An understanding of bone pain: A narrative review

• Published in: Bone (New York, N.Y.) Vol. 134; p. 115272
• Main Authors: Oostinga, Douwe, Steverink, Jasper G., van Wijck, Albert J.M., Verlaan, Jorrit-Jan
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.05.2020
• Subjects: A-delta fiber; Bone Diseases; Bone pain; C-fiber; Central sensitization; Chronic Pain; Humans; Pain Management; Periosteum; Peripheral sensitization; Quality of Life; Sensory nerve sprouting; Sensory Receptor Cells; PGE2; PR; A-delta fiber; P2X-R; BDNF; Peripheral sensitization; Central sensitization; NGF; BR; NF200; TrkA; TNF-α; NSAIDs; NMDA-R; Bone pain; Sensory nerve sprouting; TrpV1; C-fiber; ASIC3; ATP; CGRP; SP; ASIC1
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/j.bone.2020.115272

Skeletal pathologies are often accompanied by bone pain, which has negative effects on the quality of life and functional status of patients. Bone pain can be caused by a wide variety of injuries and diseases including (poorly healed) fractures, bone cancer, osteoarthritis and also iatrogenic by skeletal interventions. Orthopedic interventions are considered to be the most painful surgical procedures overall. Two major groups of medication currently used to attenuate bone pain are NSAIDs and opioids. However, these systemic drugs frequently introduce adverse events, emphasizing the need for alternative therapies that are directed at the pathophysiological mechanisms underlying bone pain. The periosteum, cortical bone and bone marrow are mainly innervated by sensory A-delta fibers and C-fibers. These fibers are mostly present in the periosteum rendering this structure most sensitive to nociceptive stimuli. A-delta fibers and C-fibers can be activated upon mechanical distortion, acidic environment and increased intramedullary pressure. After activation, these fibers can be sensitized by inflammatory mediators, phosphorylation of acid-sensing ion channels and cytokine receptors, or by upregulation of transcription factors. This can result in a change of pain perception such that normally non-noxious stimuli are now perceived as noxious. Pathological conditions in the bone can produce neurotrophic factors that bind to receptors on A-delta fibers and C-fibers. These fibers then start to sprout and increase the innervation density of the bone, making it more sensitive to nociceptive stimuli. In addition, repetitive painful stimuli cause neurochemical and electrophysiological alterations in afferent sensory neurons in the spinal cord, which leads to central sensitization, and can contribute to chronic bone pain. Understanding the pathophysiological mechanisms underlying bone pain in different skeletal injuries and diseases is important for the development of alternative, targeted pain treatments. These pain mechanism-based alternatives have the potential to improve the quality of life of patients suffering from bone pain without introducing undesirable systemic effects. •A-delta fibers and C-fibers innervate bone with highest density in the periosteum.•Mechanical, acidic and pressure stimuli activate A-delta fibers and C-fibers.•Neurotrophic factors cause peripheral sensitization and nerve sprouting.•Central sensitization amplifies the perception and intensity of bone pain.•A better understanding of bone pain might help to develop mechanism-based therapies.