8-Hydroxy-2′-deoxyguanosine as a biomarker of oxidative stress in acute exacerbation of chronic obstructive pulmonary disease

被引:30
作者
Liu, Xing [1 ]
Deng, Kaili [1 ]
Chen, Sixia [1 ]
Zhang, Yunshi [2 ]
Yao, Jing [1 ]
Weng, Xiaoqin [1 ]
Zhang, Yang [1 ]
Gao, Tianming [1 ]
Feng, Ganzhu [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 2, Dept Resp Med, Nanjing, Jiangsu, Peoples R China
[2] Xuzhou Infect Dis Hosp, Dept TB, Xuzhou, Jiangsu, Peoples R China
关键词
8-Hydroxy-2 '-deoxyguanosine; chronic obstructive pulmonary disease; acute exacerbation; oxidative stress; DNA-DAMAGE; SUPEROXIDE-DISMUTASE; AIRWAY INFLAMMATION; LUNG INFLAMMATION; RISK-FACTORS; COPD; PATHOGENESIS; 8-OHDG; ASTHMA; DIAGNOSIS;
D O I
10.3906/sag-1807-106
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/aim: 8-Hydroxy-2'-deoxyguanosine (8-OHdG) is a biomarker of oxidative stress and has been implicated in many diseases. The aim of this study was to investigate the clinical value of plasma 8-OHdG level in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD). Materials and methods: A total of 154 subjects were enrolled in this study, including 20 healthy volunteers, 24 COPD patients in the stable phase, and 110 AECOPD patients. Peripheral blood samples, demographic information, and clinical characteristics were collected from all subjects at the time of being recruited into the study. Plasma 8-OIidG level was detected by enzyme-linked immunosorbent assay. Results: 8-OHdG was increased in patients with AECOPD compared to healthy subjects and patients with stable COPD, especially in smokers. It also increased with the GOLD stage, mMRC grade, CAT score, and group level of combined COPT) assessment. Additionally, further analysis revealed that 8-OHdG was negatively correlated with FEV1, FEV1% predicted, and FEV1/FVC and positively correlated with C-reactive protein, procalcitonin, and neutrophil CD64. Conclusion: 8-OHdG is associated with spirometric severity, symptomatic severity, exacerbation risk, and inflammatory biomarkers in AECOPD patients, suggesting it as a promising biomarker for reflecting disease severity and guiding the choice of optimal therapeutic decision.
引用
收藏
页码:93 / 100
页数:8
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