ArticlePDF Available

Diabetic Peripheral Neuropathy and Neurodynamics

Authors:
Submit Manuscript | http://medcraveonline.com
Introduction
Neuropathic pain is an important problem because of its complex
natural history, multiple possible etiologies, and poor response to
standard physical therapy modalities. Disorders of the peripheral
nerve system (PNS) are heterogeneous and may involve motor
bers, sensory bers, small myelinated and unmyelinated bers and
autonomic nerve bers, with variable anatomical distribution (single
nerves, several different nerves, symmetrical affection of all nerves,
plexus, or root lesions). Furthermore, pathological processes may
result in either demyelination, axonal degeneration or both. In order
to reach an exact diagnosis of any neuropathy electrophysiological
studies are crucial to obtain information about these variables.1
As a consequence of ongoing spontaneous activity arising from
the periphery, Spino Thalamic Tract neurons develop increased
background activity, enlarged receptive elds and increased responses
to afferent impulses, including normally innocuous tactile stimuli. This
phenomenon is called central sensitization. Central sensitization is an
important mechanism of persistent neuropathic pain. Additionally,
hyperalgesic/allodynic responses in uninjured neural tissues may
be the result of alterations in central nervous system processing of
afferent information (i.e. central sensitization).2 It is known that
after a peripheral nerve lesion, peripheral sensitization aberrant
regeneration may occur. Neurons become unusually sensitive and
develop spontaneous pathological activity, abnormal excitability, and
heightened sensitivity to chemical, thermal and mechanical stimuli.3
The positive and negative symptoms associated with
musculoskeletal presentations of peripheral neuropathic pain are
produced by sensitized nociceptors in neural connective tissues,
hypersensitive AIGS, a sensitized pain neuromatrix, myelin changes,
and axonal degeneration (Nee & Butler, 2006). That is, some areas
of the brain associated with sensory perception, emotion, attention,
cognition and motor learning are activated during pain experience.4
Diabetic poly neuropathy is one of the most common long-term
complications of diabetes affecting 50% of all diabetic patients.
For example, subclinical diabetic peripheral neuropathy can be
detected by electrophysiological tests, which are useful to verify the
range and extent of the nerve lesion involved in the early stage of
diabetic peripheral neuropathy.5 Other ndings suggest that thalamic
neurons can act as central generators or ampliers of pain in diabetes.6
To this point and although there are multiple methods for detecting
and monitoring DPN, nerve conduction studies (NCS) are generally
considered to be the most sensitive and reproducible.7 In hereditary
neuropathy, for example, electrophysiological studies are also used
to distinguish axonal neuropathies from demyelinating neuropathies,
though overlap and ‘intermediate’ patterns have become well
recognized.8
The electrophysiological changes are not always concordant
with clinical manifestations.5 The most common clinical and
electrophysiological manifestation of diabetic neuropathy is the
sensory disturbance, which is more severe in lower limbs.5 The
information provided by electrodiagnosis has a functional character,
telling the practitioner how the nerve and muscle are functioning.
Nerve conduction studies (NCS) and qualitative sensory testing
(QST) are important part of the complete electrodiagnostic exam.
However, in pain syndromes, conventional studies may give normal
results when large bers are not involved, and the use of autonomic
measures in such conditions is particularly relevant.8
According to Vinik et al.9 the main drawback of NCS is that small
myelinated and unmyelinated nerve bers, which are affected early
in the disease course of diabetic neuropathy, do not contribute to the
sensory action potential detected by routine NCS. Electrophysiological
data must, therefore, always be evaluated in a clinical context. Evoked
potentials, on the other hand have the capability of revealing clinically
unsuspected pathology when demyelinating diseases are suggested.
Rehabilitation programs tend to be emphasized and combined
with pharmacotherapy in daily practice.10 Traditional approaches use
Transcutaneous electrical nerve stimulation (TENS) and interferential
current (IFC) to relieve stiffness, improve mobility, relieve neuropathic
pain, reduce edema, and heal resistant foot ulcers.11 Neuro dynamic,
i.e., the mobilization of the peripheral nervous system, is a physical
approach to the treatment of pain; the method relies on inuencing
pain physiology via mechanical treatment of neural tissues and the
non-neural structures surrounding the nervous system.2,13 Through
clinical reasoning the nervous system seems to be the logical place
for treatment and explanations, although previous descriptions of this
method have not claried the relevant mechanics and physiology,
Int Phys Med Rehab J. 2018;3(1):5657 56
© 2018 Domingues et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,
which permits unrestricted use, distribution, and build upon your work non-commercially.
