Validity of continuous glucose monitoring for categorizing glycemic responses to diet: implications for use in personalized nutrition.

Research output: Contribution to journalJournal articleResearchpeer-review

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Validity of continuous glucose monitoring for categorizing glycemic responses to diet : implications for use in personalized nutrition. / Jordi Merino, PhD; Linenberg, I; Bermingham, KM; Ganesh, S; Bakker, E; Delahanty, LM; Chan, Andrew; Capdevila, Pujol J; Wolf, Jonathan; Al, Khatib H; Franks, PW; Spector, TD; Ordovas, Jose; Berry, Sarah; Valdes, Ana M.

In: The American journal of clinical nutrition, Vol. 115, No. 6, 2022, p. 1569-1576.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jordi Merino, P, Linenberg, I, Bermingham, KM, Ganesh, S, Bakker, E, Delahanty, LM, Chan, A, Capdevila, PJ, Wolf, J, Al, KH, Franks, PW, Spector, TD, Ordovas, J, Berry, S & Valdes, AM 2022, 'Validity of continuous glucose monitoring for categorizing glycemic responses to diet: implications for use in personalized nutrition.', The American journal of clinical nutrition, vol. 115, no. 6, pp. 1569-1576. https://doi.org/10.1093/ajcn/nqac026

APA

Jordi Merino, P., Linenberg, I., Bermingham, KM., Ganesh, S., Bakker, E., Delahanty, LM., Chan, A., Capdevila, P. J., Wolf, J., Al, K. H., Franks, PW., Spector, TD., Ordovas, J., Berry, S., & Valdes, A. M. (2022). Validity of continuous glucose monitoring for categorizing glycemic responses to diet: implications for use in personalized nutrition. The American journal of clinical nutrition, 115(6), 1569-1576. https://doi.org/10.1093/ajcn/nqac026

Vancouver

Jordi Merino P, Linenberg I, Bermingham KM, Ganesh S, Bakker E, Delahanty LM et al. Validity of continuous glucose monitoring for categorizing glycemic responses to diet: implications for use in personalized nutrition. The American journal of clinical nutrition. 2022;115(6):1569-1576. https://doi.org/10.1093/ajcn/nqac026

Author

Jordi Merino, PhD ; Linenberg, I ; Bermingham, KM ; Ganesh, S ; Bakker, E ; Delahanty, LM ; Chan, Andrew ; Capdevila, Pujol J ; Wolf, Jonathan ; Al, Khatib H ; Franks, PW ; Spector, TD ; Ordovas, Jose ; Berry, Sarah ; Valdes, Ana M. / Validity of continuous glucose monitoring for categorizing glycemic responses to diet : implications for use in personalized nutrition. In: The American journal of clinical nutrition. 2022 ; Vol. 115, No. 6. pp. 1569-1576.

Bibtex

@article{e8f70cefc2cb4ab790cfccdfaf7909e1,
title = "Validity of continuous glucose monitoring for categorizing glycemic responses to diet: implications for use in personalized nutrition.",
abstract = "BackgroundContinuous glucose monitor (CGM) devices enable characterization of individuals' glycemic variation. However, there are concerns about their reliability for categorizing glycemic responses to foods that would limit their potential application in personalized nutrition recommendations.ObjectivesWe aimed to evaluate the concordance of 2 simultaneously worn CGM devices in measuring postprandial glycemic responses.MethodsWithin ZOE PREDICT (Personalised Responses to Dietary Composition Trial) 1, 394 participants wore 2 CGM devices simultaneously [n = 360 participants with 2 Abbott Freestyle Libre Pro (FSL) devices; n = 34 participants with both FSL and Dexcom G6] for ≤14 d while consuming standardized (n = 4457) and ad libitum (n = 5738) meals. We examined the CV and correlation of the incremental area under the glucose curve at 2 h (glucoseiAUC0-2 h). Within-subject meal ranking was assessed using Kendall τ rank correlation. Concordance between paired devices in time in range according to the American Diabetes Association cutoffs (TIRADA) and glucose variability (glucose CV) was also investigated.ResultsThe CV of glucoseiAUC0-2 h for standardized meals was 3.7% (IQR: 1.7%-7.1%) for intrabrand device and 12.5% (IQR: 5.1%-24.8%) for interbrand device comparisons. Similar estimates were observed for ad libitum meals, with intrabrand and interbrand device CVs of glucoseiAUC0-2 h of 4.1% (IQR: 1.8%-7.1%) and 16.6% (IQR: 5.5%-30.7%), respectively. Kendall τ rank correlation showed glucoseiAUC0-2h-derived meal rankings were agreeable between paired CGM devices (intrabrand: 0.9; IQR: 0.8-0.9; interbrand: 0.7; IQR: 0.5-0.8). Paired CGMs also showed strong concordance for TIRADA with a intrabrand device CV of 4.8% (IQR: 1.9%-9.8%) and an interbrand device CV of 3.2% (IQR: 1.1%-6.2%).ConclusionsOur data demonstrate strong concordance of CGM devices in monitoring glycemic responses and suggest their potential use in personalized nutrition.This trial was registered at clinicaltrials.gov as NCT03479866.",
author = "{Jordi Merino}, PhD and I Linenberg and KM Bermingham and S Ganesh and E Bakker and LM Delahanty and Andrew Chan and Capdevila, {Pujol J} and Jonathan Wolf and Al, {Khatib H} and PW Franks and TD Spector and Jose Ordovas and Sarah Berry and Valdes, {Ana M.}",
year = "2022",
doi = "10.1093/ajcn/nqac026",
language = "English",
volume = "115",
pages = "1569--1576",
journal = "American Journal of Clinical Nutrition",
issn = "0002-9165",
publisher = "American Society for Nutrition",
number = "6",

}

RIS

TY - JOUR

T1 - Validity of continuous glucose monitoring for categorizing glycemic responses to diet

T2 - implications for use in personalized nutrition.

