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Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults

BACKGROUND: Lipoprotein (a) [Lp(a)] is an apoB100-containing lipoprotein with high levels being positively associated with atherosclerotic cardiovascular disease. Lp(a) levels are genetically determined. However, previous studies report a negative association between Lp(a) and saturated fatty acid i...

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Autores principales: Matveyenko, Anastasiya, Seid, Heather, Kim, Kyungyeon, Ramakrishnan, Rajasekhar, Thomas, Tiffany, Matienzo, Nelsa, Reyes-Soffer, Gissette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478368/
https://www.ncbi.nlm.nih.gov/pubmed/37670291
http://dx.doi.org/10.1186/s12944-023-01884-2
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author Matveyenko, Anastasiya
Seid, Heather
Kim, Kyungyeon
Ramakrishnan, Rajasekhar
Thomas, Tiffany
Matienzo, Nelsa
Reyes-Soffer, Gissette
author_facet Matveyenko, Anastasiya
Seid, Heather
Kim, Kyungyeon
Ramakrishnan, Rajasekhar
Thomas, Tiffany
Matienzo, Nelsa
Reyes-Soffer, Gissette
author_sort Matveyenko, Anastasiya
collection PubMed
description BACKGROUND: Lipoprotein (a) [Lp(a)] is an apoB100-containing lipoprotein with high levels being positively associated with atherosclerotic cardiovascular disease. Lp(a) levels are genetically determined. However, previous studies report a negative association between Lp(a) and saturated fatty acid intake. Currently, apoB100 lowering therapies are used to lower Lp(a) levels, and apheresis therapy is FDA approved for patients with extreme elevations of Lp(a). The current study analyzed the association of free-living diet components with plasma Lp(a) levels. METHODS: Dietary composition data was collected during screening visits for enrollment in previously completed lipid and lipoprotein metabolism studies at Columbia University Irving Medical Center via a standardized protocol by registered dietitians using 24 hour recalls. Data were analyzed with the Nutrition Data System for Research (Version 2018). Diet quality was calculated using the Healthy Eating Index (HEI) score. Fasting plasma Lp(a) levels were measured via an isoform-independent ELISA and apo(a) isoforms were measured using gel electrophoresis. RESULTS: We enrolled 28 subjects [Black (n = 18); Hispanic (n = 7); White (n = 3)]. The mean age was 48.3 ± 12.5 years with 17 males. Median level of Lp(a) was 79.9 nmol/L (34.4–146.0) and it was negatively associated with absolute (grams/day) and relative (percent of total calories) intake of dietary saturated fatty acids (SFA) (R = -0.43, P = 0.02, SFA …(% CAL): R = -0.38, P = 0.04), palmitic acid intake (R = -0.38, P = 0.05), and stearic acid intake (R = -0.40, P = 0.03). Analyses of associations with HEI score when stratified based on Lp(a) levels > or ≤ 100 nmol/L revealed no significant associations with any of the constituent factors. CONCLUSIONS: Using 24 hour recall, we confirm previous findings that Lp(a) levels are negatively associated with dietary saturated fatty acid intake. Additionally, Lp(a) levels are not related to diet quality, as assessed by the HEI score. The mechanisms underlying the relationship of SFA with Lp(a) require further investigation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01884-2.
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spelling pubmed-104783682023-09-06 Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults Matveyenko, Anastasiya Seid, Heather Kim, Kyungyeon Ramakrishnan, Rajasekhar Thomas, Tiffany Matienzo, Nelsa Reyes-Soffer, Gissette Lipids Health Dis Research BACKGROUND: Lipoprotein (a) [Lp(a)] is an apoB100-containing lipoprotein with high levels being positively associated with atherosclerotic cardiovascular disease. Lp(a) levels are genetically determined. However, previous studies report a negative association between Lp(a) and saturated fatty acid intake. Currently, apoB100 lowering therapies are used to lower Lp(a) levels, and apheresis therapy is FDA approved for patients with extreme elevations of Lp(a). The current study analyzed the association of free-living diet components with plasma Lp(a) levels. METHODS: Dietary composition data was collected during screening visits for enrollment in previously completed lipid and lipoprotein metabolism studies at Columbia University Irving Medical Center via a standardized protocol by registered dietitians using 24 hour recalls. Data were analyzed with the Nutrition Data System for Research (Version 2018). Diet quality was calculated using the Healthy Eating Index (HEI) score. Fasting plasma Lp(a) levels were measured via an isoform-independent ELISA and apo(a) isoforms were measured using gel electrophoresis. RESULTS: We enrolled 28 subjects [Black (n = 18); Hispanic (n = 7); White (n = 3)]. The mean age was 48.3 ± 12.5 years with 17 males. Median level of Lp(a) was 79.9 nmol/L (34.4–146.0) and it was negatively associated with absolute (grams/day) and relative (percent of total calories) intake of dietary saturated fatty acids (SFA) (R = -0.43, P = 0.02, SFA …(% CAL): R = -0.38, P = 0.04), palmitic acid intake (R = -0.38, P = 0.05), and stearic acid intake (R = -0.40, P = 0.03). Analyses of associations with HEI score when stratified based on Lp(a) levels > or ≤ 100 nmol/L revealed no significant associations with any of the constituent factors. CONCLUSIONS: Using 24 hour recall, we confirm previous findings that Lp(a) levels are negatively associated with dietary saturated fatty acid intake. Additionally, Lp(a) levels are not related to diet quality, as assessed by the HEI score. The mechanisms underlying the relationship of SFA with Lp(a) require further investigation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-023-01884-2. BioMed Central 2023-09-05 /pmc/articles/PMC10478368/ /pubmed/37670291 http://dx.doi.org/10.1186/s12944-023-01884-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Matveyenko, Anastasiya
Seid, Heather
Kim, Kyungyeon
Ramakrishnan, Rajasekhar
Thomas, Tiffany
Matienzo, Nelsa
Reyes-Soffer, Gissette
Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title_full Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title_fullStr Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title_full_unstemmed Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title_short Association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
title_sort association of free-living diet composition with plasma lipoprotein(a) levels in healthy adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478368/
https://www.ncbi.nlm.nih.gov/pubmed/37670291
http://dx.doi.org/10.1186/s12944-023-01884-2
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