Influence of organic and inorganic soil pollutants on modifiable cerebrovascular disease risk factors
Growing evidence indicates that chronic exposure to organic and inorganic soil pollutants may contribute to the development of cerebrovascular disease (CeVD) by modulating key, potentially reversible cardiometabolic risk factors. While the vascular consequences of air and water pollution are increasingly recognized, contaminated soils remain an underappreciated environmental reservoir of toxicants with potential health effects. Inorganic pollutants such as lead and cadmium, together with organic compounds including polycyclic aromatic hydrocarbons and polychlorinated biphenyls, can enter the human body through ingestion, inhalation of resuspended particulates, or, for some compounds, dermal absorption. Once absorbed, these pollutants disrupt metabolic and vascular homeostasis through converging mechanisms involving oxidative stress, endothelial dysfunction, and chronic low-grade inflammation. These processes promote the development of hypertension, insulin resistance, hyperglycemia, and dyslipidemia—well-established, modifiable risk factors for CeVD. Organic pollutants may further exacerbate metabolic toxicity through endocrine-disrupting effects and activation of the aryl hydrocarbon receptor, amplifying their cerebrovascular relevance. This review synthesizes experimental, epidemiological, and mechanistic evidence linking exposure to organic and inorganic soil pollutants with adverse alterations in blood pressure regulation, glucose metabolism, and lipid homeostasis. Despite growing concern, a critical knowledge gap remains in defining pollutant-specific associations with discrete cerebrovascular outcomes, largely due to limited integrative studies combining environmental exposure assessment with clinical biomarkers and longitudinal health data. Moreover, populations in industrially burdened or low-resource settings experience disproportionate exposure risks, reinforcing health inequities. Strengthening soil pollution surveillance, advancing remediation strategies, and incorporating environmental exposure histories into cardiovascular risk assessment may represent an upstream approach to reducing the global burden of CeVD.
- Lu Y, Song S, Wang R, et al. Impacts of soil and water pollution on food safety and health risks in China. Environ Int. 2015;77:5-15. doi: 10.1016/j.envint.2014.12.010
- Zhao FJ, Ma Y, Zhu YG, Tang Z, McGrath SP. Soil contamination in China: Current status and mitigation strategies. Environ Sci Technol. 2015;49(2):750-759. doi: 10.1021/es5047099
- Jaishankar M, Tseten T, Anbalagan N, Mathew BB, Beeregowda KN. Toxicity, mechanism and health effects of some heavy metals. Interdiscip Toxicol. 2014;7(2):60-72. doi: 10.2478/intox-2014-0009
- Landrigan PJ, Fuller R, Acosta NJR, et al. The Lancet Commission on pollution and health. Lancet. 2018;391(10119):462-512. doi: 10.1016/S0140-6736(17)32345-0
- Bhatnagar A. Environmental Determinants of Cardiovascular Disease. Circ Res. 2017;121(2):162-180. doi: 10.1161/CIRCRESAHA.117.306458
- Tellez-Plaza M, Navas-Acien A, Caldwell KL, Menke A, Muntner P, Guallar E. Reduction in cadmium exposure in the United States population, 1988-2008: the contribution of declining smoking rates. Environ Health Perspect. 2012;120(2):204-209. doi: 10.1289/ehp.1104020
