利用胎儿循环集总模型了解主动脉缩窄胎儿的血流动力学变化。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-05-30 eCollection Date: 2025-05-01 DOI:10.1371/journal.pcbi.1013096
Inmaculada Villanueva-Baxarias, Anna Pellisé-Tintoré, María Pérez-Rodríguez, Laura Nogué, Pooja Vaziraani, Iris Soveral, Fàtima Crispi, Olga Gómez, Patricia Garcia-Canadilla, Oscar Camara, Bart Bijnens, Gabriel Bernardino
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引用次数: 0

摘要

主动脉缩窄(CoA)是一种常见的先天性心脏缺陷,其特征是主动脉狭窄。在产前,由于右心室失调和动脉导管(DA)扩张作为适应性机制发生,它对血流动力学有轻微的影响,但它们对CoA血流动力学的影响尚不清楚。为了研究这一点,我们建立了胎儿循环的闭合d计算模型,并模拟了不同的CoA心血管重构模式,包括主动脉峡(AoI)狭窄、心室失调和DA扩张。我们的研究结果显示轻度AoI狭窄(参考直径的80%)需要高达1.7右/左心室舒张末期容积比和115% DA扩张来维持生理压力、壁剪切应力和器官灌注。相比之下,严重的狭窄(AoI直径的20%)需要高达5左右心室舒张末期容积比和125%的DA扩张,突出了产前心室不成比例和DA扩张共存的必要性,以补偿AoI狭窄。通过7名对照和9名CoA患者的超声测量证实了这些生理区域。我们比较了不同胎儿胎盘解剖部位的血压、速度和容量流速。AoI速度表现为逆行血流峰值延迟,顺行舒张速度增加,AoI变窄更大,有助于诊断CoA。其他速度和压力的差异极小。在不同程度的AoI狭窄中,AoI、二尖瓣和主动脉瓣的体积流速下降,大脑中动脉和脐动脉保持稳定,DA、三尖瓣和肺动脉的体积流速增加。因此,我们证实,在胎儿CoA中,血流重新分配以确保脑和胎盘的灌注,除了AoI的舒张速度增加外,胎儿血流动力学(血压和速度)没有明显改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding the hemodynamic changes in fetuses with coarctation of the aorta using a lumped model of fetal circulation.

Coarctation of the aorta (CoA) is a common congenital heart defect characterized by aortic narrowing. Prenatally, it has mild hemodynamic effects as right ventricular disproportion and ductus arteriosus (DA) dilation occur as adaptive mechanisms, but their impact on CoA hemodynamics remains poorly understood. To investigate this, we built a closed 0D computational model of fetal circulation and simulated different CoA cardiovascular remodeling patterns, including aortic isthmus (AoI) narrowing, ventricular disproportion, and DA dilation. Our results showed mild AoI narrowing (80% of reference diameter) required up to 1.7 right/left ventricular end-diastolic volume ratio and 115% DA dilation to maintain physiological pressures, wall shear stresses, and organ perfusion. In contrast, severe narrowing (20% of reference AoI diameter) required up to 5 right/left ventricular end-diastolic volume ratio and 125% DA dilation, highlighting the necessity of co-occurrence of prenatal ventricular disproportion and DA dilation to compensate for AoI narrowing. These physiological regions were validated with ultrasonographic measurements from 7 controls and 9 CoA patients. We compared blood pressures, velocities, and volumetric flow rates across different fetoplacental anatomical sites. AoI velocity showed a delayed retrograde flow peak and increased antegrade diastolic velocity with greater AoI narrowing, which may aid in diagnosing CoA. Minimal differences were observed in other velocities and pressures. Volumetric flow rates across varying degrees of AoI narrowing decreased in the AoI and mitral and aortic valves, remained stable in the middle cerebral and umbilical arteries, and increased in the DA and tricuspid and pulmonary valves. Therefore, we corroborated that in fetal CoA a redistribution of blood flow occurs to ensure perfusion of the brain and placenta, without a significant alteration in fetal hemodynamics (blood pressure and velocities) except for increased diastolic velocities in the AoI.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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