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DOI: 10.1055/s-0040-1718236
Interfascicular Gliding Dysfunction Relation with Focal Neuropathy in Diabetic Patients with Carpal Tunnel Syndrome
Abstract
Carpal tunnel syndrome (CTS), a common neuropathy of the upper limb, is highly prevalent in diabetic patients. Recent findings indicate that changes in median nerve elasticity and its gliding characteristics may contribute to the development of CTS. Normally, each nerve should be able to adapt to the positional changes by passive movement relative to the surrounding tissues. This ability is provided by a gliding apparatus around the nerve trunk in the surrounding soft tissue. The fascicles of nerve trunks can also glide against each other (interfascicular gliding). Sonoelastography indicates that nerve elasticity is decreased in patients with CTS compared to healthy patients. Moreover, decreased nerve elasticity in diabetes mellitus type II is associated with increased neuropathy, especially in peripheral nerves. Biomechanical factors, oxidative stress, and microvascular defects are also observed in diabetic neuropathy and account for different complications. A reduction in the elasticity of peripheral nerves may be related to decreased interfascicular gliding because of the biomechanical changes that occur in neuropathy. Surgical treatments, including nerve release and reduction of carpal tunnel pressure, improve peripheral gliding but do not resolve disease symptoms completely. According to the evidence, interfascicular gliding dysfunction is the most important factor in the pathogenesis of CTS in diabetic patients. Available evidence suggests that biomechanical variations affect interfascicular gliding more than peripheral gliding in diabetic patients. Decreased nerve elasticity is strongly correlated with decreased interfascicular gliding. It is further hypothesized that the concurrent use of antioxidants and pharmacological treatment (neuroprotection) such as alpha lipoic acid with carpal tunnel release in diabetic patients may alleviate the interfascicular gliding dysfunction and improve median neve elasticity. Decreased nerve elasticity and interfascicular gliding dysfunction play significant roles in the pathogenesis of CTS in diabetic patients.
Publication History
Article published online:
04 October 2020
© 2020. Society of Indian Hand & Microsurgeons. This article is published by Thieme.
Thieme Medical and Scientific Publishers Private Ltd.
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References
- 1 Bahrmann A, Zieschang T, Neumann T, Hein G, Oster P. [Carpal tunnel syndrome in diabetes mellitus] (in German). Med Klin (Munich) 2010; 105 (03) 150-154
- 2 Perkins BA, Olaleye D, Bril V. Carpal tunnel syndrome in patients with diabetic polyneuropathy. Diabetes Care 2002; 25 (03) 565-569
- 3 Thomsen NO, Cederlund RI, Andersson GS, Rosén I, Björk J, Dahlin LB. Carpal tunnel release in patients with diabetes: a 5-year follow-up with matched controls. J Hand Surg Am 2014; 39 (04) 713-720
- 4 Gül Yurdakul F, Bodur H, Öztop Çakmak Ö. et al. On the severity of carpal tunnel syndrome: diabetes or metabolic syndrome. J Clin Neurol 2015; 11 (03) 234-240
- 5 Chaudhuri KR, Davidson AR, Morris IM. Limited joint mobility and carpal tunnel syndrome in insulin-dependent diabetes. Br J Rheumatol 1989; 28 (03) 191-194
- 6 Dyck PJ, Kratz KM, Karnes JL. et al. The prevalence by staged severity of various types of diabetic neuropathy, retinopathy, and nephropathy in a population-based cohort: the Rochester Diabetic Neuropathy Study. Neurology 1993; 43 (04) 817-824
