Shiozawa Aki, Szabo Shelagh M, Bolzani Anna, Cheung Antoinette, Choi Hyon K
From Takeda Pharmaceuticals International Inc., Deerfield, Illinois; Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA; Redwood Outcomes, Vancouver, British Columbia, Canada.
A. Shiozawa, Associate Director, MPH, Takeda Pharmaceuticals International Inc.; S.M. Szabo, Principal, MSc, Redwood Outcomes; A. Bolzani, Research Associate, MSc, Redwood Outcomes; A. Cheung, Research Associate, MPH, Redwood Outcomes; H.K. Choi, Professor, Director, MD, DrPH, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School.
J Rheumatol. 2017 Mar;44(3):388-396. doi: 10.3899/jrheum.160452. Epub 2017 Feb 1.
Lowering serum uric acid (SUA) levels can essentially cure gout; however, this is not widely practiced. To summarize epidemiologic evidence related to this causal link, we conducted a systematic review of the published literature reporting the association between SUA level and incident and recurrent gout (i.e., gout flares).
We systematically searched Medline, EMBASE, and the Cochrane Database of Systematic Reviews using separate search strategies for incident gout and recurrent gout. We screened 646 abstracts to identify 8 eligible articles reporting gout incidence and 913 abstracts to identify 18 articles reporting recurrent gout.
For both gout incidence and recurrence, a graded trend was observed where the risk was increased with higher SUA levels. Gout incidence rates per 1000 person-years from population-based studies ranged from 0.8 (SUA ≤ 6 mg/dl) to 70.2 cases (SUA ≥ 10 mg/dl). Recurrent gout risk in clinical cohorts ranged from 12% (SUA ≤ 6 mg/dl) to 61% (SUA ≥ 9 mg/dl) among those receiving urate-lowering therapy (ULT), and 3.7% (SUA 6-7 mg/dl) to 61% (SUA > 9.3 mg/dl) after successful ULT. Retrospective database studies also showed a graded relationship, although the strength of the association was weaker. Studies reporting mean flares or time-to-flare according to SUA showed similar findings.
This systematic review confirms that higher SUA levels are associated with increased risk of incident and recurrent gout in a graded manner. Although few prospective cohorts have evaluated incident and recurrent gout according to SUA, the existing evidence underscores the need to treat to SUA targets, as recommended by the American College of Rheumatology and the European League Against Rheumatism.
降低血清尿酸(SUA)水平可从根本上治愈痛风;然而,这一做法并未得到广泛应用。为总结与这种因果关系相关的流行病学证据,我们对已发表文献进行了系统回顾,这些文献报告了SUA水平与痛风发作及复发(即痛风发作)之间的关联。
我们使用针对痛风发作和复发性痛风的单独检索策略,系统检索了Medline、EMBASE和Cochrane系统评价数据库。我们筛选了646篇摘要以确定8篇报告痛风发病率的合格文章,并筛选了913篇摘要以确定18篇报告复发性痛风的文章。
对于痛风发作和复发,均观察到一种分级趋势,即SUA水平越高,风险越高。基于人群研究的每1000人年痛风发病率范围为0.8(SUA≤6mg/dl)至70.2例(SUA≥10mg/dl)。在接受降尿酸治疗(ULT)的患者中,临床队列中的复发性痛风风险范围为12%(SUA≤6mg/dl)至61%(SUA≥9mg/dl),在ULT成功后为3.7%(SUA 6 - 7mg/dl)至61%(SUA>9.3mg/dl)。回顾性数据库研究也显示出分级关系,尽管关联强度较弱。根据SUA报告平均发作次数或发作时间的研究显示了类似的结果。
这项系统评价证实,较高的SUA水平与痛风发作及复发风险增加呈分级关联。尽管很少有前瞻性队列根据SUA评估痛风发作和复发,但现有证据强调了按照美国风湿病学会和欧洲抗风湿病联盟的建议,将SUA降至目标水平进行治疗的必要性。