Review Article | Open Access
Amirah Mustapa, Maria Justine, Nadia Mohd Mustafah, Nursuriati Jamil, Haidzir Manaf, "Postural Control and Gait Performance in the Diabetic Peripheral Neuropathy: A Systematic Review", BioMed Research International, vol. 2016, Article ID 9305025, 14 pages, 2016. https://doi.org/10.1155/2016/9305025
Postural Control and Gait Performance in the Diabetic Peripheral Neuropathy: A Systematic Review
Purpose. The aim of this paper is to review the published studies on the characteristics of impairments in the postural control and gait performance in diabetic peripheral neuropathy (DPN). Methods. A review was performed by obtaining publication of all papers reporting on the postural control and gait performance in DPN from Google Scholar, Ovid, SAGE, Springerlink, Science Direct (SD), EBSCO Discovery Service, and Web of Science databases. The keywords used for searching were “postural control,” “balance,” “gait performance,” “diabetes mellitus,” and “diabetic peripheral neuropathy.” Results. Total of 4,337 studies were hit in the search. 1,524 studies were screened on their titles and citations. Then, 79 studies were screened on their abstract. Only 38 studies were eligible to be selected: 17 studies on postural control and 21 studies on the gait performance. Most previous researches were found to have strong evidence of postural control impairments and noticeable gait deficits in DPN. Deterioration of somatosensory, visual, and vestibular systems with the pathologic condition of diabetes on cognitive impairment causes further instability of postural and gait performance in DPN. Conclusions. Postural instability and gait imbalance in DPN may contribute to high risk of fall incidence, especially in the geriatric population. Thus, further works are crucial to highlight this fact in the hospital based and community adults.
Diabetic peripheral neuropathy (DPN) is a debilitating microvascular complication among the patients with Type 2 Diabetes Mellitus (T2DM). Approximately 49.3% of T2DM patients have DPN in Iran . A study in Sri Lanka found 48.1% of DPN diagnosed using Diabetic Neuropathy Symptom (DNS) score among 528 diabetic patients . A study in India reported that every fifth individual diagnosed with T2DM is likely to have DPN . In Malaysia, about 14.4% of 215 T2DM patients in Kelantan were reported to have DPN . These figures are alarming as the local prevalence of diabetes is increasing from 11.6% in the year 2006  to 15.2% in the year 2011  due to the aging of the population.
DPN is explained by the presence of signs and symptoms of peripheral nerve dysfunction in diabetic patients after nondiabetes causes have been excluded . DPN affects the proximal and distal peripheral sensory and motor nerves [8, 9]. Sensory neuropathy is prominent in DPN with an exhibition of numbness and prickling sensation in a stocking-glove pattern that starts from the feet and spreads proximally . DPN also affects the autonomic nervous system, known as diabetic autonomic neuropathy [8, 9, 11] with manifestation on the exercise intolerance, orthostatic hypotension, and sudden death .
The most common symptoms of DPN are numbness, tingling, and pain that may worsen during the evening. It begins in the toes towards plantar of the feet, ankles, and lower shins with the association of night cramps  and unsteadiness in walking . Gradually DPN will affect distal muscle strength and deteriorates normal walking function . Alteration of the peripheral nerve due to DPN is the chief contributor to postural instability  and high gait variability that may increase the likelihood of fall incidence .
Individuals with DPN are 15 times more likely to experience fall compared to the healthy subjects . Falls are marked as a dangerous health issue in DPN especially in the geriatric population . Therefore, knowledge of the factors that influence falls such as postural control deficit and gait instability in DPN patients is essential. Thus, the aim of this paper is to give an in-depth review of the published studies on the characteristics of impairments in the postural control and gait performance in DPN.
2.1. Search Strategy
To provide a comprehensive review of postural control and gait performance in DPN, an electronic search was performed within the Google Scholar, Ovid, SAGE, Springerlink, Science Direct (SD), EBSCO Discovery Service, and Web of Science databases until April 1, 2016. The keywords used for literature search were “postural control,” “balance,” “gait performance,” “diabetes mellitus,” and “diabetic peripheral neuropathy.” The searching was limited to English, academic journal, and human studies only.
