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1.
Neurol Sci ; 41(8): 2249-2253, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32240416

ABSTRACT

In the last years, change in multiple sclerosis (MS) therapeutic scenario has highlighted the need for an improved doctor-patient communication in advance of treatment initiation in order to allow patient's empowerment in the decision-making process. AIMS: The aims of our project were to review the strategies used by Italian MS specialists to inform patients about treatment options and to design a multicentre shared document that homogenizes the information about disease-modifying treatment (DMTs) and the procedure of taking informed consent in clinical practice. RESULTS: The new resource, obtained by consensus among 31 neurologists from 27 MS Centres in Italy with the supervision of a medico-legal advisor, received the aegis of Italian Neurological Society (SIN) and constitutes a step toward a standardized decision process around DMTs in MS.


Subject(s)
Informed Consent , Multiple Sclerosis , Consensus , Humans , Italy , Multiple Sclerosis/therapy , Physician-Patient Relations
2.
Eur J Neurol ; 23(3): 630-40, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26756166

ABSTRACT

BACKGROUND AND PURPOSE: Depression is common amongst subjects with multiple sclerosis (MS), and several investigations have explored different determinants of this condition, including physical disability, psychological and psychosocial factors. The brain derived neurotrophic factor (BDNF) Val66Met polymorphism has been associated with depression. The aim of this study was to analyze the influence of disease-related factors, BDNF Val66Met polymorphism and perception of disease on the severity of depression in MS. METHOD: In total, 136 MS patients (88 women) were recruited and genotyped for BDNF rs6265 polymorphism at nucleotide 196 (G/A) using 'high resolution melting'. Depressive symptoms were assessed by the Multiple Sclerosis Depression Rating Scale. Perception of health status was assessed using the SF-36 questionnaire. RESULTS: A multivariable linear regression model showed that the best predictors of depression were the SF-36 General health (ß = -0.209; P = 0.013), Mental health (ß = -0.410; P < 0.001) and Social activity (ß = -0.195; P = 0.035) scores; physical disability (assessed by the Extended Disability Status Scale score) was directly correlated to depression severity on univariate analysis, but it was not a relevant predictor of depression on multivariate analysis; other variables directly related to the disease (treatment, annual relapsing rate) and the BDNF Val66Met polymorphism were not significantly associated with depression. CONCLUSION: Perception of the health status is the principal predictor of depressive symptoms in our sample. This result supports the hypothesis that the subjective interpretation of the disease's consequences is one of the main factors in determining depression in MS.


Subject(s)
Brain-Derived Neurotrophic Factor/genetics , Depression/psychology , Multiple Sclerosis/psychology , Adult , Depression/etiology , Depression/genetics , Female , Humans , Male , Middle Aged , Multiple Sclerosis/complications , Multiple Sclerosis/genetics , Polymorphism, Genetic
3.
Eur Neurol ; 70(1-2): 10-5, 2013.
Article in English | MEDLINE | ID: mdl-23652573

ABSTRACT

OBJECTIVES: In this prospective study, we used one diagnostic protocol to establish an early diagnosis in patients with ocular palsies in absence of other neurological findings. MATERIALS AND METHODS: The study was performed on a consecutive series of 132 patients who visited our Neurological Department for ptosis and/or diplopia in absence of other neurological signs, using the same diagnostic protocol. RESULTS: An etiological diagnosis was made in 74% of cases during a mean time of 17 ± 23 months from symptom onset. Myasthenia gravis was the most common diagnosis (n = 60, 45.5%). Thirty-four cases (26%) remained undiagnosed in spite of a follow-up lasting 32 ± 33 months on average. CONCLUSIONS: Identifying the cause of an isolated ocular palsy can be difficult, and an extended follow-up time does not aid in further establishment of the diagnosis.


