Ulnar Nerve Conduction Study of the First Dorsal Interosseous Muscle in Korean Subjects
Article information
Abstract
Objective
To derive normative values for ulnar nerve conduction study of the active recording electrode on the first dorsal interosseous muscle (FDI) and the reference electrode on the proximal phalanx of the thumb.
Method
Ulnar nerve motor conduction study with FDI and abductor digiti minimi muscle (ADM) recording was performed in 214 hands of 107 healthy subjects. Ulnar NCS was performed with 2 different recording electrode montages (ADM-base of 5th finger; FDI-thumb) and differences in latency and amplitude were compared. Using this technique, the initial positivity of ulnar compound muscle action potential (CMAP) was not observed in any response with FDI recording.
Results
The maximal values for distal motor latency to the ADM and FDI muscle were 3.8 ms and 4.4 ms, respectively. The maximal difference of distal motor latency between the bilateral FDI recordings was 0.6 ms. The maximal ipsilateral latency difference between ADM and FDI was 1.4 ms.
Conclusion
Placement of the reference electrode on the thumb results in a CMAP without an initial positivity and the normative values obtained may be useful in the diagnosis of ulnar neuropathy at the wrist.
INTRODUCTION
Ulnar nerve problems commonly arise in the regions of the elbow and/or wrist. Ulnar neuropathy at the elbow is the second most common entrapment neuropathy in the upper limb.1 However, ulnar neuropathy at the wrist (UNW) is a rare disease entity and is sometimes confused with ulnar neuropathy at the elbow.2 Various techniques have been developed to diagnose UNW.2-10 Among these, ulnar nerve conduction study on the first dorsal inter osseous muscle (FDI) is very useful.3 Preston and Shapiro suggested that ulnar motor nerve conduction study with FDI recording should be done in all patients with suspected UNW. However, the short-coming of FDI recording is the initial positive deflection of compound muscle action potential (CMAP), which poses a problem in measuring distal motor onset latency.
In 1990, Wertsch et al. demonstrated that the initial positive deflection was strongly influenced by the position of the reference recording electrode, and the reference electrode placement on the thumb could avoid an initial positive deflection that may be seen when the reference is placed on the index finger (Fig. 1, 2).11 Phongsamart et al. also demonstrated that the CMAP waveform shape and onset latency could be affected by the different reference electrode position.12 Recent researchers also used the base of the thumb as a reference electrode for FDI recording.10,12-14
This study was designed to derive normative values of ulnar nerve conduction study with the recording electrode on the FDI muscle and the reference electrode on the proximal phalanx of thumb.
MATERIALS AND METHODS
Nerve conduction study (NCS) was performed in 214 hands of 107 healthy subjects consisting of 54 women and 53 men (mean age, 42.6±11.2 years). None of the subjects had symptoms and signs of systemic or neurologic disease. Subjects that fulfilled any American Association of Neuromuscular & Electrodiagnostic Medicine criteria for ulnar neuropathy on the elbow were also excluded. This study was approved by the local ethical committee and was performed with consent from each healthy subject and patient.
Ulnar motor nerve conduction study was performed separately with both abductor digiti minimi (ADM) and FDI muscles in healthy subjects and patients with UNW. The active recording electrodes were placed over the belly of each muscle and the reference electrodes were applied on the base of the proximal phalanx bone of the fifth digit for the ADM and the proximal phalanx of the thumb for the FDI. The ulnar nerve was stimulated at the wrist (8 cm proximal to the active recording electrode for ADM), 3 cm distal to the medial epicondyle, and 7 cm proximal to medial epicondyle with the elbow placed in 90 degrees flexion. Stimulation was applied with sufficient intensity to evoke a supramaximal response at each stimulation site. Surface recording and stimulation electrodes were used for this study. Distal onset latency and baseline-to-peak amplitude of the ulnar CMAP to ADM and FDI were measured. Ipsilateral distal latency difference between FDI and ADM was calculated. Side-to-side differences in latency and amplitude to each muscle were also calculated.
