Heo G, Kim S H, Chang M J
Department of Pharmaceutical Medicine and Regulatory Science, College of Medicine and Pharmacy, Yonsei University, Incheon, Korea.
Division of Pediatric Neurology, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.
J Clin Pharm Ther. 2017 Dec;42(6):758-764. doi: 10.1111/jcpt.12578. Epub 2017 Jun 18.
The ketogenic diet (KD) is an effective high-fat, adequate-protein, low-carbohydrate diet for patients with refractory epilepsy. The aim of this study was to investigate the potential effects of the KD and other dietary therapies on the concentrations of anticonvulsants in patients with epilepsy.
Patients with epilepsy who were treated with the KD and other dietary therapies for more than 30 days with at least one measurement performed both before and during the diet were evaluated. The mean serum concentrations and the mean serum concentrations per weight per daily dose per bioavailability (F) of anti-epileptic drugs (AEDs) before and during the treatment were assessed. We also compared the rates of events out of reference ranges of the AEDs between before and during the KD and other dietary therapies. We compared the serum albumin, alanine transaminase and aspartate transaminase data of patients with valproic acid before and during the KD.
One-hundred thirty-nine patients including 81 male patients were enrolled. The median age of the patients was 2.91 (0.15-15.46) years. The median duration of the dietary therapies was 153 (35-2307) days. After the dietary therapies, the serum concentrations of carbamazepine, lamotrigine, levetiracetam, topiramate and valproic acid decreased, whereas that of phenobarbital slightly increased. However, statistical significance was found only with valproic acid (67.07±25.89 μg/mL vs 51.00±20.19 μg/mL, P<.05). The serum concentrations per weight per daily dose per drug F significantly decreased for valproic acid (1.38±1.39×10 vs 0.82±0.82×10 μg d mL F ) and phenobarbital (6.66±7.20×10 vs 4.75±4.07×10 μg d mL F , P<.05). The rate of occurrence of events out of reference ranges significantly increased with valproic acid (36.08% vs 57.23%, P<.05).
Most anti-epileptic drug serum concentrations remained stable during the KD and other related dietary therapies except those of valproic acid. Therefore, serum concentrations of valproic acid should be monitored when the KD and other dietary therapies are concomitantly administered.
生酮饮食(KD)是一种对难治性癫痫患者有效的高脂肪、适量蛋白质、低碳水化合物饮食。本研究旨在探讨KD及其他饮食疗法对癫痫患者抗惊厥药物浓度的潜在影响。
对接受KD及其他饮食疗法治疗超过30天且在饮食前后至少进行过一次测量的癫痫患者进行评估。评估治疗前后抗癫痫药物(AEDs)的平均血清浓度以及每生物利用度(F)每日每剂量每体重的平均血清浓度。我们还比较了KD及其他饮食疗法前后AEDs超出参考范围的事件发生率。比较了KD前后使用丙戊酸患者的血清白蛋白、丙氨酸转氨酶和天冬氨酸转氨酶数据。
共纳入139例患者,其中男性81例。患者的中位年龄为2.91(0.15 - 15.46)岁。饮食疗法的中位持续时间为153(35 - 2307)天。饮食疗法后,卡马西平、拉莫三嗪、左乙拉西坦、托吡酯和丙戊酸的血清浓度降低,而苯巴比妥的血清浓度略有升高。然而,仅丙戊酸具有统计学意义(67.07±25.89μg/mL对51.00±20.19μg/mL,P<0.05)。丙戊酸每体重每每日剂量每药物F的血清浓度显著降低(1.38±1.39×10对0.82±0.82×10μg·d·mL·F),苯巴比妥也显著降低(6.66±7.20×10对4.75±4.07×10μg·d·mL·F,P<0.05)。丙戊酸超出参考范围的事件发生率显著增加(36.08%对57.23%,P<0.05)。
除丙戊酸外,大多数抗癫痫药物血清浓度在KD及其他相关饮食疗法期间保持稳定。因此,当同时进行KD及其他饮食疗法时,应监测丙戊酸的血清浓度。