Subject(s)
Oculomotor Nerve Diseases/diagnosis , Oculomotor Nerve Diseases/etiology , Adult , Blepharoptosis/diagnosis , Blepharoptosis/etiology , Diplopia/diagnosis , Diplopia/etiology , Female , Humans , Male , Middle Aged , Prospective Studies
4.
J Neurol Sci ; 424: 117430, 2021 05 15.
Article in English | MEDLINE | ID: mdl-33838554

ABSTRACT

The prevalence of trigeminal neuralgia (TN) in patients with Multiple Sclerosis (MS) is higher than in the general population and its management can be particularly challenging due to a number of reasons including high recurrence rates, lack of MS-specific treatment guidelines and uncertainties about pain pathophysiology. Aim of this cross-sectional, multicentre survey was to gather information on the current treatment modalities and options of MS-related TN across 23 Italian MS centres. Initial medical management (carbamazepine or oxcarbazepine) of MS-related TN was fairly homogeneous throughout Italian centres. The most commonly available surgical procedure was microvascular decompression, but the frequency and types of surgical procedures available locally differed considerably throughout MS centers, and were unavailable in one quarter of them. This survey reveals some of the issues that could hamper an optimal patient management and underlines the need for a consensus on MS-related TN to support health-care professionals in their approach to this challenging condition and to facilitate the development of local guidelines aimed at ensuring equity in access to care and treatment optimization.


Subject(s)
Multiple Sclerosis , Trigeminal Neuralgia , Cross-Sectional Studies , Health Services Accessibility , Humans , Italy/epidemiology , Multiple Sclerosis/complications , Multiple Sclerosis/epidemiology , Multiple Sclerosis/therapy , Retrospective Studies , Treatment Outcome , Trigeminal Neuralgia/epidemiology , Trigeminal Neuralgia/etiology , Trigeminal Neuralgia/therapy
5.
J Neurosci Res ; 88(5): 1106-12, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19885866

ABSTRACT

The aim of this study was to investigate the role of Brain Derived Neurotrophic Factor (BDNF) and inflammatory factors in the development of cognitive dysfunctions in Multiple Sclerosis (MS). We correlated peripheral blood mononuclear cell (PBMC) production of BDNF, Tumor Necrosis Factor-alpha (TNF-alpha), Interleukin (IL)-6 and IL-10 with performances on specific neuropsychological tasks in a selected series of MS patients. We studied a sample of 30 patients with relapsing-remitting (RR)MS, segregated by gender and matched for age, education, disease duration, type of immunomodulating therapy, degree of disability and overall cognitive status. We found that low BDNF levels were correlated with increased time of execution on a divided attention and visual scanning task whereas high levels of IL-6 were correlated with low Mini Mental State Examination scores. We did not observe any significant correlations between IL-10, TNF-alpha levels and cognitive performances in our patients. In conclusion our study shows a correlation between low BDNF and high IL-6 production by PBMCs and poorer performances in cognitive tasks in RRMS patients suggesting a possible role of these factors in cognitive impairment in MS.


Subject(s)
Cognition Disorders/metabolism , Cytokines/metabolism , Leukocytes, Mononuclear/metabolism , Multiple Sclerosis, Relapsing-Remitting/metabolism , Nerve Growth Factors/metabolism , Adult , Biomarkers/analysis , Biomarkers/metabolism , Brain/immunology , Brain/metabolism , Brain/pathology , Brain-Derived Neurotrophic Factor/metabolism , Cognition Disorders/immunology , Cognition Disorders/physiopathology , Cohort Studies , Encephalitis/immunology , Encephalitis/metabolism , Encephalitis/physiopathology , Female , Humans , Interleukin-10/metabolism , Interleukin-6/metabolism , Magnetic Resonance Imaging , Male , Middle Aged , Multiple Sclerosis, Relapsing-Remitting/complications , Multiple Sclerosis, Relapsing-Remitting/immunology , Neuropsychological Tests , Statistics as Topic , Tumor Necrosis Factor-alpha/metabolism
6.
J Neurooncol ; 98(3): 407-9, 2010 Jul.
Article in English | MEDLINE | ID: mdl-19957009

ABSTRACT

Multiple sclerosis (MS) is a T-cell autoimmune disease of the central nervous system (CNS). Predominance of women in autoimmune diseases suggests that sex hormones may play a role in disease susceptibility. A possible role for prolactin, a neuroendocrine peptide with powerful immunomodulatory properties, is suggested in MS. We describe the case of a 32-year-old man affected by relapsing-remitting MS who experienced the first MS clinical event during the development of a prolactin-secreting adenoma and the only two MS relapses during adenoma recurrence. Prolactin may have facilitated the inflammatory process and triggered MS clinical attacks, suggesting a role of prolactin in immunomodulation and therefore in autoimmune disease course.


