OBJECTIVES To investigate the incidence of hyperreflexia in patients with Guillain-Barré syndrome (GBS), and its relation with electrodiagnosis of acute motor axonal neuropathy (AMAN), antiganglioside GM1 antibody, and Campylobacter jejuni infection. It was reported that patients with AMAN in northern China often had hyperreflexia in the recovery phase.
METHODS In 54 consecutive Japanese patients with GBS, sequential findings of tendon reflexes were reviewed. By electrodiagnostic criteria, patients were classified as having AMAN or acute inflammatory demyelinating polyneuropathy (AIDP). Anti-GM1 and anti-C jejuni antibodies were measured by enzyme linked immunosorbent assays.
RESULTS Seven (13%) patients developed hyperreflexia with the spread of the myotatic reflex to other segments in the early recovery phase, one of whom already had hyperreflexia in the acute progressive phase. Of the seven patients, six had AMAN and all seven had anti-GM1 antibodies, whereas only two had anti-C jejuni antibodies. Hyperreflexia was more often found in patients with AMAN than AIDP (6/23v 1/18, p=0.002), and in patients with anti-GM1 antibodies than without them (7/26v 0/28, p=0.01). Hyperreflexic patients had milder peak disabilities than patients without hyperreflexia (p=0.03). Increased motor neuron excitability in the hyperreflexic patients was supported by increased soleus H-reflex amplitudes and the appearance of H-reflexes in the small hand or foot muscles.
CONCLUSIONS Hyperreflexia often occurs in patients with GBS especially with AMAN, anti-GM1 antibodies, and milder disease. Increased motor neuron excitability further characterises the subgroup of patients with GBS with AMAN and anti-GM1 antibodies.
- Guillain-Barré syndrome
- acute motor axonal neuropathy
- anti-GM1 antibody
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Guillain-Barré syndrome (GBS) is an immune mediated polyneuropathy clinically characterised by acute symmetric muscle weakness and areflexia.1 Whereas most GBS is demyelinating neuropathy (acute inflammatory demyelinating polyneuropathy, AIDP) in western countries,2 3 an axonal form of GBS, termed acute motor axonal neuropathy (AMAN), has been recognised in northern China4 5 and in other countries.6 7 It is suggested that AMAN is associated with pure motor axonal involvement, antiganglioside GM1 antibodies, or precedingCampylobacter jejuniinfection.7-9
Chinese patients with AMAN are reported to often develop hyperreflexia during the early phase of recovery,4 5 and other studies described patients with acute motor neuropathy with preserved tendon reflexes.10-12 Preserved or exaggerated tendon reflexes do not usually occur in patients with AIDP and in patients with other peripheral neuropathies. We, therefore, investigated the incidence of hyperreflexia and its relation with electrophysiological subtypes (AMAN or AIDP), anti-GM1 antibodies, or C jejuniinfection in consecutive patients with GBS in Japan.
Patients and methods
Fifty four patients with GBS who were seen at Chiba University Hospital and its affiliated hospitals between January 1992 and April 1998 were studied. The mean age was 40.1 years (range 3 to 78 years). Their first neurological examination and electrodiagnostic study were done within 2 weeks of onset. They fulfilled the clinical criteria for GBS,1 except for two patients who had normal or brisk tendon reflexes in the first examination. The two patients were diagnosed as having AMAN because of electrophysiological evidence of motor axonal loss. Clinical disability was evaluated with the Hughes functional grading scale13 and patients were followed up for 3 months after onset. Hyperreflexia was regarded as present when there were increased amplitudes of tendon reflexes, abnormal reflex spread (finger jerks after tendon tapping of the biceps brachii or brachioradialis muscle, or thigh adduction after patella tendon tapping), and decreased reflex threshold (biceps contraction after tendon tapping of the brachioradialis, or quadriceps contraction after tapping of the midportion of the patella). Hoffmann’s and Babinski’s signs were also examined.
Nerve conduction and H-reflex studies were done sequentially using the conventional procedures. AMAN or AIDP was diagnosed based on the electrodiagnostic criteria described by Ho et al.14 When, besides the AMAN pattern, amplitude reduction of sensory nerve action potentials was present, the patients were classified as having acute motor-sensory axonal neuropathy (AMSAN). When nerve conduction studies were done more than once within 2 weeks of onset, the results of the last study were used for the electrodiagnostic classification.
