Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 38
Filter
1.
Neurol Res Pract ; 2: 8, 2020.
Article in English | MEDLINE | ID: mdl-33324914

ABSTRACT

INTRODUCTION: Cerebrospinal fluid (CSF) analysis is important for detecting inflammation of the nervous system and the meninges, bleeding in the area of the subarachnoid space that may not be visualized by imaging, and the spread of malignant diseases to the CSF space. In the diagnosis and differential diagnosis of neurodegenerative diseases, the importance of CSF analysis is increasing. Measuring the opening pressure of CSF in idiopathic intracranial hypertension and at spinal tap in normal pressure hydrocephalus constitute diagnostic examination procedures with therapeutic benefits.Recommendations (most important 3-5 recommendations on a glimpse): The indications and contraindications must be checked before lumbar puncture (LP) is performed, and sampling CSF requires the consent of the patient.Puncture with an atraumatic needle is associated with a lower incidence of postpuncture discomfort. The frequency of postpuncture syndrome correlates inversely with age and body mass index, and it is more common in women and patients with a history of headache. The sharp needle is preferably used in older or obese patients, also in punctures expected to be difficult.In order to avoid repeating LP, a sufficient quantity of CSF (at least 10 ml) should be collected. The CSF sample and the serum sample taken at the same time should be sent to a specialized laboratory immediately so that the emergency and basic CSF analysis program can be carried out within 2 h.The indication for LP in anticoagulant therapy should always be decided on an individual basis. The risk of interrupting anticoagulant therapy must be weighed against the increased bleeding risk of LP with anticoagulant therapy.As a quality assurance measure in CSF analysis, it is recommended that all cytological, clinical-chemical, and microbiological findings are combined in an integrated summary report and evaluated by an expert in CSF analysis. CONCLUSIONS: In view of the importance and developments in CSF analysis, the S1 guideline "Lumbar puncture and cerebrospinal fluid analysis" was recently prepared by the German Society for CSF analysis and clinical neurochemistry (DGLN) and published in German in accordance with the guidelines of the AWMF (https://www.awmf.org). /uploads/tx_szleitlinien/030-141l_S1_Lumbalpunktion_und_Liquordiagnostik_2019-08.pdf). The present article is an abridged translation of the above cited guideline. The guideline has been jointly edited by the DGLN and DGN.

2.
J Neurol ; 264(3): 453-466, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28005176

ABSTRACT

BACKGROUND: It has long been known that the majority of patients with multiple sclerosis (MS) display an intrathecal, polyspecific humoral immune response to a broad panel of neurotropic viruses. This response has measles virus, rubella virus and varicella zoster virus as its most frequent constituents and is thus referred to as the MRZ reaction (MRZR). OBJECTIVE: Re-evaluation of the specificity of MRZR as a marker of MS. METHODS: Structured review of the existing English-, German- and Spanish-language literature on MRZR testing, with evaluation of MRZR in a cohort of 43 unselected patients with MS and other neurological diseases as a proof of principle. RESULTS: A positive MRZ reaction, defined as a positive intrathecal response to at least two of the three viral agents, was found in 78% of MS patients but only in 3% of the controls (p < 0.00001), corresponding to specificity of 97%. Median antibody index values were significantly lower in non-MS patients (measles, p < 0.0001; rubella, p < 0.006; varicella zoster, p < 0.02). The 30 identified original studies on MRZR reported results from 1478 individual MRZR tests. A positive MRZR was reported for 458/724 (63.3%) tests in patients with MS but only for 19/754 (2.5%) tests in control patients (p < 0.000001), corresponding to cumulative specificity of 97.5% (CI 95% 96-98.4), cumulative sensitivity of 63.3% (CI 95% 59.6-66.8) (or 67.4% [CI 95% 63.5-71.1] in the adult MS subgroup), a positive likelihood ratio of 25.1 (CI 95% 16-39.3) and a negative likelihood ratio of 0.38 (CI 95% 0.34-0.41). Of particular note, MRZR was absent in 52/53 (98.1%) patients with neuromyelitis optica or MOG-IgG-positive encephalomyelitis, two important differential diagnoses of MS. CONCLUSION: MRZR is the most specific laboratory marker of MS reported to date. If present, MRZR substantially increases the likelihood of the diagnosis of MS. Prospective and systematic studies on the diagnostic and prognostic impact of MRZR testing are highly warranted.


