Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles

Research output: Contribution to journalJournal articleResearchpeer-review

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Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles. / Castro-Mejía, Josué L.; Khakimov, Bekzod; Aru, Violetta; Lind, Mads V.; Garne, Eva; Paulová, Petronela; Tavakkoli, Elnaz; Hansen, Lars H.; Smilde, Age K.; Holm, Lars; Engelsen, Søren B.; Nielsen, Dennis S.

In: Microorganisms, Vol. 10, No. 11, 2156, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Castro-Mejía, JL, Khakimov, B, Aru, V, Lind, MV, Garne, E, Paulová, P, Tavakkoli, E, Hansen, LH, Smilde, AK, Holm, L, Engelsen, SB & Nielsen, DS 2022, 'Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles', Microorganisms, vol. 10, no. 11, 2156. https://doi.org/10.3390/microorganisms10112156

APA

Castro-Mejía, J. L., Khakimov, B., Aru, V., Lind, M. V., Garne, E., Paulová, P., Tavakkoli, E., Hansen, L. H., Smilde, A. K., Holm, L., Engelsen, S. B., & Nielsen, D. S. (2022). Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles. Microorganisms, 10(11), [2156]. https://doi.org/10.3390/microorganisms10112156

Vancouver

Castro-Mejía JL, Khakimov B, Aru V, Lind MV, Garne E, Paulová P et al. Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles. Microorganisms. 2022;10(11). 2156. https://doi.org/10.3390/microorganisms10112156

Author

Castro-Mejía, Josué L. ; Khakimov, Bekzod ; Aru, Violetta ; Lind, Mads V. ; Garne, Eva ; Paulová, Petronela ; Tavakkoli, Elnaz ; Hansen, Lars H. ; Smilde, Age K. ; Holm, Lars ; Engelsen, Søren B. ; Nielsen, Dennis S. / Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles. In: Microorganisms. 2022 ; Vol. 10, No. 11.

Bibtex

@article{8189fb2208344435a1049a585736c0ee,
title = "Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles",
abstract = "Increasing evidence indicates that the gut microbiome (GM) plays an important role in dyslipidemia. To date, however, no in-depth characterization of the associations between GM with lipoproteins distributions (LPD) among adult individuals with diverse BMI has been conducted. To determine such associations, we studied blood-plasma LPD, fecal short-chain fatty acids (SCFA) and GM of 262 Danes aged 19–89 years. Stratification of LPD segregated subjects into three clusters displaying recommended levels of lipoproteins and explained by age and body-mass-index. Higher levels of HDL2a and HDL2b were associated with a higher abundance of Ruminococcaceae and Christensenellaceae. Increasing levels of total cholesterol and LDL-1 and LDL-2 were positively associated with Lachnospiraceae and Coriobacteriaceae, and negatively with Bacteroidaceae and Bifidobacteriaceae. Metagenome-sequencing showed a higher abundance of biosynthesis of multiple B-vitamins and SCFA metabolism genes among healthier LPD profiles. Metagenomic-assembled genomes (MAGs) affiliated to Eggerthellaceae and Clostridiales were contributors of these genes and their relative abundance correlated positively with larger HDL subfractions. The study demonstrates that differences in composition and metabolic traits of the GM are associated with variations in LPD among the recruited subjects. These findings provide evidence for GM considerations in future research aiming to shed light on mechanisms of the GM–dyslipidemia axis.",
keywords = "H-NMR, gut microbiota, HDL, lipoproteins distribution, SCFAs",
author = "Castro-Mej{\'i}a, {Josu{\'e} L.} and Bekzod Khakimov and Violetta Aru and Lind, {Mads V.} and Eva Garne and Petronela Paulov{\'a} and Elnaz Tavakkoli and Hansen, {Lars H.} and Smilde, {Age K.} and Lars Holm and Engelsen, {S{\o}ren B.} and Nielsen, {Dennis S.}",
note = "Publisher Copyright: {\textcopyright} 2022 by the authors.",
year = "2022",
doi = "10.3390/microorganisms10112156",
language = "English",
volume = "10",
journal = "Microorganisms",
issn = "2076-2607",
publisher = "M D P I AG",
number = "11",

}

RIS

TY - JOUR

T1 - Gut Microbiome and Its Cofactors Are Linked to Lipoprotein Distribution Profiles

AU - Castro-Mejía, Josué L.

