The effect of polycyclic aromatic hydrocarbon biomarkers on cardiovascular diseases
-
Nie Qigang
Abstract
Polycyclic aromatic hydrocarbon (PAHs) are part of particulate matter (PM), which is produced from incomplete combustion of organic matter. Biomarkers mean biological indicators, molecules that indicate a normal or abnormal process in the body and may be a sign of a condition or disease. Studies show that PAHs increase the risk of cardiovascular diseases through processes such as oxidative stress, inflammation and atherosclerosis. The present study focused on the evaluation of health effects PAHs biomarkers on cardiovascular diseases (CVD). In this narrative study, data were collected from databases such as Scopus, PubMed, Web of science and Google Scholar in the period 1975–2023. After screening, duplicate and irrelevant articles were removed. Finally, 68 articles related to the effect of PAHs on CVD were included in the study. In addition to the articles found through the search in databases, another 18 articles from the references of the selected articles were included. According to the finding in during the biotransformation of PAH, a number of metabolites are made, such as phenols, diols, quinones, and epoxides. Phenolic isomers have the highest percentage and biomarkers used for their detection include 2-OHNAP used to trace naphthalene from heating processed food, 3-OHPHEN used to trace phenanthrene from diesel, 2-OHFLU used to trace fluorene and 1-OHPYR used to trace pyrene from cigarette and hookah smoke. According to the result, increasing blood pressure and heart rate and causing atherosclerosis are the main complications due to exposure to PAH metabolite on cardiovascular system. The most important agents that causes this affects including increased homocysteine, cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), serum biomarkers of C-reactive protein, and triglycerides. Result this study showed that cardiovascular diseases risk is increased by exposure to PAH biomarkers from smoking, car emissions, occupational exposure, and incinerators. Therefore, strict controls should be implemented for sources of PAH production and exposure.
Acknowledgments
The authors are grateful to Ahvaz Jundishapur University of Medical Sciences for providing necessary facilities to perform this research.
-
Ethical approval: The conducted research is not related to either human or animal use.
-
Informed consent: Not applicable.
-
Disclosure: No potential conflict of interest was reported by the authors.
-
Consent to participate: ‘Not applicable’ for that specific section.
-
Author contributions: NQ, AA, A-AR-C, AT-J, M-JM, MA-G, EF, PA, S-KM, PK, FM-K, MH and FK were principal investigators of the study and drafted the manuscript. NQ, AA, M-JM, and FK were advisors of the study. NQ, AA, A-AR-C, AT-J, M-JM, MA-G, EF, PA, S-KM, PK, FM-K, MH and FK performed the statistical analysis. All authors contributed to the design and data analysis and assisted in the preparation of the final version of the manuscript. All authors read and approved the final version of the manuscript.
-
Competing interests: The authors declare that they have no competing interests.
-
Research funding: This work wasn’t financially supported.
-
Data availability: Not applicable.
