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Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity
The present study aimed to explore the influence of sirtuin 1 (SIRT1) polymorphisms (rs12778366 and rs3758391) on diabetic foot (DF) susceptibility and severity in patients with type 2 diabetes mellitus (T2DM). This case–control study recruited 142 patients with DF, 148 patients with T2DM, and 148 h...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076161/ https://www.ncbi.nlm.nih.gov/pubmed/29995800 http://dx.doi.org/10.1097/MD.0000000000011455 |
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author | Peng, Yi Zhang, Guishan Tang, Hongxia Dong, Luling Gao, Chunbin Yang, Xiuhong Peng, Ying Xu, Yanrong |
author_facet | Peng, Yi Zhang, Guishan Tang, Hongxia Dong, Luling Gao, Chunbin Yang, Xiuhong Peng, Ying Xu, Yanrong |
author_sort | Peng, Yi |
collection | PubMed |
description | The present study aimed to explore the influence of sirtuin 1 (SIRT1) polymorphisms (rs12778366 and rs3758391) on diabetic foot (DF) susceptibility and severity in patients with type 2 diabetes mellitus (T2DM). This case–control study recruited 142 patients with DF, 148 patients with T2DM, and 148 healthy controls. SIRT1 gene polymorphisms were sequenced by polymerase chain reaction (PCR) and direct sequencing method. The relative expression of SIRT1 mRNA was estimated using quantitative real-time PCR (qRT-PCR) assay. Odds ratio (OR) with 95% confidence interval (95% CI) were used to represent the association of SIRT1 polymorphisms with DF susceptibility and severity. The results were adjusted using logistic regression analysis. C allele of rs12778366 polymorphism was significantly correlated with reduced DF susceptibility which deriving from healthy controls (adjusted OR = 0.364, 95% CI = 0.158–0.835) so was patients with T2DM (P = .047, OR = 0.591, 95%CI = 0.349–0.998), but the results became nonsignificant adjusted by clinical features (adjusted OR = 0.654, 95% CI = 0.391–1.094). We failed to find any significant association between rs3758391 polymorphisms and T2DM, DF susceptibility. No significant association has been discovered between SIRT1 polymorphisms and DF severity or characteristics. In addition, compared to healthy control and T2DM cases, patients with DF exhibited significant downregulation of SIRT1. The 2 studied polymorphisms had no effects on its gene expression (P > .05 for all). SIRT1 rs12778366 polymorphism C allele might act as a protective factor for DF onset. |
format | Online Article Text |
id | pubmed-6076161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-60761612018-08-17 Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity Peng, Yi Zhang, Guishan Tang, Hongxia Dong, Luling Gao, Chunbin Yang, Xiuhong Peng, Ying Xu, Yanrong Medicine (Baltimore) Research Article The present study aimed to explore the influence of sirtuin 1 (SIRT1) polymorphisms (rs12778366 and rs3758391) on diabetic foot (DF) susceptibility and severity in patients with type 2 diabetes mellitus (T2DM). This case–control study recruited 142 patients with DF, 148 patients with T2DM, and 148 healthy controls. SIRT1 gene polymorphisms were sequenced by polymerase chain reaction (PCR) and direct sequencing method. The relative expression of SIRT1 mRNA was estimated using quantitative real-time PCR (qRT-PCR) assay. Odds ratio (OR) with 95% confidence interval (95% CI) were used to represent the association of SIRT1 polymorphisms with DF susceptibility and severity. The results were adjusted using logistic regression analysis. C allele of rs12778366 polymorphism was significantly correlated with reduced DF susceptibility which deriving from healthy controls (adjusted OR = 0.364, 95% CI = 0.158–0.835) so was patients with T2DM (P = .047, OR = 0.591, 95%CI = 0.349–0.998), but the results became nonsignificant adjusted by clinical features (adjusted OR = 0.654, 95% CI = 0.391–1.094). We failed to find any significant association between rs3758391 polymorphisms and T2DM, DF susceptibility. No significant association has been discovered between SIRT1 polymorphisms and DF severity or characteristics. In addition, compared to healthy control and T2DM cases, patients with DF exhibited significant downregulation of SIRT1. The 2 studied polymorphisms had no effects on its gene expression (P > .05 for all). SIRT1 rs12778366 polymorphism C allele might act as a protective factor for DF onset. Wolters Kluwer Health 2018-07-13 /pmc/articles/PMC6076161/ /pubmed/29995800 http://dx.doi.org/10.1097/MD.0000000000011455 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | Research Article Peng, Yi Zhang, Guishan Tang, Hongxia Dong, Luling Gao, Chunbin Yang, Xiuhong Peng, Ying Xu, Yanrong Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title | Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title_full | Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title_fullStr | Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title_full_unstemmed | Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title_short | Influence of SIRT1 polymorphisms for diabetic foot susceptibility and severity |
title_sort | influence of sirt1 polymorphisms for diabetic foot susceptibility and severity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076161/ https://www.ncbi.nlm.nih.gov/pubmed/29995800 http://dx.doi.org/10.1097/MD.0000000000011455 |
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