Jing Wang, Chunfeng Li, Wen Li, Yexiao Tao, Yong Li
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引用次数: 0
摘要
目的:子痫前期(PE子痫前期(PE)会增加产妇和胎儿出现多种不良结局的风险。本研究旨在探讨心外膜脂肪组织(EAT)厚度与子痫前期和出生体重之间的相关性:这是一项单中心回顾性研究,选取了 221 名 PE 患者,并选取了 81 名无高血压和蛋白尿的妇女作为对比。在 11-13 孕周进行首次产前检查时,对她们进行超声心动图检查并测量 EAT 厚度。在随后的随访中,记录了出生体重:结果:EAT 厚度明显升高(6.60 ± 1.34 vs. 5.71 ± 1.79 mm,P = 0.001),C 反应蛋白也明显升高(OR 4.097,95% CI,2.323-7.224,P 结论:EAT 厚度和 C 反应蛋白的升高可用于鉴别胎儿是否患有先天性心脏病:EAT 厚度可用于识别有严重 PE 风险和低出生体重的孕妇。它是重度 PE 的独立风险因素,但不是轻度 PE 的重要标志。
Epicardial adipose tissue thickness associated with preeclampsia and birth weight in early pregnancy.
Objective: Preeclampsia (PE) increases the risk of many adverse maternal and fetal outcomes. This study was to investigate the correlation between epicardial adipose tissue (EAT) thickness and PE and birth weight.
Methods: This was a single-center retrospective study, 221 patients with PE were selected, and 81 women without hypertension and proteinuria were selected as a comparison. Echocardiogram was performed in their first prenatal examinations at 11-13 gestational weeks, and the thickness of EAT was measured. At the subsequent follow-up, the birth weight was recorded.
Results: EAT thickness was significantly elevated (6.60 ± 1.34 vs. 5.71 ± 1.79 mm, p < 0.001) in severe PE compared to mild PE. In the multivariate analysis, EAT thickness (OR 5.671, 95% CI, 1.991-16.150, p = 0.001), and C reactive protein (OR 4.097, 95% CI, 2.323-7.224, p < 0.001) were found as significant independent predictors of severe PE after adjusting for other risk factors. Linear regression analysis showed that hs-CRP, EAT thickness, and severe PE significantly negatively affected birth weight.
Conclusion: EAT thickness can be used to identify pregnant women with severe PE risks and low birth weight. It is an independent risk factor for severe PE but is not a valuable sign of mild PE.
期刊介绍:
Hypertension in Pregnancy is a refereed journal in the English language which publishes data pertaining to human and animal hypertension during gestation. Contributions concerning physiology of circulatory control, pathophysiology, methodology, therapy or any other material relevant to the relationship between elevated blood pressure and pregnancy are acceptable. Published material includes original articles, clinical trials, solicited and unsolicited reviews, editorials, letters, and other material deemed pertinent by the editors.