| Literature DB >> 29429076 |
Abstract
The high prevalence of osteoporosis, observed in multiple sclerosis (MS) patients, has been attributed to reduced mobility and or the use of disease-modifying drugs. However, MS-impaired cardiovascular autonomic nervous system (ANS) function has the potential of reducing bone mass density (BMD) by altering the expression and/or function of the neuronal, systemic, and local mediators of bone remodeling. This review describes the complex regulation of bone homeostasis with a focus on MS, providing evidence that ANS dysfunction and low BMD are intertwined with MS inflammatory and neurodegenerative processes, and with other MS-related morbidities, including depression, fatigue, and migraine. Strategies for improving ANS function could reduce the prevalence of MS osteoporosis and slow the rate of MS progression, with a significant positive impact on patients' quality of life.Entities:
Keywords: Autonomic; Bone mass density; Bone remodeling; Clinical morbidities; Inflammatory mediators; Leptin; Migraine; Multiple sclerosis; Neurodegeneration; Osteoporosis; Vitamin D
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Year: 2018 PMID: 29429076 DOI: 10.1007/s12017-018-8481-2
Source DB: PubMed Journal: Neuromolecular Med ISSN: 1535-1084 Impact factor: 3.843