- Ngwa EN, Kengne AP, Tiedeu-Atogho B, Mofo-Mato EP, Sobngwi E. Persistent organic pollutants as risk factors fortype 2 diabetes. Diabetol Metab Syndr. 2015;7:41. doi: 10.1186/s13098-015-0031-6
- Lin W, Huang Z, Zhang W, Ren Y. Investigating the neurotoxicity of environmental pollutants using zebrafish as a model organism: A review and recommendations for future work. Neurotoxicology. 2023;94:235-244.doi: 10.1016/j.neuro.2022.12.009
- Marrugat J, Arboix A, Garcia-Eroles L, et al. Estimacion de la incidencia poblacional y la mortalidad de la enfermedad cerebrovascular establecida isquemica y hemorragica en 2002 [The estimated incidence and case fatality rate of ischemic and hemorrhagic cerebrovascular disease in 2002 in Catalonia]. Rev Esp Cardiol. 2007;60(6):573-580. doi: 10.1157/13107113
- Grandjean P, Landrigan PJ. Neurobehavioural effects of developmental toxicity. Lancet Neurol. 2014;13(3):330-338. doi: 10.1016/S1474-4422(13)70278-3
- Paz-Ferreiro J, Gasco G, Mendez A, Reichman SM. Soil Pollution and Remediation. Int J Environ Res Public Health. 2018;15(8):1657. doi: 10.3390/ijerph15081657
- Moeckel C, Breivik K, Nost TH, Sankoh A, Jones KC, Sweetman A. Soil pollution at a major West African E-waste recycling site: Contamination pathways and implications for potential mitigation strategies. Environ Int. 2020;137:105563. doi: 10.1016/j.envint.2020.105563
- Kumar B, Verma VK, Mishra M, et al. Assessment of persistent organic pollutants in soil and sediments from an urbanized flood plain area. Environ Geochem Health. 2021;43(9):3375-3392. doi: 10.1007/s10653-021-00839-9
- Teng Y, Zhou Q, Miao X, Chen Y. Assessment of soil organic contamination in a typical petrochemical industry park in China. Environ Sci Pollut Res Int. 2015;22(13):10227-10234. doi: 10.1007/s11356-015-4219-y
- Das S, Helmus R, Dong Y, et al. Organic contaminants in bio-based fertilizer treated soil: Target and suspect screening approaches. Chemosphere. 2023;337:139261. doi: 10.1016/j.chemosphere.2023.139261
- Sun J, Pan L, Tsang DCW, et al. Polychlorinated biphenyls in agricultural soils from the Yangtze River Delta of China: Regional contamination characteristics, combined ecological effects and human health risks. Chemosphere. 2016;163:422-428. doi: 10.1016/j.chemosphere.2016.08.038
- Sun J, Pan L, Zhan Y, et al. Contamination of phthalate esters, organochlorine pesticides and polybrominated diphenyl ethers in agricultural soils from the Yangtze River Delta of China. Sci Total Environ. 2016;544:670-676. doi: 10.1016/j.scitotenv.2015.12.012
- Chen Y, Wang C, Wang Z. Residues and source identification of persistent organic pollutants in farmland soils irrigated by effluents from biological treatment plants. Environ Int. 2005;31(6):778-783. doi: 10.1016/j.envint.2005.05.024
- Zhang L, Dong L, Shi S, Zhou L, Zhang T, Huang Y. Organochlorine pesticides contamination in surface soils from two pesticide factories in Southeast China. Chemosphere. 2009;77(5):628-633. doi: 10.1016/j.chemosphere.2009.08.055
- Luo X, Wu C, Lin Y, et al. Soil heavy metal pollution from Pb/Zn smelting regions in China and the remediation potential of biomineralization. J Environ Sci (China). 2023;125:662-677. doi: 10.1016/j.jes.2022.01.029
