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ISSN: 2155-9562
Journal of Neurology & Neurophysiology
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Diversity of Neuromyelitis Optica: Inner City Hospital Experience and Review of Literature

Harini Sarva1*, Ariel Antezana2, Johanne Policard3, Diana Rojas-Soto3, Yassir El-Sherif4, Ilya Kister2, Steven Pulitzer5 and Yaacov Anziska3

1Department of Neurology, Beth Israel Medical Center, New York, NY, USA

2NYU MS Center, Department of Neurology, New York University School of Medicine, New York, NY, USA

3Department of Neurology, SUNY Downstate Medical Center, Brooklyn, New York and Kings County Hospital, Brooklyn, New York, USA

4Staten Island University Hospital, Staten Island, NY, USA

5Department of Radiology, Kings County Hospital, Brooklyn, New York, USA

Corresponding Author:
Harini Sarva
Beth Israel Medical Center, New York, NY 10003, USA
Tel: 212-844-6050
Fax: 212-844-8461
E-mail: [email protected]

Received date: December 27, 2013; Accepted date: January 27, 2014; Published date: February 06, 2014

Citation: Sarva H, Antezana A, Policard J, Soto DR, Sherif YE, et al. (2014) Diversity of Neuromyelitis Optica: Inner City Hospital Experience and Review of Literature. J Neurol Neurophysiol 5:189. doi:10.4172/2155-9562.1000189

Copyright: © 2014 Sarva H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Neuromyelitis Optica (NMO) is a potentially devastating, complex autoimmune disease of the central nervous
system that differs clinically and pathologically from the more common Multiple Sclerosis (MS). In this paper, we
briefly describe our clinical experience with NMO patients treated in an inner city hospital in central Brooklyn, New
York, and offer a an up-to-date discussion of diagnosis, treatment, and prognosis of this rare condition.

Keywords

NMO; Pathology; Diagnosis; Treatment

Introduction

Neuromyelitis Optica (NMO) is an autoimmune disorder of the central nervous system usually associated with autoantibodies against Aquaporin 4 water channel (Anti-AQP4 Ab). The disease was traditionally defined as optic neuritis (ON) and longitudinally extensive transverse myelitis (LETM) [1]. However, within the last few years, a broader spectrum of presentations was identified and referred to as ‘NMO spectrum disorders’ (NMOSD) [2]. NMOSD are unified by the presence of the anti-Aquaporin 4 antibody and encompass the following syndromes: isolated or recurrent LETM; isolated, recurrent or bilateral ON; and cerebral syndromes with ‘NMO – typical’ brain lesions [3]. Although NMO was previously and usually considered to be a variant of MS, it is being increasingly recognized as a distinct clinical entity with a unique pathophysiology and differing epidemiology, genetics, treatment, and outcomes from MS [3].

Kings County Hospital Experience

In a three year span, we diagnosed and treated 12 inpatients with NMO in Kings County Hospital, Brooklyn, New York. Table 1 summarizes the demographic features, clinical presentations, antibody status, treatment, and outcomes of our 12 cases. All of our cases were positive for Anti-AQP4 Ab. Ten of the 12 cases were classified as full-fledged NMO [4], while two cases, including one pediatric patient, fell into the NMOSD category. Two of the patients presented to our institution after having multiple relapses and having been misdiagnosed with MS. The age of our patients ranged from seven to 53 years with a mean age of 34 (±15) years. All of our patients were women. Eighty-three percent of our patients were Afro-Caribbean. More than 50 percent of our patients had an extended disability status score (EDSS) 6.5 or higher at last follow-up (required bilateral assistance to walk, or worse). Seventy-five percent of our patients needed aid with their activities of daily leaving (ADLs). Three of our 12 patients had intractable vomiting, which was the presenting symptom in two patients and developed later in the course of the third.

