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血管内皮生长因子基因序列变异及其表达与复发性流产的关系。

Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss.

机构信息

Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India; Department of Clinical Biochemistry, University of Kashmir Jammu and Kashmir, India.

Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.

出版信息

Reprod Biomed Online. 2021 Dec;43(6):1035-1044. doi: 10.1016/j.rbmo.2021.08.009. Epub 2021 Aug 20.

Abstract

RESEARCH QUESTION

What is the association between VEGF gene sequence variants and its mRNA expression in recurrent pregnancy loss (RPL)? Vascular endothelial growth factor (VEGF) has a prominent role in pregnancy and affects pregnancy outcome. The association of VEGF gene 1154G>A, 634G>C and 583C>T polymorphic variations with cases of RPL and full-term fertile women as controls was investigated.

DESIGN

Two hundred women with RPL and 240 women healthy controls were included. The restriction fragment length polymorphism method was used for genotyping and quantitative real-time polymerase chain reaction was used for analysis of mRNA expression.

RESULTS

In VEGF 1154G>A, significant differences were found in homozygous AA genotype between case and control participants. The variant allele A frequency was significantly more abundant in RPL cases (0.41) than controls (0.19) (P < 0.0001). Only RPL cases with the multi-generation family history of miscarriages and those without any history showed significant differences of combined genotype GA+AA (P < 0.0001). In VEGF 634 G>C, CC genotype and allele C showed significantly increased frequency in RPL cases compared with healthy controls (P < 0.0001). The association between VEGF-1154 G>A SNP and VEGF-A mRNA expression levels was significant in RPL cases (P = 0.004). Also in VEGF-583 C>T, CT genotypes were seen significantly associated with cases (P = 0.003). The heterozygous genotype GA was significantly (P = 0.03) associated with upregulation and downregulation of VEGF mRNA, whereas the homozygous variant genotype AA only leads to low expression levels of VEGF mRNA in patients with RPL.

CONCLUSIONS

All the variants of VEGF play a vital role in an increased susceptibility to RPL. Also, VEGF-1154, AA genotypes are associated with its altered low mRNA expression in women with RPL and seem to affect pregnancy outcome.

摘要

研究问题

血管内皮生长因子(VEGF)基因序列变异与复发性妊娠丢失(RPL)中其 mRNA 表达之间的关系如何?血管内皮生长因子(VEGF)在妊娠中起重要作用,并影响妊娠结局。本研究旨在探讨 VEGF 基因 1154G>A、634G>C 和 583C>T 多态性变异与 RPL 病例和足月生育妇女作为对照的关系。

设计

纳入 200 例 RPL 患者和 240 例健康对照者。采用限制性片段长度多态性方法进行基因分型,采用实时定量聚合酶链反应分析 mRNA 表达。

结果

在 VEGF 1154G>A 中,病例组和对照组之间纯合 AA 基因型存在显著差异。变异等位基因 A 的频率在 RPL 病例(0.41)中明显高于对照组(0.19)(P<0.0001)。只有具有多代流产家族史和无家族史的 RPL 病例的 GA+AA 联合基因型存在显著差异(P<0.0001)。在 VEGF 634G>C 中,CC 基因型和 C 等位基因在 RPL 病例中的频率明显高于健康对照组(P<0.0001)。VEGF-1154 G>A SNP 与 RPL 病例中 VEGF-A mRNA 表达水平之间存在显著相关性(P=0.004)。在 VEGF-583 C>T 中,CT 基因型与病例明显相关(P=0.003)。杂合基因型 GA 与 VEGF mRNA 的上调和下调显著相关(P=0.03),而 RPL 患者中纯合变异基因型 AA 仅导致 VEGF mRNA 的低表达水平。

结论

所有 VEGF 变体在增加 RPL 易感性方面发挥重要作用。此外,VEGF-1154 AA 基因型与 RPL 妇女中其改变的低 mRNA 表达相关,并且似乎影响妊娠结局。

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