Diabetic peripheral neuropathy and neuro dynamics
Volume 3 Issue 1 - 2018
Márcio Domingues
Centre of Investigation in Social Science, Lusofona University,
Portugal
Correspondence: Márcio Domingues, Centre of Investigation
in Social Science, Lusofona University, Portugal,
Tel (+351)217515500, Fax (+351)217577006,
Email marcio.domingues@live.com.pt
Received: December 28, 2017 | Published: February 02,2018
Abstract
Diabetic peripheral neuropathy is a common, disabling, and costly complication of
diabetes mellitus. In order to reach an exact diagnosis of electrophysiological studies
and the evaluation of diabetic neuropathy it is crucial to obtain information about these
variables. The information provided by electrodiagnosis is functional and not static,
telling the practitioner how nerve and muscle are functioning. It is known that after a
peripheral nerve, peripheral sensitization aberrant regeneration may occur alongside
this the mobilization of the nervous system is an essential approach to physical
treatment of pain. Neurodynamics encompasses interactions between mechanics
and physiology of the nervous system. Alongside this, neurodynamic as a physical
innovative therapy has been seldom used and in fact may be beneficial in preserving
nerve function thus preventing the adverse effects of intraneural edema. That is, the
rationale for the use of neurodynamic diagnosis and treatment is that it is considered
capable of detecting the increased nerve structure associated with these conditions.
International Physical Medicine & Rehabilitation Journal
Mini review Open Access
Diabetic peripheral neuropathy and neuro dynamics 57
Copyright:
©2018 Domingues
Citation: Domingues M. Diabetic peripheral neuropathy and neuro dynamics. Int Phys Med Rehab J. 2018;3(1):5657. DOI: 10.15406/ipmrj.2018.03.00075
including interactions between these two components. Within this
reasoning it is important to determine and develop clinical research
to ascertain the diagnostic value of neurodynamic sequencing in
damaged neural tissue.
Conclusion
Neurodynamic may be benecial in preserving nerve function by
limiting intraneural uid accumulation, thus preventing the adverse
effects of intra neural edema.13 The rationale for using neurodynamic
in diagnosis and treatment is that they are considered capable of
detecting the increased nerve mechanosensitivity associated with
these conditions.14,15
Acknowledgements
None.
Conict of interest
This manuscript has no conict of interest with any parts.
References
1. Crone C, Krarup C. Neurophysiological approach to disorders of pe-
ripheral nerve. Handb Clin Neurol. 2013;115:81–114.
2. Butler D. The sensitive nervous system. Noingroup Publications. Ade-
laide: Australia; 2000. p. 1–430.
3. Purves D, Augustine GJ, Fitzpatrick D, et al. Neuroscience. 5th ed.
Sunderland, USA: Sinauer Associates; 2012.
4. Melzack R. Evolution of the neuromatrix theory of pain. Pain Practice.
2005;5(2):85–94.
5. Liu MS, Hu BL, Cui LY, et al. Clinical and neurophysiological features
of 700 patients with diabetic peripheral neuropathy. Zhonghua Nei Ke
Za Zhi. 2005;44(3):173–176.
6. Fischer TZ, Waxman SG. Neuropathic pain in diabetes--evidence for a
central mechanism, Nat Rev Neurol. 2010;6(8):462–466.
7. Pan H, Jian F, Lin J, et al. F-wave latencies in patients with diabetes
mellitus. Muscle Nerve. 2014;49(6):804–808.
8. Krarup C. An update on electrophysiological studies in neuropathy.
Curr Opin Neurol. 2003;16(5):603–612.
9. Vinik AI, Kong X, Megerian JT, et al. Diabetic nerve conduction
abnormalities in the primary care setting. Diabetes Technol Ther.
2006;8(6):654–662.
