Wang L, Gu Y, Wu G
Heart Lung and Blood Vessel Medical Institute, Beijing 100029.
Zhonghua Yi Xue Za Zhi. 1999 Aug;79(8):603-6.
To explore the association of variance at XbaI site of apolipoprotein B (ApoB) gene and atherosclerotic cerebral infarction (ACI) in Chinese Han population.
Using polymerase chain reaction (PCR) techniques, we studied the restrict fragment length polymorphism (RFLP) at XbaI site of ApoB gene in 150 patients with ACI and 301 healthy age, sex-matched individuals from a population of Chinese Han nationality in Beijing.
In both ACI group and control group, X-X- genotype was the most frequent one (frequency: 0.907, 0.948) and we did not find X+X+ genotype. The distribution of genotypes in the two groups was at the Hardy-Weiberg equilibriums. The frequency of rare allele X+ was significantly lower in Chinese Han than that reported in Caucasians (0.027 vs 0.418, 0.454, 0.479, P < 0.01). The higher frequency of rare allele X+ was found in the ACI group as compared with the control group (0.053 vs 0.027, P < 0.05). markedly increased levels of TC (5.3 +/- 1.3), (4.9 +/- 1.3) mmol/L (P < 0.05), and low levels of Apo-AI, Apo-AI/ApoB in the ACI group were observed (1.02 +/- 0.34), (1.26 +/- 0.40) g/L, (P < 0.01); X+X- genotype was associated with higher levels of ApoB compared with the levels of X-X- genotype in the ACI group (0.89 +/- 0.29) g/L, (0.78 +/- 0.17) g/L (P < 0.05).
X+ allele of ApoB gene may be associated with ACI to some extent in the Chinese population, and presumbly through its effect on ApoB metabolism it increases the susceptibility to ACI.
探讨载脂蛋白B(ApoB)基因XbaI位点的多态性与中国汉族人群动脉粥样硬化性脑梗死(ACI)的关系。
采用聚合酶链反应(PCR)技术,研究了150例ACI患者及301例来自北京汉族人群、年龄和性别匹配的健康对照者ApoB基因XbaI位点的限制性片段长度多态性(RFLP)。
ACI组和对照组中,X-X-基因型最为常见(频率分别为0.907、0.948),未发现X+X+基因型。两组基因型分布均符合Hardy-Weinberg平衡。中国汉族人群中稀有等位基因X+的频率显著低于白种人报道的频率(0.027比0.418、0.454、0.479,P<0.01)。ACI组稀有等位基因X+的频率高于对照组(0.053比0.027,P<0.05)。ACI组TC水平显著升高(5.3±1.3)、(4.9±1.3)mmol/L(P<0.05),Apo-AI、Apo-AI/ApoB水平降低(1.02±0.34)、(1.26±0.40)g/L(P<0.01);ACI组中,X+X-基因型的ApoB水平高于X-X-基因型(0.89±0.29)g/L,(0.78±0.17)g/L(P<0.05)。
在中国人群中,ApoB基因的X+等位基因可能在一定程度上与ACI相关,推测其通过影响ApoB代谢增加了ACI的易感性。