Subject(s)
Hyperprolactinemia/complications , Multiple Sclerosis/etiology , Adult , Brain/pathology , Humans , Magnetic Resonance Imaging/methods , Male , Multiple Sclerosis/pathology
7.
Eur Rev Med Pharmacol Sci ; 24(6): 3267-3273, 2020 03.
Article in English | MEDLINE | ID: mdl-32271444

ABSTRACT

OBJECTIVE: Multiple Sclerosis (MS) is an inflammatory and neurodegenerative disease that affect both white and gray matter. The relapsing and the eventually progressive course of MS is heterogeneous; thus, a confident long-term prediction of individual prognosis is not possible yet. Recent studies have demonstrated the role of long non-coding RNA (lncRNAs) as potential biomarkers that could provide information to predict disease activity and progression. PATIENTS AND METHODS: By qRT-PCR, we analysed the lncRNAs expression in the serum of 16 secondary progressive MS (SP-MS), 12 primary progressive (PP-MS) patients and 8 healthy controls. RESULTS: We found that TUG1 was upregulated in SP-MS, while the comparison of PP-MS vs. controls showed a downregulation of non-protein coding RNA 188 (LRRC75A-AS1) and a significant upregulation of two lncRNAs: long intergenic non-protein coding RNA 293 (LINC00293) and RP11-29G8.3. Moreover, we performed an in-silico analysis using DIANA-LncBase v2 and HMDD v3.0 software, in order to predict the possible interaction of these four lncRNAs with miRNAs. We identified 21 miRNAs prediction targets possibly involved in MS. CONCLUSIONS: Our data indicate a regulatory function of these lncRNAs in autoimmune and inflammatory processes related to MS suggesting their potential role in progressive MS pathogenesis.


Subject(s)
Gene Expression Profiling , Multiple Sclerosis/genetics , Multiple Sclerosis/pathology , RNA, Long Noncoding/genetics , Female , Humans , Male , Middle Aged , Multiple Sclerosis/blood , Pilot Projects , Real-Time Polymerase Chain Reaction
8.
Clin Immunol ; 131(1): 70-83, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19097824

ABSTRACT

In pregnant women affected by multiple sclerosis (MS) we observed increased percentages of CD4(+)CD25(+)Foxp3(+) T regulatory cells at the 1st and the 2nd trimester of gestation that was associated with a decreased T-bet expression in CD4(+) T cells. In women showing clinical relapse and/or new lesions at MRI after delivery we found, a higher expression of T-bet, pSTAT1 and pSTAT3 in CD4(+), CD8(+) T cells and CD14(+) cells, associated with an increase of IFNgamma and IL17 production by PBMC at the 3rd trimester of gestation and after delivery. Our data suggest that the expansion of circulating CD4(+)CD25(+)Foxp3(+) regulatory T cells and the lower expression of T-bet in CD4(+) T cells may account for the decreased MS activity during pregnancy. The expression of T-bet, pSTAT1 and pSTAT3 in peripheral blood CD4(+) and CD8(+) T cells and monocytes could be useful to identify MS patients who will develop a relapse after delivery.


Subject(s)
Forkhead Transcription Factors/blood , Multiple Sclerosis, Relapsing-Remitting/blood , Pregnancy Complications/blood , STAT1 Transcription Factor/blood , STAT3 Transcription Factor/blood , T-Box Domain Proteins/blood , T-Lymphocytes, Regulatory/immunology , Adult , Enzyme-Linked Immunosorbent Assay , Female , Flow Cytometry , Forkhead Transcription Factors/biosynthesis , Forkhead Transcription Factors/immunology , Humans , Interferon-gamma/blood , Interferon-gamma/immunology , Interleukin-10/blood , Interleukin-10/immunology , Interleukin-17/blood , Interleukin-17/immunology , Longitudinal Studies , Multiple Sclerosis, Relapsing-Remitting/immunology , Postpartum Period/blood , Postpartum Period/immunology , Pregnancy , Pregnancy Complications/immunology , STAT1 Transcription Factor/biosynthesis , STAT1 Transcription Factor/immunology , STAT3 Transcription Factor/biosynthesis , STAT3 Transcription Factor/immunology , T-Box Domain Proteins/biosynthesis , T-Box Domain Proteins/immunology
9.
Clin Exp Immunol ; 158(1): 106-14, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19737237

