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Helicobacter pylori infection may influence prevalence and disease course in myelin oligodendrocyte glycoprotein antibody associated disorder (MOGAD) similar to MS but not AQP4-IgG associated NMOSD
by
Pandit, Lekha
, Sudhir, Akshatha
, D’Cunha, Anita
, Malli, Chaithra
in
Age
/ Antibodies
/ Antibodies, Bacterial
/ Aquaporin 4
/ Aquaporins
/ Autoimmune diseases
/ Children
/ Demyelination
/ Developing countries
/ Disease
/ Disease Progression
/ Education
/ environmental factor
/ Environmental factors
/ Enzyme-linked immunosorbent assay
/ Females
/ Gender
/ Glycoproteins
/ Helicobacter Infections - epidemiology
/ Helicobacter pylori
/ Humans
/ Hygiene
/ Hypotheses
/ Immune system
/ Immunoglobulin G
/ Immunology
/ Infections
/ LDCs
/ MOGAD
/ Multiple sclerosis
/ Multivariate analysis
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein
/ NMOSD
/ Oligodendrocyte-myelin glycoprotein
/ Prevalence
/ Serology
/ Socioeconomic factors
/ Socioeconomic status
/ Variables
2023
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Helicobacter pylori infection may influence prevalence and disease course in myelin oligodendrocyte glycoprotein antibody associated disorder (MOGAD) similar to MS but not AQP4-IgG associated NMOSD
by
Pandit, Lekha
, Sudhir, Akshatha
, D’Cunha, Anita
, Malli, Chaithra
in
Age
/ Antibodies
/ Antibodies, Bacterial
/ Aquaporin 4
/ Aquaporins
/ Autoimmune diseases
/ Children
/ Demyelination
/ Developing countries
/ Disease
/ Disease Progression
/ Education
/ environmental factor
/ Environmental factors
/ Enzyme-linked immunosorbent assay
/ Females
/ Gender
/ Glycoproteins
/ Helicobacter Infections - epidemiology
/ Helicobacter pylori
/ Humans
/ Hygiene
/ Hypotheses
/ Immune system
/ Immunoglobulin G
/ Immunology
/ Infections
/ LDCs
/ MOGAD
/ Multiple sclerosis
/ Multivariate analysis
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein
/ NMOSD
/ Oligodendrocyte-myelin glycoprotein
/ Prevalence
/ Serology
/ Socioeconomic factors
/ Socioeconomic status
/ Variables
2023
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Helicobacter pylori infection may influence prevalence and disease course in myelin oligodendrocyte glycoprotein antibody associated disorder (MOGAD) similar to MS but not AQP4-IgG associated NMOSD
by
Pandit, Lekha
, Sudhir, Akshatha
, D’Cunha, Anita
, Malli, Chaithra
in
Age
/ Antibodies
/ Antibodies, Bacterial
/ Aquaporin 4
/ Aquaporins
/ Autoimmune diseases
/ Children
/ Demyelination
/ Developing countries
/ Disease
/ Disease Progression
/ Education
/ environmental factor
/ Environmental factors
/ Enzyme-linked immunosorbent assay
/ Females
/ Gender
/ Glycoproteins
/ Helicobacter Infections - epidemiology
/ Helicobacter pylori
/ Humans
/ Hygiene
/ Hypotheses
/ Immune system
/ Immunoglobulin G
/ Immunology
/ Infections
/ LDCs
/ MOGAD
/ Multiple sclerosis
/ Multivariate analysis
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein
/ NMOSD
/ Oligodendrocyte-myelin glycoprotein
/ Prevalence
/ Serology
/ Socioeconomic factors
/ Socioeconomic status
/ Variables
2023
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Helicobacter pylori infection may influence prevalence and disease course in myelin oligodendrocyte glycoprotein antibody associated disorder (MOGAD) similar to MS but not AQP4-IgG associated NMOSD
Journal Article
Helicobacter pylori infection may influence prevalence and disease course in myelin oligodendrocyte glycoprotein antibody associated disorder (MOGAD) similar to MS but not AQP4-IgG associated NMOSD
2023
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Overview
(
persists after colonizing the gut in childhood, and potentially regulates host immune system through this process. Earlier studies have shown that
infection in childhood, may protect against MS in later life. Such an association was not seen with AQP4-IgG positive NMOSD, while the association with MOGAD is unclear.
To evaluate frequency of
among patients with MOGAD, MS, NMOSD and matched controls and its effect on disease course. To ascertain whether childhood socio economic factors were linked to prevalence of
infection.
In all, 99 patients diagnosed to have MOGAD, 99 AQP4 IgG+ NMOSD, 254MS and 243 matched controls were included. Patient demographics, diagnosis, age at disease onset, duration and the last recorded expanded disability status scale (EDSS) were obtained from our records. Socioeconomic and educational status was queried using a previously validated questionnaire. Serum
IgG was detected using ELISA kits (Vircell, Spain).
Frequency of
IgG was significantly lower among MOGAD (28.3% vs 44%, p-0.007) and MS (21.2% vs 44%, p-0.0001) but not AQP4-IgG+ NMOSD patients (42.4% vs 44%, p-0.78) when compared to controls. Frequency of
IgG in MOGAD & MS patients combined (MOGAD-MS) was significantly lower than those with NMOSD (23.2% vs 42.4%, p- 0.0001). Seropositive patients with MOGAD- MS were older (p-0.001. OR -1.04, 95% CI- 1.01- 1.06) and had longer disease duration (p- 0.04, OR- 1.04, 95% CI- 1.002- 1.08) at time of testing. Educational status was lower among parents/caregivers of this study cohort (p- 0.001, OR -2.34, 95% CI- 1.48-3.69) who were
IgG
In developing countries
infection may be a significant environmental factor related to autoimmune demyelinating CNS disease. Our preliminary data suggests that
may exert a differential influence - a largely protective role for MS-MOGAD but not NMOSD and may influence disease onset and course. This differential response maybe related to immuno-pathological similarities between MOGAD and MS in contrast to NMOSD. Our study further underscores the role of
as a surrogate marker for poor gut hygiene in childhood and its association with later onset of autoimmune diseases.
Publisher
Frontiers Media SA,Frontiers Media S.A
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