Subject(s)
Antibodies, Viral/cerebrospinal fluid , Herpesvirus 3, Human/immunology , Measles virus/immunology , Multiple Sclerosis/cerebrospinal fluid , Rubella virus/immunology , Biomarkers/cerebrospinal fluid , Humans , Multiple Sclerosis/virology
3.
Int J Pharm ; 457(2): 395-406, 2013 Dec 05.
Article in English | MEDLINE | ID: mdl-24148666

ABSTRACT

Taste masking and moisture protection of oral dosage forms contribute significantly to the therapeutic effect of pharmaceutical and nutraceutical formulations either by ensuring patient compliance or by providing stability through shelf life of the dosage form. Among different types of taste, bitter taste is the most relevant for patient acceptance because of the extremely high sensitivity. As hydrolysis is the most common mode of degradation of an active ingredient, moisture protection plays a vital role in the stability of the active during manufacturing and storage. Optimized oral dosage forms need to reliably hinder the release of bitter drug molecules in the mouth or ensure stability of the active compound, while also ensuring fast drug release in the stomach to enable early therapeutic onset. Besides different formulation concepts, film coating is found to be the most effective and commonly used approach for taste masking and moisture protection. Film coating can be achieved through the use of water-soluble, cationic, anionic or neutral insoluble polymers from different chemical structures. Cationic polymers provide efficient moisture protection as well as taste masking without influencing the release of the drug in the gastric fluids. Polymers may be sprayed onto various types of cores from dispersions or solutions in organic, solvents or water in drum or fluidzed bed coaters. Applied quantities need insuring complete coating thickness ranging from 0.5 to 50 µm or more finally. Insulating excipients, such as hydrophobic plasticizers, lipids, pigments or other insoluble substances will influence the functionality of films. Organoleptic tests are still common in testing the quality of taste-masked formulations. Recently, multi-channel taste sensors have been developed to quantify different types of taste. Dynamic vapor sorption technique and studies at elevated temperature provide effective concepts study the efficacy of the formulations. Efficient taste masking and reliable moisture protection of solid oral dosage forms can be achieved by film coating implementing the options of pharmaceutical polymers and processes.


Subject(s)
Pharmaceutical Preparations/chemistry , Taste , Chemistry, Pharmaceutical , Drug Stability , Humans , Pharmaceutical Preparations/administration & dosage , Pharmaceutical Preparations/analysis , Polymers/chemistry , Technology, Pharmaceutical , Water/chemistry
4.
Z Rheumatol ; 71(7): 572-82, 2012 Sep.
Article in German | MEDLINE | ID: mdl-22930108

ABSTRACT

Antirheumatic medication is of crucial importance within the treatment concept of chronic inflammatory disorders. Side effects may affect various organ systems, among which are neurologic manifestations. If patients have comorbidities involving the nervous system this should be taken into consideration before choosing an individual immunosuppressant or immunomodulatory compound, as any worsening of the underlying neurologic disease should be avoided. In this article, relevant neurologic disorders will be described with respect to the clinical manifestations, differential diagnosis and treatment. In the second part, pharmaceuticals and biologicals which are frequently used as part of an antirheumatic regimen are discussed with respect to the potential to induce side effects specifically related to the nervous system.


