From the Departments of Neurology (M.A.S., R.B., S.B., R.L., A.Y.H., G.B.) and Medicine (E.A.M.), Massachusetts General Hospital, Boston; University of Cincinnati (A.J.E.), OH; Rush University (C.G.G.), Chicago, IL; Michigan State University (J.L.G.), East Lansing; Struthers Parkinson's Center (S.A.P.), Minneapolis, MN; Boston University (M.H.S.-H.), MA; University of Rochester (A.R.), NY; University of Miami (J.M.H.), FL; Brigham and Women's Hospital (G.C.C.), Boston, MA; Yale University School of Medicine (D.S.R.), New Haven, CT; and Department of Nutrition (A.A.), Harvard School of Public Health, Boston, MA.
Neurology. 2019 Oct 1;93(14):e1328-e1338. doi: 10.1212/WNL.0000000000008194. Epub 2019 Sep 4.
To investigate whether women and men with Parkinson disease (PD) differ in their biochemical and clinical responses to long-term treatment with inosine.
The Safety of Urate Elevation in Parkinson's Disease (SURE-PD) trial enrolled 75 people with early PD and baseline serum urate below 6 mg/dL and randomized them to 3 double-blinded treatment arms: oral placebo or inosine titrated to produce mild (6.1-7.0 mg/dL) or moderate (7.1-8.0 mg/dL) serum urate elevation for up to 2 years. Parkinsonism, serum urate, and plasma antioxidant capacity were measured at baseline and repeatedly on treatment; CSF urate was assessed once, at 3 months. Here in secondary analyses results are stratified by sex.
Inosine produced an absolute increase in average serum urate from baseline that was 50% greater in women (3.0 mg/dL) than in men (2.0 mg/dL), consistent with expected lower baseline levels in women. Similarly, only among women was CSF urate significantly greater on mild or moderate inosine (+87% [ < 0.001] and +98% [ < 0.001], respectively) than on placebo (in contrast to men: +10% [ = 0.6] and +14% [ = 0.4], respectively). Women in the higher inosine dosing group showed a 7.0 Unified Parkinson's Disease Rating Scale (UPDRS) points/year lower rate of decline vs placebo ( = 0.01). In women, slower rates of UPDRS change were associated with greater increases in serum urate ( = -0.52; = 0.001), and with greater increases in plasma antioxidant capacity ( = -0.44; = 0.006). No significant associations were observed in men.
Inosine produced greater increases in serum and CSF urate in women compared to men in the SURE-PD trial, consistent with the study's design and with preliminary evidence for slower clinical decline in early PD among women treated with urate-elevating doses of inosine.
NCT00833690.
This study provides Class II evidence that inosine produced greater urate elevation in women than men and may slow PD progression in women.
研究女性和男性帕金森病(PD)患者在长期使用肌苷治疗时的生化和临床反应是否存在差异。
安全性尿酸升高在帕金森病(SURE-PD)试验纳入了 75 名早期 PD 患者和基线血清尿酸水平低于 6mg/dL,并将他们随机分为 3 个双盲治疗组:口服安慰剂或肌苷滴定至产生轻度(6.1-7.0mg/dL)或中度(7.1-8.0mg/dL)血清尿酸升高,持续 2 年。帕金森病、血清尿酸和血浆抗氧化能力在基线和治疗期间重复测量;CSF 尿酸在 3 个月时评估一次。在这里,二次分析结果按性别分层。
肌苷使平均血清尿酸从基线水平绝对升高,女性升高 3.0mg/dL,高于男性升高 2.0mg/dL,这与女性预期的基线水平较低相一致。同样,只有女性在轻度或中度肌苷(分别增加 87%[<0.001]和 98%[<0.001])上的 CSF 尿酸明显高于安慰剂(而男性分别增加 10%[=0.6]和 14%[=0.4])。高肌苷剂量组的女性 UPDRS 评分(统一帕金森病评定量表)每年下降 7.0 分,与安慰剂相比(=0.01)。在女性中,UPDRS 变化率较慢与血清尿酸升高呈正相关(= -0.52;=0.001),与血浆抗氧化能力升高呈正相关(= -0.44;=0.006)。在男性中未观察到显著相关性。
在 SURE-PD 试验中,与男性相比,女性肌苷治疗时血清和 CSF 尿酸升高幅度更大,这与研究设计一致,也与女性用尿酸升高剂量肌苷治疗的早期 PD 临床进展较慢的初步证据一致。
临床试验.gov 标识符:NCT00833690。
本研究提供了 II 级证据,表明肌苷在女性中引起的尿酸升高幅度大于男性,并且可能减缓女性 PD 的进展。