Role of Amniotic Fluid Toxicity in the Pathophysiology of Myelomeningocele: A Narrative Literature Review.

amniotic fluid myelomeningocele neuroepithelium spinal cord damage toxicity

Journal

Prenatal diagnosis
ISSN: 1097-0223
Titre abrégé: Prenat Diagn
Pays: England
ID NLM: 8106540

Informations de publication

Date de publication:
06 Oct 2024
Historique:
revised: 06 09 2024
received: 28 05 2024
accepted: 23 09 2024
medline: 7 10 2024
pubmed: 7 10 2024
entrez: 6 10 2024
Statut: aheadofprint

Résumé

Myelomeningocele is a birth defect whose clinical manifestations are due both to incomplete neural tube closure and the progressive destruction of exposed neuroepithelium during pregnancy. Two hypotheses have been formulated to explain the spinal cord damage in utero: mechanical trauma and chemical factors. The objective of this review was to summarize the current insights about the potential role of amniotic fluid in spinal cord damage in myelomeningocele. Numerous histological and clinical data on animals and humans strongly suggest a progressive degeneration of neural tissue including loss of neural cells, astrogliosis, inflammation, and loss of normal architecture. However, few data have been published about the direct toxicity of amniotic fluid in this neural degeneration, including the potentially toxic effect of meconium. Finally, the chemical and cellular modifications of amniotic fluid composition in myelomeningocele could reflect both the process (toxic effect of meconium) and the consequences of neuroepithelium destruction (release of neural cells). Fetal surgery not only stops the leakage of the cerebrospinal fluid but also reduces the toxic effect of amniotic fluid by restoring the intrauterine environment. Identification of amniotic fluid neurotoxic factors could lead to the development of therapeutic agents designed to protect spinal tissue and improve fetal myelomeningocele outcomes.

Identifiants

pubmed: 39370541
doi: 10.1002/pd.6681
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Author(s). Prenatal Diagnosis published by John Wiley & Sons Ltd.

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Auteurs

Yoann Athiel (Y)

Department of Fetal Medicine, Armand Trousseau Hospital, AP-HP, DMU ORIGYNE, National Reference Center for Rare Disease: Spin@, Sorbonne University, Paris, France.
Stem Cell Biotechnologies Unit, INSERM 976, CIC-BT, AP-HP, Saint-Louis Hospital, Université Paris Cité, Paris, France.

Jean-Marie Jouannic (JM)

Department of Fetal Medicine, Armand Trousseau Hospital, AP-HP, DMU ORIGYNE, National Reference Center for Rare Disease: Spin@, Sorbonne University, Paris, France.
Working Group Spina Bifida and Other Dysraphisms, European Reference Network ITHACA, Paris, France.

Matthieu Lépine (M)

Stem Cell Biotechnologies Unit, INSERM 976, CIC-BT, AP-HP, Saint-Louis Hospital, Université Paris Cité, Paris, France.

Corentin Maillet (C)

Department of Fetal Medicine, Armand Trousseau Hospital, AP-HP, DMU ORIGYNE, National Reference Center for Rare Disease: Spin@, Sorbonne University, Paris, France.
Stem Cell Biotechnologies Unit, INSERM 976, CIC-BT, AP-HP, Saint-Louis Hospital, Université Paris Cité, Paris, France.

Timothée de Saint Denis (T)

Department of Pediatric Orthopedic and Reconstructive Surgery, Armand Trousseau Hospital, AP-HP, Sorbonne University, Paris, France.

Jérôme Larghero (J)

Stem Cell Biotechnologies Unit, INSERM 976, CIC-BT, AP-HP, Saint-Louis Hospital, Université Paris Cité, Paris, France.

Lucie Guilbaud (L)

Department of Fetal Medicine, Armand Trousseau Hospital, AP-HP, DMU ORIGYNE, National Reference Center for Rare Disease: Spin@, Sorbonne University, Paris, France.
Stem Cell Biotechnologies Unit, INSERM 976, CIC-BT, AP-HP, Saint-Louis Hospital, Université Paris Cité, Paris, France.
Working Group Spina Bifida and Other Dysraphisms, European Reference Network ITHACA, Paris, France.

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