Tracing the influence of prenatal risk factors on the offspring retina: Focus on development and putative long-term consequences

IF 4.4 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL European Journal of Clinical Investigation Pub Date : 2024-06-12 DOI:10.1111/eci.14266
Filipa I. Baptista, António F. Ambrósio
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Abstract

Background

Pregnancy represents a window of vulnerability to fetal development. Disruptions in the prenatal environment during this crucial period can increase the risk of the offspring developing diseases over the course of their lifetime. The central nervous system (CNS) has been shown to be particularly susceptible to changes during crucial developmental windows. To date, research focused on disruptions in the development of the CNS has predominantly centred on the brain, revealing a correlation between exposure to prenatal risk factors and the onset of neuropsychiatric disorders. Nevertheless, some studies indicate that the retina, which is part of the CNS, is also vulnerable to in utero alterations during pregnancy. Such changes may affect neuronal, glial and vascular components of the retina, compromising retinal structure and function and possibly impairing visual function.

Methods

A search in the PubMed database was performed, and any literature concerning prenatal risk factors (drugs, diabetes, unbalanced diet, infection, glucocorticoids) affecting the offspring retina were included.

Results

This review collects evidence on the cellular, structural and functional changes occurring in the retina triggered by maternal risk factors during pregnancy. We highlight the adverse impact on retinal development and its long-lasting effects, providing a critical analysis of the current knowledge while underlining areas for future research.

Conclusions

Appropriate recognition of the prenatal risk factors that negatively impact the developing retina may provide critical clues for the design of preventive strategies and for early therapeutic intervention that could change retinal pathology in the progeny.

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追踪产前风险因素对后代视网膜的影响:关注发育和可能的长期后果。
背景:孕期是胎儿发育的脆弱期。在这一关键时期,产前环境的破坏会增加后代一生中罹患疾病的风险。事实证明,中枢神经系统(CNS)尤其容易受到关键发育窗口期变化的影响。迄今为止,有关中枢神经系统发育紊乱的研究主要集中在大脑方面,揭示了暴露于产前危险因素与神经精神疾病发病之间的相关性。然而,一些研究表明,视网膜作为中枢神经系统的一部分,在怀孕期间也很容易受到子宫内变化的影响。这些变化可能会影响视网膜的神经元、胶质细胞和血管成分,损害视网膜的结构和功能,并可能损害视觉功能:方法:在PubMed数据库中进行搜索,纳入所有与影响后代视网膜的产前风险因素(药物、糖尿病、不均衡饮食、感染、糖皮质激素)有关的文献:本综述收集了有关孕期母体风险因素引发视网膜细胞、结构和功能变化的证据。我们强调了对视网膜发育的不利影响及其持久性影响,对现有知识进行了批判性分析,同时强调了未来研究的领域:结论:适当识别对视网膜发育产生负面影响的产前风险因素,可为设计预防策略和早期治疗干预提供重要线索,从而改变后代的视网膜病理学。
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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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Issue Information [225Ac]Ac-PSMA for the treatment of metastatic castration-resistant prostate cancer: A systematic review and meta-analysis. Machine learning for stroke in heart failure with reduced ejection fraction but without atrial fibrillation: A post-hoc analysis of the WARCEF trial. Structural aspects of CEACAM1 interactions. Clinical measures in chronic neuropathic pain are related to the Kennedy and endocannabinoid pathways.
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