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PhenX 工具包妊娠和分娩数据集。

The PhenX Toolkit pregnancy and birth collections.

机构信息

RTI International, San Francisco, CA, USA.

出版信息

Ann Epidemiol. 2012 Nov;22(11):753-8. doi: 10.1016/j.annepidem.2012.08.004. Epub 2012 Sep 3.

DOI:10.1016/j.annepidem.2012.08.004
PMID:22954959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4508122/
Abstract

PURPOSE

Pregnancy and childbirth are normal conditions, but complications and adverse outcomes are common. Both genetic and environmental factors influence the course of pregnancy. Genetic epidemiologic research into pregnancy outcomes could be strengthened by the use of common measures, which would allow data from different studies to be combined or compared. Here, we introduce perinatal researchers to the PhenX Toolkit and the Collections related to pregnancy and childbirth.

METHODS

The Pregnancy and Birth Collections were drawn from measures in the PhenX Tooklit. The lead author selected a list of measures for each Collection, which was reviewed by the remaining authors and revised on the basis of their comments. We chose the measures we thought were most relevant for perinatal research and had been linked most strongly to perinatal outcomes.

RESULTS

The Pregnancy and Birth Health Conditions Collection includes 24 measures related to pregnancy and fertility history, maternal complications, and infant complications. The Pregnancy and Birth Outcome Risk Factors Collection includes 43 measures of chemical, medical, psychosocial, and personal factors associated with pregnancy outcomes.

CONCLUSIONS

The biological complexity of pregnancy and its sensitivity to environmental and genomic influences suggest that multidisciplinary approaches are needed to generate new insights or practical interventions. To fully exploit new research methods and resources, we encourage the biomedical research community to adopt standard measures to facilitate pooled or meta-analyses.

摘要

目的

妊娠和分娩是正常的生理状态,但并发症和不良结局较为常见。遗传和环境因素均会影响妊娠过程。对妊娠结局进行遗传流行病学研究,可以采用通用的测量方法来加强研究,从而能够合并或比较来自不同研究的数据。在这里,我们向围产期研究人员介绍 PhenX 工具包以及与妊娠和分娩相关的集合。

方法

妊娠和分娩集合从 PhenX 工具包中的测量方法中提取。主要作者为每个集合选择了一组测量方法,其余作者对该列表进行了审查,并根据意见进行了修订。我们选择了我们认为与围产期研究最相关、与围产期结局关联最紧密的测量方法。

结果

妊娠和分娩健康状况集合包括 24 项与妊娠和生育史、孕产妇并发症以及婴儿并发症相关的测量方法。妊娠和分娩结局风险因素集合包括 43 项与妊娠结局相关的化学、医疗、心理社会和个人因素的测量方法。

结论

妊娠的生物学复杂性及其对环境和基因组影响的敏感性表明,需要采用多学科方法来产生新的见解或实际干预措施。为了充分利用新的研究方法和资源,我们鼓励生物医学研究界采用标准测量方法,以促进合并或荟萃分析。

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Research standardization tools: pregnancy measures in the PhenX Toolkit.研究标准化工具:PhenX工具包中的妊娠测量指标
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Using the PhenX Toolkit to Add Standard Measures to a Study.使用PhenX工具包为研究添加标准测量方法。
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2
Invited commentary: consolidating data harmonization--how to obtain quality and applicability?特邀评论:整合数据协调——如何获得质量和适用性?
Am J Epidemiol. 2011 Aug 1;174(3):261-4; author reply 265-6. doi: 10.1093/aje/kwr194. Epub 2011 Jul 11.
3
The PhenX Toolkit: get the most from your measures. PhenX 工具包:充分利用您的测量结果。
Am J Epidemiol. 2011 Aug 1;174(3):253-60. doi: 10.1093/aje/kwr193. Epub 2011 Jul 11.
4
Genome-wide significance and replication of the chromosome 12p11.22 locus near the PTHLH gene for peripartum cardiomyopathy.甲状旁腺激素样激素(PTHLH)基因附近12号染色体p11.22位点在围产期心肌病中的全基因组显著性及复制研究
Circ Cardiovasc Genet. 2011 Aug 1;4(4):359-66. doi: 10.1161/CIRCGENETICS.110.959205. Epub 2011 Jun 10.
5
Genomics in the post-GWAS era.后 GWAS 时代的基因组学。
Semin Liver Dis. 2011 May;31(2):215-22. doi: 10.1055/s-0031-1276641. Epub 2011 May 2.
6
An evolutionary genomic approach to identify genes involved in human birth timing.一种进化基因组学方法,用于鉴定与人类出生时间相关的基因。
PLoS Genet. 2011 Apr;7(4):e1001365. doi: 10.1371/journal.pgen.1001365. Epub 2011 Apr 14.
7
The genetics of pre-eclampsia and other hypertensive disorders of pregnancy.子痫前期和其他妊娠高血压疾病的遗传学。
Best Pract Res Clin Obstet Gynaecol. 2011 Aug;25(4):405-17. doi: 10.1016/j.bpobgyn.2011.02.007. Epub 2011 Mar 22.
8
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.利用连锁、单倍型共享和关联分析绘制新的自发性早产易感性基因 IGF1R。
PLoS Genet. 2011 Feb 3;7(2):e1001293. doi: 10.1371/journal.pgen.1001293.
9
Genetic causes of myocardial infarction: new insights from genome-wide association studies.心肌梗死的遗传病因:全基因组关联研究的新见解。
Dtsch Arztebl Int. 2010 Oct;107(40):694-9. doi: 10.3238/arztebl.2010.0694. Epub 2010 Oct 8.
10
Interplay of cytokine polymorphisms and bacterial vaginosis in the etiology of preterm delivery.细胞因子多态性与细菌性阴道病在早产发病机制中的相互作用。
J Reprod Immunol. 2010 Dec;87(1-2):82-9. doi: 10.1016/j.jri.2010.06.158. Epub 2010 Oct 20.