Assessment of Osteoprotegerin and Receptor Activator of Nf-Κb Ligand in Malaysian Male Patients with Chronic Obstructive Pulmonary Disease: A Cross-Sectional Study.

Bitar Ahmad N, Al-Mansoub Majed A, Syed-Sulaiman Syed A, Saqallah Fadi G, Hyder-Ali Irfhan A B, Alshehade Salah A, Hayat-Khan Amer
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Abstract

Unassigned: Background: Limited information exists regarding the pathophysiological interactions between osteoporosis and chronic obstructive pulmonary disease (COPD). Objective: To study the association of Osteoprotegerin (OPG) and receptor activator of nuclear factor kappa-Β ligand (RANKL) in male COPD patients. Methods: An observational clinical study was conducted at Penang General Hospital in Malaysia. Participants were divided into three groups: COPD patients with osteoporosis, COPD patients without osteoporosis, and healthy participants of the same age groups. Serum OPG (sOPG) and RANKL (sRANKL) levels were investigated. Results: The mean age of COPD patients was 64.10 ± 10.04 years. COPD patients had lower body mass index (23.22 ± 6.43) than healthy participants (27.32 ± 6.80). The T-score was significantly lower among COPD patients than healthy participants (p = 0.018). The sOPG concentration among healthy participants was significantly higher (361.90 ± 29.10 pg/mL, p < 0.001) than in the other groups, while the sRANKL concentration was not significantly different. The serum OPG/RANKL concentration was markedly higher in the control group than in the COPD patient group (p < 0.05). The COPD patients with osteoporosis had significantly lower pulmonary parameters (forced expiratory volume in the first [FEV]1% and FEV1/[forced vital capacity] (FVC), p < 0.01) and more dyspnea (modified medical research council = 2.60 ± 0.78 versus 1.90 ± 0.70, p < 0.01) than did the patients without osteoporosis. Furthermore, patients with severe COPD had a 3 times greater risk of developing osteoporosis (OR = 2.997 [95% CI = 2.181, 4.118], p < 0.001), while spirometric parameters had a significant inverse relationship with osteoporosis (FEV1% OR = 0.970, [95% CI = 0.954, 0.986], p = 0.001; FEV1/FVC OR = 0.984, (95% CI = 0.970, 0.999], p = 0.035). Conclusion: The study concluded that COPD patients had lower sOPG levels, leading to decreased OPG/RANKL ratio and faster bone resorption. Low bone mineral density was associated with more severe COPD. (Rev Invest Clin. 2024;76(6):262-73).

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评估马来西亚男性慢性阻塞性肺疾病患者的骨保护素和Nf-Κb配体受体激活剂:一项横断面研究。
背景:关于骨质疏松症和慢性阻塞性肺疾病(COPD)之间的病理生理相互作用的信息有限。目的:探讨骨保护素(OPG)与核因子κ κ受体激活因子-Β配体(RANKL)在男性COPD患者中的相关性。方法:在马来西亚槟城总医院进行观察性临床研究。参与者被分为三组:合并骨质疏松的COPD患者、无骨质疏松的COPD患者和同年龄组的健康参与者。检测血清OPG (sOPG)和RANKL (sRANKL)水平。结果:COPD患者的平均年龄为64.10±10.04岁。COPD患者的体重指数(23.22±6.43)低于健康受试者(27.32±6.80)。COPD患者的t评分明显低于健康受试者(p = 0.018)。健康组的sOPG浓度(361.90±29.10 pg/mL, p < 0.001)显著高于其他组,而sRANKL浓度无显著差异。对照组血清OPG/RANKL浓度明显高于COPD患者组(p < 0.05)。COPD合并骨质疏松患者肺参数(首发用力呼气量[FEV]1%和FEV1/[用力肺活量](FVC), p < 0.01)明显低于无骨质疏松患者,呼吸困难(修正医学研究委员会= 2.60±0.78比1.90±0.70,p < 0.01)明显高于无骨质疏松患者。此外,重度COPD患者发生骨质疏松的风险是COPD患者的3倍(OR = 2.997 [95% CI = 2.181, 4.118], p < 0.001),肺活量测定参数与骨质疏松呈显著负相关(FEV1% OR = 0.970, [95% CI = 0.954, 0.986], p = 0.001;FEV1/FVC OR = 0.984, (95% CI = 0.970, 0.999), p = 0.035。结论:COPD患者sOPG水平较低,导致OPG/RANKL比值降低,骨吸收加快。低骨密度与更严重的COPD相关。[j] .中国医学工程学报,2009;36(6):662 - 663。
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CiteScore
3.00
自引率
0.00%
发文量
60
审稿时长
>12 weeks
期刊介绍: The Revista de Investigación Clínica – Clinical and Translational Investigation (RIC-C&TI), publishes original clinical and biomedical research of interest to physicians in internal medicine, surgery, and any of their specialties. The Revista de Investigación Clínica – Clinical and Translational Investigation is the official journal of the National Institutes of Health of Mexico, which comprises a group of Institutes and High Specialty Hospitals belonging to the Ministery of Health. The journal is published both on-line and in printed version, appears bimonthly and publishes peer-reviewed original research articles as well as brief and in-depth reviews. All articles published are open access and can be immediately and permanently free for everyone to read and download. The journal accepts clinical and molecular research articles, short reports and reviews. Types of manuscripts: – Brief Communications – Research Letters – Original Articles – Brief Reviews – In-depth Reviews – Perspectives – Letters to the Editor
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