All nerve conduction studies were performed with a Nicolet Viking IV Electrodiagnostic System (Nicolet Instrument Corp., Madison, USA). For the ulnar motor nerve conduction study of the FDI muscle, the filter was set at a low-frequency filter of 2 Hz and high-frequency filter of 10 kHz, and sensitivity and sweep speed were set at 5 mV/division and 1ms/division, respectively. The skin temperature was maintained above 32℃ with a thermal sensor placed on the surface of the FDI.
Statistical analysis
We considered the maximal value for the latency and latency difference as the upper normal limit, and the minimal value for amplitude as the lower normal limit. The values of distal motor latency to FDI and ADM, ipsilateral latency differences between ADM and FDI, side-to-side latency difference of ADM and FDI responses, and CMAP amplitudes recorded over ADM and FDI were presented as mean, standard deviation, median, minimal and maximal, and 5th or 95th percentile value. Paired t-test was used to test for side-to-side differences and independent t-test for gender differences. To build the models between the electrophysiogic parameters and independent variables, such as age, height, weight and BMI, multiple regression analysis was performed in the forward stepwise method. A p-value of less than 0.05 was considered statistically significant. The statistical package SPSS version 12.0 was used for the analysis of all data.
RESULTS
The demographic data of all healthy subjects are presented (Table 1). Normative values for the electrophysiologic study for UNW as the maximal value, 95 percentile value, and mean+2SD of latency of ADM and FDI, and the minimal value, 5 percentile value, and mean-2SD of amplitude of ADM and FDI are presented (Table 2). The mean and range for distal motor latency to ADM and FDI by decade are presented in Table 3 and the mean and range for baseline-to-negative peak amplitudes of ADM and FDI according to each decade of age are presented in Table 4. There was a tendency for the CMAP amplitudes of both muscles to decrease with advancing age, but no association was observed between minimal value and age. There was no significant right-left difference in CMAP amplitudes of ADM, but there was a significant right-left amplitude difference for FDI recordings, in which mean CMAP amplitude was 14.6 mV in the right and 13.6 mV in the left (p<0.05).
According to the forward stepwise multiple regression analysis performed on the distal motor latency to ADM (DML_ADM) and FDI (DML_FDI), the models for multiple linear regression were yDML_ADM=1.455+0.11×age+0.006×height (p=0.000; R2=0.184) and yDML_FDI= 01.426+0.013×age+0.01×height (p=0.000; R2=0.180), respectively. For CMAP amplitude of ADM (AMP_ADM) and FDI (AMP_FDI), the models for multiple linear regression were yAMP_ADM=14.657-0.064age (p=0.000; R2=0.105) and yAMP_FDI=17.296-0.075×age (p=0.000; R2=0.067), respectively. For side-to-side latency difference to ADM (SIDE_ADM) and FDI (SIDE_FDI), the equations for multiple linear regression were ySIDE_ADM=0.182-0.004×age (p=0.018; R2=0.061) and ySIDE_FDI=0.260-0.006×age (p=0.03; R2=0.094), respectively. For ipsilateral latency difference between FDI and ADM, there was no significant variable among age, height, weight, and BMI. There was no initial small positive deflection in any ulnar nerve conduction study with FDI recording.
