Corneal confocal microscopy differentiates inflammatory from diabetic neuropathy

GND
1034210726
ORCID
0000-0002-5720-8393
Zugehörige Organisation
Department of Neurology and Center for Translational and Behavioral Neurosciences (C-TNBS), University Hospital Essen, University Duisburg-Essen, Essen, Germany
Fleischer, Michael;
Zugehörige Organisation
Department of Neurology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany
Lee, Inn;
Zugehörige Organisation
Department of Neurology and Center for Translational and Behavioral Neurosciences (C-TNBS), University Hospital Essen, University Duisburg-Essen, Essen, Germany
Erdlenbruch, Friedrich;
GND
1168481546
LSF
59277
Zugehörige Organisation
Department of Cardiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany
Hinrichs, Lena;
Zugehörige Organisation
Weill Cornell Medicine-Qatar, Educator City, Doha, Qatar
Petropoulos, Ioannis N.;
ORCID
0000-0002-7188-8903
Zugehörige Organisation
Weill Cornell Medicine-Qatar, Educator City, Doha, Qatar
Malik, Rayaz A.;
ORCID
0000-0002-0614-6989
Zugehörige Organisation
Department of Neurology, Palacky University, Olomouc, Czech Republic
Hartung, Hans-Peter;
GND
114711496
Zugehörige Organisation
Department of Neurology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany
Kieseier, Bernd C.;
GND
123343909
ORCID
0000-0002-1650-8875
LSF
58465
Zugehörige Organisation
Department of Neurology and Center for Translational and Behavioral Neurosciences (C-TNBS), University Hospital Essen, University Duisburg-Essen, Essen, Germany
Kleinschnitz, Christoph;
GND
1023934205
Zugehörige Organisation
Department of Neurology and Center for Translational and Behavioral Neurosciences (C-TNBS), University Hospital Essen, University Duisburg-Essen, Essen, Germany
Stettner, Mark

Background: Immune-mediated neuropathies, such as chronic inflammatory demyelinating polyneuropathy (CIDP) are treatable neuropathies. Among individuals with diabetic neuropathy, it remains a challenge to identify those individuals who develop CIDP. Corneal confocal microscopy (CCM) has been shown to detect corneal nerve fiber loss and cellular infiltrates in the sub-basal layer of the cornea. The objective of the study was to determine whether CCM can distinguish diabetic neuropathy from CIDP and whether CCM can detect CIDP in persons with coexisting diabetes.

Methods: In this multicenter, case-control study, participants with CIDP ( n = 55) with ( n = 10) and without ( n = 45) diabetes; participants with diabetes ( n = 58) with ( n = 28) and without ( n = 30) diabetic neuropathy, and healthy controls ( n = 58) underwent CCM. Corneal nerve fiber density (CNFD), corneal nerve fiber length (CNFL), corneal nerve branch density (CNBD), and dendritic and non-dendritic cell density, with or without nerve fiber contact were quantified.

Results: Dendritic cell density in proximity to corneal nerve fibers was significantly higher in participants with CIDP with and without diabetes compared to participants with diabetic neuropathy and controls. CNFD, CNFL, and CNBD were equally reduced in participants with CIDP, diabetic neuropathy, and CIDP with diabetes.

Conclusions: An increase in dendritic cell density identifies persons with CIDP. CCM may, therefore, be useful to differentiate inflammatory from non-inflammatory diabetic neuropathy.

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