2.2. Study Selection
All identified titles and citations retrieved by the search strategy were screened to select relevant studies. Two reviewers independently checked the titles and abstracts of all the selected articles. In discrepancy case between the reviewers, a consensus meeting was done to make a final decision on the articles selection. Then, the selection criteria were applied to all potentially relevant full text of articles. Articles were eligible if they met the following inclusion criteria:(1)The studies and reports that provided data on the postural control and gait performance in DPN.(2)The study that indicated cross-sectional and case-control (narrative review and single case studies were excluded).(3)The study population, that is, patients with diabetic neuropathy or DPN (studies on patients with diabetes mellitus without identified into DPN were excluded).
2.3. Data Extraction
The full text of the articles was gathered and reviewed if the study was appropriate. Data on the study characteristics (study design, author, and year), population (age, gender, and number), the methodology used, and the characteristics of postural control and gait performance in DPN were extracted. The PRISMA guidelines for reporting literature searching were utilized in this study .
3. Results and Discussion
4,337 studies were hit in the search (Figure 1). 1,524 studies were screened on their titles and citations. Then, 79 studies were screened on their abstract. Only 38 studies were eligible to be selected: 17 studies on postural control and 21 studies on the gait performance. Figure 1 displays the process of selecting the studies.
3.1. Study Characteristics
|EO: eyes open, EC: eyes closed, BMS: Balance Master System, LOS: limits of stability, mCTSIB: Modified Clinical Test of Sensory Interaction on Balance, COP: Centre of Pressure, COM: Centre of Mass, COG: Centre of Gravity, A/P: anterior/posterior, M/L: medial/lateral, MAO: Mean Amplitude Oscillation, ASO: Average Speed Oscillation, ST: Semitandem, MVEL: mean velocity of body sway, and VFY: physiological ankle control to hip postural control.|
|SE: standard environment, CE: challenging environment, A/P: anterior/posterior, M/L: medial/lateral, EO: eyes open, EC: eyes closed, and BOS: base of support.|
3.2. Participants Characteristics
This study reviewed 883 DPN participants and various methods were used to identify DPN among the participants. Some studies evaluated DPN by recording nerve conduction velocity (NCV) [17, 21, 27, 29] through amplitude and latency tests of sensory (sural) and motor (peroneal and tibial) nerves [27, 38]. Additionally, the Michigan Neuropathy Screening Instrument (MNSI) test with score higher than eight [22, 35, 45] included a test of vibration sensitivity using a tuning fork set at 128 Hz; tendon reflexes, muscle strength in the lower extremities [20, 50], and the somatosensory test using Semmes-Weinstein monofilaments examination (SMWE) were used to diagnose DPN [19, 28, 37, 38, 49, 53, 54]. The presence of DPN also was assessed by using the modified Neuropathy Disability Score (mNDS) NDS > 5 [42, 48] and the vibration perception threshold (VPT)  with <25 volts [24, 29, 30, 34, 40, 46, 55]. mDNS consists of clinical testing of (1) sensory modalities (pinprick, light touch, vibration, and pain), (2) the anatomic level below which light touch sensation is impaired, (3) muscle strength, and (4) ankle jerk. The total score varies between 0 and 33. A total score of 0 is graded as no DPN, 1–9 as mild, 10–18 as moderate, and 19–33 as severe DPN .
3.3. Instruments and Methods Used for Postural Control Assessment
Three studies used static posturography on a standard platform [20, 24] and a GS-10 Anima gravicorder (Anima Corporation, Tokyo, Japan) to assess postural control . Additionally, the Physilog system (BioAGM, CH) was used to measure linear accelerations at the trunk and ankle levels of postural control . A study used dual force platform with a touch plate, positioned at the participants’ right side at 90 cm height from the floor and examined under three touch conditions, no touch (NT), light touch (LT), and heavy touch (HT) to measure postural control . Dynamometric platform (Kistler) also was used to calculate sway area in EO and EC, while platform producing a horizontal sinusoidal in the AP direction, alternately with EO and EC, was used to measure dynamic balance . Similarly, Sliding Linear Investigative Platform, a horizontal translating force platform , and standing on foam rubber mat (40407.5 cm thick) in EO and EC  were used to assess postural sway. A recent study that used traditional body sway parameters from COG plots includes COG (AP) sway, COG (ML) sway, and COG sway with two 15-second trials of stood upright with feet together as close as possible and with arms crossed over chest in EO and EC . Force platform measurements (Kistler) [17, 18, 27, 29] and Wii Balance Board®  were used to evaluate the COP fluctuations to identify postural sway. Some studies also evaluate COP through a static balance test carried out in EO and EC conditions [17, 26].