References
1. Vichi, S, Pizzale, L, Conte, LS, Buxaderas, S, López-Tamames, E. Simultaneous determination of volatile and semi-volatile aromatic hydrocarbons in virgin olive oil by headspace solid-phase microextraction coupled to gas chromatography/mass spectrometry. J Chromatogr A 2005;1090:146–54. https://doi.org/10.1016/j.chroma.2005.07.007.Search in Google Scholar PubMed
2. Goudarzi, G, Alavi, N, Babaei, AA, Geravandi, S, Idani, E, Salmanzadeh, S, et al.. Investigation of ambient polycyclic aromatic hydrocarbons in a populated middle eastern city. Polycycl Aromat Comp 2020;42:1978–93. https://doi.org/10.1080/10406638.2020.1823857.Search in Google Scholar
3. Israa Ibrahim, L, Neran Adnan, A. Measuring pollution based on total petroleum hydrocarbons and total organic carbon in Tigris River, Maysan Province, Southern Iraq. Casp J Environ Sci 2021;19:535–45.Search in Google Scholar
4. Li, T, Wang, Y, Guo, S, Li, X, Xu, Y, Wang, Y, et al.. Effect of polarity-reversal on electrokinetic enhanced bioremediation of Pyrene contaminated soil. Electrochim Acta 2016;187:567–75. https://doi.org/10.1016/j.electacta.2015.11.097.Search in Google Scholar
5. Rafiee, A, Hoseini, M, Akbari, S, Mahabee-Gittens, EM. Exposure to polycyclic aromatic hydrocarbons and adverse reproductive outcomes in women: current status and future perspectives. Rev Environ Health 2024;39:305–11. https://doi.org/10.1515/reveh-2022-0182.Search in Google Scholar PubMed PubMed Central
6. Freeman, DJ, Cattell, FC. Woodburning as a source of atmospheric polycyclic aromatic hydrocarbons. Environ Sci Technol 1990;24:1581–5. https://doi.org/10.1021/es00080a019.Search in Google Scholar
7. Westerholm, RN, Alsberg, TE, Frommelin, ÅB, Strandell, ME, Rannug, U, Winquist, L, et al.. Effect of fuel polycyclic aromatic hydrocarbon content on the emissions of polycyclic aromatic hydrocarbons and other mutagenic substances from a gasoline-fueled automobile. Environ Sci Technol 1988;22:925–30. https://doi.org/10.1021/es00173a010.Search in Google Scholar PubMed
8. Goudarzi, G, Idani, E, Alavi, N, Salmanzadeh, S, Babaei, AA, Geravandi, S, et al.. Association of polycyclic aromatic hydrocarbons of the outdoor air in Ahvaz, southwest Iran during warm-cold season. Toxin Rev 2017;36:282–9. https://doi.org/10.1080/15569543.2017.1304422.Search in Google Scholar
9. Cervena, T, Vrbova, K, Rossnerova, A, Topinka, J, Rossner, PJr. Short-term and long-term exposure of the MucilAir™ model to polycyclic aromatic hydrocarbons. Altern Lab Anim 2019;47:9–18. https://doi.org/10.1177/0261192919841484.Search in Google Scholar PubMed
10. McGregor, DB. Risk of cancer of the colon and rectum in firemen. Canada: desLibris; 2007:20–33 pp.Search in Google Scholar
11. Rottapel, RE, Hudson, LB, Folta, SC. Cardiovascular health and African-American women: a qualitative analysis. Am J Health Behav 2021;45:735–45. https://doi.org/10.5993/ajhb.45.4.12.Search in Google Scholar PubMed
12. Shmakova, N, Puzin, S, Zarariy, N, Abol, А. The characteristics of the impaired functions and life limitations of the disabled people due to the coronary heart disease. J Popul Ther Clin Pharmacol 2022;29:e62–70. https://doi.org/10.47750/jptcp.2022.888.Search in Google Scholar PubMed
13. Goudarzi, G, Geravandi, S, Alavi, N, Idani, E, Salmanzadeh, S, Yari, AR, et al.. Association between cancer risk and polycyclic aromatic hydrocarbons’ exposure in the ambient air of Ahvaz, southwest of Iran. Int J Biometeorol 2018;62:1461–70. https://doi.org/10.1007/s00484-018-1543-1.Search in Google Scholar PubMed