10. Akyuz G, Kenis O. Physical therapy modalities and rehabilitation te-
chniques in the treatment of neuropathic pain. Int J Phys Med Rehabil.
2013;93(3):253-259.
11. Kalra S, Kalra B, Sharma N. Prevention and management of diabetes:
The role of the physiotherapist. Diabetes Voice. 2007;52(3):12–14.
12. Shacklock M. Clinical Neurodynamics: a new system of musculoskele-
tal treatment. UK: Elsevier; 2005.
13. Brown CL, Gilbert KK, Brismee JM, et al. The effects of neurodynamic
mobilization on uid dispersion within the tibial nerve at the ankle: an
unembalmed cadaveric study. J Man Manip Ther. 2011;19(1):26–34.
14. Nee RJ, Bulter D. Management of peripheral neuropathic pain: Inte-
grating neurobiology, neurodynamics, and clinical evidence. Physical
Therapy in Sport. 2006;7(1):36–49.
15. Wainner RS, Gill H. Diagnosis and nonoperative management of cervi-
cal radiculopathy. J Ortho Sports Phys Ther. 2000;30(12):728–744.
... Diffusion Tensor Imaging (DTI) may be used as the assessment tool in the peripheral nerve related disease and also monitor reinnervation through fractional anisotropy (FA), apparent diffusion coefficient (ADC) [15]. Hyperglycemia leads to the altered nerve biomechanics due to fluid accumulation in the nerve [16] which can be targeted through nerve mobilization (NM) in the form of the neurodynamics and the nerve massage [17][18][19] [20,21]. The purpose of current research is to explore the effect of NM on the DTI parameters in healthy individuals and in DPN patients. ...
Article
Full-text available
Background: Diabetic neuropathy is the commonest chronic disabling complication of diabetes which may lead to amputation and compromising patient's quality of life. It is characterized by pain, sensation loss associated with neural edema. Diffusion tensor imaging parameter i.e. fraction anisotropy determines the free water proton diffusion in the healthy nerve. Since the diabetes leads to altered mechanosensitivity of the posterior tibial nerve thereby, might interferes with the water molecules movement. Therefore the present clinical trial will provide the evidence of improving the diffusion tensor imaging in the diabetic neuropathy directly by targeting the nerve through nerve mobilization treatment. Methods: Participants with Type II Diabetes Mellitus induced peripheral neuropathy will be selected randomly on the basis of eligibility criteria and informed consent will be taken. Participants will be recruited into three groups. Group A (experimental group A) will receive neural mobilization technique, Group B (experimental group B) will receive conventional therapy and Group C (control group) will receive sham treatment for 3 weeks. MRI technique, Visual analogue scale and neuropathy specific quality of life questionnaire will be used as assessment tools. Assessment will be taken at baseline and post intervention. Conclusion: this clinical trial will provide the evidence of efficacy of nerve mobilization in determining the diffusion tensor imaging (DTI) changes in the posterior tibial nerve in patients with diabetic neuropathy. This trial will also be the first one in itself to look at the treatment induced DTI changes in the peripheral nerve. Trial registration: Clinical Trial Registry of India (CTRI/2019/06/019552).
Article
Background MR-DTI parameters namely fractional anisotropy (FA) and apparent diffusion coefficient values (ADC) of diffusion imaging demonstrate the directional preference and speed of diffusion of water molecules. The purpose of this case report is to explore the effect of massage, passive neural mobilization and transcutaneous electrical nerve stimulation on MR-DTI of the tibial nerve in a patient with type 2 diabetes mellitus having chronic distal symmetrical sensorimotor neuropathy. Case Description A 63-year-old male with type 2 diabetes mellitus diagnosed with chronic symmetrical sensorimotor diabetic peripheral neuropathy on the basis of medical examination and electrophysiological testing. Altered mechanosensitivity of the tibial nerve was confirmed through neurodynamic testing. MR-DTI revealed severe damage of the tibial nerve as shown by chaotic diffusion of water molecules and damaged microstructural integrity. Intervention A total six sessions over 3 weeks including nerve massage in a longitudinal and transverse direction; passive neural mobilization consisting of sliders and tensioners of the tibial nerve; and followed by 15 minutes of continuous transcutaneous electrical nerve stimulation directed along the nerve course. Outcome FA and ADC values, pain,neuropathy quality of life and range of motion data were collected pre and post intervention. Analysis revealed clinical improvement in all the outcome measures. Conclusion This case report identified improvement in radiological MR-DTI outcomes following rehabilitation in a patient with diabetic peripheral neuropathy.
