Despite 30 years of research there are still significant unknowns and controversies associated with multifocal motor neuropathy (MMN) including disease pathophysiology, diagnostic criteria and treatment. Foremost relates to the underlying pathophysiology, specifically whether MMN represents an axonal or demyelinating neuropathy and whether the underlying pathophysiology is focused at the node of Ranvier. In turn, this discussion promotes consideration of therapeutic approaches, an issue that becomes more directed in this evolving era of precision medicine. It is generally accepted that MMN represents a chronic progressive immune-mediated motor neuropathy clinically characterised by progressive asymmetric weakness and electrophysiologically by partial motor conduction block. Anti-GM1 IgM antibodies are identified in at least 40% of patients. There have been recent developments in the use of neuromuscular ultrasound and MRI to aid in diagnosing MMN and in further elucidation of its pathophysiological mechanisms. The present Review will critically analyse the knowledge accumulated about MMN over the past 30 years, culminating in a state-of-the-art approach to therapy.
- PERIPHERAL NEUROPATHOLOGY
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Despite 30 years of research there are still significant unknowns and controversies associated with multifocal motor neuropathy (MMN) including disease pathophysiology, diagnostic criteria and treatment (table 1). Foremost relates to the underlying pathophysiology, specifically whether MMN represents an axonal or demyelinating neuropathy and whether the underlying pathophysiology is focused at the node of Ranvier. In turn, this discussion promotes consideration of therapeutic approaches, an issue that becomes more directed in this evolving era of precision medicine. In terms of knowns, it is generally accepted that MMN represents a chronic progressive immune-mediated motor neuropathy, clinically characterised by progressive asymmetric weakness and electrophysiologically by partial motor conduction block. While MMN may be considered rare with prevalence estimated at 0.6 to 2 per 100 000 population,1 2 it is likely to be an under-recognised entity. In addition to improved understanding of the basic mechanisms there have also been recent developments in the use of neuromuscular ultrasound and MRI to aid in diagnosing MMN and in further elucidation of its pathophysiological mechanisms. As such, the present Review will critically analyse the knowledge accumulated about MMN over the past 30 years, culminating in a state-of-the-art approach to therapy.
Classically MMN presents as an asymmetrical upper limb pure motor multiple mononeuropathy, with often prominent wasting despite a short history of weakness. MMN more commonly affects males, with a male-to-female ratio of 2.7:1. Age at symptom onset can range between 20 and 70 years with a mean age of 40 years.1 3 4 The first symptom is most commonly distal upper limb weakness but with relative sparing of finger flexors.1 Foot drop is the first symptom in a third of patients. Many with initial lower limb involvement later develop upper limb symptoms. Involvement of the non-dominant upper limb is more frequently reported. Fasciculations and cramps are prominent and observed in up to 40% of patients, and in some cases may generate local muscle hypertrophy. Aggravation of weakness by cold is common and reported in 83% of cases in one study.5 Deep tendon reflexes are usually reduced in the affected limb, but may also be normal.
The presence of sensory symptoms, signs or neurophysiological abnormalities particularly at diagnosis or early in disease should raise significant diagnostic uncertainty and prompt further investigation including consideration of targeted nerve biopsy. However, in one case series, 22% had abnormal vibration sense in the distal lower limb, with these cases having had a longer median disease duration compared with those without sensory findings.1
Involvement beyond the limbs is rare, with scattered reports of phrenic and cranial nerve involvement.6 Diagnostic criteria for MMN were proposed by the European Federation of Neurological Societies and the Peripheral Nerve Society and published in 2010 (box 1 lists the clinical criteria for MMN).7
Clinical criteria for multifocal motor neuropathy as proposed by the EuropeanFederation of Neurological Societies7
Core criteria—both must be present
Slowly progressive or stepwise progressive, focal, asymmetrical limb weakness, that is, motor involvement in the motor nerve distribution of at least two nerves, for more than 1 month. If symptoms and signs are present in the distribution of one nerve only a possible diagnosis can be made
No objective sensory abnormalities except for minor vibration sense abnormalities in the lower limbs
Supportive clinical criteria
Predominant upper limb involvement
Decreased or absent tendon reflexes in the affected limb
Absence of cranial nerve involvement
Cramps and fasciculations in the affected limb
