雌二醇水平与有创伤后应激障碍和无创伤后应激障碍绝经前妇女脉搏波速度的差异相关。

IF 2.2 3区 医学 Q3 PHYSIOLOGY American journal of physiology. Regulatory, integrative and comparative physiology Pub Date : 2025-03-01 Epub Date: 2025-01-17 DOI:10.1152/ajpregu.00262.2024
Chasity Corbin, Chowdhury Ibtida Tahmin, Chowdhury Tasnova Tahsin, Zynab Ahmed, Redeat Wattero, Azhaar Mohamed, Susan B Racette, Daniel Duprez, Ida T Fonkoue
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引用次数: 0

摘要

动脉僵硬是众所周知的心血管疾病的危险因素。虽然已知雌二醇(E2)具有心脏保护作用,但现有数据表明,由于创伤后应激障碍(PTSD),绝经前女性患心血管疾病的风险不断增加。本研究旨在探讨E2对有或无临床诊断为PTSD的创伤暴露绝经前妇女动脉顺应性的影响。我们假设E2与PTSD患者(PTSD+, n=45)和非PTSD患者(PTSD-, n=47)的脉搏波速度(PWV)之间存在差异。在两次单独的研究访问中测量雌二醇和PWV。血清E2水平通过定量夹心酶联免疫分析法(ELISA)测定,由于非正态分布,采用对数变换。颈动脉至股动脉压扁式血压计测量PWV。我们的分析显示E2和PWV之间的总体相关性较弱且不显著(r=-0.119, p=0.350)。然而,在检查各组时,我们发现E2和PWV在PTSD中呈负相关(r=-0.466, p=0.004)。相反,我们发现PTSD+患者E2水平与PWV之间存在意想不到的正相关(r=0.360, p=0.037)。此外,多元线性回归显示,即使在考虑了月经周期、年龄、BMI、舒张压和PTSD症状严重程度后,E2仍可预测PTSD患者的PWV (R2= 0.670, p=0.005)。有趣的是,我们还发现PTSD+组E2水平低于PTSD-组(1.4±0.4 vs 1.6±0.4 pg/mL, p=0.022)。这些发现表明,PTSD可能抑制E2对绝经前女性动脉顺应性的保护作用。
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Estradiol levels are differentially associated with pulse wave velocity in trauma-exposed premenopausal women with and without PTSD.

Arterial stiffness is a well-known risk factor for cardiovascular disease. Although estradiol (E2) is known to be cardioprotective, the available data point to a growing cardiovascular disease risk in women before menopause due to posttraumatic stress disorder (PTSD). The present study aimed to investigate the effects of E2 on arterial compliance in trauma-exposed premenopausal women, with and without a clinical diagnosis of PTSD. We hypothesized that E2 will be differentially associated with pulse wave velocity (PWV) in women with PTSD (PTSD+, n = 45) and without PTSD (PTSD-, n = 47). Estradiol and PWV were measured during two separate study visits. Serum E2 levels were measured via the quantitative sandwich enzyme-linked immunoassay technique (ELISA) and log-transformed due to non-normal distribution. Carotid to femoral applanation tonometry was used to measure PWV. Our analyses revealed an overall weak and nonsignificant correlation between E2 and PWV (r = -0.119, P = 0.350). However, when examining each group, we found a negative association between E2 and PWV in PTSD- (r = -0.466, P = 0.004). In contrast, we found an unexpected positive association between E2 levels and PWV in PTSD+ (r = 0.360, P = 0.037). Furthermore, a multiple linear regression revealed that E2 was predictive of PWV in PTSD- only, even after accounting for the phase of the menstrual cycle, age, body mass index, diastolic blood pressure, and PTSD symptom severity (R2 = 0.670, P = 0.005). Interestingly, we also found lower levels of E2 in PTSD+ than PTSD- (1.4 ± 0.4 vs. 1.6 ± 0.4 pg/mL, P = 0.022). These findings suggest that PTSD may inhibit the protective effects of E2 on arterial compliance in women before menopause.NEW & NOTEWORTHY In trauma-exposed premenopausal women, we found that serum estradiol (E2) was a predictor of pulse wave velocity (PWV) only in the absence of a posttraumatic stress disorder (PTSD) diagnosis, even after accounting for the phase of the menstrual cycle, age, body mass index, diastolic blood pressure, and PTSD symptom severity. Moreover, E2 levels were lower in women with PTSD than in those without PTSD. We collected E2 and PWV during two separate visits and controlled for the menstrual cycle phase in our analyses.

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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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