14. Wuraola, M, Kamyshnikova, LA, Veysalov, SE, Sviridova, MS, Obolonkova, NI, Gayvoronskaya, MA, et al.. Investigation on the association of cardiovascular markers with severity of chronic pyelonephritis. Arch Razi Inst 2022;77:315–21. https://doi.org/10.22092/ARI.2021.356614.1883.Search in Google Scholar PubMed PubMed Central
15. Bassey, IE, Akpan, UO, Nehemiah, ED, Arekong, R, Okonkwo, OL, Udoh, AE. Cardiovascular disease risk factors and cardiac markers among male cement workers in Calabar, Nigeria. J Chem Health Risks 2017;7:85–94.Search in Google Scholar
16. Goli, F, Ghorbani-Zavareh, N, Sadeghi, M, Amirpur, A, Roohafza, H. From the heart to heart; the communicative problems and resources in the cardiology service. Int J Body Mind Cult 2022;8:216–34.Search in Google Scholar
17. Portugal-Cohen, M, Oron, M, Cohen, D, Ma’or, Z. Antipollution skin protection–a new paradigm and its demonstration on two active compounds. Clin Cosmet Invest Dermatol 2017;10:185. https://doi.org/10.2147/ccid.s129437.Search in Google Scholar
18. Dastoorpoor, M, Sekhavatpour, Z, Masoumi, K, Mohammadi, MJ, Aghababaeian, H, Khanjani, N, et al.. Air pollution and hospital admissions for cardiovascular diseases in Ahvaz, Iran. Sci Total Environ 2019;652:1318–30. https://doi.org/10.1016/j.scitotenv.2018.10.285.Search in Google Scholar PubMed
19. Hameed, S, Abdulqader Jasim, H, Sharief, M. Effect of serum level of human epididymis protein 4 and interleukin-6 as biomarkers in patients with adnexal mass. Arch Razi Inst 2022;77:1659–71. https://doi.org/10.22092/ARI.2022.358329.2194.Search in Google Scholar PubMed PubMed Central
20. Hisamuddin, NH, Jalaludin, J. Children’s exposure to polycyclic aromatic hydrocarbon (PAHs): a review on urinary 1-hydroxypyrene and associated health effects. Rev Environ Health 2023;38:151–68. https://doi.org/10.1515/reveh-2021-0013.Search in Google Scholar PubMed
21. Vasan, RS. Biomarkers of cardiovascular disease: molecular basis and practical considerations. Circulation 2006;113:2335–62. https://doi.org/10.1161/circulationaha.104.482570.Search in Google Scholar
22. Siddeek, RAT, Gupta, A, Gupta, S, Goyal, B, Gupta, AK, Agrawal, S, et al.. Evaluation of platelet distribution width as novel biomarker in gall bladder cancer. J Carcinog 2020;19:1–8. https://doi.org/10.4103/jcar.jcar_12_20. PMID: 33033461.Search in Google Scholar PubMed PubMed Central
23. Domínguez-Morueco, N, Schuhmacher, M, Sierra, J, Nadal, M, Domingo, JL. Assessment of PAH loss in passive air samplers by the effect of temperature. Atmos Pollut Res 2016;7:142–6. https://doi.org/10.1016/j.apr.2015.08.005.Search in Google Scholar
24. Daurbekov, T, Koysultanov, M, Alyautdinova, A, Sozonov, A, Kuzn, NKI, Kuzn, I. Features of the organization of activities in the field of prevention of cardiovascular disease. J Comp Med Res 2022;13:49–52. https://doi.org/10.5455/jcmr.2022.13.01.08.Search in Google Scholar
25. Besis, A, Tsolakidou, A, Balla, D, Samara, C, Voutsa, D, Pantazaki, A, et al.. Toxic organic substances and marker compounds in size-segregated urban particulate matter-Implications for involvement in the in vitro bioactivity of the extractable organic matter. Environ Pollut 2017;230:758–74. https://doi.org/10.1016/j.envpol.2017.06.096.Search in Google Scholar PubMed
26. Isaac, P, Martínez, FL, Bourguignon, N, Sánchez, LA, Ferrero, MA. Improved PAHs removal performance by a defined bacterial consortium of indigenous Pseudomonas and actinobacteria from Patagonia, Argentina. Int Biodeterior Biodegrad 2015;101:23–31. https://doi.org/10.1016/j.ibiod.2015.03.014.Search in Google Scholar
27. Boehm, PD. Polycyclic aromatic hydrocarbons (PAHs). Environmental forensics. US: Elsevier; 1964:313–37 pp. https://doi.org/10.1016/B978-0-12-507751-4.X5021-6.Search in Google Scholar