- Oyebamiji AO, Olaolorun OA, Popoola OJ, Zafar T. Assessment of heavy metal pollution in soils of Jebba Area, Nigeria: Concentrations, source analysis and implications for ecological and human health risks. Sci Total Environ. 2024;945:173860. doi: 10.1016/j.scitotenv.2024.173860
- Enjavinejad SM, Zahedifar M, Moosavi AA, Khosravani P. Integrated application of multiple indicators and geographic information system-based approaches for comprehensive assessment of environmental impacts of toxic metals-contaminated agricultural soils and vegetables. Sci Total Environ. 2024;926:171747. doi: 10.1016/j.scitotenv.2024.171747
- Kapwata T, Mathee A, Sweijd N, et al. Spatial assessment of heavy metals contamination in household garden soils in rural Limpopo Province, South Africa. Environ Geochem Health. 2020;42(12):4181-4191. doi: 10.1007/s10653-020-00535-0
- Shezi B, Street RA, Webster C, Kunene Z, Mathee A. Heavy Metal Contamination of Soil in Preschool Facilities around Industrial Operations, Kuils River, Cape Town (South Africa). Int J Environ Res Public Health. 2022;19(7):4380. doi: 10.3390/ijerph19074380
- Marrugo-Negrete J, Pinedo-Hernandez J, Diez S. Assessment of heavy metal pollution, spatial distribution and origin in agricultural soils along the Sinu River Basin, Colombia. Environ Res. 2017;154:380-388. doi: 10.1016/j.envres.2017.01.021
- Ngole-Jeme VM. Heavy metals in soils along unpaved roads in south west Cameroon: Contamination levels and health risks. Ambio. 2016;45(3):374-386. doi: 10.1007/s13280-015-0726-9
- Adeniyi M, Fabunmi O, Olaniyan O, Adetunji C, Seriki S. Electroencephalographic findings of young adult males during prolonged unipedal orthostasis. Neurosci Res Notes. 2023:6(2):177.1–177.8. doi: 10.31117/neuroscirn.v6i2.177.
- Pavuk M, Serio TC, Cusack C, Cave M, Rosenbaum PF, Birnbaum LS. Hypertension in Relation to Dioxins and Polychlorinated Biphenyls from the Anniston Community Health Survey Follow-Up. Environ Health Perspect. 2019;127(12):127007. doi: 10.1289/EHP5272
- Goncharov A, Bloom M, Pavuk M, Birman I, Carpenter DO. Blood pressure and hypertension in relation to levels of serum polychlorinated biphenyls in residents of Anniston, Alabama. J Hypertens. 2010;28(10):2053-2060. doi: 10.1097/HJH.0b013e32833c5f3e
- Cheng C, Li X, Wu B, Liu B, Li L, Yu Y. Serum level of dioxin-like polychlorinated biphenyls and blood pressure in primarynschool children. Ecotoxicol Environ Saf. 2025;298:118278. doi: 10.1016/j.ecoenv.2025.118278
- Goncharov A, Pavuk M, Foushee HR, Carpenter DO. Anniston Environmental Health Reseach Consortium. Blood pressure in relation to concentrations of PCB congeners and chlorinated pesticides. Environ Health Perspect. 2011;119(3):319-325. doi: 10.1289/ehp.1002830
- İlhan S, Ateşşahin D, Ateşşahin A, Mutlu E, Onat E, Şahna E. 2,3,7,8-Tetrachlorodibenzo-p-dioxin-induced hypertension: the beneficial effects of melatonin. Toxicol Ind Health. 2015;31(4):298-303. doi: 10.1177/0748233712472521
- Kopf PG, Huwe JK, Walker MK. Hypertension, cardiac hypertrophy, and impaired vascular relaxation induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin are associated with increased superoxide. Cardiovasc Toxicol. 2008;8(4):181-193. doi: 10.1007/s12012-008-9027-x
- Bae S, Hong YC. Exposure to bisphenol A from drinking canned beverages increases blood pressure: randomized crossover trial. Hypertension. 2015;65(2):313-319. doi: 10.1161/HYPERTENSIONAHA.114.04261
