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计算模型捕捉了高血压妊娠和产后期间的心脏生长情况。

Computational model captures cardiac growth in hypertensive pregnancies and in the postpartum period.

机构信息

Department of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, United States.

出版信息

Am J Physiol Heart Circ Physiol. 2024 Jun 1;326(6):H1491-H1497. doi: 10.1152/ajpheart.00104.2024. Epub 2024 Apr 26.

Abstract

Heart growth in the pregnant patient helps maintain cardiovascular function while supporting the growing fetus. However, in some cases, the cardiovascular demand of pregnancy can trigger life-threatening conditions, including hypertensive disorders of pregnancy and peripartum cardiomyopathy. The mechanisms that control heart growth throughout pregnancy are unclear, and treating these diseases remains elusive. We previously developed a computational model that accounts for hormonal and hemodynamic interactions throughout pregnancy and demonstrated its ability to capture realistic cardiac growth in normal rat pregnancy. In this study, we evaluated whether this model could capture heart growth beyond normal pregnancy. After further validation of our normal pregnancy predictions, we tested our model predictions of three rat studies of hypertensive pregnancies. We next simulated the postpartum period and examined the impact of lactation on cardiac growth in rats. We demonstrate that our multiscale model can capture cardiac growth associated with new-onset hypertension during pregnancy and lactation status in the postpartum period. We conclude by elaborating on the potential clinical utility of our model in the future. Our multiscale model predicts appropriate heart growth beyond normal pregnancy, including elevated heart weights in rats with induced hypertension during pregnancy and in lactating mice and decreased heart weight in nonlactating mice. Our model captures distinct mechanisms that result in similar organ-level growth, highlighting its potential to distinguish healthy from diseased pregnancy-induced growth.

摘要

妊娠患者的心脏生长有助于维持心血管功能,同时为不断发育的胎儿提供支持。然而,在某些情况下,妊娠的心血管需求可能会引发危及生命的情况,包括妊娠高血压疾病和围产期心肌病。控制妊娠期间心脏生长的机制尚不清楚,这些疾病的治疗仍然难以捉摸。我们之前开发了一个计算模型,该模型考虑了整个妊娠期间的激素和血液动力学相互作用,并证明了其捕捉正常大鼠妊娠中真实心脏生长的能力。在这项研究中,我们评估了该模型是否可以捕捉正常妊娠以外的心脏生长。在进一步验证了我们对正常妊娠的预测之后,我们测试了我们对三种高血压妊娠大鼠研究的模型预测。接下来,我们模拟了产后阶段,并检查了哺乳对大鼠心脏生长的影响。我们证明,我们的多尺度模型可以捕捉与妊娠和哺乳期新发高血压相关的心脏生长。最后,我们阐述了我们的模型在未来的潜在临床应用。我们的多尺度模型预测了正常妊娠以外的适当心脏生长,包括诱导高血压的大鼠在妊娠和哺乳期的心脏重量增加,以及非哺乳期的小鼠心脏重量减轻。我们的模型捕捉到了导致相似器官水平生长的不同机制,突出了其区分健康和患病妊娠诱导生长的潜力。

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