3.4. Instruments and Methods Used for Gait Performance Assessment
Portable electronic GAITRite walkway system  and electronic baropodometry treadmill (FootWalk Pro AM CUBE, France) with a sampling frequency of 200 Hz, equipped with the software FootWork Pro , were used to calculate spatiotemporal gait parameters, while other studies assessed gait by walking along an 11 m pathway called the Walk Ratio at preferred and maximum speeds to measure cadence . Walking speed was assessed by measuring the time taken to walk a 10-metre distance following a 3-metre predistance to assure constant velocity  and equipped with the Physilog1 system to walk with a preferred walking speed . A study used gait analyzer system (LEGSys BioSensics LLC, Cambridge, Massachusetts) wearable sensors attached to the right and left anterior shins, the right and left anterior thighs, and posteriorly to the lower back for gait analysis . Another study asked participants to walk on a motorized treadmill at a constant speed of 1 m/s and filmed them with a 60 Hz video camera and automatic digitizing software (Peak Performance, Englewood, CO) for gait analysis . One study performed gait analysis by using a nonslippery steel-covered pathway 8 m long with the conductive material under the heel and toes of each foot to provide accurate temporal values corresponding to the onset and offset of right and left single support and double support phases . Gait analysis was performed by using a 6.7 m long pressure sensitive carpet (GAITRite1, CIR System, Havertown, USA) with three different locomotion speeds slow speed, preferred speed, and maximal speed in EO and during preferred walking in EC  and by wearing flat-soled athletic shoes (New Balance Athletic Shoe Inc., Boston, MA) .
Gait stability was analyzed with a baropodometer (FootWalk Pro, AM CUBE, France; sampling rate of 200 Hz) consisting of a 2 m pressure platform and a 6 m walkway (total of 8 m), which permits gait acceleration and deceleration in the initial and final 3 m walked on the walkway at a comfortable and self-selected speed in conditions EO and EC and walking with EO and narrow base of support (NB) , while kinematic and kinetic data were acquired by using (1) single camera motion capture , (2) a BTS motion capture system (six cameras, 60–120 Hz) synchronized with two Bertec force plates (FP4060-10) and integrated with two Imago plantar pressure systems (0.64 cm2 resolution, 150 Hz) , (3) a Vicon 512 Motion Analysis System (Oxford Metrics Ltd., Oxford, England) with six cameras operating at a sampling frequency of 100 Hz and a force plate (Kistler, Switzerland) embedded into a 10 m walkway operating at a sampling frequency of 400 Hz , (4) a portable data logger based on Tattletale Model 8 hardware (Onset Computer, Inc., Pocasset, MA), which consisted of a fully programmable microprocessor, an 8-channel 12-bit A/D converter , (5) GaitMeter™, a portable and inertia sensing motion analysis system attached to the anterior mid shins , and (6) 2D digital optical recording system, which consisted of a 25 Hz interlaced digital video camera (50 frames/s) (MX5, Adimec, Holland) with a 12.5 mm lens (Ernitec) . A study used the Vifor (video force) system to identify patterns of gait and kinetic data in the sagittal and frontal planes during walking .
