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Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients
Background: Cardiovascular mortality in dialysis population remains very high. Saturated fatty acids (SFA) contribute to atherosclerosis and to cardiovascular risk. Aim: The aim of this study was to evaluate the relationship between mortality in dialysis patients and the serum SFA content. Methods:...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457217/ https://www.ncbi.nlm.nih.gov/pubmed/36078983 http://dx.doi.org/10.3390/jcm11175051 |
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author | Sikorska-Wisniewska, Malgorzata Mika, Adriana Sledzinski, Tomasz Chmielewski, Michal |
author_facet | Sikorska-Wisniewska, Malgorzata Mika, Adriana Sledzinski, Tomasz Chmielewski, Michal |
author_sort | Sikorska-Wisniewska, Malgorzata |
collection | PubMed |
description | Background: Cardiovascular mortality in dialysis population remains very high. Saturated fatty acids (SFA) contribute to atherosclerosis and to cardiovascular risk. Aim: The aim of this study was to evaluate the relationship between mortality in dialysis patients and the serum SFA content. Methods: Survival of 54 patients on dialysis was assessed. A total of 21 SFA from patients’ sera were measured by gas chromatography-mass spectrometry (GC-MS). Diet was assessed by food frequency questionnaire FFQ-6. The SFA content is presented as fatty acid proportion (%). Results: During the observation time (median 66 months) 22 patients died. There was a significant relationship between elevated SFA (above SFA mean) and mortality (log-rank 3.13; p = 0.0017). Moreover, patients who ingested foods rich in SFA, according to FFQ-6, had a higher mortality risk (log-rank 2.24; p = 0.03). The hazard ratio for mortality associated with increased SFA content equalled 4.47 (1.63–12.26). Addition of age and inflammation (hsCRP > 5 mg/L) into the Cox model did not modify this relationship. However, SFA content turned out to be significantly higher in patients with diabetes mellitus and cardiovascular disease, as compared to patients free from these co-morbidities. Their addition to the model attenuated the relationship between SFA and mortality, making it statistically insignificant. Conclusion: The serum content of SFA turned out to be a strong predictor of mortality in dialysis patients. However, given the significant associations between SFA, DM, and CVD, interventional studies with controlled SFA intake are needed to evaluate the causal links between SFA, co-morbidities and survival. |
format | Online Article Text |
id | pubmed-9457217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94572172022-09-09 Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients Sikorska-Wisniewska, Malgorzata Mika, Adriana Sledzinski, Tomasz Chmielewski, Michal J Clin Med Article Background: Cardiovascular mortality in dialysis population remains very high. Saturated fatty acids (SFA) contribute to atherosclerosis and to cardiovascular risk. Aim: The aim of this study was to evaluate the relationship between mortality in dialysis patients and the serum SFA content. Methods: Survival of 54 patients on dialysis was assessed. A total of 21 SFA from patients’ sera were measured by gas chromatography-mass spectrometry (GC-MS). Diet was assessed by food frequency questionnaire FFQ-6. The SFA content is presented as fatty acid proportion (%). Results: During the observation time (median 66 months) 22 patients died. There was a significant relationship between elevated SFA (above SFA mean) and mortality (log-rank 3.13; p = 0.0017). Moreover, patients who ingested foods rich in SFA, according to FFQ-6, had a higher mortality risk (log-rank 2.24; p = 0.03). The hazard ratio for mortality associated with increased SFA content equalled 4.47 (1.63–12.26). Addition of age and inflammation (hsCRP > 5 mg/L) into the Cox model did not modify this relationship. However, SFA content turned out to be significantly higher in patients with diabetes mellitus and cardiovascular disease, as compared to patients free from these co-morbidities. Their addition to the model attenuated the relationship between SFA and mortality, making it statistically insignificant. Conclusion: The serum content of SFA turned out to be a strong predictor of mortality in dialysis patients. However, given the significant associations between SFA, DM, and CVD, interventional studies with controlled SFA intake are needed to evaluate the causal links between SFA, co-morbidities and survival. MDPI 2022-08-28 /pmc/articles/PMC9457217/ /pubmed/36078983 http://dx.doi.org/10.3390/jcm11175051 Text en © 2022 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 Sikorska-Wisniewska, Malgorzata Mika, Adriana Sledzinski, Tomasz Chmielewski, Michal Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title | Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title_full | Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title_fullStr | Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title_full_unstemmed | Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title_short | Associations between Serum Saturated Fatty Acids Content and Mortality in Dialysis Patients |
title_sort | associations between serum saturated fatty acids content and mortality in dialysis patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457217/ https://www.ncbi.nlm.nih.gov/pubmed/36078983 http://dx.doi.org/10.3390/jcm11175051 |
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