Understanding fetal factors that contribute to preterm birth: Sjögren-Larsson syndrome as a model

Author:

Staps Pippa1ORCID,Hogeveen Marije2,Fuijkschot Joris2,van Drongelen Joris3,Willemsen Michèl A.A.P.1

Affiliation:

1. Department of Pediatric Neurology , Radboud University Medical Center, Donders Institute for Brain Cognition and Behaviour , Nijmegen , The Netherlands

2. Department of Pediatrics , Radboud University Medical Center, Amalia Children’s Hospital , Nijmegen , The Netherlands

3. Department of Obstetrics , Radboud University Medical Center , Nijmegen , The Netherlands

Abstract

Abstract Aim: Preterm birth is the world’s leading cause of neonatal death. Unfortunately, the pathophysiology of preterm birth remains poorly understood. Sjögren-Larsson syndrome is a rare, neurometabolic disorder caused by a fatty aldehyde dehydrogenase deficiency. A majority of patients with Sjögren-Larsson syndrome is born preterm. Methods: Data of all known Dutch patients with Sjögren-Larsson syndrome and all cases reported in literature were analyzed to learn from preterm birth in context of this rare disease. Results: Exact gestational age was known in 33 Dutch patients; 24 (73%) of them were born preterm, with a median gestational age of 36 weeks. The literature search confirmed our findings: 13 (59%) of 22 cases was born preterm. Conclusions: Preterm birth is a hallmark of Sjögren-Larsson syndrome, presumably caused by the abnormal lipid metabolism of the fetus. At least five additional rare genetic disorders (namely Ehlers-Danlos syndrome, ichthyosis prematurity syndrome, congenital analbuminemia, osteogenesis imperfecta type II and restrictive dermopathy) were found in literature that lead to preterm birth of the affected fetus. These disorders are in fact “experiments of nature” and as such they shed new lights on the mechanisms causing preterm birth.

Publisher

Walter de Gruyter GmbH

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects;International Journal of Molecular Sciences;2022-01-21

2. Sjögren-Larsson Syndrome;Neurocutaneous Disorders;2022

3. A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia;British Journal of Biomedical Science;2020-10-30

4. Sjögren‐Larsson syndrome: The mild end of the phenotypic spectrum;JIMD Reports;2020-03-25

5.

Sjogren-Larsson Syndrome: Mechanisms and Management

;The Application of Clinical Genetics;2020-01

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