Corneal confocal microscopy differentiates inflammatory from diabetic neuropathy
Language English Country England, Great Britain Media electronic
Document type Journal Article, Multicenter Study
PubMed
33832507
PubMed Central
PMC8033689
DOI
10.1186/s12974-021-02130-1
PII: 10.1186/s12974-021-02130-1
Knihovny.cz E-resources
- Keywords
- Chronic inflammatory demyelinating neuropathy, Diabetes mellitus, corneal confocal microscopy,
- MeSH
- Polyradiculoneuropathy, Chronic Inflammatory Demyelinating diagnosis epidemiology MeSH
- Dendrites pathology MeSH
- Diabetes Mellitus, Type 2 diagnosis epidemiology MeSH
- Diabetic Neuropathies diagnosis epidemiology MeSH
- Diagnosis, Differential MeSH
- Adult MeSH
- Microscopy, Confocal methods standards MeSH
- Middle Aged MeSH
- Humans MeSH
- Nerve Fibers pathology MeSH
- Cornea pathology MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
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.
Brain and Mind Centre University of Sydney Sydney Australia
Department of Cardiology University Hospital Essen University Duisburg Essen Essen Germany
Department of Neurology Medical Faculty Heinrich Heine University Düsseldorf Germany
Department of Neurology Palacky University Olomouc Czech Republic
See more in PubMed
Querol L, Crabtree M, Herepath M, Priedane E, Viejo Viejo I, Agush S, Sommerer P. 2020. Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP). J Neurol PubMed
McLeod JG, Pollard JD, Macaskill P, Mohamed A, Spring P, Khurana V. Prevalence of chronic inflammatory demyelinating polyneuropathy in New South Wales, Australia. Ann Neurol. 1999;46(6):910–3. 10.1002/1531-8249(199912)46:6<910::AID-ANA14>3.0.CO;2-2. PubMed
Chaudhary UJ, Rajabally YA. 2020. Underdiagnosis and diagnostic delay in chronic inflammatory demyelinating polyneuropathy. J Neurol, DOI: 10.1007/s00415-020-10287-7 PubMed PMC
Liberatore G, Manganelli F, Doneddu PE, Cocito D, Fazio R, Briani C, Filosto M, Benedetti L, Mazzeo A, Antonini G, Cosentino G, Jann S, Cortese A, Marfia GA, Clerici AM, Siciliano G, Carpo M, Luigetti M, Lauria G, Rosso T, Cavaletti G, Santoro L, Peci E, Tronci S, Ruiz M, Cotti Piccinelli S, Schenone A, Leonardi L, Toscano A, Mataluni G, Spina E, Gentile L, Nobile-Orazio E. 2020. Chronic inflammatory demyelinating polyradiculoneuropathy: can a diagnosis be made in patients not fulfilling electrodiagnostic criteria? Eur J Neurol PubMed
Stino AM, Naddaf E, Dyck PJ, Dyck PJB. 2020. Chronic inflammatory demyelinating polyradiculoneuropathy-Diagnostic pitfalls and treatment approach. Muscle Nerve PubMed
Rajabally YA, Stettner M, Kieseier BC, Hartung HP, Malik RA. CIDP and other inflammatory neuropathies in diabetes - diagnosis and management. Nat Rev Neurol. 2017;13(10):599–611. doi: 10.1038/nrneurol.2017.123. PubMed DOI
Doneddu PE, Cocito D, Manganelli F, Fazio R, Briani C, Filosto M, Benedetti L, Bianchi E, Jann S, Mazzeo A, Antonini G, Cosentino G, Marfia GA, Cortese A, Clerici AM, Carpo M, Schenone A, Siciliano G, Luigetti M, Lauria G, Rosso T, Cavaletti G, Beghi E, Liberatore G, Santoro L, Spina E, Peci E, Tronci S, Ruiz M, Cotti Piccinelli S, Verrengia EP, Gentile L, Leonardi L, Mataluni G, Piccolo L, Nobile-Orazio E. Frequency of diabetes and other comorbidities in chronic inflammatory demyelinating polyradiculoneuropathy and their impact on clinical presentation and response to therapy. J Neurol Neurosurg Psychiatry. 2020;91(10):1092–1099. doi: 10.1136/jnnp-2020-323615. PubMed DOI
