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Mylip 基因 rs3757354 及 ABCA1 基因 2230806 位点单核苷酸多态性与早发型子痫前期的相关性研究:一项候选基因病例对照研究。

Novel associations of SNPs MYLIP rs3757354 and ABCA1 2230806 gene with early-onset-preeclampsia: A case-control candidate genetic study.

机构信息

The First Hospital of Jilin University, Department of Obstetrics, Changchun, Jilin Province 130021, China.

Institute of Genetic Technology, Yinfeng Bilogical Group, Yinfeng Gene Technology Company Limited, Jinan, Shandong Province 250014, China.

出版信息

Pregnancy Hypertens. 2021 Mar;23:185-190. doi: 10.1016/j.preghy.2020.12.005. Epub 2020 Dec 24.

DOI:10.1016/j.preghy.2020.12.005
PMID:33450693
Abstract

OBJECTIVE

To investigate the association between MYLIP rs3757354 and ABCA1 2230806 single nucleotide polymorphisms in women with preeclampsia in China.

STUDY DESIGN

The case-control study involved 205 patients with preeclampsia and 145 controls. All women with preeclampsia were divided into two groups: 78 patients with early-onset preeclampsia and 127 with late-onset preeclampsia.

MAIN OUTCOME MEASURE

MYLIP rs3757354 and ABCA1 rs2230806 SNPs were analyzed through multiplex PCR for targeted next-generation sequencing technology. A secondary outcome was lipid profile changes and liver function in women with PE.

RESULTS

Maternal age (OR: 1.073, 95% CI = 1.006-1.145), BMI (OR: 1.118, 95% CI = 1.040-1.201), TG/HDL-C (OR: 1.536, 95% CI = 1.080-2.183), and TT genotype of SNP rs3757354 (OR: 3.238, 95% CI = 1.313-7.990) were associated with EOPE risk. Our study found that patients with TT genotype of ABCA1 rs2230806 had more severe hepatic dysfunction and higher HDL levels in the EOPE group compared with CC/CT genotype. There was no association between rs2230806 and the risk of PE.

CONCLUSION

The polymorphisms of rs3757354 are associated with the risk of EOPE in Chinese pregnant women. The TT genotype in ABCA1 rs2230806 is a strong predictive risk for elevated aminotransferase levels in pregnant women with EOPE.

摘要

目的

探讨中国子痫前期患者 MYLIP rs3757354 和 ABCA1 2230806 单核苷酸多态性的相关性。

研究设计

病例对照研究纳入了 205 例子痫前期患者和 145 例对照。所有子痫前期患者分为两组:78 例早发型子痫前期患者和 127 例晚发型子痫前期患者。

主要观察指标

通过多重 PCR 靶向下一代测序技术分析 MYLIP rs3757354 和 ABCA1 rs2230806 SNP。次要观察指标为子痫前期患者的血脂谱和肝功能变化。

结果

母亲年龄(OR:1.073,95%CI=1.006-1.145)、BMI(OR:1.118,95%CI=1.040-1.201)、TG/HDL-C(OR:1.536,95%CI=1.080-2.183)和 SNP rs3757354 的 TT 基因型(OR:3.238,95%CI=1.313-7.990)与 EOPE 风险相关。我们的研究发现,与 CC/CT 基因型相比,ABCA1 rs2230806 的 TT 基因型患者的 EOPE 组肝功能更严重,HDL 水平更高。ABCA1 rs2230806 与 PE 风险无关。

结论

rs3757354 多态性与中国孕妇 EOPE 风险相关。ABCA1 rs2230806 的 TT 基因型是预测 EOPE 孕妇转氨酶水平升高的强风险因素。

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