Inocente Clara, Arnulf Isabelle, Bastuji Hélène, Thibault-Stoll Anne, Raoux Aude, Reimão Rubens, Lin Jian-Sheng, Franco Patricia
Integrative Physiology of Brain Arousal System, CRNL, INSERM-U1028, CNRS UMR5292, University Lyon1, Lyon, France.
Clin Neuropharmacol. 2012 Mar-Apr;35(2):55-60. doi: 10.1097/WNF.0b013e318246879d.
Narcolepsy is a rare disabling sleep disorder characterized by excessive daytime sleepiness and cataplexy (sudden loss of muscle tone). Drugs such as pitolisant, which block histamine H3 autoreceptors, constitute a newly identified class of stimulants because they increase brain histamine and enhance wakefulness in animal and human adult narcolepsy.
We report our experience with the off-label use of pitolisant in 4 teenagers with narcolepsy/cataplexy with severe daytime sleepiness, refractory to available treatments (modafinil, methylphenidate, mazindol, sodium oxybate, and D-amphetamine).
All teenagers developed their disease during childhood (11.3 ± 2.4 years; 50% boys) and were 17.3 ± 0.8 years old at the time of pitolisant therapy. Pitolisant treatment was increased from 10 to 30 mg (n = 1) and 40 mg (n = 3). The adapted Epworth Sleepiness Score decreased from 14.3 ± 1.1 to 9.5 ± 2.9 (P = 0.03) with pitolisant alone to 7 ± 3.4 when combined with mazindol (n = 1), methylphenidate (n = 1), or sodium oxybate plus modafinil (n = 1). Mean sleep onset latency increased from 31 ± 14 minutes to 36 ± 8 minutes (P = 0.21) on the maintenance of wakefulness test. The severity and frequency of cataplexy were slightly improved. Adverse effects were minor (insomnia, headache, hot flushes, leg pain, and hallucinations) and transitory, except for insomnia, which persisted in 2 teenagers. The benefit was maintained after a mean of 13 months.
Pitolisant could constitute an acceptable alternative for the treatment of refractory sleepiness in teenagers with narcolepsy.
发作性睡病是一种罕见的致残性睡眠障碍,其特征为日间过度嗜睡和猝倒(肌肉张力突然丧失)。诸如匹莫林这类阻断组胺H3自身受体的药物,构成了一类新发现的兴奋剂,因为它们能增加脑内组胺并增强动物及成年发作性睡病患者的清醒度。
我们报告了4例发作性睡病/猝倒且日间严重嗜睡、现有治疗(莫达非尼、哌甲酯、马吲哚、羟丁酸钠和右旋苯丙胺)无效的青少年患者使用匹莫林的经验。
所有青少年均在儿童期发病(11.3±2.4岁;50%为男孩),开始使用匹莫林治疗时年龄为17.3±0.8岁。匹莫林治疗剂量从10毫克增加至30毫克(1例)和40毫克(3例)。匹莫林单用时,改良爱泼沃斯嗜睡量表评分从14.3±1.1降至9.5±2.9(P=0.03),与马吲哚(1例)、哌甲酯(1例)或羟丁酸钠加莫达非尼(1例)联用时降至7±3.4。在维持觉醒试验中,平均入睡潜伏期从31±14分钟增至36±8分钟(P=0.21)。猝倒的严重程度和发作频率略有改善。不良反应轻微(失眠、头痛、潮热、腿痛和幻觉)且为一过性,除失眠外,2例青少年的失眠症状持续存在。平均13个月后仍维持疗效。
匹莫林可作为治疗青少年发作性睡病难治性嗜睡的一种可接受的替代药物。