Patient Age Sex Race/Country Initial Presentation Anti-AQP4 EDSS Preventative Treatment Outcome
1 49 F Black/Haiti Paraparesis, bilateral ON, Urinary Retention. + 6 Oral steroids Wheelchair bound, legally blind and incontinent to urine.
2 25 F Hispanic/Dominican Republic Unilateral ON and TM + 2 Mycophenolate Mophetyl (initially failed steroids and azathioprine) Fully Functional, mild decrease in visual acuity.
3 25 F African American/US Nausea, vomiting, hyponatremia, progressed to quadriparesis. + 4.5 Azathioprine Requires some assistance with long distances but mostly functional
4 41 F Black/Haiti Severe TM with progressive quadriplegia + 7 Azathioprine wheelchair bound; requires assistance for most of her activities. Residual pseudoatetosis.
5 19 F Black/Haiti TM Paraparesis – sensory loss + 7 Oral Steroids after receiving IVIG and PLEX Bilateral assistance for walking; requires assistance in most of her activities of daily living
6 26 F Black/Granada ON + 6.5 Rituximab (failed repeat steroids and IVIG, PLEX, and azathioprine) Bilateral support and some assistance with her self-care
7 52 F Black/Haiti Hiccup, vomiting, quadriparesis + 10 NA Patient died despite aggressive immune suppressive treatment in the acute phase
8 46 F Hispanic/Mexico Recurrent paraparesis, Urinary Retention + 7.5 Azathioprine Wheelchair bound with some retention of self-care.
9 36 F Black/US Hemiparesis progressed to quadriparesis + 7.5 Azathioprine quadriparetic, requiring assistance in most of her activities of daily living
10 53 F Black/Haiti Paraparesis, Urinary incontinence + 4.0 Oral Steroids Functional in most of his activities
11 12 F Black/Granada Intractable vomiting, hiccups, quadriparesis, diplopia, autonomic instability. + 6.0 Oral steroids+Azathioprine Requires some assistance with ADLs
12 7 F African Diplopia, constipation + 3.5 Oral steroids Mostly fully functional

Table 1: Kings county patients.

Only three of our 12 patients responded to treatment with IV methylprednisolone for acute relapses, resulting in partial recovery of function. One patient (Patient 6 in the table) failed treatment with steroids, plasmapharesis, and intravenous immunoglobulin, and consequently became blind due to recurrent and devastating optic neuritis attacks. Two of our five patients treated with azathioprine prophylactically had mild disability and four of our patients were maintained on oral steroids alone. We encountered two pediatric cases, one of them presented with intractable vomiting, hiccups, and weight loss, which was attributed to vomiting and the other - with brainstem signs and symptoms.

The MRIs of our patients were consistent with NMO. Figures 1-6 show the most prominent radiologic findings in our patients.

Figure

Figure 1: Longitudinally Extensive Transverse Myelitis. MRI T2-weighted sagittal (left) and axial (right) views of the cervical spine showing an intramedullary hyperintense lesion from C2 to C7.

Figure

Figure 2: Extension of Spinal Lesion to Brainstem. MRI T2(left) and T1 (right) contrast weighted sagittal views of the cervical spine with an extensive enhancing lesion from the lower medulla to the C4 spinal level.

Figure

Figure 3: Brainstem Lesions in NMO. MRI sagittal view showing nonenhancing hyperintense lesions of the upper medulla and lower pons.

Figure

Figure 4: Hypothalamic NMO Lesion. T2-weighted FLAIR axial view showing bilateral hyperintense signals of the hypothalami.

Figure

Figure 5: Optic Nerve Enhancement in NMO. MRI coronal view of the orbits revealed bilateral enhancement of the optic nerves.

Figure

Figure 6: Extent of Eye Involvement in NMO. T2 (left) T1 (right) weighted MRI axial view of the orbits with thin cuts revealed atrophy of the left optic nerve and diffuse contrast enhancement of the right optic nerve, the right and middle portion of the optic chiasm, and the anterior aspect of right optic tract compatible with acute right optic neuritis.