28. Ravindra, K, Sokhi, R, Van Grieken, R. Atmospheric polycyclic aromatic hydrocarbons: source attribution, emission factors and regulation. Atmos Environ 2008;42:2895–921. https://doi.org/10.1016/j.atmosenv.2007.12.010.Search in Google Scholar
29. Menzie, CA, Potocki, BB, Santodonato, J. Exposure to carcinogenic PAHs in the environment. Environ Sci Technol 1992;26:1278–84. https://doi.org/10.1021/es00031a002.Search in Google Scholar
30. Brunekreef, B, Janssen, N, de Hartog, JJ, Oldenwening, M, Meliefste, K, Hoek, G, et al.. Personal, indoor, and outdoor exposures to PM2. 5 and its components for groups of cardiovascular patients in Amsterdam and Helsinki. Res Rep 2005:1–70.Search in Google Scholar
31. Arenas-Huertero, F, Apátiga-Vega, E, Miguel-Pérez, G, Villeda-Cuevas, D, Trillo-Tinoco, J. Molecular markers associated with the biological response to aromatic hydrocarbons from urban air in humans. Air Pollut New Dev 2011;2:87–112. https://doi.org/10.5772/17999.Search in Google Scholar
32. Oliveira, M, Slezakova, K, Alves, MJ, Fernandes, A, Teixeira, JP, Delerue-Matos, C, et al.. Polycyclic aromatic hydrocarbons at fire stations: firefighters’ exposure monitoring and biomonitoring, and assessment of the contribution to total internal dose. J Hazard Mater 2017;323:184–94. https://doi.org/10.1016/j.jhazmat.2016.03.012.Search in Google Scholar PubMed
33. Li, Z, Mulholland, JA, Romanoff, LC, Pittman, EN, Trinidad, DA, Lewin, MD, et al.. Assessment of non-occupational exposure to polycyclic aromatic hydrocarbons through personal air sampling and urinary biomonitoring. J Environ Monit 2010;12:1110–8. https://doi.org/10.1039/c000689k.Search in Google Scholar PubMed
34. Adlkofer, F, Scherer, G, Conze, C, Angerer, J, Lehnert, G. Significance of exposure to benzene and other toxic compounds through environmental tobacco smoke. J Cancer Res Clin Oncol 1990;116:591–8. https://doi.org/10.1007/bf01637079.Search in Google Scholar PubMed
35. Rengarajan, T, Rajendran, P, Nandakumar, N, Lokeshkumar, B, Rajendran, P, Nishigaki, I. Exposure to polycyclic aromatic hydrocarbons with special focus on cancer. Asian Pac J Trop Biomed 2015;5:182–9. https://doi.org/10.1016/s2221-1691(15)30003-4.Search in Google Scholar
36. Phillips, DH. Polycyclic aromatic hydrocarbons in the diet. Mutat Res Genet Toxicol Environ Mutagen 1999;443:139–47. https://doi.org/10.1016/s1383-5742(99)00016-2.Search in Google Scholar PubMed
37. Sun, Y, Xie, Z, Wu, K, Lan, J, Li, T, Yuan, D. Speciation, distribution and migration pathways of polycyclic aromatic hydrocarbons in a typical underground river system in Southwest China. J Hydrol 2021;596:125690. https://doi.org/10.1016/j.jhydrol.2020.125690.Search in Google Scholar
38. Xu, B, Liu, F, Alfaro, D, Jin, Z, Liu, Y, Liu, Y, et al.. Polycyclic aromatic hydrocarbons in fine road dust from a coal-utilization city: spatial distribution, source diagnosis and risk assessment. Chemosphere 2022;286:131555. https://doi.org/10.1016/j.chemosphere.2021.131555.Search in Google Scholar PubMed
39. Caldwell, J, Gardner, I, Swales, N. An introduction to drug disposition: the basic principles of absorption, distribution, metabolism, and excretion. Toxicol Pathol 1995;23:102–14. https://doi.org/10.1177/019262339502300202.Search in Google Scholar PubMed
40. Mitchell, C. Distribution and retention of benzo (a) pyrene in rats after inhalation. Toxicol Lett 1982;11:35–42. https://doi.org/10.1016/0378-4274(82)90102-3.Search in Google Scholar PubMed
