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可能存在于编码 A-激酶锚定蛋白 10 的 AKAP10 基因中的 1936A>G(I646V)多态性对 1936A>G(I646V)多态性的新生儿的反作用。

Possible counter effect in newborns of 1936A>G (I646V) polymorphism in the AKAP10 gene encoding A-kinase-anchoring protein 10.

机构信息

Department of Neonatal Diseases, Pomeranian Medical University, Szczecin, Poland.

出版信息

J Perinatol. 2012 Mar;32(3):230-4. doi: 10.1038/jp.2011.85. Epub 2011 Jun 23.

Abstract

OBJECTIVE

Cyclic adenosine monophosphate/protein kinase A (PKA) is important in embryonic development. The human AKAP10 gene is polymorphic: 1936A>G results in changes to a PKA-binding domain and increased targeting to mitochondria. Previous studies found G1936 as 'deleterious' in adults, and this study investigates whether this holds true in preterm birth.

STUDY DESIGN

Study group consisted of 80 preterm newborns (PTNs) born before the 38th gestation week. Control group consisted of 123 full-term healthy newborns born after the 37th gestation week with uncomplicated pregnancies. Genomic DNA was extracted from umbilical blood and AKAP10 genotypes were identified by PCR/restriction enzyme.

RESULT

Significant differences in frequencies of 1936A>G genotypes/alleles between both groups were found. PTNs had increased frequency (55%) of AA homozygotes (odds ratio, AA versus AG+GG: 2.63 (95% confidence interval: 1.33 to 5.20), P=0.006) after adjustments: mothers with previous PTNs, smoking, first pregnancy, first delivery and Cesarean section.

CONCLUSION

Results suggest G1936 is preventative factor against preterm birth, in contrast with previously asserted negative effects in adults.

摘要

目的

环磷酸腺苷/蛋白激酶 A(PKA)在胚胎发育中很重要。人类 AKAP10 基因是多态性的:1936A>G 导致 PKA 结合域发生变化,并增加了向线粒体的靶向性。先前的研究发现 G1936 在成年人中是“有害的”,本研究调查了这是否在早产中也是如此。

研究设计

研究组由 80 名胎龄小于 38 周的早产儿(PTN)组成。对照组由 123 名胎龄大于 37 周且无并发症的足月健康新生儿组成。从脐血中提取基因组 DNA,并通过 PCR/限制性内切酶鉴定 AKAP10 基因型。

结果

两组之间 1936A>G 基因型/等位基因的频率存在显著差异。PTN 中 AA 纯合子的频率增加(55%)(优势比,AA 与 AG+GG:2.63(95%置信区间:1.33 至 5.20),P=0.006),调整后:母亲有先前的 PTN、吸烟、首次妊娠、首次分娩和剖宫产。

结论

结果表明 G1936 是预防早产的因素,与先前在成年人中断言的负面影响相反。

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