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The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults
Inpatient populations are at increased risk of hyperglycemia due to factors such as medications, physical inactivity and underlying illness, which increases morbidity and mortality. Unfortunately, clinicians have limited tools available to prospectively identify those at greatest risk. We evaluated...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046412/ https://www.ncbi.nlm.nih.gov/pubmed/35477971 http://dx.doi.org/10.1038/s41598-022-10683-1 |
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author | Fry, Jean L. Munson, Brooke D. Thompson, Katherine L. Fry, Christopher S. Paddon-Jones, Douglas Arentson-Lantz, Emily J. |
author_facet | Fry, Jean L. Munson, Brooke D. Thompson, Katherine L. Fry, Christopher S. Paddon-Jones, Douglas Arentson-Lantz, Emily J. |
author_sort | Fry, Jean L. |
collection | PubMed |
description | Inpatient populations are at increased risk of hyperglycemia due to factors such as medications, physical inactivity and underlying illness, which increases morbidity and mortality. Unfortunately, clinicians have limited tools available to prospectively identify those at greatest risk. We evaluated the ability of 10 common genetic variants associated with development of type 2 diabetes to predict impaired glucose metabolism. Our research model was a simulated inpatient hospital stay (7 day bed rest protocol, standardized diet, and physical inactivity) in a cohort of healthy older adults (n = 31, 65 ± 8 years) with baseline fasting blood glucose < 100 mg/dL. Participants completed a standard 75 g oral glucose tolerance test (OGTT) at baseline and post-bed rest. Bed rest increased 2-h OGTT blood glucose and insulin independent of genetic variant. In multiple regression modeling, the transcription factor 7-like 2 (TCF7L2) rs7903146 T allele predicted increases in 2-h OGTT blood glucose (p = 0.039). We showed that the TCF7L2 rs7903146 T allele confers risk for loss of glucose tolerance in nondiabetic older adults following 7 days of bed rest. |
format | Online Article Text |
id | pubmed-9046412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90464122022-04-29 The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults Fry, Jean L. Munson, Brooke D. Thompson, Katherine L. Fry, Christopher S. Paddon-Jones, Douglas Arentson-Lantz, Emily J. Sci Rep Article Inpatient populations are at increased risk of hyperglycemia due to factors such as medications, physical inactivity and underlying illness, which increases morbidity and mortality. Unfortunately, clinicians have limited tools available to prospectively identify those at greatest risk. We evaluated the ability of 10 common genetic variants associated with development of type 2 diabetes to predict impaired glucose metabolism. Our research model was a simulated inpatient hospital stay (7 day bed rest protocol, standardized diet, and physical inactivity) in a cohort of healthy older adults (n = 31, 65 ± 8 years) with baseline fasting blood glucose < 100 mg/dL. Participants completed a standard 75 g oral glucose tolerance test (OGTT) at baseline and post-bed rest. Bed rest increased 2-h OGTT blood glucose and insulin independent of genetic variant. In multiple regression modeling, the transcription factor 7-like 2 (TCF7L2) rs7903146 T allele predicted increases in 2-h OGTT blood glucose (p = 0.039). We showed that the TCF7L2 rs7903146 T allele confers risk for loss of glucose tolerance in nondiabetic older adults following 7 days of bed rest. Nature Publishing Group UK 2022-04-27 /pmc/articles/PMC9046412/ /pubmed/35477971 http://dx.doi.org/10.1038/s41598-022-10683-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fry, Jean L. Munson, Brooke D. Thompson, Katherine L. Fry, Christopher S. Paddon-Jones, Douglas Arentson-Lantz, Emily J. The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title | The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title_full | The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title_fullStr | The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title_full_unstemmed | The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title_short | The T allele of TCF7L2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
title_sort | t allele of tcf7l2 rs7903146 is associated with decreased glucose tolerance after bed rest in healthy older adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046412/ https://www.ncbi.nlm.nih.gov/pubmed/35477971 http://dx.doi.org/10.1038/s41598-022-10683-1 |
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