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  • Mini Review   
  • J Clin Exp Neuroimmunol, Vol 8(3)

During the COVID-19 Pandemic and Neuromyelitis Optica Therapy, Treatment Options for Patients with Neuromyelitis Optica Spectrum Disorder

Uqbah Iqbal*
Department of Neuroimmunology, Aristotle University of Thessaloniki, Thessaloniki, Greece
*Corresponding Author: Uqbah Iqbal, Department of Neuroimmunology, Aristotle University of Thessaloniki, Thessaloniki, Greece, Email: Iqbal_U@gmail.com

Received: 05-Apr-2023 / Manuscript No. JCENI-23-94361 / Editor assigned: 10-Apr-2023 / PreQC No. JCENI-23-94361(PQ) / Reviewed: 24-Apr-2023 / QC No. JCENI-23-94361 / Revised: 02-May-2023 / Manuscript No. JCENI-23-94361(R) / Published Date: 30-May-2023

Abstract

Neuromyelitis Optica (NMO) or device disease is a central nervous system inflammatory disorder characterized by optic neuritis and transverse myelitis episodes. In 1894, a doctor in Lyon, France, named Eugene device, described the condition. Afterward, it was thought that there was no clinical involvement beyond the optic nerve and spinal cord and that the disorder might be a variant of Acute Disseminated Encephalomyelitis (ADEM) when monophasic and a variant of classic Multiple Sclerosis (MS) when relapsing. However, NMO cases have frequently been associated with symptoms in other neurological axes.

Keywords: Neuromyelitis optica; Disorder; Optic nerve; Spinal cord

Keywords

Neuromyelitis optica; Disorder; Optic nerve; Spinal cord

Introduction

Citation4 the prognosis of NMO has been poor without appropriate treatment, as many patients were left with severe disability and many died within weeks or months. Additionally, NMO is currently considered an entity distinct from classic multiple sclerosis due to its clinical manifestations, antibodies and radiological and pathological features that differ from MS. Citation5 As a result, early detection and treatment of NMO are crucial. In this article we audit the pathogenesis and clinical signs of NMO with an accentuation on the optic nerve and spinal rope contribution and then some. Treatment and clinicopathological correlation are also discussed [1].

The treatment strategies for numerous autoimmune diseases have been affected by the ongoing Coronavirus (COVID-19) pandemic, which is a worldwide health emergency of international significance.

Literature Review

The management of Neuromyelitis Optica Spectrum Disorder (NMOSD) relies heavily on immunomodulatory and immunosuppressive treatments, which may put patients at risk for COVID-19 infections [2]. It is still up for debate which NMOSD management strategy is best for the COVID-19 era. However, in order to provide the best possible care for NMOSD patients during the COVID-19 period, we investigated the evidence that NMOSD Disease Modifying Treatments (DMTs) are currently used and highlighted a number of scenarios, such as the treatment of relapses and the introduction and maintenance of DMTs [3].

Extremely severe respiratory condition the coronavirus known as Covid 2 (SARS-CoV-2) is the third member of the coronaviridae family to be linked to flare ups of an extremely severe respiratory condition. This study discusses the challenges of managing Neuromyelitis Optica Spectrum Disorder (NMOSD) acute relapses during the COVID-19 era and offers algorithms for adjusting the use of prospective Disease Modifying Therapy (DMT) at this crucial time. Since the disease was identified as a pandemic (IM), concerns have been expressed regarding individuals with immune-mediated disorders who require treatment with immunomodulators.

The Neuromyelitis Optica Spectrum Disorder (NMOSD) is a group of inflammatory, immunologically mediated CNS disorders characterized by the development of Auto-Reactive Antibodies (Abs) against distinct neuroglial components. The most common autoantibodies are those against water channel Aquaporin-4 (Anti AQP-4 IgG1), but there are also overlapping antibodies against Glial Fibrillary Acidic Protein (GFAP) and Myelin Oligodendrocyte Glycoprotein IgG (Anti-MOG). Cell Mediated Immunity (CMI), plays a role in the pathophysiology because T-lymphocytes are polarized toward the helper T cells Th-17 and Th-2. A significant pathophysiologic role is also played by Interleukin (IL) 6, a cytokine that is specifically linked to the severity of relapses, CNS damage, and degree of disability. Relapses are closely linked to disability in NMOSD, so effective relapse management and a decrease in relapse frequency is essential [4,5].