- 7 Thomas PK. Classification, differential diagnosis, and staging of diabetic peripheral neuropathy. Diabetes 1997; 46 (Suppl. 02) S54-S57
- 8 Boulton AJM, Malik RA, Arezzo JC, Sosenko JM. Diabetic somatic neuropathies. Diabetes Care 2004; 27 (06) 1458-1486
- 9 Younger DS, Rosoklija G, Hays AP, Trojaborg W, Latov N. Diabetic peripheral neuropathy: a clinicopathologic and immunohistochemical analysis of sural nerve biopsies. Muscle Nerve 1996; 19 (06) 722-727
- 10 Dyck PJ, Albers JW, Andersen H. et al. Toronto Expert Panel on Diabetic Neuropathy. Diabetic polyneuropathies: update on research definition, diagnostic criteria and estimation of severity. Diabetes Metab Res Rev 2011; 27 (07) 620-628
- 11 Huizinga MM, Peltier A. Painful diabetic neuropathy: a management-centered review. Clin Diabetes 2007; 25 (01) 6-15
- 12 Vinik AI, Mehrabyan A. Diabetic neuropathies. Med Clin North Am 2004; 88 (04) 947-999, xi
- 13 Sandireddy R, Yerra VG, Areti A, Komirishetty P, Kumar A. Neuroinflammation and oxidative stress in diabetic neuropathy: futuristic strategies based on these targets. Int J Endocrinol 2014; 2014: 674987
- 14 Østergaard L, Finnerup NB, Terkelsen AJ. et al. The effects of capillary dysfunction on oxygen and glucose extraction in diabetic neuropathy. Diabetologia 2015; 58 (04) 666-677
- 15 Herder C, Bongaerts BW, Rathmann W. et al. Association of subclinical inflammation with polyneuropathy in the older population: KORA F4 study. Diabetes Care 2013; 36 (11) 3663-3670
- 16 Verrotti A, Prezioso G, Scattoni R, Chiarelli F. Autonomic neuropathy in diabetes mellitus. Front Endocrinol (Lausanne) 2014; 5: 205
- 17 Bilir B, Ekiz Bilir B, Yilmaz I. et al. Association of apelin, endoglin and endocan with diabetic peripheral neuropathy in type 2 diabetic patients. Eur Rev Med Pharmacol Sci 2016; 20 (05) 892-898
- 18 Condorelli RA, Vicari E, Calogero AE. La Vignera S. Male accessory gland inflammation prevalence in type 2 diabetic patients with symptoms possibly reflecting autonomic neuropathy. Asian J Androl 2014; 16 (05) 761-766
- 19 Vinik AI, Erbas T, Casellini CM. Diabetic cardiac autonomic neuropathy, inflammation and cardiovascular disease. J Diabetes Investig 2013; 4 (01) 4-18
- 20 Stolinski C. Structure and composition of the outer connective tissue sheaths of peripheral nerve. J Anat 1995; 186 (pt 1) 123-130
- 21 Topp KS, Boyd BS. Structure and biomechanics of peripheral nerves: nerve responses to physical stresses and implications for physical therapist practice. Phys Ther 2006; 86 (01) 92-109
- 22 Kohrs RT, Zhao C, Sun YL. et al. Tendon fascicle gliding in wild type, heterozygous, and lubricin knockout mice. J Orthop Res 2011; 29 (03) 384-389
- 23 Aboonq MS. Pathophysiology of carpal tunnel syndrome. Neurosciences (Riyadh) 2015; 20 (01) 4-9
- 24 Ozkul Y, Sabuncu T, Kocabey Y, Nazligul Y. Outcomes of carpal tunnel release in diabetic and non-diabetic patients. Acta Neurol Scand 2002; 106 (03) 168-172
- 25 Wehbé MA, Schlegel JM. Nerve gliding exercises for thoracic outlet syndrome. Hand Clin 2004; 20 (01) 51-55, vi
- 26 Hough AD, Moore AP, Jones MP. Reduced longitudinal excursion of the median nerve in carpal tunnel syndrome. Arch Phys Med Rehabil 2007; 88 (05) 569-576
- 27 Lundborg G, Dahlin LB. Anatomy, function, and pathophysiology of peripheral nerves and nerve compression. Hand Clin 1996; 12 (02) 185-193
- 28 Millesi H, Zöch G, Rath T. The gliding apparatus of peripheral nerve and its clinical significance. Ann Chir Main Memb Super 1990; 9 (02) 87-97
- 29 Miyamoto H, Halpern EJ, Kastlunger M. et al. Carpal tunnel syndrome: diagnosis by means of median nerve elasticity–improved diagnostic accuracy of US with sonoelastography. Radiology 2014; 270 (02) 481-486