Response in terms of disability or muscle strength to immunomodulatory treatment
Upper motor neuron signs
Marked bulbar involvement
Sensory impairment more marked than minor vibration loss in the lower limbs
Diffuse symmetrical weakness during the initial weeks
Copyright 2010 Peripheral Nerve Society. Used with permission from, John Wiley and Sons.7
Identification of motor conduction block (CB) is the key neurophysiological criterion in the diagnosis of MMN (box 2).7 The two most commonly affected nerves are the median and ulnar nerves,3 in their forearm segments and not at typical compression sites. The CB observed in MMN is unique in that it affects motor fibres exclusively with normal sensory conduction through the same segment in mixed nerves.2 3 Additionally the block is focal and occurs abruptly and, at least in the earliest stages of the disease, motor conduction distal to the site of block may remain normal.3
Electrophysiological criteria for conduction block7
1. Definite motor conduction block (CB)*
Negative peak compound motor action potential (CMAP) area reduction on proximal vs distal stimulation of at least 50% whatever the nerve segment length (median, ulnar and peroneal). Negative peak CMAP amplitude on stimulation of the distal part of the segment with motor CB must be >20% of the lower limit of normal and >1 mV and increase of proximal to distal negative peak CMAP duration must be ≤30%
2. Probable motor CB*
Negative peak CMAP area reduction of at least 30% over a long segment of an upper limb nerve with increase of proximal to distal negative peak CMAP duration ≤30%
Negative peak CMAP area reduction of at least 50% (same as definite) with an increase of proximal to distal negative peak CMAP duration >30%
3. Normal sensory nerve conduction in upper limb segments with CB (see exclusion criteria)
Copyright 2010 Peripheral Nerve Society. Used with permission from, John Wiley and Sons.7
*Evidence for CB must be found at sites distinct from common entrapment or compression syndromes.
The criteria for definite CB have been debated at length, with different criteria for different nerves depending on difficulty of obtaining consistent compound motor action potentials (CMAPs) from appropriate sites.2 3 8–10 For example defining CB as definite in the tibial nerve requires a greater CMAP decrement than in the forearm segment of the median nerve. There is evidence that CMAP decrement for the detection of block may be more accurately measured from CMAP area decrement, rather than amplitude.9
Phase cancellation due to temporal dispersion leading to spurious CB is a common finding in demyelinating neuropathies and can be a significant issue in the diagnosis of CB in MMN.9 Currently there are no reliable and reproducible techniques for assessing proximal sites of CB. Needle stimulation of motor roots is difficult to undertake with significant chance of false-positive recordings and is not well tolerated. Many criteria for CB in MMN also include a stipulation of the maximal amount of temporal dispersion that is allowable. Similarly, CB is very difficult to delineate reliably when the distal evoked CMAP amplitude is less than 1 mV.3
Electromyography (EMG) almost always reveals significant chronic denervation and reinnervation of muscles supplied by nerves with CB, demonstrating that axonal degeneration is a significant feature of MMN even from the earliest onset of the disease.3
There have been reports of MMN with typical clinical features but no CB identified.4 A possible reason is very proximal or distal locations of CB where routine electrophysiology is unable to detect block. Another possibility is conduction studies were performed only in clinically affected limbs while CB may be found also in nerves innervating muscles with normal strength. There does not appear to be any significant differences in clinical characteristics and treatment response between those with and without focal block.4
In a patient who presents with symptoms of weakness suggestive of a lower motor neuron (LMN) syndrome, apart from MMN, other diagnoses to consider include amyotrophic lateral sclerosis (ALS) and particularly the LMN variant of progressive muscular atrophy (PMA), late onset forms of spinal muscular atrophy (SMA), monomelic amyotrophy including Hirayama disease, focal and pure motor variants of chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal acquired demyelinating sensory and motor neuropathy (MADSAM) often referred to as the Lewis-Sumner Syndrome, distal hereditary motor neuropathies and hereditary neuropathy with liability to pressure palsy (HNPP).11 The acute motor axonal neuropathy (AMAN) variant of Guillain-Barré syndrome (GBS) is a consideration in pure motor presentations with an acute onset. There have been reported cases of MMN presenting abruptly though this is unusual.12 Monitoring often reveals progression in MMN beyond 1 month, whereas AMAN tends to exhibit a monophasic course with plateau by 4 weeks from symptom onset followed by a period of recovery.