3.5. Characteristics of Postural Control Impairments in the DPN
Postural control is defined as the control of body’s position in space for balance purpose. Postural control is obtained from sensory feedbacks of the body which are the vestibular, visual, and somatosensory system . Postural control in static conditions is known as postural steadiness while in the dynamic volitional perturbations it is noted as postural stability . Postural instability was significantly associated with DPN compared to the DM only and control group through imbalance of standing in two studies [29, 33]. But, Simoneau et al. (1994) further tested the postural stability under EO/head straight, EO/head back, EC/head straight, and EC/head back condition . de Souza Fortaleza et al.  reported a significant difference in the Mean Amplitude Oscillation (MAO) A/P EO and EC, MAO-M/L EC and Semitandem (ST), and Average Speed Oscillation (ASO), ASO-M/L ST, were identified as the factor of postural instability among DPN group . A study by Fulk et al. (2010) revealed diabetic with and without DPN requires accelerations to detect a 1 mm and 4 mm displacement, and DPN may not be the only cause of impaired balance in people with DM . Turcot et al. (2009) revealed significantly higher anterior-posterior range of lumbar acceleration and ankle accelerations for DPN group compared with other groups, interpreting greater postural instability. This study also suggested visual deficit as contributing factors of greater postural instability in DPN . Supportingly, several studies also supported that the absence of visual and vestibular senses lead to worsening of posture control [18, 21, 22, 29].
Postural instability in DPN occurs due to deficits of systems that work to control balance. Reducing accurate feedback of the proprioception sense along with the deterioration of somatosensory , visual [18, 21, 22, 29], and vestibular systems causes postural instability and larger postural sway . Interruption of the afferent and efferent neuron function through the termination of the tibial, sural, and deep peroneal nerves in the mechanoreceptors of the capsule and ligaments at the ankle joint  lead to diminishing function of proprioceptive and tactile sensation in maintaining postural stability . However, review by Bonnet and Lepeut (2011) questioned whether peripheral neuropathy may exaggerate postural control mechanisms as they found contrast result from five studies regarding the issues of neuropathy problem in disruption of postural control . Visual dysfunction in DM occurs when peripheral vision is occluded with high blood glucose level in the blood vessels of the retina . DM affect vestibular function as the vestibular system is sensitive to high blood glucose and insulin level, which cause DPN group exhibited impaired ability to detect short, whole body anterior translation with large sway area .
Postural sway is defined as the response of the postural muscle activity in stimulating a continuous to-and-fro movement of the body against the point of gravity while standing . Dixit et al. (2015)  found a significant difference with greater sway amplitude on firm and foam surface in EO, EC, and EO on foam and EC on foam conditions in DPN group. Fahmy et al. (2014) also demonstrated that DPN group had significantly lower equilibrium scores, lower balance score of the Berg Balance Scale (BBS), and more postural sway than the control group . One study noted that trace surfaces were significantly larger; trace length was significantly longer and the mean velocity of body sway (MVEL) was faster in EO and EC in the DPN group than the other groups , while another study demonstrated the velocity of body sway and velocity variance and the anteroposterior mean position of the body (VFY), fast Fourier transformation on (FFTX), and fast Fourier transformation on (FFTY) planes frequencies of body oscillation on and planes were significantly higher in DPN group compared to the DM without DPN and control group . Body sway (COG (AP) sway, COG (ML) sway, and COG sway) in EO and EC in DPN group was significantly higher by 74% with EO and 87% with EC than controls . Boucher et al. (1995) found significant postural sway through investigating five postural dependent variables (anteroposterior, mediolateral, and scalar ranges of sway, sway speed, and dispersion of sway) in DPN group than the control group . Decrease in postural sway at low-medium frequencies suggested lower reliance on vestibular system. Also, this study noted that DPN group showed better balance and sway compensation performance after balance training . One study concluded that DPN group had a significantly larger Centre of Pressure-Centre of Mass (COP-COM) amplitudes in the eyes closed (EC) condition compared with the eyes open (EO) condition in anteroposterior (A/P) and mediolateral (M/L) directions than the control group . A study by Dickstein et al. (2003) noted significant longer postural response latencies and smaller scaling of initial response magnitude in DPN group compared to the control group . Normal adult maintains their posture by an anterior-posterior sway pattern which is known as ankle strategy, resembling an inverted pendulum: the fulcrum is the ankle, and the head is the opposite end of the pendulum. However, DPN group exhibited reduced ability of the ankle strategy to resist postural sway against gravity as proven by the finding of larger trace surface of posturography in DPN group compared to the control and diabetic without DPN group . Consistently, postural sway in DPN occurs following the inability of the postural and lower limb muscles to provide an adequate activity level of muscles and joint. Muscle strength reduction is associated with relatively high glucose level and potentially less glucose uptake and hyperglycemia in muscles, which can contribute to lower capability in resisting postural sway [17, 30]. Abnormality of the postural sway is recognized and expected if there is any deterioration of one sensory input and/or motor output. Evidently, postural sway requires high demands on the peripheral nervous system. Therefore, impairments of the afferent and the efferent pathways in DPN are suggested to cause many considerable changes in postural sway reaction . In spite of that, review by Bonnet and Ray (2011) partially agreed with findings of DPN being the fundamental reason causing larger postural sway in diabetic patients than controls in quiet stance and affecting more if visual or vestibular systems are deteriorated .