- 30 Yoshii Y, Ishii T, Tanaka T, Tung WL, Sakai S. Detecting median nerve strain changes with cyclic compression apparatus: a comparison of carpal tunnel syndrome patients and healthy controls. Ultrasound Med Biol 2015; 41 (03) 669-674
- 31 Ogur T, Yakut ZI, Teber MA. et al. Ultrasound elastographic evaluation of the median nerve in pregnant women with carpal tunnel syndrome. Eur Rev Med Pharmacol Sci 2015; 19 (01) 23-30
- 32 Aslan H, Analan PD. Effects of chronic flexed wrist posture on the elasticity and crosssectional area of the median nerve at the carpal tunnel among chronic stroke patients. Med Ultrason 2018; 1 (01) 71-75
- 33 Yagci I, Kenis-Coskun O, Ozsoy T, Ozen G, Direskeneli H. Increased stiffness of median nerve in systemic sclerosis. BMC Musculoskelet Disord 2017; 18: 434
- 34 Kowalska B, Sudoł-Szopińska I. Normal and sonographic anatomy of selected peripheral nerves. Part I: sonohistology and general principles of examination, following the example of the median nerve. J Ultrason 2012; 12 (49) 120-130
- 35 Kowalska B, Sudoł-Szopińska I. Ultrasound assessment on selected peripheral nerve pathologies. Part I: entrapment neuropathies of the upper limb - excluding carpal tunnel syndrome. J Ultrason 2012; 12 (50) 307-318
- 36 Park G-Y, Kwon DR. Application of real-time sonoelastography in musculoskeletal diseases related to physical medicine and rehabilitation. Am J Phys Med Rehabil 2011; 90 (11) 875-886
- 37 Xiang X, Yan F, Yang Y. et al. Quantitative assessment of healthy skin elasticity: reliability and feasibility of shear wave elastography. Ultrasound Med Biol 2017; 43 (02) 445-452
- 38 Brownlee M. The pathobiology of diabetic complications: a unifying mechanism. Diabetes 2005; 54 (06) 1615-1625
- 39 Dahlin LB. Aspects on pathophysiology of nerve entrapments and nerve compression injuries. Neurosurg Clin N Am 1991; 2 (01) 21-29
- 40 Samii A, Unger J, Lange W. Vascular endothelial growth factor expression in peripheral nerves and dorsal root ganglia in diabetic neuropathy in rats. Neurosci Lett 1999; 262 (03) 159-162
- 41 Malik RA, Tesfaye S, Newrick PG. et al. Sural nerve pathology in diabetic patients with minimal but progressive neuropathy. Diabetologia 2005; 48 (03) 578-585
- 42 Chen RJ, Lin CC, Ju MS. In situ biomechanical properties of normal and diabetic nerves: an efficient quasi-linear viscoelastic approach. J Biomech 2010; 43 (06) 1118-1124
- 43 Onur MR, Poyraz AK, Ucak EE, Bozgeyik Z, Özercan IH, Ogur E. Semiquantitative strain elastography of liver masses. J Ultrasound Med 2012; 31 (07) 1061-1067
- 44 Ishibashi F, Taniguchi M, Kojima R, Kawasaki A, Kosaka A, Uetake H. Elasticity of the tibial nerve assessed by sonoelastography was reduced before the development of neuropathy and further deterioration associated with the severity of neuropathy in patients with type 2 diabetes. J Diabetes Investig 2016; 7 (03) 404-412
- 45 Tesfaye S, Selvarajah D. Advances in the epidemiology, pathogenesis and management of diabetic peripheral neuropathy. Diabetes Metab Res Rev 2012; 28 (Suppl. 01) 8-14
- 46 Misra UK, Kalita J, Nair PP. Diagnostic approach to peripheral neuropathy. Ann Indian Acad Neurol 2008; 11 (02) 89-97
- 47 Vincent AM, Edwards JL, McLean LL. et al. Mitochondrial biogenesis and fission in axons in cell culture and animal models of diabetic neuropathy. Acta Neuropathol 2010; 120 (04) 477-489
- 48 Maccarrone M, Brüne B. Redox regulation in acute and chronic inflammation. Cell Death Differ 2009; 16 (08) 1184-1186
- 49 Dyck PJ, Giannini C. Pathologic alterations in the diabetic neuropathies of humans: a review. J Neuropathol Exp Neurol 1996; 55 (12) 1181-1193
