Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010 Oct;6(10):599-606.
doi: 10.1038/nrrheum.2010.107. Epub 2010 Jul 27.

Assessment of mechanisms in localized and widespread musculoskeletal pain

Affiliations
Review

Assessment of mechanisms in localized and widespread musculoskeletal pain

Thomas Graven-Nielsen et al. Nat Rev Rheumatol. 2010 Oct.

Abstract

The aim of this Review is to give a short presentation of the manifestations, assessment methods, and mechanisms underlying localized and widespread musculoskeletal pain, deep somatic tissue hyperalgesia and chronification. Hyperalgesia can be explained by increased pain sensitivity of nociceptors located in deep tissue (peripheral sensitization) or by increased responses from dorsal horn neurons (central sensitization). The spreading of pain and sensitization is related to increased synaptic activity in central neurons and to changes in descending control from supraspinal centers. Manifestations related to the different aspects of sensitization can be assessed quantitatively using sensory tests, such as pressure algometry (quantitative palpation) and cuff-algometry. Repeated pressure stimulation can evaluate the degree of temporal summation, which is a proxy for the level of central sensitization, as is expanded referred muscle pain area. The transition of acute localized musculoskeletal pain into chronic widespread pain is related to the progression of peripheral and central sensitization. This sensitization for the chronification of pain should be assessed by adequate pain biomarkers. Furthermore, pain prevention should target early intervention strategies and new anti-hyperalgesic compounds should be developed.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Man Ther. 1996 Dec;1(5):258-265 - PubMed
    1. Basic Clin Pharmacol Toxicol. 2005 Jul;97(1):52-7 - PubMed
    1. Exp Brain Res. 2002 Jun;144(4):475-82 - PubMed
    1. Pain. 2001 Aug;93(2):107-114 - PubMed
    1. Eur J Pain. 2008 Nov;12(8):1078-89 - PubMed