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本文引用的文献

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Corticotropin-releasing hormone affects short immobilization stress-induced changes in lung cytosolic and membrane glucocorticoid binding sites.促肾上腺皮质激素释放激素影响短时间束缚应激引起的肺胞质和膜糖皮质激素结合位点的变化。
Cell Mol Neurobiol. 2013 May;33(4):503-11. doi: 10.1007/s10571-013-9916-9. Epub 2013 Feb 21.
2
Variation in the maternal corticotrophin releasing hormone-binding protein (CRH-BP) gene and birth weight in Blacks, Hispanics and Whites.黑人、西班牙裔和白种人群中母源促肾上腺皮质激素释放激素结合蛋白(CRH-BP)基因与出生体重的差异。
PLoS One. 2012;7(9):e43931. doi: 10.1371/journal.pone.0043931. Epub 2012 Sep 11.
3
Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn.CRHR1 变异与新生儿持续性肺动脉高压有关。
Pediatr Res. 2012 Feb;71(2):162-7. doi: 10.1038/pr.2011.24. Epub 2011 Dec 21.
4
Multiple courses of antenatal corticosteroids for preterm birth study: 2-year outcomes.多疗程产前皮质类固醇治疗早产研究:2 年结局。
Pediatrics. 2010 Nov;126(5):e1045-55. doi: 10.1542/peds.2010-0857. Epub 2010 Oct 18.
5
Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.胎儿炎症和凝血途径基因多态性与 2 岁时神经发育迟缓的关系。
Am J Obstet Gynecol. 2010 Jul;203(1):83.e1-83.e10. doi: 10.1016/j.ajog.2010.01.047. Epub 2010 Apr 24.
6
Effect of mutations of the human serpin protein corticosteroid-binding globulin on cortisol-binding, thermal and protease sensitivity.人丝氨酸蛋白酶抑制剂蛋白皮质醇结合球蛋白突变对皮质醇结合、热和蛋白酶敏感性的影响。
J Steroid Biochem Mol Biol. 2010 May;120(1):30-7. doi: 10.1016/j.jsbmb.2010.03.014. Epub 2010 Mar 11.
7
11beta-Hydroxysteroid dehydrogenase type 1 is an important regulator at the interface of obesity and inflammation.11β-羟类固醇脱氢酶 1 是肥胖症和炎症交界处的重要调节因子。
J Steroid Biochem Mol Biol. 2010 Mar;119(1-2):56-72. doi: 10.1016/j.jsbmb.2009.12.013. Epub 2010 Jan 5.
8
Microarray analysis of placental tissue in intrauterine growth restriction.宫内生长受限胎盘组织的基因芯片分析。
Clin Endocrinol (Oxf). 2010 Feb;72(2):241-7. doi: 10.1111/j.1365-2265.2009.03659.x. Epub 2009 Jun 22.
9
Prenatal inflammation and lung development.产前炎症与肺发育
Semin Fetal Neonatal Med. 2009 Feb;14(1):2-7. doi: 10.1016/j.siny.2008.08.011. Epub 2008 Oct 8.
10
Chromosome 17: association of a large inversion polymorphism with corticosteroid response in asthma.17号染色体:一种大型倒位多态性与哮喘中皮质类固醇反应的关联。
Pharmacogenet Genomics. 2008 Aug;18(8):733-7. doi: 10.1097/FPC.0b013e3282fe6ebf.

新生儿类固醇代谢及关键呼吸功能基因的遗传变异与单疗程和多疗程皮质类固醇的围产期结局

Neonatal Genetic Variation in Steroid Metabolism and Key Respiratory Function Genes and Perinatal Outcomes in Single and Multiple Courses of Corticosteroids.

作者信息

Borowski K S, Clark E A S, Lai Y, Wapner R J, Sorokin Y, Peaceman A M, Iams J D, Leveno K J, Harper M, Caritis S N, Miodovnik M, Mercer B M, Thorp J M, O'Sullivan M J, Ramin S M, Carpenter M W, Rouse D J, Sibai B

机构信息

Departments of Obstetrics and Gynecology, University of Iowa, Iowa City, Iowa.

University of Utah, Salt Lake City, Utah.

出版信息

Am J Perinatol. 2015 Oct;32(12):1126-32. doi: 10.1055/s-0035-1549217. Epub 2015 May 8.

DOI:10.1055/s-0035-1549217
PMID:26445141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4860012/
Abstract

OBJECTIVE

The aim of the study is to evaluate the association of steroid metabolism and respiratory gene polymorphisms in neonates exposed to antenatal corticosteroids (ACS) with respiratory outcomes, small for gestational age (SGA), and response to repeat ACS.

STUDY DESIGN

This candidate gene study is a secondary analysis of women enrolled in a randomized controlled trial of single versus weekly courses of ACS. Nineteen single nucleotide polymorphisms (SNPs) in 13 steroid metabolism and respiratory function genes were evaluated. DNA was extracted from placenta or fetal cord serum and analyzed with TaqMan genotyping. Each SNP was evaluated for association via logistic regression with respiratory distress syndrome (RDS), continuous positive airway pressure (CPAP)/ventilator use (CPV), and SGA.

RESULTS

CRHBP, CRH, and CRHR1 minor alleles were associated with an increased risk of SGA. HSD11B1 and SCNN1B minor alleles were associated with an increased likelihood of RDS. Carriage of minor alleles in SerpinA6 was associated with an increased risk of CPV. CRH and CRHR1 minor alleles were associated with a decreased likelihood of CPV.

CONCLUSION

Steroid metabolism and respiratory gene SNPs are associated with respiratory outcomes and SGA in patients exposed to ACS. Risks for respiratory outcomes are affected by minor allele carriage as well as by treatment with multiple ACS.

摘要

目的

本研究旨在评估产前接受糖皮质激素(ACS)治疗的新生儿中,类固醇代谢和呼吸基因多态性与呼吸结局、小于胎龄儿(SGA)以及重复使用ACS的反应之间的关联。

研究设计

这项候选基因研究是对参与ACS单疗程与每周疗程随机对照试验的女性进行的二次分析。评估了13个类固醇代谢和呼吸功能基因中的19个单核苷酸多态性(SNP)。从胎盘或胎儿脐带血清中提取DNA,并使用TaqMan基因分型进行分析。通过逻辑回归评估每个SNP与呼吸窘迫综合征(RDS)、持续气道正压通气(CPAP)/呼吸机使用(CPV)和SGA之间的关联。

结果

CRHBP、CRH和CRHR1的次要等位基因与SGA风险增加相关。HSD11B1和SCNN1B的次要等位基因与RDS可能性增加相关。SerpinA6中次要等位基因的携带与CPV风险增加相关。CRH和CRHR1的次要等位基因与CPV可能性降低相关。

结论

在接受ACS治疗的患者中,类固醇代谢和呼吸基因SNP与呼吸结局和SGA相关。呼吸结局的风险受次要等位基因携带以及多次使用ACS治疗的影响。