Chasity Corbin, Chowdhury Ibtida Tahmin, Chowdhury Tasnova Tahsin, Zynab Ahmed, Redeat Wattero, Azhaar Mohamed, Susan B Racette, Daniel Duprez, Ida T Fonkoue
{"title":"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。","authors":"Chasity Corbin, Chowdhury Ibtida Tahmin, Chowdhury Tasnova Tahsin, Zynab Ahmed, Redeat Wattero, Azhaar Mohamed, Susan B Racette, Daniel Duprez, Ida T Fonkoue","doi":"10.1152/ajpregu.00262.2024","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>+</sup>, <i>n</i> = 45) and without PTSD (PTSD<sup>-</sup>, <i>n</i> = 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 (<i>r</i> = -0.119, <i>P</i> = 0.350). However, when examining each group, we found a negative association between E2 and PWV in PTSD<sup>-</sup> (<i>r</i> = -0.466, <i>P</i> = 0.004). In contrast, we found an unexpected positive association between E2 levels and PWV in PTSD<sup>+</sup> (<i>r</i> = 0.360, <i>P</i> = 0.037). Furthermore, a multiple linear regression revealed that E2 was predictive of PWV in PTSD<sup>-</sup> only, even after accounting for the phase of the menstrual cycle, age, body mass index, diastolic blood pressure, and PTSD symptom severity (<i>R</i><sup>2</sup> = 0.670, <i>P</i> = 0.005). Interestingly, we also found lower levels of E2 in PTSD<sup>+</sup> than PTSD<sup>-</sup> (1.4 ± 0.4 vs. 1.6 ± 0.4 pg/mL, <i>P</i> = 0.022). These findings suggest that PTSD may inhibit the protective effects of E2 on arterial compliance in women before menopause.<b>NEW & NOTEWORTHY</b> 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.</p>","PeriodicalId":7630,"journal":{"name":"American journal of physiology. Regulatory, integrative and comparative physiology","volume":" ","pages":"R235-R241"},"PeriodicalIF":2.2000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Estradiol levels are differentially associated with pulse wave velocity in trauma-exposed premenopausal women with and without PTSD.\",\"authors\":\"Chasity Corbin, Chowdhury Ibtida Tahmin, Chowdhury Tasnova Tahsin, Zynab Ahmed, Redeat Wattero, Azhaar Mohamed, Susan B Racette, Daniel Duprez, Ida T Fonkoue\",\"doi\":\"10.1152/ajpregu.00262.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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<sup>+</sup>, <i>n</i> = 45) and without PTSD (PTSD<sup>-</sup>, <i>n</i> = 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 (<i>r</i> = -0.119, <i>P</i> = 0.350). However, when examining each group, we found a negative association between E2 and PWV in PTSD<sup>-</sup> (<i>r</i> = -0.466, <i>P</i> = 0.004). In contrast, we found an unexpected positive association between E2 levels and PWV in PTSD<sup>+</sup> (<i>r</i> = 0.360, <i>P</i> = 0.037). Furthermore, a multiple linear regression revealed that E2 was predictive of PWV in PTSD<sup>-</sup> only, even after accounting for the phase of the menstrual cycle, age, body mass index, diastolic blood pressure, and PTSD symptom severity (<i>R</i><sup>2</sup> = 0.670, <i>P</i> = 0.005). Interestingly, we also found lower levels of E2 in PTSD<sup>+</sup> than PTSD<sup>-</sup> (1.4 ± 0.4 vs. 1.6 ± 0.4 pg/mL, <i>P</i> = 0.022). These findings suggest that PTSD may inhibit the protective effects of E2 on arterial compliance in women before menopause.<b>NEW & NOTEWORTHY</b> 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.</p>\",\"PeriodicalId\":7630,\"journal\":{\"name\":\"American journal of physiology. Regulatory, integrative and comparative physiology\",\"volume\":\" \",\"pages\":\"R235-R241\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of physiology. Regulatory, integrative and comparative physiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1152/ajpregu.00262.2024\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Regulatory, integrative and comparative physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpregu.00262.2024","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/17 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
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.
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.