AU - Jordi Merino, PhD

AU - Linenberg, I

AU - Bermingham, KM

AU - Ganesh, S

AU - Bakker, E

AU - Delahanty, LM

AU - Chan, Andrew

AU - Capdevila, Pujol J

AU - Wolf, Jonathan

AU - Al, Khatib H

AU - Franks, PW

AU - Spector, TD

AU - Ordovas, Jose

AU - Berry, Sarah

AU - Valdes, Ana M.

PY - 2022

Y1 - 2022

N2 - BackgroundContinuous glucose monitor (CGM) devices enable characterization of individuals' glycemic variation. However, there are concerns about their reliability for categorizing glycemic responses to foods that would limit their potential application in personalized nutrition recommendations.ObjectivesWe aimed to evaluate the concordance of 2 simultaneously worn CGM devices in measuring postprandial glycemic responses.MethodsWithin ZOE PREDICT (Personalised Responses to Dietary Composition Trial) 1, 394 participants wore 2 CGM devices simultaneously [n = 360 participants with 2 Abbott Freestyle Libre Pro (FSL) devices; n = 34 participants with both FSL and Dexcom G6] for ≤14 d while consuming standardized (n = 4457) and ad libitum (n = 5738) meals. We examined the CV and correlation of the incremental area under the glucose curve at 2 h (glucoseiAUC0-2 h). Within-subject meal ranking was assessed using Kendall τ rank correlation. Concordance between paired devices in time in range according to the American Diabetes Association cutoffs (TIRADA) and glucose variability (glucose CV) was also investigated.ResultsThe CV of glucoseiAUC0-2 h for standardized meals was 3.7% (IQR: 1.7%-7.1%) for intrabrand device and 12.5% (IQR: 5.1%-24.8%) for interbrand device comparisons. Similar estimates were observed for ad libitum meals, with intrabrand and interbrand device CVs of glucoseiAUC0-2 h of 4.1% (IQR: 1.8%-7.1%) and 16.6% (IQR: 5.5%-30.7%), respectively. Kendall τ rank correlation showed glucoseiAUC0-2h-derived meal rankings were agreeable between paired CGM devices (intrabrand: 0.9; IQR: 0.8-0.9; interbrand: 0.7; IQR: 0.5-0.8). Paired CGMs also showed strong concordance for TIRADA with a intrabrand device CV of 4.8% (IQR: 1.9%-9.8%) and an interbrand device CV of 3.2% (IQR: 1.1%-6.2%).ConclusionsOur data demonstrate strong concordance of CGM devices in monitoring glycemic responses and suggest their potential use in personalized nutrition.This trial was registered at clinicaltrials.gov as NCT03479866.

AB - BackgroundContinuous glucose monitor (CGM) devices enable characterization of individuals' glycemic variation. However, there are concerns about their reliability for categorizing glycemic responses to foods that would limit their potential application in personalized nutrition recommendations.ObjectivesWe aimed to evaluate the concordance of 2 simultaneously worn CGM devices in measuring postprandial glycemic responses.MethodsWithin ZOE PREDICT (Personalised Responses to Dietary Composition Trial) 1, 394 participants wore 2 CGM devices simultaneously [n = 360 participants with 2 Abbott Freestyle Libre Pro (FSL) devices; n = 34 participants with both FSL and Dexcom G6] for ≤14 d while consuming standardized (n = 4457) and ad libitum (n = 5738) meals. We examined the CV and correlation of the incremental area under the glucose curve at 2 h (glucoseiAUC0-2 h). Within-subject meal ranking was assessed using Kendall τ rank correlation. Concordance between paired devices in time in range according to the American Diabetes Association cutoffs (TIRADA) and glucose variability (glucose CV) was also investigated.ResultsThe CV of glucoseiAUC0-2 h for standardized meals was 3.7% (IQR: 1.7%-7.1%) for intrabrand device and 12.5% (IQR: 5.1%-24.8%) for interbrand device comparisons. Similar estimates were observed for ad libitum meals, with intrabrand and interbrand device CVs of glucoseiAUC0-2 h of 4.1% (IQR: 1.8%-7.1%) and 16.6% (IQR: 5.5%-30.7%), respectively. Kendall τ rank correlation showed glucoseiAUC0-2h-derived meal rankings were agreeable between paired CGM devices (intrabrand: 0.9; IQR: 0.8-0.9; interbrand: 0.7; IQR: 0.5-0.8). Paired CGMs also showed strong concordance for TIRADA with a intrabrand device CV of 4.8% (IQR: 1.9%-9.8%) and an interbrand device CV of 3.2% (IQR: 1.1%-6.2%).ConclusionsOur data demonstrate strong concordance of CGM devices in monitoring glycemic responses and suggest their potential use in personalized nutrition.This trial was registered at clinicaltrials.gov as NCT03479866.

U2 - 10.1093/ajcn/nqac026

DO - 10.1093/ajcn/nqac026

M3 - Journal article

C2 - 35134821

VL - 115

SP - 1569

EP - 1576

JO - American Journal of Clinical Nutrition

JF - American Journal of Clinical Nutrition

SN - 0002-9165

IS - 6

ER -

ID: 347793132