Subject(s)
Antirheumatic Agents/adverse effects , Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Brain Diseases/chemically induced , Brain Diseases/diagnosis , Nervous System Diseases/chemically induced , Nervous System Diseases/diagnosis , Arthritis, Rheumatoid/complications , Brain Diseases/prevention & control , Diagnosis, Differential , Humans , Nervous System Diseases/prevention & control
5.
Mult Scler ; 17(4): 478-86, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21148265

ABSTRACT

BACKGROUND: Patient-reported quality of life (QOL) is an outcome measure in clinical trials in multiple sclerosis (MS), but translated QOL instruments may affect the actual comparability of data. OBJECTIVES: We aimed to investigate possible differences in QOL in MS between cultures and countries. We employed the Functional Assessment of Multiple Sclerosis (FAMS) Version 4 questionnaire, which is a state-of-the-art QOL instrument. METHODS: Some 484 MS patients from Austria (145), Germany (144), and Poland (195) aged 20-60 years, and stratified for sex and disease severity as measured by the Expanded Disability Status Scale (EDSS) score completed the respective FAMS translation and a socio-demographic questionnaire. RESULTS: Analysis of variance and post-hoc Scheffé-test showed that 64% of the FAMS items were answered significantly differently (p < 0.001) between the three countries. A multivariate regression analysis including all the available disease-related and socio-demographic variables revealed the factors age, EDSS score, employment, social contacts, MS course, and country to be significant predictors of both the total FAMS score and the score for items answered differently between the three countries. CONCLUSIONS: Differences exist in the QOL of MS patients from Austria, Germany, and Poland which seem to lie beyond the impact of disease severity. They appear to be related to culture or other country-specific factors, as country was an independent predictor of differently answered items of the FAMS and thus also of the whole FAMS. QOL instruments should consider this aspect to faithfully reflect subjective information such as patient-reported benefit of treatment in multinational clinical trials.


Subject(s)
Cross-Cultural Comparison , Multiple Sclerosis/psychology , Quality of Life/psychology , Adult , Analysis of Variance , Austria , Chi-Square Distribution , Cross-Sectional Studies , Disability Evaluation , Female , Germany , Humans , Male , Middle Aged , Poland , Severity of Illness Index , Surveys and Questionnaires
6.
Mult Scler ; 15(2): 189-92, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18971221

ABSTRACT

BACKGROUND: Rituximab, a monoclonal antibody against the B-cell-specific surface protein CD20, is being evaluated for treatment of multiple sclerosis and neuromyelitis optica. Both diseases are restricted to the brain and cerebrospinal fluid (CSF). Whereas the ability of rituximab to deplete B cells in peripheral blood and tissue is well known, little information is available about the ability of rituximab to penetrate the barriers separating brain and CSF from the serum compartment. OBJECTIVE: To measure rituximab levels in serum and CSF of rituximab-treated patients and correlate them with CSF and response markers. METHODS: Fourteen paired serum/CSF samples of patients with autoimmune nervous system disorder were analyzed for up to 43 weeks after rituximab application. RESULTS: Rituximab remains detectable within the CSF after i.v. application for up to 24 weeks. Furthermore, levels of rituximab in CSF correlate significantly with the integrity of the blood CSF barrier.


Subject(s)
Antibodies, Monoclonal/pharmacokinetics , Blood-Brain Barrier , Immunologic Factors/pharmacokinetics , Multiple Sclerosis/drug therapy , Neuromyelitis Optica/drug therapy , Aged , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal/cerebrospinal fluid , Antibodies, Monoclonal, Murine-Derived , B-Lymphocytes/cytology , B-Lymphocytes/drug effects , Female , Flow Cytometry , Humans , Immunologic Factors/administration & dosage , Immunologic Factors/cerebrospinal fluid , Injections, Intravenous , Lymphocyte Count , Male , Multiple Sclerosis/cerebrospinal fluid , Multiple Sclerosis/immunology , Neuromyelitis Optica/cerebrospinal fluid , Neuromyelitis Optica/immunology , Rituximab , Young Adult
7.
J Neurol Neurosurg Psychiatry ; 79(10): 1134-6, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18270237