DISCUSSION
UNW has diverse clinical findings including pure sensory, pure motor, and combined motor and sensory symptoms according to the location of lesion in the wrist. Electrophysiologic evaluation for suspected UNW has to include nerve conduction studies to evaluate motor fibers to ADM and FDI and sensory fibers to 5th digit. Preston and Shapiro15 recommended a routine nerve conduction study protocol for ulnar neuropathy at the wrist as follows: 1) ulnar motor study recording ADM; 2) ulnar motor study recording FDI (bilateral studies); 3) short segment increment study of ulnar motor nerve across the wrist recording FDI; 4) Median motor study recording APB; 5) median and ulnar F responses; 6) ulnar sensory response recording digit 5 (bilateral studies); 7) median sensory response recording digit 2 or 3; 8) dorsal ulnar cutaneous sensory response (bilateral studies); and 9) lumbrical-interosseous distal latency comparison study. Among these, it is essential to perform the ulnar motor conduction study recording the FDI in patients with lesions of deep palmar motor branches. Distal latency to FDI, side-to-side latency difference to FDI, and ipsilateral latency difference between FDI and ADM are often helpful in the diagnosis of UNW and their normal criteria are 4.5 msec, 2.0 msec, and 1.3 msec, respectively, reported by Olney and Wilbourn.3 These criteria have been recited in many electrodiagnostic texts. However, their method using the 2nd metacarpophalangeal joint as a reference electrode brought about a problem in measuring the distal motor latency to FDI, which was an initial positive deflection. This initial positive deflection is influenced not by the position of active recording electrode on FDI but by the position of the reference recording electrode, and the change of reference electrode placement to the thumb from the index finger can avoid this initial deflection. As the ulnar nerve conduction study is performed in the FDI, the thumb over the index finger is preferred by many as a reference electrode position because the initial positive deflection can be avoided.10,12-14 This situation required the development of new normal criteria for the diagnosis of UNW using the modified ulnar motor nerve conduction study with FDI recording. We performed ulnar motor nerve conduction study to the FDI with the reference electrode placed on the thumb in 214 hands of 107 healthy persons and obtained the maximal values as the normal criteria to compare with Olney and Wilbourn's study.3 There was no significant difference in the distal latency to FDI and ADM. However, our study revealed that the ipsilateral latency difference between FDI and ADM, side-to-side latency difference to ADM, and side-to-side latency difference to FDI were shorter than those of Olney and Wilbourn's study (Table 2).3 We postulate that the shorter side-to-side latency to ADM or FDI in our study may be caused by the differences of stimulation site and the different position of reference recording electrode. Olney and Wilbourn's study used the proximal wrist crease as stimulation site, which may cause differences in stimulation distance between both sides.3 In this study, the ulnar nerve was stimulated a point 8 cm proximal to the active recording electrode site on the ADM for both ADM and FDI recordings which allowed a more uniform stimulation distance compared to Olney and Wilbourn's findings.3 Also, the change of reference electrode placement to the thumb from the index finger would be helpful to eliminate the measurement error by the initial positive deflection. The maximal values considered as the normal upper limit of distal latency to FDI, side-to-side latency difference to FDI, and ipsilateral latency difference between FDI and ADM were 4.4 ms, 0.6 ms, and 1.4 ms, respectively. The CMAP amplitudes of ADM and FDI recordings in this study were all greater than those of the previous study, and in contrast to the previous study, our study revealed smaller minimal amplitude of ADM than the FDI: ADM, 7.0 mA; FDI, 8.4 mA.
We analyzed our electrophysiologic and demographic data with the forward stepwise multiple regression method and formulated regression equations. Although all equations were statistically significant (p<0.000), the small coefficients of determination (R2, 0.061-0.184) of each formula and the small regression coefficients (0.004-0.11) indicated that this model was inadequate for explaining the variation of many dependent variables useful for diagnosing UNW. In particular, equations for distal latency to and amplitude of FDI, side-to-side latency difference to ADM and FDI showed a very small coefficient of determination and regression coefficients. Also, there was no statistically significant correlation in the ipsilateral latency difference between FDI and ADM with age, height, weight, and BMI. The results of regression analysis suggest that these parameters may be useful in the diagnosis of UNW regardless of age, sex, height, weight, and BMI.
CONCLUSION
In conclusion, considering the current trend of the thumb being used as a reference in the ulnar nerve conduction study to FDI, the results of our study may be very meaningful in the diagnosis of UNW. Although the maximal values are used as normal upper criteria for latency to compare with the previous study, the 95th percentile or 'mean+SD' values may be applied as normal criteria. However, as these values can increase sensitivity and decrease specificity of UNW, they should be used with caution. Because the incidence of UNW is rare, using the maximal values may be a safer method that can decrease false positives.
Further studies need to be performed in patients suspected with UNW to prove the usefulness of ulnar nerve conduction studies of the recording electrode on the FDI muscle and the reference electrode on the proximal phalanx of the thumb.