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Combined association of walking pace and grip strength with incident type 2 diabetes
The current study aims to investigate the combined association of walking pace and grip strength with incident type 2 diabetes (T2D). A total of 205 738 participants (mean age 56.6 ± 8.1 years, 115 139 [56.0%] women) without diagnosed or unknown diabetes at baseline from the UK Biobank study were in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544034/ https://www.ncbi.nlm.nih.gov/pubmed/35612725 http://dx.doi.org/10.1111/sms.14197 |
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author | Boonpor, Jirapitcha Parra‐Soto, Solange Petermann‐Rocha, Fanny Ho, Frederick K Celis‐Morales, Carlos Gray, Stuart R. |
author_facet | Boonpor, Jirapitcha Parra‐Soto, Solange Petermann‐Rocha, Fanny Ho, Frederick K Celis‐Morales, Carlos Gray, Stuart R. |
author_sort | Boonpor, Jirapitcha |
collection | PubMed |
description | The current study aims to investigate the combined association of walking pace and grip strength with incident type 2 diabetes (T2D). A total of 205 738 participants (mean age 56.6 ± 8.1 years, 115 139 [56.0%] women) without diagnosed or unknown diabetes at baseline from the UK Biobank study were included in this prospective study. Walking pace was self‐reported as slow, average, or brisk. Grip strength was measured using a dynamometer and classified as weak, average, and strong. The combined association of walking pace and grip strength with incident T2D was investigated using Cox‐proportional hazards models with a 2‐year landmark analysis. The additive interaction was conducted by estimating relative excess risk due to interaction (RERI). After the median follow‐up period of 5.4 years (interquartile range: 4.8–6.5), 5082 (2.5%) participants were diagnosed with T2D. Compared to brisk‐strong individuals (reference group), people who were slow‐weak had a higher risk of T2D (hazard ratio: 1.64 [95% CI, 1.42–1.89]) after adjusting for all covariates. There were dose–response gradients across both walking pace and grip strength variables. There was a modest amount of negative additive interaction (RERI; −0.06 [95% CI, −0.16; −0.01]. To conclude, slower pace and weaker grip strength were associated with a higher risk of developing T2D, independent of sociodemographics, lifestyle, and adiposity. Combining walking pace and grip strength might be a practical approach to screening people who are at increased risk of developing T2D. |
format | Online Article Text |
id | pubmed-9544034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95440342022-10-14 Combined association of walking pace and grip strength with incident type 2 diabetes Boonpor, Jirapitcha Parra‐Soto, Solange Petermann‐Rocha, Fanny Ho, Frederick K Celis‐Morales, Carlos Gray, Stuart R. Scand J Med Sci Sports Original Articles The current study aims to investigate the combined association of walking pace and grip strength with incident type 2 diabetes (T2D). A total of 205 738 participants (mean age 56.6 ± 8.1 years, 115 139 [56.0%] women) without diagnosed or unknown diabetes at baseline from the UK Biobank study were included in this prospective study. Walking pace was self‐reported as slow, average, or brisk. Grip strength was measured using a dynamometer and classified as weak, average, and strong. The combined association of walking pace and grip strength with incident T2D was investigated using Cox‐proportional hazards models with a 2‐year landmark analysis. The additive interaction was conducted by estimating relative excess risk due to interaction (RERI). After the median follow‐up period of 5.4 years (interquartile range: 4.8–6.5), 5082 (2.5%) participants were diagnosed with T2D. Compared to brisk‐strong individuals (reference group), people who were slow‐weak had a higher risk of T2D (hazard ratio: 1.64 [95% CI, 1.42–1.89]) after adjusting for all covariates. There were dose–response gradients across both walking pace and grip strength variables. There was a modest amount of negative additive interaction (RERI; −0.06 [95% CI, −0.16; −0.01]. To conclude, slower pace and weaker grip strength were associated with a higher risk of developing T2D, independent of sociodemographics, lifestyle, and adiposity. Combining walking pace and grip strength might be a practical approach to screening people who are at increased risk of developing T2D. John Wiley and Sons Inc. 2022-06-03 2022-09 /pmc/articles/PMC9544034/ /pubmed/35612725 http://dx.doi.org/10.1111/sms.14197 Text en © 2022 The Authors. Scandinavian Journal of Medicine & Science In Sports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Boonpor, Jirapitcha Parra‐Soto, Solange Petermann‐Rocha, Fanny Ho, Frederick K Celis‐Morales, Carlos Gray, Stuart R. Combined association of walking pace and grip strength with incident type 2 diabetes |
title | Combined association of walking pace and grip strength with incident type 2 diabetes |
title_full | Combined association of walking pace and grip strength with incident type 2 diabetes |
title_fullStr | Combined association of walking pace and grip strength with incident type 2 diabetes |
title_full_unstemmed | Combined association of walking pace and grip strength with incident type 2 diabetes |
title_short | Combined association of walking pace and grip strength with incident type 2 diabetes |
title_sort | combined association of walking pace and grip strength with incident type 2 diabetes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544034/ https://www.ncbi.nlm.nih.gov/pubmed/35612725 http://dx.doi.org/10.1111/sms.14197 |
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