1986
DOI: 10.1016/0002-9378(86)90092-x
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Cortisol levels in human pregnancy in relation to parity and age

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Cited by 36 publications
(20 citation statements)
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“…This might be explained by the relative youthfulness of our sample, ranging from 16 to 44 years of age, in which the proposed 'age-related increase in HPA axis activity' is not apparent yet. We also found higher cortisol levels in nulliparous women compared to multiparous women, which is a replication of earlier findings (Vleugels et al 1986;Conde & Figueiredo 2014). Self-reported pre-pregnancy BMI was inversely associated with cortisol.…”
Section: Biological Factorssupporting
confidence: 89%
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“…This might be explained by the relative youthfulness of our sample, ranging from 16 to 44 years of age, in which the proposed 'age-related increase in HPA axis activity' is not apparent yet. We also found higher cortisol levels in nulliparous women compared to multiparous women, which is a replication of earlier findings (Vleugels et al 1986;Conde & Figueiredo 2014). Self-reported pre-pregnancy BMI was inversely associated with cortisol.…”
Section: Biological Factorssupporting
confidence: 89%
“…Pregnancy itself has been stated a 'controlled inflammatory process' in which cortisol and CRP levels are correlated, allowing an appropriate environment to allow pregnancy, and dysregulation might result in adverse obstetric outcomes (Wilder 1998, Mor & Cardenas 2010. In pregnancy, higher cortisol levels were found in nulliparous women compared to multiparous women (Vleugels et al 1986;Conde & Figueiredo 2014), and lower cortisol levels were reported in women with a higher body mass index (BMI) . Furthermore, environmental factors such as smoking behavior also appear to influence cortisol levels (Dušková et al 2012).…”
Section: Introductionmentioning
confidence: 99%
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“…Experimental studies comparing gestating and non-gestating infected mice confirm that gestation promotes inflammatory response to infection (such as TNF␣ production; Rivera et al, 1995) without modifying the course of infection (Carlier et al, 1987;Cardoni and Antunez, 2004a). However, as observed by our team but not by others (Salas et al, 2007), primiparity might be an additional factor contributing to parasite transmission, since, higher levels of cortisol (an immunosuppressive hormone) and lower levels of prolactin (an immunostimulatory hormone) are produced in primiparas compared to multiparas (Vleugels et al, 1986). Of interest, infected mothers with fewer previous pregnancies produced less IFN-␥ than did infected mothers with more previous pregnancies (Hermann et al, 2004), which might contribute to increase parasitemia and congenital transmission.…”
Section: 3supporting
confidence: 79%
“…Non-specific immunosuppression and hormonal changes such as increased cortisol levels in primigravidae women have been implicated. 4 Although there is some evidence of a general immunosuppression in cellular immunity in pregnant women, 5 two studies have shown no difference in antibody responses to malaria antigens between pregnant and non-pregnant women. 6,7 Recent evidence suggest that gravidity-dependent changes in cytokine levels, 8 and the acquisition of antibodies that block parasite binding to the placenta could play an important role in protection against placental malaria.…”
Section: Introductionmentioning
confidence: 99%