ABSTRACT

Coeliac disease (CD) is considered a T cell-mediated autoimmune disease, and up-regulation of T-bet and phosphorylated signal transducers and activators of transcription (pSTAT)1, key transcription factors for the development of T helper type 1 (Th1) cells, has been described in the mucosa of patients with untreated CD. Using transcription factor analysis, we investigated whether T-bet and pSTAT1 expressions are up-regulated in the peripheral blood of CD patients and correlate with disease activity. Using flow cytometry, we analysed T-bet, pSTAT1 and pSTAT3 expression in CD4(+), CD8(+) T cells, CD19(+) B cells and monocytes from peripheral blood of 15 untreated and 15 treated CD patients and 30 controls, and longitudinally in five coeliac patients before and after dietary treatment. We evaluated using enzyme-linked immunosorbent assay (ELISA), interferon (FN)-gamma, interleukin (IL)-17 and IL-10 production by peripheral blood mononuclear cell (PBMC) cultures. T-bet expression in CD4(+), CD8(+) T cells, CD19(+) B cells and monocytes and IFN-gamma production by PBMC was higher in untreated than in treated CD patients and controls. pSTAT1 expression was higher in CD4(+)T cells, B cells and monocytes from untreated than from treated CD patients and controls. pSTAT3 was increased only in monocytes from untreated patients compared with CD-treated patients and controls. The data obtained from the longitudinal evaluation of transcription factors confirmed these results. Flow cytometric analysis of pSTAT1 and T-bet protein expression in peripheral blood mononuclear cells could be useful and sensible markers in the follow-up of CD patients to evaluate disease activity and response to dietary treatment.


Subject(s)
Celiac Disease/blood , Leukocytes, Mononuclear/metabolism , STAT1 Transcription Factor/analysis , T-Box Domain Proteins/analysis , Acute Disease , Adult , Analysis of Variance , Antigens, CD19/immunology , B-Lymphocytes/immunology , B-Lymphocytes/metabolism , Biomarkers/blood , CD4-Positive T-Lymphocytes/metabolism , CD8-Positive T-Lymphocytes/metabolism , Case-Control Studies , Celiac Disease/diet therapy , Diet, Gluten-Free , Female , Flow Cytometry/methods , Humans , Interferon-gamma/analysis , Interleukin-10/analysis , Interleukin-17/analysis , Male , Middle Aged , STAT3 Transcription Factor/blood
10.
Mult Scler Relat Disord ; 35: 176-181, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31394405

ABSTRACT

BACKGROUND: Multiple sclerosis (MS) is a chronic, immune-mediated, inflammatory, neurodegenerative disorder. Many studies are investigating the potential role of body fluid biomarkers as prognostic factors for early identification of patients presenting with clinical isolated syndrome (CIS) at high risk for conversion to MS or to recognize RRMS patients at high risk for progression. OBJECTIVES: To evaluate the correlation between levels of BAFF, chitinase 3-like 1 (CHI3L1), sCD163, Osteopontin (OPN), both on serum and cerebral spinal fluid (CSF), and the disease activity and progression. We also want to explore a possible relationship between serological and CSF biomarker's levels. PATIENTS AND METHODS: We enrolled 82 patients between June 2014 and June 2016. Seventy-one received a diagnosis of demyelinating disease of CNS (46 RRMS and 25 CIS), while 11 were affected by other neurological diseases. All patients underwent a neural axis MRI, lumbar puncture and blood samples. Levels of BAFF, CHI3L1, sCD163, OPN on serum and CSF were analyzed by Luminex xMAP system, with a kit 11-plex ad hoc. RESULTS: The CSF CHI3L1, sCD163 and OPN levels were significantly higher in MS patients than in controls. We did not find significant differences in serum CHI3L1, sCD163 and OPN levels, nor CSF or serum BAFF levels between patient and control groups. We found significantly higher CSF level of sCD163 and CHI3L1 in all patients' subgroups compared with controls, while OPN was higher in CIS and RR subgroups. We did not find significant differences for serum and CSF levels of all the markers between patients with or without clinical or radiological disease activity. CSF sCD163 and CHI3L1 levels was significant higher in CIS patients who converted to MS (p < 0.05). Using ROC curve analysis, CSF sCD163 resulted the best predictive factor. CSF CHI3L1 and OPN levels resulted useful independent predictors too. Combined ROCs of those three analytes demonstrated a better predictive value, with sCD163 and CHI3L1 resulting as the best combination. CONCLUSIONS: CSF sCD163 CHI3L1 and OPN levels were higher in MS patients whereas serum CHI3L1, sCD163 and OPN levels did not show differences compared with controls. This finding confirms the high CSF specificity with regards to the analysis of processes, inflammatory and non-inflammatory, that occur within the CNS.


