Neuromodulation as a Potential Disease-Modifying Therapy for Osteoarthritis

被引:8
作者
Cruz, Carlos J. [1 ,2 ]
Dewberry, L. Savannah [1 ]
Otto, Kevin J. [1 ,3 ,4 ,5 ,6 ]
Allen, Kyle D. [1 ,2 ,7 ]
机构
[1] Univ Florida, J Crayton Pruitt Family Dept Biomed Engn, Biomed Sci Bldg,1275 Ctr Dr, Gainesville, FL 32611 USA
[2] Pain Res & Intervent Ctr Excellence, Gainesville, FL 32610 USA
[3] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 USA
[4] Univ Florida, Dept Neurol, Gainesville, FL USA
[5] Univ Florida, Dept Elect & Comp Engn, Gainesville, FL USA
[6] Univ Florida, Dept Neurosci, Gainesville, FL USA
[7] Univ Florida, Dept Orthopaed & Rehabil, Gainesville, FL 32611 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Osteoarthritis; Vagus nerve stimulation; Neuroimmune axis; AUTONOMIC NERVOUS-SYSTEM; SPINAL-CORD STIMULATION; DORSAL-ROOT GANGLION; HEART-RATE-VARIABILITY; KNEE OSTEOARTHRITIS; ELECTRICAL-STIMULATION; CONDUCTION BLOCK; NEUROPATHIC PAIN; BLOOD-PRESSURE; WEIGHT-LOSS;
D O I
10.1007/s11926-022-01094-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of Review The following review discusses the therapeutic potential of targeting the autonomic nervous system (ANS) for osteoarthritis (OA) treatment and encourages the field to consider the candidacy of bioelectronic medicine as a novel OA treatment strategy. Recent Findings The study of OA pathogenesis has focused on changes occurring at the joint level. As such, treatments for OA have been aimed at the local joint environment, intending to resolve local inflammation and decrease pain. However, OA pathogenesis has shown to be more than joint wear and tear. Specifically, OA-related peripheral and central sensitization can prompt neuroplastic changes in the nervous system beyond the articular joint. These neuroplastic changes may alter physiologic systems, like the neuroimmune axis. In this way, OA and related comorbidities may share roots in the form of altered neuroimmune communication and autonomic dysfunction. Summary ANS modulation may be able to modify OA pathogenesis or reduce the impact of OA comorbidities. Moreover, blocking chronic nociceptive drive from the joint may help to prevent maladaptive nervous system plasticity in OA.
引用
收藏
页码:1 / 11
页数:11
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