Sex-specific neuroprotection: Does BDNF shield girls from autism?

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Takshashila Wankhade , Nayan Thakre , Manasi Tadas , Raj Katariya , Milind Umekar , Nandkishor Kotagale , Brijesh Taksande
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Abstract

Autism Spectrum Disorder (ASD) exhibits a clear male bias, with males being approximately four times more likely to be affected than females. This difference has sparked curiosity about possible neurological elements that provide protection to females. One such neurological element that has shown promise is brain-derived neurotrophic factor (BDNF), essential for neuronal development, synaptic plasticity, and neuroprotection. ASD may be less common in females due to increased BDNF levels, which may be influenced by sex-specific epigenetic control and estrogen hormone. Research studies indicate that increased baseline BDNF in females promotes neurodevelopmental resilience and mitigates the environmental and genetic risk factors linked to ASD. Also, this protective impact may be enhanced by the regulatory function of estrogen in BDNF expression and the interaction of BDNF with X-linked genes. The processes by which BDNF contributes to sex differences are still not well understood despite strong evidence. Interpreting results is made more difficult by the variability of ASD symptoms and variations in study methodologies. In addition to that, it is yet unknown whether increased BDNF levels represent compensatory processes or actually provide protection. Longitudinal studies that monitor BDNF expression across developmental stages and look at sex-specific treatment approaches that target BDNF pathways should be the main focus of future research. Thus, a thorough understanding of how BDNF prevents sex differences in ASD may pave the way for innovative strategies destined to diminish the risk of ASD. In this milieu, this review explores the current research, highlighting the complex relationship between sex differences, BDNF, and the incidence of ASD.

Abstract Image

性别特异性神经保护:BDNF能保护女孩远离自闭症吗?
自闭症谱系障碍(ASD)表现出明显的男性偏见,男性受影响的可能性大约是女性的四倍。这一差异引发了人们对可能的神经学因素的好奇,这些因素为女性提供了保护。脑源性神经营养因子(brain-derived neurotrophic factor, BDNF)是其中一种显示出前景的神经学元素,它对神经元发育、突触可塑性和神经保护至关重要。由于BDNF水平升高,ASD在女性中可能不太常见,这可能受到性别特异性表观遗传控制和雌激素激素的影响。研究表明,女性基线BDNF增加可促进神经发育恢复力,并减轻与ASD相关的环境和遗传风险因素。此外,雌激素对BDNF表达的调节功能以及BDNF与x连锁基因的相互作用可能会增强这种保护作用。尽管有强有力的证据,但BDNF导致性别差异的过程仍未得到很好的理解。由于ASD症状的可变性和研究方法的变化,解释结果变得更加困难。除此之外,尚不清楚BDNF水平的增加是代表代偿过程还是实际上提供保护。在发育阶段监测BDNF表达的纵向研究,以及针对BDNF通路的性别特异性治疗方法,应该是未来研究的重点。因此,彻底了解BDNF如何防止ASD中的性别差异,可能为旨在降低ASD风险的创新策略铺平道路。在此背景下,本文回顾了目前的研究,强调性别差异、BDNF和ASD发病率之间的复杂关系。
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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
65
审稿时长
37 days
期刊介绍: Molecular and Cellular Neuroscience publishes original research of high significance covering all aspects of neurosciences indicated by the broadest interpretation of the journal''s title. In particular, the journal focuses on synaptic maintenance, de- and re-organization, neuron-glia communication, and de-/regenerative neurobiology. In addition, studies using animal models of disease with translational prospects and experimental approaches with backward validation of disease signatures from human patients are welcome.
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