scholarly journals Multiple Sclerosis and Celiac Disease

Author(s):  
Carlos Hernndez-Lahoz ◽  
Luis Rodrigo
2008 ◽  
Vol 9 (4) ◽  
pp. 289-293 ◽  
Author(s):  
C Núñez ◽  
B Dema ◽  
M C Cénit ◽  
I Polanco ◽  
C Maluenda ◽  
...  

2008 ◽  
Vol 69 (12) ◽  
pp. 837-839 ◽  
Author(s):  
Giovanni Frisullo ◽  
Viviana Nociti ◽  
Raffaele Iorio ◽  
Agata Katia Patanella ◽  
Alessandro Marti ◽  
...  

2009 ◽  
Vol 15 (11) ◽  
pp. 1368-1371 ◽  
Author(s):  
Bassem Yamout ◽  
Jinan Usta ◽  
Salam Itani ◽  
Shadi Yaghi

Multiple sclerosis (MS) is a demyelinating disease of uncertain etiology. Many genetic and environmental risk factors have been associated with this disease including certain human leukocyte antigen haplotypes, Epstein-Barr virus infection, and vitamin D deficiency. We report a 30-year-old woman with MS, the product of consanguineous marriage, and three siblings with three different autoimmune diseases: idiopathic thrombocytopenic purpura, celiac disease, and Behçet’s disease.


2011 ◽  
Vol 31 (1) ◽  
pp. 240-244
Author(s):  
İrem Fatma ULUDAĞ ◽  
Uğur KULU ◽  
Ufuk ŞENER ◽  
Yaşar ZORLU ◽  
Işın GÖKÇÖL ERDOĞAN

2020 ◽  
Vol 26 (13) ◽  
pp. 1801-1803 ◽  
Author(s):  
Maksim Son ◽  
Lynn McEwan ◽  
Manaf Ubaidat ◽  
Keith Bovell ◽  
Sarah A Morrow

Teriflunomide is an oral monotherapy used to treat relapsing multiple sclerosis. Although teriflunomide may be associated with gastrointestinal symptoms, these events are mild and self-limiting. We present a 39-year-old female who developed severe diarrhea and lost 20 pounds within 3 weeks of starting teriflunomide. Despite discontinuing teriflunomide and undergoing cholestyramine washout, her symptoms persisted. Celiac disease on genetic testing was positive, but no anti-transglutaminase and anti-endomysial antibodies were detected. She underwent colonoscopy and biopsy was consistent with lymphocytic colitis. Remission was achieved within days of starting budenoside. Our case describes a rare, but serious, gastrointestinal adverse event of teriflunomide.


2012 ◽  
Vol 113 (08) ◽  
pp. 495-497
Author(s):  
M. Khoshbaten ◽  
M. Farhoudi ◽  
M. Nikanfar ◽  
H. Ayromlou ◽  
S. Shaafi ◽  
...  

2008 ◽  
Vol 14 (5) ◽  
pp. 698-700 ◽  
Author(s):  
A Nicoletti ◽  
F Patti ◽  
S Lo Fermo ◽  
A Sciacca ◽  
P Laisa ◽  
...  

We evaluated the presence of IgA and IgG celiac disease–related antibodies in a sample of 217 patients with multiple sclerosis (MS) and in a sample of 200 controls not affected by neurological disorders. None of the 217 patients with MS presented IgG and IgA anti-gliadin, anti-endomysial antibodies, anti-tissue transglutaminase and anti-reticulin, whereas only one of the selected controls presented specific antibodies; this subject resulted to be effectively affected by celiac disease. Our data did not show an increased frequency of celiac disease among patients with MS.


2021 ◽  
Vol 3 (2) ◽  
pp. 73-74
Author(s):  
Irina Blumenstein

Recent studies have shown that a number of common autoimmune diseases have perturbations of their intestinal microbiome (dysbiosis). These include: Celiac Disease (CeD), Multiple Sclerosis (MS), Rheumatoid Arthritis (RA), Sjogren’s Syndrome (SS), and Type 1 diabetes (T1D). All of these have intestinal microbiomes that are different from healthy controls. There have been numerous studies using animal models of single probiotics (monoclonal) or mixtures of probiotics (polyclonal) and even complete microbiota transfer (fecal microbial transfer-FMT) to inhibit or delay the onset of autoimmune diseases such as the aforementioned common ones. However, proportionally, fewer clinical trials have utilized monoclonal therapies or FMT than polyclonal therapies for treating autoimmune diseases, even though bacterial mono-therapies do inhibit the development of autoimmune diseases and/or delay the onset of autoimmune diseases in rodent models of those autoimmune diseases. In this review then, we review the previously completed and currently ongoing clinical trials that are testing bacterial therapies (FMT, monoclonal, and polyclonal) to treat common autoimmune diseases and discuss the successes in using bacterial monotherapies to treat rodent models of these common autoimmune diseases.


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