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Difficulty in identification of patients with active secondary progressive multiple sclerosis by clinical classification tools

Difficulty in identification of patients with active secondary progressive multiple sclerosis by clinical classification tools

Source : https://doi.org/10.1111/ene.15227

This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between...


Conclusion: We propose to lessen the emphasis on the label “SPMS” in favor of the more open term “active progressive disease” to simplify the process of identification of patients who may benefit from immune therapy.

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Polymorphisms CYP2R1 rs10766197 and CYP27B1 rs10877012 in Multiple Sclerosis: A Case-Control Study

Polymorphisms CYP2R1 rs10766197 and CYP27B1 rs10877012 in Multiple Sclerosis: A Case-Control Study

Source : https://www.hindawi.com/journals/jir/2021/7523997/

Background . Multiple sclerosis (MS) is a chronic autoimmune inflammatory disease. Low vitamin D levels have been reported to be a risk factor for MS, and genetic variances could be...


Conclusion: Lower serum 25(OH) vitamin D levels were observed in MS patients than in controls, although these levels were not associated with disease progression. Carriers of genotypes of CYP2R1 rs10766197 had an increased risk of MS. None of these polymorphisms was associated with severe progression of MS.

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Primary Progressive Multiple Sclerosis in a Portuguese Patient With Neurofibromatosis Type 1

Primary Progressive Multiple Sclerosis in a Portuguese Patient With Neurofibromatosis Type 1

Source : https://www.cureus.com/articles/80177-primary-progressive-multiple-sclerosis-in-a-portuguese-patient-with-neurofibromatosis-type-1

Neurofibromatosis type 1 (NF1) is a frequent genetic neurocutaneous syndrome and multiple sclerosis (MS) is an acquired demyelinating disease of the central nervous system. The association of both these diseases...


The genetic study revealed a new mutation in the NF1 gene that was not previously reported. We intend to discuss the genetic and autoimmune mechanisms by which MS and NF1 appear to be related and draw attention to this association because a timely diagnosis of MS is important to prevent further disability in NF1 patients.

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Conclusion: Using data from EHR as input, SPOKEsigs describe patients at both the clinical and biological levels. We provide a clinical use case for detecting MS up to 5 years prior to their documented diagnosis in the clinic and illustrate the biological features that distinguish the prodromal MS state.

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Stress Signal ULBP4, an NKG2D Ligand, Is Upregulated in Multiple Sclerosis and Shapes CD8 + T-Cell Behaviors. - Abstract - Europe PMC

Stress Signal ULBP4, an NKG2D Ligand, Is Upregulated in Multiple Sclerosis and Shapes CD8 + T-Cell Behaviors. - Abstract - Europe PMC

Source : https://europepmc.org/article/pmc/pmc8656234

Background and objectives We posit the involvement of the natural killer group 2D (NKG2D) pathway in multiple sclerosis (MS) pathology via the presence of specific NKG2D ligands (NKG2DLs). We aim...


Discussion: Our study provides new evidence for the involvement of NKG2D and its ligand ULBP4 in MS pathology. Our results point to ULBP4 as a viable target to specifically block 1 component of the NKG2D pathway without altering immune surveillance involving other NKG2DL.