Cardiovascular Autonomic Dysfunction: Link Between Multiple Sclerosis Osteoporosis and Neurodegeneration

Neuromolecular Med. 2018 Mar;20(1):37-53. doi: 10.1007/s12017-018-8481-2. Epub 2018 Feb 10.

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.

Keywords: Autonomic; Bone mass density; Bone remodeling; Clinical morbidities; Inflammatory mediators; Leptin; Migraine; Multiple sclerosis; Neurodegeneration; Osteoporosis; Vitamin D.

Publication types

  • Review

MeSH terms

  • Adiponectin / metabolism
  • Autonomic Nervous System / physiopathology*
  • Bone Density / physiology
  • Bone Remodeling / physiology*
  • Brain / metabolism
  • Cardiovascular System / physiopathology*
  • Depression / etiology
  • Depression / physiopathology
  • Endocannabinoids / metabolism
  • Fatigue / etiology
  • Fatigue / physiopathology
  • Humans
  • Inflammation
  • Leptin / physiology
  • Migraine Disorders / etiology
  • Migraine Disorders / physiopathology
  • Multiple Sclerosis / complications*
  • Multiple Sclerosis / metabolism
  • Nerve Degeneration / etiology*
  • Nerve Degeneration / metabolism
  • Neuropeptide Y / metabolism
  • Osteocalcin / physiology
  • Osteopontin / physiology
  • Osteoporosis / etiology*
  • Osteoporosis / metabolism
  • Osteoprotegerin / physiology
  • Parathyroid Hormone / metabolism
  • RANK Ligand / physiology
  • Serotonin / metabolism
  • Vitamin D / metabolism

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • BGLAP protein, human
  • Endocannabinoids
  • LEP protein, human
  • Leptin
  • Neuropeptide Y
  • Osteoprotegerin
  • Parathyroid Hormone
  • RANK Ligand
  • SPP1 protein, human
  • TNFRSF11B protein, human
  • TNFSF11 protein, human
  • Osteocalcin
  • Osteopontin
  • Vitamin D
  • Serotonin