- Bae S, Kim JH, Lim YH, Park HY, Hong YC. Associations of bisphenol A exposure with heart rate variability and blood pressure. Hypertension. 2012;60(3):786-793. doi: 10.1161/HYPERTENSIONAHA.112.197715
- Bae S, Lim YH, Lee YA, Shin CH, Oh SY, Hong YC. Maternal Urinary Bisphenol A Concentration During Midterm Pregnancy and Children’s Blood Pressure at Age 4. Hypertension. 2017;69(2):367-374. doi: 10.1161/HYPERTENSIONAHA.116.08281
- Xiong Q, Liu X, Shen Y, et al. Elevated serum Bisphenol A level in patients with dilated cardiomyopathy. Int J Environ Res Public Health. 2015;12(5):5329-5337. doi: 10.3390/ijerph120505329
- Perry HM Jr, Erlanger MW, Perry EF. Effect of a second metal on cadmium-induced hypertension. Arch Environ Health. 1983;38(2):80-85. doi: 10.1080/00039896.1983.10543985
- Rossi KA, Almenara CCP, Simoes RP, et al. Short-term Effects of Cadmium Exposure on Blood Pressure and Vascular Function in Wistar Rats. Biol Trace Elem Res. 2024;202(6):2645-2656. doi: 10.1007/s12011-023-03851-5
- Puri VN. Cadmium induced hypertension. Clin Exp Hypertens. 1999;21(1-2):79-84. doi: 10.3109/10641969909068651
- Pinheiro Junior JEG, Moraes PZ, Rodriguez MD, et al. Cadmium exposure activates NADPH oxidase, renin-angiotensin system and cyclooxygenase 2 pathways in arteries, inducing hypertension and vascular damage. Toxicol Lett. 2020;333:80-89. doi: 10.1016/j.toxlet.2020.07.027
- Gambelunghe A, Sallsten G, Borne Y, et al. Low-level exposure to lead, blood pressure, and hypertension in a population-based cohort. Environ Res. 2016;149:157-163. doi: 10.1016/j.envres.2016.05.015
- Glenn BS, Bandeen-Roche K, Lee BK, Weaver VM, Todd AC, Schwartz BS. Changes in systolic blood pressure associated with lead in blood and bone. Epidemiology. 2006;17(5):538-544. doi: 10.1097/01.ede.0000231284.19078.4b
- Hara A, Thijs L, Asayama K, et al. Blood pressure in relation to environmental lead exposure in the national health and nutrition examination survey 2003 to 2010. Hypertension. 2015;65(1):62-69. doi: 10.1161/HYPERTENSIONAHA.114.04023
- Chen CJ, Hsueh YM, Lai MS, et al. Increased prevalence of hypertension and long-term arsenic exposure. Hypertension. 1995;25(1):53-60.
- Ameer SS, Engstrom K, Harari F, Concha G, Vahter M, Broberg K. The effects of arsenic exposure on blood pressure and early risk markers of cardiovascular disease: Evidence for population differences. Environ Res. 2015;140:32-36. doi: 10.1016/j.envres.2015.03.010
- Khatun M, Haque N, Siddique AE, et al. Arsenic Exposure-Related Hypertension in Bangladesh and Reduced Circulating Nitric Oxide Bioavailability. Environ Health Perspect. 2024;132(4):47003. doi: 10.1289/EHP13018
- Kaufman JA, Mattison C, Fretts AM, et al. Arsenic, blood pressure, and hypertension in the Strong Heart Family Study. Environ Res. 2021;195:110864. doi: 10.1016/j.envres.2021.110864
- Wang Q, Tian H, Wang W, Liu S, Zhang A. The Relationship of Arsenic Exposure with Hypertension and Wide Pulse Pressure: Preliminary Evidence from Coal-Burning Arsenicosis Population in Southwest China. Toxics. 2023;11(5):443. doi: 10.3390/toxics11050443
- Ige SF, Adeniyi MJ, Joanna AO, Oluwaseyi DA. Allium cepa juice prevented oxidative stress-mediated metabolic disorder following chronic lead acetate exposure in male rats. Albanian J Med Health Sci. 2019;50(1):11.
