4.4 Article

Small-Fiber Neuropathy Is Associated With Corneal Nerve and Dendritic Cell Alterations: An In Vivo Confocal Microscopy Study

期刊

CORNEA
卷 34, 期 9, 页码 1114-1119

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/ICO.0000000000000535

关键词

corneal nerve alterations; clinical imaging; axonal degeneration; polyneuropathy; confocal microscopy

资金

  1. German Research Foundation [HE 6743/2-1, SFB 643: B10, CU 47/6-1, CU 47/4-1]
  2. GEROK-Programme University Hospital of Cologne
  3. EU FP7 STRONG
  4. Dr Gabriele Lederle-Foundation, Taufkirchen

向作者/读者索取更多资源

Purpose:In patients with small-fiber neuropathy (SFN), noninvasive diagnostic tests that allow accurate monitoring of disease progression are urgently needed. The aim of this study was to assess corneal trigeminal small sensory nerves and immune cells by in vivo corneal confocal microscopy (CCM) in SFN.Methods:In this prospective single-center study, 14 patients with histologically confirmed SFN were analyzed. CCM parameters [corneal nerve fiber density (NFD); the total number of nerves, main trunks, and branches; nerve tortuosity; and dendritic cell density] were compared with 14 age-matched healthy controls and correlated with clinical symptoms, disease course, and histopathological findings.Results:Corneal NFD (15,489.3 5927.6 m/mm(2) vs. 22,687.1 +/- 4328.7 m/mm(2); P = 0.001) and the total number of nerves (10.4 +/- 4.6/frame vs. 18.5 +/- 4.8/frame; P < 0.0001) were significantly reduced in patients with SFN. In contrast, nerve tortuosity was significantly increased (2.2 +/- 0.3 vs. 1.7 +/- 0.5; P = 0.02). Corneal NFD did not correlate with intraepidermal NFD ( = -0.158; P = 0.5) or clinical symptoms (cold P = 0.1; prickling P = 0.2; burning P = 0.8; formication P = 0.7; stabbing P = 0.4; rubbing 0.1; pressure P = 0.1). The average dendritic cell density was increased in SFN (33.5 +/- 57.5 cells/mm(2) vs. 16.1 +/- 13.7 cells/mm(2)) but did not reach significance (P = 0.7).Conclusions:CCM provides parameters that reliably indicate injury to sensory afferents of the trigeminal nerve in patients with SFN. Our data suggest that CCM may serve both as a noninvasive diagnostic test and as a surrogate marker in SFN.

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