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Psicofarmacología 48

  • Text
  • Marcadores
  • Glucocorticoides
  • Eritematoso
  • Lupus
  • Psicosis
  • Snc
  • Desarrollo
  • Receptores
  • Transportadores
  • Gaba
  • Neurotransmision
  • Ciclado
  • Swich
  • Seguridad
  • Isrs
  • Litio
  • Estabilizadores
  • Antidepresivos
  • Tratamiento
  • Bipolar
Revista Latinoamericana de psicofarmacología y neurociencia.

Laura Scévola,

Laura Scévola, Estefanía Calvet, Valeria Stella, Julia Teitelbaum, María Marletta, Miguel Vallejos 12. Fields RA, Sibbitt WL, Toubbeh H, Bankhurst AD. Neuropsychiatric lupus erythematosus, cerebral infarctions, and anticardiolipin antibodies. Ann Rheum Dis 1990;49(2) 114–7. 13. Manual diagnostico y estadístico de los trastornos mentales, Editorial Masson 1995. 14. Karassa FB, Ioannidis JPA, Touloumi G, Boki K, Moutsopoulos HM. Risk factors for central nervous system involment in systemic lupus erythematosus. QJM 2000;93(3):169-74. 15. Lopez-Medrano F, Cervera R, Trejo O, Font J, Ingelmo M. Steroid induced psychosis in systemic lupus erythematosus: a possible role of serum albumin level. Ann Rheum Dis 2002;61(6):562-3. 16. Sato T, Uchiumi T, Ozawa T, Kikuchi M, Nakano M, Kominami R, et al. Autoantibodies against ribosomal proteins found with high frequency in patients with systemic lupus erythematosus with active disease. J Rheumatol 1991;18(11):1681-4. 17. Nojima Y, Minota S, Yamada A, Takaku F, Aotsuka S, Yokohari R. Correlation of antibodies to ribosomal P protein with psychosis in patients with systemic lupus erythematosus. Ann Rheum Dis 1992;51(9):1053-5. 18. Teh LS, Isenberg DA. Antiribosomal P protein antibodies in systemic lupus erythematosus. A reappraisal. Arthritis Rheum 1994;37(3):307-15. 19. Arnett FC, Reveille JD, Moutsopoulos HM, Georgescu L, Elkon KB. Ribosomal P autoantibodies in systemic lupus erythematosus. Frequencies in different ethnic groups and clinical and immunogenetic associations. Arthritis Rheum 1996;39(11):1833- 9. 20. Teh LS, Doherty DG, Williams BD. HLA-DRB genes and antiribosomal P antibodies in systemic lupus erythematosus. Br J Rheumatol 1994;33(12):1125-6. 21. Yoshio T, Masuyama JI, Minota S, Kaneko N, Iwamoto M, Okazaki H, et al. A close temporal relationship of liver disease to antiribosomal P0 protein antibodies and central nervous system disease in patients with systemic lupus erythematosus. J Rheumatol. 1998;25(4):681-8. 22. Arnett FC, Reveille JD, Moutsopoulos HM, Georgescu L, Elkon KB. Ribosomal P autoantibodies in systemic lupus erythematosus. Frequencies in different ethnic groups and clinical and immunogenetic association. Arthritis Rheum 1996;39(11):1833–9. 23. Derksen RHWM, van Dam AP, Gmelig Meyling FHJ, Bijlsma JWJ, Smeenk RJT. A prospective study of antiribosomal P proteins in two cases of familial lupus and recurrent psychosis. Ann Rheum Dis 1990;49(10):779 –82. 24. Schneebaum AB, Singleton JD, West SG, Blodgett JK, Allen LG, Cheronis JC, et al. Association of psychiatric manifestation with antibodies to ribosomal P proteins in systemic lupus erythematosus. Am J Med 1991;90(1): 54–62. 25. Van Dam A, Nossent H, de Jong J, Meilof J, ter Borg EJ, Swaak T, et al. Diagnostic value of antibodies against ribosomal phosphoproteins. A cross sectional and longitudinal study. J Rheumatol 1991;18(7):1026–34. 26. Teh LS, Hay EM, Amos N, Black D, Huddy A, Creed F, et al. Anti-P antibodies are associated with psychiatric and focal cerebral disorders in patients with systemic lupus erythematosus. Br J Rheumatol 1993;32(4):287–90. 