Department of Cardiology, Institute of Cardiovascular Diseases, the First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Biofactors. 2013 May-Jun;39(3):315-25. doi: 10.1002/biof.1073. Epub 2013 Jan 28.
The interactions between single nucleotide polymorphisms (SNPs) and high body mass index (BMI) on serum lipid profiles are limited. This study was undertaken to detect the interactions of 10 SNPs and high BMI on serum lipid traits in an isolated population. A total of 978 normal BMI (< 24 kg/m2) and 751 high BMI (≥ 24 kg/m2) subjects of Bai Ku Yao were randomly selected from our previous stratified randomized cluster samples. Genotypes of rs2066715, rs1044925, low density lipoprotein receptor (LDL-R) Ava||, rs2070895, rs2000813, rs1801133, rs3757354, rs505151, rs2016520, and rs5888 SNPs were determined by polymerase chain reaction and restriction fragment length polymorphism combined with gel electrophoresis, and then confirmed by direct sequencing. The interactions were detected by factorial design covariance analysis. The genotypic and allelic frequencies of rs2070895 and rs505151 were different between normal and high BMI subjects, the genotypic frequency of rs2000813 and allelic frequency of rs3757354 were also different between normal and high BMI subjects (P < 0.01). The levels of total cholesterol (TC), apolipoprotein (Apo) A1 (rs2066715); TC, low-density lipoprotein cholesterol (LDL-C), ApoA1, ApoB, and ApoA1/ApoB (rs2070895); triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), and ApoA1 (rs2000813); TC, HDL-C, LDL-C, ApoA1, and ApoB (rs1801133); HDL-C and ApoA1 (rs3757354) in normal BMI subjects were different among the genotypes (P < 0.01). The levels of LDL-C, ApoB, and ApoA1/ApoB (rs2066715); HDL-C, ApoA1, ApoB, and ApoA1/ApoB (rs2070895); TC, HDL-C, ApoA1, and ApoB (rs2000813); TC, TG, HDL-C, LDL-C, ApoA1, and ApoB (rs1801133); TC, TG, and ApoB (rs3757354); TG (rs505151); TG and ApoA1 and ApoB (rs2016520); and TC, HDL-C, LDL-C, ApoA1, and ApoB (rs5888) in high BMI subjects were also different among the genotypes (P < 0.01). The SNPs of rs2066715 (LDL-C and ApoA1/ApoB); rs2070895 (TC, LDL-C, ApoA1, and ApoB); rs2000813 (ApoB); rs1801133 (TC, TG, and LDL-C); rs3757354 (TC and TG); rs505151 (TG, HDL-C, ApoB, and ApoA1/ApoB); rs2016520 (TG and ApoA1/ApoB); and rs5888 (TG, ApoA1, and ApoB) interacted with high BMI to influence serum lipid levels (P < 0.01). The differences in serum lipid levels between normal and high BMI subjects might partly result from different interactions of several SNPs and high BMI.
单核苷酸多态性 (SNP) 与高体重指数 (BMI) 之间的相互作用对血清脂质谱的影响有限。本研究旨在检测 10 个 SNP 与高 BMI 对一个隔离人群血清脂质特征的相互作用。从我们之前的分层随机聚类样本中,随机选择了 978 名正常 BMI(<24kg/m2)和 751 名高 BMI(≥24kg/m2)的白裤瑶受试者。通过聚合酶链反应和限制性片段长度多态性与凝胶电泳相结合的方法,确定了 rs2066715、rs1044925、低密度脂蛋白受体 (LDL-R) Ava||、rs2070895、rs2000813、rs1801133、rs3757354、rs505151、rs2016520 和 rs5888 等 SNP 的基因型,并通过直接测序进行了验证。通过因子设计协方差分析检测相互作用。正常和高 BMI 组 rs2070895 和 rs505151 的基因型和等位基因频率不同,rs2000813 的基因型频率和 rs3757354 的等位基因频率也不同(P<0.01)。正常 BMI 组 rs2066715 的总胆固醇 (TC)、载脂蛋白 (Apo)A1;rs2070895 的 TC、低密度脂蛋白胆固醇 (LDL-C)、ApoA1、ApoB 和 ApoA1/ApoB;rs2000813 的甘油三酯 (TG)、高密度脂蛋白胆固醇 (HDL-C)和 ApoA1;rs1801133 的 TC、HDL-C、LDL-C、ApoA1 和 ApoB;rs3757354 的 HDL-C 和 ApoA1 的水平在不同基因型之间存在差异(P<0.01)。正常 BMI 组 rs2066715 的 LDL-C、ApoB 和 ApoA1/ApoB;rs2070895 的 HDL-C、ApoA1、ApoB 和 ApoA1/ApoB;rs2000813 的 TC、HDL-C、ApoA1 和 ApoB;rs1801133 的 TC、TG、HDL-C、LDL-C、ApoA1 和 ApoB;rs3757354 的 TC、TG 和 ApoB;rs505151 的 TG;rs2016520 的 TG 和 ApoA1/ApoB;rs5888 的 TC、HDL-C、LDL-C、ApoA1 和 ApoB 的水平在不同基因型之间也存在差异(P<0.01)。高 BMI 组 rs2066715 的 LDL-C 和 ApoA1/ApoB;rs2070895 的 TC、LDL-C、ApoA1 和 ApoB;rs2000813 的 ApoB;rs1801133 的 TC、TG 和 LDL-C;rs3757354 的 TC 和 TG;rs505151 的 TG、HDL-C、ApoB 和 ApoA1/ApoB;rs2016520 的 TG 和 ApoA1/ApoB;rs5888 的 TG、ApoA1 和 ApoB 与高 BMI 相互作用影响血清脂质水平(P<0.01)。正常和高 BMI 组之间血清脂质水平的差异可能部分是由几个 SNP 和高 BMI 的不同相互作用造成的。