25 research outputs found

    Time Parameters of the Blink Reflex in Normal Subjects

    No full text
    Our study was aimed at estimating normal time values for the EMG waves recorded in the blink reflex test. The group examined included 400 healthy subjects (226 women and 174 men, with mean age about 50 years). There was no significant difference between the ages of the male and female subjects. The mean latency of the R1 wave in the response was 10.3 msec, while R2 was obtained after 32.5 msec, on average. The contralateral response component R2c was observed after 34.4 msec, on average. Gender did not influence the results, while age had a significant effect on R1 (P = 0.029) and R2c (P = 0.0003). The older the subject, the longer the latencies of the above waves. The data obtained on a rather large sampling of the tested subjects can be useful as normography for medical and neurophysiological purposes.У своєму дослідженні ми оцінювали нормальні часові параметри хвиль ЕМГ, що реєструвалися при тестуванні рефлексу кліпання. До обстеженої групи ввійшли 400 здорових осіб (226 жінок та 174 чоловіки, середній вік близько 50 років) без істотної різниці віку в групах чоловіків і жінок. Середній латентний період (ЛП) хвилі R1 у складі досліджуваної рефлекторної відповіді складав 10.30, а хвилі R2 – 32.51 мс. Контралатеральний компонент відповіді R2c виникав із середнім ЛП 34.43 мс. Стать обстежених не впливала істотно на ці значення; в той же час останні демонстрували значну залежність від віку (R1, P = 0.029; R2c, P = 0.0003; чим старші були обстежені, тим довші були вказані ЛП). Результати, отримані на досить великій дослідженій групі здорових осіб, можуть бути корисними як нормографічні дані для медичних та нейрофизіологічних цілей

    Segurança Na Mudança Direta De Natalizumabe Para Fingolimode Em Um Grupo De Pacientes Com Esclerose Múltipla E Positivos Para Jcv

    Get PDF
    To assess safety of the switch between natalizumab and fingolimod without a washout period. Methods: Prospective data on 25 JCV positive patients who underwent this medication switch were collected and analyzed. Results: After a median period of nine months from the medication switch, there were no safety issues to report. The patients had good disease control and no adverse events were reported. Conclusion: Washout may not be necessary in daily practice when switching from natalizumab to fingolimod. Expertise on multiple sclerosis management, however, is essential for drug switching. © 2016, Associacao Arquivos de Neuro-Psiquiatria. All Rights Reserved.74865065

    The role of subfractions of high density lipoprotein in reverse cholesterol transport The rabbit as an experimental model

    No full text
    SIGLEAvailable from British Library Document Supply Centre- DSC:DX181243 / BLDSC - British Library Document Supply CentreGBUnited Kingdo

    How Do We Manage And Treat A Patient With Multiple Sclerosis At Risk Of Tuberculosis?

    No full text
    Tuberculosis continues to be a serious health problem worldwide. The disease continues to be underdiagnosed and not properly treated. In conditions that affect the immune system, such as multiple sclerosis (MS), latent tuberculosis may thrive and reactivate during the use of immunomodulatory and immunosuppressive drugs. Among the best treatment options for patients with latent or active tuberculosis who have MS are IFN-β, glatiramer acetate and mitoxantrone. Drugs leading to a reduced number and/or function of lymphocytes should be avoided or used with caution. Tuberculosis must always be investigated