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Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients

Gender differences in the burden of cardiovascular disease (CVD) have been observed worldwide. In this study, plasmatic levels of trimethylamine (TMA) and blood oxidative biomarkers have been evaluated in 358 men (89 controls and 269 CVD patients) and 189 women (64 control and 125 CVD patients). The...

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Autores principales: Bordoni, Laura, Fedeli, Donatella, Piangerelli, Marco, Pelikant-Malecka, Iwona, Radulska, Adrianna, Samulak, Joanna J., Sawicka, Angelika K., Lewicki, Lukasz, Kalinowski, Leszek, Olek, Robert A., Gabbianelli, Rosita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460342/
https://www.ncbi.nlm.nih.gov/pubmed/32717906
http://dx.doi.org/10.3390/biomedicines8080238
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author Bordoni, Laura
Fedeli, Donatella
Piangerelli, Marco
Pelikant-Malecka, Iwona
Radulska, Adrianna
Samulak, Joanna J.
Sawicka, Angelika K.
Lewicki, Lukasz
Kalinowski, Leszek
Olek, Robert A.
Gabbianelli, Rosita
author_facet Bordoni, Laura
Fedeli, Donatella
Piangerelli, Marco
Pelikant-Malecka, Iwona
Radulska, Adrianna
Samulak, Joanna J.
Sawicka, Angelika K.
Lewicki, Lukasz
Kalinowski, Leszek
Olek, Robert A.
Gabbianelli, Rosita
author_sort Bordoni, Laura
collection PubMed
description Gender differences in the burden of cardiovascular disease (CVD) have been observed worldwide. In this study, plasmatic levels of trimethylamine (TMA) and blood oxidative biomarkers have been evaluated in 358 men (89 controls and 269 CVD patients) and 189 women (64 control and 125 CVD patients). The fluorescence technique was applied to determine erythrocyte membrane fluidity using 1,6-diphenyl-1,3,5-hexatriene (DPH) and Laurdan, while lipid hydroperoxides were assessed by diphenyl−1-pyrenylphosphine (DPPP). Results show that levels of plasmatic TMA were higher in healthy men with respect to healthy women (p = 0.0001). Significantly lower TMA was observed in male CVD patients (0.609 ± 0.104 μM) compared to healthy male controls (0.680 ± 0.118 μM) (p < 0.001), while higher levels of TMA were measured in female CVD patients (0.595 ± 0.115 μM) with respect to female controls (0.529 ± 0.073 μM) (p < 0.001). DPPP was significantly higher in healthy control men than in women (p < 0.001). Male CVD patients displayed a lower value of DPPP (2777 ± 1924) compared to healthy controls (5528 ± 2222) (p < 0.001), while no significant changes were measured in females with or without CVD (p > 0.05). Membrane fluidity was significantly higher (p < 0.001) in the hydrophobic bilayer only in control male subjects. In conclusion, gender differences were observed in blood oxidative biomarkers, and DPPP value might be suggested as a biomarker predictive of CVD only in men.
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spelling pubmed-74603422020-09-02 Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients Bordoni, Laura Fedeli, Donatella Piangerelli, Marco Pelikant-Malecka, Iwona Radulska, Adrianna Samulak, Joanna J. Sawicka, Angelika K. Lewicki, Lukasz Kalinowski, Leszek Olek, Robert A. Gabbianelli, Rosita Biomedicines Article Gender differences in the burden of cardiovascular disease (CVD) have been observed worldwide. In this study, plasmatic levels of trimethylamine (TMA) and blood oxidative biomarkers have been evaluated in 358 men (89 controls and 269 CVD patients) and 189 women (64 control and 125 CVD patients). The fluorescence technique was applied to determine erythrocyte membrane fluidity using 1,6-diphenyl-1,3,5-hexatriene (DPH) and Laurdan, while lipid hydroperoxides were assessed by diphenyl−1-pyrenylphosphine (DPPP). Results show that levels of plasmatic TMA were higher in healthy men with respect to healthy women (p = 0.0001). Significantly lower TMA was observed in male CVD patients (0.609 ± 0.104 μM) compared to healthy male controls (0.680 ± 0.118 μM) (p < 0.001), while higher levels of TMA were measured in female CVD patients (0.595 ± 0.115 μM) with respect to female controls (0.529 ± 0.073 μM) (p < 0.001). DPPP was significantly higher in healthy control men than in women (p < 0.001). Male CVD patients displayed a lower value of DPPP (2777 ± 1924) compared to healthy controls (5528 ± 2222) (p < 0.001), while no significant changes were measured in females with or without CVD (p > 0.05). Membrane fluidity was significantly higher (p < 0.001) in the hydrophobic bilayer only in control male subjects. In conclusion, gender differences were observed in blood oxidative biomarkers, and DPPP value might be suggested as a biomarker predictive of CVD only in men. MDPI 2020-07-23 /pmc/articles/PMC7460342/ /pubmed/32717906 http://dx.doi.org/10.3390/biomedicines8080238 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bordoni, Laura
Fedeli, Donatella
Piangerelli, Marco
Pelikant-Malecka, Iwona
Radulska, Adrianna
Samulak, Joanna J.
Sawicka, Angelika K.
Lewicki, Lukasz
Kalinowski, Leszek
Olek, Robert A.
Gabbianelli, Rosita
Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title_full Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title_fullStr Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title_full_unstemmed Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title_short Gender-Related Differences in Trimethylamine and Oxidative Blood Biomarkers in Cardiovascular Disease Patients
title_sort gender-related differences in trimethylamine and oxidative blood biomarkers in cardiovascular disease patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460342/
https://www.ncbi.nlm.nih.gov/pubmed/32717906
http://dx.doi.org/10.3390/biomedicines8080238
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