Electrophysiological evaluation of carpal tunnel syndrome female patients after vitamin D replacement

Avaliação eletrofisiológica de pacientes do sexo feminino com síndrome do túnel do carpo após reposição de vitamina D

Abstract

Objective:

The effects of vitamin D on the central and peripheral nervous system continue to be investigated today. In the present study, we aimed to evaluate pain and electrophysiologic response in patients with carpal tunnel syndrome (CTS) who have undergone replacement therapy due to vitamin D deficiency.

Methods:

Fifty female patients diagnosed with mild and moderate CTS and accompanied by vitamin D deficiency were included in this study. Nerve conduction study (NCS) was performed before and after vitamin D replacement, and the patient’s pain was evaluated with Visual Analogue Scale (VAS).

Results:

When NCS were compared before and after treatment, there was a statistically significant improvement in the median distal sensory onset latency (DSOL) and sensory conduction velocity (CV) and motor distal latencies (DML) values (p=0.001; p<0.001; p=0.001, respectively). At the same time, there was a decrease in the VAS values in patients (p<0.001). When the two groups were compared there was an improvement in DSOL and sensory CV in both groups, but in DML only in moderate CTS group.

Conclusion:

In this study, it was shown that mild and moderate CTS patients had an improvement in pain and electrophysiological parameters after vitamin D replacement. Replacing vitamin D in early stages of CTS may be beneficial.

Keywords:
carpal tunnel syndrome; vitamin D treatment; nerve conduction velocity

Resumo

Objetivo:

Os efeitos da vitamina D no sistema nervoso central e periférico continuam sendo investigados atualmente. Neste estudo, objetivamos avaliar a dor e a resposta eletrofisiológica em pacientes com síndrome do túnel do carpo (STC) submetidos a terapia de reposição devido à deficiência de vitamina D.

Métodos:

Cinquenta pacientes do sexo feminino diagnosticadas com STC leve e moderada e acompanhadas de deficiência de vitamina D foram incluídas neste estudo. O estudo da condução nervosa (ECN) foi realizado antes e após a reposição da vitamina D, e a dor do paciente foi avaliada com a Escala Visual Analógica (EVA).

Resultados:

Quando a ECN foi comparada antes e após o tratamento, houve uma melhora estatisticamente significativa na latência mediana do início sensorial distal (DSOL) e nos valores de velocidade de condução sensorial (VC) e latência distal motora (LDM) (p=0,001; p<0,001; p=0,001, respectivamente). Ao mesmo tempo, houve uma diminuição dos valores da EVA nos pacientes (p<0,001). Quando os dois grupos foram comparados, houve uma melhora no DSOL e no VC sensorial em ambos, mas no LDM apenas no grupo STC moderado.

Conclusão:

Neste estudo, foi demonstrado que pacientes com STC leve e moderada apresentaram melhora da dor e parâmetros eletrofisiológicos após a reposição de vitamina D. A substituição da vitamina D nos estágios iniciais da STC pode ser benéfica.

Palavras-chave:
síndrome do túnel carpal; tratamento com vitamina D; velocidade de condução sensorial

Carpal tunnel syndrome (CTS) is the most common peripheral nerve entrapment caused by an impairment in the nerve functions, due to the compression of the median nerve at the wrist level^1,2. CTS can be caused by systemic, anatomic and idiopathic causes³. Treatment is medical (splinting, steroid injections) or surgical decompression of carpal tunnel². Vitamin D deficiency is an independent risk factor, that increases the symptoms of CTS⁴.

Vitamin D deficiency is worldwide seen as a pandemic condition, and its main cause is inadequate synthesis⁵. Vitamin D is a steroid molecule and it is synthesized from 7-dehydrocholesterol by the action of ultraviolet B rays in the epidermis⁶. Experimental animal model studies demonstrated that vitamin D increases myelination after peripheral nerve injury and reduces neuronal injury^7,8. Vitamin D deficiency may cause hyperinnervation and hypersensitivity in the nerve fibers and increases pain sensation and pain perception in the pathological process⁹.