41. Hall, M, Forrester, LM, Parker, DK, Grover, PL, Wolf, CR. Relative contribution of various forms of cytochrome P450 to the metabolism of benzo [a] pyrene by human liver microsomes. Carcinogenesis 1989;10:1815–21. https://doi.org/10.1093/carcin/10.10.1815.Search in Google Scholar PubMed
42. Kao, J, Hall, J, Shugart, LR, Holland, JM. An in vitro approach to studying cutaneous metabolism and disposition of topically applied xenobiotics. Toxicol Appl Pharmacol 1984;75:289–98. https://doi.org/10.1016/0041-008x(84)90211-4.Search in Google Scholar PubMed
43. Smoke, T, Smoking, I. IARC monographs on the evaluation of carcinogenic risks to humans. IARC, Lyon 2004;1:1–1452.Search in Google Scholar
44. Conney, A. Pharmacological implications of microsomal enzyme induction. Pharmacol Rev 1967;19:317–66.Search in Google Scholar
45. Flesher, JW, Lehner, AF. Structure, function and carcinogenicity of metabolites of methylated and non-methylated polycyclic aromatic hydrocarbons: a comprehensive review. Toxicol Mech Methods 2016;26:151–79. https://doi.org/10.3109/15376516.2015.1135223.Search in Google Scholar PubMed
46. Hanzlik, RP, Hogberg, K, Judson, CM. Microsomal hydroxylation of specifically deuterated monosubstituted benzenes. Evidence for direct aromatic hydroxylation. Biochemistry 1984;23:3048–55. https://doi.org/10.1021/bi00308a031.Search in Google Scholar PubMed
47. Keysell, G, Booth, J, Sims, P. Glutathione conjugates as metabolites of benz [a] anthracene. Xenobiotica 1975;5:439–48. https://doi.org/10.3109/00498257509056114.Search in Google Scholar PubMed
48. Foth, H, Kahl, R, Kahl, G. Pharmacokinetics of low doses of benzo [a] pyrene in the rat. Food Chem Toxicol 1988;26:45–51. https://doi.org/10.1016/0278-6915(88)90040-3.Search in Google Scholar PubMed
49. Jandacek, RJ, Tso, P. Factors affecting the storage and excretion of toxic lipophilic xenobiotics. Lipids 2001;36:1289–305. https://doi.org/10.1007/s11745-001-0844-z.Search in Google Scholar PubMed
50. Yang, SK, Selkirk, JK, Plotkin, EV, Gelboin, HV. Kinetic analysis of the metabolism of benzo (a) pyrene to phenols, dihydrodiols, and quinones by high-pressure chromatography compared to analysis by aryl hydrocarbon hydroxylase assay, and the effect of enzyme induction. Cancer Res 1975;35:3642–50.Search in Google Scholar
51. Kim, JH, Stansbury, KH, Walker, NJ, Trush, MA, Strickland, PT, Sutter, TR. Metabolism of benzo [a] pyrene and benzo [a] pyrene-7, 8-diol by human cytochrome P450 1B1. Carcinogenesis 1998;19:1847–53. https://doi.org/10.1093/carcin/19.10.1847.Search in Google Scholar PubMed
52. Wei, Q, Gu, J, Cheng, L, Bondy, ML, Jiang, H, Hong, WK, et al.. Benzo (a) pyrene diol epoxide-induced chromosomal aberrations and risk of lung cancer. Cancer Res 1996;56:3975–9.Search in Google Scholar
53. Gelboin, HV. Benzo [alpha] pyrene metabolism, activation and carcinogenesis: role and regulation of mixed-function oxidases and related enzymes. Physiol Rev 1980;60:1107–66. https://doi.org/10.1152/physrev.1980.60.4.1107.Search in Google Scholar PubMed
54. Meeker, JD, Barr, DB, Serdar, B, Rappaport, SM, Hauser, R. Utility of urinary 1-naphthol and 2-naphthol levels to assess environmental carbaryl and naphthalene exposure in an epidemiology study. J Expo Sci Environ Epidemiol 2007;17:314–20. https://doi.org/10.1097/00001648-200611001-00787.Search in Google Scholar
55. Shah, SD, Ogunyoku, TA, Miller, JW, Cocker, DR. On-road emission rates of PAH and n-alkane compounds from heavy-duty diesel vehicles. Environ Sci Technol 2005;39:5276–84. https://doi.org/10.1021/es048086+.10.1021/es048086+Search in Google Scholar PubMed