Diagnostic Criteria

The two main sets of diagnostic criteria are the Mayo Clinic Diagnostic Criteria and the National Multiple Sclerosis Task Force Criteria [4], both of which require clinical events of optic neuritis and myelitis. The revised NMO criteria set forth by the Mayo Clinic require both transverse myelitis and ON. The supporting criteria, of which two must be met, include the following: brain MRI that is non-diagnostic for MS at initial presentation; spinal cord lesion on MRI that extends for three or more segments; and Anti-AQP4 Ab IgG seropositivity. The National Multiple Sclerosis Task Force requires all three of the following in an unspecified time interval: optic neuritis in one or both eyes; clinically complete or incomplete transverse myelitis extending over three vertebral segments on MRI; and no alternative inflammatory disease such as systemic lupus erythematosis, sarcoidosis, or Sjogren’s syndrome. The Mayo Clinic, however, recognizes that collagen vascular diseases and other autoimmune diseases can occur concurrently with NMO and should not preclude the diagnosis of NMO. One or two minor criteria must also be met per the National Multiple Sclerosis Task Force guidelines: either Anti-AQP4 Ab IgG seropositivity and/ or supporting neuroimaging (a normal brain MRI; or a MRI which has nonspecific T2 lesions inconsistent with McDonald’s MS criteria, such as hypothalamic lesions or brainstem lesions extending upwards from spinal lesions.) [4].

Epidemiology

The worldwide prevalence of NMO varies from 0.52 to 4.4 in 100,000 [5]. It has a female preponderance, ranging from 2:1 to 10:1, depending on the case series. In our case series, all of our patients were women. Mean disease onset is around age 40, as is the case in our series (mean age of 39 years) [4]. Many of the earlier epidemiological studies were done in the Asian and Afro-Caribbean populations.. Although NMO is overrepresented in these populations relative to MS, most patients with NMO in the developed world are white [3]. In a multicenter French epidemiological study of 125 patients, 87 percent of the patients were white. Of the remaining non-white population, 45 percent originated from Sub-Saharan Africa, 37 percent from Asia, and 18 percent from Latin America [6].

The frequency of NMO in non-whites is quite high compared to MS. NMO is the cause of nearly 40 percent of the demyelinating diseases in Thailand [7], 20-30 percent in the Japanese, 27 percent among the West Indian population, and approximately 20 percent among Indians [3]. Cuban study of 89 patients with NMO showed equal prevalence among Cuban whites, Blacks, and mixed racial patients [8]. Another study among 178 Caribbean patients showed reduced prevalence of seropositivity with anti-aquaporin 4 antibodies in those of African ancestry compared with those of white ancestry, but those of African ancestry had a worse prognosis with more frequent attacks and severe disability [9]. In a recent US study of 187 NMO patients, 36.9 percent of NMO patients were of African descent (which constitutes approximately 12 percent of the US population at large) [10]. In our series, half of the patients were of Afro-Caribbean descent and only one patient did not have black ancestry. This probably reflects the demographics of our catchment area.

Clinical Findings

The classic NMO findings are optic neuritis and acute transverse myelitis, occurring either separately or together. However, the definition of NMO has expanded to include cerebral and neuroendocrine syndromes, even without optic neuritis or myelitis [2]. Optic neuritis may be unilateral or bilateral, sometimes affecting the chiasm, causing severe visual disability and even complete loss of vision. Usually, the optic neuritis attack is more severe in NMO than in MS and ocular coherence tomography demonstrates a greater loss of retinal nerve fiber layer, ganglion cell layer, and inner plexiform layer of the retina compared with MS [11]. Spinal cord attacks are also typically more frequent and severe than in MS. Typical symptoms of myelitis are bilateral sensory complaints, bowel or bladder dysfunction, paraparesis or paraplegia, and in some cases of cervical myelitis, quadriparesis or quadriplegia. Paralysis is rare in MS myelitis and should raise suspicion of NMO. Neuropathic pain and Lhermitte’s phenomenon (‘electric shock’-like paresthesias after neck flexion, suggestive of cervical spine pathology) [12,13] are frequently seen. Eight of our 12 patients had at some point in their disease course either symptoms of ON or LETM and two of the eight had both ON and LETM during their disease course. A recent case series of NMO patients recorded frequent, paroxysmal tonic spasms, or dystonia, mostly in a single limb, of short duration, occurring at any point in the disease course. All patients responded to treatment with carbamazepine [14]. In a retrospective study comparing 29 NMO patients with 66 MS patients, 85 percent of the NMO patients had more severe pain, needing multiple pain medications and reporting poorer quality of life [12]. In approximately 40-45 percent of patients with anti-aquaporin 4 antibodies, refractory nausea, vomiting, or hiccups occur, due to lesions in the brainstem affecting the area postrema [4], but only in 12 percent did they occur as the initial presentation [15]. In our series 25 percent of the patients had intractable nausea and vomiting. Extension of spinal lesions into the brainstem may cause neurogenic respiratory failure and death, as may have been the case in patient 7 of our series. Other uncommon presentations include endocrinopathies, due to hypothalamic lesions, exeplefied by patient 3, who experienced central diabetes insipidus. Cerebral syndromes such as encephalopathy, and coma due to tumefactive lesions, have also been reported, and appear to be more common in children [4].