MMN is an important diagnosis to consider given there is at least partially effective treatment available. Some features are atypical for MMN, particularly the presence of bulbar or respiratory involvement, or sensory involvement. Differential diagnoses can generally be differentiated from MMN by appropriate imaging of the cervical spinal cord (Hirayama disease), electrophysiological (MADSAM, PMA), genetical (SMA, HNPP and a proportion of dHMN), serological (AMAN typically associated with IgG antibodies against GM1 and GD1a) and in some cases cerebrospinal fluid analysis (MADSAM, CIDP and variants, GBS).11 Although in some cases the diagnosis is still difficult and serial assessment and even trials of therapy with appropriate monitoring are required.
MRI and neuromuscular ultrasound
A supportive criterion for the diagnosis of MMN is the detection of diffuse nerve swelling of the brachial plexus by MRI.7 Nerve ultrasound is also emerging as a tool to identify such abnormalities and possible sites of proximal CB.
MRI of the cervical nerve roots and brachial plexus can demonstrate abnormalities of cervical root and plexus T2 hyperintensity and enlargement in MMN in between 35% to 50% of patients.13 14 Such abnormalities can also be seen in other inflammatory neuropathies such as CIDP. An abnormal MRI did not correlate with specific clinical characteristics or response to treatment in MMN patients.13
High-resolution ultrasound (HRUS) is an emerging tool in the assessment of peripheral nerve pathology. Multifocal nerve enlargement can be identified in the brachial plexus, nerve roots and peripheral nerves, with these changes demonstrated in nerves both with and without clinical and electrophysiological abnormalities.15 One study found significantly increased cross-sectional areas (CSA) in median, ulnar and tibial nerves in MMN patients compared with controls.16 Intra-nerve variability and asymmetry of CSA was seen in the median nerve of MMN patients, suggestive of significant focality of nerve abnormalities.
A comparative study of MRI and HRUS of the cervical nerve roots and brachial plexus in treatment-naïve patients with CIDP or MMN demonstrated MRI findings of nerve enlargement and/or T2 hyperintensity in 50% of MMN patients and HRUS finding of nerve enlargement in 67%.14 Imaging abnormalities on either modality were seen in 79% of MMN patients, half of this group having both abnormal MRI and HRUS, 36% with only HRUS abnormalities and 14% with only MRI findings.
Ultrasound studies have shown promise in assisting with differentiating MMN from ALS. Studies of motor-containing peripheral nerves, cervical nerve roots and/or brachial plexus have found increased CSA measurements in MMN compared with ALS patients.17–19 Ultrasound protocols and models were also proposed to differentiate MMN and ALS, with sensitivities greater than 87% and specificities approaching 100% being shown. Apart from peripheral nerve CSA, a recent study using nerve ultrasound showed that median and ulnar nerve CSA distal-proximal ratios may be useful in differentiating ALS from MMN.20 However it is unclear whether HRUS can distinguish between MMN and motor variants of CIDP.
Imaging abnormalities in MMN are generally multifocal and may correlate with sites of CB but can also be identified in nerves that do not have clinical or electrophysiological abnormalities detected.15 17 18 21 This suggests that pathology may be more widespread than is evident by clinical and electrophysiological assessment alone, with imaging abnormalities potentially detectable at an earlier stage of disease course. Furthermore, diagnostic protocols consisting of examination at specific sites can be useful as shown in HRUS-based studies.18 19 HRUS-based assessment is likely to be a cheaper, safer and more accessible technique than MRI. However, both techniques require expertise at operation and interpretation and require population-based normal values to be defined for them to be part of an objective assessment.
MMN is thought to be an immune-mediated neuropathy. The pathophysiological mechanism behind CB was initially hypothesised as due to focal demyelination, but there is increasing evidence that functional disturbances at the node of Ranvier may be the cause of block. The term ‘nodo-paranodopathy’ encompasses neuropathies due to dysfunction at nodes and paranodes.22 Schwann cell dysfunction at the paranodal region may be an important component of nodo-paranodopathy with very focal demyelination in this region necessary to open up the paranode to immune attack.