27. Yoshio T, Masuyama J-I, Ikeda M, Tamai K, Hachiya T, Emori T, et al. Quantification of antiribosomal P0 protein antibodies by ELISA with recombinant P0 fusion protein and their association with central nervous system disease in systemic lupus erythematosus. J Rheumatol 1995;22(9):1681–7. 28. West SG, Emlen W, Wener MH, Kotzin BL. Neuropsychiatric lupus erythematosus: a 10-year prospective study on the value of diagnostic tests. Am J Med 1995;99(2):153–62. 29. Watanabe T, Sato T, Uchiumi T, Arakawa M. Neuropsychiatric manifestation in patients with systemic lupus erythematosus: diagnostic and predictive value of longitudinal examination of anti-ribosomal P antibody. Lupus 1996;5(3): 178–83. 30. Press J, Palayew K, Laxer RM, Elkon K, Eddy A, Rakoff D, et al. Antiribosomal p antibodies in pediatric patients with systemic lupus erythematosus and psychosis. Arthritis Rheum 1996;39(4):671–6. 31. Isshi K, Hirohata S. Association of antiribosomal P protein antibodies with neuropsychiatric systemic lupus erythematosus. Arthritis Rheum 1996;39(9):1483–90. 32. Tzioufas AG, Tzortzakis NG, Panou-Pomonis E, Boki KA, Sakarellos-Daitsiotis M, Sakarellos C et al. The clinical relevance of antibodies to ribosomal-P common epitope in two targeted systemic lupus erythematosus populations: a large cohort of consecutive patients and patients with active central nervous system disease. Ann Rheum Dis 2000;59(2):99–104. 33. Iverson GL. Are antibodies to ribosomal P proteins a clinically useful predictor of neuropsychiatric manifestations in patients with systemic lupus erythematosus? Lupus 1996;5(6):634–5. 34. Caponi L, Pegoraro S, Di Bartolo V, Rovero P, Revoltella R, Bombardieri S. Autoantibodies directed against ribosomal P proteins: use of a multiple antigen peptide as the coating agent in ELISA. J Immunol Methods 1995;179(2): 193–202. 35. Cuchacovich R, Espinoza LR. Clinical and serological associations of ribosomal P autoantibodies in systemic lupus erythematosus: prospective evaluation in a large cohort of Italian patients. Rheumatology 2003;42(9): 1115-7. 36. Hanly JG, Walsh NM, Fisk JD, Eastwood B, Hong C, Sherwood G, et al. Cognitive impairment and autoantibodies in systemic lupus erythematosus. Br J Rheumatol 1993;32(4): 291–6. 37. Isshi K, Hirohata S. Differential roles of the antiribosomal P antibody and anti-neuronal antibody in the pathogenesis of central nervous system involvement in systemic lupus erythematosus. Arthritis Rheum 1998; 41(10): 1819–27. 38. Bonfa E, Elkon KB. Clinical and serological associations of the antiribosomal P protein antibody. Arthritis Rheum 1986;29(8):981–5. 39. Bonfa E, Golombek SJ, Kaufman LD, Skelly S, Weissbach H, Brot N, et al. Association between lupus psychosis and anti-ribosomal P-protein antibodies. N Engl J Med 1987;317(5): 265–71. 40. Lijnen HR. Plasmin and matrix metalloproteinases in vascular remodeling. Thromb Haemost 2001;86(1):324 –33. 41. Kalela A, Koivu TA, Sisto T, Kanervisto J, Höyhtyä M, Sillanaukee P , et al. Serum matrix metalloproteinase-9 concentration in angiographically assessed coronary artery disease. Scand J Clin Lab Invest 2002;62(5):337–42. 42. Ainiala H, Hietaharju A, Dastidar P, Loukkola J, Lehtimäki T, Peltola J , et al. Increased serum matrix metalloproteinase 9 levels in systemic lupus erythematosus patients with neuropsychiatric manifestations and brain magnetic resonance imaging abnormalities. Arthritis Rheum 2004;50(3):858 –65. 43. Hanly JG. Neuropsychiatric lupus. Rheum Dis Clin North Am 2005;31(2):273-98. 44. Small P, Mass MF, Kohler PF, Harbeck RJ. Central nervous system involvement in SLE. Diagnostic profile and clinical features. Arthritis Rheum 1977;20(3):869 –78. 