Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
J Atheroscler Thromb. 2010 Apr 30;17(4):356-60. doi: 10.5551/jat.2451. Epub 2010 Apr 7.
Ezetimibe is known to target Niemann-Pick Type C1 Like1 (NPC1L1), a key protein in intestinal cholesterol absorption, and thus to decrease serum LDL-cholesterol (LDL-C) levels. The response of serum LDL-C levels to ezetimibe was reported to differe among NPC1L1 haplotypes.We analyzed NPC1L1 genotypes in Japanese and investigated differences in markers of cholesterol synthesis/absorption among the genotypes.
Blood samples were collected from 42 adult volunteers to measure markers of cholesterol synthesis (lathosterol) and absorption (sitosterol and campesterol) by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Based on a study by Hegele RA et al. in Canada, we selected three SNPs (1735 C>G, 25342 A>C and 27677 T>C (numbers relative to the transcription start site)) and analyzed them using PCR-RFLP.
The frequencies of genotypes were as follows: 1735 C/G (46%)>C/C (35%)>G/G (19%), 25342 A/A (97%)>A/C (3%)>C/C (0%) and 27677 T/T (97%)>T/C (3%)>C/C (0%). Serum campesterol levels were significantly higher in the 1735 G/G group than 1735 C/G+C/C group, but lathosterol levels showed no significant differences between the genotypes.
Our results revealed differences in the frequency of the NPC1L1 polymorphism between Japanese and Canadians. In Japanese, the 1735 G/G group showed enhanced cholesterol absorption from the intestine, as compared to the 1735 C/G+C/C group.
依泽替米贝靶向作用于 NPC1L1,这是肠道胆固醇吸收的关键蛋白,可降低血清 LDL-胆固醇(LDL-C)水平。据报道,依泽替米贝对血清 LDL-C 水平的反应因 NPC1L1 单倍型而异。我们分析了日本人 NPC1L1 基因型,并研究了基因型之间胆固醇合成/吸收标志物的差异。
采集 42 名成年志愿者的血样,采用液相色谱-串联质谱法(LC-MS/MS)测定胆固醇合成标志物(羊毛甾醇)和吸收标志物(豆甾醇和菜油甾醇)。基于加拿大 Hegele RA 等人的研究,我们选择了三个 SNP(1735 C>G、25342 A>C 和 27677 T>C(相对于转录起始位点的编号)),并通过 PCR-RFLP 进行分析。
基因型频率如下:1735 C/G(46%)>C/C(35%)>G/G(19%),25342 A/A(97%)>A/C(3%)>C/C(0%)和 27677 T/T(97%)>T/C(3%)>C/C(0%)。1735 G/G 组血清菜油甾醇水平明显高于 1735 C/G+C/C 组,但基因型之间羊毛甾醇水平无显著差异。
我们的研究结果揭示了日本人 NPC1L1 多态性的频率与加拿大人不同。在日本人中,与 1735 C/G+C/C 组相比,1735 G/G 组表现出更强的肠道胆固醇吸收能力。