4.6 Article

Reduced intraepidermal nerve fiber density in patients with chronic ischemic pain in peripheral arterial disease

期刊

PAIN
卷 155, 期 9, 页码 1784-1792

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/j.pain.2014.06.003

关键词

Chronic ischemic pain; Peripheral arterial disease; Intraepidermal nerve fiber density; Quantitative sensory testing; Pain questionnaires

资金

  1. Research Funds of the University Hospitals of Munich and Wurzburg

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Chronic ischemic pain in peripheral arterial disease (PAD) is a leading cause of pain in the lower extremities. A neuropathic component of chronic ischemic pain has been shown independent of coexisting diabetes. We aimed to identify a morphological correlate potentially associated with pain and sensory deficits in PAD. Forty patients with symptomatic PAD (Fontaine stages II-IV), 20 with intermittent claudication (CI), and 20 with critical limb ischemia (CLI) were enrolled; 12 volunteers served as healthy controls. All patients were examined using pain scales and questionnaires. All study participants underwent quantitative sensory testing (QST) at the distal calf and skin punch biopsy at the distal leg for determination of intraepidermal nerve fiber density (IENFD). Additionally, S100beta serum levels were measured as a potential marker for ischemic nerve damage. Neuropathic pain questionnaires revealed slightly higher scores and more pronounced pain-induced disability in CLI patients compared to CI patients. QST showed elevated thermal and mechanical detection pain thresholds as well as dynamic mechanical allodynia, particularly in patients with advanced disease. IENFD was reduced in PAD compared to controls (P < 0.05), more pronounced in the CLI subgroup (CLI: 1.3 +/- 0.5 fibers/mm, CI: 2.9 +/- 0.5 fibers/mm, controls: 5.3 +/- 0.6 fibers/mm). In particular, increased mechanical and heat pain thresholds negatively correlated with lower IENFD. Mean S100beta levels were in the normal range but were higher in advanced disease. Patients with chronic ischemic pain had a reduced IENFD associated with impaired sensory functions. These findings support the concept of a neuropathic component in ischemic pain. (C) 2014 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.

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