Subject(s)
Biomarkers/cerebrospinal fluid , Demyelinating Diseases/diagnosis , Multiple Sclerosis/diagnosis , Adult , Antigens, CD/blood , Antigens, CD/cerebrospinal fluid , Antigens, Differentiation, Myelomonocytic/blood , Antigens, Differentiation, Myelomonocytic/cerebrospinal fluid , B-Cell Activating Factor/blood , B-Cell Activating Factor/cerebrospinal fluid , Biomarkers/blood , Chitinase-3-Like Protein 1/blood , Chitinase-3-Like Protein 1/cerebrospinal fluid , Demyelinating Diseases/blood , Demyelinating Diseases/cerebrospinal fluid , Disease Progression , Female , Humans , Male , Middle Aged , Multiple Sclerosis/blood , Multiple Sclerosis/cerebrospinal fluid , Osteopontin/blood , Osteopontin/cerebrospinal fluid , Prognosis , Receptors, Cell Surface/blood
11.
J Neurol Sci ; 372: 33-39, 2017 Jan 15.
Article in English | MEDLINE | ID: mdl-28017240

ABSTRACT

Gait impairment is one of the most frequent and life-altering consequences of Multiple sclerosis (MS), frequently associated with lower limb spasticity. Focal muscle vibration (fMV) is a technique that applies a vibratory stimulus to a specific muscle or its tendon, reducing spasticity. The aim of our study is to evaluate the efficacy of fMV in ameliorating gait impairment in MS patients with severe lower limb spasticity, measured by Gait Analysis (GA) and objective and patient-oriented scales scores. Fourteen patients affected by Secondary Progressive MS (SPMS) with a lower limb spasticity with a low or no response to antispastic drugs, received repetitive fMV (r-fMV) over the quadriceps and the lumbar paraspinal muscles. The effect of r-fMV on gait was measured by a GA evaluation and objective and patient-oriented scales scores, performed before r-fMV (T0), and 1week (T1) and 1month (T2) after the last session of r-fMV. After the r-fMV the most of spatio-temporal parameters calculated by GA were improved. Moreover, clinical evaluation related results showed an improvement of SM patients' quality of life. In conclusion, r-fMV improves gait function in MS patients affected by severe spasticity of lower limb, non-responsive to common oral antispastic drugs.


Subject(s)
Gait Disorders, Neurologic/etiology , Gait Disorders, Neurologic/rehabilitation , Multiple Sclerosis/complications , Muscle, Skeletal/physiology , Vibration/therapeutic use , Adult , Biomechanical Phenomena , Disability Evaluation , Female , Follow-Up Studies , Humans , Male , Middle Aged , Mood Disorders/etiology , Severity of Illness Index , Time Factors
14.
Am J Surg ; 161(4): 466-9, 1991 Apr.
Article in English | MEDLINE | ID: mdl-1827961

ABSTRACT

Surgically induced immunosuppression may play a role in cancer, because of the possible existence of micrometastases at the time of surgical removal of tumors. Antitumor immune reactions are mediated by interleukin-2 (IL-2). IL-2 acts on a specific IL-2 cell surface receptor; moreover, a soluble form of IL-2 receptor (sIL-2R) can be released in the blood. This study was carried out to evaluate the effect of surgery on sIL-2R serum levels in patients with operable solid tumors. A total of 48 patients with cancer and 11 controls who underwent major surgery for non-neoplastic disease were evaluated before and 7 days after surgery. Serum mean levels of sIL-2R were significantly higher after than before surgery in both the cancer and control groups. No correlation was seen between surgery-induced changes in sIL-2R and in T lymphocyte subsets. Because of its capacity of binding to IL-2, the increased blood concentrations of sIL-2R could reduce the IL-2 availability and negatively affect antitumor immune reactions.


Subject(s)
Neoplasms/surgery , Receptors, Interleukin-2/analysis , T-Lymphocyte Subsets/pathology , Breast Neoplasms/blood , Breast Neoplasms/surgery , Cholelithiasis/blood , Cholelithiasis/surgery , Colonic Neoplasms/blood , Colonic Neoplasms/surgery , Female , Humans , Leukocyte Count , Lung Neoplasms/blood , Lung Neoplasms/surgery , Male , Middle Aged , Neoplasms/blood , Rectal Neoplasms/blood , Rectal Neoplasms/surgery , Stomach Neoplasms/blood , Stomach Neoplasms/surgery , T-Lymphocytes, Helper-Inducer/pathology , T-Lymphocytes, Regulatory/pathology
15.
Minerva Chir ; 32(9): 577-82, 1977 May 15.
Article in Italian | MEDLINE | ID: mdl-865701