Article
Full-text available
To evaluate the effects of neurodynamic mobilization on the fluid dynamics of the tibial nerve in cadavers. Evidence showing patients benefit from neural mobilization is limited. Mechanisms responsible for changes in patient symptoms are unclear. Bilateral lower limbs of six unembalmed cadavers (n = 12) were randomized into matched pairs and dissected to expose the tibial nerve proximal to the ankle. Dye composed of Toulidine blue and plasma was injected into the nerve. The longitudinal dye spread was measured pre- and post-mobilization. The experimental group received the intervention consisting of 30 repetitions of passive ankle range of motion over the course of 1 minute. The matched control limb received no mobilization. Data were analysed using a 2×2 repeated measures ANOVA with subsequent t-tests for pairwise comparisons. Mean dye spread was 23.8±10.2 mm, a change of 5.4±4.7% in the experimental limb as compared to 20.7±6.0 mm, a change of -1.5±3.9% in the control limb. The ANOVA was significant (P⩽0.02) for interaction between group (experimental/control) and time (pre-mobilization/post-mobilization). t-test results were significant between pre- and post-mobilization of the experimental leg (P = 0.01), and between control and experimental limbs post-mobilization (P⩽0.02). Passive neural mobilization induces dispersion of intraneural fluid. This may be clinically significant in the presence of intraneural edema found in pathological nerves such as those found in compression syndromes.
Article
Full-text available
Qualitative, comprehensive literature review. To discuss and summarize the current peer-reviewed literature related to the management of patients with cervical radiculopathy. Cervical radiculopathy is a lesion of the cervical spinal nerve root with a reported prevalence of 3.3 cases per 1000 people; peak annual incidence is 2.1 cases per 1000 and occurs in the fourth and fifth decades of life. Nerve root injury has the potential to produce significant functional limitations and disability. A search of the MEDLINE, CINAHL, and Web of Science databases for the periods 1966, 1982, and 1996, respectively, to December 1999 was conducted using selected keywords and MeSH headings. The bibliography of all retrieved articles were searched and pertinent articles were obtained. The Cochrane Database of Systematic Reviews was also searched. Literature related to the diagnosis, prognosis, and treatment of cervical radiculopathy were thoroughly reviewed and summarized using a critical appraisal approach. Although cervical radiculopathy remains largely a clinical diagnosis, the true diagnostic accuracy of the clinical examination for cervical radiculopathy is unknown. Imaging and electrophysiologic tests are capable of detecting clinically significant problems in many patients and each modality has inherent strengths and weaknesses; technical as well as practical factors affect the choice of procedure. The natural course of cervical radiculopathy appears to be generally favorable but no prognostic or risk factors have been firmly established and the efficacy of various nonoperative treatments for the condition is unknown. A clear definition of terms and further research are required to establish definitive diagnostic criteria and effective treatment for the management of patients with cervical radiculopathy.
Article
Neuropathic pain is an important problem because of its complex natural history, unclear etiology, and poor response to standard physical therapy modalities. It causes severe disability unrelated to its etiology. The primary goal of neuropathic pain management is to investigate the underlying cause, to make the differential diagnosis, to eliminate risk factors, and to reduce pain. The physician should also be aware of functional, and psychological conditions of the patient. Therefore, a multimodal management plan in neuropathic pain is essential. In this article, we aimed to reflect a diverse point of view about various physical therapy modalities and rehabilitation techniques. For this purpose, we searched articles about physical therapy modalities and rehabilitation techniques in PubMED database and presented various studies according to their relevance. New rehabilitation techniques seem promising however there is a requirement for more randomized controlled trials with larger patient groups. In this review, we suggest that physical therapy modalities and rehabilitation techniques are very important options and must be considered with pharmacotherapy.
