Abstract
Increasing evidence suggests that a high-velocity, low-amplitude (HVLA) thrust directed at a dysfunctional vertebral segment in people with subclinical spinal pain alters various neurophysiological measures, including somatosensory evoked potentials (SEPs). We hypothesized that an HVLA thrust applied to a clinician chosen vertebral segment based on clinical indicators of vertebral dysfunction, in short, segment considered as “relevant” would significantly reduce the N30 amplitude compared to an HVLA thrust applied to a predetermined vertebral segment not based on clinical indicators of vertebral dysfunction or segment considered as “non-relevant”. In this double-blinded, active-controlled, parallel-design study, 96 adults with recurrent mild neck pain, ache, or stiffness were randomly allocated to receiving a single thrust directed at either a segment considered as “relevant” or a segment considered as “non-relevant" in their upper cervical spine. SEPs of median nerve stimulation were recorded before and immediately after a single HVLA application delivered using an adjusting instrument (Activator). A linear mixed model was used to assess changes in the N30 amplitude. A significant interaction between the site of thrust delivery and session was found (F1,840 = 9.89, p < 0.002). Pairwise comparisons showed a significant immediate decrease in the N30 complex amplitude after the application of HVLA thrust to a segment considered “relevant” (− 16.76 ± 28.32%, p = 0.005). In contrast, no significant change was observed in the group that received HVLA thrust over a segment considered “non-relevant” (p = 0.757). Cervical HVLA thrust applied to the segment considered as “relevant” altered sensorimotor parameters, while cervical HVLA thrust over the segment considered as “non-relevant” did not. This finding supports the hypothesis that spinal site targeting of HVLA interventions is important when measuring neurophysiological responses. Further studies are needed to explore the potential clinical relevance of these findings.
Subject terms: Neuroscience, Sensorimotor processing, Health care, Musculoskeletal system, Neurophysiology
Introduction
A recent narrative review explored the effects of high-velocity, low-amplitude (HVLA) thrusts delivered to vertebral segments1. The article differentiated between HVLA thrusts applied to clinician chosen vertebral segment based on clinical indicators of vertebral dysfunction, in short segments considered as “relevant” vs HVLA thrusts delivered to predetermined vertebral segments not based on clinical indicators of vertebral dysfunction or segments considered as “non-relevant”1. Four of the eight included studies (i.e., 50%), which examined the effects of HVLA thrusts on segments considered as “non-relevant”, found a positive change in neuromuscular control measures1. In contrast, 14 of the 18 (i.e., 78%) of the studies which examined HVLA thrust to segment considered as “relevant” reported improvements in measures of neuromuscular control1. This raises the interesting question of whether the site of a HVLA thrust matters, and if so, how it might matter.
The term joint dysfunction is an umbrella term that can encompass anything from a infected joint to an arthritic join. However, for the purposes of this study the type of vertebral dysfunction we are talking about are the type of biomechanical lesions of the vertebral column that chiropractors and other manual therapists might apply their HVLA thrusts. Chiropractors do not usually randomly apply HVLA thrust at a segment of the spine. Usually, they will assess the spine for areas of the spine characterized by tight vertebral muscles, reduced intervertebral movement and tenderness to touch2. This type of joint dysfunction is often referred to as a vertebral subluxation in chiropractic profession3–6. Vertebral subluxation is a term recognised as biomechanical lesions of the vertebral column by the World Health Organization (ICD-10-CM code M99.1)7. However, other professions have used many other names, thus for the purposes of this study we will simply refer to it as joint dysfunction.
Neurophysiological measures are a novel and attractive means of examining the importance of applying HVLA vertebral thrusts to a segment considered as “relevant” vs segment considered as “non-relevant”. Electroencephalography (EEG) represents a low-cost, non-invasive, and safe neurophysiological measurement tool to examine brain activity related to HVLA vertebral thrusts administration. EEG enables virtually real-time assessment of central nervous system changes induced by HVLA thrusts and has been used in previous studies examining the changes of HVLA vertebral thrusts directed at segments considered as “relevant”8,9. Numerous other studies have also used EEG in combination with somatosensory stimulation before and after HVLA thrusts directed at segments considered as “relevant”8,10–13. These studies found that HVLA thrusts applied to segments considered as “relevant” alter the amplitudes of several SEP peaks, in particular, the N20 and N30 peaks8,10–13. The most consistent change following HVLA thrusts directed at vertebrae considered as “relevant” is a reduction in the amplitude of the N30 SEP peak8,10–13.
Animal studies have clearly shown that the contact site for an HVLA thrust can have a significant effect on the magnitude of sensory input arising from muscle spindles in the paraspinal muscles14. However, it is also important to take into account the known alterations that occur to these paraspinal muscles and other tissues around a dysfunctional vertebral segment in humans, which may influence the neurophysiological effects of an HVLA thrust directed at a “relevant” vs “non-relevant” vertebra. There are, for example, known maladaptive plastic changes in the deep paraspinal muscles following a spinal injury in animal models15–20. Rapid atrophy16,17, muscle fibrosis, extensive fatty infiltration, changes in muscle fibre types15,18–21, and even changes to muscle spindles22 have all been found within the deep paraspinal muscles at various time-frames after a spinal injury in various animal models. Multiple studies in humans support such maladaptive plastic changes also occur in humans when their spines dysfunction or are injured23–26. These local paraspinal muscle changes coincide with 'smudging' within the primary sensorimotor cortices27,28 and have led scientists to conclude that disrupted or reduced proprioceptive signaling from deep paraspinal muscles likely plays a pivotal role in driving the long-term cortical reorganization and changes in the top-down control of the sensorimotor systems, and that this plays a vital role in driving the recurrence and chronicity of spinal pain29. With such clear evidence that maladaptive dysfunction of the deep paraspinal muscles can occur15–20,22, an HVLA thrust directed at such a dysfunctional vertebral segment that is surrounded by poorly functioning paraspinal muscles could produce a different physiological response compared to an HVLA thrust applied to a fully functioning vertebral segment with healthy paraspinal muscles and tissues. To test this hypothesis, the present study aimed to compare the changes in response to HVLA thrust directed to a vertebral segment considered as “relevant” with the changes in response to an HVLA thrust directed to a segment considered as “non-relevant”, using the most consistent neurophysiological measure, i.e., the N30 SEP amplitude, in adults with subclinical neck pain. We hypothesized that the group receiving HVLA thrust directed at a “relevant” vertebra would show a significant decrease in N30 SEP complex amplitude8,10–13.
