Gómez-Isla Teresa, Blesa Rafael, Boada Merce, Clarimón Jordi, Del Ser Teodoro, Domenech Gemma, Ferro Jose M, Gómez-Ansón Beatriz, Manubens Jose M, Martínez-Lage Jose M, Muñoz David, Peña-Casanova Jordi, Torres Ferran
Neurology Department, Hospital Santa Cruz y San Pablo and Centro de Investigación Biomédica en Red (CIBERNED), Lisboa, Spain.
Alzheimer Dis Assoc Disord. 2008 Jan-Mar;22(1):21-9. doi: 10.1097/WAD.0b013e3181611024.
Amnestic mild cognitive impairment represents, in many cases, the earliest clinical phases of Alzheimer disease. Anti-inflammatory agents have epidemiologic support as drugs potentially beneficial in Alzheimer disease. In vivo studies have shown that Triflusal and its active metabolite 2-hydroxy-4-trifluoromethyl-benzoic acid have potent anti-inflammatory actions in the central nervous system.
We conducted a randomized, double-blind, placebo-controlled trial of Triflusal in patients with amnestic mild cognitive impairment. Subjects were randomly assigned to receive 900 mg of Triflusal or placebo for 18 months. The primary outcome was a change in Cognitive subscale of the Alzheimer Disease Assessment Scale; conversion to dementia was a secondary outcome.
A slow rate of recruitment forced a premature cessation of the study. Two hundred and fifty-seven subjects were enrolled and followed-up for an average of 13 months. The significance level was not reached for the primary outcome even though a trend in favor of Triflusal was observed. However, there was a significant difference in the probability of progression to dementia of Alzheimer's type with a lower risk in the Triflusal compared with the placebo group (hazard ratio, 2.10; 95% confidence interval, 1.10-4.01; P=0.024).
In this study, Triflusal therapy was associated with a significant lower rate of conversion to dementia that is likely to be clinically relevant. Because the trial was prematurely halted, these results should be interpreted with caution and require further confirmation.
在许多情况下,遗忘型轻度认知障碍是阿尔茨海默病最早的临床阶段。抗炎药作为可能对阿尔茨海默病有益的药物,有流行病学依据支持。体内研究表明,曲氟尿苷及其活性代谢物2-羟基-4-三氟甲基苯甲酸在中枢神经系统具有强大的抗炎作用。
我们对遗忘型轻度认知障碍患者进行了一项曲氟尿苷的随机、双盲、安慰剂对照试验。受试者被随机分配接受900毫克曲氟尿苷或安慰剂,为期18个月。主要结局是阿尔茨海默病评估量表认知子量表的变化;转化为痴呆是次要结局。
招募速度缓慢迫使研究提前终止。共纳入257名受试者,平均随访13个月。尽管观察到有利于曲氟尿苷的趋势,但主要结局未达到显著性水平。然而,与安慰剂组相比,曲氟尿苷组进展为阿尔茨海默型痴呆的概率存在显著差异,风险较低(风险比,2.10;95%置信区间,1.10 - 4.01;P = 0.024)。
在本研究中,曲氟尿苷治疗与显著较低的痴呆转化率相关,这可能具有临床意义。由于试验提前终止,这些结果应谨慎解释,需要进一步证实。