The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study

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The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study. / Nestel, Nathalie; Hvass, Josephine D; Bahl, Martin Iain; Hansen, Lars Hestbjerg; Krych, Lukasz; Nielsen, Dennis Sandris; Dragsted, Lars Ove; Roager, Henrik Munch.

In: Frontiers in Nutrition, Vol. 7, 594850, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nestel, N, Hvass, JD, Bahl, MI, Hansen, LH, Krych, L, Nielsen, DS, Dragsted, LO & Roager, HM 2021, 'The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study', Frontiers in Nutrition, vol. 7, 594850. https://doi.org/10.3389/fnut.2020.594850

APA

Nestel, N., Hvass, J. D., Bahl, M. I., Hansen, L. H., Krych, L., Nielsen, D. S., Dragsted, L. O., & Roager, H. M. (2021). The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study. Frontiers in Nutrition, 7, [594850]. https://doi.org/10.3389/fnut.2020.594850

Vancouver

Nestel N, Hvass JD, Bahl MI, Hansen LH, Krych L, Nielsen DS et al. The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study. Frontiers in Nutrition. 2021;7. 594850. https://doi.org/10.3389/fnut.2020.594850

Author

Nestel, Nathalie ; Hvass, Josephine D ; Bahl, Martin Iain ; Hansen, Lars Hestbjerg ; Krych, Lukasz ; Nielsen, Dennis Sandris ; Dragsted, Lars Ove ; Roager, Henrik Munch. / The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study. In: Frontiers in Nutrition. 2021 ; Vol. 7.

Bibtex

@article{6d83249c5c544b66848e1ec38b6a7b0f,
title = "The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study",
abstract = "The gut microbiome has combined with other person-specific information, such as blood parameters, dietary habits, anthropometrics, and physical activity been found to predict personalized postprandial glucose responses (PPGRs) to various foods. Yet, the contributions of specific microbiome taxa, measures of fermentation, and abiotic factors in the colon to glycemic control remain elusive. We tested whether PPGRs 60 min after a standardized breakfast was associated with gut microbial α-diversity (primary outcome) and explored whether postprandial responses of glucose and insulin were associated with specific microbiome taxa, colonic fermentation as reflected by fecal short-chain fatty acids (SCFAs), and breath hydrogen and methane exhalation, as well as abiotic factors including fecal pH, fecal water content, fecal energy density, intestinal transit time (ITT), and stool consistency. A single-arm meal trial was conducted. A total of 31 healthy (24 female and seven male) subjects consumed a standardized evening meal and a subsequent standardized breakfast (1,499 kJ) where blood was collected for analysis of postprandial glucose and insulin responses. PPGRs to the same breakfast varied across the healthy subjects. The largest inter-individual variability in PPGRs was observed 60 min after the meal but was not associated with gut microbial α-diversity. In addition, no significant associations were observed between postprandial responses and specific taxa of the gut microbiome, measures of colonic fermentation, ITT, or other abiotic factors. However, fasting glucose concentrations were negatively associated with ITT, and fasting insulin was positively associated with fasting breath hydrogen. In conclusion, the gut microbiome, measures of colonic fermentation, and abiotic factors were not shown to be significantly associated with variability in postprandial responses, suggesting that contributions of the gut microbiome, colonic fermentation, and abiotic factors to PPGRs may be subtle in healthy adults.",
keywords = "Faculty of Science, Gut microbiome, Personalized nutrition, Individuality, Intestinal transit time, Abiotic factors, Colonic fermentation",
author = "Nathalie Nestel and Hvass, {Josephine D} and Bahl, {Martin Iain} and Hansen, {Lars Hestbjerg} and Lukasz Krych and Nielsen, {Dennis Sandris} and Dragsted, {Lars Ove} and Roager, {Henrik Munch}",
note = "CURIS 2021 NEXS 065",
year = "2021",
doi = "10.3389/fnut.2020.594850",
language = "English",
volume = "7",
journal = "Frontiers in Nutrition",
issn = "2296-861X",
publisher = "Frontiers",

}

RIS

TY - JOUR

T1 - The gut microbiome and abiotic factors as potential determinants of postprandial glucose responses: A single-arm meal study