Methods
Design and setting
This study was a double-blinded, randomized, active-controlled, parallel study conducted at the New Zealand College of Chiropractic, New Zealand. The study was approved by the New Zealand Health and Disability Ethics Committees (19/CEN/202), and the protocol was prospectively registered with the Australian New Zealand Clinical Trials Registry (ACTRN12620000175976, 17/02/2020). All participants gave written informed consent, which conformed to the Declaration of Helsinki.
Participants
Participants were recruited through convenience sampling targeting the student and staff population at the New Zealand College of Chiropractic. Participants were included if they had a history of recurring and ongoing neck pain, aches, stiffness, or discomfort for which they had not sought treatment and were between the ages of 18 and 50 years. All participants were required to be pain-free at the time of the study. This requirement was intended to (1) avoid the confounding effect of current pain, (2) avoid any confounding effect from current or past treatment for more severe spinal problems and (3) ensure they were likely to actually need HVLA thrusts i.e., without a history of spinal problems there may not be any clinical reason to provide HVLA to their spines. Participants were excluded if they had no evidence of spinal dysfunction upon assessment by the chiropractor, had metal implants in their skull, had a history of severe neck pain (i.e., numeric pain rating scale ≥ 7/10), or had serious spinal pathology (i.e., malignancy, fracture, infection, hematoma, or cervical arterial dissection). If any of the participants had received previous chiropractic care for anything other than their neck pain, ache or tension, they were excluded if they had received HVLA thrusts within seven days of the day of data collection. Those who had received previous HVLA thrusts greater than seven days for anything other than their neck pain prior to data collection were not excluded.
Sample size calculations were made based on data from our unpublished pilot study wherein we investigated changes in SEPs before and after a single session of relevant HVLA thrust using a similar protocol. We calculated a required sample size of 84 using G*Power (version 3.1.9.4) based on the statistical t-tests (Means: Difference between two independent means [two groups]) to observe an Effect size d of 0.6212775 with α = 0.05, power β = 0.8, and an allocation ratio of 1. To compensate for the dropouts, we recruited 96 participants.
Randomization and blinding
Participants were allocated to either the “relevant” HVLA thrust or the “non-relevant” HVLA thrust group using an online randomization program (QMinim, Microsoft Corp., Redmond, WA, USA). A randomization sequence with 1:1 allocation was done with age (< 35 years or ≥ 35) and gender as a priori covariates. Participants and the investigators who collected or analyzed the data were blinded to group allocation, while the chiropractors who delivered the intervention were unable to be blinded due to the nature of the intervention. To ensure effective blinding of investigators, all recorded data were anonymized and given a code a priori. The investigators were kept blinded until the final analysis was completed.
Study procedure
Following an initial screening, each participant’s cervical spine was assessed by a registered and experienced (> 10 years) chiropractor for the presence and site of spinal dysfunction/subluxation (i.e., “relevant” sites)2. Eligible participants came in for a single session comprising of SEP recording before and immediately after the HVLA thrust intervention. During the session, the participants were seated comfortably in a chair and were asked to focus their gaze on a fixed target on the wall and be relaxed to minimize the contamination of EEG signals.
Somatosensory evoked potentials
SEPs were evoked by stimulating the median nerve of the dominant hand using electrical pulses from an electrical stimulator (Digitimer DS7AH, Hertfordshire, UK). After positioning the stimulating electrodes (Neuroline 700, AMBU A/S, Ballerup, DK) on the wrist, the intensity was slowly increased until the motor threshold, the lowest current intensity that produces a visible twitch of the thumb, was reached. A total of 1000 monophasic electrical pulses at a frequency of 2.3 Hz having 0.2 ms width were given to the median nerve.
EEG
The EEG from 25 channels (frontal and frontal-central: FP1, FPz, FP2, F7, F3, Fz, F4, F8, FC5, FC1, FC2, FC6, AF7, AF3, AF4, AF8, F5, F1, F2, F6, FC3, FCZ, FC4, FT7, FT8) was recorded at a sampling rate of 2048 Hz using REFA amplifier (TMSi, Twente, NL). The ground electrode was placed at AFz. The electrode impedance was kept below 10 kΩ. During EEG recording, participants were asked to reduce eye blinks, eye movements and facial movements. Offline analysis of the EEG data was performed using custom scripts in MATLAB 2020a (The MathWorks, Inc., Natick, MA, USA) that utilised EEGLAB (version 2019)30, ERPLAB (version 2019)31, FieldTrip (version 20180912)32, and MATLAB functions33. At the start and end of the EEG recording, an additional 10 s of data was recorded to minimize the filtering artefacts in preprocessing. The standardized early-stage EEG processing pipeline (PREP) pipeline34 was utilized to determine faulty channels, discard line noise and acquire the average referenced data.
Interventions
HVLA thrust directed at cervical vertebrae considered as “relevant”
We defined the “relevant” HVLA thrust intervention as a high-velocity, low-amplitude thrust directed at a dysfunctional cervical spinal segment. The chiropractor determined each cervical spinal site to be “relevant” (i.e. dysfunctional) based on an examination which identified restricted intervertebral motion and pain provocation with motion palpation and palpable, asymmetric local hypertonic musculature, and any blocked or unusual joint play/end-feel of the spinal joints1,35. Participants in this group were eligible to have more than one site of dysfunction, yet only a single site was chosen for the HVLA thrust. In the instance of multiple sites of dysfunction, the chiropractor always defaulted to choose the more superior/cranial HVLA thrust to establish consistency with the HVLA thrust methodology.
The “relevant” HVLA thrust intervention involved the chiropractor delivering a single administration of HVLA thrust with an Activator instrument on the site of “relevant” cervical dysfunction (Fig. 1). The Activator instrument is a hand-held device that delivers fast, precise, and low-force thrust to the spine36. This device was preferred over manual delivery of HVLA thrust for the purposes of consistency with HVLA thrust administration, as its use would reduce the amount of variability in HVLA thrust parameters (i.e., force, amplitude, and duration).
