author_facet Umi Partan, Radiyati
Hidayat, Rachmat
Umi Partan, Radiyati
Hidayat, Rachmat
author Umi Partan, Radiyati
Hidayat, Rachmat
spellingShingle Umi Partan, Radiyati
Hidayat, Rachmat
Journal of Physics: Conference Series
The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
General Physics and Astronomy
author_sort umi partan, radiyati
spelling Umi Partan, Radiyati Hidayat, Rachmat 1742-6588 1742-6596 IOP Publishing General Physics and Astronomy http://dx.doi.org/10.1088/1742-6596/1246/1/012035 <jats:title>Abstract</jats:title> <jats:p>Tumour necrosis factor alpha (TNF-α) is an important regulator of bone metabolism. Polymorphisms in the promoter region of the TNF-α gene at position 308 have been identified. We investigated whether these polymorphisms and circulating TNF-a levels were related to BMD in osteoporosis caused by COPD. We conducted this study to analyse the relationship between genetic polymorphism of tumour necrosis factor (TNF)-a -308 G/A and levels of pro-inflammatory cytokines, bone turnover marker levels, and the incidence of osteoporosis in COPD patients. This study was conducted on 70 COPD patients. BMD and bone area of the femoral neck and lumbar spines were measured using dual energy X-ray absorptiometry (Stratos ®). Blood cytokines (TNF-a, interleukin (IL)-6, IL-17, IL-1b) and Ctelopeptide (CTX), receptor activator of nuclear factor kB (RANKL), and osteoprotegerin (OPG) were analysed using ELISA. Polymorphism of the TNF-α gene -308 G/A was assayed by PCR-RFLP. The levels of cytokines were significantly increased in the osteoporosis group compared to those without. Polymorphism was significantly different between COPD with osteoporosis and COPD without. The frequency of the GA and AA genotypes was significantly increased in patients with osteoporosis. To conclude, there is a relationship between the TNF-a -308 G/A polymorphism and high levels of TNF-a, IL-1β, IL-6, IL-17, CTX, and the incidence of osteoporosis in patients with COPD.</jats:p> The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis Journal of Physics: Conference Series
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title The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_unstemmed The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_full The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_fullStr The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_full_unstemmed The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_short The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_sort the relationship between tnf-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in copd patients with osteoporosis
topic General Physics and Astronomy
url http://dx.doi.org/10.1088/1742-6596/1246/1/012035
publishDate 2019
physical 012035
description <jats:title>Abstract</jats:title> <jats:p>Tumour necrosis factor alpha (TNF-α) is an important regulator of bone metabolism. Polymorphisms in the promoter region of the TNF-α gene at position 308 have been identified. We investigated whether these polymorphisms and circulating TNF-a levels were related to BMD in osteoporosis caused by COPD. We conducted this study to analyse the relationship between genetic polymorphism of tumour necrosis factor (TNF)-a -308 G/A and levels of pro-inflammatory cytokines, bone turnover marker levels, and the incidence of osteoporosis in COPD patients. This study was conducted on 70 COPD patients. BMD and bone area of the femoral neck and lumbar spines were measured using dual energy X-ray absorptiometry (Stratos ®). Blood cytokines (TNF-a, interleukin (IL)-6, IL-17, IL-1b) and Ctelopeptide (CTX), receptor activator of nuclear factor kB (RANKL), and osteoprotegerin (OPG) were analysed using ELISA. Polymorphism of the TNF-α gene -308 G/A was assayed by PCR-RFLP. The levels of cytokines were significantly increased in the osteoporosis group compared to those without. Polymorphism was significantly different between COPD with osteoporosis and COPD without. The frequency of the GA and AA genotypes was significantly increased in patients with osteoporosis. To conclude, there is a relationship between the TNF-a -308 G/A polymorphism and high levels of TNF-a, IL-1β, IL-6, IL-17, CTX, and the incidence of osteoporosis in patients with COPD.</jats:p>
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author Umi Partan, Radiyati, Hidayat, Rachmat