ABSTRACT

BACKGROUND: A polyspecific, intrathecal humoral immune response against neurotropic viruses such as measles, rubella and varicella zoster virus (MRZ reaction, MRZR) is present in 80-100% of patients with multiple sclerosis (MS), but has not to date been evaluated in patients with neuromyelitis optica (NMO). AIMS: To evaluate whether MRZR distinguishes NMO and MS. METHODS: 20 patients with NMO and 42 with MS were included. The intrathecal synthesis of antibodies against measles, rubella and varicella zoster virus was detected by calculation of the respective antibody indices (AI). RESULTS: A positive MRZ reaction, as defined by a combination of at least two positive AIs, was found in 37/42 MS, but in only 1/20 NMO patients (p<0.0001). Median AI values differed significantly between the groups (p<0.0005). CONCLUSIONS: The polyspecific antiviral humoral immune response characteristic for MS is widely missing in NMO, irrespective of the NMO-IgG status of the patients. Our findings further strengthen the case for NMO being pathologically distinct from MS.


Subject(s)
Antibodies, Viral/immunology , Multiple Sclerosis/diagnosis , Multiple Sclerosis/immunology , Neuromyelitis Optica/diagnosis , Neuromyelitis Optica/immunology , Adult , Aged , Chickenpox/immunology , Diagnosis, Differential , Female , Fluorescent Antibody Technique, Indirect , Humans , Magnetic Resonance Imaging , Male , Measles/immunology , Middle Aged , Optic Nerve/immunology , Optic Nerve/pathology , Rubella/immunology
8.
Acta Neurol Scand ; 117(6): 399-403, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18031564

ABSTRACT

OBJECTIVE: To study the time course of immunoglobulin, B and plasma cells in the blood and cerebrospinal fluid (CSF) before and during rituximab treatment in a patient with severe relapsing-remitting multiple sclerosis (MS) in relation to clinical and MRI findings. METHODS: Immunoglobulins in the CSF were measured by nephelometry and detected by isoelectrical focussing. CSF and blood cell subtypes from seven time points were analysed by flow cytometry. RESULTS: Treatment with rituximab induced a dramatic and sustained improvement in clinical and MRI findings over a follow-up period of 20 months. By contrast, the initially completely suppressed B and plasma cells in both the blood and CSF reappeared after 5 and 10 months, CSF cells being the first to reappear. Interestingly, intrathecal IgG synthesis persisted throughout the study period. DISCUSSION: Although highly effective in this case, the clinical effect in larger series and the mechanism of rituximab in MS deserves further evaluation.


Subject(s)
Antibodies, Monoclonal/therapeutic use , B-Lymphocytes/immunology , Immunoglobulin G/biosynthesis , Multiple Sclerosis/drug therapy , Adult , Antibodies, Monoclonal, Murine-Derived , Antibody Formation , Humans , Immunoglobulin G/blood , Immunoglobulin G/cerebrospinal fluid , Magnetic Resonance Imaging , Male , Multiple Sclerosis/diagnosis , Multiple Sclerosis/immunology , Plasma Cells/immunology , Rituximab , Treatment Outcome
9.
HNO ; 55(12): 961-3, 2007 Dec.
Article in German | MEDLINE | ID: mdl-17103202

ABSTRACT

In a 9-year-old boy with sudden sensorineural loss of hearing in the lower registers in both ears, serology showed elevated levels of antibodies against Borrelia burgdorferi and examination of the CSF revealed a positive antibody index against Borrelia burgdorferi. The boy was treated with antibiotics for 2 weeks. Audiometry performed 4 weeks after treatment was completely normal. Inner ear involvement in Lyme disease has often been discussed. Treating these patients with antibiotics may lead to an improvement in some.


