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Myo-inositol: a potential prophylaxis against premature onset of labour and preterm birth

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NUTRITION RESEARCH REVIEWS
卷 36, 期 1, 页码 60-68

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CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0954422421000299

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Myo-inositol; Preterm birth; Labour-onset; Preterm pre-labour rupture of membranes; Placenta

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The incidence of preterm birth is increasing globally, and myo-inositol supplementation may have a positive impact on reducing this risk. However, the molecular mechanisms by which myo-inositol affects preterm labor remain unclear. This paper presents hypotheses on the role of uteroplacental myo-inositol in human parturition and explores potential molecular mechanisms through which myo-inositol may inhibit preterm labor onset.
The incidence of preterm birth (PTB), delivery before 37 completed weeks of gestation, is rising in most countries. Several recent small clinical trials of myo-inositol supplementation in pregnancy, which were primarily aimed at preventing gestational diabetes, have suggested an effect on reducing the incidence of PTB as a secondary outcome, highlighting the potential role of myo-inositol as a preventive agent. However, the underlying molecular mechanisms by which myo-inositol might be able to do so remain unknown; these may occur through directly influencing the onset and progress of labour, or by suppressing stimuli that trigger or promote labour. This paper presents hypotheses outlining the potential role of uteroplacental myo-inositol in human parturition and explains possible underlying molecular mechanisms by which myo-inositol might modulate the uteroplacental environment and inhibit preterm labour onset. We suggest that a physiological decline in uteroplacental inositol levels to a critical threshold with advancing gestation, in concert with an increasingly pro-inflammatory uteroplacental environment, permits spontaneous membrane rupture and labour onset. A higher uteroplacental inositol level, potentially promoted by maternal myo-inositol supplementation, might affect lipid metabolism, eicosanoid production and secretion of pro-inflammatory chemocytokines that overall dampen the pro-labour uteroplacental environment responsible for labour onset and progress, thus reducing the risk of PTB. Understanding how and when inositol may act to reduce PTB risk would facilitate the design of future clinical trials of maternal myo-inositol supplementation and definitively address the efficacy of myo-inositol prophylaxis against PTB.

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