ABSTRACT

Six cases of perforation of the small intestine, one secondary to anaphylactoid purpura and five spontaneous, are reported. Ingestion of an iced drink acted as a trigger in two cases. A vascular genesis is put forward to explain the aetiopathogenesis of two cases and it is noted that perforation of this type is present in the final ileal ansa, at the mesenterial margin. In three cases, histology revealed the presence of double refraction crystal. These came from vegetal residues and are probably capable of penetrating from the lumen into the mucosa causing a foreign body reaction, abscess and subsequent perforation. In these cases, perforation occurred in an ansa located further away than the last ileal ansa (about 3 m) and on the mesenterial margin. Intestinal resection and subsequent end-to-end, single layer anastomosis were performed in all cases.


Subject(s)
Intestinal Perforation , Intestine, Small , Child, Preschool , Enteritis/complications , Female , Foreign Bodies/complications , Humans , IgA Vasculitis/complications , Intestinal Perforation/etiology , Intestinal Perforation/surgery , Male , Middle Aged , Peptic Ulcer Perforation/surgery
16.
Minerva Chir ; 30(23-24): 1175-92, 1975.
Article in Italian | MEDLINE | ID: mdl-1223693

ABSTRACT

Eight cases of pancreatic traumas are considered and the literature reviewed. Personal cases include: 1 contusion treated nedically; 2 cases of complete rupture (1 of which primary treated with double jejunal pancreatic anastomosis); 1 associated with splenic rupture, treated with distal pancreatectomy and splenectomy; 1 contusion of the head associated with hepatic lesions treated with suture of the lesions external derived and cholecystostomy; 4 contusions without lesion of the duct associated with other visceral lesions (stomach, duodenum, spleen, liver), treated surgically by suture of the lesion, and drainage of the omental bursa. As regards diagnosis, the only pathognomonic examination is amylasaemia. Paracentesis proved important in cases of haemoperitoneum. Long-term results were observed by scintigraphy and through starch and maltose load curves. Scintigraphy pointed to the presence of functional deficiency in areas which seemed to be only contused or actually normal. It is therefore concluded, especially in cases of complete rupture, that therapy should be kept as conservative as possible (Duodenal pancreatic anastomosis). The purpose of this is to prevent fistulas of the residual stump, fostered by the pressure in Oddi's sphincter, and to lease the pancreatic tissue as operative as possible. This is particularly important if patients are young.


Subject(s)
Pancreas/injuries , Abdominal Injuries/diagnosis , Abdominal Injuries/diagnostic imaging , Adult , Child , Child, Preschool , Emergencies , Female , Humans , Male , Palpation , Pancreas/surgery , Radiography , Radionuclide Imaging , Rupture , Splenic Rupture/etiology
20.
J Neuroimmunol ; 225(1-2): 149-52, 2010 Aug 25.
Article in English | MEDLINE | ID: mdl-20510468

ABSTRACT

Elevated anti-Epstein-Barr virus (EBV) antibody levels are present in serum of Multiple sclerosis (MS) patients but literature lacks of studies comparing anti-EBV antibody levels between MS and other neurological diseases. We evaluate anti-VCA IgG and IgM, anti-EBNA1 IgG, anti-Cytomegalovirus IgG and IgM titres in serum and cerebrospinal fluid (CSF) of 267 MS, 50 Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) and 88 Amyotrophic Lateral Sclerosis (ALS) patients. We found increased titres of anti-EBV-IgG in serum and CSF of MS subjects as compared to CIDP and ALS patients thus providing additional evidence for a possible involvement of EBV in MS.


Subject(s)
Amyotrophic Lateral Sclerosis , Herpesvirus 4, Human/immunology , Multiple Sclerosis , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating , Adult , Aged , Amyotrophic Lateral Sclerosis/blood , Amyotrophic Lateral Sclerosis/cerebrospinal fluid , Amyotrophic Lateral Sclerosis/virology , Antibodies/blood , Antibodies/cerebrospinal fluid , Female , Humans , Male , Middle Aged , Multiple Sclerosis/blood , Multiple Sclerosis/cerebrospinal fluid , Multiple Sclerosis/virology , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/blood , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/cerebrospinal fluid , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/virology
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