阿尔茨海默病和骨质疏松症之间的潜在联系。

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY Biogerontology Pub Date : 2025-01-20 DOI:10.1007/s10522-024-10181-z
Fariha Nasme, Jyotirmaya Behera, Prisha Tyagi, Nabendu Debnath, Jeff C Falcone, Neetu Tyagi
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引用次数: 0

摘要

阿尔茨海默病(AD)和骨质疏松症(OP)构成了不同但相互关联的健康挑战,都对老龄化人口产生了重大影响。AD是一种以记忆障碍和认知能力下降为特征的神经退行性疾病,主要与大脑中异常折叠的β淀粉样蛋白(a β)肽和神经原纤维缠结的积累有关。OP是一种以低骨密度为特征的骨骼疾病,涉及骨重塑失调,并与骨折风险增加有关。最近的研究揭示了AD和OP之间有趣的联系,强调了共同的病理生理调控途径的共同病理特征。在这篇文章中,我们阐明了调节AD和OP病理的信号机制,并对导致这些疾病的复杂因素网络提供了见解。我们还研究了骨源性因素在阿尔茨海默病进展中的作用,强调了大脑和骨骼系统之间双向交流的可行性。AD患者大脑中淀粉样斑块的存在与血管性痴呆中脑Aβ的积累相似,这表明需要进一步研究共同的分子机制。此外,我们还讨论了骨源性microrna可能调节AD病理进展的作用,为骨骼因素在神经退行性疾病中的作用提供了新的视角。这里提出的见解应该有助于研究人员探索针对老年人群神经退行性和骨骼疾病的创新治疗方法。
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The potential link between the development of Alzheimer's disease and osteoporosis.

Alzheimer's disease (AD) and osteoporosis (OP) pose distinct but interconnected health challenges, both significantly impacting the aging population. AD, a neurodegenerative disorder characterized by memory impairment and cognitive decline, is primarily associated with the accumulation of abnormally folded amyloid beta (Aβ) peptides and neurofibrillary tangles in the brain. OP, a skeletal disorder marked by low bone mineral density, involves dysregulation of bone remodeling and is associated with an increased risk of fractures. Recent studies have revealed an intriguing link between AD and OP, highlighting shared pathological features indicative of common regulatory pathophysiological pathways. In this article, we elucidate the signaling mechanisms that regulate the pathology of AD and OP and offer insights into the intricate network of factors contributing to these conditions. We also examine the role of bone-derived factors in the progression of AD, underscoring the plausibility of bidirectional communication between the brain and the skeletal system. The presence of amyloid plaques in the brain of individuals with AD is akin to the accumulation of brain Aβ in vascular dementia, pointing towards the need for further investigation of shared molecular mechanisms. Moreover, we discuss the role of bone-derived microRNAs that may regulate the pathological progression of AD, providing a novel perspective on the role of skeletal factors in neurodegenerative diseases. The insights presented here should help researchers engaged in exploring innovative therapeutic approaches targeting both neurodegenerative and skeletal disorders in aging populations.

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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
期刊最新文献
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