Article
Neuropathic pain is an important problem because of its complex natural history, unclear etiology, and poor response to standard physical therapy agents. It causes severe disability unrelated to its etiology. The primary goals of the management of neuropathic pain are to detect the underlying cause, to define the differential diagnosis and eliminate risk factors, and to reduce the pain. The physician should also know the functional and psychologic conditions of the patient. Therefore, a multimodal management plan in neuropathic pain is essential. This review aimed to reflect a diverse point of view about various physical therapy modalities and rehabilitation techniques. Physical therapy modalities and rehabilitation techniques are important options and must be considered when pharmacotherapy alone is not sufficient. In addition, psychosocial support and cognitive behavioral therapy could also be taken into consideration. It has been suggested that the importance of pain rehabilitation techniques will increase in time and these will take a larger part in the management of neuropathic pain. However, it is now early to comment on these methods because of the lack of adequate publications.
Article
Introduction: To evaluate the sensitivity of electrophysiologic assessments, we compared F-waves and motor and sensory nerve conduction studies (MNCS and SNCS) in patients with diabetes mellitus (DM). Methods: We tested median, ulnar, tibial, and fibular nerves in 132 DM patients divided into those with and without clinical evidence of polyneuropathy. Results: Of 64 asymptomatic patients, 2 (3%) had MNCS or SNCS abnormalities, both of whom had F-wave changes, whereas 21 (33%) had only delayed F-waves, for a combined yield of 23 (36%). The corresponding values for 68 symptomatic patients consisted of 43 (63%), 14 (21%), and 57 (84%). In both groups, F-wave latency had a higher (P<0.05) frequency of abnormality than MNCS in all nerves. F-wave study also surpassed SNCS in lower limb nerves. Conclusions: F-waves of the tibial and fibular nerves are the most sensitive measure to detect subclinical or overt diabetic polyneuropathy. Muscle Nerve 49: 804-808, 2014.
Article
Disorders of the peripheral nerve system (PNS) are heterogeneous and may involve motor fibers, sensory fibers, small myelinated and unmyelinated fibers and autonomic nerve fibers, with variable anatomical distribution (single nerves, several different nerves, symmetrical affection of all nerves, plexus, or root lesions). Furthermore pathological processes may result in either demyelination, axonal degeneration or both. In order to reach an exact diagnosis of any neuropathy electrophysiological studies are crucial to obtain information about these variables. Conventional electrophysiological methods including nerve conduction studies and electromyography used in the study of patients suspected of having a neuropathy and the significance of the findings are discussed in detail and more novel and experimental methods are mentioned. Diagnostic considerations are based on a flow chart classifying neuropathies into eight categories based on mode of onset, distribution, and electrophysiological findings, and the electrophysiological characteristics in each type of neuropathy are discussed.
Article
Hyperexcitability of and aberrant spontaneous impulse generation by damaged first-order sensory neurons and their peripheral axons are well-established processes that strongly contribute to pain associated with diabetic neuropathy. Studies in the past 5 years, however, suggest that, as in many neuropathic pain disorders, central neuropathic mechanisms can also contribute to pain experienced with diabetes. These studies have demonstrated that thalamic dysfunction occurs in patients with diabetes mellitus, and that in experimental models of this disease neurons in the ventral posterolateral thalamus can become hyperexcitable, firing at abnormally high frequencies and generating aberrant spontaneous activity. In this article, we discuss these findings, which suggest that thalamic neurons can act as central generators or amplifiers of pain in diabetes.
Article
The review concentrates on the use of clinical neurophysiology in peripheral nerve disorders covered in the present issue. It is pertinent to distinguish different types of involvement of fibers in diabetic neuropathy, including the involvement of small and large fibers, to outline the diagnostic criteria of inflammatory neuropathies, and to describe the spectrum of peripheral nerve pathophysiology in inherited neuropathies. Painful neuropathies represent a particular challenge to clinical neurophysiology since it is mainly small fibers, which are difficult to study, that are affected. Electrodiagnostic studies have relevance in distinguishing neuropathies with different etiologies in diabetes mellitus, and different strategies and methods are necessary to study patients with autonomic and small-fiber involvement. The involvement of motor or sensory fibers, or both, and primary axonal or demyelinative pathology are important questions relating to immune-mediated neuropathies studied in the context of the specificity of antibodies against various neuronal and Schwann-cell structures. In hereditary neuropathy, electrophysiological studies are also used to distinguish axonal neuropathies from demyelinating neuropathies, though overlap and 'intermediate' patterns have become well recognized. In pain syndromes, conventional electrophysiological studies may give normal results if large fibers are not involved, and the use of autonomic measures in these situations has particular relevance. The usefulness of electrodiagnostic measures depends on the clinical, diagnostic, or pathophysiological question involved, and the strategy employed should reflect the advantages and limitations of these methods. If adequate consideration is paid to these properties, then such studies have a central role in the diagnosis and adequate treatment of patients with neuromuscular disorders.