HVLA thrusts directed at cervical vertebrae considered as “non-relevant”
The “non-relevant” HVLA thrust intervention refers to a thrust directed at a non-dysfunctional spinal segment that had no signs of dysfunction upon examination by a chiropractor1. This intervention involved the delivery of a single HVLA thrust application via the Activator instrument. The non-dysfunctional vertebra targeted was always the one that was furthest away from the dysfunctional vertebra, yet within the cervical spinal region. In the event that there was more than one site of cervical dysfunction, the chiropractor avoided providing HVLA thrust at any site of dysfunction yet aimed to be furthest from the relevant segment. HVLA thrust was delivered by the same chiropractor who provided the relevant HVLA thrust intervention to ensure consistency.
Both groups received HVLA thrusts directed at a vertebra in the upper cervical spine. The main reason for this is that there are differences in the physiology of the upper and lower cervical spine that could introduce confounding variables that we wanted to avoid. Unlike the lower cervical spine, where muscles span multiple segments, the upper cervical spine has many small deep paraspinal muscles that cross individual spinal segments. Additionally, the deep paraspinal muscles of the upper cervical spine are rich in muscle spindles, which a crucial for mechanoreception and known to respond to the HVLA thrust. Therefore, to maintain as much consistency in the intervention level across groups the most cephalic segment was chosen for both groups, i.e., the most cephalic segment that either was or was not deemed dysfunctional.
Data processing
Most of the GUIs and codes used were the same as in Navid et al.8,33. The mastoid channel ipsilateral to the dominant hand was used as the reference channel. The data was filtered with a 2nd order Butterworth band-pass filter with a frequency range from 1 to 500 Hz. SEPs were extracted from − 100 ms to 150 ms with respect to the stimulus. The pre-stimulus period was used for baseline correction. The post-stimulus period used was 150 ms and entails the cortex's response this study concentrates on. Contralaterally to the dominant hand, the trial-rejected, averaged, eyeblink-cleaned, and noise-cleaned event-related potential of either F3 for right-handed or F4 for left-handed participants was plotted and scanned for the components P22 and N30. This was done with a GUI for component marking.
Statistical analysis
A linear mixed model was used to identify the effects of intervention site selection on the N30 amplitude. The intervention (“relevant” and “non-relevant”) and session (pre and post) were used as fixed factors. The between-paticipant variance was estimated using random intercept in the model. The models were implemented using lme4 package (version 1.1.23) in R (version 3.5.1)37. The pairwise comparisons were obtained using the emmeans package version 1.4.838, adjusted for multiple comparisons using Tukey's honestly significant difference test. The significance threshold was set at p < 0.05.
Results
Ninety-six participants met the eligibility criteria and were enrolled in the study between February 2020 and March 2020. The participant recruitment flow diagram is given in Fig. 2. The demographic characteristics of included participants in each group are given in Table 1.
Table 1.
Variables | HVLA thrust applied to segments considered as “relevant” | HVLA thrust applied to segments considered as “non-relevant” |
---|---|---|
Gender | ||
Male, number (%) | 20 (47) | 17 (40) |
Female, number (%) | 23 (53) | 26 (60) |
Age, years (mean ± SD) | 24.41 ± 5.05 | 24.83 ± 5.57 |
SD standard deviation.
HVLA thrust site selection
The cervical spinal site of HVLA thrust administration in the “relevant” HVLA thrust group was most often C1 (n = 25), followed by C2 (n = 14) and C3 (n = 4). No patient in this group received HVLA thrust at a cervical spinal level caudal to C3. In the “non-relevant” HVLA thrust group, the most common site of HVLA thrust was C3 (n = 17), followed by C2 (n = 16), C1 (n = 8), C5 (n = 1), and C6 (n = 1). In the “non-relevant” HVLA thrust group, the maximum distance from the dysfunctional segment to the non-dysfunctional, manipulated segment was two vertebral segments.
N30 complex amplitude
The mixed model showed a significant interaction between the site of intervention and session (F1,84 = 9.89, p = 0.002) (Table 2).
Table 2.
F | Df | Df.res | Pr (> F) | |
---|---|---|---|---|
Intervention | 1.28 | 1 | 84 | 0.262 |
Session | 3.06 | 1 | 84 | 0.084 |
Intervention: session | 9.89 | 1 | 84 | 0.002 |
Pairwise comparisons (Table 3) revealed that there was a significant decrease in the N30 amplitude immediately after HVLA thrust was applied to segments considered as “relevant” (N30 complex difference % = − 16.76 ± 28.32%, p = 0.005), whereas the N30 amplitude displayed a non-significant increase after HVLA thrust was applied to segments considered as “non-relevant” (N30 complex difference % = 19.58 ± 55.09%, p = 0.0757).
Table 3.
Contrast | Estimate ± SE | 95% CI | t. ratio | p-value |
---|---|---|---|---|
“Non-relevant” post – “non-relevant” pre | 0.12 ± 0.12 | [− 0.19, 0.43] | 0.99 | 0.757 |
“Relevant” post – “relevant” pre | − 0.41 ± 0.12 | [− 0.72, − 0.10] | − 3.46 | 0.005 |
Figure 3 shows the distribution and differences of the N30 amplitude before and immediately after the interventions such that the N30 amplitude significantly decreased immediately after HVLA thrust was applied to segment considered as relevant.
Discussion
This randomized controlled trial was the first study to compare the immediate changes in response to the application of an HVLA thrust at a cervical vertebra considered as “relevant” versus an HVLA thrust directed at a cervical vertebra considered as “non-relevant” on human brain activity as measured by the N30 SEP complex amplitude. The present study found a significant decrease in the N30 SEP complex amplitude (about − 17%) immediately after an HVLA thrust applied to a cervical segment considered as “relevant” (i.e., a dysfunctional segment), whereas a non-significant increase in the N30 SEP complex amplitude was recorded immediately after an HVLA thrust applied to a cervical segment considered as “non-relevant” (i.e., a non-dysfunctional segment). According to previous research, a decrease in the N30 SEP complex amplitude is suggestive of changes in sensorimotor function occurring within the prefrontal cortex12. Therefore, the current study findings suggest that applying the HVLA thrust at a dysfunctional segment may induce greater level of sensorimotor integrative changes than applying an HVLA thrust at a non-dysfunctional site.
