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Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion
Low bile acid excretion (BAE) is associated with a higher risk of coronary artery disease (CAD) and cerebrovascular disease (stroke). This study investigated BAE in patients with peripheral vascular disease (PVD) and carotid artery disease (CA) and those without these diseases, compared to patients...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451290/ https://www.ncbi.nlm.nih.gov/pubmed/37627820 http://dx.doi.org/10.3390/bioengineering10080935 |
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author | Charach, Lior Charach, Gideon Karniel, Eli Galin, Leonid Bar Ziv, Dorin Grossman, Lior Kaye, Irit Grosskopf, Itamar |
author_facet | Charach, Lior Charach, Gideon Karniel, Eli Galin, Leonid Bar Ziv, Dorin Grossman, Lior Kaye, Irit Grosskopf, Itamar |
author_sort | Charach, Lior |
collection | PubMed |
description | Low bile acid excretion (BAE) is associated with a higher risk of coronary artery disease (CAD) and cerebrovascular disease (stroke). This study investigated BAE in patients with peripheral vascular disease (PVD) and carotid artery disease (CA) and those without these diseases, compared to patients with CAD, stroke, or no evidence of atherosclerosis. Patients with complaints of chest pain-suspected CAD, syncope, stroke/TIA, severe headache, intermittent claudication, or falls were enrolled. All received a 4-day standard diet with 490 mg of cholesterol and internal standard copper thiocyanate. Fecal BAE was measured using gas–liquid chromatography. One hundred and three patients, sixty-eight (66%) men and thirty-five women (34%), mean age range 60.9 ± 8.9 years, were enrolled in this prospective, 22-year follow-up study. Regression analysis showed that advanced age, total BAE, and excretion of the main fractions were the only significant independent factors that predicted prolonged survival (p < 0.001). Twenty-two years’ follow-up revealed only 15% of those with BAE <262.4 mg/24 h survived, compared to >60% of participants without atherosclerosis and a mean BAE of 676 mg/24 h. BAE was lower in patients with polyvascular atherosclerosis than in those with involvement of 1–3 vascular beds. Pearson correlations were found between total BAE and various fractions of BA, as well as HDL cholesterol. BAE and short-term survival were decreased among patients with PVD compared to those with CAD or stroke. Low BAE should be considered a valuable and independent risk factor for PVD. |
format | Online Article Text |
id | pubmed-10451290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104512902023-08-26 Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion Charach, Lior Charach, Gideon Karniel, Eli Galin, Leonid Bar Ziv, Dorin Grossman, Lior Kaye, Irit Grosskopf, Itamar Bioengineering (Basel) Article Low bile acid excretion (BAE) is associated with a higher risk of coronary artery disease (CAD) and cerebrovascular disease (stroke). This study investigated BAE in patients with peripheral vascular disease (PVD) and carotid artery disease (CA) and those without these diseases, compared to patients with CAD, stroke, or no evidence of atherosclerosis. Patients with complaints of chest pain-suspected CAD, syncope, stroke/TIA, severe headache, intermittent claudication, or falls were enrolled. All received a 4-day standard diet with 490 mg of cholesterol and internal standard copper thiocyanate. Fecal BAE was measured using gas–liquid chromatography. One hundred and three patients, sixty-eight (66%) men and thirty-five women (34%), mean age range 60.9 ± 8.9 years, were enrolled in this prospective, 22-year follow-up study. Regression analysis showed that advanced age, total BAE, and excretion of the main fractions were the only significant independent factors that predicted prolonged survival (p < 0.001). Twenty-two years’ follow-up revealed only 15% of those with BAE <262.4 mg/24 h survived, compared to >60% of participants without atherosclerosis and a mean BAE of 676 mg/24 h. BAE was lower in patients with polyvascular atherosclerosis than in those with involvement of 1–3 vascular beds. Pearson correlations were found between total BAE and various fractions of BA, as well as HDL cholesterol. BAE and short-term survival were decreased among patients with PVD compared to those with CAD or stroke. Low BAE should be considered a valuable and independent risk factor for PVD. MDPI 2023-08-07 /pmc/articles/PMC10451290/ /pubmed/37627820 http://dx.doi.org/10.3390/bioengineering10080935 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Charach, Lior Charach, Gideon Karniel, Eli Galin, Leonid Bar Ziv, Dorin Grossman, Lior Kaye, Irit Grosskopf, Itamar Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title | Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title_full | Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title_fullStr | Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title_full_unstemmed | Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title_short | Peripheral Vascular Disease and Carotid Artery Disease Are Associated with Decreased Bile Acid Excretion |
title_sort | peripheral vascular disease and carotid artery disease are associated with decreased bile acid excretion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451290/ https://www.ncbi.nlm.nih.gov/pubmed/37627820 http://dx.doi.org/10.3390/bioengineering10080935 |
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