Jallon P, Picard F
Epilepsy Unit, Hôpital Cantonal, Geneva, Switzerland.
Drug Saf. 2001;24(13):969-78. doi: 10.2165/00002018-200124130-00004.
Bodyweight gain is a common and frequent undesirable effect associated with the use of anticonvulsant drugs. This has been observed for many years with valproic acid (sodium valproate) and carbamazepine, and also, more recently, with some of the newer anticonvulsants such as vigabatrin and gabapentin. Very often bodyweight gain in children, adolescents and adults with epilepsy taking such anticonvulsants results in cosmetic adverse effects. On the other hand, bodyweight gain is disturbing to general health, with a possible increase in the risk of diabetes mellitus or heart disease. Other potential adverse effects, such as the association of obesity with polycystic ovaries, have been reported with the use of valproic acid. Potential mechanisms of anticonvulsant-associated bodyweight gain are not yet clear and differ between drugs used. The involvement of lowered blood glucose level, which may stimulate eating through an effect on the hypothalamus, constitutes one of the possible mechanisms. Lowered blood glucose levels may result from a competition between the binding of the drug and long chain fatty acids. An increased availability of the latter stimulates insulin production and lowers the serum glucose levels. Another possible explanation for lowered blood glucose may be a deficiency in carnitine directly caused by the drug, that would result in a reduction of fatty acid metabolism and an increase in glucose consumption. An enhancing effect of gamma-aminobutyric acid-mediated neurotransmission may increase appetite for carbohydrates and reduce energy expenditure. An antidiuretic hormone-like effect or effects on norepinephrine (noradrenaline) or serotonin-mediated neurotransmission are more rarely considered. Many studies on anticonvulsant-associated bodyweight gain illustrate how we could better define the risk factors for the development of anticonvulsant-induced bodyweight gain and uncover the mechanisms behind it.
体重增加是使用抗惊厥药物常见且频繁出现的不良后果。多年来,丙戊酸(丙戊酸钠)和卡马西平都有此现象,最近,一些新型抗惊厥药物如氨己烯酸和加巴喷丁也出现了这种情况。服用此类抗惊厥药物的儿童、青少年和成人癫痫患者体重增加,常常会产生美容方面的不良影响。另一方面,体重增加对整体健康也有不良影响,可能会增加患糖尿病或心脏病的风险。使用丙戊酸还报告了其他潜在的不良影响,如肥胖与多囊卵巢的关联。抗惊厥药物相关体重增加的潜在机制尚不清楚,且不同药物之间存在差异。血糖水平降低可能是其中一种机制,它可能通过影响下丘脑刺激进食。血糖水平降低可能是由于药物与长链脂肪酸结合的竞争所致。后者可用性增加会刺激胰岛素分泌并降低血清葡萄糖水平。血糖降低的另一个可能解释可能是药物直接导致肉碱缺乏,这会导致脂肪酸代谢减少和葡萄糖消耗增加。γ-氨基丁酸介导的神经传递增强作用可能会增加对碳水化合物的食欲并减少能量消耗。抗利尿激素样作用或对去甲肾上腺素(去甲肾上腺素)或5-羟色胺介导的神经传递的影响较少被考虑。许多关于抗惊厥药物相关体重增加的研究表明,我们如何能够更好地确定抗惊厥药物引起体重增加的风险因素,并揭示其背后的机制。