AU - Nestel, Nathalie

AU - Hvass, Josephine D

AU - Bahl, Martin Iain

AU - Hansen, Lars Hestbjerg

AU - Krych, Lukasz

AU - Nielsen, Dennis Sandris

AU - Dragsted, Lars Ove

AU - Roager, Henrik Munch

N1 - CURIS 2021 NEXS 065

PY - 2021

Y1 - 2021

N2 - The gut microbiome has combined with other person-specific information, such as blood parameters, dietary habits, anthropometrics, and physical activity been found to predict personalized postprandial glucose responses (PPGRs) to various foods. Yet, the contributions of specific microbiome taxa, measures of fermentation, and abiotic factors in the colon to glycemic control remain elusive. We tested whether PPGRs 60 min after a standardized breakfast was associated with gut microbial α-diversity (primary outcome) and explored whether postprandial responses of glucose and insulin were associated with specific microbiome taxa, colonic fermentation as reflected by fecal short-chain fatty acids (SCFAs), and breath hydrogen and methane exhalation, as well as abiotic factors including fecal pH, fecal water content, fecal energy density, intestinal transit time (ITT), and stool consistency. A single-arm meal trial was conducted. A total of 31 healthy (24 female and seven male) subjects consumed a standardized evening meal and a subsequent standardized breakfast (1,499 kJ) where blood was collected for analysis of postprandial glucose and insulin responses. PPGRs to the same breakfast varied across the healthy subjects. The largest inter-individual variability in PPGRs was observed 60 min after the meal but was not associated with gut microbial α-diversity. In addition, no significant associations were observed between postprandial responses and specific taxa of the gut microbiome, measures of colonic fermentation, ITT, or other abiotic factors. However, fasting glucose concentrations were negatively associated with ITT, and fasting insulin was positively associated with fasting breath hydrogen. In conclusion, the gut microbiome, measures of colonic fermentation, and abiotic factors were not shown to be significantly associated with variability in postprandial responses, suggesting that contributions of the gut microbiome, colonic fermentation, and abiotic factors to PPGRs may be subtle in healthy adults.

AB - The gut microbiome has combined with other person-specific information, such as blood parameters, dietary habits, anthropometrics, and physical activity been found to predict personalized postprandial glucose responses (PPGRs) to various foods. Yet, the contributions of specific microbiome taxa, measures of fermentation, and abiotic factors in the colon to glycemic control remain elusive. We tested whether PPGRs 60 min after a standardized breakfast was associated with gut microbial α-diversity (primary outcome) and explored whether postprandial responses of glucose and insulin were associated with specific microbiome taxa, colonic fermentation as reflected by fecal short-chain fatty acids (SCFAs), and breath hydrogen and methane exhalation, as well as abiotic factors including fecal pH, fecal water content, fecal energy density, intestinal transit time (ITT), and stool consistency. A single-arm meal trial was conducted. A total of 31 healthy (24 female and seven male) subjects consumed a standardized evening meal and a subsequent standardized breakfast (1,499 kJ) where blood was collected for analysis of postprandial glucose and insulin responses. PPGRs to the same breakfast varied across the healthy subjects. The largest inter-individual variability in PPGRs was observed 60 min after the meal but was not associated with gut microbial α-diversity. In addition, no significant associations were observed between postprandial responses and specific taxa of the gut microbiome, measures of colonic fermentation, ITT, or other abiotic factors. However, fasting glucose concentrations were negatively associated with ITT, and fasting insulin was positively associated with fasting breath hydrogen. In conclusion, the gut microbiome, measures of colonic fermentation, and abiotic factors were not shown to be significantly associated with variability in postprandial responses, suggesting that contributions of the gut microbiome, colonic fermentation, and abiotic factors to PPGRs may be subtle in healthy adults.

KW - Faculty of Science

KW - Gut microbiome

KW - Personalized nutrition

KW - Individuality

KW - Intestinal transit time

KW - Abiotic factors

KW - Colonic fermentation

U2 - 10.3389/fnut.2020.594850

DO - 10.3389/fnut.2020.594850

M3 - Journal article

C2 - 33585532

VL - 7

JO - Frontiers in Nutrition

JF - Frontiers in Nutrition

SN - 2296-861X

M1 - 594850

ER -

ID: 256633504