in patients with MS and treated with rigor.141112511260Noseworthy, J.H., Lucchinetti, C., Rodriguez, M., Weinshenker, B.G., Multiple sclerosis (2000) N Engl J Med, 343 (13), pp. 938-952Wingerchuk, D.M., Carter, J.L., Multiple sclerosis: Current and emerging disease-modifying therapies and treatment strategies (2014) Mayo Clin Proc, 89 (2), pp. 225-240Happe, L.E., Choosing the best treatment for multiple sclerosis: Comparative effectiveness, safety, and other factors involved in disease-modifying therapy choice (2013) Am J Manag Care, 19 (17), pp. s332-s342Freedman, M.S., Selchen, D., Arnold, D.L., Treatment optimization in MS: Canadian MS Working Group updated recommendations (2013) Can J Neurol Sci, 40 (3), pp. 307-323Norbis, L., Miotto, P., Alagna, R., Cirillo, D.M., Tuberculosis: Lights and shadows in the current diagnostic landscape (2013) New Microbiol, 36 (2), pp. 111-120Fritsche, A., Engel, R., Buhl, D., Zellweger, J.P., Mycobacterium bovis tuberculosis: From animal to man and back (2004) Int J Tuberc Lung Dis, 8 (7), pp. 903-904De Jong, B.C., Antonio, M., Gagneux, S., Mycobacterium africanum-review of an important cause of human tuberculosis in West Africa (2010) PLoS Negl Trop Dis, 4, p. e744Panteix, G., Gutierrez, M.C., Boschiroli, M.L., Pulmonary tuberculosis due to Mycobacterium microti: A study of six recent cases in France (2010) J Med Microbiol, 59, pp. 984-989Buonora, N., Chiavarini, M., Salmasi, L., Impact of immigration on burden of tuberculosis in Umbria: A low-incidence Italian region with high immigrants rates (2013) J Prev Med Hyg, 54 (1), pp. 29-34Lawn, S.D., Zumla, A.I., Tuberculosis (2011) Lancet, 378 (9785), pp. 57-72Corbett, E.L., Watt, C.J., Walker, N., The growing burden of tuberculosis: Global trends and interactions with the HIV epidemic (2003) Arch Intern Med, 163 (9), pp. 1009-1021Frieden, T.R., Six components necessary for effective public health program implementation (2014) Am J Public Health, 104 (1), pp. 17-22Frieden, T.R., Sterling, T.R., Munsiff, S.S., Tuberculosis (2003) Lancet, 362 (9387), pp. 887-889Dye, C., Making wider use of the world's most widely used vaccine: Bacille Calmette-Guerin revaccination reconsidered (2013) J R Soc Interface, 10 (87), p. 20130365Barreto, M.L., Cunha, S.S., Pereira, S.M., Neonatal BCG protection against tuberculosis lasts for 20 years in Brazil (2005) Int J Tuberc Lung Dis, 9 (10), pp. 1171-1173Chiang, C.Y., Riley, L.W., Exougenous reinfection in tuberculosis (2005) Lancet Infect Dis, 5 (10), pp. 629-636Ramakrishnan, L., Revisiting the role of the granuloma in tuberculosis (2012) Nat Rev Immunol, 12 (5), pp. 352-366Schwander, S., Dheda, K., Human lung immunity against Mycobacterium tuberculosis: Insights into pathogenesis and protection (2011) Am J Respir Crit Care Med, 183 (6), pp. 696-707Rajni Rao, N., Meena, L.S., Biosynthesis and virulent behavior of lipids produced by Mycobacterium tuberculosis: LAM and cord factor: An overview (2011) Biotechnol Res Int, 2011, p. 274693Walzl, G., Ronacher, K., Hanekom, W., Immunological biomarkers of tuberculosis (2011) Nat Rev Immunol, 11 (5), pp. 343-354Bozzano, F., Marras, F., De Maria, A., Immunology of tuberculosis (2014) Mediterr J Hematol Infect Dis, 6 (1), p. e2014027Coelho Filho, J.C., Takenami, I., Arruda, S., Revisiting the Rich's formula: An update about granulomas in human tuberculosis (2013) Braz J Infect Dis, 17 (2), pp. 234-238Prezzemolo, T., Giggino, G., La Manna, M.P., Functional signatures of human CD4 and CD8 T cell responses to Mycobacterium tuberculosis (2014) Front Immunol, 5, p. 