56. Zhu, L, Wang, J. Sources and patterns of polycyclic aromatic hydrocarbons pollution in kitchen air, China. Chemosphere 2003;50:611–8. https://doi.org/10.1016/s0045-6535(02)00668-9.Search in Google Scholar PubMed
57. Chetiyanukornkul, T, Toriba, A, Kameda, T, Tang, N, Hayakawa, K. Simultaneous determination of urinary hydroxylated metabolites of naphthalene, fluorene, phenanthrene, fluoranthene and pyrene as multiple biomarkers of exposure to polycyclic aromatic hydrocarbons. Anal Bioanal Chem 2006;386:712–8. https://doi.org/10.1007/s00216-006-0628-6.Search in Google Scholar PubMed
58. Helen, SG, Goniewicz, ML, Dempsey, D, Wilson, M, Jacob, PIII, Benowitz, NL. Exposure and kinetics of polycyclic aromatic hydrocarbons (PAHs) in cigarette smokers. Chem Res Toxicol 2012;25:952–64. https://doi.org/10.1021/tx300043k.Search in Google Scholar PubMed PubMed Central
59. Kuusimäki, L, Peltonen, Y, Mutanen, P, Peltonen, K, Savela, K. Urinary hydroxy-metabolites of naphthalene, phenanthrene and pyrene as markers of exposure to diesel exhaust. Int Arch Occup Environ Health 2004;77:23–30. https://doi.org/10.1007/s00420-003-0477-y.Search in Google Scholar PubMed
60. Keyte, IJ, Albinet, A, Harrison, RM. On-road traffic emissions of polycyclic aromatic hydrocarbons and their oxy-and nitro-derivative compounds measured in road tunnel environments. Sci Total Environ 2016;566:1131–42. https://doi.org/10.1016/j.scitotenv.2016.05.152.Search in Google Scholar PubMed
61. Ravindra, K, Bencs, L, Wauters, E, De Hoog, J, Deutsch, F, Roekens, E, et al.. Seasonal and site-specific variation in vapour and aerosol phase PAHs over Flanders (Belgium) and their relation with anthropogenic activities. Atmos Environ 2006;40:771–85. https://doi.org/10.1016/j.atmosenv.2005.10.011.Search in Google Scholar
62. Tolos, WP, Shaw, PB, Lowry, LK, MacKenzie, BA, Deng, J-F, Markel, HL. 1-Pyrenol: a biomarker for occupational exposure to polycyclic aromatic hydrocarbons. Appl Occup Environ Hyg 1990;5:303–9. https://doi.org/10.1080/1047322x.1990.10389643.Search in Google Scholar
63. Toriba, A, Hayakawa, K. Biomarkers of exposure to polycyclic aromatic hydrocarbons and related compounds. J Health Sci 2007;53:631–8. https://doi.org/10.1248/jhs.53.631.Search in Google Scholar
64. Rabadán-Diehl, C, Alam, D, Baumgartner, J. Household air pollution in the early origins of CVD in developing countries. Global Heart 2012;7:235–42. https://doi.org/10.1016/j.gheart.2012.06.014.Search in Google Scholar PubMed
65. Hadrup, N, Mielżyńska-Švach, D, Kozłowska, A, Campisi, M, Pavanello, S, Vogel, U. Association between a urinary biomarker for exposure to PAH and blood level of the acute phase protein serum amyloid A in coke oven workers. Environ Health 2019;18:1–9. https://doi.org/10.1186/s12940-019-0523-1.Search in Google Scholar PubMed PubMed Central
66. Clark, JDIII, Serdar, B, Lee, DJ, Arheart, K, Wilkinson, JD, Fleming, LE. Exposure to polycyclic aromatic hydrocarbons and serum inflammatory markers of cardiovascular disease. Environ Res 2012;117:132–7. https://doi.org/10.1016/j.envres.2012.04.012.Search in Google Scholar PubMed PubMed Central
67. Asweto, CO. Cardiovascular health risk posed by polycyclic aromatic hydrocarbon and ultrafine particles. J Clin Exp Tox 2018;2:1–5. https://doi.org/10.4066/2630-4570.009.Search in Google Scholar
68. Cho, HM, Kang, DR, Kim, HC, Oh, SM, Kim, B-K, Suh, I. Association between fibrinogen and carotid atherosclerosis according to smoking status in a Korean male population. Yonsei Med J 2015;56:921–7. https://doi.org/10.3349/ymj.2015.56.4.921.Search in Google Scholar PubMed PubMed Central
