Nakayama K, Bayasgalan T, Yamanaka K, Kumada M, Gotoh T, Utsumi N, Yanagisawa Y, Okayama M, Kajii E, Ishibashi S, Iwamoto S
Division of Human Genetics, Center for Community Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke-city, Tochigi, 329-0498 Japan.
J Med Genet. 2009 Jun;46(6):370-4. doi: 10.1136/jmg.2008.064063. Epub 2009 Mar 11.
Recent genome wide association studies discovered seven novel loci that influence plasma concentrations of triglycerides, high density lipoprotein (HDL) and low density lipoprotein (LDL) cholesterol in Europeans. To date, large scale replication studies using populations with known differences in genome-wide linkage disequilibrium (LD) pattern have not been undertaken.
To address this issue, we tested associations between single nucleotide polymorphisms (SNPs) within the seven novel loci and plasma lipid profiles in 21 010 Japanese individuals.
Multiple linear regression analyses showed that the rs3812316 in MLXIPL was strongly associated with triglyceride concentrations (p approximately 3.0x10(-11), 7.1 mg/dl decrease per minor C allele) and that rs599839 in CELSR2/PSRC1/SORT1 was strongly associated with LDL cholesterol concentrations (p approximately 3.1x10(-11), 4.7 mg/dl decrease per minor G allele) in the Japanese population. SNPs near ANGPTL3, TRIB1 and GALNT2 showed evidence for associations with triglyceride concentrations (3.6x10(-6)<p<5.1x10(-5)). SNP near TRIB1 showed association with LDL cholesterol concentrations (p approximately 1.2x10(-5)). On the other hand, SNPs in NCAN/CILP2/PBX4 and MVK/MMAB were not associated with any plasma lipid profiles in the Japanese population. Ethnic differences in LD pattern would explain the lack of association between these two loci and plasma lipid concentrations in the Japanese population.
Associations between the novel loci and plasma lipid concentrations were generally conserved in the Japanese population, with the exception of NCAN/CILP2/PBX4 and MVK/MMAB.
近期全基因组关联研究发现了7个新的基因位点,它们影响欧洲人的甘油三酯、高密度脂蛋白(HDL)和低密度脂蛋白(LDL)胆固醇的血浆浓度。迄今为止,尚未开展针对全基因组连锁不平衡(LD)模式存在已知差异人群的大规模重复研究。
为解决这一问题,我们在21010名日本个体中检测了这7个新基因位点内的单核苷酸多态性(SNP)与血浆脂质谱之间的关联。
多元线性回归分析显示,在日本人群中,MLXIPL基因中的rs3812316与甘油三酯浓度密切相关(p约为3.0×10⁻¹¹,每一个次要C等位基因使甘油三酯浓度降低7.1mg/dl),CELSR2/PSRC1/SORT1基因中的rs599839与LDL胆固醇浓度密切相关(p约为3.1×10⁻¹¹,每一个次要G等位基因使LDL胆固醇浓度降低4.7mg/dl)。ANGPTL3、TRIB1和GALNT2附近的SNP显示出与甘油三酯浓度相关的证据(3.6×10⁻⁶ < p < 5.1×10⁻⁵)。TRIB1附近的SNP与LDL胆固醇浓度相关(p约为1.2×10⁻⁵)。另一方面,NCAN/CILP2/PBX4和MVK/MMAB中的SNP与日本人群的任何血浆脂质谱均无关联。LD模式的种族差异可以解释这两个基因位点与日本人群血浆脂质浓度缺乏关联的原因。
除NCAN/CILP2/PBX4和MVK/MMAB外,新基因位点与血浆脂质浓度之间的关联在日本人群中总体上是保守的。