重庆汉族男性载脂蛋白B基因MspⅠ、XbaⅠ、EcoRⅠ多态性与血脂水平的相关性
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重庆医科大学公共卫生与管理学院,重庆医科大学公共卫生与管理学院,重庆医科大学检验医学院,重庆市九龙坡区第一人民医院检验科,重庆医科大学公共卫生与管理学院

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国家自然科学基金(81202274).


Relationship between ApoB gene MspⅠ/XbaⅠ/EcoRⅠ polymorphisms and serum lipid level in male Han population in Chongqing, China
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School of Public Health and Management,Chongqing Medical University,School of Public Health and Management,Chongqing Medical University,College of Laboratory Medicine,Chongqing Medical University,Department of Clinical Laboratory,First People’s Hospital of Jiu Longpo District,School of Public Health and Management,Chongqing Medical University

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Supported by National Natural Science Foundation of China (81202274).

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    摘要:

    目的 探讨重庆汉族男性载脂蛋白B基因(apolipoprotein B, ApoB)MspⅠ、XbaⅠ、EcoRⅠ位点的多态性与血脂水平的关系。方法 采用基因芯片技术,检测血脂异常组157人和健康对照组180人载脂蛋白B基因MspⅠ、XbaⅠ、EcoRⅠ位点的多态性,并分析其与血脂水平的关系。结果 血脂异常组和健康对照组组内比较,MspⅠ 位点M+M-基因型的总胆固醇(TC)水平高于M+M+基因型[异常组:(6.54±0.58) vs (5.58±0.83) mmol/L, P<0.01; 对照组:(5.43±0.17) vs (4.39±0.62) mmol/L, P<0.01)];XbaⅠ位点X+X-基因型的高密度脂蛋白胆固醇(HDL-C)水平和低密度脂蛋白胆固醇(LDL-C)水平分别低于和高于X-X-基因型[异常组HDL-C:(1.08±0.27) vs (1.22±0.44) mmol/L, P=0.03; LDL-C:(3.88±0.63) vs (3.46±0.83) mmol/L, P=0.01; 对照组HDL-C:(1.31±0.43) vs (1.48±0.37) mmol/L, P=0.04; LDL-C:(3.19±0.54) vs (2.94±0.59) mmol/L, P=0.02];EcoRⅠ位点E+E-基因型的HDL-C水平低于E+E+基因型[异常组:(1.01±0.18) vs (1.21±0.43) mmol/L, P=0.01; 对照组:(1.27±0.20) vs (1.47±0.40) mmol/L, P=0.03]。血脂异常组和对照组组间比较,异常组X+X-基因型HDL-C 水平和LDL-C水平分别低于和高于对照组X+X-基因型[HDL-C:(1.08±0.27) vs (1.31±0.43) mmol/L, P=0.01; LDL-C:(3.88±0.63) vs (3.19±0.54) mmol/L, P<0.01];异常组E+E-基因型HDL-C水平低于对照组E+E-基因型[(1.01±0.18) vs (1.27±0.20) mmol/L, P<0.01]。多元线性回归分析结果显示,MspⅠ多态性与TC呈正相关,XbaⅠ多态性与HDL-C呈负相关、与LDL-C呈正相关。结论 ApoB基因MspⅠ和XbaⅠ多态性对血脂水平有一定的影响,M+M-基因型有使TC水平升高的趋势,X+X-基因型有使HDL-C水平降低、LDL-C水平升高的趋势。

    Abstract:

    Objective To explore the relationship between apolipoprotein B (ApoB) gene MspⅠ/XbaⅠ/EcoRⅠ polymorphisms and the levels of serum lipid in male Han population in Chongqing. Methods The ApoB gene MspⅠ/XbaⅠ/EcoRⅠpolymorphisms were detected by gene chip technology in 157 dyslipidemia cases and 180 healthy controls; and their relationship with serum lipids was analyzed in the dyslipidemia group and the controls. Results In both dyslipidemia group and control group, the total cholesterol (TC) levels with M+M- genotype at MspⅠ locus were significantly higher than those with M+M+ genotype (dyslipidemia group: [6.54±0.58] vs [5.58±0.83] mmol/L, P<0.01; control group: [5.43±0.17] vs [4.39±0.62] mmol/L, P<0.01); the high density lipoprotein cholesterol (HDL-C) levels with X+X- genotype at XbaⅠ locus were significantly lower than those with X-X- genotype, whereas the low density lipoprotein cholesterol (LDL-C) levels were significantly higher than those with X-X- genotype (dyslipidemia group HDL-C: [1.08±0.27] vs [1.22±0.44] mmol/L, P=0.03; LDL-C: [3.88±0.63] vs [3.46±0.83] mmol/L, P=0.01; control group HDL-C: [1.31±0.43] vs [1.48±0.37] mmol/L, P=0.04; LDL-C: [3.19±0.54] vs [2.94±0.59] mmol/L, P=0.02); the HDL-C levels with E+E- genotype at EcoRⅠ locus were significantly lower than those with E+E+ genotype (dyslipidemia group: [1.01±0.18] vs [1.21±0.43] mmol/L, P=0.01; control group: [1.27±0.20] vs [1.47±0.40] mmol/L, P=0.03). The HDL-C levels in dyslipidemia group with X+X- genotype were significantly lower than the control group with X+X- genotype, but the LDL-C levels were significantly higher than the control group with X+X- genotype (HDL-C: [1.08±0.27] vs [1.31±0.43] mmol/L, P=0.01; LDL-C: [3.88±0.63] vs [3.19±0.54] mmol/L, P<0.01); the HDL-C levels in the dyslipidemia group with E+E- genotype were significantly lower than those in the control group ([1.01±0.18] vs [1.27±0.20] mmol/L, P<0.01). The multiple linear regression analysis showed that ApoB gene MspⅠ polymorphism was positively correlated with TC; XbaⅠpolymorphism was negatively correlated with HDL-C and positively correlated with LDL-C. Conclusion The ApoB gene MspⅠ and XbaⅠ polymorphisms may be associated with the levels of serum lipids. There is a tendency that the M+M- genotype can increase TC levels and the X+X- genotype can reduce HDL-C levels and increase LDL-C levels.

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  • 收稿日期:2014-12-12
  • 最后修改日期:2015-02-28
  • 录用日期:2015-04-13
  • 在线发布日期: 2015-09-14
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