AU - Khakimov, Bekzod

AU - Aru, Violetta

AU - Lind, Mads V.

AU - Garne, Eva

AU - Paulová, Petronela

AU - Tavakkoli, Elnaz

AU - Hansen, Lars H.

AU - Smilde, Age K.

AU - Holm, Lars

AU - Engelsen, Søren B.

AU - Nielsen, Dennis S.

N1 - Publisher Copyright: © 2022 by the authors.

PY - 2022

Y1 - 2022

N2 - Increasing evidence indicates that the gut microbiome (GM) plays an important role in dyslipidemia. To date, however, no in-depth characterization of the associations between GM with lipoproteins distributions (LPD) among adult individuals with diverse BMI has been conducted. To determine such associations, we studied blood-plasma LPD, fecal short-chain fatty acids (SCFA) and GM of 262 Danes aged 19–89 years. Stratification of LPD segregated subjects into three clusters displaying recommended levels of lipoproteins and explained by age and body-mass-index. Higher levels of HDL2a and HDL2b were associated with a higher abundance of Ruminococcaceae and Christensenellaceae. Increasing levels of total cholesterol and LDL-1 and LDL-2 were positively associated with Lachnospiraceae and Coriobacteriaceae, and negatively with Bacteroidaceae and Bifidobacteriaceae. Metagenome-sequencing showed a higher abundance of biosynthesis of multiple B-vitamins and SCFA metabolism genes among healthier LPD profiles. Metagenomic-assembled genomes (MAGs) affiliated to Eggerthellaceae and Clostridiales were contributors of these genes and their relative abundance correlated positively with larger HDL subfractions. The study demonstrates that differences in composition and metabolic traits of the GM are associated with variations in LPD among the recruited subjects. These findings provide evidence for GM considerations in future research aiming to shed light on mechanisms of the GM–dyslipidemia axis.

AB - Increasing evidence indicates that the gut microbiome (GM) plays an important role in dyslipidemia. To date, however, no in-depth characterization of the associations between GM with lipoproteins distributions (LPD) among adult individuals with diverse BMI has been conducted. To determine such associations, we studied blood-plasma LPD, fecal short-chain fatty acids (SCFA) and GM of 262 Danes aged 19–89 years. Stratification of LPD segregated subjects into three clusters displaying recommended levels of lipoproteins and explained by age and body-mass-index. Higher levels of HDL2a and HDL2b were associated with a higher abundance of Ruminococcaceae and Christensenellaceae. Increasing levels of total cholesterol and LDL-1 and LDL-2 were positively associated with Lachnospiraceae and Coriobacteriaceae, and negatively with Bacteroidaceae and Bifidobacteriaceae. Metagenome-sequencing showed a higher abundance of biosynthesis of multiple B-vitamins and SCFA metabolism genes among healthier LPD profiles. Metagenomic-assembled genomes (MAGs) affiliated to Eggerthellaceae and Clostridiales were contributors of these genes and their relative abundance correlated positively with larger HDL subfractions. The study demonstrates that differences in composition and metabolic traits of the GM are associated with variations in LPD among the recruited subjects. These findings provide evidence for GM considerations in future research aiming to shed light on mechanisms of the GM–dyslipidemia axis.

KW - H-NMR

KW - gut microbiota

KW - HDL

KW - lipoproteins distribution

KW - SCFAs

U2 - 10.3390/microorganisms10112156

DO - 10.3390/microorganisms10112156

M3 - Journal article

C2 - 36363749

AN - SCOPUS:85141722316

VL - 10

JO - Microorganisms

JF - Microorganisms

SN - 2076-2607

IS - 11

M1 - 2156

ER -

ID: 326731145