The H-reflex in the soleus muscle was recorded after submaximum stimulation delivered to the tibial nerve at the knee.15Stimulus duration was 1.0 ms and the rate was 0.5 Hz. Patients lay in the prone position with the ankle joint maintained at approximately 120°. The ratio of the peak to peak maximum H-reflex to the maximum compound muscle action potential (H/M ratio) was measured. Whether the H-reflex was elicited in the abductor pollicis brevis or abductor hallucis muscle, was also examined after stimulation at the wrist or ankle respectively. The H/M ratio control data were obtained from 15 normal volunteers aged 21 to 52 years (mean 38.6 years).
ANTI-GM1 ANTIBODY ASSAY
Serum samples obtained in the first 4 weeks after onset were frozen at −80°C until used. The serum samples were tested for the presence of IgG and IgM antibodies to GM1 by the enzyme linked immunosorbent assay as described elsewhere.16 Well characterised human serum with high IgG anti-GM1 antibody titre was the internal control. Antibody titre was the highest serum dilution at which the optical density at 492 nm was 0.1 or more. Serum was considered positive when the titre was 1:500 or more.
ANTI-CAMPYLOBACTER JEJUNI ANTIBODY ASSAY
IgG anti-C jejuni antibody was measured by the enzyme linked immunosorbent assay as described elsewhere.17 Serum was considered positive when the titre was 1:2000 or more. The IgG anti-C jejuniantibody assay is sufficiently sensitive and specific for serological evidence of C jejuni infection, even if IgM and IgA antibodies are not determined.17 All anti-GM1 and anti-C jejuni antibody assays were done by one investigator (MK) who was blinded to the clinical and electrophysiological data.
Differences in percentages were tested with χ2 or Fisher’s exact test, and in medians with the Mann-WhitneyU test using Stat View 4.5 software.
TENDON REFLEX AND H-REFLEX
In the first examination (3 to 14 days after onset, mean 7.9 days), 52 of the 54 patients had areflexia (n=44) or hyporeflexia (n=8). Of the remaining two patients, one had normal reflexes, and the other, hyperreflexia (patient 6 in tables 1 and 2). During weeks 3 to 4, seven patients (13%), including patient 6, developed hyperreflexia (table 1). Hyperreflexia was associated with abnormal reflex spread and decreased reflex threshold. Hoffmann’s sign were present in four patients, but none had Babinski’s sign.
Figure 1 shows the soleus H/M ratios of patients with GBS in the acute (weeks 1 to 3) and recovery (weeks 5 to 8) phases, and those of the normal controls. In the acute phase, H reflexes were recordable in only 10 patients, including six who developed hyperreflexia. patients with GBS had low H/M ratios, except for patient 4, who had a high ratio of 0.77 (fig 2). In the recovery phase, the H/M ratios were significantly higher in patients with GBS with hyperreflexia and significantly lower in the other patients with GBS, compared with the ratios of the normal subjects. Of the seven patients with hyperreflexia, H-reflexes were elicited in the abductor pollicis brevis in four and in the abductor hallucis in three (fig 3).
Patients were classified as having AMAN (n=23), AIDP (n=18), or AMSAN (n=2), or were unclassified (n=11). Of the seven patients with hyperreflexia, six had AMAN and one AIDP (table 1). Sequential findings of patella tendon reflexes in AMAN and patients with AIDP are shown in fig 4. In the acute phase (week 1 or 2), 65% of AMAN, and 100% of patients with AIDP showed absence of patella tendon reflexes. During the early recovery phase (weeks 4 to 6), 34% of patients with AMAN and 12% of patients with AIDP had normal or brisk patella tendon reflexes. Most patients (88%) with AIDP still had areflexia 3 months after the onset. Two patients with AMSAN had areflexia up to 3 months after the onset. Hyperreflexia was significantly more frequent in AMAN (table2).
Positive anti-GM1 antibodies were found in 28 (52%) patients; 21 had IgG alone, four IgM alone, and three had both classes. All the seven patients with hyperreflexia had anti-GM1 antibodies, most of which were of IgG class (table 1). Hyperreflexia was significantly more frequent in patients with than without anti-GM1 antibodies (table 2).