Nerve excitability studies of MMN showed excitability parameters consistent with hyperpolarisation, as also seen in postischaemic nerves, including greater axonal superexcitability distal to the site of CB.23 Depolarisation at the site of CB may result in this observation via intracellular sodium (Na+) accumulation possibly due to sodium channel or Na+/potassium (K+)-pump dysfunction. Recent mathematical modelling by Garg and colleagues suggested reductions of Na+ and K+ ion channel function along the axon distal to CB.24 These functional disturbances of the axonal membrane have been hypothesised to lead to increased ectopic generation manifesting as positive symptomatology such as fasciculations and cramps.23 A further study in which polarising direct currents were delivered at sites of CB, as determined by inching studies, showed that blocks may be depolarising, hyperpolarising or both.25 Assessing axonal excitability at the sites of CB was based on response to the polarising current applied, with hyperpolarisation expected to worsen and depolarisation to improve CB at sites of membrane hyperpolarisation, with the opposite applying for sites of depolarisation. The authors hypothesised that their findings may reflect disease evolution over time with depolarising preceding the later development of hyperpolarising blocks.
CB in MMN has been demonstrated to be activity-dependent. One study showed transient reduction in proximal-to-distal CMAP ratios following maximal voluntary contraction (MVC).26 There was also reduction in force generated by affected muscles post-contraction. Transient CB or temporal dispersion was seen post-MVC in six MMN patients without overt CB identified on routine electrodiagnostic tests.27 Another study of 19 MMN patients failed to demonstrate activity-dependent CB.28 However in nerve segments with pre-existing CB, MVC resulted in temporal dispersion. Apart from differences in methodology, the different findings between studies may reflect the nature or degree of the underlying block. The mechanism for these changes is likely nodal sodium channel dysfunction, Na+/K+-pump hyperactivity or other nodal/paranodal functional disturbance.
Eighty-three per cent of MMN patients report cold paresis.5 This suggests a prominent functional disturbance rather than focal demyelination, as cold tends to improve symptoms and CB secondary to demyelination. Cooling of human nerves has been shown to induce axonal depolarisation, likely due to reduced activity of temperature-sensitive Na+/K+-pump.29 In MMN, depolarising CBs may be exacerbated via this mechanism with corresponding symptom exacerbation. A study comparing the effect of cooling on excitability parameters in motor and sensory axons found significant differences between them.30 In motor axons, cooling resulted in changes consistent with axonal depolarisation, including fanning-in of threshold electrotonus (as defined by a decrease in threshold change of the threshold electrotonus waveforms) and steepening of current-voltage relation (I/V) slopes.30 31 These findings may reflect differences in ion channel subtypes expressed on motor and sensory axons, with their involvements in MMN possibly explaining its pure motor manifestations. Nerve excitability studies and the phenomenon of cold paresis indicate that MMN cannot be explained by demyelination alone, thereby supporting the concept of it being a nodo-paranodopathy.
The presence of anti-GM1 IgM antibodies was first described in MMN in 1988. These antibodies are present in at least 40% of cases.1 3 32 Sensitivity is low and they are detectable in a proportion of neurologically normal, ALS and other neuropathy patients. However in the setting of high positive titres and when an immune-mediated motor neuropathy is suspected, specificity can exceed 90%.32 In MMN, these antibodies are likely produced by a limited number of B cell clones.33
The factors leading to development of MMN are not well understood. A genetic predisposition to autoimmunity is suggested by an increased frequency of other autoimmune diseases present in MMN patients and their first-degree relatives as well as higher frequencies of the human leucocyte antigen-DRB1*15 haplotype, which is also associated with multiple sclerosis and CIDP, among MMN patients relative to controls.34 35 A preceding infectious trigger may play a role, potentially through molecular mimicry of ganglioside or other epitopes, though there is not yet any clear evidence supporting this. A small study found antibodies against Campylobacter jejuni were more frequent than expected in MMN patients, but this was not supported by a later study.36 37 IgM monoclonal gammopathy has been identified in 7% of MMN patients compared with 2% of healthy controls.38 The significance of this finding is not clear and may represent B cell autoimmunity or a concomitant lymphoproliferative disorder which may or may not be pathogenetically connected.