Subject(s)
Hearing Loss, Sensorineural/diagnosis , Hearing Loss, Sensorineural/etiology , Labyrinth Diseases/diagnosis , Labyrinth Diseases/etiology , Lyme Disease/complications , Lyme Disease/diagnosis , Child , Humans , Male
10.
Fortschr Neurol Psychiatr ; 74(9): 497-502, 2006 Sep.
Article in German | MEDLINE | ID: mdl-16947099

ABSTRACT

Fatigue describes the presence of a pronounced and advanced state of weariness. People with fatigue need more energy and it takes more effort to perform different activities than expected when compared to the patients disability. Fatigue can be observed in up to 92 % of patients suffering from multiple sclerosis. In the presented study, the German fatigue severity scale (dFSS) was established following the English "Fatigue Severity Scale". We enrolled 20 patients suffering from a primary relapsing multiple sclerosis and compared them to 20 healthy controls. Fatigue was detected if at least 4 points were reached in the dFSS. The dFSS demonstrated high validity and reliability. The dFSS is able to differentiate patients with fatigue from healthy controls. As consequence, the dFSS can be used to evaluate fatigue in German speaking individuals. The presented data demonstrated a good internal consistence. The scale is able to measure fatigue in an economic and rapid fashion. Therefore, it can be used in clinical situations for measuring fatigue in German speaking individuals.


Subject(s)
Multiple Sclerosis/diagnosis , Multiple Sclerosis/physiopathology , Muscle Fatigue/physiology , Adult , Factor Analysis, Statistical , Female , Germany , Humans , Language , Male , Multiple Sclerosis, Chronic Progressive/physiopathology , Reproducibility of Results
11.
Drug Dev Ind Pharm ; 32(6): 709-18, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16885126

ABSTRACT

A multiparticulate drug delivery system was studied in which the drug release of a model drug theophylline could be modulated by interactions of ammonio methacrylate polymer and anions. The system consisted of a EUDRAGIT NE coated anionic core, layered with drug and further layered with EUDRAGIT RS. The effects of different anions like chloride, succinate, citrate, and acetate as well as the thickness of the polymer layers on the in vitro drug release were studied. It was seen that succinate and acetate anions had permeability enhancing effects and citrate and chloride anions had permeability retarding effects on the polymer. The results indicate that changing these variables would enable us to get a desired release profile and hence the proposed system could be a viable alternative to existing technologies for the development of a controlled drug delivery system.


Subject(s)
Acrylic Resins/chemistry , Delayed-Action Preparations , Methacrylates/chemistry , Polymers/chemistry , Theophylline/chemistry , Cations , Citrates/chemistry , Osmolar Concentration , Permeability , Sodium Acetate/chemistry , Sodium Chloride/chemistry , Sodium Citrate , Solubility , Technology, Pharmaceutical/methods , Time Factors
12.
Acta Neurol Scand ; 113(6): 433-6, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16674611

ABSTRACT

BACKGROUND: Interferon-beta (INF-beta) is effective and used in reducing exacerbation frequency and disease progression in multiple sclerosis. In certain circumstances, INF-beta can lead to rare side effects. AIMS OF THE STUDY: We report the case of a 34-year-old female patient satisfying the McDonald criteria of multiple sclerosis without showing typical pathologic changes in cerebrospinal fluid (CSF). After introduction of INF-beta treatment, she quickly developed further progression of her disseminated neurological symptoms and finally an ischemic cerebral infarction. METHODS: Evaluation of the patient included arterial angiography, magnetic resonance and positron emission tomography, histopathological assessment as well as a broad spectrum of serum and CSF analysis. RESULTS: All diagnostic evaluations and the clinical course revealed evidences for a primary angiitis of the CNS. We discuss the possible worsening due to inappropriate INF-beta treatment in cerebral angiitis promoting severe cerebrovascular insufficiency. CONCLUSION: The authors suggest that all diagnostic multiple sclerosis criteria including typical CSF findings should be ascertained before INF-beta treatment is initiated.