Efron N, Edwards K, Roper N, Pritchard N, Sampson GP, Shahidi AM, Vagenas D, Russell A, Graham J, Dabbah MA, Malik RA. Repeatability of measuring corneal subbasal nerve fiber length in individuals with type 2 diabetes. Eye Contact Lens. 2010;36(5):245–248. doi: 10.1097/ICL.0b013e3181eea915. PubMed DOI
Hertz P, Bril V, Orszag A, Ahmed A, Ng E, Nwe P, Ngo M, Perkins BA. Reproducibility of in vivo corneal confocal microscopy as a novel screening test for early diabetic sensorimotor polyneuropathy. Diab Med. 2011;28(10):1253–1260. doi: 10.1111/j.1464-5491.2011.03299.x. PubMed DOI
Smith AG, Kim G, Porzio M, Allen B, Koach M, Mifflin M, Digre K, Keung BM, Singleton JR. Corneal confocal microscopy is efficient, well-tolerated, and reproducible. J Peripheral Nervous Syst. 2013;18(1):54–58. doi: 10.1111/jns5.12008. PubMed DOI
Malik RA, Kallinikos P, Abbott CA, van Schie CH, Morgan P, Efron N, Boulton AJ. Corneal confocal microscopy: a non-invasive surrogate of nerve fibre damage and repair in diabetic patients. Diabetologia. 2003;46(5):683–688. doi: 10.1007/s00125-003-1086-8. PubMed DOI
Perkins BA, Lovblom LE, Bril V, Scarr D, Ostrovski I, Orszag A, Edwards K, Pritchard N, Russell A, Dehghani C, Pacaud D, Romanchuk K, Mah JK, Jeziorska M, Marshall A, Shtein RM, Pop-Busui R, Lentz SI, Boulton AJM, Tavakoli M, Efron N, Malik RA. Corneal confocal microscopy for identification of diabetic sensorimotor polyneuropathy: a pooled multinational consortium study. Diabetologia. 2018;61(8):1856–1861. doi: 10.1007/s00125-018-4653-8. PubMed DOI PMC
Ferdousi M, Kalteniece A, Azmi S, Petropoulos IN, Ponirakis G, Alam U, Asghar O, Marshall A, Fullwood C, Jeziorska M, Abbott C, Lauria G, Faber CG, Soran H, Efron N, Boulton AJM, Malik RA. 2020. Diagnosis of neuropathy and risk factors for corneal nerve loss in type 1 and type 2 diabetes: a corneal confocal microscopy study. Diabetes Care PubMed PMC
Chen X, Graham J, Dabbah MA, Petropoulos IN, Ponirakis G, Asghar O, Alam U, Marshall A, Fadavi H, Ferdousi M, Azmi S, Tavakoli M, Efron N, Jeziorska M, Malik RA. Small nerve fiber quantification in the diagnosis of diabetic sensorimotor polyneuropathy: comparing corneal confocal microscopy with intraepidermal nerve fiber density. Diab Care. 2015;38(6):1138–1144. doi: 10.2337/dc14-2422. PubMed DOI PMC
Pritchard N, Edwards K, Russell AW, Perkins BA, Malik RA, Efron N. Corneal confocal microscopy predicts 4-year incident peripheral neuropathy in type 1 diabetes. Diab Care. 2015;38(4):671–675. doi: 10.2337/dc14-2114. PubMed DOI
Tavakoli M, Marshall A, Pitceathly R, Fadavi H, Gow D, Roberts ME, Efron N, Boulton AJ, Malik RA. Corneal confocal microscopy: a novel means to detect nerve fibre damage in idiopathic small fibre neuropathy. Exp Neurol. 2010;223(1):245–250. doi: 10.1016/j.expneurol.2009.08.033. PubMed DOI PMC
Tavakoli M, Marshall A, Banka S, Petropoulos IN, Fadavi H, Kingston H, Malik RA. Corneal confocal microscopy detects small-fiber neuropathy in Charcot-Marie-Tooth disease type 1A patients. Muscle Nerve. 2012;46(5):698–704. doi: 10.1002/mus.23377. PubMed DOI PMC
Kemp HI, Petropoulos IN, Rice ASC, Vollert J, Maier C, Sturm D, Schargus M, Peto T, Hau S, Chopra R, Malik RA. Use of Corneal Confocal Microscopy to Evaluate Small Nerve Fibers in Patients With Human Immunodeficiency Virus. JAMA Ophthalmol. 2017;135(7):795–800. doi: 10.1001/jamaophthalmol.2017.1703. PubMed DOI PMC