180Brighenti, S., Andersson, J., Local immune responses in human tuberculosis: Learning from the site of infection (2012) J Infect Dis, 205, pp. S316-S324Feng, C.G., Kaviratne, M., Rothfuchs, A.G., NK cell-derived IFN-gamma differentially regulates innate resistance and neutrophil response in T cell-deficient hosts infected with Mycobacterium tuberculosis (2006) J Immunol, 177 (10), pp. 7086-7093Cole, S.T., Brosch, R., Parkhill, J., Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence (1988) Nature, 393 (6685), pp. 537-544Hoffmann, C., Leis, A., Niederweis, M., Disclosure of the mycobacterial outer membrane: Cryo-electron tomography and vitreous sections reveal the lipid bilayer structure (2008) Proc Natl Acad Sci USA, 105 (10), pp. 3963-3967Delogu, G., Sali, M., Fadda, G., The biology of mycobacterium tuberculosis infection (2013) Mediterr J Hematol Infect Dis, 5, p. e2013070Boshoff, H.I., Lun, D.S., Systems biology approaches to understanding mycobacterial survival mechanisms (2010) Drug Discov Today Dis Mech, 7 (1), pp. e75-82Abdallah, A.M., Gey Van Pittius, N.C., Champion, P.A., Type VII secretion-mycobacteria show the way (2007) Nat Rev Microbiol, 5 (11), pp. 883-891Houben, E.N., Bestebroer, J., Ummels, R., Composition of the type VII secretion system membrane complex (2012) Mol Microbiol, 86 (2), pp. 472-484Volkman, H.E., Pozos, T.C., Zheng, J., Tuberculous granuloma induction via interaction of a bacterial secreted protein with host epithelium (2010) Science, 327 (5964), pp. 466-469Korch, S.B., Contreras, H., Clark-Curtiss, J.E., Three Mycobacterium tuberculosis Rel toxin-antitoxin modules inhibit mycobacterial growth and are expressed in infected human macrophages (2009) J Bacteriol, 191 (5), pp. 1618-1630Fox, W., Ellard, G.A., Mitchison, D.A., Studies on the treatment of tuberculosis undertaken by the British Medical Research Council tuberculosis units 1946-1986, with relevant subsequent publications (1999) Int J Tuberc Lung Dis, 3, pp. S231-S279Hernandez, C., Cetner, A.S., Jordan, J.E., Tuberculosis in the age of biologic therapy (2008) J Am Acad Dermatol, 59 (3), pp. 363-380Esmail, H., Barry, C.E., III, Young, D.B., Wilkinson, R.J., The ongoing challenge of latent tuberculosis (2014) Philos Trans R Soc Lond B Biol Sci, 369 (1645), p. 20130437Rich, A.R., (1951) The Pathogenesis of Tuberculosis. 2 Edition, , Charles ThomasIL USA:Hosoglu, S., Ayaz, C., Et Al. G.Mf, Tuberculous meningitis in adults: An eleven-year review (1998) Int J Tuberc Lung Dis, 2 (7), pp. 553-557Be, N.A., Kim, K.S., Bishai, W.R., Jain, S.K., Pathogenesis of central nervous system tuberculosis (2009) Curr Mol Med, 9 (2), pp. 94-99Ghosh, K., Patwardhan, M., Pradhan, V., Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas (2009) Rheumatol Int, 29 (9), pp. 1047-1050Pradhan, V., Patwardhan, M., Athavale, A., Mycobacterium tuberculosis triggers autoimmunity (2012) Indian J Tuberc, 59 (1), pp. 49-51Lee, J., Reinke, E.K., Zozulya, A.L., Mycobacterium bovis bacille Calmette-Guérin infection in the CNS suppresses experimental autoimmune encephalomyelitis and Th17 responses in an IFN-gamma-independent manner (2008) J Immunol, 181 (9), pp. 6201-6212Bible, E., Multiple sclerosis: Disease activity is reduced in CIS after BCG vaccination (2014) Nat Rev Neurol, 10 (2), p. 62Wucherpfennig, K.W., Mechanisms for the induction of autoimmunity by infectious agents (2001) J Clin Invest, 108 (8), pp. 1097-1104Chodisetti, S.B., Rai, P.K., Gowthaman, U., Potential T cell epitopes of Mycobacterium tuberculosis that can instigate molecular mimicry against host: Implications in