For static balance alteration, a study by Palma et al. (2013) revealed that DPN group showed poor balance under both EO and EC conditions, with a significantly greater COP ratio in the CE condition . Nardone et al. (2006) also concluded that DPN group are unstable during quiet stance compared to the control group with slight increase of the head AP displacement despite displacement of the feet during dynamic balance task . In addition, DPN also demonstrated significant high reaction time and reduce movement velocity, which noted slow sensory processing and motor planning deficits . Indeed, DPN affects somatosensory input that is a proprioceptive and tactile sensation and motor output, that is, reaction time and muscle strength that contribute to abnormal postural control .
3.6. Characteristics of Gait Performance in the DPN
Temporal-spatial parameters were significantly affected in DPN group [34, 37]. There were smaller step length [39, 45, 47, 49, 54], reduced duration of single support [39, 47], higher duration of double support [45, 47, 51], decreased gait velocity [38, 42, 47, 49, 51], lowered cadence [47, 54], increased step width-to-step length ratio , increased step time and step time variability [43, 49], and greater gait variability [51, 54] in the DPN group compared to the control group. DPN group had a significant reduction in gait speed and single stance time and increased double support time in experimental of walking with EO, EC, and EO and narrow base of support (BOS) compared to the control group . The changes in this gait parameter were concluded as the factors of gait instability. Furthermore, DPN group significantly walked slower with shorter steps than control that causes increase in gait variability [13, 44].
Katoulis et al. (1997) demonstrated that alteration of gait parameters during walking among DPN group is a sequence of smaller maximum knee joint angle in the sagittal plane, higher maximum value of the anteroposterior forces, and higher maximum frontal plane ankle joint moment in DPN group compared to the normal group . In addition, lower range of motion at the hips (frontal plane, by 25%), hips and knees (transverse plane, 31% and 32%), ankles (sagittal plane, 22%), and first metatarsophalangeal joints (sagittal plane, 32%), with less foot rotation (24%) identified gait alterations in people with clinically severe peripheral neuropathy and related plantar foot ulcer history . The maximum value of the vertical component of GRF was found to be higher () in the two control groups compared with the DPN group .
Brown et al. (2014) also reported that maximum joint strengths of the knee were significantly less in both diabetic with and diabetic without DPN and less strength of ankle in DPN group compared to the control group. This author suggested that reduced strength of knee and ankle may cause a disturbance in perturbation response in balance, potentially increasing the risk of falling . Additionally, Sawacha et al. (2009) noted that trunk and lower limb joint mobility (in static and dynamic states) were more reduced in diabetics with and without DPN in each plane with DPN significantly demonstrating lower ranges of motion. Furthermore, both diabetic only and DPN groups showed significant reductions in each joint moment and velocity during gait . Gait variability and the coefficient of variation of gait velocity were significantly higher in the DPN group when barefoot walking over long distances. Furthermore, there was a high correlation between neuropathy severity and gait unsteadiness demonstrated during the barefoot walking/long walking distance condition . DPN with a history of fall demonstrated decreased speed, greater step width (SW), shorter step length (SL), and greater SW-to-SL ratio (SW : SL) on both surfaces compared to the DPN with no history of fall .