Gangliosides are glycosphingolipids attached to sialic acid moieties. GM1 is ubiquitously abundant and found in the central and peripheral nervous system.39 In peripheral nerves, it is found in the axolemma and myelin predominantly at nodal and paranodal regions and concentrated at cholesterol-enriched domains of plasma membranes. Gangliosides serve several functions including maintaining tight junctions, ion channel clustering with maintenance of potassium channels in paranodal/internodal regions and sodium channels at nodes, and cellular calcium homeostasis.39–41
Studies have suggested that anti-GM1 antibodies are pathogenic through both direct and indirect mechanisms (figure 1). Anti-GM1 antibodies can cause direct functional disturbance via increase in potassium current at paranodes and disruption of calcium-signalling pathways.41 42 They can also cause indirect nerve dysfunction via the classical complement pathway.43 In animal studies, complement activation and membrane attack complex formation result in disruption of nodal sodium channel clusters and paranodal potassium channel clusters.42 44 These alterations can lead to suppression of sodium current and leakage of driving current. Complement deposition and activation was prevented by addition of immunoglobulins.43 A human induced-pluripotent stem cell (IPSC)-derived model of MMN showed both antibody-mediated complement-dependent and complement-independent disruption of motor neuron calcium homeostasis and axonal damage.41 Disruptions were reduced with immunoglobulin application. Though providing novel insights, the findings of this human in vitro model of MMN must be interpreted with its limitations in mind, which include the absence of glial cells and in particular Schwann cells and the relative immaturity of neurons studied.
Using indirect immunofluorescence on rat teased nerve fibres incubated with sera of 11 MMN patients, Garg et al identified only one patient with a paranodal staining pattern despite 55% of patients being anti-GM1 IgM positive.24 In contrast, 9 of 11 CIDP patients with CB showed staining at the node, paranode and/or myelin. This supports the notion that MMN and CIDP have differing disease mechanisms and target antigens. Though not supportive, this study does not rule out MMN as a possible nodo-paranodopathy. Differences between the human and rat epitope may limit antibody binding, and intravenous immunoglobulin (IVIG) given as treatment may also influence findings.
The focality of abnormalities raises questions as to the pathophysiological mechanisms resulting in such selectivity. Serum from patients with MMN has been shown to disrupt the blood-nerve barrier,45 with motor nerves more susceptible than sensory nerves. There is no significant difference in quantity of GM1 found on motor or sensory nerves, but differences in composition of ceramide moieties of gangliosides may modulate antibody binding affinity and susceptibility to antibody-mediated damage of motor and sensory nerves.46 GM1 serves a crucial role in maintaining the integrity of motor nerves but not as significantly for sensory nerves.40 Incubation of human IPSC-derived sensory neurons with MMN patient sera resulted in binding of anti-GM1 antibodies to sensory neurites.41 However, the sensory neurites do not undergo damage as seen in motor neurites. This suggests that motor neurons are more vulnerable to anti-ganglioside antibody-mediated injury than sensory neurons. A possible explanation is the presence of cofactors on motor neurons, but absent on sensory neurons, playing a critical role in unmasking epitopes and facilitating nodal dysfunction and nerve injury.41
Other antibodies and target antigens
In a human IPSC-derived model, Harschnitz et al found that there was significantly increased IgM binding to neurites following incubation with either anti-GM1 IgM positive or negative MMN patient sera compared with controls.41 The antibody target of both sera groups appeared to be GM1. This finding is likely in part due to technical factors which limit sensitivity of anti-GM1 antibody detection. Several studies have shown increased detection rates of anti-GM1 IgM in combination with the glycolipid galactocerebroside (GalC), with increased sensitivity up to 81% but with a slight drop in specificity.47 48 The addition of GalC likely enhances antibody binding possibly through better exposure of GM1 epitopes.
Another possibility in anti-GM1 antibody-negative cases is the presence of antibodies directed at other antigens. Several studies have sought to identify these. The nodal proteins gliomedin and neurofascin-186 (NF186) have been proposed as potential targets given their role in nodal sodium channel clustering. Notturno et al showed 62% of MMN patients had antibodies to gliomedin or NF186 using synthetic rat peptides. However this was not supported by cell binding assays using transfected cells.49 Two studies which additionally examined for antibodies against paranodal proteins contactin-1 and neurofascin-155 using human proteins did not detect antibodies against these in any MMN patient.50 51 The likely reason for these opposing results is the use of different proteins in their assays, rat in the first and human in the subsequent two studies. Pestronk et al proposed antibodies against heparin disaccharide NS6S as associated with acquired chronic motor neuropathies.52 They were present in 43% of patients with a motor neuropathy and 57% with MMN. Nobile-Orazio et al identified 23% of MMN patients with anti-NS6S IgM antibodies but this was not statistically significant compared with controls.47 Therefore anti-NS6S antibodies’ diagnostic and pathogenic significance remains uncertain.