author_facet Umi Partan, Radiyati, Hidayat, Rachmat, Umi Partan, Radiyati, Hidayat, Rachmat
author_sort umi partan, radiyati
container_issue 1
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container_title Journal of Physics: Conference Series
container_volume 1246
description <jats:title>Abstract</jats:title> <jats:p>Tumour necrosis factor alpha (TNF-α) is an important regulator of bone metabolism. Polymorphisms in the promoter region of the TNF-α gene at position 308 have been identified. We investigated whether these polymorphisms and circulating TNF-a levels were related to BMD in osteoporosis caused by COPD. We conducted this study to analyse the relationship between genetic polymorphism of tumour necrosis factor (TNF)-a -308 G/A and levels of pro-inflammatory cytokines, bone turnover marker levels, and the incidence of osteoporosis in COPD patients. This study was conducted on 70 COPD patients. BMD and bone area of the femoral neck and lumbar spines were measured using dual energy X-ray absorptiometry (Stratos ®). Blood cytokines (TNF-a, interleukin (IL)-6, IL-17, IL-1b) and Ctelopeptide (CTX), receptor activator of nuclear factor kB (RANKL), and osteoprotegerin (OPG) were analysed using ELISA. Polymorphism of the TNF-α gene -308 G/A was assayed by PCR-RFLP. The levels of cytokines were significantly increased in the osteoporosis group compared to those without. Polymorphism was significantly different between COPD with osteoporosis and COPD without. The frequency of the GA and AA genotypes was significantly increased in patients with osteoporosis. To conclude, there is a relationship between the TNF-a -308 G/A polymorphism and high levels of TNF-a, IL-1β, IL-6, IL-17, CTX, and the incidence of osteoporosis in patients with COPD.</jats:p>
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spelling Umi Partan, Radiyati Hidayat, Rachmat 1742-6588 1742-6596 IOP Publishing General Physics and Astronomy http://dx.doi.org/10.1088/1742-6596/1246/1/012035 <jats:title>Abstract</jats:title> <jats:p>Tumour necrosis factor alpha (TNF-α) is an important regulator of bone metabolism. Polymorphisms in the promoter region of the TNF-α gene at position 308 have been identified. We investigated whether these polymorphisms and circulating TNF-a levels were related to BMD in osteoporosis caused by COPD. We conducted this study to analyse the relationship between genetic polymorphism of tumour necrosis factor (TNF)-a -308 G/A and levels of pro-inflammatory cytokines, bone turnover marker levels, and the incidence of osteoporosis in COPD patients. This study was conducted on 70 COPD patients. BMD and bone area of the femoral neck and lumbar spines were measured using dual energy X-ray absorptiometry (Stratos ®). Blood cytokines (TNF-a, interleukin (IL)-6, IL-17, IL-1b) and Ctelopeptide (CTX), receptor activator of nuclear factor kB (RANKL), and osteoprotegerin (OPG) were analysed using ELISA. Polymorphism of the TNF-α gene -308 G/A was assayed by PCR-RFLP. The levels of cytokines were significantly increased in the osteoporosis group compared to those without. Polymorphism was significantly different between COPD with osteoporosis and COPD without. The frequency of the GA and AA genotypes was significantly increased in patients with osteoporosis. To conclude, there is a relationship between the TNF-a -308 G/A polymorphism and high levels of TNF-a, IL-1β, IL-6, IL-17, CTX, and the incidence of osteoporosis in patients with COPD.</jats:p> The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis Journal of Physics: Conference Series
spellingShingle Umi Partan, Radiyati, Hidayat, Rachmat, Journal of Physics: Conference Series, The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis, General Physics and Astronomy
title The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_full The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_fullStr The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_full_unstemmed The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_short The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
title_sort the relationship between tnf-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in copd patients with osteoporosis
title_unstemmed The relationship between TNF-α gene polymorphism, pro-inflammatory cytokines and bone turnover markers in COPD patients with osteoporosis
topic General Physics and Astronomy
url http://dx.doi.org/10.1088/1742-6596/1246/1/012035