Association Between Serum Total Bilirubin Level and Lung Function Decline in Patients with COPD: Results from a Pooled Study

被引:3
作者
Dai, Cuiqiong [1 ]
Wang, Zihui [1 ]
Deng, Zhishan [1 ]
Wu, Fan [1 ]
Yang, Huajing [1 ]
Xiao, Shan [1 ]
Wen, Xiang [1 ]
Zheng, Youlan [1 ]
Xu, Jianwu [1 ]
Lu, Lifei [1 ]
Zhao, Ningning [1 ]
Huang, Peiyu [1 ]
Zhou, Yumin [1 ]
Ran, Pixin [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Hlth, Natl Clin Res Ctr Resp Dis,State Key Lab Resp Dis, 195 Dongfeng Xi Rd, Guangzhou 510000, Peoples R China
基金
美国国家科学基金会;
关键词
total bilirubin; COPD; lung function; GOLD stage; decline; OBSTRUCTIVE PULMONARY-DISEASE; HEME OXYGENASE-1; GILBERT-SYNDROME; RISK; ANTIOXIDANT; CANCER;
D O I
10.2147/COPD.S360485
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Serum total bilirubin has been reported to have antioxidant properties against chronic respiratory diseases. The objective of our study is to evaluate the association of total bilirubin (TB) with annual lung function decline in COPD patients with different GOLD stages. Methods: This study used pooled data from two observational and prospective cohorts of 612 COPD patients whose TB levels were measured at baseline. The associations between TB and postbronchodilator FEV1, FEV(1)pred, FVC, FVCpred, FEV1/FVC, and the rate of their decline were all determined using linear regression models in the total population and strata of GOLD stages. Results: Serum TB was positively related to FEV1 and FVC in the total group 03 0.02, 95% CI 0.001 similar to 0.02, P = 0.025 and beta 0.02, 95% CI 0.002 similar to 0.03, P = 0.022, respectively). Additionally, TB was inversely associated with the annual decline in FEV1 and FEV(1)pred (beta 4.91, 95% CI 1.68 similar to 8.14, P = 0.025 and beta 0.21, 95% CI 0.06 similar to 0.36, P = 0.022, respectively) when adjusted for multivariables. After stratification, the significant associations merely persisted in COPD patients with GOLD 2 and GOLD 3-4. Conclusion: Increased TB level was related to less annual decline in FEV1 as well as FEV(1)pred in moderate-to-severe COPD but not mild COPD, which indicated the different status of TB in different COPD severity and the possible role as potential biomarker merely in moderate-to-severe COPD. Future researches to determine whether TB could be served as biomarker for COPD and the mechanisms should be focused on some target patients with a certain disease severity.
引用
收藏
页码:1031 / 1039
页数:9
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