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Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes
BACKGROUND: In this proof-of-concept study, we evaluated if monogenic diabetes resulting from mutations of the HNF-1α gene (HNF1A-MODY) has a distinctive continuous glucose monitoring (CGM) glucotype, in comparison to type 1 diabetes (T1D). METHODS: Using CGM data from 5 subjects with HNF1A-MODY and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074392/ https://www.ncbi.nlm.nih.gov/pubmed/37035501 http://dx.doi.org/10.1210/jendso/bvad038 |
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author | Steenkamp, Devin W Cheney, Michael C Ju, Zhihui Rodbard, David Wolpert, Howard A |
author_facet | Steenkamp, Devin W Cheney, Michael C Ju, Zhihui Rodbard, David Wolpert, Howard A |
author_sort | Steenkamp, Devin W |
collection | PubMed |
description | BACKGROUND: In this proof-of-concept study, we evaluated if monogenic diabetes resulting from mutations of the HNF-1α gene (HNF1A-MODY) has a distinctive continuous glucose monitoring (CGM) glucotype, in comparison to type 1 diabetes (T1D). METHODS: Using CGM data from 5 subjects with HNF1A-MODY and 115 subjects with T1D, we calculated multiple glucose metrics, including measures of within- and between-day variability (such as coefficient variation for each hour [CV(b_1h)]). RESULTS: The MODY and T1D cohorts had minimum CV(b_1h) of 11.3 ± 4.4 and 18.0 ± 4.9, respectively (P = .02) and maximum CV(b_1h) of 33.9 ± 5.0 and 50.3 ± 10, respectively (P < .001). All subjects with HNF1A-MODY had a minimum %CV(b_1h) ≤ 17.3% and maximum %CV(b_1h) ≤ 37.1%. In contrast, only 12 of 115 subjects with T1D had both a minimum and maximum %CV(b_1h) below these thresholds (P < .001). CONCLUSION: HNF1A- MODY is characterized by a low hourly, between-day glucose variability. CGM-derived glucose metrics may have potential applicability for screening for atypical diabetes phenotypes in the T1D population. |
format | Online Article Text |
id | pubmed-10074392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100743922023-04-06 Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes Steenkamp, Devin W Cheney, Michael C Ju, Zhihui Rodbard, David Wolpert, Howard A J Endocr Soc Brief Report BACKGROUND: In this proof-of-concept study, we evaluated if monogenic diabetes resulting from mutations of the HNF-1α gene (HNF1A-MODY) has a distinctive continuous glucose monitoring (CGM) glucotype, in comparison to type 1 diabetes (T1D). METHODS: Using CGM data from 5 subjects with HNF1A-MODY and 115 subjects with T1D, we calculated multiple glucose metrics, including measures of within- and between-day variability (such as coefficient variation for each hour [CV(b_1h)]). RESULTS: The MODY and T1D cohorts had minimum CV(b_1h) of 11.3 ± 4.4 and 18.0 ± 4.9, respectively (P = .02) and maximum CV(b_1h) of 33.9 ± 5.0 and 50.3 ± 10, respectively (P < .001). All subjects with HNF1A-MODY had a minimum %CV(b_1h) ≤ 17.3% and maximum %CV(b_1h) ≤ 37.1%. In contrast, only 12 of 115 subjects with T1D had both a minimum and maximum %CV(b_1h) below these thresholds (P < .001). CONCLUSION: HNF1A- MODY is characterized by a low hourly, between-day glucose variability. CGM-derived glucose metrics may have potential applicability for screening for atypical diabetes phenotypes in the T1D population. Oxford University Press 2023-03-17 /pmc/articles/PMC10074392/ /pubmed/37035501 http://dx.doi.org/10.1210/jendso/bvad038 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Brief Report Steenkamp, Devin W Cheney, Michael C Ju, Zhihui Rodbard, David Wolpert, Howard A Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title | Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title_full | Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title_fullStr | Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title_full_unstemmed | Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title_short | Proof-of-concept Application of Continuous Glucose Monitoring Data Analytics to Identify Diabetes Glucotypes |
title_sort | proof-of-concept application of continuous glucose monitoring data analytics to identify diabetes glucotypes |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074392/ https://www.ncbi.nlm.nih.gov/pubmed/37035501 http://dx.doi.org/10.1210/jendso/bvad038 |
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