PerampaAIAN
Annals of Indian Academy of Neurology
  Users Online: 9412 Home | About the Journal | InstructionsCurrent Issue | Back IssuesLogin      Print this page Email this page  Small font size Default font size Increase font size

Table of Contents
EDITORIAL COMMENTARY
Year : 2022  |  Volume : 25  |  Issue : 2  |  Page : 181-182
 

Central Nervous System (CNS) and systemic autoimmune disease: Coexistence or more?


Department of Neurology, All India Institute of Medical Sciences, New Delhi, India

Date of Submission09-Dec-2021
Date of Acceptance10-Dec-2021
Date of Web Publication09-Feb-2022

Correspondence Address:
Deepti Vibha
Department of Neurology, All India Institute of Medical Sciences, Room No. 707, Neurosciences Center, New Delhi - 110 029
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/aian.aian_1054_21

Rights and Permissions

 



How to cite this article:
Vibha D, Singh RK. Central Nervous System (CNS) and systemic autoimmune disease: Coexistence or more?. Ann Indian Acad Neurol 2022;25:181-2

How to cite this URL:
Vibha D, Singh RK. Central Nervous System (CNS) and systemic autoimmune disease: Coexistence or more?. Ann Indian Acad Neurol [serial online] 2022 [cited 2022 Jul 1];25:181-2. Available from: https://www.annalsofian.org/text.asp?2022/25/2/181/337446




Dear Sir,

The central nervous system (CNS) autoimmune and demyelinating diseases have been known to be associated with systemic autoimmune diseases. However, their magnitude of association and the underlying common genetic and/or environmental predisposition is still a subject of ongoing research. The study published by Malli et al.[1] in the current issue emphasizes the need for more hospital- and community-based disease-specific registries to answer this conundrum. The study has specifically looked at primary demyelinating diseases of the CNS and classified patients into multiple sclerosis (MS), anti-aquaporin 4 (AQP4)-positive, anti-myelin oligodendrocyte glycoprotein-positive, and seronegative non-MS cases. They have studied the frequency of concomitant autoimmune disorders, anti-nuclear antibody (ANA), and antithyroid antibody (ATAb) in the cohort Mangalore Demyelinating Disease Registry (MANDDIR).

The association of MS with other autoimmune diseases has been shown in earlier cohorts.[2],[3] The criticism of such associations has been linked to the mere serological association than any clinical implication. Another challenge is that some of the newer treatment modalities, like alemtuzumab, used in MS can itself cause diseases like Goodpasture syndrome and thyroid diseases. Longitudinal studies can answer if there is a mere serological coexistence, and if their early detection would alter the course of the disease by timely intervention. Such registries, as well as population-based data, are available in the developed world,[4] and the contribution of environmental and genetic factors warrant similar studies in the Indian subcontinent. It has been shown that MS patients have an increased risk of rheumatoid arthritis, psoriasis, thyroid diseases, ankylosing spondylitis, dermatomyositis, Sjögren's syndrome (SS), systemic lupus erythematosus (SLE), systemic sclerosis, inflammatory bowel disease, myasthenia gravis, uveitis, and pemphigoid.[4],[5],[6] There have been very few earlier registry-based data in MS from India.[7],[8] These have shown comparable prevalence and clinical features. Studies have also shown the association of neuromyelitis optica (NMO) and neuromyelitis optica spectrum disorders (NMOSD) with systemic sclerosis[9] and other systemic connective tissue diseases (CTD).[10] AQP4 antibody was detectable in 78% of the patients with CTD and NMOSD but in none of the patients with CTD and neurological disorders other than NMO, longitudinally extensive transverse myelitis (LETM), or optic neuritis (ON). This strengthens the concept that the AQP4 antibody is responsible for the pathogenesis of these neurological conditions and is not simply a part of a group of antibodies associated with other connective tissue disorders.

The current study found ATAb as the commonest association in about a quarter of the patients of MS as well as healthy controls. It is, therefore, imperative that longitudinal cohorts provide associations if any. This would help in channelizing the constrained resources toward the management of clinical problems, rather than advising a 'panel' of antibody tests. A positive result would create anxiety and stress for the patients, a challenge for the treating clinician, and would add to the cost of the disease. On the other hand, early detection of another autoimmune disease, which would impact the clinical course, would be empowering the clinician. The detection of the neurological findings in rheumatological diseases has a profound bearing, especially, SLE, sarcoidosis, and Sjögren syndrome, as it warrants aggressive and prolonged immunosuppression.[6] Whether the reverse is true still needs to be explored. As more and more antibodies are added to the list of the 'autoimmune panel,' results from registries and population-based studies may provide answers to how much diagnostic cost needs to be added up. This publication from this registry has sown the seed and the preliminary efforts also need to be applauded so that the registry matures and provides more robust results.



 
   References Top

1.
Malli C, Pandit L, D'Çunha MA, Sudhir A. Coexistence of autoantibodies and other autoimmune diseases with multiple sclerosis and related disorders – Experience from the Mangalore demyelinating disease registry (MANDDIR). Ann Indian Acad Neurol 2021. doi: 10.4103/aian.AIAN_170_21.  Back to cited text no. 1
    
2.
Dobson R, Giovannoni G. Autoimmune disease in people with multiple sclerosis and their relatives: A systematic review and meta-analysis. J Neurol 2013;260:1272–85.  Back to cited text no. 2
    
3.
Barcellos LF, Kamdar BB, Ramsay PP, DeLoa C, Lincoln RR, Caillier S, et al. Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: A descriptive study. Lancet Neurol 2006;5:924–31.  Back to cited text no. 3
    
4.
Marrie RA, Reider N, Cohen J, Stuve O, Sorensen PS, Cutter G, et al. A systematic review of the incidence and prevalence of autoimmune disease in multiple sclerosis. Mult Scler 2015;21:282–93.  Back to cited text no. 4
    
5.
Farez MF, Balbuena Aguirre ME, Varela F, Köhler AA, Correale J. Autoimmune disease prevalence in a multiple sclerosis cohort in Argentina. Mult Scler Int 2014;2014:828162.  Back to cited text no. 5
    
6.
Pavlakis PP. Rheumatologic disorders and the nervous system. Continuum (Minneap Minn) 2020;26:591–610.  Back to cited text no. 6
    
7.
Pandit L, Kundapur R. Prevalence and patterns of demyelinating central nervous system disorders in urban Mangalore, South India. Mult Scler 2014;20:1651–3.  Back to cited text no. 7
    
8.
Singhal A, Bhatia R, Srivastava MVP, Prasad K, Singh MB. Multiple sclerosis in India: An institutional study. Mult Scler Relat Disord 2015;4:250–7.  Back to cited text no. 8
    
9.
Pittock SJ, Lennon VA, de Seze J, Vermersch P, Homburger HA, Wingerchuk DM, et al. Neuromyelitis optica and non-organ-specific autoimmunity. Arch Neurol 2008;65:78–83.  Back to cited text no. 9
    
10.
Jarius S, Jacobi C, de Seze J, Zephir H, Paul F, Franciotta D, et al. Frequency and syndrome specificity of antibodies to aquaporin-4 in neurological patients with rheumatic disorders. Mult Scler 2011;17:1067–73.  Back to cited text no. 10
    




 

Top
Print this article  Email this article

    

 
   Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Article in PDF (300 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    References

 Article Access Statistics
    Viewed370    
    Printed11    
    Emailed0    
    PDF Downloaded27    
    Comments [Add]    

Recommend this journal