- 50 Kundalić B, Ugrenović S, Jovanović I. et al. Morphometric analysis of connective tissue sheaths of sural nerve in diabetic and nondiabetic patients. BioMed Res Int 2014; 2014: 870930
- 51 Boyd BS, Dilley A. Altered tibial nerve biomechanics in patients with diabetes mellitus. Muscle Nerve 2014; 50 (02) 216-223
- 52 Taser F, Deger AN, Deger H. Comparative histopathological evaluation of patients with diabetes, hypothyroidism and idiopathic carpal tunnel syndrome. Turk Neurosurg 2017; 27 (06) 991-997
- 53 Deger AN, Deger H, Taser F. The role of neoangiogenesis and vascular endothelial growth factor in the development of carpal tunnel syndrome in patients with diabetes. Niger J Clin Pract 2016; 19 (02) 189-195
- 54 Ebrahimzadeh MH, Mashhadinejad H, Moradi A, Kachooei AR. Carpal tunnel release in diabetic and non-diabetic patients. Arch Bone Jt Surg 2013; 1 (01) 23-27
- 55 Zimmerman M, Dahlin E, Thomsen NO, Andersson GS, Björkman A, Dahlin LB. Outcome after carpal tunnel release: impact of factors related to metabolic syndrome. J Plast Surg Hand Surg 2017; 51 (03) 165-171
- 56 Mozaffarian K, Owjimehr M, Eskandari Sani B, Mokarami F, Sharifzadeh R. Carpal tunnel release outcomes in diabetic versus non-diabetic patients. Shafa Ortho J 2015; 2 (02) e1234
- 57 Afshar A, Tabrizi A, Tajbakhsh M, Navaeifar N. Subjective outcomes of carpal tunnel release in patients with diabetes and patients without diabetes. J Hand Microsurg 2019; doi: DOI: 10.1055/s-0039-1697059.
- 58 Recio-Pinto E, Rechler MM, Ishii DN. Effects of insulin, insulin-like growth factor-II, and nerve growth factor on neurite formation and survival in cultured sympathetic and sensory neurons. J Neurosci 1986; 6 (05) 1211-1219
- 59 Ishii DN, Lupien SB. Insulin-like growth factors protect against diabetic neuropathy: effects on sensory nerve regeneration in rats. J Neurosci Res 1995; 40 (01) 138-144
- 60 Plastino M, Fava A, Carmela C. et al. Insulin resistance increases risk of carpal tunnel syndrome: a case-control study. J Peripher Nerv Syst 2011; 16 (03) 186-190
- 61 Ozkul Y, Sabuncu T, Yazgan P, Nazligul Y. Local insulin injection improves median nerve regeneration in NIDDM patients with carpal tunnel syndrome. Eur J Neurol 2001; 8 (04) 329-334
- 62 Greene DA, De Jesus Jr PV, Winegrad AI. Effects of insulin and dietary myoinositol on impaired peripheral motor nerve conduction velocity in acute streptozotocin diabetes. J Clin Invest 1975; 55 (06) 1326-1336
- 63 Cameron NE, Cotter MA. Effects of antioxidants on nerve and vascular dysfunction in experimental diabetes. Diabetes Res Clin Pract 1999; 45 (2,3) 137-146
- 64 Cameron NE, Cotter MA, Archibald V, Dines KC, Maxfield EK. Anti-oxidant and pro-oxidant effects on nerve conduction velocity, endoneurial blood flow and oxygen tension in non-diabetic and streptozotocin-diabetic rats. Diabetologia 1994; 37 (05) 449-459
- 65 Di Geronimo G, Caccese AF, Caruso L, Soldati A, Passaretti U. Treatment of carpal tunnel syndrome with alpha-lipoic acid. Eur Rev Med Pharmacol Sci 2009; 13 (02) 133-139
- 66 Mijnhout GS, Kollen BJ, Alkhalaf A, Kleefstra N, Bilo HJ. Alpha lipoic Acid for symptomatic peripheral neuropathy in patients with diabetes: a meta-analysis of randomized controlled trials. Int J Endocrinol 2012; 2012: 456279
- 67 Boriani F, Granchi D, Roatti G, Merlini L, Sabattini T, Baldini N. Alpha-lipoic acid after median nerve decompression at the carpal tunnel: a randomized controlled trial. J Hand Surg Am 2017; 42 (04) 236-242
- 68 Monroy Guízar EA, García Benavides L, Ambriz Plascencia AR. et al. Effect of alpha-lipoic acid on clinical and neurophysiologic recovery of carpal tunnel syndrome: a double-blind, randomized clinical trial. J Med Food 2018; 21 (05) 521-526