Ferdousi M, Azmi S, Petropoulos IN, Fadavi H, Ponirakis G, Marshall A, Tavakoli M, Malik I, Mansoor W, Malik RA. Corneal Confocal Microscopy Detects Small Fibre Neuropathy in Patients with Upper Gastrointestinal Cancer and Nerve Regeneration in Chemotherapy Induced Peripheral Neuropathy. PLoS One. 2015;10(10):e0139394. doi: 10.1371/journal.pone.0139394. PubMed DOI PMC
Rousseau A, Cauquil C, Dupas B, Labbé A, Baudouin C, Barreau E, Théaudin M, Lacroix C, Guiochon-Mantel A, Benmalek A, Labetoulle M, Adams D. Potential role of in vivo confocal microscopy for imaging corneal nerves in transthyretin familial amyloid polyneuropathy. JAMA Ophthalmol. 2016;134:983–989. doi: 10.1001/jamaophthalmol.2016.1889. PubMed DOI
Pagovich OE, Vo ML, Zhao Z, Petropoulos IN, Yuan M, Lertsuwanroj B, Ciralsky J, Lai E, Kiss S, D'Amico DJ, Mezey JG, Malik RA, Crystal RG. 2018. Corneal Confocal Microscopy: Neurologic Disease Biomarker in Friedreich's Ataxia. Ann Neurol PubMed
Leppin K, Behrendt AK, Reichard M, Stachs O, Guthoff RF, Baltrusch S, Eule JC, Vollmar B. Diabetes mellitus leads to accumulation of dendritic cells and nerve fiber damage of the subbasal nerve plexus in the cornea. Invest Ophthalmol Vis Sci. 2014;55(6):3603–3615. doi: 10.1167/iovs.14-14307. PubMed DOI
Stettner M, Hinrichs L, Guthoff R, Bairov S, Petropoulos IN, Warnke C, Hartung HP, Malik RA, Kieseier BC. Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy. Ann Clin Transl Neurol. 2016;3(2):88–100. doi: 10.1002/acn3.275. PubMed DOI PMC
Pitarokoili K, Sturm D, Labedi A, Greiner T, Eitner L, Kumowski N, Enax-Krumova EK, Fisse AL, Maier C, Gold R, Tegenthoff M, Schmidt-Wilcke T, Yoon MS. Neuroimaging markers of clinical progression in chronic inflammatory demyelinating polyradiculoneuropathy. Ther Adv Neurol Disord. 2019;12:1756286419855485. doi: 10.1177/1756286419855485. PubMed DOI PMC
Athanasopoulos D, Motte J, Fisse AL, Grueter T, Trampe N, Sturm D, Tegenthoff M, Sgodzai M, Klimas R, Querol L, Gold R, Pitarokoili K. Longitudinal study on nerve ultrasound and corneal confocal microscopy in NF155 paranodopathy. Ann Clin Transl Neurol. 2020;7(6):1061–1068. doi: 10.1002/acn3.51061. PubMed DOI PMC
Hughes RA, Bouche P, Cornblath DR, Evers E, Hadden RD, Hahn A, Illa I, Koski CL, Leger JM, Nobile-Orazio E, Pollard J, Sommer C, Van den Bergh P, van Doorn PA, van Schaik IN. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society. Eur J Neurol. 2006;13(4):326–332. doi: 10.1111/j.1468-1331.2006.01278.x. PubMed DOI
Tesfaye S, Boulton AJ, Dyck PJ, Freeman R, Horowitz M, Kempler P, Lauria G, Malik RA, Spallone V, Vinik A, Bernardi L, Valensi P. Diabetic neuropathies: update on definitions, diagnostic criteria, estimation of severity, and treatments. Diab Care. 2010;33(10):2285–2293. doi: 10.2337/dc10-1303. PubMed DOI PMC
Rajabally YA, Peric S, Cobeljic M, Afzal S, Bozovic I, Palibrk A, Basta I. Chronic inflammatory demyelinating polyneuropathy associated with diabetes: a European multicentre comparative reappraisal. J Neurol Neurosurg Psychiatry. 2020;91(10):1100–1104. doi: 10.1136/jnnp-2020-322971. PubMed DOI
Lotan I, Hellman MA, Steiner I. Diagnostic criteria of chronic inflammatory demyelinating polyneuropathy in diabetes mellitus. Acta Neurol Scand. 2015;132(4):278–283. doi: 10.1111/ane.12394. PubMed DOI