Vitamin D3 and Vitamin D2, which accelerate the neuronal regeneration process, were approved by the FDA⁷. The role of calcitriol in treatment of the nervous system will be better understood if it is noted that the nervous system and ectoderm have a common embryologic origin⁷. Therapeutic and protective effects of vitamin D are reduction in oxidative stress and provision of neuroplasticity and neuroprotection^10,11.

In recent years, the role of vitamin D deficiency in the etiology of acute-chronic central and peripheral neurological diseases has been investigated, and the effectiveness and treatment of vitamin D replacement has been demonstrated. For example, in diabetic sensory neuropathy, topical and oral vitamin D therapy reduce the pain¹². The role of vitamin D in the recovery of CTS remains unknown. In this study, we aimed to evaluate the effect of vitamin D replacement on pain and electrophysiological response in CTS patients with vitamin deficiency.

METHODS

This cohort study was retrospectively conducted with CTS patients, who had a diagnosis of vitamin D deficiency and were admitted to the Yozgat Bozok University departments of Neurology and Physical Therapy and Rehabilitation from 2017 to 2018. Patients with CTS who were not on neuropathic pain treatment and could not use splint because of discomfort were selected. Patients with a vitamin D level above 20 ng/mL, who did not use vitamin therapy regularly, and patients receiving recurrent vitamin treatments were excluded from the study. Patients who have severe CTS were the main exclusion criteria for this study. Other exclusions were patients on dialysis, malignancy, severe liver failure, coronary artery disease, cerebrovascular disease, diabetes mellitus, hypothyroidism, hyperparathyroidism, and/or vitamin B12 deficiency, cervical hernia, prior CTS surgery, or steroid injections. For each patient, body mass index (BMI) was calculated according to the World Health Organization (WHO) classification, based on patient’s height and weight.

The Ethics Committee gave its approval before the study was started. It was conducted according to the principles of the Declaration of Helsinki.

Biochemical analysis

Laboratory examinations, including a screening analysis of 25-dihydroxyvitamin D levels, were performed using venous blood samples from 9:00 to 10:00. All serum 25-dihydroxyvitamin D (ng/ml) concentrations were analysed using an electrochemiluminescent immunosassay technique with Coba e601 analyzer (Roche Diagnostics GmbH; Mannheim, Germany). In all adults with vitamin D deficiency, 6000 IU/day or 50.000 IU/week of vitamin D2 or vitamin D3 was given for eight weeks and also supplemented in maintenance therapy.

Assessment of peripheral neuropathy and pain

Visual analogue scale

Visual Analogue Scale (VAS) was used to measure the pain score: 1-3: mild; 4-6: moderate; 7-8: severe; 9-10: extremely severe¹³. Symptom duration, pain severity, and methodology of vitamin D treatment were questioned in face-to-face interviews.

Electrophysiological evaluation

All CTS patients who regularly used 3-month vitamin D treatment underwent conventional sensory and motor nerve conduction studies, performed by the neurologist who was blinded to the first nerve conduction study (NCS) results. Median and ulnar nerves were studied in both limbs, with respect to sensory and motor conduction studies using a Medelec Synergy electromyography (EMG) machine (Medelec Synergy, Oxford Instruments, Surrey, UK). The filter settings used a 20-2,000 Hz bandpass for the sensory nerve studies and a 2-10,000 Hz bandpass for the motor nerve studies. The sweep speed was set at 1 ms per division. The bar electrodes recordings were used for motor nerve studies and sensory studies. A ground electrode was appropriately placed between the stimulating and recording electrodes. The skin temperature of the hand was maintained at or above 32°C. Nerve conduction studies have been performed using standard techniques, and bipolar superficial electrodes based on a guideline¹⁴. Sensory nerve conduction studies were performed with antidromic methods. Recordings were performed with supramaximal stimulation. All the studies were performed in a warm room, with the temperature maintained at 26-28°C. The age and temperature of patients were considered in the diagnostic parameters of CTS by NCS evaluation¹⁵.

Median distal sensory onset latency (DSOL): the stimulation delivered on the median nerve at the wrist activates sensory action potentials at the index finger. We used a fixed 13 cm distance from the bar recording electrode. The cutoff value was 3.5 ms.

