Bratincsak Andras, Limm-Chan Blair N, Nerurkar Vivek R, Ching Lauren L, Reddy Venu D, Lim Eunjung, Shohet Ralph V, Melish Marian E
Kapi'olani Medical Specialists, Hawai'i Pacific Health, Honolulu, HI, United States.
Hawai'i Residency Program, University of Hawai'i, Honolulu, HI, United States.
Contemp Clin Trials. 2018 Feb;65:33-38. doi: 10.1016/j.cct.2017.11.014. Epub 2017 Dec 5.
Kawasaki disease (KD) is the most common acquired heart disease in children of the developed world, and triggers progressive coronary artery lesions (CAL) in 30% of cases if left untreated. Despite standard anti-inflammatory treatment for KD, CAL (dilation or aneurysm) still occurs in 5-10% of children, increasing their risk for fatal coronary artery complications. CAL is mediated by enhanced matrix metalloproteinase activity and elastin breakdown induced by the inflammatory process in the coronary artery wall. Doxycycline is an effective inhibitor of matrix metalloproteinases, and has been shown to reduce elastin breakdown and CAL in a mouse model of KD, but has not been evaluated in patients.
We aim to evaluate the efficacy of doxycycline in the prevention of CAL in children during the acute phase of KD.
This is a phase II prospective, randomized, double-blinded, clinical trial in two steps. In Step 1, any child older than 1month with the diagnosis of KD will be included. Children with KD will be included in Step 2 if they develop coronary artery dilation (z-score≥2.5) within 20days from the onset of fever. Study subjects in Step 2 will be randomized to receive a 3-week course of doxycycline or placebo.
The efficacy of a 3-week doxycycline course during the acute phase of KD will be evaluated by measuring the decline in coronary artery z-scores from baseline with doxycycline treatment compared to placebo.
This study was registered on clinicaltrials.gov (NCT01917721).
川崎病(KD)是发达国家儿童中最常见的后天性心脏病,若不治疗,30%的病例会引发进行性冠状动脉病变(CAL)。尽管对KD采用了标准抗炎治疗,但仍有5%-10%的儿童会出现CAL(扩张或动脉瘤),增加了其发生致命冠状动脉并发症的风险。CAL是由冠状动脉壁炎症过程诱导的基质金属蛋白酶活性增强和弹性蛋白分解介导的。强力霉素是一种有效的基质金属蛋白酶抑制剂,在KD小鼠模型中已显示可减少弹性蛋白分解和CAL,但尚未在患者中进行评估。
我们旨在评估强力霉素在KD急性期儿童中预防CAL的疗效。
这是一项分两步进行的II期前瞻性、随机、双盲临床试验。在第一步中,将纳入任何年龄大于1个月且诊断为KD的儿童。如果KD患儿在发热开始后20天内出现冠状动脉扩张(z评分≥2.5),则将其纳入第二步。第二步的研究对象将被随机分配接受为期3周的强力霉素疗程或安慰剂。
通过测量与安慰剂相比,强力霉素治疗后冠状动脉z评分相对于基线的下降情况,来评估KD急性期为期3周的强力霉素疗程的疗效。
本研究已在clinicaltrials.gov上注册(NCT01917721)。