Dunnigan SK, Ebadi H, Breiner A, Katzberg HD, Lovblom LE, Perkins BA, Bril V. Conduction slowing in diabetic sensorimotor polyneuropathy. Diab Care. 2013;36(11):3684–3690. doi: 10.2337/dc13-0746. PubMed DOI PMC
Herrmann DN, Ferguson ML, Logigian EL. Conduction slowing in diabetic distal polyneuropathy. Muscle Nerve. 2002;26(2):232–237. doi: 10.1002/mus.10204. PubMed DOI
Dunnigan SK, Ebadi H, Breiner A, Katzberg HD, Lovblom LE, Perkins BA, Bril V. Comparison of diabetes patients with "demyelinating" diabetic sensorimotor polyneuropathy to those diagnosed with CIDP. Brain Behav. 2013;3(6):656–663. doi: 10.1002/brb3.177. PubMed DOI PMC
Mitsuma S, Van den Bergh P, Rajabally YA, Van Parijs V, Martin-Lamb D, Sonoo M, Inaba A, Shimizu T, Isose S, Sato Y, Komori T, Misawa S, Kuwabara S. Effects of low frequency filtering on distal compound muscle action potential duration for diagnosis of CIDP: A Japanese-European multicenter prospective study. Clin Neurophysiol. 2015;126(9):1805–1810. doi: 10.1016/j.clinph.2014.11.027. PubMed DOI
Rajabally YA, Martin-Lamb D, Nicolas G. Compound muscle action potential amplitude and distal potential duration in axonal neuropathy. Muscle Nerve. 2014;49(1):146–147. doi: 10.1002/mus.24065. PubMed DOI
Jann S, Bramerio MA, Beretta S, Koch S, Defanti CA, Toyka KV, Sommer C. Diagnostic value of sural nerve matrix metalloproteinase-9 in diabetic patients with CIDP. Neurology. 2003;61(11):1607–1610. doi: 10.1212/01.WNL.0000096174.86850.7F. PubMed DOI
Sommer C, Koch S, Lammens M, Gabreels-Festen A, Stoll G, Toyka KV. Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP. Neurology. 2005;65(12):1924–1929. doi: 10.1212/01.wnl.0000188879.19900.b7. PubMed DOI
Mayer WJ, Mackert MJ, Kranebitter N, Messmer EM, Gruterich M, Kampik A, Kook D. Distribution of antigen presenting cells in the human cornea: correlation of in vivo confocal microscopy and immunohistochemistry in different pathologic entities. Curr Eye Res. 2012;37(11):1012–1018. doi: 10.3109/02713683.2012.696172. PubMed DOI
Chen W, Hara K, Tian Q, Zhao K, Yoshitomi T. Existence of small slow-cycling Langerhans cells in the limbal basal epithelium that express ABCG2. Exp Eye Res. 2007;84(4):626–634. doi: 10.1016/j.exer.2006.11.006. PubMed DOI
Mayer WJ, Irschick UM, Moser P, Wurm M, Huemer HP, Romani N, Irschick EU. Characterization of antigen-presenting cells in fresh and cultured human corneas using novel dendritic cell markers. Invest Ophthalmol Vis Sci. 2007;48(10):4459–4467. doi: 10.1167/iovs.06-1184. PubMed DOI
Alkhawajah NM, Dunnigan SK, Bril V. Comparison of monoclonal gammopathy of undetermined significance-associated neuropathy and chronic inflammatory demyelinating polyneuropathy patients. J Neurol. 2014;261(8):1485–1491. doi: 10.1007/s00415-014-7357-0. PubMed DOI PMC
Nabi S, Kahlon P, Bozorgnia F, Arshad A, Saleem A, Kuriakose P. Analyzing Relationship Between Monoclonal Gammopathy of Undetermined Significance (MGUS) with Different Types of Neuropathy: An Observational Study. Indian J Hematol Blood Transfus. 2016;32(2):186–192. doi: 10.1007/s12288-015-0547-9. PubMed DOI PMC
Magy L, Chassande B, Maisonobe T, Bouche P, Vallat JM, Leger JM. Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 cases. Eur J Neurol. 2003;10(6):677–685. doi: 10.1046/j.1468-1331.2003.00687.x. PubMed DOI