Laboratory Studies

The initial test to detect Anti-AQP4 Ab in serum was indirect immunefluorescence (IIF). IIF using tissue substrates had a sensitive of 54 to 73 percent and a specificity of 91 percent [16]. The cell-based assay using human embryonic kidney (HEK) cells has a sensitivity of 91 percent and a specificity of 100 percent [16]. A number of newer techniques that are available: radioimmunoprecipitation (RIPA), fluoroimmunoprecipitation (FIPA), enzyme-linked immunoabsorbent assays (ELISA), and cell based assays - reach specificity of 85-100 percent [16].

Cerebrospinal Fluid (CSF) studies may demonstrate mild pleocytosis (50-1000 × 106 with neutrophilic and eosinophilic predominance during acute relapse). Oligoclonal bands, commonly found in MS are absent in most NMO cases [17].

Radiology

Orbital MRI shows enhancement of one or both optic nerves and sometimes of the chiasm and optic tracts during attacks of optic neuritis. In a study comparing MRI features of optic neuritis in patients with NMO and MS, those with NMO had a more frequent enhancement of both optic nerves, the posterior aspect of the optic nerve, the chiasm, and optic tracts [18]. Figures 5 and 6 are in accordance with this description of optic nerve lesions in NMO. MRI of the spinal cord during acute myelitis typically shows an expensile central lesion at least three spinal segments in length, as in our Figures 1 and 2, unlike MS myelitis, which is associated with lesions that are 1-2 vertebral segments long and located in the periphery of the cord [4]. Chronic NMO spine lesions may become patchy or disappear with time. Thus, smaller cord lesions during a quiescent phase or “normal cord MRI” does not preclude the diagnosis of NMO [19].

Although orbital and spine MRI provide strong evidence for NMO, distinctive features on brain MRI may further support the diagnosis. Lesions in the hypothalamus (Figure 4) and areas surrounding the third and fourth ventricles and the aqueduct of Sylvius are considered to be characteristic of NMO. [20] Corpus callosal lesions are typically linear and follow the border of the corpus callosum, rather than being perpendicular to the callosum, as in MS [4,21]. It should be born in mind that ‘NMO distinctive’ brain lesions are seen in only a minority of NMO patients. The most common finding is ‘non-specific’ punctate white matter lesions [22], as recorded in the NMO Consortium Study of 151 NMO patients, in which 47 percent had nonspecific white matter lesions and 12.6 percent had “typical” MS lesions [10].

Treatment

The European Federation of Neurological Societies published a consortium paper in 2010 outlining the treatment of NMO and divided into acute treatment of relapses and preventative therapy [23].

Acute management consists of high doses of intravenous steroids, such as methylprednisolone 1 g for 5-10 days with careful monitoring of side effects, especially if patients have diabetes mellitus, hypertension, or neuro-psychiatric illnesses. For those patients, who do not effectively respond to high dose steroids, plasma exchange (PLEX) should be strongly considered. The usual dose course is seven cycles. In a randomized study, plasma exchange demonstrated moderate to significant improvement in neurological disability compared to sham treatment in patients with acute demyelinating disease of the CNS [24]. Intravenous immunoglobulin (IVIG) can be considered as an alternative treatment of patients unresponsive to methylprednisolone and/or PLEX. A recent retrospective study of 10 patients with NMO, unresponsive to either IV methylprednisolone or PLEX, showed that 45.5 percent of patients improved after IVIG and the remaining were no worse after treatment [25]. Intravenous chemotherapy, such as cyclophosphamide [26] or mitoxantrone should also be considered in severe cases [27].

Preventative therapy to prevent relapses is always required in NMOSD (unless there are strong contraindications). The commonly used drugs are azathioprine, mycophenolate mophetil, and rituximab, alone or in combination with oral steroids. Less commonly used are cyclophosphamide, mitoxantrone, and methotrexate. A consensus expert opinion on prophylactic treatment in NMO was recently published [28].

