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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Potential relationships between transaminase abnormality and valproic acid clearance or serum carnitine concentrations in Japanese epileptic patients.
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Potential relationships between transaminase abnormality and valproic acid clearance or serum carnitine concentrations in Japanese epileptic patients.

机译:日本癫痫患者转氨酶异常与丙戊酸清除率或血清肉碱浓度之间的潜在关系。

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摘要

This study tested the hypothesis that the determinants of mild liver injury are prerequisites for more severe idiosyncratic hepatotoxicity. This study verified whether the possible risk factors for rare idiosyncratic valproic acid (VPA)-induced hepatotoxicity, VPA clearance and/or serum carnitine concentrations are common to those for a mild elevation in transaminases in VPA-treated patients. VPA clearance was calculated in 172 Japanese patients with epilepsy, using a non-linear mixed-effects regression program. Carnitine concentrations were determined in a subset of 60 patients. The relationships between VPA clearance, carnitine concentration and levels of transaminases and ammonia were evaluated by Pearson's correlation coefficients. The final model of VPA apparent clearance (CL/F) was as follows: CL/F (L h(-1) = 0.012 x (BW/40)(0.34) x dose(0.55) x 0.90(gender) x 1.32(PHT) x 1.11(CBZ) x 1.12(PB), where BW = total body weight (kg); gender = 1 if female, 0 if male; PHT/CBZ/PB = 1 if phenytoin, carbamazepine, or phenobarbital, respectively, is coadministrated, otherwise 0. Either a higher VPA clearance or acyl/free carnitine ratio and a lower total and/or free carnitine concentration, but not VPA concentration, were associated with the mild elevation in transaminases or ammonia. These results support the initial hypothesis, while also helping to clarify the mechanism of severe idiosyncratic hepatotoxicity with VPA.
机译:这项研究检验了以下假设:轻度肝损伤的决定因素是更严重的特发性肝毒性的先决条件。这项研究证实了罕见的特异丙戊酸(VPA)引起的肝毒性,VPA清除率和/或血清肉碱浓度的可能危险因素是否与经VPA治疗的患者转氨酶轻度升高有关。使用非线性混合效应回归程序计算了172名日本癫痫患者的VPA清除率。在60例患者中确定了肉碱浓度。通过皮尔逊相关系数评估VPA清除率,肉碱浓度以及转氨酶和氨水平之间的关系。 VPA表观清除率(CL / F)的最终模型如下:CL / F(L h(-1)= 0.012 x(BW / 40)(0.34)x剂量(0.55)x 0.90(性别)x 1.32( PHT)x 1.11(CBZ)x 1.12(PB),其中BW =体重(千克);如果女性,则性别= 1;如果男性,则为0;如果苯妥英钠,卡马西平或苯巴比妥,则PHT / CBZ / PB = 1,较高的VPA清除率或酰基/游离肉碱比例和较低的总和/或游离肉碱浓度(而不是VPA浓度)与转氨酶或氨的轻度升高相关,这些结果支持最初的假设。 ,同时也有助于阐明VPA引起的严重特发性肝毒性的机制。

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