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Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease

BACKGROUND: Heavy metal pollutants such as cadmium (Cd), lead (Pb), and mercury (Hg) are rarely the subjects of cardiovascular research although they have been suspected for decades to negatively impact the circulatory system. METHODS: Apart from detailed anamnestic data, urinary levels of Cd and fu...

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Autores principales: Sponder, Michael, Fritzer-Szekeres, Monika, Marculescu, Rodrig, Mittlböck, Martina, Uhl, Maria, Köhler-Vallant, Birgit, Strametz-Juranek, Jeanette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027918/
https://www.ncbi.nlm.nih.gov/pubmed/24868163
http://dx.doi.org/10.2147/VHRM.S61510
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author Sponder, Michael
Fritzer-Szekeres, Monika
Marculescu, Rodrig
Mittlböck, Martina
Uhl, Maria
Köhler-Vallant, Birgit
Strametz-Juranek, Jeanette
author_facet Sponder, Michael
Fritzer-Szekeres, Monika
Marculescu, Rodrig
Mittlböck, Martina
Uhl, Maria
Köhler-Vallant, Birgit
Strametz-Juranek, Jeanette
author_sort Sponder, Michael
collection PubMed
description BACKGROUND: Heavy metal pollutants such as cadmium (Cd), lead (Pb), and mercury (Hg) are rarely the subjects of cardiovascular research although they have been suspected for decades to negatively impact the circulatory system. METHODS: Apart from detailed anamnestic data, urinary levels of Cd and full blood levels of Pb and Hg were measured in 53 female (mean age: 68.04±7.03 years) and 111 male (mean age: 60.68±11.43 years) nonsmoking or never-smoking patients with angiographically verified and precisely quantified coronary artery disease (CAD). RESULTS: Although Cd was quantifiable in 68.3% of subjects, only 34.1% of these patients exceeded the critical 1 μg/L Human Biomonitoring (HBM)-I level. Median Pb (20 μg/L) and Hg (0.55 μg/L) levels were lower than the HBM-I, as well as reference levels of Pb. Wine consumption was the main source for Pb, fish and wine consumption for Hg, and previous nicotine abuse for Cd. There was no correlation between Cd, Pb, or Hg and severity of CAD although severity correlated positively with atherosclerosis parameters (uric acid, creatinine, triglycerides, blood urea nitrogen, C-reactive protein) and negatively with high density lipoprotein cholesterol. CONCLUSION: Cd levels detected in CAD patients were high compared to German and European reference levels but it could not be proven that urine levels of Cd and blood levels of Hg or Pb played a major role in the genesis of CAD, particularly when compared to well-known biomarkers such as blood pressure, glucose, and lipids.
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spelling pubmed-40279182014-05-27 Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease Sponder, Michael Fritzer-Szekeres, Monika Marculescu, Rodrig Mittlböck, Martina Uhl, Maria Köhler-Vallant, Birgit Strametz-Juranek, Jeanette Vasc Health Risk Manag Original Research BACKGROUND: Heavy metal pollutants such as cadmium (Cd), lead (Pb), and mercury (Hg) are rarely the subjects of cardiovascular research although they have been suspected for decades to negatively impact the circulatory system. METHODS: Apart from detailed anamnestic data, urinary levels of Cd and full blood levels of Pb and Hg were measured in 53 female (mean age: 68.04±7.03 years) and 111 male (mean age: 60.68±11.43 years) nonsmoking or never-smoking patients with angiographically verified and precisely quantified coronary artery disease (CAD). RESULTS: Although Cd was quantifiable in 68.3% of subjects, only 34.1% of these patients exceeded the critical 1 μg/L Human Biomonitoring (HBM)-I level. Median Pb (20 μg/L) and Hg (0.55 μg/L) levels were lower than the HBM-I, as well as reference levels of Pb. Wine consumption was the main source for Pb, fish and wine consumption for Hg, and previous nicotine abuse for Cd. There was no correlation between Cd, Pb, or Hg and severity of CAD although severity correlated positively with atherosclerosis parameters (uric acid, creatinine, triglycerides, blood urea nitrogen, C-reactive protein) and negatively with high density lipoprotein cholesterol. CONCLUSION: Cd levels detected in CAD patients were high compared to German and European reference levels but it could not be proven that urine levels of Cd and blood levels of Hg or Pb played a major role in the genesis of CAD, particularly when compared to well-known biomarkers such as blood pressure, glucose, and lipids. Dove Medical Press 2014-05-13 /pmc/articles/PMC4027918/ /pubmed/24868163 http://dx.doi.org/10.2147/VHRM.S61510 Text en © 2014 Sponder et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Sponder, Michael
Fritzer-Szekeres, Monika
Marculescu, Rodrig
Mittlböck, Martina
Uhl, Maria
Köhler-Vallant, Birgit
Strametz-Juranek, Jeanette
Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title_full Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title_fullStr Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title_full_unstemmed Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title_short Blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
title_sort blood and urine levels of heavy metal pollutants in female and male patients with coronary artery disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027918/
https://www.ncbi.nlm.nih.gov/pubmed/24868163
http://dx.doi.org/10.2147/VHRM.S61510
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