In a retrospective study of 99 patients with NMO, those treated with azathioprine had a 74 percent decrease in the annual relapse rate, regardless of concomitant prednisone treatment [29]. This drug takes three to six months to show effect. The authors recommended treating patients with at least 2.5mg/kg/day to have optimal benefit. It is also recommended to measure patients’ thiopurine methyltransferase (TPMT) levels prior to initiating therapy, as patients with deficient enzyme activity have a risk of toxicity and severe infections. Azathioprine carries a black box of warning of hematologic malignancies in patients on chronic treatment [30].

Rituximab is a chimeric anti-CD20 monoclonal antibody approved for the treatment of non-Hodgkin’s Lymphoma, rheumatoid arthritis, and other autoimmune diseases. Several open label studies showed that two doses of Rituximab 1 g every two weeks at six month intervals [31], not only decreased the number of relapses significantly but also considerably improved disability scores. A recent retrospective study analyzing five years of experience using Rituximab showed an 86 percent reduction in the annual relapse rate (ARR). Sixty percent of the treated patients were relapse-free during this period of time, and no serious adverse events leading to discontinuation were observed [32]. Mycophenylate mofetil 1 g twice a day was effective in some case series [33]. There is limited data with regard to the use of Mitoxantrone and Cyclophosphamide [30]. A small study of seven patients with chemotherapy refractory disease and considerable disability demonstrated that maintenance plasmaphereses not only improved disability, but stabilized disease over the course of seven years [33]. Two novel agents also have shown promise in treatment of recalcitrant cases of NMO: eculizumab, a monoclonal IgG that neutralises the complement protein C5 [34,35] and Tocilizumab, an inhibitor of IL-6 receptors [36].

Among emergent treatments, mention should be made of a nonpathogenic, recombinant monoclonal antibody against aquaporin 4, ¨aquaporumab,¨ that selectively blocks pathogenic NMO-IgG binding to AQP4. Thus, in the absence of effector function, aquaporumab lacks functionality for complement- and cell-mediated cytotoxicity. Aquaporumab was evaluated in vitro, ex’vivo, and in vivo using cell cultures as well as mice [37]. There have been no human studies with this agent to date.

Interferon beta, commonly used to treat MS, should be avoided in NMO, in view of reports documenting worsening of disease activity in interferon beta-treated NMO patients, possibly due to the switching of the immune response to a more autoantibody-favoring Th2 dominated arm [38]. Natalizumab, an alpha-4 integrin antagonist and a potent MS drug, exacerbated NMO in a small study [39] as did another MS therapy, fingolimod [40]. These dramatic differences in response to treatment in MS and NMO highlight the absolute imperative of establishing a correct diagnosis at the earliest stage of the disease.

Prognosis

Earlier reports suggested that ninety percent of NMO patients have a relapsing course, and that the recovery from relapses is typically slow and incomplete [3]. Approximately 50 percent of patients in these original series were blind within five years [3]. Predictors of worse prognosis include number of attacks in the first two years; severity of the first attack; and presence of concurrent autoimmune disorders, such as systemic lupus erythematous. [3] Seventy-five percent of the patients in our cohort had very high EDSS scores at the time of diagnosis and treatment initiation, consistent with a poor prognosis as previously reported. Our cohort also suggests that those treated in underprivileged hospitals rather than in tertiary care centers may have a worse prognosis, which may be due in part to delays in diagnosis and a suboptimal follow up. It is advisable to refer NMO patients to specialty MS clinics whenever possible.

Importantly, secondary progression, which is seen in 90 percent of untreated MS patients [41], is generally not part of the NMO course. An important clinical corollary of this observation is that aborting attacks results in disease remission [42]. In contrast, in MS, there is often disease progression without relapses [41].

Conclusion

As seen from our case series and a review of the literature, NMO is a potentially devastating disease that involves optic nerves, spinal cord, and the brain. Recovery from relapses is often disappointing, and the cumulative nervous system damage sustained during the attacks contributes heavily to long-term disability. Consequently, treatments, which can decrease the number of relapses, should be initiated as early as possible in the disease course, with the aim of reducing the chances of significant disability [4]. In a patient with an inflammatory disorder of the central nervous system, NMO should be considered in the differential, and timely treatment is likely to decrease morbidity and mortality.

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