- Ige SF, Adeniyi MJ, Ademilua OB, Fatola AO, Adeyemi IA. Allium Cepa Remediates Oxidative Stress-Mediated Hepatic DNA Damage in Cadmium-Exposed Rats through Enhanced p53 Expression and Inhibition of Bcl2. Int J Biomed Sci. 2020;16(2):11-17. doi: 10.59566/ijbs.2020.16011
- Adeniyi MJ, Fabunmi OA, Awosika A. Unravelling the interplay between Harmattan wind and baroreflex functions: Implications on environmental health and cardiovascular pathophysiology. Explor Med. 2024;5(5):584-600. doi: 10.37349/emed.2024.00242
- Warner M, Rauch S, Brambilla P, Signorini S, Mocarelli P, Eskenazi B. Prenatal dioxin exposure and glucose metabolism in the Seveso Second Generation study. Environ Int. 2020;134:105286. doi: 10.1016/j.envint.2019.105286
- Hoyeck MP, Blair H, Ibrahim M, et al. Long-term metabolic consequences of acute dioxin exposure differ between male and female mice. Sci Rep. 2020;10(1):1448. doi: 10.1038/s41598-020-57973-0
- Matteo G, Hoyeck MP, Blair HL, et al. Prolonged Low-Dose Dioxin Exposure Impairs Metabolic Adaptability to High-Fat Diet Feeding in Female but Not Male Mice. Endocrinology. 2021;162(6):bqab050. doi: 10.1210/endocr/bqab050
- Moghaddam HS, Samarghandian S, Farkhondeh T. Effect of bisphenol A on blood glucose, lipid profile and oxidative stress indices in adult male mice. Toxicol Mech Methods.
2015;25(7):507-513. doi: 10.3109/15376516.2015.1056395
- Susiarjo M, Xin F, Bansal A, et al. Bisphenol a exposure disrupts metabolic health across multiple generations in the mouse. Endocrinology. 2015;156(6):2049-2058. doi: 10.1210/en.2014-2027
- Bansal A, Rashid C, Xin F, et al. Sex- and Dose-Specific Effects of Maternal Bisphenol A Exposure on Pancreatic Islets of First- and Second-Generation Adult Mice Offspring. Environ Health Perspect. 2017;125(9):097022. doi: 10.1289/EHP1674
- Weber LW, Lebofsky M, Greim H, Rozman K. Key enzymes of gluconeogenesis are dose-dependently reduced in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-treated rats. Arch Toxicol. 1991;65(2):119-123. doi: 10.1007/BF02034937
- Baker NA, Karounos M, English V, et al. Coplanar polychlorinated biphenyls impair glucose homeostasis in lean C57BL/6 mice and mitigate beneficial effects of weight loss on glucose homeostasis in obese mice. Environ Health Perspect. 2013;121(1):105-110. doi: 10.1289/ehp.1205421
- Zhang S, Wu T, Chen M, et al. Chronic Exposure to Aroclor 1254 Disrupts Glucose Homeostasis in Male Mice via Inhibition of the Insulin Receptor Signal Pathway. Environ Sci Technol. 2015;49(16):10084-10092. doi: 10.1021/acs.est.5b01597
- Xi Z, Fang L, Xu J, et al. Exposure to Aroclor 1254 persistently suppresses the functions of pancreatic β-cells and deteriorates glucose homeostasis in male mice. Environ Pollut. 2019;249:822-830. doi: 10.1016/j.envpol.2019.03.101
- Kim HY, Kwon WY, Kim YA, et al. Polychlorinated biphenyls exposure-induced insulin resistance is mediated by lipid droplet enlargement through Fsp27. Arch Toxicol. 2017;91(6):2353-2363. doi: 10.1007/s00204-016-1889-2
- Nguyen J, Patel A, Gensburg A, Bokhari R, Lamar P, Edwards J. Diabetogenic and Obesogenic Effects of Cadmium in Db/Db Mice and Rats at a Clinically Relevant Level of Exposure. Toxics. 2022;10(3):107. doi: 10.3390/toxics10030107
