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在正常妊娠期间,血管性血友病因子相关参数会发生复杂变化。

Complex changes in von Willebrand factor-associated parameters are acquired during uncomplicated pregnancy.

作者信息

Drury-Stewart Danielle N, Lannert Kerry W, Chung Dominic W, Teramura Gayle T, Zimring James C, Konkle Barbara A, Gammill Hilary S, Johnsen Jill M

机构信息

Research Institute, Puget Sound Blood Center, Seattle, Washington, United States of America.

Research Institute, Puget Sound Blood Center, Seattle, Washington, United States of America; Department of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS One. 2014 Nov 19;9(11):e112935. doi: 10.1371/journal.pone.0112935. eCollection 2014.

Abstract

BACKGROUND

The coagulation protein von Willebrand Factor (VWF) is known to be elevated in pregnancy. However, the timing and nature of changes in VWF and associated parameters throughout pregnancy are not well understood.

OBJECTIVES

To better understand the changes in VWF provoked by pregnancy, we studied VWF-associated parameters in samples collected over the course of healthy pregnancies.

METHODS

We measured VWF antigen (VWF:Ag), VWF propeptide (VWFpp), Factor VIII (FVIII), and ADAMTS13 activity in samples collected from 46 women during pregnancy and at non-pregnant baseline. We also characterized pregnant vs. non-pregnant VWF multimer structure in 21 pregnancies, and performed isoelectric focusing (IEF) of VWF in two pregnancies which had samples from multiple trimesters.

RESULTS

VWF:Ag and FVIII levels were significantly increased during pregnancy. ADAMTS13 activity was unchanged. VWFpp levels increased much later in pregnancy than VWF:Ag, resulting in a progressive decrease in VWFpp:Ag ratios. FVIII:VWF ratios also decreased in pregnancy. Most pregnancies exhibited a clear loss of larger VWF multimers and altered VWF triplet structure. Further evidence of acquired VWF qualitative changes in pregnancy was found in progressive, reversible shifts in VWF IEF patterns over gestation.

CONCLUSIONS

These data support a new view of pregnancy in which VWF can acquire qualitative changes associated with advancing gestational age. Modeling supports a scenario in which both increased VWF production and doubling of the VWF half-life would account for the data observed. We propose that gestation induces a prolongation in VWF survival, which likely contributes to increased total VWF levels and altered VWF structure.

摘要

背景

已知凝血蛋白血管性血友病因子(VWF)在孕期会升高。然而,孕期VWF及其相关参数变化的时间和性质尚不清楚。

目的

为了更好地理解孕期引发的VWF变化,我们研究了健康孕期不同阶段采集样本中与VWF相关的参数。

方法

我们测量了46名女性孕期及非孕期基线样本中的VWF抗原(VWF:Ag)、VWF前体肽(VWFpp)、凝血因子VIII(FVIII)和ADAMTS13活性。我们还对21例孕期样本的VWF多聚体结构进行了孕、非孕特征分析,并对两个有多个孕期样本的孕妇进行了VWF的等电聚焦(IEF)分析。

结果

孕期VWF:Ag和FVIII水平显著升高。ADAMTS13活性无变化。VWFpp水平在孕期比VWF:Ag升高得晚得多,导致VWFpp:Ag比值逐渐降低。孕期FVIII:VWF比值也降低。大多数孕期样本显示较大的VWF多聚体明显减少,VWF三联体结构改变。在孕期VWF等电聚焦模式的渐进性、可逆性变化中发现了VWF定性变化的进一步证据。

结论

这些数据支持了一种关于孕期的新观点,即VWF可获得与孕周增加相关的定性变化。模型支持一种情景,即VWF产生增加和VWF半衰期加倍都可以解释观察到的数据。我们提出,孕期可诱导VWF存活期延长,这可能导致VWF总水平增加和VWF结构改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e9d/4237360/bddef6c336be/pone.0112935.g001.jpg

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