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降尿酸药物初始剂量与成年男性痛风患者痛风发作的相关性。

Association between the initial dose urate-lowering drugs and gout flares in adult males with gout.

机构信息

Department of Rheumatology, Xingtai People's Hospital, Xingtai, China.

Department of Pediatric Rheumatology, Xingtai People's Hospital, Xingtai, China.

出版信息

Rheumatology (Oxford). 2024 May 3;63(6):1599-1606. doi: 10.1093/rheumatology/kead437.

Abstract

OBJECTIVES

Frequent gout attacks in the initial introduction of urate-lowering therapy (ULT) are significant causes of poor drug adherence and ULT discontinuation. Initial low-dose urate-lowering drugs may be effective in reducing gout flares, however robust evidence is sparse. The aim of this study was therefore to assess the association of initial dose urate-lowering drugs with gout flares in adult males with gout during the initial introduction of ULT.

METHODS

This cohort study obtained data on consecutive gout patients from a single-centre gout cohort study from August 2017 to October 2020. A standard questionnaire was applied to collect demographic and clinical information, and biochemical parameters were tested on the same day. The primary endpoint was to estimate the association of initial dose febuxostat with gout flares, using Cox hazard models with inverse probability of treatment weighting (IPTW).

RESULTS

A total of 582 gout patients were included in this study. During the 6-week follow-up, 71 (12.2%) patients suffered gout flares. In the main analysis using Cox hazard models with IPTW, compared with colchicine prophylaxis, initial low-dose febuxostat alone had no statistical significance with the increased risk of gout flares [hazard ratio (HR) 1.26; 95% CI 0.58, 2.72], while initial high-dose febuxostat was associated with an increased risk of gout flares (HR 3.08; 95% CI 1.34, 7.07).

CONCLUSIONS

This observational study demonstrated that initial low-dose febuxostat was equally effective in preventing gout flares as colchicine prophylaxis, while initial high-dose febuxostat alone was associated with an increased risk of gout flares.

摘要

目的

在降尿酸治疗(ULT)初始引入时频繁发生痛风发作是导致药物依从性差和 ULT 停药的重要原因。初始低剂量降尿酸药物可能有效减少痛风发作,但缺乏有力证据。因此,本研究旨在评估在 ULT 初始引入时,男性痛风患者初始降尿酸药物剂量与痛风发作之间的关联。

方法

本队列研究从 2017 年 8 月至 2020 年 10 月的单中心痛风队列研究中获取连续痛风患者的数据。应用标准问卷收集人口统计学和临床信息,并在同一天检测生化参数。主要终点是使用逆概率治疗加权(IPTW)的 Cox 风险模型估计初始剂量非布司他与痛风发作的相关性。

结果

本研究共纳入 582 例痛风患者。在 6 周的随访期间,71 例(12.2%)患者发生痛风发作。在使用 IPTW 的 Cox 风险模型的主要分析中,与秋水仙碱预防相比,单独使用初始低剂量非布司他与痛风发作风险增加无统计学意义[风险比(HR)1.26;95%置信区间(CI)0.58,2.72],而初始高剂量非布司他与痛风发作风险增加相关(HR 3.08;95%CI 1.34,7.07)。

结论

这项观察性研究表明,与秋水仙碱预防相比,初始低剂量非布司他在预防痛风发作方面同样有效,而单独使用初始高剂量非布司他与痛风发作风险增加相关。

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