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肺功能受损会增加痛风风险:来自英国生物银行一项大型队列研究的证据。

Impaired pulmonary function increases the risk of gout: evidence from a large cohort study in the UK Biobank.

作者信息

Kang Zijian, Zhang Jianzheng, Zhu Chen, Zhu Ying, Jiang Hanlei, Tong Qiang, Dai Sheng-Ming

机构信息

Department of Rheumatology and Immunology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Senior Department of Orthopedics, The Forth Medical Center of Chinese PLA General Hospital, Beijing, China.

出版信息

BMC Med. 2024 Dec 31;22(1):606. doi: 10.1186/s12916-024-03836-8.

Abstract

BACKGROUND

Pulmonary function is increasingly recognized as a key factor in metabolic diseases. However, its link to gout risk remains unclear. The study aimed to investigate the relationship between pulmonary function and the risk of developing gout and the underlying biological mechanisms.

METHODS

Our study included 420,002 participants with complete pulmonary function data from the UK Biobank. Logistic regression was used to evaluate gout prevalence among individuals with different pulmonary function statuses. Propensity score matching (PSM) created balanced groups, while Cox regression gauged the risk association between reduced lung capacity and gout compared with normal function. Mendelian randomization (MR) analysis was used to verify causal associations. Non-linear correlations were assessed with restricted cubic spline (RCS) analysis, and mediation analysis was used to explore the role of blood biomarkers. Mediation analyses were used to investigate the potential mediating role of biomarkers in the association.

RESULTS

Cross-sectional analysis revealed a higher prevalence of gout in individuals with preserved ratio of impaired spirometry (PRISm) of 6.31% and chronic obstructive pulmonary disease (COPD) of 6.26% than in those with normal pulmonary function (3.45%). After adjustment for covariates, both PRISm (odds ratio [OR] 1.24, 95% confidence interval [CI] 1.17-1.31) and COPD (OR 1.14, 95% CI 1.07-1.22) were significantly associated with gout. Longitudinal analysis confirmed that impaired pulmonary function significantly increased the risk of developing gout (hazard ratio [HR] 1.32, 95% CI 1.24-1.40). MR further revealed a potential causal effect of decreased pulmonary function on an increased risk of gout. Subgroup analysis revealed significant interactions between impaired pulmonary function and several factors, including body mass index (BMI), levels of physical activity, and diabetes status, in their associations with the risk of gout. RCS analysis showed a nonlinear relationship between pulmonary function indicators and gout incidence, characterized by an inverse S-shaped curve. Mediation analysis revealed that urate levels (49.1% mediation proportion), C-reactive protein (CRP) levels (6.62%), monocyte counts (1.33%), and neutrophil counts (4.85%) significantly mediated the relationship between pulmonary function and the risk of gout.

CONCLUSIONS

Our study revealed a significant association between impaired pulmonary function and an increased risk of developing gout. The association might be partially mediated by biomarkers including urate levels, inflammatory markers, and immune cell counts.

摘要

背景

肺功能日益被认为是代谢性疾病的关键因素。然而,其与痛风风险的联系仍不明确。本研究旨在探讨肺功能与痛风发生风险之间的关系及其潜在的生物学机制。

方法

我们的研究纳入了来自英国生物银行的420,002名拥有完整肺功能数据的参与者。采用逻辑回归评估不同肺功能状态个体的痛风患病率。倾向得分匹配(PSM)创建了平衡组,而Cox回归评估了肺功能降低与痛风之间的风险关联,并与正常功能进行比较。采用孟德尔随机化(MR)分析来验证因果关联。使用受限立方样条(RCS)分析评估非线性相关性,并使用中介分析来探讨血液生物标志物的作用。中介分析用于研究生物标志物在该关联中的潜在中介作用。

结果

横断面分析显示,肺活量降低比例保留(PRISm)组痛风患病率为6.31%,慢性阻塞性肺疾病(COPD)组为6.26%,均高于肺功能正常组(3.45%)。在调整协变量后,PRISm(优势比[OR] 1.24,95%置信区间[CI] 1.17 - 1.31)和COPD(OR 1.14,95% CI 1.07 - 1.22)均与痛风显著相关。纵向分析证实,肺功能受损显著增加了患痛风的风险(风险比[HR] 1.32,95% CI 1.24 - 1.40)。MR进一步揭示了肺功能降低对痛风风险增加的潜在因果效应。亚组分析显示,肺功能受损与痛风风险的关联中,与体重指数(BMI)、身体活动水平和糖尿病状态等几个因素之间存在显著交互作用。RCS分析显示肺功能指标与痛风发病率之间呈非线性关系,特征为反S形曲线。中介分析表明,尿酸水平(中介比例49.1%)、C反应蛋白(CRP)水平(6.62%)、单核细胞计数(1.33%)和中性粒细胞计数(4.85%)显著介导了肺功能与痛风风险之间的关系。

结论

我们的研究揭示了肺功能受损与痛风发生风险增加之间存在显著关联。这种关联可能部分由包括尿酸水平、炎症标志物和免疫细胞计数在内的生物标志物介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f097/11686989/d8fc91dd0cd8/12916_2024_3836_Fig1_HTML.jpg

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