Subject(s)
Interferon-beta/adverse effects , Multiple Sclerosis, Relapsing-Remitting/diagnosis , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Stroke/chemically induced , Vasculitis, Central Nervous System/complications , Vasculitis, Central Nervous System/diagnosis , Adjuvants, Immunologic/adverse effects , Adult , Brain/blood supply , Brain/diagnostic imaging , Brain/pathology , Cerebral Angiography , Cerebral Arteries/diagnostic imaging , Cerebral Arteries/drug effects , Cerebral Arteries/pathology , Cerebrovascular Circulation/drug effects , Diagnostic Errors , Disease Progression , Female , Humans , Iatrogenic Disease/prevention & control , Magnetic Resonance Imaging , Multiple Sclerosis, Relapsing-Remitting/cerebrospinal fluid , Nerve Fibers, Myelinated/pathology , Positron-Emission Tomography , Stroke/diagnosis , Stroke/physiopathology , Vasculitis, Central Nervous System/physiopathology
13.
Acta Neurol Scand ; 113(5): 347-9, 2006 May.
Article in English | MEDLINE | ID: mdl-16629772

ABSTRACT

We report the case of a 22-years old genotypic women suffering from a relapsing-remitting multiple sclerosis (MS) according to the Poser criteria. In this patient, a gender change had been performed by androgen-supplementation and surgical intervention. During gender change, the patient experienced further relapses. Different immunomodulatory and immunosuppressive treatment strategies did not stabilise the course of MS in this patient. Actually, an escalating therapy with mitoxantrone has been initiated. During the observation period the patient received long-term testosterone-supplementation. Testosterone levels were elevated in the serum of this genotypic female MS patient under such a hormonal treatment compared to normal ranges before. The clinical course of the patient is presented in this case. As there are several studies investigating an immunomodulatory impact of hormones on the course of MS or experimental allergic encephalomyelitis, we discuss the presented case and a possible influence of androgens in this patient.


Subject(s)
Androgens/administration & dosage , Genitalia, Female/surgery , Multiple Sclerosis, Chronic Progressive/physiopathology , Multiple Sclerosis, Relapsing-Remitting/physiopathology , Testosterone/administration & dosage , Adult , Disease Progression , Female , Follow-Up Studies , Humans , Multiple Sclerosis, Chronic Progressive/surgery , Multiple Sclerosis, Relapsing-Remitting/surgery
14.
Nervenarzt ; 77(6): 711-5, 2006 Jun.
Article in German | MEDLINE | ID: mdl-16550412

ABSTRACT

Fatal familial insomnia (FFI) is a hereditary prion disease caused by a mutation in codon 178 of the prion protein gene PRNP on chromosome 20. It is characterized by disturbed night sleep, resulting in daily vigilance perturbations and a variety of other neurological symptoms. We present the case of a 46-year-old woman deteriorating despite immunosuppressive treatment which was initiated suspecting cerebral vasculitis as the cause of her progressive neurological symptoms. The correct diagnosis was established only post mortem. Based on the case presented here, we discuss typical clinical symptoms and imaging findings. In particular, we outline how modern diagnostic methods such as positron emission tomography with [(15)O]H(2)O and [(18)F]FDG and single photon emission computed tomography can add valuable information to results from conventionally performed imaging techniques and genetic testing.


Subject(s)
Fluorodeoxyglucose F18 , Immunosuppressive Agents/therapeutic use , Insomnia, Fatal Familial/diagnosis , Insomnia, Fatal Familial/drug therapy , Positron-Emission Tomography/methods , Tomography, Emission-Computed, Single-Photon/methods , Water , Fatal Outcome , Female , Humans , Middle Aged , Oxygen Radioisotopes , Radiopharmaceuticals
15.
Nervenarzt ; 77(4): 481-92; quiz 493-4, 2006 Apr.
Article in German | MEDLINE | ID: mdl-16496104

ABSTRACT

Cerebrospinal fluid analysis is the method of choice in CNS infection and provides the basis for appropriate treatment. Due to the proximity of CSF and CNS, the infectious agent may be detected directly by microscopy or antigen or nucleic acid detection--the latter by polymerase chain reaction--in native CSF or after culture. Furthermore, intrathecal antibody synthesis against the infectious agent may identify the cause of infection. This indirect antigen detection method requires correction for a systemic antibody response and a blood-CSF barrier disturbance. The following text gives an overview of appropriate detection methods and their relevance to the most important CNS infections.