autoimmune pathogenesis (2012) BMC Immunology, 13, p. 13Moseley, P., Stress proteins and the immune response (2000) Immunopharmacology, 48 (3), pp. 299-302Mycko, M.P., Brosnan, C.F., Raine, C.S., Transcriptional profiling of microdissected areas of active multiple sclerosis lesions reveals activation of heat shock protein genes (2012) J Neurosci Res, 90 (10), pp. 1941-1948Wiendl, H., Hohlfeld, R., Therapeutic approaches in multiple sclerosis: Lessons from failed and interrupted treatment trials (2002) BioDrugs, 6, pp. 183-200Shaik, J., Pillay, M., Jeena, P., The role of interferon gamma release assays in the monitoring of response to anti-tuberculosis treatment in children (2013) Paediatr Respir Rev, 13, pp. S1526-0542Beamer, G.L., Cyktor, J., Carruthers, B., Turner, J., H-2 alleles contribute to antigen 85-specific interferon-gamma responses during Mycobacterium tuberculosis infection (2011) Cell Immunol, 271 (1), pp. 53-61Todd, P.A., Goa, K.L., Interferon gamma-1b A review of its pharmacology and therapeutic potential in chronic granulomatous disease (1992) Drugs, 43 (1), pp. 111-122Nikfar, S., Rahimi, R., Abdollahi, M., A meta-analysis of the efficacy and tolerability of interferon-b in multiple sclerosis, overall and by drug and disease type (2010) Clin Ther, 32 (11), pp. 1871-1888Aharoni, R., The mechanism of action of glatiramer acetate in multiple sclerosis and beyond (2013) Autoimmun Rev, 12 (5), pp. 543-553Dheda, K., Schwander, S.K., Zhu, B., The immunology of tuberculosis: From bench to bedside (2010) Respirology, 15 (3), pp. 433-450Musabak, U., Demirkaya, S., Genç, G., Serum adiponectin TNF-A IL-12p70 and IL-13 levels in multiple sclerosis and the effects of different therapy regimens (2011) Neuroimmunomodulation, 18 (1), pp. 57-66Winkelmann, A., Loebermann, M., Reisinger, E.C., Zettl, U.K., Multiple sclerosis treatment and infections issues: Update 2013 (2014) Clin Exp Immunol, 175 (3), pp. 425-438Kappos, L., Radue, E.W., O'Connor, P., A placebo-controlled trial of oral fingolimod in relapsing multiple sclerosis (2010) N Engl J Med, 362 (5), pp. 387-401Connor, L.M., Harvie, M.C., Rich, F.J., A key role for lung-resident memory lymphocytes in protective immune responses after BCG vaccination (2010) Eur J Immunol, 40 (9), pp. 2482-2492Kappos, L., Bates, D., Edan, G., Natalizumab treatment for multiple sclerosis: Updated recommendations for patient selection and monitoring (2011) Lancet Neurol, 10 (8), pp. 745-758Abonia, J.P., Hallgren, J., Jones, T., Alpha-4 integrins and VCAM-1, but not MAdCAM-1, are essential for recruitment of mast cell progenitors to the inflamed lung (2006) Blood, 108 (5), pp. 1588-1594Mulero, P., Caminero, A.B., Neri Crespo, M.J., Latent tuberculosis seems not to reactivate in multiple sclerosis patients on natalizumab (2012) J Neuroimmunol, 243 (1-2), pp. 103-105Dahdaleh, D., Altmann, D.M., Malik, O., Nicholas, R.S., Breathlessness night sweats and weight loss on natalizumab (2012) Lancet, 380 (9843), pp. 726-727Anderson, C., Hopkins, S., Adeboyeku, D., Maguire, H., Tuberculosis in London: Not unexpected (2013) Lancet, 381 (9862), p. 201Boumpas, D.T., Paliogianni, F., Anastassiou, E.D., Balow, J.E., Glucocorticosteroid action on the immune system: Molecular and cellular aspects (1991) Clin Exp Rheumatol, 9 (4), pp. 413-423Gold, R., Buttgereit, F., Toyka, K.V., Mechanism of action of glucocorticosteroid hormones: Possible implications for therapy of neuroimmunological disorders (2001) J Neuroimmunol, 117 (1-2), pp. 1-8Critchley, J.A., Young, F., Orton, L., Garner, P., Corticosteroids for prevention