Comparison with the literature
The present study adds to the limited research regarding HVLA thrust site selection39. Studies using animal models have demonstrated one can maximize proprioceptive afferent inputs and muscle spindle responses coming from a specific spinal segment when HVLA thrusts are directed at that same spinal segment with velocities greater than 20–30 mm/s and with thrust rates greater than 300N/s14,40. In one animal study, the authors created spinal dysfunction with a facet fixation model41 and found that such spinal fixations altered paraspinal sensory responses during “relevant” HVLA thrusts at these levels. However, there is paucity of evidence of differences in neurophysiologic changes in humans following HVLA thrust applied to segments considered as “relevant” versus HVLA thrust applied to segments considered as “non-relevant”. The current study, therefore, adds to the limited research regarding HVLA thrust site selection in the cervical spine in humans. The present study has the potential to offer insights into practical decision-making for chiropractors when choosing between HVLA thrust at one cervical site versus another. The current findings support that chiropractors' selection of which cervical site to apply HVLA thrust may be relevant with respect to subsequent sensorimotor changes. A recent systematic review reported that spinal manipulation applied to suspected relevant sites did not yield a superior result for clinical outcome measures compared to spinal manipulation applied to non-relevant sites in nine of 10 included studies39. However, the study was limited in that the included studies demonstrated variability in what constituted a relevant site of spinal manipulation, and in some instances, both the treatment and control groups received a potentially relevant HVLA thrust. In three of the included studies42–44, two different HVLA techniques were compared, yet potentially targeted dysfunctional, hypomobile, or symptomatic spinal segments, resulting in improved pain and disability outcomes. Although the between-group HVLA techniques varied, the segment(s) to which HVLA thrust was applied could represent relevant sites42–44.
Two of the nine studies45,46 compared two groups receiving HVLA thrust manipulation of spinal levels pre-determined by the experimental design rather than clinical context. For example, Romero del Rey et al.45 compared HVLA manipulation of either C1-C2 with HVLA thrust manipulation C3-4, C7-T1 and T5-6, while Bautista-Aguirre et al.46 compared HVLA thrust manipulation of C7 with HVLA manipulation of T1. In both of these studies, the sites of HVLA thrusts were therefore not chosen according to patient-specific clinical findings; hence all groups potentially received non-relevant HVLA manipulations45,46. In these studies, there were no significant between-group differences in pain outcome scores, pressure pain thresholds, or upper extremity grip strength.
Four of the nine studies47–50 tested whether applying an HVLA thrust to the most tender lumbar47,48 or cervical49 segment, or hypomobile segment based on end play assessment50 (i.e., HVLA thrust on “relevant” vertebral segment would lead to better clinical outcomes compared to applying a general HVLA thrust at a pre-determined cervical or thoracic spinal segment (i.e., HVLA thrust on “non-relevant” vertebral segment). In all four of these studies, there were no differences in pain scores (pain intensity, pressure pain threshold, disability and global perceived change) or stiffness after the relevant HVLA lumbar or cervical segment manipulation compared with the non-relevant HVLA thoracic manipulation47–49 or cervical manipulation50. For all HVLA groups, the pain measures improved47–49. In the tenth study51, the authors compared an HVLA thrust aiming to improve the mobility of a dysfunctional (hypomobile) thoracic segment with a less specific thoracic HVLA manipulation provided in the direction of normal mobility. In this study, the relevant thrust significantly reduced cervical pain compared to the non-relevant HVLA manipulative thrust51. Given the above limited and conflicting findings, it remains unclear whether it is therapeutically important to aim to apply HVLA thrust to a “relevant” or “non-relevant” vertebral site when treating spinal pain or dysfunction.
Previous measures used in studies examining the relevance of HVLA thrusts site selection have had inherent limitations. The most commonly measured outcomes, such as pain intensity, range of motion, or disability, may be influenced by patient expectations or may not be expected to change with only a single application of HVLA vertebral thrusts39. Few studies have used imaging tests to examine this question, and while study designs using radiography to examine changes in intervertebral motion may be useful52, these are hindered by the necessity of exposure of participants to ionizing radiation. Newer magnetic resonance imaging studies (e.g. examining disc diffusion) are promising53 but may be limited by cost.
Possible mechanisms
The present findings provide evidence that cervical HVLA thrust directed to a vertebral segment considered as “relevant” produces distinct neurophysiological changes evident via EEG via decreased N30 SEP complex amplitude. Previous studies have shown decreases in N30 SEP peak amplitudes following relevant HVLA thrust in subclinical spinal pain populations10,11,54. This amplitude reduction is attributed to changes in somatosensory processing at the cortical level, particularly within the prefrontal cortex12. Other neural generators of the N30 amplitude complex include the primary sensory cortex, basal ganglia, thalamus, premotor areas, and primary motor cortex55–61. The frontal N30 peak is thought to reflect early sensorimotor integration62,63.
Drawing from the insights in the literature on animal fixation model41, where spinal fixations were observed to modify sensory responses in paraspinal muscles during “relevant” HVLA thrusts, along with our current findings, we infer that the neurophysiological mechanisms associated with these “relevant” HVLA thrusts likely involve the activation of these paraspinal proprioceptive sensory responses, particularly in the presence of dysfunction. Paraspinal tissue dysfunction has, as discussed earlier, been noted to occur following a spinal injury15–20. This paraspinal tissue dysfunction includes rapid atrophy of deep paraspinal muscles16,17, deep paraspinal muscle fibrosis, extensive fatty infiltration of such muscles, changes in muscle fibre types within such muscles15,18–21 and even changes to muscle spindles themselves within the deep paraspinal muscles at the injured segment22. These local paraspinal muscle changes coincide with 'smudging' within the primary sensorimotor cortices27,28 and have led scientists to conclude that disrupted or reduced proprioceptive signalling from deep paraspinal muscles likely plays a pivotal role in driving the long-term cortical reorganisation and changes in the top-down control of the sensorimotor systems and that this plays a vital role in driving the recurrence and chronicity of back pain29. As applying an HVLA thrust is known to activate muscle spindles in surrounding paraspinal muscles14,40, it, therefore, seems plausible that applying the HVLA thrust at such dysfunctional segments could result in different clinical effects, as compared to applying an HVLA manipulation to a healthy vertebral segment, with non-fibrotic, non-fatty infiltrated paraspinal segments. The current study would support this notion.
