血管紧张素转化酶基因插入或缺失多态性与健康新生儿胰岛素敏感性关系的研究

血管紧张素转化酶基因插入或缺失多态性与健康新生儿胰岛素
敏感性关系的研究
韩彤妍;崔蕴璞;王新利;叶鸿瑁;朴梅花;童笑梅;李松
【期刊名称】《发育医学电子杂志》
【年(卷),期】2014(000)001
【摘要】目的：研究血管紧张素转化酶（ACE）基因插入或缺失（I /D）多态性与健康新生儿胰岛素敏感性的关系。

方法180例健康新生儿（孕周>33周，1分钟Apgar 评分>7分）在出生时测量体重、身长，生后2~3天上午8～9时哺乳前取足跟血，测空腹血糖（FG）和空腹胰岛素（FI）水平，提取 DNA 进行 ACE 基因
分型，用 FI 和内稳态模式评估值（HOMA）衡量胰岛素敏感性。

结果 ACE基因
分布符合 Hardy-Weinberg 平衡定律（χ2=0.188，P =0.910）。

不同 ACE 基因型间出生体格无差异。

DD 基因型的 HOMA 对数值最高（0.21±0.45），但与 ID 和 II 基因型相比差异无显著性。

DD 基因型与≥1个 I 等位基因（即 ID+II 基因型）比较，DD 基因型 FI 对数值较高（0.93±0.41比0.76±0.36, P=0.018），DD 基因型的 HOMA 对数值较高（0.21±0.45比0.01±0.38, P=0.010）。

结论在健康
新生儿， D 等位基因与相对差的胰岛素敏感性相关。

这可能是解释远期胰岛素抵
抗与 D 等位基因相关的线索。

%Objective Our goal was to investigate the relationship between angiotensin-converting enzyme gene
insertion/deletion polymorphism and the insulin sensitivity in healthy newborns. Method One hundred eighty healthy newborns, all of whom
had a 1-minute Apgar score of >7 and gestational age >33 weeks, were enrolled in the study. Fasting glucose and insulin levels were measured on
day 2 or 3 after birth, and angiotensin-converting enzyme genotype was determined.Result The observed frequency distribution of angiotensin-converting enzyme genotypes did not deviate from that predicted by Hardy-Weinberg equilibrium in this group. There were no statistically significant differences in birth size and shape in different angiotensin-converting enzyme genotypes. Those carriers of the genotype homozygous for the deletion allele had the highest logarithmically transformed homeostasis model assessment (HOMA) compared with those who were heterozygous or homozygous for the insertion polymorphism. When compared with those with ≥1 insertion allele, those of the genotype homozygous for the deletion allele had significantly higher logarithmically transformed fasting insulin and logarithmically transformed homeostasis model assessment results. Regarding birth weight, birth length, ponderal index, and fasting glucose concentration, there were no significant differences between the genotype homozygous for the deletion allele and the genotypes heterozygous or homozygous for the insertion allele. Conclusion In this study, the deletion allele was associated with relatively impaired insulin sensitivity in healthy neonates. It may be a clue to explain the association between the deletion allele and insulin resistance in the long-term.
【总页数】5页(P1-5)
【作者】韩彤妍;崔蕴璞;王新利;叶鸿瑁;朴梅花;童笑梅;李松
【作者单位】北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191;北京医科大学第三医院儿科，北京 100191【正文语种】中文
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