Subject(s)
Central Nervous System Infections/diagnosis , Cerebrospinal Fluid/microbiology , Cerebrospinal Fluid/virology , Encephalitis/diagnosis , Meningitis/diagnosis , AIDS Dementia Complex/cerebrospinal fluid , AIDS Dementia Complex/diagnosis , AIDS-Related Opportunistic Infections/cerebrospinal fluid , AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/etiology , Antibodies/cerebrospinal fluid , Antigens/cerebrospinal fluid , Central Nervous System Infections/cerebrospinal fluid , Central Nervous System Infections/etiology , Encephalitis/cerebrospinal fluid , Encephalitis/etiology , Meningitis/cerebrospinal fluid , Meningitis/etiology , Microscopy , Nucleic Acids/cerebrospinal fluid , Polymerase Chain Reaction , Sensitivity and Specificity
16.
Mult Scler ; 12(1): 66-71, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16459721

ABSTRACT

Intravenous immunoglobulins (IVIG) have been effective in reducing multiple sclerosis (MS) disease activity and improving disability scores. However, the mechanism by which this beneficial effect is achieved remains unclear. An effect of IVIG on pro- and anti-inflammatory cytokines which are thought to play a role in the disease process - has been postulated in a number of animal and ex vivo studies. Hence, we performed a study on 34 patients with secondary progressive (SP) MS being treated with monthly IVIG or placebo for two years according to the protocol of the ESIMS study. Clinical outcome measures and cytokine production (interferon gamma, tumour necrosis factor alpha, interleukin-4 and -10) were recorded in all patients and compared with respect to the treatment group. Against our expectations, IVIG did not reduce the relapse rate or the progression of disability or cytokine production. Our data argue against an enduring immunomodulating effect of IVIG, at least in SPMS.


Subject(s)
Cytokines/blood , Immunoglobulins, Intravenous/therapeutic use , Lymphocytes/immunology , Multiple Sclerosis, Chronic Progressive/drug therapy , Multiple Sclerosis, Chronic Progressive/immunology , Adult , Female , Humans , Immunologic Factors/therapeutic use , Lymphocytes/drug effects , Male , Middle Aged , Multiple Sclerosis, Chronic Progressive/blood , Recurrence
17.
Acta Neurol Scand ; 112(4): 207-13, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16146488

ABSTRACT

OBJECTIVES: A number of neurological syndromes may be evoked by involvement of the nervous system due to systemic diseases such as lupus erythematodes, sarcoidosis, Behçet's disease and Sjögren's syndrome (SS) and may be confounded with another chronic inflammatory disease which is restricted to the central nervous system, e.g. multiple sclerosis (MS). Because of different treatment strategies, it is important to distinguish between these different autoimmune diseases. RESULTS: Neither clinical signs nor additional analyses such as serological findings or cerebrospinal fluid (CSF) analysis are able to differentiate between the diseases with certainty. Nevertheless, taking all findings together, diagnosis may be possible. CONCLUSION: Here we compare typical clinical and CSF findings in MS, neurosarcoidosis, neurolupus, neuro-Behçet and nervous system involving SS with special emphasis on those findings allowing differentiation of the respective diseases by reviewing the literature.