Median motor distal latency (DML): The median nerve stimulation was delivered at the wrist to activate the compound muscle action potential at the thenar eminence. We used a fixed 7 cm distance from the bar recording electrodes that were placed over the belly of the abductor pollicis brevis (APB) muscle (the recording electrode), and just distal to the metacarpophalangeal joint (the reference electrode). The cutoff value was 4.4 ms.

All NCS’s were performed on the same device and by the same person, using the same technique; the NCS and 25(OH)D results were evaluated by the blind neurologist. Patients were classified as follows: mild CTS (median sensory conduction velocity [SCV] slowed in the finger-wrist nerve segment with normal DML), moderate CTS (median SCV slowed in the finger-wrist nerve segment with increased DML).

Statistical analysis

All analyses were carried out using the Statistical Package for the Social Sciences (SPSS) program for Windows (version 20.0, released in 2011; IBM Corp. Armonk, New York, USA). The main characteristics of patients were evaluated with descriptive and analytical statistics. Categorical variables were compared by chi-square test. The mean values of the continuous variables were compared using the independent-samples or paired-samples Student’s t-test as appropriate. The normal distribution of continuous variables was tested using a Kolmogorov-Smirnov test. Normally distributed paired data were analyzed with a paired t-test, whereas skewed paired data were analyzed using the Wilcoxon test. Data were expressed as mean±SD or median (minimum-maximum). The Spearman correlation coefficient was used to evaluate the correlation between the improvement in 25(OH)D and the NCS. P-values<0.05 were considered to be statistically significant.

RESULTS

Fifty female patients with vitamin D deficiency were included in the study with results of bilateral median nerve conduction studies. Among the subjects, there were 45 hands with mild CTS (54.87%), and 37 hands with moderate CTS (45.12%). In both groups, the age, VAS score, BMI, vitamin D levels of CTS patients were summarized in Table 1. The mean age was 48.04±6.03 (range 36-60) in the mild CTS group, and 45.97±7.97 (range 31-56) in the moderate CTS group. BMI was 30.30±5.99 in the mild CTS group and 31.70±5.73 in the moderate CTS group, and there was no statistically significant difference between the mild and moderate CTS groups regarding their demographic characteristics (p>0.05).

Table 1.
Demographic characterics of mild and moderate CTS groups at baseline.

Variables	Mild CTS (n=45)	ModerateCTS (n=37)	p-value
Age (years)	48.04±6.03	45.97±7.97	0.380
Body mass index (kg/m2)	30.30±5.99	31.70±5.73	0.288
Serum vitamin D level (ng/mL)	11.75±4.53	11.64±3.55	0.727
VAS	6.64±1.13	7.24±0.85	0.051
Duration of symptoms (months)	5.97±2.27	13.59±2.24	<0.001

• VAS: visual analog scale; CTS: carpal tunnel syndrome; bold values are statistically significant..

Considering all subjects, the pre- and post-treatment vitamin D levels were 11.70±4.09 (range 3.30‒20.00) and 35.48±15.30 (range 14.90‒60.00), respectively. The improvement in vitamin D levels after a 3-month treatment was found to be statistically significant (p<0.001).

Baseline nerve conduction values and control values (at the third post-treatment month) of the mild and moderate CTS groups are presented in Tables 2 and 3. In the mild CTS group, shortening of DSOL and increase in conduction velocity were statistically significant (p=0.003; p<0.001, respectively). In moderate CTS group, sensory amplitudes and sensory conduction velocity increased, and there was a shortening in DML (p=0.037; p=0.005; p=0.001, respectively). Improvements in other parameters were not statistically significant in two groups (p>0.05).

Table 2.
Nerve conduction studies results before and after 3 months of vitamin D suppplementation in the mild CTS.

Mild CTS patients	Before replacement	After replacement	p-value
Median distal sensory onset latency (DSOL) (ms)	2.93±0.26	2.81±0.36	0.003
Median distal motor latency (DML) (ms)	3.39±0.28	3.51±0.84	0.138
Sensory amplitude (µV)	26.28±4.95	26.77±6.73	0.61
Motor amplitude (wrist) (mV)	8.84±1.79	9.20±2.04	0.21
Median sensory conduction velocity (m/s)	43.67±3.11	47.25±5.77	<0.001
Median motor conduction velocity (m/s)	55.74±2.88	55.71±2.79	0.94
Serum vitamin D level (ng/mL)	11.75±4.53	37.97±16.02	<0.001
VAS	6.64±1.13	4.53±0.69	<0.001

• VAS: visual analog scala; CTS: Carpal tunnel syndrome; bold values indicate a statistically significant difference with a p-value under 0.05.