Article
To study the clinical and electrophysiological features of diabetic peripheral neuropathy in 700 patients to elucidate the relationships between them and evaluate the value of electromyography in the diagnosis of diabetic peripheral neuropathy. Standard sensory and motor nerve conduction studies were performed in the 700 patients, sensory nerve conduction velocity (SCV), amplitude of sensory nerve action potential (SNAP), distal motor latency (DML) and amplitude of compound muscle action potential (CMAP) of median nerve, ulnar nerve, posterior tibial nerve and common peroneal nerve were studied simultaneously. Needle electromyogram (EMG) test was performed in 239 patients. (1) The most common symptoms of peripheral neuropathy were numbness and pain in limbs, while impaired or lost tendon reflexes were the most common abnormal signs in lower limbs. (2) The abnormal rate of nerve conduction studies was 72.4% in the 700 patients. Slow SCV, prolonged DML and decreased amplitude of SNAP and CMAP were detected. (3) More severe abnormal nerve conduction was found in lower limbs than in upper limbs. The abnormal degree was more severe in sensory nerve than in motor nerve and severity was more in amplitude than in conduction velocity (P < 0.05). (4) Abnormal motor and/or sensory nerve conduction was detected in 67.3% of the patients with clinical manifestations of neuropathy and 5.1% patients without signs or symptoms of neuropathy, while motor or sensory nerve conduction was normal in 27.6% patients with manifestations of neuropathy. Needle EMG showed neurogenic lesion in 4.6% of the patients with normal motor and sensory nerve conduction. (5) polyneuropathy is the most common type of diabetic neuropathy and carpal tunnel syndrome the next. The most common clinical and electrophysiological manifestation of diabetic neuropathy is sensory disturbance, which is more severe in lower limbs. The electrophysiological changes are not always accordant with clinical manifestations. Subclinical diabetic peripheral neuropathy can be detected by electrophysiological tests, which are useful to verify the range and extent of the nerve lesion involved in the early stage of diabetic peripheral neuropathy. Needle EMG is not recommended for screening diabetic neuropathy.
Article
Nerve conduction studies (NCS) are the most objective measure of nerve function, and their use is recommended in the clinical and epidemiological evaluation of diabetic polyneuropathy (DPN). The purpose of this study was to utilize automated NCS technology to characterize nerve conduction of patients with diabetes in primary care settings. The Diabetes cohort was drawn from 28 community clinics. The Control cohort consisted of subjects without diabetes and without evidence of neuropathy. Bilateral peroneal NCS were performed with an automated NCS instrument (NC-stat, NeuroMetrix, Inc., Waltham, MA). Neuropathic symptoms were quantified using an abbreviated form of the NTSS-6 questionnaire. Risk factors for abnormal NCS were determined using multivariate regression modeling. Data were collected for 172 control subjects and 1,358 subjects with diabetes. Statistically significant differences in peroneal NCS were found. Of the Diabetes cohort, 75.1% had at least one NCS abnormality, and 53.2% had bilateral abnormalities. Of the asymptomatic patients, 45% had bilateral NCS abnormalities. By contrast, 40% of those with clinically significant symptoms lacked bilateral NCS abnormalities. Independent predictors for bilateral NCS abnormalities were age, height, weight, hemoglobin A1c (HbA1c), and duration of diabetes. Up to 16% of the variance in NCS measurements was explained by HbA1c, duration of diabetes, and several demographic variables. This study suggests that automated NCS can provide nerve conduction confirmation of DPN in primary care settings and has clinical utility. These findings have important implications for the clinical and epidemiological evaluation of DPN.