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A clustering analysis of lipoprotein diameters in the metabolic syndrome

BACKGROUND: The presence of smaller low-density lipoproteins (LDL) has been associated with atherosclerosis risk, and the insulin resistance (IR) underlying the metabolic syndrome (MetS). In addition, some research has supported the association of very low-, low- and high-density lipoprotein (VLDL H...

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Autores principales: Frazier-Wood, Alexis C, Glasser, Stephen, Garvey, W Timothy, Kabagambe, Edmond K, Borecki, Ingrid B, Tiwari, Hemant K, Tsai, Michael Y, Hopkins, Paul N, Ordovas, Jose M, Arnett, Donna K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260106/
https://www.ncbi.nlm.nih.gov/pubmed/22182248
http://dx.doi.org/10.1186/1476-511X-10-237
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author Frazier-Wood, Alexis C
Glasser, Stephen
Garvey, W Timothy
Kabagambe, Edmond K
Borecki, Ingrid B
Tiwari, Hemant K
Tsai, Michael Y
Hopkins, Paul N
Ordovas, Jose M
Arnett, Donna K
author_facet Frazier-Wood, Alexis C
Glasser, Stephen
Garvey, W Timothy
Kabagambe, Edmond K
Borecki, Ingrid B
Tiwari, Hemant K
Tsai, Michael Y
Hopkins, Paul N
Ordovas, Jose M
Arnett, Donna K
author_sort Frazier-Wood, Alexis C
collection PubMed
description BACKGROUND: The presence of smaller low-density lipoproteins (LDL) has been associated with atherosclerosis risk, and the insulin resistance (IR) underlying the metabolic syndrome (MetS). In addition, some research has supported the association of very low-, low- and high-density lipoprotein (VLDL HDL) particle diameters with components of the metabolic syndrome (MetS), although this has been the focus of less research. We aimed to explore the relationship of VLDL, LDL and HDL diameters to MetS and its features, and by clustering individuals by their diameters of VLDL, LDL and HDL particles, to capture information across all three fractions of lipoprotein into a unified phenotype. METHODS: We used nuclear magnetic resonance spectroscopy measurements on fasting plasma samples from a general population sample of 1,036 adults (mean ± SD, 48.8 ± 16.2 y of age). Using latent class analysis, the sample was grouped by the diameter of their fasting lipoproteins, and mixed effects models tested whether the distribution of MetS components varied across the groups. RESULTS: Eight discrete groups were identified. Two groups (N = 251) were enriched with individuals meeting criteria for the MetS, and were characterized by the smallest LDL/HDL diameters. One of those two groups, one was additionally distinguished by large VLDL, and had significantly higher blood pressure, fasting glucose, triglycerides, and waist circumference (WC; P < .001). However, large VLDL, in the absence of small LDL and HDL particles, did not associate with MetS features. These associations held after additionally controlling for VLDL, LDL and HDL particle concentrations. CONCLUSIONS: While small LDL diameters remain associated with IR and the MetS, the occurrence of these in conjunction with a shift to overall larger VLDL diameter may identify those with the highest fasting glucose, TG and WC within the MetS. If replicated, the association of this phenotype with more severe IR-features indicated that it may contribute to identifying of those most at risk for incident type II diabetes and cardiometabolic disease.
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spelling pubmed-32601062012-01-18 A clustering analysis of lipoprotein diameters in the metabolic syndrome Frazier-Wood, Alexis C Glasser, Stephen Garvey, W Timothy Kabagambe, Edmond K Borecki, Ingrid B Tiwari, Hemant K Tsai, Michael Y Hopkins, Paul N Ordovas, Jose M Arnett, Donna K Lipids Health Dis Research BACKGROUND: The presence of smaller low-density lipoproteins (LDL) has been associated with atherosclerosis risk, and the insulin resistance (IR) underlying the metabolic syndrome (MetS). In addition, some research has supported the association of very low-, low- and high-density lipoprotein (VLDL HDL) particle diameters with components of the metabolic syndrome (MetS), although this has been the focus of less research. We aimed to explore the relationship of VLDL, LDL and HDL diameters to MetS and its features, and by clustering individuals by their diameters of VLDL, LDL and HDL particles, to capture information across all three fractions of lipoprotein into a unified phenotype. METHODS: We used nuclear magnetic resonance spectroscopy measurements on fasting plasma samples from a general population sample of 1,036 adults (mean ± SD, 48.8 ± 16.2 y of age). Using latent class analysis, the sample was grouped by the diameter of their fasting lipoproteins, and mixed effects models tested whether the distribution of MetS components varied across the groups. RESULTS: Eight discrete groups were identified. Two groups (N = 251) were enriched with individuals meeting criteria for the MetS, and were characterized by the smallest LDL/HDL diameters. One of those two groups, one was additionally distinguished by large VLDL, and had significantly higher blood pressure, fasting glucose, triglycerides, and waist circumference (WC; P < .001). However, large VLDL, in the absence of small LDL and HDL particles, did not associate with MetS features. These associations held after additionally controlling for VLDL, LDL and HDL particle concentrations. CONCLUSIONS: While small LDL diameters remain associated with IR and the MetS, the occurrence of these in conjunction with a shift to overall larger VLDL diameter may identify those with the highest fasting glucose, TG and WC within the MetS. If replicated, the association of this phenotype with more severe IR-features indicated that it may contribute to identifying of those most at risk for incident type II diabetes and cardiometabolic disease. BioMed Central 2011-12-19 /pmc/articles/PMC3260106/ /pubmed/22182248 http://dx.doi.org/10.1186/1476-511X-10-237 Text en Copyright ©2011 Frazier-Wood et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Frazier-Wood, Alexis C
Glasser, Stephen
Garvey, W Timothy
Kabagambe, Edmond K
Borecki, Ingrid B
Tiwari, Hemant K
Tsai, Michael Y
Hopkins, Paul N
Ordovas, Jose M
Arnett, Donna K
A clustering analysis of lipoprotein diameters in the metabolic syndrome
title A clustering analysis of lipoprotein diameters in the metabolic syndrome
title_full A clustering analysis of lipoprotein diameters in the metabolic syndrome
title_fullStr A clustering analysis of lipoprotein diameters in the metabolic syndrome
title_full_unstemmed A clustering analysis of lipoprotein diameters in the metabolic syndrome
title_short A clustering analysis of lipoprotein diameters in the metabolic syndrome
title_sort clustering analysis of lipoprotein diameters in the metabolic syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260106/
https://www.ncbi.nlm.nih.gov/pubmed/22182248
http://dx.doi.org/10.1186/1476-511X-10-237
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