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日本血脂异常患者中NPC1L1基因(rs2072183、rs217434和rs217428)的基因多态性及频率

Gene polymorphism and frequencies of the NPC1L1 gene (rs2072183, rs217434 and rs217428) in Japanese patients with dyslipidemia.

作者信息

Kashiwabara Y, Kobayashi Y, Koba S, Kohyama N, Ohbayashi M, Murayama J-I, Hirano T, Kobayashi Y, Yamamoto T

机构信息

Department of Pharmacotherapeutics, Division of Clinical Pharmacy, School of Pharmacy, Showa University, Tokyo, Japan.

出版信息

J Clin Pharm Ther. 2014 Oct;39(5):551-4. doi: 10.1111/jcpt.12176. Epub 2014 May 26.

Abstract

WHAT IS KNOWN AND OBJECTIVE

Niemann-Pick C1-Like 1 (NPC1L1) plays a pivotal role in intestinal cholesterol absorption. Ezetimibe is known as an inhibitor for NPC1L1 and decreases concentration of low-density lipoprotein cholesterol (LDL-C) in blood. Responses of the decrease of serum LDL-C levels to ezetimibe have been reported to be different among NPC1L1 variants. However, there are still limited data concerning the genetic variation in the NPC1L1 gene, specifically, in Japanese patients with dyslipidemia. The purpose of this study is to elucidate genotype and allele frequencies of the NPC1L1 gene in Japanese patients with dyslipidemia.

METHODS

Written informed consent was obtained from all participants. All patients were administered ezetimibe at the dose of 10 mg for once a day either alone or coadministered with statins. Patient's data were retrospectively obtained from their medical records. Genomic DNA was extracted from whole blood samples and analysed three NPC1L1 SNPs (rs2072183, rs217428 and rs217434) by the direct sequencing method.

RESULTS AND DISCUSSION

We found that there is a significant difference of genotype frequencies between healthy Japanese and dyslipidemic subjects in rs2072183. No significant differences were observed in rs217428 and rs217434; however, comparison of our data with literature reports suggests that there are significant differences in the frequencies of rs217428 and rs217434 between Canadian and Japanese dyslipidemic patients.

WHAT IS NEW AND CONCLUSION

Our study is the first report concerning the genotype and allele frequencies of the gene coding for NPC1L1 in Japanese patients with dyslipidemia. The most notable result was to demonstrate that there exists a significant difference in rs2072183 variant between healthy Japanese and dyslipidemic subjects and also found that there exists genetic variation of rs2072183 between Japanese and Canadian patients with dyslipidemia. Our results are expected to facilitate research in the proper use of ezetimibe-based mono- or combination therapies. Further studies will be required to evaluate the effects of rs2072183 on the efficacy of LDL cholesterol reduction by ezetimibe.

摘要

已知信息与研究目的

尼曼-匹克C1样蛋白1(NPC1L1)在肠道胆固醇吸收中起关键作用。依折麦布是已知的NPC1L1抑制剂,可降低血液中低密度脂蛋白胆固醇(LDL-C)的浓度。据报道,NPC1L1基因变异患者对依折麦布降低血清LDL-C水平的反应存在差异。然而,关于NPC1L1基因的遗传变异,特别是日本血脂异常患者的相关数据仍然有限。本研究的目的是阐明日本血脂异常患者中NPC1L1基因的基因型和等位基因频率。

方法

所有参与者均获得书面知情同意。所有患者均接受10mg依折麦布治疗,每日一次,单独使用或与他汀类药物联合使用。患者数据通过回顾其病历获得。从全血样本中提取基因组DNA,并采用直接测序法分析三个NPC1L1单核苷酸多态性(SNP,rs2072183、rs217428和rs217434)。

结果与讨论

我们发现,在rs2072183位点,健康日本人和血脂异常患者的基因型频率存在显著差异。在rs217428和rs217434位点未观察到显著差异;然而,将我们的数据与文献报道进行比较表明,加拿大和日本血脂异常患者在rs217428和rs217434的频率上存在显著差异。

新发现与结论

我们的研究是关于日本血脂异常患者中编码NPC1L1的基因的基因型和等位基因频率的首次报道。最显著的结果是证明健康日本人和血脂异常患者在rs2072183变异上存在显著差异,并且还发现日本和加拿大血脂异常患者在rs2072183上存在遗传变异。我们的结果有望促进基于依折麦布的单一或联合治疗合理使用的研究。需要进一步研究来评估rs2072183对依折麦布降低LDL胆固醇疗效的影响。

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