- Jacquet A, Arnaud J, Hininger-Favier I, et al. Impact of chronic and low cadmium exposure of rats: sex specific disruption of glucose metabolism. Chemosphere. 2018;207:764-773. doi: 10.1016/j.chemosphere.2018.05.099
- Fitzgerald R, Olsen A, Nguyen J, Wong W, El Muayed M, Edwards J. Pancreatic Islets Accumulate Cadmium in a Rodent Model of Cadmium-Induced Hyperglycemia. Int J Mol Sci. 2020;22(1):360. doi: 10.3390/ijms22010360
- Tyrrell JB, Hafida S, Stemmer P, Adhami A, Leff T. Lead (Pb) exposure promotes diabetes in obese rodents. J Trace Elem Med Biol. 2017;39:221-226. doi: 10.1016/j.jtemb.2016.10.007
- Wan H, Wang B, Cui Y, et al. Low-level lead exposure promotes hepatic gluconeogenesis and contributes to the elevation of fasting glucose level. Chemosphere. 2021;276:130111. doi: 10.1016/j.chemosphere.2021.130111
- Paul DS, Walton FS, Saunders RJ, Styblo M. Characterization of the impaired glucose homeostasis produced in C57BL/6 mice by chronic exposure to arsenic and high-fat diet. Environ Health Perspect. 2011;119(8):1104-1109. doi: 10.1289/ehp.1003324
- Liu S, Guo X, Wu B, Yu H, Zhang X, Li M. Arsenic induces diabetic effects through beta-cell dysfunction and increased gluconeogenesis in mice. Sci Rep. 2014;4:6894. doi: 10.1038/srep06894
- Postiglione A, Napoli C. Hyperlipidaemia and atherosclerotic cerebrovascular disease. Curr Opin Lipidol. 1995;6(4):236-242. doi: 10.1097/00041433-199508000-00008
- Jeremiah AM. Plasma Lipid Profile and Uric Acid in High Fat Fed Female Rats Treated with Oral Contraceptive. Biomed J Sci & Tech Res. 2017;1(2):526-535. doi: 10.26717/bjstr.2017.01.000238
- Brewster DW, Bombick DW, Matsumura F. Rabbit serum hypertriglyceridemia after administration of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). J Toxicol Environ Health. 1988;25(4):495-507. doi: 10.1080/15287398809531227
- Brewster DW, Matsumura F. Differential effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin on adipose tissue lipoprotein lipase activity in the guinea pig, rat, hamster, rabbit, and mink. Comp Biochem Physiol C Comp Pharmacol Toxicol. 1989;93(1):49-53. doi: 10.1016/0742-8413(89)90009-1
- Brewster DW, Matsumura F. Reduction of adipose tissue lipoprotein lipase activity as a result of in vivo administration of 2,3,7,8-tetrachlorodibenzo-p-dioxin to the guinea pig. Biochem Pharmacol. 1988;37(11):2247-2253. doi: 10.1016/0006-2952(88)90588-6
- Wang B, Wang S, Zhao Z, et al. Bisphenol A exposure in relation to altered lipid profile and dyslipidemia among Chinese adults: A repeated measures study. Environ Res. 2020;184:109382. doi: 10.1016/j.envres.2020.109382
- Marmugi A, Lasserre F, Beuzelin D, et al. Adverse effects of long-term exposure to bisphenol A during adulthood leading to hyperglycaemia and hypercholesterolemia in mice. Toxicology. 2014;325:133-143. doi: 10.1016/j.tox.2014.08.006
- Samarghandian S, Azimi-Nezhad M, Shabestari MM, Azad FJ, Farkhondeh T, Bafandeh F. Effect of chronic exposure to cadmium on serum lipid, lipoprotein and oxidative stress indices in male rats. Interdiscip Toxicol. 2015;8(3):151-154. doi: 10.1515/intox-2015-0023
- Guo L, Zhao P, Xue S, Zhu Z. Association of urinary bisphenol A with hyperlipidemia and all-cause mortality: NHANES 2003-2016. PLoS One. 2024;19(7):e0304516. doi: 10.1371/journal.pone.0304516
