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Patients with CYP3A4∗1G genetic polymorphism consumed significantly lower amount of sufentanil in general anesthesia during lung resection

机译:CYP3A4 * 1G基因多态性患者在肺切除过程中全麻的舒芬太尼用量显着降低

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摘要

CYP3A4, an isoform of cytochrome P450 enzymes, is responsible for the metabolism of 45% to 60% of currently prescribed drugs. It has been shown that CYP3A4∗1G, a single nucleotide polymorphism (SNP), affects the enzymatic activity of CYP3A4. Sufentanil, a synthetic opioid commonly used for the induction and maintenance of general anesthesia, analgesia, and sedation, is mainly metabolized by CYP3A4. So far, the impact of CYP3A4∗1G on sufentanil metabolism has not been investigated. In the present study, we first determined the frequency of CYP3A4∗1G polymorphism in patients of Chinese Han nationality who underwent lung resection, and then compared the amount of sufentanil used in general anesthesia during the surgical procedure between wild type and mutant patients.DNA sequencing was performed to genotype the CYP3A4∗1G allele in 191 patients. The sufentanil dosages consumed in general anesthesia were recorded and compared between wild-type and mutant patients.The frequency of the CYP3A4∗1G variant allele was 0.202 (77/382). No significant difference was observed in age, body weight, or operation time between wild-type and mutant patients. The amount of sufentanil consumed by patients with the point mutation was significantly lower than that in the wild type group. No significant difference in sufentanil dosages was observed between females and males within wild type or within mutant group.High frequency of CYP3A4∗1G variants was detected in patients of Chinese Han nationality. Significantly lower amount of sufentanil was consumed in mutant patients compared with wild type subjects, likely a result of impaired CYP3A4 activity due to the point mutation. These findings suggest genotyping of CYP3A4 might be of value in providing guidance for the use of sufentanil.
机译:CYP3A4是细胞色素P450酶的一种同工型,可导致目前处方药的45%至60%的代谢。已经显示CYP3A4 * 1G是一种单核苷酸多态性(SNP),会影响CYP3A4的酶活性。 Sufentanil是一种通常用于诱导和维持全身麻醉,镇痛和镇静作用的合成阿片类药物,主要通过CYP3A4代谢。到目前为止,尚未研究CYP3A4 * 1G对舒芬太尼代谢的影响。在本研究中,我们首先确定了接受肺切除的中国汉族患者的CYP3A4 * 1G多态性的频率,然后比较了野生型和突变型患者在手术过程中全麻中使用的舒芬太尼的量。对191例患者进行了CYP3A4 * 1G等位基因基因分型。记录在全身麻醉中使用的舒芬太尼剂量并在野生型和突变型患者之间进行比较.CYP3A4 * 1G变异等位基因的频率为0.202(77/382)。在野生型和突变型患者之间,年龄,体重或手术时间均无明显差异。点突变患者消耗的舒芬太尼量显着低于野生型组。在野生型或突变组中,男女之间的舒芬太尼剂量没有显着差异。在中国汉族患者中检测到CYP3A4 * 1G变异体的高频率。与野生型受试者相比,突变型患者的舒芬太尼消耗量明显减少,这可能是由于点突变导致CYP3A4活性受损的结果。这些发现表明CYP3A4的基因分型可能在提供舒芬太尼使用指导方面具有价值。

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