There have been few studies examining the pathological changes of affected nerves. Kaji and colleagues described a patient who had their medial pectoral nerve removed for pathological examination, with this being just distal to the site of CB in the brachial plexus.21 Demyelinating features of large-diameter axons that were thinly myelinated or devoid of myelin and small onion bulbs were seen with reduced fibre density. Inflammatory cell infiltrates were not seen. Auer et al reported a case of a lower motor neuron syndrome suggestive of MMN with electrophysiological findings consistent with demyelination in the brachial plexuses but with no CB identified.53 Proximal right ulnar nerve biopsy demonstrated features consistent with chronic demyelination with onion bulbs and an absence of inflammatory cells.
In contrast, Taylor and colleagues identified multifocal fibre degeneration and loss (particularly of large fibres) and significant numbers of regenerative clusters in fascicular nerve biopsies taken at sites of CB in eight nerves from seven MMN patients.54 There were no features to suggest demyelination including no onion-bulb formation. Small perivascular lymphocytic infiltrates were seen in two nerves. The authors hypothesised that MMN was an axonopathy without demyelination and that the CB was an antibody-mediated channelopathy focused at the nodes of Ranvier.
These two disparate findings, one of chronic demyelination and the other of multifocal fibre degeneration and regeneration, raise several possibilities. One possibility is that different pathological alterations occur at different sites of affected nerves, with chronic demyelinating changes at sites distal to CB perhaps secondary to the primary insult causing CB. Another possibility is that different underlying pathological mechanisms result in different pathological changes. Focal and motor variants of CIDP can have a clinical presentation very similar to that of MMN and also demonstrate motor CB on electrophysiological studies. However, nerve pathology in focal motor CIDP would be expected to demonstrate demyelination as its prominent feature (figure 2).
In terms of sensory nerve pathology, a study examining sensory nerve biopsies from 11 patients found very minor demyelinating features.55 These findings suggest that sensory nerves may also undergo insult though of much lesser severity compared with motor nerves. However, given the lack of sensory symptoms and electrophysiological abnormalities in MMN, and in the cases biopsied, and these very minor pathological changes seen, it is difficult to make any strong inferences although sensory involvement in late stage disease has been reported in a significant number of cases.1 3
Given its likely immunopathogenic basis, immunomodulating agents have been used extensively in the treatment of MMN. IVIG is currently the first-line treatment with evidence from several randomised controlled trials (RCT) demonstrating benefit. RCT evidence supporting non-immunoglobulin agents are however lacking.
A beneficial effect of IVIG in improving muscle strength was first described in 1992. To date there have been five RCTs of IVIG use in MMN, all demonstrating a clear benefit. Four were part of a Cochrane meta-analysis which demonstrated an improvement in muscle strength in 78% of patients treated with IVIG compared with only 4% on placebo.56 Thirty-nine per cent of IVIG-treated patients had improvement in disability but this was not statistically significant, which is likely due to lack of a good disability scale suitable for the unusual distribution of weakness in MMN. The final RCT was a double-blind crossover study with 44 patients randomised to two groups, one receiving 12 weeks of IVIG followed by 12 weeks of placebo and the other receiving the same treatments in reverse order.57 Mean maximal grip strength of the affected hand increased by 3.75% with IVIG and decreased 31.38% with placebo. Worsening disability was seen in 35.7% of subjects on placebo but not after crossing over to IVIG. This was compared with 11.9% whose disability worsened while on IVIG but not during their placebo period. Sixty-nine per cent of subjects were switched prematurely from placebo to open-label IVIG due to substantial functional deterioration on placebo. The authors concluded that IVIG treatment in MMN clearly improved muscle strength and disability.
In the long-term, most patients require maintenance IVIG to prevent clinical worsening. Despite continued IVIG, a significant proportion of patients exhibit disease progression with reduced muscle strength though still better than before treatment.1 8 58–60 The IVIG dose required for maintenance increases with time. Serial electrophysiological assessment have demonstrated evidence of reinnervation and demyelination/axonal loss although CB may persist despite clinical improvement.60 IVIG, though beneficial, is only able to partially control the disease process and slow axon loss.
Cats et al showed that more severe disability or weakness was associated with axon loss and years untreated.1 Axon loss was the most significant determinant of muscle weakness followed by years untreated in another study.61 A study using higher maintenance doses of IVIG showed that IVIG can significantly reduce axonal degeneration and also promote reinnervation.62 As such, early diagnosis and treatment institution is of utmost importance to minimise axonal loss and disability accrual.