Gait in DPN is known as a conservative gait performance that occurs with high double support time, slow speed, and shorter steps as an attempt to keep stability in walking. This pattern is exhibited by DPN because of the reduction of proprioception sensory feedbacks from the lower extremities  and weakness of ankle plantar flexor and dorsiflexor muscles [41, 47, 49, 54]. Less dorsiflexion mobility and increased plantarflexion mobility were associated with a decrease in muscle strength of the dorsiflexors and plantiflexors, which may affect speed of the gait cycle . Moreover, the improper input of vestibular and visual systems also cause CNS to lose coordination in gait and may cause decreased gait speed and wider step length [51, 64]. Moreover, lack of sensation towards pain and pressure with repetition of high pressure on the forefoot during the push-off phase of gait may result in inflammation and then develop ulceration among neuropathies . Consequently, foot pain may cause antalgic gait with smaller steps in DPN patients . In fact, diminished sensory feedback with a further contribution of vision impairments, muscle weakness, and lack of neuromuscular control of distal joints in neuropathic patients results in increase of gait instability .
Additionally, diminished sensory information makes gait control more cognitively dependent in diabetic neuropathic persons than in control subject , due to the inability of the brain to respond on the dual tasking in walking . Type 2 DM is associated with the dysregulation of glycemic variability that might contribute to brain atrophy and cognitive impairments . Diabetes significantly causes impairment in information processing speed, memory, and attention with attribute effect on the mood states . Furthermore, individuals with diabetic retinopathy have shown reduced performance on cognitive tests of fluid intelligence, information processing speed, and ability to maintain attention and concentration . de Mettelinge et al. (2013) found older adults with diabetes with impaired cognitive function walked slower, took shorter strides, and had reduced double support time and increased gait variability compared with participants with intact cognitive function. Therefore, gait was further affected by reduced cognitive function, irrespective of the presence of neuropathy . Cognitive and attention impairments have an important role in the maintenance of balance and postural control as the brain gives the command to the limb muscles to stabilize the body . Thus, diabetic patients with cognitive and attention impairments will have balance deficit in walking and lead to a high risk of fall incidence. Relatively, study by Pan and Bai (2014) has reviewed appropriate balance training including proprioception, ankle strategy, and vestibular training as an intervention to reduce fall risk among elderly with DPN .
This systematic review evaluated 38 studies, investigating characteristics of postural control and gait performance impairments in 883 DPN participants. A huge number of articles published about this study reflect the importance of investigations and researches in this aspect. Pandemic prevalence of DPN and the well-known fall incidence require understanding of the postural control and gait performance changes which DPN patients are confronted with. Overall, this review has made an endeavor to state two points. First, DPN patients have been demonstrated with postural instability and gait imbalance that contribute to fall incidence. Lastly, DPN patients exhibited significant deficit in sensorimotor function, balance, and gait. Cognitive and attention impairments also have an important role in maintaining balance in gait performance as the brain gives the command to the limbs muscles to stabilize the body. Therefore, cognitive impairment will result in delay or slow response of dual tasking action. Consequently, this condition may lead to many deleterious effects if individuals with cognitive impairment do dual tasking in mobility such as walking or turning. Holistic managements are required to cope and prevent this problem. In particular, the practice of physiotherapy requires theory-based knowledge and evidence-based practice. Thus, further works in this aspect are crucial to providing evidence to support the need for balance and gait training that can be used by physiotherapists in the clinical practice as one of the primary strategies of rehabilitation in DPN patients.
There are no studies that noted on confounding factors of aging in stable posture and gait performance among DPN participants. Plus, the limited number of published studies regarding the dual cognitive or motor tasking on the gait performance in the DPN causes difficulty in reviewing the effect of DPN on the dual tasking in the gait performance. Future studies about the dual tasking on the gait performance should be considered.
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors thank the Ministry of Education, Malaysia, for funding the research project through the Niche Research Grant Scheme (NRGS-KPM) (Ref. no. 600-RMI/NRGS 5/3 (10/2013)) and the Research Management Institute (RMI), Universiti Teknologi MARA (UiTM), for the administrative support.
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