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Neurosteroid involvement in threatened preterm labour

INTRODUCTION: The neurosteroid allopregnanolone modulates oxytocin expression in the brain, and its effects arise from its action on the GABA(A) receptor. Whether neurosteroid levels and the function of the GABA(A) receptor are involved in the risk of preterm labour in pregnant women is unknown. MET...

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Detalles Bibliográficos
Autores principales: Turkmen, Sahruh, Bäckström, Torbjörn, Kangas Flodin, Yvonne, Bixo, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8029533/
https://www.ncbi.nlm.nih.gov/pubmed/33855217
http://dx.doi.org/10.1002/edm2.216
Descripción
Sumario:INTRODUCTION: The neurosteroid allopregnanolone modulates oxytocin expression in the brain, and its effects arise from its action on the GABA(A) receptor. Whether neurosteroid levels and the function of the GABA(A) receptor are involved in the risk of preterm labour in pregnant women is unknown. METHODS: Pregnant women with (n = 16) or without (n = 20) threatened preterm labour (TPL) in gestational week 33 + 6 days to 37 + 0 days were studied prospectively with procedures including foetal heart rate monitoring, vaginal examination, ultrasound examination and blood tests to determine allopregnanolone, progesterone and oxytocin levels. The GABA(A) receptor function in both groups was measured with a saccadic eye velocity test (SEVT). RESULTS: Plasma oxytocin levels were higher in the TPL group than in the control group (41.5 vs. 37.0 pmol/L, respectively, p = .021). Although the allopregnanolone and progesterone levels in both groups did not differ, there was a negative association between blood oxytocin and allopregnanolone (as predictor) levels in the TPL group (B: −3.2, 95% confidence interval (CI): −5.5 to −0.9, p = .012). As a predictor of TPL, progesterone was associated with cervix maturity (odds ratio: 1.02, 95% CI: 1.00–1.04, p = .038). SEVT showed that the women in both groups had similar GABA(A) receptor functions. In both groups, body mass index correlated with peak saccadic eye velocity (r = .34, p = .044) and negatively with allopregnanolone (r = −.41, p = .013). CONCLUSIONS: Neurosteroid levels were unchanged in the peripheral blood of women with TPL, despite the increase in available oxytocin. Although the function of the GABA(A) receptor was unchanged in women with TPL, to ensure reliable results, saccadic eye velocity should be investigated during a challenge test with a GABA(A) receptor agonist.