-Melander, M.; Havulinna, A.S.; Silander, K.; Sharma, A.; Guiducci, C.; Perola, M.; Jula, A.; Sinisalo, J.; et al. A multilocus genetic risk score for coronary heart disease: Case-control and prospective cohort analyses. Lancet 2010, 376, 1393–1400. [Google Scholar] [CrossRef]
  23. Stenlund, H.; Lönnberg, G.; Jenkins, P.; Norberg, M.; Persson, M.; Messner, T.; Boman, K.; Pearson, T.; Wall, S.; Nyström, L.; et al. Fewer deaths from cardiovascular disease than expected from the Systematic Coronary Risk Evaluation chart in a Swedish population. Eur. J. Cardiovasc. Prev. Rehabil. 2009. [Google Scholar] [CrossRef] [PubMed]
  24. Lloyd-Jones, D.M.; Wilson, P.W.; Larson, M.G.; Beiser, A.; Leip, E.P.; D’Agostino, R.B.; Lévy, D. Framingham risk score and prediction of lifetime risk for coronary heart disease. Am. J. Cardiol. 2004, 94, 20–24. [Google Scholar] [CrossRef] [PubMed]
  25. Shakhtshneider, E.V.; Kulikov, I.V.; Maksimov, V.N.; Ragino, Y.I.; Ivanova, M.V.; Voevoda, M.I. CETP Gene Polymorphism in the Caucasian Population of West Siberia and in Groups Contrast by Total Serum Cholesterol Levels. Bull. Exp. Biol. Med. 2014, 157, 364–367. [Google Scholar] [CrossRef]
  26. Li, Y.Y.; Wu, X.Y.; Xu, J.; Qian, Y.; Zhou, C.W.; Wang, B. ApoA5 -1131T/C, FgB -455G/A, -148C/T and CETP Taq1B gene polymorphisms and coronary artery disease in the Chinese population: A meta-analysis of 15,055 subjects. Mol. Biol. Rep. 2013, 40, 1997–2014. [Google Scholar] [CrossRef]
  27. Maksimov, V.N.; Orlov, P.S.; Ivanova, A.A.; Lozhkina, N.G.; Kuimov, A.D.; Savchenko, S.V.; Novoselov, V.P.; Voevoda, M.I.; Malyutina, S.K. Complex Evaluation of the Significance of Populational Genetic Markers Associated with Myocardial Infarction and Risk Factors. Russ. J. Cardiol. 2017, 33–41. [Google Scholar] [CrossRef]
  28. Cai, G.; Shi, G.; Huang, Z. Gender specific effect of CETP rs 708272 polymorphism on lipid and atherogenic index of plasma levels but not on the risk of coronary artery disease: A case-control study. Medicine (Baltimore) 2018, 97, e13514. [Google Scholar] [CrossRef]
  29. Regitz-Zagrosek, V.; Kararigas, G. Mechanistic Pathways of Sex Differences in Cardiovascular Disease. Physiol. Rev. 2017, 97, 1–37. [Google Scholar] [CrossRef]
  30. Mehta, L.S.; Beckie, T.M.; DeVon, H.A.; Grines, C.L.; Krumholz, H.M.; Johnson, M.N.; Lindley, K.J.; Vaccarino, V.; Wang, T.Y.; Watson, K.E.; et al. Acute myocardial infarction in women. A scientific statement from the American Heart Association. Circulation 2016, 133, 916–947. [Google Scholar] [CrossRef]
  31. Balaian, N.M.; Shebzukhova, M.M.; Grachev, N.S.; Muradianc, A.A.; Shostak, N.A. A comparison of gender differences in clinical and angiographic characteristics in young adults with myocardial infarction. Bull. RSMU 2016, 5, 41–47. [Google Scholar] [CrossRef]
Table 1. Characteristics of study subjects from the population of Western Siberia (Russia).
Table 1. Characteristics of study subjects from the population of Western Siberia (Russia).
MalesFemalesBoth Sexes
Number of subjects150316283132
Age, years56.6 ± 0.256.5 ± 0.256.5 ± 0.1
TC, mg/dL235.5 ± 1.4253.4 ± 1.5244.8 ± 1.1
HDL-C, mg/dL57.9 ± 0.460.8 ± 0.559.4 ± 0.3
LDL-C, mg/dL115.9 ± 1.2127.6 ± 1.3122 ± 0.9
TGs, mg/dL136.1 ± 2143.1 ± 2.1139.8 ± 1.5
Index of atherogenicity2.8 ± 0.032.9 ± 0.032.8 ± 0.03
Fasting glucose, mmol/L5.7 ± 0.065.7 ± 0.065.7 ± 0.04
Body mass index, kg/m226.5 ± 0.129.7 ± 0.128.1 ± 0.1
Waist circumference, cm94.8 ± 0.392.3 ± 0.493.5 ± 0.2
Systolic blood pressure, mmHg143.1 ± 0.6143.6 ± 0.6143.4 ± 0.4
Diastolic blood pressure, mmHg90 ± 0.389.8 ± 0.389.9 ± 0.2
Heart rate, bpm71.5 ± 0.371.7 ± 0.371.6 ± 0.2
* Continuous variables are presented as mean ± standard error. TGs, triglycerides; TC, total cholesterol; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol.
Table 2. Frequencies of alleles and genotypes of rs708272.
Table 2. Frequencies of alleles and genotypes of rs708272.
MalesFemalesBoth Sexes
%%%
Genotypes
AA0.22
n = 334
0.21
n = 336
0.21
n = 670
AG0.47
n = 707
0.50
n = 815
0.49
n = 1522
GG0.31
n = 463
0.29
n = 477
0.30
n = 940
Alleles
A0.45710.45660.4568
G0.54280.54330.5431
n: the number of individuals (3132 total).
Table 3. Analysis of rs708272 association with parameters of the blood lipid profile and with results of the clinical examination in the white population of Western Siberia (n = 3132).
Table 3. Analysis of rs708272 association with parameters of the blood lipid profile and with results of the clinical examination in the white population of Western Siberia (n = 3132).
SexGenotypeTC, mg/dLHDL-C, mg/dLLDL-C, mg/dLTGs, mg/dLIndex of AtherogenicityFasting Glucose, mM BMI, kg/m2Systolic BP, mmHgDiastolic BP, mmHgHeart Rate, bpm
MalesAA238.5 ± 359.6 ± 0.8115.3 ± 2.5140.5 ± 4.72.72 ± 0.075.85 ± 0.1426.4 ± 0.2144 ± 1.390.2 ± 0.871.8 ± 0.7
AG236.3 ± 2.158.2 ± 0.6116.8 ± 1.7135.2 ± 2.82.78 ± 0.055.57 ± 0.0726.5 ± 0.2143.5 ± 0.990.5 ± 0.571.6 ± 0.5
GG232.1 ± 2.456.2 ± 0.7114.9 ± 2.1134.5 ± 3.72.86 ± 0.075.79 ± 0.1126.4 ± 0.2141.8 ± 1.189.1 ± 0.671.2 ± 0.6
p 0.3170.006 *0.5780.6310.2260.060.9480.4280.2650.734
FemalesAA251.5 ± 3.365.3 ± 1.7123.7 ± 3.1137.7 ± 4.62.62 ± 0.075.69 ± 0.1229.6 ± 0.3144.6 ± 1.490.3 ± 0.771.2 ± 0.6
AG254.9 ± 2.359.9 ± 0.5128.7 ± 1.9146.3 ± 3.12.94 ± 0.055.75 ± 0.0929.8 ± 0.9143 ± 0.989.5 ± 0.571.9 ± 0.4
GG252.3 ± 2.759.1 ± 0.6128.3 ± 2.3141.5 ± 3.62.99 ± 0.075.59 ± 0.0929.6 ± 0.3144.1 ± 1.190 ± 0.671.8 ± 0.5
p 0.426<0.001 *0.3140.152<0.001 *0.4520.8380.3540.4610.532
Both sexesAA245 ± 2.262.5 ± 1119.5 ± 2139.1 ± 3.32.67 ± 0.055.77 ± 0.0928 ± 0.2144.3 ± 190.3 ± 0.571.5 ± 0.4
AG246.2 ± 1.659.1 ± 0.4123.2 ± 1.3141.1 ± 2.12.87 ± 0.045.67 ± 0.0628.3 ± 0.1143.2 ± 0.690 ± 0.371.7 ± 0.3
GG242.4 ± 1.857.7 ± 0.5121.7 ± 1.6138 ± 2.62.93 ± 0.055.68 ± 0.0728 ± 0.2143 ± 0.889.6 ± 0.471.5 ± 0.4
p 0.426<0.001 *0.3140.152<0.001 *0.4520.8380.3540.4610.532
The data are presented as mean ± standard error. BMI, body mass index; BP, blood pressure. * Statistically significant.
Table 4. The association of rs708272 with myocardial infarction in the white population of Western Siberia (n = 3132).
Table 4. The association of rs708272 with myocardial infarction in the white population of Western Siberia (n = 3132).
SexGenotypeSubgroupMyocardial Infarction CasesOR (95% CI)p
n%n%
MalesAA32322.51115.70.641 (0.333–1.235)0.238
AG68047.42738.60.696 (0.426–1.139)0.177
GG43130.13245.71.960 (1.208–3.178)0.008 *
FemalesAA32320.71319.40.923 (0.497–1.711)0.878
AG781503450.71.029 (0.631–1.678)1.000
GG45729.32029.91.028 (0.602–1.754)0.892
Both sexesAA64621.62417.50.770 (0.491–1.206)0.287
AG146148.96144.50.838 (0.594–1.183)0.337
GG88029.55238.01.465 (1.028–2.087)0.036 *
* Statistically significant. OR: odds ratio, CI: confidence interval.