of mortality in people with tuberculosis: A systematic review and meta-analysis (2013) Lancet Infect Dis, 13 (3), pp. 223-237Segal, B.H., Sneller, M.C., Infectious complications of immunosuppressive therapy in patients with rheumatic diseases (1997) Rheum Dis Clin North Am, 23 (2), pp. 219-237Jick, S.S., Lieberman, E.S., Rahman, M.U., Choi, H.K., Glucocorticoid use, other associated factors, and the risk of tuberculosis (2006) Arthritis Rheum, 55, pp. 19-26Cline, J.C., Davis, S.M., Risks of infection or reactivation of tuberculosis associated with chronic corticosteroid therapy (1997) Ann Pharmacother, 31 (6), pp. 775-776Tam, L.S., Li, E.K., Wong, S.M., Szeto, C.C., Risk factors and clinical features for tuberculosis among patients with systemic lupus erythematosus in Hong Kong (2002) Scand J Rheumatol, 31 (5), pp. 296-300Hirata, N., Koerner, M.M., Tenderich, G., Influence of cytoimmunological state on the development of tuberculosis in heart transplant recipients (2001) Surg Today, 31 (6), pp. 482-486Tiede, I., Fritz, G., Strand, S., CD28-dependent Rac1 activation is the molecular target of azathioprine in primary human CD4+ T lymphocytes (2003) J Clin Invest, 111 (8), pp. 1133-1145Casetta, I., Iuliano, G., Filippini, G., Azathioprine for multiple sclerosis (2009) J Neurol Neurosurg Psychiatry, 80 (2), pp. 131-132Casetta, I., Iuliano, G., Filippini, G., Azathioprine for multiple sclerosis (2007) Cochrane Database Syst Rev, 4, p. CD003982Ludeman, S.M., The chemistry of the metabolites of cyclophosphamide (1999) Curr Pharm des, 5 (8), pp. 627-643Agency, B.C., (2013) Cancer Drug Manual: Cyclophosphamide, pp. 1-12Binymin, K., Cooper, R.G., Late reactivation of spinal tuberculosis by low-dose methotrexate therapy in a patient with rheumatoid arthritis (2001) Rheumatology (Oxford), 40 (3), pp. 341-342Zorlu, M., Kiskac, M., Karatoprak, C., Pott's disease and hypercalcemia in a patient with rheumatoid arthritis receiving methotrexate monotherapy (2013) Indian J Pharmacol, 45 (6), pp. 631-633Mor, A., Bingham, C.O., III, Kishimoto, M., Methotrexate combined with isoniazid treatment for latent tuberculosis is well tolerated in patients with rheumatoid arthritis: Experience from an urban arthritis clinic (2008) Ann Rheumatol Dis, 67 (4), pp. 462-465Wehenkel, A., Fernandez, P., Bellinzoni, M., The structure of PknB in complex with mitoxantrone, an ATP-competitive inhibitor, suggests a mode of protein kinase regulation in mycobacteria (2006) FEBS Lett, 580 (13), pp. 3018-3022Martinelli Boneschi, F., Vacchi, L., Rovaris, M., Mitoxantrone for multiple sclerosis (2013) Cochrane Database Syst Rev, 5, p. CD002127Darlington, P.J., Boivin, M.N., Bar-Or, A., Harnessing the therapeutic potential of mesenchymal stem cells in multiple sclerosis (2011) Expert Rev Neurother, 11 (9), pp. 1295-1303Russo, R.L., Dulley, F.L., Suganuma, L., Tuberculosis in hematopoietic stem cell transplant patients: Case report and review of the literature (2010) Int J Infect Dis, 14, pp. e187-e191Akan, H., Arslan, O., Akan, O.A., Tuberculosis in stem cell transplant patients (2006) J Hosp Infect, 62 (4), pp. 421-426De La Câmara, R., Martino, R., Granados, E., Tuberculosis after hematopoietic stem cell transplantation: Incidence, clinical characteristics and outcome (2000) Bone Marrow Transplant, 26 (3), pp. 291-298. , Spanish Group on Infectious Complications in Hematopoietic TransplantationHolloman, J., Ho, C.C., Hukki, A., The development of hematopoietic and mesenchymal stem cell transplantation as an effective treatment for multiple sclerosis (2013) Am J Stem Cell, 