Effects of hormonal contraceptive phase and progestin generation on stress-induced cortisol and progesterone release.

Cortisol Hormonal contraception Progesterone Progestin generation Progestins Stress

Journal

Neurobiology of stress
ISSN: 2352-2895
Titre abrégé: Neurobiol Stress
Pays: United States
ID NLM: 101643409

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 31 10 2018
revised: 24 01 2019
accepted: 28 02 2019
entrez: 3 4 2019
pubmed: 3 4 2019
medline: 3 4 2019
Statut: epublish

Résumé

The stress response differs between women using hormonal contraception and naturally cycling women. Yet, despite ample evidence showing that the stress response differs across the menstrual cycle in naturally cycling women, limited work has investigated whether the stress response differs across the hormonal contraceptive cycle, during which synthetic hormones are taken most of the month but not all of it. To induce a stress response, women using hormonal contraception completed the cold pressor test during either the active phase, when hormones are present, or during the inactive phase, when hormones are not present. Saliva was collected and assayed for free cortisol and progesterone levels prior to stress onset, immediately after stress termination, and 15-min post stress onset. Free cortisol and progesterone increased to a similar degree across both hormonal contraceptive phases in response to the cold pressor test. Post-hoc investigation indicates that the progestin "generation" (classification of synthetic progestins based on the compounds they are derived from) can differentially affect the free steroid response to cold pressor test stress, with the largest effects observed in women using formulations containing second-generation progestins. These findings indicate that progestin generation, particularly second-generation progestins, may have a more impactful influence on the stress response than hormonal contraceptive cycle phase. Potential mechanisms driving this effect and need for additional research are discussed.

Identifiants

pubmed: 30937356
doi: 10.1016/j.ynstr.2019.100151
pii: S2352-2895(18)30085-7
pii: 100151
pmc: PMC6430619
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100151

Subventions

Organisme : NIA NIH HHS
ID : R01 AG025340
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG038043
Pays : United States

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Auteurs

Alexandra Ycaza Herrera (AY)

University of Southern California, Davis School of Gerontology, USA.

Sophia Faude (S)

University of Southern California, USA.

Shawn E Nielsen (SE)

University of Southern California, Davis School of Gerontology, USA.

Mallory Locke (M)

University of Southern California, USA.

Mara Mather (M)

University of Southern California, Davis School of Gerontology, USA.
University of Southern California, Department of Psychology, USA.
University of Southern California, Neuroscience Graduate Program, USA.

Classifications MeSH