- Azais-Braesco V, Macaire JP, Bellenand P, Robertson LW, Pascal G. Effects of two prototypic polychlorinated biphenyls (PCBs) on lipid composition of rat liver and serum. J Nutr Biochem. 1990;1(7):350-354. doi: 10.1016/0955-2863(90)90002-3
- Aminov Z, Haase RF, Pavuk M, Carpenter DO; Anniston Environmental Health Research Consortium. Analysis of the effects of exposure to polychlorinated biphenyls and chlorinated pesticides on serum lipid levels in residents of Anniston, Alabama. Environ Health. 2013;12:108. doi: 10.1186/1476-069X-12-108
- Kania-Korwel I, Wu X, Wang K, Lehmler HJ. Identification of lipidomic markers of chronic 3,3’,4,4’,5-pentachlorobiphenyl (PCB 126) exposure in the male rat liver. Toxicology. 2017;390:124-134. doi: 10.1016/j.tox.2017.09.005
- Arsenescu V, Arsenescu RI, King V, Swanson H, Cassis LA. Polychlorinated biphenyl-77 induces adipocyte differentiation and proinflammatory adipokines and promotes obesity and atherosclerosis. Environ Health Perspect. 2008;116(6):761-768. doi: 10.1289/ehp.10554
- Kim JY, Kim SJ, Bae MA, Kim JR, Cho KH. Cadmium exposure exacerbates severe hyperlipidemia and fatty liver changes in zebrafish via impairment of high-density lipoproteins functionality. Toxicol In Vitro. 2018;47:249-258. doi: 10.1016/j.tiv.2017.11.007
- Zhou Z, Lu YH, Pi HF, et al. Cadmium Exposure is Associated with the Prevalence of Dyslipidemia. Cell Physiol Biochem. 2016;40(3-4):633-643. doi: 10.1159/000452576
- Zhang Y, Liu W, Zhang W, et al. Association between blood lead levels and hyperlipidemiais: Results from the NHANES (1999-2018). Front Public Health. 2022;10:981749. doi: 10.3389/fpubh.2022.981749
- Kristal-Boneh E, Coller D, Froom P, Harari G, Ribak J. The association between occupational lead exposure and serum cholesterol and lipoprotein levels. Am J Public Health. 1999;89(7):1083-1087. doi: 10.2105/ajph.89.7.1083
- Kuo CC, Su PH, Sun CW, Liu HJ, Chang CL, Wang SL. Early life arsenic exposure promotes atherogenic lipid metabolism in adolescence: A 15-year birth cohort follow-up study in central Taiwan. Environ Int. 2018;118:97-105. doi: 10.1016/j.envint.2018.05.033
- Qu C, Huang R. Linking the Low-Density Lipoprotein-Cholesterol (LDL) Level to Arsenic Acid, Dimethylarsinic, and Monomethylarsonic: Results from a National Population-Based Study from the NHANES, 2003-2020. Nutrients. 2022;14(19):3993. doi: 10.3390/nu14193993
- Yue Y, Nair N, Quinones S, Kordas K, Desai G. Associations of total urinary arsenic with total cholesterol and highdensity lipoprotein among 12-17-year-old participants from the 2009-2016 NHANES cycles: A cross-sectional study. Int J Hyg Environ Health. 2022;242:113950. doi: 10.1016/j.ijheh.2022.113950
- Karim MR, Rahman M, Islam K, et al. Increases in oxidized low-density lipoprotein and other inflammatory and adhesion molecules with a concomitant decrease in highdensity lipoprotein in the individuals exposed to arsenic in Bangladesh. Toxicol Sci. 2013;135(1):17-25. doi: 10.1093/toxsci/kft130
- Segura B, Jurado MA, Freixenet N, Bargallo N, Junque C, Arboix A. White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a casecontrol study. BMC Neurol. 2010;10:64. doi: 10.1186/1471-2377-10-64