Clinical and research implications
The decrease in N30 amplitude noted in the present study suggests that the neurological activity within the network responsible for generating the N30 component (i.e., basal ganglia, thalamus, premotor cortex, prefrontal cortex and motor-cortex) decreases in response to HVLA thrust applied to cervical segment considered as “relevant”55–61. However, in light of the findings by Lelic et al.12 that showed when relevant HVLA thrusts were applied to research participants, the decrease in the N30 SEP complex amplitude appeared to reflect mainly changes in sensorimotor function occurring within the prefrontal cortex, the decrease in the N30 SEP complex amplitude found in the current study most likely also reflects alterations in sensorimotor function within the prefrontal cortex. Accordingly, relevant HVLA thrust may influence sensorimotor integration and related neuromuscular functions. Future studies can explore the clinical relevance of these findings.
Strengths, limitations and future research
A strength of the study was the large sample size which supports the fact that is unlikely that the observed reduction in N30 complex amplitude in the relevant HVLA thrust group occurred by chance. Limitations of the study include that a single cervical HVLA thrust application may not reflect the long-term care performed in clinical practice. However, this protocol design was intended to avoid repeatedly exposing the “non-relevant” HVLA thrust group to HVLA thrust directed at the non-dysfunctional segment for a longer period. Another limitation is that the changes in N30 SEP complex amplitudes were only measured immediately after one thrust application and not several time periods after the HVLA thrust application. Therefore, it is unclear how long the effects on N30 complex amplitude last after the HVLA thrust.
There are several potentially important differences between spinal regions that preclude our ability to generalize the current study findings to other regions of the spine (i.e., thoracic, lumbar, or sacroiliac joints). Importantly, the density of mechanoreceptors is higher in the cervical region64,65. HVLA thrust is known to activate muscle spindles in surrounding paraspinal muscles14,40. Therefore, mechanoreceptors such as muscle spindles are believed to sense the impulse provided by HVLA thrust and trigger subsequent neurophysiological changes1 and thus may produce greater responses, as evident via EEG. The height of cervical vertebrae and, therefore, the corresponding motion segments are smaller, thus potentially requiring a greater degree of precision or lower degree of force application with HVLA thrust. There is also a difference in innervation; for example, cranial nerve five has an anatomical relationship to the upper cervical spine and may be implicated in cases of neck pain66, whereas cranial nerves are unrelated to the other spinal regions. The current study should therefore be replicated in other regions of the spine to determine if the findings are consistent or dependent upon the spinal region.
The results of this study may not be generalizable to other methods of HVLA thrust administration. As the current study used an instrument to administer HVLA thrust (Activator), the delivery of force could be both lower in magnitude and/or more localized to a specific vertebrae or motion segment. While little is known about this topic, it is possible that other forms of HVLA thrust applied manually could lead to a broader biomechanical effect on the spinal target53 and potentially a less predictable neurophysiological response. However, in the current study, the HVLA thrust delivered via the Activator instrument led to a significant decrease in the N30 SEP peak complex, similar to what has been found following HVLA thrusts delivered manually as well8,10–13. In these previous studies, HVLA thrusts were likewise targeted at dysfunctional segments, thus representing HVLA thrusts. The current study did not measure several clinical variables, such as baseline or post-HVLA thrust changes in pain severity or range of motion. Accordingly, it is not known if the observed changes in N30 amplitude correlate with measures of clinical improvement such as reduced pain, pain pressure thresholds, reduced stiffness, or improved mobility. Future studies could replicate the present design while including clinical outcomes alongside EEG. In addition, a longitudinal design with multiple HVLA thrust interventions may enable the examination of potential long-term or progressive changes in neurophysiological measures.
The present study may only be generalizable to younger adults as the mean age for each group was 24 to 25 years. It is unknown if age-related degenerative changes in the cervical spine would interfere with mechanoreception related to HVLA thrust or the observed subsequent neurophysiological changes. In addition, the current study may not be generalizable to people with severe neck pain, such as cervical radiculopathy or disc herniation, as only individuals with milder symptoms were included. The current study could be replicated in an older population or individuals with more severe neck pain syndromes for comparison.
Regarding the blinding of the chiropractor providing the HVLA thrust, it could be noted that an alternative approach could have involved a different chiropractor conducting the assessments on all participants and subsequently informing the treating chiropractor about the specific site for the HVLA thrust without disclosing its relevance. However, for the sake of maintaining consistency and minimizing potential variability in technique application, the same chiropractor was deliberately chosen to perform both the assessments and the HVLA thrust intervention. This decision was further supported by the utilization of standardized instrument-assisted thrusting with Activator, which aimed to reduce potential sources of variation. Despite this, it is important to acknowledge that not blinding the treating chiropractor may introduce a source of bias. In order to mitigate potential bias, we took measures to blind both the participants and the assessors involved in the study. This additional step was implemented to enhance the rigor and integrity of our methodology.
Conclusion
This randomized controlled trial was the first to investigate the immediate changes in response to an HVLA thrust site selection in the cervical spine using a neurophysiological EEG outcome measure and found evidence that HVLA thrust directed at a cervical site considered as dysfunctional significantly reduces N30 amplitude immediately after such intervention. In contrast, HVLA thrust directed at a cervical site considered as non-dysfunctional causes no significant change. The present findings suggest that clinicians' selection of where to apply cervical HVLA thrust is likely to be relevant with regards to affecting the subsequent sensorimotor response. Further research is needed to correlate these changes with clinical outcomes, repeat the study design in other spinal regions and patient populations, and examine both potential changes at short, medium and long terms, as well as the longitudinal response to multiple HVLA thrust sessions.
Acknowledgements
The authors thank all the students and staff from the New Zealand College of Chiropractic who volunteered to participate in this study.
Author contributions
Conceptualisation: I.K.N., K.H., H.H.; data curation: I.K.N., C.M., I.A.; formal analysis: M.S.N., C.M.; funding acquisition: H.H.; investigation: I.K.N., C.M., I.A.; methodology: M.S.N., C.M.; project administration: I.K.N., M.S.N., K.H., H.H.; resources: I.K.N., K.H., H.H.; software, M.S.N., C.M.; supervision: I.K.N., M.S.N., I.A.,K.H., H.H.; validation: M.S.N., C.M.; visualisation: M.S.N.; writing—original draft preparation, I.K.N.,M.S.N., C.M., N.K., R.J.T., K.H.; writing—review and editing, I.K.N., M.S.N., C.M., I.A., N.K., K.H., R.J.T., H.H.
Funding
This study was funded by Australian Spinal Research Foundation (ASRF) (Grant no. TRG2019-3) and the Centre for Chiropractic Research Supporters Program at the New Zealand College of Chiropractic.
Data availability
The numerical data supporting the conclusions of this article will be made available by the authors without undue reservation. Interested individuals can obtain this data by making a reasonable request to the corresponding author, Imran Khan Niazi. The Local Ethics Committee adhering to local data protection laws, does not allow the sharing of individuals’ raw data.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
These authors contributed equally: Imran Khan Niazi and Muhammad Samran Navid.
Contributor Information
Imran Khan Niazi, Email: Imran.niazi@nzchiro.co.nz.
Heidi Haavik, Email: Heidi.haavik@nzchiro.co.nz.
References
- 1.Haavik H, et al. The contemporary model of vertebral column joint dysfunction and impact of high-velocity, low-amplitude controlled vertebral thrusts on neuromuscular function. Eur. J. Appl. Physiol. 2021;121:2675–2720. doi: 10.1007/s00421-021-04727-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Triano JJ, et al. Review of methods used by chiropractors to determine the site for applying manipulation. Chiropr. Man. Ther. 2013;21:36. doi: 10.1186/2045-709X-21-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Cooperstein, R., Haneline, M. & Young, M. In Association of Chriopractic Colleges Educational Conference - Research Agenda Conference (ACC-RAC) (The Journal of Chiropractic Education, Vol. 24(1), 88, Las Vegas, Nevada, United States, 2010).
- 4.Cooperstein R, Young M, Haneline M. Interexaminer reliability of cervical motion palpation using continuous measures and rater confidence levels. J. Can. Chiropr. Assoc. 2013;57:156. [PMC free article] [PubMed] [Google Scholar]
- 5.Niazi IK, et al. Changes in H-reflex and V-waves following spinal manipulation. Exp. Brain Res. 2015;233:1165–1173. doi: 10.1007/s00221-014-4193-5. [DOI] [PubMed] [Google Scholar]
- 6.Holt K, et al. Interexaminer reliability of a multidimensional battery of tests used to assess for vertebral subluxations. Chiropr. J. Aust. 2018;46:100–117. [Google Scholar]
- 7.Organization, W. H. WHO guidelines on basic training and safety in chiropractic (2005).
- 8.Navid MS, et al. Investigating the effects of chiropractic spinal manipulation on EEG in stroke patients. Brain Sci. 2020;10:253. doi: 10.3390/brainsci10050253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Navid MS, et al. The effects of chiropractic spinal manipulation on central processing of tonic pain-a pilot study using standardized low-resolution brain electromagnetic tomography (sLORETA) Sci. Rep. 2019;9:1–12. doi: 10.1038/s41598-019-42984-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Haavik-Taylor H, Murphy B. Cervical spine manipulation alters sensorimotor integration: A somatosensory evoked potential study. Clin. Neurophysiol. 2007;118:391–402. doi: 10.1016/j.clinph.2006.09.014. [DOI] [PubMed] [Google Scholar]
- 11.Haavik Taylor H, Murphy B. The effects of spinal manipulation on central integration of dual somatosensory input observed following motor training: A crossover study. J. Manip. Physiol. Ther. 2010;33:261–272. doi: 10.1016/j.jmpt.2010.03.004. [DOI] [PubMed] [Google Scholar]
- 12.Lelic D, et al. Manipulation of dysfunctional spinal joints affects sensorimotor integration in the prefrontal cortex: A brain source localization study. Neural Plast. 2016;2016:3704964. doi: 10.1155/2016/3704964. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Haavik H, et al. Impact of spinal manipulation on cortical drive to upper and lower limb muscles. Brain Sci. 2017;7:2. doi: 10.3390/brainsci7010002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Reed WR, Long CR, Kawchuk GN, Pickar JG. Neural responses to the mechanical characteristics of high velocity, low amplitude spinal manipulation: Effect of specific contact site. Man. Ther. 2015;20:797–804. doi: 10.1016/j.math.2015.03.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Brown SH, et al. ISSLS prize winner: Adaptations to the multifidus muscle in response to experimentally induced intervertebral disc degeneration. Spine. 2011;36:1728–1736. doi: 10.1097/BRS.0b013e318212b44b. [DOI] [PubMed] [Google Scholar]
- 16.Hodges P, Holm AK, Hansson T, Holm S. Rapid atrophy of the lumbar multifidus follows experimental disc or nerve root injury. Spine. 2006;31:2926–2933. doi: 10.1097/01.brs.0000248453.51165.0b. [DOI] [PubMed] [Google Scholar]
- 17.Hodges PW, Galea MP, Holm S, Holm AK. Corticomotor excitability of back muscles is affected by intervertebral disc lesion in pigs. Eur. J. Neurosci. 2009;29:1490–1500. doi: 10.1111/j.1460-9568.2009.06670.x. [DOI] [PubMed] [Google Scholar]
- 18.Hodges PW, et al. Can proinflammatory cytokine gene expression explain multifidus muscle fiber changes after an intervertebral disc lesion? Spine. 2014;39:1010–1017. doi: 10.1097/brs.0000000000000318. [DOI] [PubMed] [Google Scholar]
- 19.Hodges PW, et al. Multifidus muscle changes after back injury are characterized by structural remodeling of muscle, adipose and connective tissue, but not muscle atrophy: Molecular and morphological evidence. Spine. 2015;40:1057–1071. doi: 10.1097/brs.0000000000000972. [DOI] [PubMed] [Google Scholar]
- 20.James G, et al. Mesenchymal stem cell treatment of intervertebral disc lesion prevents fatty infiltration and fibrosis of the multifidus muscle, but not cytokine and muscle fiber changes. Spine. 2016;41:1208–1217. doi: 10.1097/brs.0000000000001669. [DOI] [PubMed] [Google Scholar]
- 21.Cooley JR, et al. Relationships between paraspinal muscle morphology and neurocompressive conditions of the lumbar spine: A systematic review with meta-analysis. BMC Musculoskelet. Disord. 2018;19:351. doi: 10.1186/s12891-018-2266-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.James G, et al. Muscle spindles of the multifidus muscle undergo structural change after intervertebral disc degeneration. Eur. Spine J. 2022;31:1879–1888. doi: 10.1007/s00586-022-07235-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Shahidi B, et al. Lumbar multifidus muscle degenerates in individuals with chronic degenerative lumbar spine pathology. J. Orthop. Res. 2017;35:2700–2706. doi: 10.1002/jor.23597. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Kang J-I, Kim S-Y, Kim J-H, Bang H, Lee I-S. The location of multifidus atrophy in patients with a single level, unilateral lumbar radiculopathy. Ann. Rehabil. Med. 2013;37:498–504. doi: 10.5535/arm.2013.37.4.498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Stevens S, Agten A, Timmermans A, Vandenabeele F. Unilateral changes of the multifidus in persons with lumbar disc herniation: A systematic review and meta-analysis. Spine J. 2020;20:1573–1585. doi: 10.1016/j.spinee.2020.04.007. [DOI] [PubMed] [Google Scholar]
- 26.Faur C, Patrascu JM, Haragus H, Anglitoiu B. Correlation between multifidus fatty atrophy and lumbar disc degeneration in low back pain. BMC Musculoskelet. Disord. 2019;20:1–6. doi: 10.1186/s12891-019-2786-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Burns E, Chipchase LS, Schabrun SM. Primary sensory and motor cortex function in response to acute muscle pain: A systematic review and meta-analysis. Eur. J. Pain. 2016;20:1203–1213. doi: 10.1002/ejp.859. [DOI] [PubMed] [Google Scholar]
- 28.Chang W-J, et al. Sensorimotor cortical activity in acute low back pain: A cross-sectional study. J. Pain. 2019;20:819–829. doi: 10.1016/j.jpain.2019.01.006. [DOI] [PubMed] [Google Scholar]
- 29.Meier ML, Vrana A, Schweinhardt P. Low back pain: The potential contribution of supraspinal motor control and proprioception. Neuroscientist. 2018 doi: 10.1177/1073858418809074. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Delorme A, Makeig S. EEGLAB: An open source toolbox for analysis of single-trial EEG dynamics including independent component analysis. J. Neurosci. Methods. 2004;134:9–21. doi: 10.1016/j.jneumeth.2003.10.009. [DOI] [PubMed] [Google Scholar]
- 31.Lopez-Calderon J, Luck SJ. ERPLAB: An open-source toolbox for the analysis of event-related potentials. Front. Hum. Neurosci. 2014;8:213. doi: 10.3389/fnhum.2014.00213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Oostenveld R, Fries P, Maris E, Schoffelen JM. FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data. Comput. Intell. Neurosci. 2011;2011:156869. doi: 10.1155/2011/156869. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Navid MS, Niazi IK, Lelic D, Drewes AM, Haavik H. The effects of filter’s class, cutoff frequencies, and independent component analysis on the amplitude of somatosensory evoked potentials recorded from healthy volunteers. Sensors. 2019;19:2610. doi: 10.3390/s19112610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Bigdely-Shamlo N, Mullen T, Kothe C, Su KM, Robbins KA. The PREP pipeline: Standardized preprocessing for large-scale EEG analysis. Front. Neuroinform. 2015;9:16. doi: 10.3389/fninf.2015.00016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Triano JJ, et al. Review of methods used by chiropractors to determine the site for applying manipulation. Chiropr. Man. Ther. 2013;21:36. doi: 10.1186/2045-709x-21-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Fuhr AW, Menke JM. Status of activator methods chiropractic technique, theory, and practice. J. Manip. Physiol. Ther. 2005;28:e1–e20. doi: 10.1016/j.jmpt.2005.01.001. [DOI] [PubMed] [Google Scholar]
- 37.R: A language and environment for statistical computing (R Foundation for Statistical Computing, 2013).
- 38.Emmeans: Estimated Marginal Means, aka Least-Squares Means v. 1.4. 8 (cran.r-project.org, 2022).
- 39.Nim CG, et al. The importance of selecting the correct site to apply spinal manipulation when treating spinal pain: Myth or reality? A systematic review. Sci. Rep. 2021;11:23415. doi: 10.1038/s41598-021-02882-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Reed WR, Cao D-Y, Long CR, Kawchuk GN, Pickar JG. Relationship between biomechanical characteristics of spinal manipulation and neural responses in an animal model: Effect of linear control of thrust displacement versus force, thrust amplitude, thrust duration, and thrust rate. Evid. Based Complement. Altern. Med. 2013;2013:492039. doi: 10.1155/2013/492039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Reed WR, Long CR, Pickar JG. Effects of unilateral facet fixation and facetectomy on muscle spindle responsiveness during simulated spinal manipulation in an animal model. J. Manip. Physiol. Ther. 2013;36:585–594. doi: 10.1016/j.jmpt.2013.08.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Karas S, et al. The effect of direction specific thoracic spine manipulation on the cervical spine: A randomized controlled trial. J. Man. Manip. Ther. 2018;26:3–10. doi: 10.1080/10669817.2016.1260674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Cleland JA, et al. Comparison of the effectiveness of three manual physical therapy techniques in a subgroup of patients with low back pain who satisfy a clinical prediction rule: A randomized clinical trial. Spine. 2009;34:2720–2729. doi: 10.1097/BRS.0b013e3181b48809. [DOI] [PubMed] [Google Scholar]
- 44.Sutlive TG, et al. Comparison of short-term response to two spinal manipulation techniques for patients with low back pain in a military beneficiary population. Mil. Med. 2009;174:750–756. doi: 10.7205/MILMED-D-02-4908. [DOI] [PubMed] [Google Scholar]
- 45.Romero del Rey R, Saavedra Hernández M, Rodríguez Blanco C, Palomeque del Cerro L, Alarcon Rodriguez R. Short-term effects of spinal thrust joint manipulation on postural sway in patients with chronic mechanical neck pain: A randomized controlled trial. Disabil. Rehabil. 2020;44:1–7. doi: 10.1080/09638288.2020.1798517. [DOI] [PubMed] [Google Scholar]
- 46.Bautista-Aguirre F, et al. Effect of cervical vs. thoracic spinal manipulation on peripheral neural features and grip strength in subjects with chronic mechanical neck pain: A randomized controlled trial. Eur. J. Phys. Rehabil. Med. 2017;53:333–341. doi: 10.23736/S1973-9087.17.04431-8. [DOI] [PubMed] [Google Scholar]
- 47.de Oliveira RF, Costa LOP, Nascimento LP, Rissato LL. Directed vertebral manipulation is not better than generic vertebral manipulation in patients with chronic low back pain: A randomised trial. J. Physiother. 2020;66:174–179. doi: 10.1016/j.jphys.2020.06.007. [DOI] [PubMed] [Google Scholar]
- 48.de Oliveira RF, Liebano RE, Costa LDCM, Rissato LL, Costa LOP. Immediate effects of region-specific and non–region-specific spinal manipulative therapy in patients with chronic low back pain: A randomized controlled trial. Phys. Ther. 2013;93:748–756. doi: 10.2522/ptj.20120256. [DOI] [PubMed] [Google Scholar]
- 49.Martínez-Segura R, De-La-Llave-Rincón AI, Ortega-Santiago R, Cleland JA, Fernandez-De-Las-Penas C. Immediate changes in widespread pressure pain sensitivity, neck pain, and cervical range of motion after cervical or thoracic thrust manipulation in patients with bilateral chronic mechanical neck pain: A randomized clinical trial. J. Orthop. Sports Phys. Ther. 2012;42:806–814. doi: 10.2519/jospt.2012.4151. [DOI] [PubMed] [Google Scholar]
- 50.Haas M, et al. Efficacy of cervical endplay assessment as an indicator for spinal manipulation. Spine. 2003;28:1091–1096. doi: 10.1097/01.BRS.0000067276.16209.DB. [DOI] [PubMed] [Google Scholar]
- 51.Karas S, Olson Hunt MJ. A randomized clinical trial to compare the immediate effects of seated thoracic manipulation and targeted supine thoracic manipulation on cervical spine flexion range of motion and pain. J. Man. Manip. Ther. 2014;22:108–114. doi: 10.1179/2042618613Y.0000000052. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Anderst WJ, et al. Intervertebral kinematics of the cervical spine before, during, and after high-velocity low-amplitude manipulation. Spine J. 2018;18:2333–2342. doi: 10.1016/j.spinee.2018.07.026. [DOI] [PubMed] [Google Scholar]
- 53.Beattie PF, Butts R, Donley JW, Liuzzo DM. The within-session change in low back pain intensity following spinal manipulative therapy is related to differences in diffusion of water in the intervertebral discs of the upper lumbar spine and L5–S1. J. Orthop. Sports Phys. Ther. 2014;44:19–29. doi: 10.2519/jospt.2014.4967. [DOI] [PubMed] [Google Scholar]
- 54.Haavik Taylor H, Murphy B. Altered central integration of dual somatosensory input following cervical spine manipulation. J. Manip. Physiol. Ther. 2010;33:178–188. doi: 10.1016/j.jmpt.2010.01.005. [DOI] [PubMed] [Google Scholar]
- 55.Allison T, et al. Human cortical potentials evoked by stimulation of the median nerve. II. Cytoarchitectonic areas generating short-latency activity. J. Neurophysiol. 1989;62:694–710. doi: 10.1152/jn.1989.62.3.694. [DOI] [PubMed] [Google Scholar]
- 56.Allison T, McCarthy G, Wood CC, Jones SJ. Potentials evoked in human and monkey cerebral cortex by stimulation of the median nerve. A review of scalp and intracranial recordings. Brain. 1991;114:2465–2503. doi: 10.1093/brain/114.6.2465. [DOI] [PubMed] [Google Scholar]
- 57.Kanovský P, Bare M, Rektor I. The selective gating of the N30 cortical component of the somatosensory evoked potentials of median nerve is different in the mesial and dorsolateral frontal cortex: Evidence from intracerebral recordings. Clin. Neurophysiol. 2003;114:981–991. doi: 10.1016/S1388-2457(03)00068-3. [DOI] [PubMed] [Google Scholar]
- 58.Mauguiere F, Desmedt JE, Courjon J. Astereognosis and dissociated loss of frontal or parietal components of somatosensory evoked potentials in hemispheric lesions. Detailed correlations with clinical signs and computerized tomographic scanning. Brain. 1983;106:271–311. doi: 10.1093/brain/106.2.271. [DOI] [PubMed] [Google Scholar]
- 59.Rossini PM, et al. Abnormalities of short-latency somatosensory evoked potentials in Parkinsonian patients. Electroencephalogr. Clin. Neurophysiol. 1989;74:277–289. doi: 10.1016/0168-5597(89)90058-0. [DOI] [PubMed] [Google Scholar]
- 60.Rossini PM, Gigli GL, Marciani MG, Zarola F, Caramia M. Non-invasive evaluation of input-output characteristics of sensorimotor cerebral areas in healthy humans. Electroencephalogr. Clin. Neurophysiol. 1987;68:88–100. doi: 10.1016/0168-5597(87)90036-0. [DOI] [PubMed] [Google Scholar]
- 61.Waberski TD, et al. N30 and the effect of explorative finger movements: A model of the contribution of the motor cortex to early somatosensory potentials. Clin. Neurophysiol. 1999;110:1589–1600. doi: 10.1016/S1388-2457(99)00092-9. [DOI] [PubMed] [Google Scholar]
- 62.Rossi S, et al. Early somatosensory processing during tonic muscle pain in humans: Relation to loss of proprioception and motor 'defensive' strategies. Clin. Neurophysiol. 2003;114:1351–1358. doi: 10.1016/S1388-2457(03)00073-7. [DOI] [PubMed] [Google Scholar]
- 63.Cebolla A-M, Palmero-Soler E, Dan B, Cheron G. Frontal phasic and oscillatory generators of the N30 somatosensory evoked potential. NeuroImage. 2011;54:1297–1306. doi: 10.1016/j.neuroimage.2010.08.060. [DOI] [PubMed] [Google Scholar]
- 64.Gilroy AM, MacPherson BR, Wikenheiser JC, Voll MM, Wesker K. Atlas of anatomy. Thieme; 2021. [Google Scholar]
- 65.Hodgkin AL, Huxley AF. A quantitative description of membrane current and its application to conduction and excitation in nerve. J. Physiol. 1952;117:500–544. doi: 10.1113/jphysiol.1952.sp004764. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Chu EC-P, Trager RJ, Chen AT-C. Concurrent Bell’s Palsy and facial pain improving with multimodal chiropractic therapy: A case report and literature review. Am. J. Case Rep. 2022;23:e937511–937511. doi: 10.12659/AJCR.937511. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The numerical data supporting the conclusions of this article will be made available by the authors without undue reservation. Interested individuals can obtain this data by making a reasonable request to the corresponding author, Imran Khan Niazi. The Local Ethics Committee adhering to local data protection laws, does not allow the sharing of individuals’ raw data.