Table 3.
Nerve conduction studies results before and after 3 months of vitamin D suppplementation in the moderate CTS.

Moderate CTS patients	Before replacement	After replacement	p-value
Median distal sensory onset latency (DSOL) (ms)	3.54±0.71	3.34±0.75	0.06
Median distal motor latency (DML) (ms)	4.72±0.80	4.50±1.46	0.001
Sensory amplitude (µV)	17.98±6.62	21.42±10.20	0.037
Motor amplitude (wrist) (mV)	8.84±1.79	9.20±2.04	0.21
Median sensory conduction velocity (m/s)	37.27±5.46	40.47±7.31	0.005
Median motor conduction velocity (m/s)	55.00±2.71	54.50±3.56	0.71*
Serum vitamin D level (ng/mL)	11.64±3.55	32.45±13.99	<0.001
VAS	7.45±0.69	6.64±0.85	<0.001

• VAS: visual analog scala; CTS: Carpal tunnel syndrome; bold values indicate a statistically significant difference with a p-value under 0.05.

For all subjects, when the correlation between vitamin D and electrophysiological values after treatment was examined, the shortening in DSOL and DML showed a moderately negative correlation (p=0.009, rho=-0.287; p=0.013, rh o=-0.272), and the increase in sensory conduction velocity showed a moderately positive correlation (p=0.019, rho=0.258). There was no significant correlation between other electrophysiological values and vitamin D levels.

In the evaluation of the electrophysiological improvement before and after the treatment in both groups, NCS recordings of 36 hands improved neurophysiologically (43.9%) as well as pain scores (p<0.001). Of these, 28 were from the mild CTS group, and 8 were from the moderate CTS group (62.2%, 21.6%). When NCS was repeated after 3 months of treatment, 25 patients (67.6%) had moderate CTS findings and 16 patients (35.6%) had mild CTS findings. All recovery percentages in two groups are presented in Table 4.

Table 4.
Alteration of mild and moderate CTS groups before and after treatment, according to electrophysiological values with table of 2x2.

Post treatment recordings of NCS values	Pre-treatment mild CTS (n=45)	Pre-treatment moderate CTS (n=37)	Total recordings of CTS (n=82)
Normal NCS n (%)	28 (62.2%)	8 (21.6%)	36 (43.9%)
Mild CTS n (%)	16 (35.6%)	25 (67.6%)	41 (50%)
Moderate CTS n (%)	1 (2.2%)	4 (10.8%)	5 (6.1%)

• NCS: nerve conduction study; CTS: Carpal tunnel syndrome.

DISCUSSION

When the electrophysiological measurements before and after treatment were evaluated in general, we found a neurophysiological improvement. In both groups, improvements in VAS and serum vitamin D levels after the treatment were found to be highly significant.

In the evaluation of mild and moderate CTS groups regarding response to vitamin D replacement, 36 patients (43.9%) were seen to reach normal electrophysiological values at the follow-up visit 3 months later (28 patients-mild, 62.2%; 8 patients-moderate, 21.6%). Pain, numbness and tingle symptoms persisted in 16 patients (35.6%) in the mild CTS group and in 25 patients (67.6%) in the moderate CTS group.

In recent years, efforts have been made to identify treatment protocols to effectively heal peripheral nerve diseases in which nerve injury is present. Although steroid injections and splint treatment have limited effects, reducing carpal tunnel edema and preventing the onset of axonal damage are the most important goals of the CTS treatment, especially in mild CTS patients². In a study evaluating the nerve conducitions before and after vitamin D treatment, no clear recovery findings were observed in this study, because of the axonal damage in the pathophysiological disorder caused by diabetes¹². A treatment option, which is developed to enhance median nerve regeneration in CTS, has not been included in the guidelines yet. Neither Vit D nor corticosteroids are proved to enhance nerve repair, and axonal damage is caused by compression and nerve degeneration².