2 (2), pp. 95-107Fox, R.J., Kita, M., Cohan, S.L., BG-12 (dimethyl fumarate): A review of mechanism of action efficacy and safety (2014) Curr Med Res Opin, 30 (2), pp. 251-262Gold, R., Kappos, L., Arnold, D.L., Placebo-controlled phase 3 study of oral BG-12 for relapsing multiple sclerosis (2012) N Engl J Med, 367 (12), pp. 1098-1107Phillips, J.T., Fox, R.J., BG-12 in multiple sclerosis (2013) Semin Neurol, 33 (1), pp. 56-65Montoya, M.C., Sancho, D., Bonello, G., Role of ICAM-3 in the initial interaction of T lymphocytes and APCs (2002) Nat Immunol, 3 (2), pp. 159-168Zeyda, M., Poglitsch, M., Geyeregger, R., Disruption of the interaction of T cells with antigen-presenting cells by the active leflunomide metabolite teriflunomide: Involvement of impaired integrin activation and immunologic synapse formation (2005) Arthritis Rheum, 52 (9), pp. 2730-2739Minagar, A., Alexander, J.S., Sahraian, M.A., Zivadinov, R., Alemtuzumab and multiple sclerosis: Therapeutic application (2010) Expert Opin Biol Ther, 10, pp. 421-429Willis, M., Robertson, N.P., Drug safety evaluation of alemtuzumab for multiple sclerosis (2014) Expert Opin Drug Saf, 13 (8), pp. 1115-1124Antohe, I., Dascalescu, A., Burcoveanu, C., Pact with the devil: Alemtuzumab therapy, immune suppression and infectious complications in chronic lymphocytic leukemia (2014) Rev Med Chir Soc Med Nat Iasi, 118, pp. 92-95Abad, S., Gyan, E., Moachon, L., Tuberculosis due to Mycobacterium bovis after alemtuzumab administration (2003) Clin Infect Dis, 37, pp. e27-e28Au, W.Y., Leung, A.Y., Tse, E.W., High incidence of tuberculosis after alemtuzumab treatment in Hong Kong Chinese patients (2008) Leuk Res, 32, pp. 547-551Bosch, W., Poowanawittayakom, N., Chaikriangkrai, K., Tuberculous hepatitis in renal transplant recipients following alemtuzumab induction therapy (2013) Transpl Infect Dis, 15, pp. E33-E39Iannone, F., Cantini, F., Lapadula, G., Diagnosis of latent tuberculosis and prevention of reactivation in rheumatic patients receiving biologic therapy: International recommendations (2014) J Rheumatol Suppl, 91, pp. 41-46Gisondi, P., Pezzolo, E., Lo Cascio, G., Girolomoni, G., Latent tuberculosis infection in patients with chronic plaque psoriasis candidate to biological therapy (2014) Br J Dermatol, , [Epub ahead of print]Kieseier, B.C., The mechanism of action of interferon-b in relapsing multiple sclerosis (2011) CNS Drugs, 25, pp. 491-502Racke, M.K., Lovett-Racke, A.E., Karandikar, N.J., The mecanism of action of glatiramer acetate treatment in multiple sclerosis (2010) Neurology, 74, pp. S25-30Chun, J., Hartung, H.P., Mechanism of action of oral fingolimod (FTY720) in multiple sclerosis (2010) Clin Neuropharmacol, 33, pp. 91-101Engelhardt, B., Kappos, L., Natalizumab: Targeting a4-integrins in multiple sclerosis (2008) Neurodegener Dis, 5, pp. 16-22Schaal, A.D., Alemtuzumab (Campath 1-H) (2005) Clin J Oncol Nurs, 9, pp. 630-63

    Efficacy, safety, and cost-effectiveness of glatiramer acetate in the treatment of relapsing–remitting multiple sclerosis

    No full text
    The current Multiple Sclerosis (MS) therapeutic landscape is rapidly growing. Glatiramer acetate (GA) remains unique given its non-immunosuppressive mechanism of action as well as its superior long-term safety and sustained efficacy data. In this review, we discuss proposed mechanisms of action of GA. Then we review efficacy data for reduction of relapses and slowing disability as well as long term safety data. Finally we discuss possible future directions of this unique polymer in the treatment of MS
    corecore