69. Hansson, GK, Libby, P. The immune response in atherosclerosis: a double-edged sword. Nat Rev Immunol 2006;6:508–19. https://doi.org/10.1038/nri1882.Search in Google Scholar PubMed
70. Xu, X, Cook, RL, Ilacqua, VA, Kan, H, Talbott, EO, Kearney, G. Studying associations between urinary metabolites of polycyclic aromatic hydrocarbons (PAHs) and cardiovascular diseases in the United States. Sci Total Environ 2010;408:4943–8. https://doi.org/10.1016/j.scitotenv.2010.07.034.Search in Google Scholar PubMed
71. Getz, GS, Krishack, PA, Reardon, CA. Serum amyloid A and atherosclerosis. Curr Opin Lipidol 2016;27:531–5. https://doi.org/10.1097/mol.0000000000000331.Search in Google Scholar PubMed
72. Wu, Y, Zhang, J, Wen, Y, Wang, H, Zhang, M, Cianflone, K. Increased acylation-stimulating protein, C-reactive protein, and lipid levels in young women with polycystic ovary syndrome. Fertil Steril 2009;91:213–9. https://doi.org/10.1016/j.fertnstert.2007.11.031.Search in Google Scholar PubMed
73. Wilson, AM, Ryan, MC, Boyle, AJ. The novel role of C-reactive protein in cardiovascular disease: risk marker or pathogen. Int J Cardiol 2006;106:291–7. https://doi.org/10.1016/j.ijcard.2005.01.068.Search in Google Scholar PubMed
74. Li, L, Roumeliotis, N, Sawamura, T, Renier, G. C-reactive protein enhances LOX-1 expression in human aortic endothelial cells: relevance of LOX-1 to C-reactive protein–induced endothelial dysfunction. Circ Res 2004;95:877–83. https://doi.org/10.1161/01.res.0000147309.54227.42.Search in Google Scholar
75. Nordestgaard, BG, Zacho, J. Lipids, atherosclerosis and CVD risk: is CRP an innocent bystander? Nutr Metabol Cardiovasc Dis 2009;19:521–4. https://doi.org/10.1016/j.numecd.2009.07.005.Search in Google Scholar PubMed
76. Horne, BD, Anderson, JL, John, JM, Weaver, A, Bair, TL, Jensen, KR, et al.. Which white blood cell subtypes predict increased cardiovascular risk? J Am Coll Cardiol 2005;45:1638–43. https://doi.org/10.1016/j.jacc.2005.02.054.Search in Google Scholar PubMed
77. Brown, DW, Giles, WH, Croft, JB. White blood cell count: an independent predictor of coronary heart disease mortality among a national cohort. J Clin Epidemiol 2001;54:316–22. https://doi.org/10.1016/s0895-4356(00)00296-1.Search in Google Scholar PubMed
78. Group, MRFITR, Hansen, LK, Grimm, JRRH, Neaton, JD. The relationship of white blood cell count to other cardiovascular risk factors. Int J Epidemiol 1990;19:881–8. https://doi.org/10.1093/ije/19.4.881.Search in Google Scholar PubMed
79. Ensrud, K, Grimm, RHJr. The white blood cell count and risk for coronary heart disease. Am Heart J 1992;124:207–13. https://doi.org/10.1016/0002-8703(92)90942-o.Search in Google Scholar PubMed
80. Ganguly, P, Alam, SF. Role of homocysteine in the development of cardiovascular disease. Nutr J 2015;14:1–10. https://doi.org/10.1186/1475-2891-14-6.Search in Google Scholar PubMed PubMed Central
81. Zhang, S, Bai, Y-Y, Luo, L-M, Xiao, W-K, Wu, H-M, Ye, P. Association between serum homocysteine and arterial stiffness in elderly: a community-based study. J Geriatr Cardiol 2014;11:32. https://doi.org/10.3969/j.issn.1671-5411.2014.01.007.Search in Google Scholar PubMed PubMed Central
82. Shenoy, V, Mehendale, V, Prabhu, K, Shetty, R, Rao, P. Correlation of serum homocysteine levels with the severity of coronary artery disease. Indian J Clin Biochem 2014;29:339–44. https://doi.org/10.1007/s12291-013-0373-5.Search in Google Scholar PubMed PubMed Central
© 2023 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Reviews
- A systematic review on the association between exposure to air particulate matter during pregnancy and the development of hypertensive disorders of pregnancy and gestational diabetes mellitus
