Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis

<p>Abstract</p> <p>Background</p> <p>Osteoporosis is one of the systemic features of COPD. A correlation between the emphysema phenotype of COPD and reduced bone mineral density (BMD) is suggested by some studies, however, the mechanisms underlying this relationship are...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs: Bai Peng, Sun Yongchang, Jin Jianmin, Hou Jia, Li Ran, Zhang Qing, Wang Yang
Formaat: Artikel
Taal:English
Gepubliceerd in: BMC 2011-12-01
Reeks:Respiratory Research
Onderwerpen:
Online toegang:http://respiratory-research.com/content/12/1/157
_version_ 1828738557198467072
author Bai Peng
Sun Yongchang
Jin Jianmin
Hou Jia
Li Ran
Zhang Qing
Wang Yang
author_facet Bai Peng
Sun Yongchang
Jin Jianmin
Hou Jia
Li Ran
Zhang Qing
Wang Yang
author_sort Bai Peng
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Osteoporosis is one of the systemic features of COPD. A correlation between the emphysema phenotype of COPD and reduced bone mineral density (BMD) is suggested by some studies, however, the mechanisms underlying this relationship are unclear. Experimental studies indicate that IL-1β, IL-6 and TNF-α may play important roles in the etiology of both osteoporosis and emphysema. The OPG/RANK/RANKL system is an important regulator of bone metabolism, and participates in the development of post-menopausal osteoporosis. Whether the OPG/RANK/RANKL pathway is involved in the pathogenesis of osteoporosis in COPD has not been studied.</p> <p>Methods</p> <p>Eighty male patients (current or former smokers) completed a chest CT scan, pulmonary function test, dual x-ray absorptiometry measurements and questionnaires. Among these subjects, thirty patients with normal BMD and thirty patients with low BMD were selected randomly for measurement of IL-1β, IL-6, TNF-α (flow cytometry) and OPG/RANK/RANKL (ELISA). Twenty age-matched healthy volunteers were recruited as controls.</p> <p>Results</p> <p>Among these eighty patients, thirty-six had normal BMD and forty-four had low BMD. Age, BMI and CAT score showed significant differences between these two COPD groups (<it>p </it>< 0.05). The low-attenuation area (LAA%) in the lungs of COPD patients was negatively correlated with lumbar vertebral BMD (r = 0.741; <it>p </it>< 0.0001). Forward logistic regression analysis showed that only LAA% (<it>p </it>= 0.005) and BMI (<it>p </it>= 0.009) were selected as explanatory variables. The level of IL-1β was significantly higher in the COPD patients as compared to the normal controls (<it>p </it>< 0.05), but the difference between the two COPD groups did not reach significance. The levels of IL-6 and TNF-α among the three groups were significantly different (<it>p </it>< 0.05). The level of RANKL and the RANKL/OPG ratio were significantly higher in COPD patients with low BMD compared to those with normal BMD and the normal controls (<it>p </it>< 0.05), and correlated negatively with lumbar vertebral BMD, but positively with LAA%.</p> <p>Conclusions</p> <p>Radiographic emphysema is correlated with low BMD in current and former smokers with COPD. IL-1β, IL-6, TNF-α, and the osteoporosis-related protein system OPG/RANK/RANKL may have some synergetic effects on emphysema and bone loss in COPD.</p>
first_indexed 2024-04-13T00:05:43Z
format Article
id doaj.art-47f5a90df35f45a6a58e764dbaafc7e2
institution Directory Open Access Journal
issn 1465-9921
language English
last_indexed 2024-04-13T00:05:43Z
publishDate 2011-12-01
publisher BMC
record_format Article
series Respiratory Research
spelling doaj.art-47f5a90df35f45a6a58e764dbaafc7e22022-12-22T03:11:15ZengBMCRespiratory Research1465-99212011-12-0112115710.1186/1465-9921-12-157Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosisBai PengSun YongchangJin JianminHou JiaLi RanZhang QingWang Yang<p>Abstract</p> <p>Background</p> <p>Osteoporosis is one of the systemic features of COPD. A correlation between the emphysema phenotype of COPD and reduced bone mineral density (BMD) is suggested by some studies, however, the mechanisms underlying this relationship are unclear. Experimental studies indicate that IL-1β, IL-6 and TNF-α may play important roles in the etiology of both osteoporosis and emphysema. The OPG/RANK/RANKL system is an important regulator of bone metabolism, and participates in the development of post-menopausal osteoporosis. Whether the OPG/RANK/RANKL pathway is involved in the pathogenesis of osteoporosis in COPD has not been studied.</p> <p>Methods</p> <p>Eighty male patients (current or former smokers) completed a chest CT scan, pulmonary function test, dual x-ray absorptiometry measurements and questionnaires. Among these subjects, thirty patients with normal BMD and thirty patients with low BMD were selected randomly for measurement of IL-1β, IL-6, TNF-α (flow cytometry) and OPG/RANK/RANKL (ELISA). Twenty age-matched healthy volunteers were recruited as controls.</p> <p>Results</p> <p>Among these eighty patients, thirty-six had normal BMD and forty-four had low BMD. Age, BMI and CAT score showed significant differences between these two COPD groups (<it>p </it>< 0.05). The low-attenuation area (LAA%) in the lungs of COPD patients was negatively correlated with lumbar vertebral BMD (r = 0.741; <it>p </it>< 0.0001). Forward logistic regression analysis showed that only LAA% (<it>p </it>= 0.005) and BMI (<it>p </it>= 0.009) were selected as explanatory variables. The level of IL-1β was significantly higher in the COPD patients as compared to the normal controls (<it>p </it>< 0.05), but the difference between the two COPD groups did not reach significance. The levels of IL-6 and TNF-α among the three groups were significantly different (<it>p </it>< 0.05). The level of RANKL and the RANKL/OPG ratio were significantly higher in COPD patients with low BMD compared to those with normal BMD and the normal controls (<it>p </it>< 0.05), and correlated negatively with lumbar vertebral BMD, but positively with LAA%.</p> <p>Conclusions</p> <p>Radiographic emphysema is correlated with low BMD in current and former smokers with COPD. IL-1β, IL-6, TNF-α, and the osteoporosis-related protein system OPG/RANK/RANKL may have some synergetic effects on emphysema and bone loss in COPD.</p>http://respiratory-research.com/content/12/1/157chronic obstructive pulmonary diseasepulmonary emphysemaosteoporosiscytokineOPG/RANK/RANKL
spellingShingle Bai Peng
Sun Yongchang
Jin Jianmin
Hou Jia
Li Ran
Zhang Qing
Wang Yang
Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
Respiratory Research
chronic obstructive pulmonary disease
pulmonary emphysema
osteoporosis
cytokine
OPG/RANK/RANKL
title Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
title_full Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
title_fullStr Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
title_full_unstemmed Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
title_short Disturbance of the OPG/RANK/RANKL pathway and systemic inflammation in COPD patients with emphysema and osteoporosis
title_sort disturbance of the opg rank rankl pathway and systemic inflammation in copd patients with emphysema and osteoporosis
topic chronic obstructive pulmonary disease
pulmonary emphysema
osteoporosis
cytokine
OPG/RANK/RANKL
url http://respiratory-research.com/content/12/1/157
work_keys_str_mv AT baipeng disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT sunyongchang disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT jinjianmin disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT houjia disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT liran disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT zhangqing disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis
AT wangyang disturbanceoftheopgrankranklpathwayandsystemicinflammationincopdpatientswithemphysemaandosteoporosis