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细胞色素 P450 2D6 多态性与系统性红斑狼疮患者血液羟氯喹水平的相关性。

Association of Polymorphisms of Cytochrome P450 2D6 With Blood Hydroxychloroquine Levels in Patients With Systemic Lupus Erythematosus.

机构信息

Catholic University of Korea and Seoul St. Mary's Hospital, Seoul, Republic of Korea.

Catholic University of Korea, Seoul, Republic of Korea.

出版信息

Arthritis Rheumatol. 2016 Jan;68(1):184-90. doi: 10.1002/art.39402.

Abstract

OBJECTIVE

To evaluate associations of genetic polymorphisms in cytochrome P450 (CYP) isoforms 2D6, 3A5, and 3A4 with blood concentrations of hydroxychloroquine (HCQ) and its metabolite, N-desethyl HCQ (DHCQ), in patients with systemic lupus erythematosus (SLE).

METHODS

SLE patients taking HCQ for >3 months were recruited and were genotyped for 4 single-nucleotide polymorphisms in CYP2D610, CYP3A53, and CYP3A4*18B. Blood HCQ and DHCQ concentrations ([HCQ] and [DHCQ]) were measured and their association with corresponding genotypes was investigated.

RESULTS

A total of 194 patients were included in the analysis. CYP2D610 polymorphisms (rs1065852 and rs1135840) were significantly associated with the [DHCQ]:[HCQ] ratio after adjustment for age, sex, dose per weight per day, and SLE Disease Activity Index score (P = 0.03 and P < 0.01, respectively). In adjusted models, the [DHCQ]:[HCQ] ratio was highest in patients with the G/G genotype of the CYP2D610 (rs1065852) polymorphism and lowest in those with the A/A genotype (P = 0.03). Similarly, the [DHCQ]:[HCQ] ratio was highest in patients with the C/C genotype of the CYP2D610 (rs1135840) polymorphism and lowest in those with the G/G genotype (P < 0.01). The CYP2D610 (rs1065852) polymorphism was significantly related to the [DHCQ] (P = 0.01). However, the polymorphisms of CYP3A53 and CYP3A418B did not show any significant association with the [HCQ], [DHCQ], or [DHCQ]:[HCQ] ratio.

CONCLUSION

Our study showed that the [DHCQ]:[HCQ] ratio was related to CYP2D6 polymorphisms in Korean lupus patients taking oral HCQ. CYP polymorphisms may explain why there is wide variation in blood HCQ concentrations. The role of an individual's CYP polymorphisms should be considered when prescribing oral HCQ.

摘要

目的

评估细胞色素 P450(CYP)同工酶 2D6、3A5 和 3A4 的遗传多态性与系统性红斑狼疮(SLE)患者羟氯喹(HCQ)及其代谢物 N-去乙基 HCQ(DHCQ)血药浓度的关系。

方法

招募服用 HCQ 超过 3 个月的 SLE 患者,并对 CYP2D610、CYP3A53 和 CYP3A4*18B 的 4 个单核苷酸多态性进行基因分型。测量血液 HCQ 和 DHCQ 浓度([HCQ]和[DHCQ]),并研究其与相应基因型的关系。

结果

共纳入 194 例患者进行分析。CYP2D610 多态性(rs1065852 和 rs1135840)在调整年龄、性别、每日每公斤剂量和 SLE 疾病活动指数评分后,与 [DHCQ]:[HCQ]比值显著相关(分别为 P=0.03 和 P<0.01)。在调整模型中,CYP2D610(rs1065852)多态性 G/G 基因型患者的 [DHCQ]:[HCQ]比值最高,A/A 基因型患者的比值最低(P=0.03)。同样,CYP2D610(rs1135840)多态性 C/C 基因型患者的 [DHCQ]:[HCQ]比值最高,G/G 基因型患者的比值最低(P<0.01)。CYP2D610(rs1065852)多态性与 [DHCQ]显著相关(P=0.01)。然而,CYP3A53 和 CYP3A418B 的多态性与 [HCQ]、[DHCQ]或 [DHCQ]:[HCQ]比值均无显著相关性。

结论

本研究表明,韩国狼疮患者服用口服 HCQ 时,[DHCQ]:[HCQ]比值与 CYP2D6 多态性相关。CYP 多态性可能解释了为什么 HCQ 血药浓度存在广泛差异。在开具口服 HCQ 时,应考虑个体 CYP 多态性的作用。

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