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Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease
OBJECTIVES: To study the effects of GSTM1, GSTT1 gene polymorphisms, and organism antioxidant capacity and related indicators such as antioxidant capacity per unit of albumin (AC/ALB) on chronic obstructive pulmonary disease (COPD). METHODS: Using polymerase chain reaction technology, GSTM1 and GSTT...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603134/ https://www.ncbi.nlm.nih.gov/pubmed/28951769 http://dx.doi.org/10.1155/2017/6232397 |
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author | Cao, Tinghui Xu, Naijin Wang, Zhen Liu, Hui |
author_facet | Cao, Tinghui Xu, Naijin Wang, Zhen Liu, Hui |
author_sort | Cao, Tinghui |
collection | PubMed |
description | OBJECTIVES: To study the effects of GSTM1, GSTT1 gene polymorphisms, and organism antioxidant capacity and related indicators such as antioxidant capacity per unit of albumin (AC/ALB) on chronic obstructive pulmonary disease (COPD). METHODS: Using polymerase chain reaction technology, GSTM1 and GSTT1 gene polymorphisms were detected in 33 COPD patients and 33 healthy people. The total antioxidant capacity (TAC) found in serum was determined using the I(2)/KI potentiometric, KMnO(4) microtitration, and H(2)O(2) potentiometric methods. The AC/ALB was defined as the TAC divided by the serum albumin concentration. Logistic regression analysis was carried out with biochemical screening indices, which was found to be closely related with the incidence of COPD. RESULTS: The GSTM1 and GSTT1 gene deletion rate in the COPD group was significantly higher than that in the control group (P < 0.05). The differences in serum TAC between the COPD and control groups, GSTM1 (+) and GSTM1 (−) groups, and GSTT1 (+) and GSTT1 (−) groups were statistically significant (P < 0.001). In addition, there was a significant difference in the AC/ALB between the COPD and control groups (P < 0.05). Logistic regression analysis showed that the incidence of COPD was closely related to the AC/ALB (P < 0.05). CONCLUSIONS: GSTM1 and GSTT1 gene polymorphisms are closely correlated with the pathogenesis of COPD, while the AC/ALB plays a decisive role in the occurrence and development of COPD. |
format | Online Article Text |
id | pubmed-5603134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56031342017-09-26 Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease Cao, Tinghui Xu, Naijin Wang, Zhen Liu, Hui Oxid Med Cell Longev Research Article OBJECTIVES: To study the effects of GSTM1, GSTT1 gene polymorphisms, and organism antioxidant capacity and related indicators such as antioxidant capacity per unit of albumin (AC/ALB) on chronic obstructive pulmonary disease (COPD). METHODS: Using polymerase chain reaction technology, GSTM1 and GSTT1 gene polymorphisms were detected in 33 COPD patients and 33 healthy people. The total antioxidant capacity (TAC) found in serum was determined using the I(2)/KI potentiometric, KMnO(4) microtitration, and H(2)O(2) potentiometric methods. The AC/ALB was defined as the TAC divided by the serum albumin concentration. Logistic regression analysis was carried out with biochemical screening indices, which was found to be closely related with the incidence of COPD. RESULTS: The GSTM1 and GSTT1 gene deletion rate in the COPD group was significantly higher than that in the control group (P < 0.05). The differences in serum TAC between the COPD and control groups, GSTM1 (+) and GSTM1 (−) groups, and GSTT1 (+) and GSTT1 (−) groups were statistically significant (P < 0.001). In addition, there was a significant difference in the AC/ALB between the COPD and control groups (P < 0.05). Logistic regression analysis showed that the incidence of COPD was closely related to the AC/ALB (P < 0.05). CONCLUSIONS: GSTM1 and GSTT1 gene polymorphisms are closely correlated with the pathogenesis of COPD, while the AC/ALB plays a decisive role in the occurrence and development of COPD. Hindawi 2017 2017-08-30 /pmc/articles/PMC5603134/ /pubmed/28951769 http://dx.doi.org/10.1155/2017/6232397 Text en Copyright © 2017 Tinghui Cao et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cao, Tinghui Xu, Naijin Wang, Zhen Liu, Hui Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title | Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_full | Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_fullStr | Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_full_unstemmed | Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_short | Effects of Glutathione S-Transferase Gene Polymorphisms and Antioxidant Capacity per Unit Albumin on the Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_sort | effects of glutathione s-transferase gene polymorphisms and antioxidant capacity per unit albumin on the pathogenesis of chronic obstructive pulmonary disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603134/ https://www.ncbi.nlm.nih.gov/pubmed/28951769 http://dx.doi.org/10.1155/2017/6232397 |
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