Our findings are similar to those from a study by Montava et al., in which facial nerve injury was induced in an experimental animal model. After 200 IU/kg/day oral vitamin D treatment, calcitriol induced functional recovery and myelination starting from the 6^th week, and myelination response was seen electrophysiologically starting from the 12^th week⁷. It has also been shown that in rat models with peroneal nerve injury, cholecalciferol and calcitriol induce peroneal nerve healing⁸. However, they found more prominent recovery in the facial nerve neuropraxia model compared to peroneal injury model. They attributed this effect to some of the unique features of the facial nerve^16,17.

Chabas et al. induced the peroneal nerve injury in two different experimental animal models and found a significant contribution of cholecalciferol and calcitriol to locomotor and electrophysiological healing. There was an increase in nerve myelination proximal and distal to the injury. Besides that, genes inducing axonogenesis and myelination associated with calcitriol were activated after vitamin D therapy. As a result, new axons and myelination were increased in the proximal and distal peroneal nerve stumps^8,18.

Vitamin D increases the production of NGF, neurotrophin 3 and glial cell line- derived neurotrophic factor (GDNF), whereas neurotrophin 4 expression decreases⁸. Vitamin D receptors are commonly expressed in neuronal tissues, because they are needed for the development of the central and peripheral nervous system beginning from the embryonic stage (). Vitamin D induces neurotrophin expression and enhances axon development. It also plays an immunomodulatory role in Wallerian degeneration^19,20.

In an animal study in which a neuropathic pain model was developed, it was shown that hyperalgesia and allodynia decreased after vitamin D supplementation, especially in the 21-day acute phase²¹. However, the necessity of clinical trials to find effective dose in the treatment was emphasized. When its role in the mechanism of pain is considered, vitamin D prevents progression of the inflammatory cascade in chronic pain. TNF and macrophage-microglia, which cause sensitization of the peripheral and central nervous system and inhibit the stimulating mechanism²². Donato and colleagues emphasized that vitamin D plays a role in anti-VEGF agent and it may be the first line treatment because it is cheap and effective in the treatment of CTS⁴.

Akyuz et al. evaluated EMG measurements after 8 weeks of vitamin D therapy in patients with chronic generalized pain, no significant improvement was found in other conductions, except for sensory amplitudes of median and ulnar nerves²³. Shehab et al. found no statistically significant difference in nerve conduction values after vitamin D treatment for 8 weeks in diabetic peripheral neuropathic patients. They stated that Vitamin D treatment resulted in symptomatic improvement, but they attributed the lack of electrophysiologic improvement to the length of diabetes exposure and the more axonal mechanism of neuropathy¹². They have mentioned that it will take more than 8 weeks to recover. Lee and Chen et al. showed that there is a decrease in VAS scores after vitamin D replacement for 3 months in diabetic neuropathic patients²⁴.

Many previous studies show that vitamin D deficiency is present in patients with CTS. When the severity of pain was evaluated by neuropathic pain scales in these patients, pain increased^23,25. In our study, interviews with treated patients demonstrated a significant decrease in pain after treatment, like in previous studies. In fact, we obtained electrophysiologically recovery in patients with CTS. DSOL is the first parameter to response to the treatment because it is also the first parameter to be affected.

One of the most important limitations of our study is the lack of male patients and absence of a control group. We believe that further information could be gathered if the evaluation included anamnesis and examination findings. A higher number of participants could have provided more reliable results and greater statistical strength. In addition, the most important point we want to emphasize is that addition of vitamin D replacement to the treatment of patients in the mild to moderate stages of CTS is a symptomatic treatment and may support electrophysiological recovery. Perhaps, considering that the long-term clinical efficacy of the applied treatment modals may be different, a longer follow-up time is required.

In conclusion, our findings suggest that replacement of the necessary and adequate dose of vitamin D during the mild to moderate stages of CTS can both improve pain and enable electrophysiologic recovery. In addition, we suggest that, because vitamin D deficiency is widespread, increasing sun exposure to increase its synthesis is needed, and then, if replacement is required, the treatment should be initiated at an early period.

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Publication Dates

• Publication in this collection
  9 Apr 2020
• Date of issue
  Apr 2020

History

• Reviewed
  13 May 2019
• Received
  03 Nov 2019
• Accepted
  12 Nov 2019