Subcutaneousimmunoglobulin (SCIG) has potential advantages over IVIG including patient convenience, avoidance of hospitalisation, potential cost benefit and better overall adverse effect profile. SCIG also results in a more stable serum IgG level thus preventing adverse events due to unphysiologically high serum IgG levels and symptom fluctuation due to end-of-dose effect with IVIG.
Several studies have described SCIG therapy in patients who have previously been on maintenance IVIG, using equivalent total monthly doses. These have shown similar efficacy between SCIG and IVIG.63 A meta-analysis examining efficacy and safety of SCIG compared with IVIG in MMN and CIDP showed no significant differences in muscle strength and a 28% reduction in relative risk of moderate or systemic adverse effects.64 A 2 year follow-up study showed SCIG was effective at maintaining clinical stability.65
An open-label trial of SCIG with 15 MMN patients used a dose ratio of 1.53:1 of SCIG-to-IVIG in patients receiving less than 2 g/kg IVIG per month, and 1:1 dosing in patients on 2 g/kg/month.66 Three of six patients receiving equivalent dose SCIG deteriorated in strength while all patients on 1.53:1 SCIG dosing remained stable. The authors proposed that SCIG dosing should be commenced at a ratio greater than 1:1. This contrasts with studies demonstrating stability with equivalent dosing.
There are reports from the 1990’s that have shown clinical benefit with use of oral or intravenous cyclophosphamide including in cases refractory to IVIG.67 However there are also descriptions of cases in which the efficacy of cyclophosphamide is equivocal or not effective at all.59
In a study of six MMN patients on maintenance IVIG, oral cyclophosphamide was added.67 All six patients showed improvement in their muscle strength, functional impairment scores and modified Rankin disability scores. They were able to increase the interval between IVIG doses, with three patients able to stop all treatment for up to 2 years before return of symptoms which responded to IVIG. Longer follow-up of these patients has not been reported
Cyclophosphamide has potentially significant adverse effects including myelosuppression, haemorrhagic cystitis, infertility, malignancies and opportunistic infections.67 Risk increases with repeated treatment which is usually necessary in MMN. In a patient who is refractory to IVIG with significant worsening of weakness and/or functional impact, treatment with cyclophosphamide may be trialled but must be considered in the context of its risk profile. Full informed consent and careful monitoring are essential. It is important to note that there is little evidence that cyclophosphamide or any therapy will reverse established disability and therefore the use of potentially harmful therapies should be avoided in this situation. Given mixed reports of benefit, an RCT would be very useful in clarifying cyclophosphamide’s efficacy, and if this is established also the ideal delivery route and dosage regimen. However, the development and application of newer therapies has made such a trial highly unlikely. Therefore, cyclophosphamide as a treatment for MMN should be considered a therapy of last resort with full informed consent in those who are progressing despite best practice treatment with IVIG and whose independence is significantly threatened by progressive MMN.
Steroids and plasma exchange
Corticosteroid efficacy in MMN has been disappointing with no benefit and in some cases clinical worsening.59 A similar situation has been observed with plasma exchange with a lack of efficacy and again with some patients exhibiting deterioration.68 The reason for these unexpected responses to steroids and plasma exchange is unknown, but may be due to an altered balance between damaging and regulatory immune components resulting in worsening clinical state.
Rituximab is a murine-human chimeric monoclonal antibody against CD20, which results in B cell depletion. Several small observational studies described benefit with rituximab, with improved muscle strength and increased interval between IVIG doses in those on maintenance IVIG.69 Other studies reported equivocal benefit in terms of maintenance IVIG requirement, with one case describing a clinical worsening 2 months following rituximab dosing.70 An open-label trial of six patients on maintenance IVIG given rituximab and followed for 12 months did not demonstrate a reduction in IVIG administration or change in grip strength, Medical Research Council sum score or disability score.71 Further studies of rituximab and other anti-CD20 monoclonal antibodies are required to determine if there is any benefit. Currently the use of rituximab in MMN cannot be supported outside of clinical trials or possibly as rescue therapy where other treatments have failed, with a low expectation of success.
