Lanza Frank, Sahba Bruce, Schwartz Howard, Winograd Steven, Torosis James, Quan Hui, Reyes Robert, Musliner Thomas, Daifotis Anastasia, Leung Albert
Houston Institute for Clinical Research, Texas 77074, USA.
Am J Gastroenterol. 2002 Jan;97(1):58-64. doi: 10.1111/j.1572-0241.2002.05446.x.
Alendronate (10 mg daily) has been shown in long term clinical trials to be an effective treatment for postmenopausal osteoporosis. A weekly dosing regimen of alendronate is preferred by both patients and physicians, as it has the potential to provide greater convenience and enhance compliance. In a 1-yr clinical trial, alendronate (70 mg once weekly) was equally efficacious and at least as well tolerated as the 10-mg daily dose in the treatment of postmenopausal osteoporosis, despite the higher unit dosage required. We conducted a randomized, double blind, placebo- and active-controlled endoscopy study to confirm the results of this clinical trial. We hypothesized that mean endoscopic gastric erosion scores would be similar in subjects receiving alendronate (70 mg once weekly) and those receiving a placebo.
Two hundred seventy-seven subjects (90 men and 187 women) were randomized to one of three treatment groups: 1) alendronate (70 mg once weekly) for 10 wk (N = 126), 2) placebo (once weekly) for 10 wk (N = 126), or 3) placebo (once weekly) for 10 wk followed by aspirin (650 mg q.i.d.) for the last week as the positive control (N = 25). Esophagogastroduodenoscopy was performed 5 to 7 days after the last dose of alendronate or matching placebo.
The mean gastric erosion scores (Lanza scale) were similar in subjects given alendronate (70 mg once weekly) and those given a placebo (0.32 vs 0.35, respectively; 95% CI for difference = -0.22-0.16, p = 0.75), whereas scores in both groups were significantly lower than in those given aspirin (3.09; p < 0.001). Endoscopic gastroduodenal ulcers occurred in no alendronate (0%), two placebo (1.7%), and five aspirin (23.8%) subjects. The mean erosion scores in the esophagus and duodenum of alendronate and placebo subjects were also similar. The incidences of upper GI symptoms were similar in the alendronate and placebo subjects and did not suggest a relationship with endoscopic lesions.
Alendronate (70 mg once weekly) was not associated with any increase in endoscopic lesions in the upper GI tract relative to a placebo.
长期临床试验表明,阿仑膦酸钠(每日10毫克)是治疗绝经后骨质疏松症的有效药物。阿仑膦酸钠每周给药方案更受患者和医生青睐,因为它可能带来更大便利并提高依从性。在一项为期1年的临床试验中,阿仑膦酸钠(每周70毫克)在治疗绝经后骨质疏松症方面疗效与每日10毫克剂量相当,且耐受性至少相同,尽管所需单位剂量更高。我们进行了一项随机、双盲、安慰剂对照和活性对照的内镜研究以证实该临床试验结果。我们假设接受阿仑膦酸钠(每周70毫克)的受试者与接受安慰剂的受试者的平均内镜下胃糜烂评分相似。
277名受试者(90名男性和187名女性)被随机分为三个治疗组之一:1)阿仑膦酸钠(每周70毫克),共10周(N = 126);2)安慰剂(每周一次),共10周(N = 126);或3)安慰剂(每周一次),共10周,最后一周给予阿司匹林(650毫克,每日四次)作为阳性对照(N = 25)。在最后一剂阿仑膦酸钠或匹配安慰剂给药后5至7天进行食管胃十二指肠镜检查。
接受阿仑膦酸钠(每周70毫克)的受试者与接受安慰剂的受试者的平均胃糜烂评分(兰扎量表)相似(分别为0.32和0.35;差异的95%置信区间 = -0.22 - 0.16,p = 0.75),而两组的评分均显著低于接受阿司匹林的受试者(3.09;p < 0.001)。阿仑膦酸钠组无内镜下胃十二指肠溃疡发生(0%),安慰剂组有2例(1.7%),阿司匹林组有5例(23.8%)。阿仑膦酸钠组和安慰剂组受试者食管和十二指肠的平均糜烂评分也相似。阿仑膦酸钠组和安慰剂组上消化道症状的发生率相似,且未显示与内镜病变有关。
与安慰剂相比,阿仑膦酸钠(每周70毫克)未导致上消化道内镜病变增加。