- Screen time and childhood attention deficit hyperactivity disorder: a meta-analysis
- The association between polycystic ovary syndrome and environmental pollutants based on animal and human study; a systematic review
- Residues of carcinogenic pesticides in food: a systematic review
- The concentration of Lithium in water resources: A systematic review, meta-analysis and health risk assessment
- Polychlorinated biphenyls and thyroid function: a scoping review
- The European Union assessments of radiofrequency radiation health risks – another hard nut to crack (Review)
- Research progresses on the effects of heavy metals on the circadian clock system
- Diagnosing and managing heat exhaustion: insights from a systematic review of cases in the desert climate of Mecca
- Para-occupational exposure to chemical substances: a systematic review
- Association of the ACE2-Angiotensin1-7–Mas axis with lung damage caused by cigarette smoke exposure: a systematic review
- Impacts and mechanisms of PM2.5 on bone
- Impacts and potential mechanisms of fine particulate matter (PM2.5) on male testosterone biosynthesis disruption
- Exposure to perfluoroalkyl and polyfluoroalkyl substances and risk of stroke in adults: a meta-analysis
- Prevalence and concentration of aflatoxin M1 and ochratoxin A in cheese: a global systematic review and meta-analysis and probabilistic risk assessment
- The effect of polycyclic aromatic hydrocarbon biomarkers on cardiovascular diseases
- Biological effects of electromagnetic fields on insects: a systematic review and meta-analysis
- Letter to the Editor
- Monkeypox and drug repurposing: seven potential antivirals to combat the viral disease
Articles in the same Issue
- Frontmatter
- Reviews
- A systematic review on the association between exposure to air particulate matter during pregnancy and the development of hypertensive disorders of pregnancy and gestational diabetes mellitus
- Screen time and childhood attention deficit hyperactivity disorder: a meta-analysis
- The association between polycystic ovary syndrome and environmental pollutants based on animal and human study; a systematic review
- Residues of carcinogenic pesticides in food: a systematic review
- The concentration of Lithium in water resources: A systematic review, meta-analysis and health risk assessment
- Polychlorinated biphenyls and thyroid function: a scoping review
- The European Union assessments of radiofrequency radiation health risks – another hard nut to crack (Review)
- Research progresses on the effects of heavy metals on the circadian clock system
- Diagnosing and managing heat exhaustion: insights from a systematic review of cases in the desert climate of Mecca
- Para-occupational exposure to chemical substances: a systematic review
- Association of the ACE2-Angiotensin1-7–Mas axis with lung damage caused by cigarette smoke exposure: a systematic review
- Impacts and mechanisms of PM2.5 on bone
- Impacts and potential mechanisms of fine particulate matter (PM2.5) on male testosterone biosynthesis disruption
- Exposure to perfluoroalkyl and polyfluoroalkyl substances and risk of stroke in adults: a meta-analysis
- Prevalence and concentration of aflatoxin M1 and ochratoxin A in cheese: a global systematic review and meta-analysis and probabilistic risk assessment
- The effect of polycyclic aromatic hydrocarbon biomarkers on cardiovascular diseases
- Biological effects of electromagnetic fields on insects: a systematic review and meta-analysis
- Letter to the Editor
- Monkeypox and drug repurposing: seven potential antivirals to combat the viral disease