Eculizumab is a humanised monoclonal antibody against the complement component C5 which acts to inhibit the terminal pathway in complement activation. Given complement activation appears to be implicated in the pathophysiology of MMN, inhibition would be expected to prevent nerve injury. Eculizumab has been proven to be beneficial in paroxysmal nocturnal haemoglobinuria, a disease in which complement activation is involved in its pathogenesis. In an open-label trial of eculizumab in 13 MMN cases, improvements in self-evaluated functional rating scale and muscle strength as measured by myometry, as well as a small but statistically significant decrease in median percentage of CB across all nerves studied, were seen.72 No change in IVIG dosing interval in those on maintenance IVIG was seen. This short-term non-blinded trial demonstrates the potential clinical benefit with eculizumab, but this needs to be established in larger RCTs with longer follow-up.
Other immunomodulatory treatments
There are reports of other immunomodulatory agents being used, including azathioprine and interferon-beta, with variable effect.8 73 Adjunctive use of mycophenolate was assessed in a RCT with 28 patients.74 No significant alteration in disease course or IVIG dose was seen. Thus, there is no compelling evidence to advocate treatment with these agents at this stage.
Currently the only treatment that has been shown to be unequivocally useful in the treatment of MMN is IVIG/SCIG. However, there is no clear consensus on treatment regimes and when to reduce, stop or commence therapy. Many cases of MMN may demonstrate stability for years without therapy and treatment may be seen as holding them stable. Therefore, understanding the trajectory of an individual’s condition is important. Regular review with nerve conduction studies and a blinded assessment of peripheral nerve function such as the neuropathy impairment score (NIS) or NIS subscore of weakness can significantly aid in treatment decisions.3 75 No treatment has been shown to reverse established atrophy. A trajectory of worsening on assessment is an indication for treatment, and this should consist of IVIG or SCIG utilising the regimens as outlined in the clinical trials. If improvement or stabilisation of a worsening trajectory is seen the maintenance dosage of IVIG/SCIG that maintains that improvement should be sought. Practice points proposed by the European Federation of Neurological Societies and the Peripheral Nerve Society suggest IVIG induction dose of 2 g/kg over 2 to 5 days, and maintenance IVIG of 1 g/kg every 2 to 4 weeks or 2 g/kg every 1 to 2 months as guided by treatment response.7 IVIG/SCIG is expensive and in short supply in many countries and therefore every effort should be made to limit the amount used to treat MMN as for all conditions. Clear cut guidelines for stopping or reducing therapy should be developed based on trials of weaning or ceasing therapy.
Other immunosuppresants/immunomodulators (cyclophosphamide, rituximab or eculizumab) have not been shown to alter the natural history of MMN reproducibly in clinical trials. Preferably these treatments should be given as part of clinical trials. However due to the rarity of MMN these are not currently underway to the best of our knowledge. Fully informed consent and careful objective monitoring is essential.
Since MMN was first described more than three decades ago, our understanding of its clinical characteristics and underlying pathophysiology have progressed. Early recognition and diagnosis of MMN is important given that the years left untreated and resultant axonal loss are poor prognostic factors.1 61 Brachial plexus MRI has been shown to be useful in diagnostic evaluation, and HRUS is also an emerging and promising technique. Testing for antibodies against GM1 with GalC in patients negative for anti-GM1 antibodies may aid evaluation. The aim once MMN is diagnosed is to institute effective treatment to slow disease progression and axonal loss. Currently IVIG/SCIG is the treatment of choice although there are still many unanswered treatment questions. Eculizumab has been proposed as a possible effective treatment, but we currently await RCT evidence regarding its efficacy.
The pathophysiology of MMN is still not fully elucidated however there is now strong evidence that MMN is not a variant of CIDP and that these two conditions can be separated pathologically. There is increasing evidence that MMN is a disorder of the paranodal or nodal regions of the node of Ranvier. However direct ultrastructural confirmation of this is lacking and should be a major goal of future research. The mechanisms by which an immune attack can result in focal motor nerve damage presumably acting at the nodes of Ranvier need further elucidation. The development of an IPSC model of MMN and other peripheral nerve disorders will greatly aid these types of experiments.
Contributors BVT, MCK, PJBD and LHvdB conceived the idea for the article. WZY drafted the manuscript. All authors revised the manuscript critically for important intellectual content and gave final approval of the version to be published.
Funding BVT was supported by a Macquarie Foundation MSRA Clinical Fellowship. This work was supported in part by funding to Forefront from the National Health and Medical Research Council of Australia (NHMRC) program grant (#1037746). MCK was supported by an NHMRC Practitioner Fellowship (#1156093).
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.