Subject(s)
Autoimmune Diseases of the Nervous System/diagnosis , Central Nervous System Diseases/diagnosis , Autoimmune Diseases of the Nervous System/cerebrospinal fluid , Autoimmune Diseases of the Nervous System/immunology , Biomarkers , Central Nervous System Diseases/cerebrospinal fluid , Central Nervous System Diseases/immunology , Chronic Disease , Diagnosis, Differential , Humans
18.
Dtsch Med Wochenschr ; 130(27): 1633-6, 2005 Jul 08.
Article in German | MEDLINE | ID: mdl-15988661

ABSTRACT

HISTORY AND ADMISSION FINDINGS: A 37-year-old woman was admitted with total loss of vision of the left eye within 24 hours. Additionally, she complained about fatigue, headache, chills, fever, muscle pain and neck stiffness since 4 days. At admission, the body temperature was 38.7 degrees C. Neurological examination revealed papilledema and meningism. INVESTIGATIONS: Ophthalmologic findings were consistent with a papillitis. The vision was lost, the pattern-shift checkerboard visual evoked potentials were not measurable. MRI of the brain and the optical nerve was without pathological findings, meningeal or cerebral Gadolinium enhancement was not present. The CSF analysis yielded a lymphocytic meningitis with 249 cells/mm (3), the glucose ratio of cerebrospinal fluid and serum was normal. DIAGNOSIS, TREATMENT AND COURSE: The papillitis was treated unsuccessfully with high-dose methylprednisolone, the left eye remained blind. Persistence of the pleocytosis under initial treatment with aciclovir and ceftriaxone, reduction of the glucose ratio of cerebrospinal fluid and serum and intrathecal immunoglobuline A -- synthesis required a change of the diagnostic and therapeutic regimen. Various common and rare differential diagnoses were considered and ruled out, a chronic meningitis of unclear aetiology with the complication of amaurosis was diagnosed. In consideration of the most probable diagnosis, a tuberculostatic therapy was initiated. A prolonged reduction of the pleocytosis and normalization of cerebrospinal fluid parameters could be observed. CONCLUSIONS: A large number of aetiologies can cause chronic meningitis; this case report reviews the most important differential diagnoses and highlights the limitations of the diagnostic work-up although various methods are available. Clinical course and symptoms of chronic meningitis are mild to moderate and may even be absent, but it can cause severe complications.


Subject(s)
Blindness/etiology , Evoked Potentials, Visual/physiology , Meningitis/complications , Meningitis/diagnosis , Meningitis/physiopathology , Adult , Brain/pathology , Chronic Disease , Female , Humans , Lymphocytes/pathology , Magnetic Resonance Imaging , Pattern Recognition, Visual
19.
Mult Scler ; 11(2): 245-8, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15794402

ABSTRACT

Glatiramer acetate (GLAT) is a well tolerated and safe immunomodulatory drug for the treatment of relapsing-remitting multiple sclerosis. The most commonly recognized side effects are localized injection site reactions consisting of pain, pruritus, mild erythema and induration, which sometimes persist for several days. We describe the first case of a biopsy-proven lymphocytic infiltration (T-cell pseudolymphoma) with the clinical appearance of a figured erythema on the ventrolateral thighs in the first four weeks under GLAT treatment, resolving without any evidence of recurrence despite ongoing therapy. A T-cell pseudolymphoma is a very rare side effect of GLAT treatment. For clinical purposes it is important to state that re-exposition after GLAT-induced pseudolymphoma is possible without permanent sequelae.


Subject(s)
Immunosuppressive Agents/adverse effects , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Peptides/adverse effects , Pseudolymphoma/chemically induced , Skin Diseases/chemically induced , Adult , Glatiramer Acetate , Humans , Hyperpigmentation/chemically induced , Hyperpigmentation/immunology , Lymphocytes/immunology , Male , Multiple Sclerosis, Relapsing-Remitting/immunology , Pseudolymphoma/immunology , Skin Diseases/immunology
SELECTION OF CITATIONS
SEARCH DETAIL
...