ANTI-C JEJUNI ANTIBODY
Positive anti-C jejuni antibodies were found in 13 (24%) patients. Hyperreflexia was present in two (15%) of the 13 patients with anti-C jejuniantibodies, and in five (14%) of 36 patients without anti-C jejuni antibody.C jejuni infection, therefore, had no relevant association with hyperreflexia.
CLINICAL FEATURES OF PATIENTS WITH HYPERREFLEXIA
The clinical manifestations of the patients with hyperreflexia were similar to those of the other patients with AMAN; less frequent cranial and sensory nerve involvement (table 1). They had, however, significantly less peak disabilities than the other patients with GBS. On the Hughes functional grading scale, the median (range) in patients with hyperreflexia was 2.5 (2.0–3.0), whereas it was 3.5 (2.0–5.0) in patients without hyperreflexia (p=0.03). Of the hyperreflexic patients, three were able to walk with aids (Hughes grade 3), and the other four were able to walk independently (Hughes grade 2). The three patients were treated with intravenous immunoglobulin infusion (2 and 4) or plasmapheresis (1). All seven patients recovered well, six being able to run 3 months after onset. Two patients (3 and 5) had moderate atrophy of the small hand muscles 3 months after onset.
Our study showed that some patients with GBS showed obvious hyperreflexia when they had the AMAN pattern, anti-GM1 antibody, and milder muscle weakness. The incidence of hyperreflexia in AMAN was 33%, whereas McKahnn et al.5found that 12 (48%) of 25 Chinese patients with AMAN showed hyperreflexia. Most of the Chinese patients were children, but our findings showed a similar incidence of hyperreflexia in AMAN that occurs in adults.
Because sensory nerve involvement in AIDP or AMAN should contribute to the areflexia, the selective involvement of motor axons in AMAN could account for the relative preservation or earlier appearance of reflexes18; but it does not account for hyperreflexia and reflex spread to other segments. Some of our patients with AMAN had electrophysiological evidence of increased motor neuron excitability shown by the increased soleus H/M ratios and the abnormal appearance of H-reflexes in the small muscles of the hands or feet. Our hyperreflexic patients had less peak disability than the other patients with GBS. We consider that hyperreflexia could be evident when motor axonal loss is less severe and sensory nerves are intact. Van der Mechéet al 19 found that, in patients with pure motor GBS, tendon reflexes were preserved up to MRC grade 3 paresis.
The mechanism that causes hyperreflexia in GBS is unknown. The abnormal reflex spread to other segments suggests a central mechanism; possibly due to the dysfunction of spinal inhibitory interneurons, or of the upper motor neurons. Because hyperreflexia was found only in patients with anti-GM1 antibodies, we speculate a possible role of this antibody. Hyperreflexia is occasionally seen in chronic motor neuropathy associated with high titre anti-GM1 antibody,20 21 and anti-GM1 serum injected in the subarachnoid space was reported to cause damage to the central axons in the spinal cord as well as nerve roots.22 In addition, the spinal nerve roots, where the blood-nerve barrier is anatomically deficient,23 are preferentially affected in GBS.24 Inflammation in the spinal roots may lead to local dysfunction of the blood-CNS barrier and allow anti-GM1 antibodies to bind with the neural structures in the spinal cord. Further study is required to clarify the mechanism of increase in motor neuron excitability in GBS.
In AMAN or anti-GM1 positive GBS, excitability of the motor neuron could increase even in the acute progressive phase. In most of our patients, hyperreflexia developed in the early recovery phase, but a few patients with AMAN had brisk reflexes in the acute phase. Moreover, patient 4 had an increased soleus H/M ratio despite the markedly low compound muscle action potential at the time when achilles tendon reflexes were absent (fig 2, on day 8), suggestive of hyperexcitability of the residual motor neurons. Several studies described patients who had acute pure motor neuropathy with preserved tendon reflexes throughout the course,10-12 and in some cases, the disorder was not diagnosed as GBS because of preserved reflexes.11 Yuki and Hirata12 described four patients with AMAN with preserved tendon reflexes (two of them had even brisk reflexes), and proposed that these patients should be treated as having GBS. Our results confirm that hyperreflexia is not a finding inconsistent with the diagnosis of GBS.
In conclusion, hyperreflexia often occurs in patients with GBS with AMAN, anti-GM1 antibody, and less severe disease. Increased motor neuron excitability further characterises the subgroup of patients with GBS with the AMAN pattern and anti-GM1 antibodies.
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