Share and Cite

MDPI and ACS Style

Semaev, S.; Shakhtshneider, E.; Orlov, P.; Ivanoshchuk, D.; Malyutina, S.; Gafarov, V.; Ragino, Y.; Voevoda, M. Association of RS708272 (CETP Gene Variant) with Lipid Profile Parameters and the Risk of Myocardial Infarction in the White Population of Western Siberia. Biomolecules 2019, 9, 739. https://doi.org/10.3390/biom9110739

AMA Style

Semaev S, Shakhtshneider E, Orlov P, Ivanoshchuk D, Malyutina S, Gafarov V, Ragino Y, Voevoda M. Association of RS708272 (CETP Gene Variant) with Lipid Profile Parameters and the Risk of Myocardial Infarction in the White Population of Western Siberia. Biomolecules. 2019; 9(11):739. https://doi.org/10.3390/biom9110739

Chicago/Turabian Style

Semaev, Sergey, Elena Shakhtshneider, Pavel Orlov, Dinara Ivanoshchuk, Sophia Malyutina, Valery Gafarov, Yuliya Ragino, and Mikhail Voevoda. 2019. "Association of RS708272 (CETP Gene Variant) with Lipid Profile Parameters and the Risk of Myocardial Infarction in the White Population of Western Siberia" Biomolecules 9, no. 11: 739. https://doi.org/10.3390/biom9110739

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop