Detection of C8/T1 radiculopathy by measuring the root motor conduction time

Abstract

Background

Root motor conduction time (RMCT) can noninvasively evaluate the status of the proximal root segment. However, its clinical application remains limited, and wider studies regarding its use are scarce. We aimed to investigate the association between C8/T1 level radiculopathy and RMCT.

Methods

This was a retrospective cross-sectional study. Subjects were extracted from a general hospital’s spine clinic database. A total of 48 C8/T1 root lesions from 37 patients were included, and 48 C8/T1 root levels from control subjects were matched for age, sex, and height. RMCT was measured in the abductor pollicis brevis muscle and the assessment of any delays owing to C8/T1 radiculopathy.

Results

The RMCT of the C8/T1 radiculopathy group was 1.7 ± 0.6 ms, which was significantly longer than that in the control group (1.2 ± 0.8 ms; p = 0.001). The delayed RMCT was independently associated with radiculopathy (adjusted odds ratio, 1.15; 95% confidence interval, 1.06–1.27; p = 0.011) after adjusting for the peripheral motor conduction time, amplitude of median compound motor nerve action potential, and shortest F-wave latency. The area under the Receiver Operating Characteristic curve for diagnosing C8/T1 radiculopathy using RMCT was 0.72 (0.61–0.82). The RMCT was significantly correlated with symptom duration (coefficient = 0.58; p < 0.001) but was not associated with the degree of arm pain.

Conclusion

Our findings illustrate the clinical applicability of the RMCT by demonstrating its utility in diagnosing radiculopathy at certain spinal levels.

Introduction

Radiculopathy is a common condition whose symptoms can include pain, sensory change, and motor weakness owing to mechanical and chemical irritation of the spinal nerve root [1, 2]. Imaging studies are essential for diagnosing radiculopathy; magnetic resonance imaging helps identify soft tissues such as discs, ligaments, and nerve roots [3], while computed tomography is primarily used to confirm abnormalities in bony structures [4]. Meanwhile, another key factor in confirming radiculopathy is electrophysiologic diagnosis [5]. In particular, electromyography (EMG) is a classical tool that was used to evaluate radiculopathy before the development of modern imaging instruments [6]; its key advantage is in its ability to detect neurophysiological changes that cannot be confirmed by imaging studies alone [7]. By applying EMG to multiple myotomes, it is possible not only to localize the abnormal spinal root level but also to estimate the temporal aspect of compression by distinguishing motor unit action potential [8]. However, the invasive nature of EMG creates a potential risk of complications such as bleeding or infection at the examination site [9]. Additionally, patient cooperation is essential for observing resting potential and interference patterns [10].

Root motor conduction time (RMCT) is a measure of the state of the proximal root segment that is obtained noninvasively by performing direct cervical stimulation and nerve conduction studies [11, 12]. Notably, RMCT is very localized since it excludes distal neural lesions and measures only the conduction time of the proximal root segment [13,14,15]. However, it also has the disadvantage of involving a somewhat complicated measurement method wherein well-trained examiners are required [16]. To date, the RMCT has been investigated in only a few disease types, such as demyelinating disease and lumbar spinal stenosis, whereas its clinical applicability in patients with radiculopathy remains unclear [17].

In this study, we hypothesized that the RMCT can be a valuable tool for the diagnosis of radiculopathy at certain spinal root levels. To that end, we investigated whether the RMCT measured in the abductor pollicis brevis (APB) muscle was significantly delayed in the presence of C8/T1 radiculopathy. Moreover, we aimed to determine the association between clinical symptoms and RMCT.

Methods

Subjects and clinical evaluations

We performed a retrospective cross-sectional study based on medical records of patients treated between June 2007 and December 2021. We extracted patients diagnosed with C8/T1 radiculopathy at our hospital through electrodiagnosis and whose RMCT was measured at the same time. All patients diagnosed with C8/T1 radiculopathy also underwent cervical x-ray and magnetic resonance imaging studies to confirm root compression and exclude other differential diagnoses. Thereafter, the final study group was selected by applying the following exclusion criteria: uncontrolled diabetes, concomitant polyneuropathy or median nerve lesion, previous cervical spine surgery, previous hand injury or surgery, unobtainable electrodiagnostic parameters, and lack of clinical information. Data from 48 C8/T1 root lesions in 37 patients were finally extracted; these included the subjective symptom duration, numerical rating scale (NRS) of the neck and arm pain, and neck disability index (NDI) score at the time of electrodiagnostic examination.

The control group consisted of a single-center healthy cohort of 190 prospectively analyzed subjects who were reported previously by the authors [18]. We controlled the potential biases between the two groups by performing propensity score matching (PSM). Consequently, 96 root levels (48 patients and 48 matched controls) were finally investigated (Fig. 1).

Fig. 1

Flowchart showing the comparative analysis of the patients and control subjects

This study was approved by the Institutional Review Board of Pohang Stroke and Spine Hospital (PSSH0475-202207-HR-011-01); informed consent was waived, given its retrospective design. The research complied with the guidelines of the Declaration of Helsinki.

Electrodiagnostic assessments

The EMG protocol for radiculopathy comprised of the following [5]: First, we examined muscles innervated by different nerves in the same myotome. Second, we assessed both proximal and distal muscles in the same myotome. Finally, we examined muscles in the myotomes adjacent to the suspected level. EMG-confirmed C8/T1 radiculopathy was defined as the presence of denervation potentials or polyphasic, long-duration, and large-amplitude motor unit action potentials in two or more of the differently innervated following muscles after other conditions were ruled out: flexor pollicis longus, flexor digitorum profundus, flexor carpi radialis, first dorsal interosseous, abductor digiti minimi, and APB [5].

For the nerve conduction study, we first recorded the sensory nerve action potentials of the median, ulnar, and superficial radial nerve in the distal arm. Electrical stimulations with 0.1 ms square wave pulses were applied for the sensory nerve conduction studies with a 10–2000 Hz filter setting. Next, we recorded compound motor nerve action potentials from the APB and abductor digiti minimi muscles and F-waves from the APB muscle. To conduct motor nerve conduction studies, each nerve was supramaximally stimulated by 0.2 ms square wave pulses with a 5–5000 Hz filter setting. We recorded nerve action potentials at least 12 times at the same nerve for study reproducibility. Surface electrodes were attached using the belly-tendon method to all recorded muscles. All nerve conduction studies were performed in the supine position. The detailed methods for individual nerve conduction studies are described in Supplementary Table 1 [5, 19].

To measure the stimulated peripheral motor conduction time (PMCT), we performed magnetic stimulation at the C7 spinous process; the ABP muscle was recorded using the surface electrodes. To provoke median motor evoked potential, we administered supramaximal stimulation (20% above the threshold) with weak isometric contraction in the APB muscle. The simulations were applied biphasic and the active pulse width was 280 µs. Then, we calculated the RMCT using the following equations, which are based on the principle that nerve excitement occurs a few centimeters distal to the anterior horn cell upon magnetic stimulation (Fig. 2) [20].

Fig. 2

Schematic diagram illustrating the measurement of C8/T1 root motor conduction time

RMCT (ms) = calculated PMCT − stimulated PMCT

Calculated PMCT (ms) = (compound muscle action potential onset latency + F-wave onset latency − 1) / 2

Stimulated PMCT (ms) = spinal motor-evoked potential onset latency

All electrodiagnostic evaluations were performed using the Cadwell Sierra Wave EMG system (Cadwell Laboratories Inc., Kennewick, WA, USA). A MagPro Compact with a C-100 circular coil (11 cm outer diameter) (MagVenture Inc, Farum, Denmark) was used for cervical magnetic stimulation. The temperature of the electrodiagnostic laboratory was maintained at approximately 23℃ to 25℃. All electrodiagnostic examinations were interpreted by experienced physiatrists.

Statistical analysis

The Shapiro-Wilk test was applied to check the normality of continuous variables. These are expressed as means ± standard deviations if normality was satisfied or as medians (interquartile ranges) if not; the independent t-test and Mann-Whitney U-test were applied for comparative analyses of these types of values, respectively. Categorical variables are expressed as frequencies (proportions); groups were compared using the chi-squared test. We established binary logistic regression models for detecting C8/T1 root lesions using data adjusted for age, sex, and height. Model 1 was a predictive model of RMCT alone, Model 2 was adjusted for the stimulated PMCT, and Model 3 was adjusted for the median compound muscle action potential and F-wave in addition to the adjustment of Model 2. The multicollinearity of the model was confirmed, as the variance inflation factor was < 10. We drew the Receiver Operating Characteristic curve and calculated the cutoff value using Youden’s J statistic. We calculated the Spearman coefficient to determine the correlation between RMCT and symptoms. All statistical analyses were performed using SPSS 22.0 (IBM Inc., Armonk, NY, USA).

For PSM, the “MatchIt” package of the R software version 4.1.2 (R Core Team, R Foundation for Statistical Computing, Vienna, Austria) was used [21]. The covariates used for matching were age, sex, and height; moreover, 1:1 matching with no replacement was performed. The nearest-neighbor method was applied with the caliper set to 0.2.

Results

Baseline characteristics of patients and controls

Table 1 summarizes the baseline characteristics of the 37 patients, 11 of whom had bilateral C8/T1 radiculopathy. The mean patient age was 61.1 years and the mean height was 166.5 cm; 75.7% were men. The patients’ median NDI score was 12.0. Among all 48 C8/T1 root levels, 25 (52.1%) were right-sided, and the median duration of symptoms was 4.0 (3.0–12.0) months. The median NRS scores of the neck and arm were 3.0 and 4.5, respectively.

Table 1 Baseline features of patients with C8/T1 level radiculopathy

After performing PSM for comparative analysis, we extracted 48 control C8/T1 root levels and confirmed that there were no significant differences in age, sex, or height between the two groups (Table 2).

Table 2 Comparison of data from patients with C8/T1 level radiculopathy and matched control subjects

RMCT at the C8/T1 level

The mean RMCT among patients with radiculopathy was 1.7 ± 0.6 ms, which was significantly longer than that among control subjects (1.2 ± 0.8 ms; p = 0.001) (Table 2; Fig. 3). Logistic regression models revealed that the delay in RMCT observed in patients with C8/T1 was independently associated with radiculopathy (per Model 3: odds ratio, 1.15; 95% confidence interval, 1.06–1.27; p = 0.011) (Table 3). The area under the Receiver Operating Characteristic curve for diagnosing C8/T1 radiculopathy using RMCT was 0.72 (0.61–0.82) with 0.83 sensitivity and 0.58 specificity (Supplementary Fig. 1). In terms of subjective symptom indices, the RMCT was significantly associated with symptom duration (coefficient = 0.58; p < 0.001) but not with the NRS of the arm (coefficient = 0.22; p = 0.139) All measured values for calculating the RMCT are presented in Supplementary Table 2.

Fig. 3

Root motor conduction time (RMCT) in each group. Patients with C8/T1 level radiculopathy showed significantly longer RMCTs than did the control group (p = 0.001)

Table 3 Logistic regression models using data from patients and matched control subjects

Discussion

We observed a significant delay in RMCT among patients with C8/T1 radiculopathy when compared to control subjects, and also demonstrated that this delay was independently associated with the presence of radiculopathy at the C8/T1 level. This finding is notable because it provided a rational basis for the applicability of RMCT in terms of diagnosing radiculopathy at a specific spinal root level.

The application of RMCT to assess radiculopathy occurring at particular levels is rare. Most relevant studies were conducted before the 2000s, with only a few published since then. Banerjee et al. [13] described magnetic spinal stimulation as a non-invasive method to evaluate lumbosacral motor radiculopathy in 26 patients and 25 control subjects; they mainly targeted the lower lumbosacral nerve roots (L5, S1, and S2) by recording from the abductor hallucis muscle. According to their results, patients with clinical motor weakness had profoundly prolonged RMCTs; therefore, they suggested that RMCT delay was related to the severity of symptoms. Golez [22] measured motor conduction time via stimulation at the L1 and S1 levels in 25 patients with lumbar spinal stenosis and 36 control subjects. That study was noteworthy because it demonstrated that neurogenic claudication increased the cauda equina motor conduction time, revealing that the clinical symptom and delay of motor conduction time were related. In our study, the RMCT showed a significant correlation with the duration of subjective symptoms, which supports Golez’s results to some extent. However, in our study, the subjective pain level in the lesional-side limb was not related to RMCT as we assumed when we primarily evaluated the motor nerve. Additionally, Seçil et al. [23] measured the cauda equina motor conduction time and showed that it was slower in the lumbar spinal stenosis group than in the control group; however, their study did not identify the relationship between the degree of motor conduction delay and symptom severity.

Our study is the first to measure RMCT in patients with cervical radiculopathy and has the advantage of being specific to a specific spinal level; moreover, we included a relatively large number of subjects compared to previous related studies. Additionally, variables such as age, sex, and height were analyzed and adjusted for using PSM, rendering the results much more reliable. Since the APB-RMCT was previously found to be affected by height in a linear model [18], for the integrity of our results, it was important that we controlled for this factor when assessing the patient and control groups.

RMCT has also been studied in patients with demyelinating neuropathy. In a previous study, a significant difference was found in the RMCT of 30 healthy subjects and 12 patients with Guillain-Barre syndrome who were diagnosed within one week [14]; hence, RMCT was deemed to be useful for the early diagnosis of focal segmental demyelinating polyneuropathy, affording this measure a novel clinical utility. In the study of Inaba et al. [24], RMCT was measured in 11 patients with chronic inflammatory demyelinating neuropathy and 10 with Guillain-Barre syndrome, wherein the authors found that the RMCT increasingly normalized as muscle strength recovered. Taken together, such studies illustrate the applicability of the RMCT to various diseases involving the motor root segment. Furthermore, measuring the RMCT is a non-invasive procedure and has the potential to be applied to additional fields given its ability to detect diseases in their early stages and to also assess functional recovery. Therefore, additional research on the use of the RMCT is warranted going forward.

This study had several limitations. It was retrospective in nature, requiring additional investigations to validate our results. Additionally, our participants were limited to Koreans; hence, validation among patients of other ethnicities is also required. Our patients comprised a single group diagnosed with C8/T1 radiculopathy that was relatively heterogeneous; future studies that analyze various subgroups of patients (such as those with acute versus chronic lesions or mild versus severe symptoms), would further clarify the relationship between RMCT and radiculopathy. Finally, there were potential limitations in terms of measurement. For example, it is difficult to apply our methods at some spinal root levels because reliable recording of the F-wave is possible only from distal muscles [25]. Moreover, it was challenging to measure the RMCT when reliable motor evoked potentials or compound muscle action potentials could not be obtained owing to severe peripheral nerve lesions in the distal limbs.

Conclusion

We demonstrated that the RMCT is delayed in the root lesions of patients with C8/T1 level radiculopathy. This noninvasive method (compared to EMG) can have an adjuvant role in diagnosing radiculopathy at certain spinal levels. Our study may be a good milestone for future clinical applications of RMCT as related to patients with radiculopathy. However, it is important to validate our results through additional multi-center, multi-ethnic studies.