Problems with NMOSD managers during the Coronavirus the ongoing pandemic of the Coronavirus has given specialists in the nervous system unprecedented opportunities to provide NMOSD patients with the best possible care [6].

Unanswered inquiries

Whether or not being open to particular DMT regimens increases the likelihood of developing severe Coronavirus disease, which may necessitate treatment interruption, temporary interference, or replacement; facilitating the reception of suitable gamble delineation systems in relation to individual patient profiles and medication properties; 2) whether, like any other infection, an asymptomatic COVID-19 infection can result in acute relapses (i.e., relapses with symptoms like fever, headache, or fatigue) [7].

Transverse myelitis Acute Transverse Myelitis (ATM) is a focal inflammation of the spinal cord with motor, sensory, and autonomic dysfunction. It has multiple potential causes. It is essential to rule out compressive lesions and secondary ATM, which include autoimmune disorders like NMO, Sjogren's syndrome, antiphospholipid syndrome, and Systemic Lupus Erythematosus (SLE); MS, ADEM, Behçet disease, and sarcoidosis are all examples of inflammation; infection; neoplasm; metabolic disorders like not having enough copper or B12; conditions of the vascular system like infarction and dural fistula; myelopathy caused by radiation [8].

The serum NMO-IgG level rose during relapse and decreased during remission or after treatment with steroids and immunosuppressive drugs like azathioprine, rituximab, and cyclophosphamide, as demonstrated by the treatment one investigation. Following intravenous methylprednisolone for acute relapse, two patients who received a combination of azathioprine and prednisolone experienced a low antibody titer for approximately a year.

When avoiding unnecessary hospital procedures to save money and reduce patient contact, think about options like delaying follow-up MRI scans and reducing the frequency of routine laboratory monitoring for stable patients. As of now, nervous system specialists who treat NMOSD patients need explicit ideas, particularly while managing people who contract coronavirus. Additional initiatives should be supported, such as avoiding unnecessary medical visits and consultations in person or replacing them with remote interventions (such as telecommunications-based checking of laboratory or MRI results).

Discussion

Neuromyelitis optica, a rare and persistent inflammatory disease of the central nervous system, results in transverse myelitis and optic neuritis occurring intermittently and monophasically, with little to no recovery. An international panel coined the term "Neuromyelitis Optica Spectrum Disorder" (NMOSD) in 2015 to make it easier for people with or without aquaporin-4 antibodies to be diagnosed at an early stage. Pain, weakness, and problems with the engine and vision are the most prevalent and debilitating side effects. Over time, remaining disability frequently restricts daily function and independence. The traditional definition of stigma is the belief that something is unfairly stigmatized by society. A recent survey conducted by the European federation of neurological associations found that many people with neurological disorders felt stigmatized. Stigma has been linked to a number of neurological conditions, such as low self-esteem, depression, anxiety, decreased health-seeking behavior, and unequal life opportunities. Information on the recurrence of disgrace among patients with neuroinflammatory and it are scant to demyelinate sicknesses. As of late, research investigated the impression of disgrace among individuals with different sclerosis (MS). Different tests showed that 20 and 80 percent of people with backsliding dispatching and essential mild MS had seen honor, respectively. Stigma was linked to low quality of life, depression, and unemployment, even in patients with mild physical disabilities [9].

Anxiety and mental health issues have an impact on abstract prosperity in NMOSD sufferers. However, shame and NMOSD have not been the focus of any studies. The study's objective was to ascertain how stigma affects NMOSD patients.

Thirteen neuroimmunology clinics in Spanish hospitals were the locations of a cross-sectional, non-interventional study called perspectives-NMO. According to Wingerchuk's 2015 eligibility requirements, in order to be eligible, you must be at least 18 years old and have been diagnosed with NMOSD. The Galician investigative review board (CEIm-G) in Santiago de Compostela, Spain, gave its approval to this study after it was carried out in accordance with the good clinical practice guidelines of the International Conference on Harmonization (ICH) and the declaration of Helsinki. Each member gave composed, completely educated assent.

Conclusion

Even in a population with low levels of physical disability and clinical stability, NMOSD stigma is widespread. To clarify the underlying mechanisms and support the connections between stigma, quality of life and mood, additional longitudinal studies are required.

References

Citation: Iqbal U (2023) During the COVID-19 Pandemic and Neuromyelitis Optica Therapy, Treatment Options for Patients with Neuromyelitis Optica Spectrum Disorder. J Clin Exp Neuroimmunol 8: 179.

Copyright: © 2023 Iqbal U. 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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