45. Trysberg E, Nylen K, Rosengren LE, Tarkowski A. Neuronal and astrocytic damage in systemic lupus erythematosus patients with central nervous system involvement. Arthritis Rheum 2003;48(10):2881–7. 46. Conti F, Alessandri C, Bompane D, Bombardieri M, Spinelli FR, Rusconi AC, et al. Autoantibody profile in systemic lupus erythematosus with psychiatric manifestations: a role for anti-endothelial-cell antibodies. Arthritis Res Ther 2004;6(4):366-72. 47. Chan TM, Yu PM, Tsang KL, Cheng IK. Endothelial cell binding by human polyclonal anti- DNA antibodies: relationship to disease activity and endothelial functional alterations. Clin Exp Immunol 1995;100(3):506-13. 48. Chan TM, Cheng IK: Identification of endothelial cell membrane proteins that bind anti-DNA antibodies from patients with systemic lupus erythematosus by direct or indirect mechanisms. J Autoimmun 1997;10(5):433-9. 49. Moscato S, Pratesi F, Bongiorni F, Scavuzzo MC, Chimenti D, Bombardieri S, et al. Endothelial cell binding by systemic lupus antibodies: functional properties and relationship with anti-DNA activity. J Autoimmun 2002;18(3):231-8. 50. Sanna G, Bertolaccini ML, Mathieu A. Central Nervous System Lupus: a clinical approach to therapy. Lupus 2003;12(12):935-42. 51. Bodani M, Kopelman MD. A psychiatric perspective on the therapy of psychosis in systemic lupus erythematosus. Lupus 2003;12(12):947-9. 52. Sherwood Brown E, Chandler PA. Mood and cognitive changes during systemic corticosteroid therapy: Primary Care Companion. J Clin Psychiatry 2001;3(1):17-21. 53. Ahmad M, Rasul FM. Steroid- induced psychosis treated with haloperidol in a patient with active chronic obstructive pulmonary disease. Am J Emerg Med 1999;17(7):735. 54. Kramer TM, Cottingham EM. Risperidone in the treatment of steroid-induced psychosis. J Child Adolesc Psychopharmacol 1999;9(4): 315-6. 55. DeSilva CC, Nurse MC, Vokey K. Steroid-induced psychosis treated with risperidone. Can J Psychiatry 2002;47(4):388-9. 56. Portela LV, Brenol JC, Walz R, Bianchin M, Tort AB, Canabarro UP, et al. Serum S100B levels in patients with lupus erythematosus: preliminary observation. Clin Diagn Lab Immunol 2002;9(1):164-6. 57. Sibbitt Jr WL, Sibbitt RR, Brooks WM. Neuroimaging in neuropsychiatric systemic lupus erythematosus [see comments]. Arthritis Rheum 1999;42(10):2026–38. 58. McCune WJ, MacGuire A, Aisen A, Gebarski S, et al. Identification of brain lesions in neuropsychiatric systemic lupus erythematosus by magnetic resonance scanning. Arthritis Rheum 1988;31(2):159–66. 59. Rovaris M, Viti B, Ciboddo G, Gerevini S, Capra R, Iannucci G, et al. Brain involvement in systemic immune mediated diseases: magnetic resonance and magnetization transfer imaging study. J Neurol Neurosurg Psychiatry 2000;68(2):170–7. 60. Graham JW, Jan W. MRI and the brain in systemic lupus erythematosus. Lupus 2003; 12(12):891–6. 61. Sibbitt Jr WL, Schmidt PJ, Hart BL, Brooks WM, et al. Fluid Attenuated Inversion Recovery (FLAIR) imaging in neuropsychiatric systemic lupus erythematosus. J Rheumatol 2003;30(9):1983–9. 62. Bell CL, Partington C, Robbins M, Graziano F, Turski P, Kornguth S, et al. Magnetic resonance imaging of central nervous system lesions in patients with lupus erythematosus. Correlation with clinical remission and antineurofilament and anticardiolipin antibody titers [see comments]. Arthritis Rheum 1991;34(4): 432 –41. 63. Gonzalez-Crespo MR, Blanco FJ, Ramos A, Ciruelo E, Mateo I, Lopez Pino MA et al. Magnetic resonance im,aging of the brain in systemic lupus erythematosus. Br J Rheumatol 1995;34(11):1055–60. 64. Cauli A, Montaldo C, Peltz MT, Nurchis P, Sanna G, Garau P, et al. Abnormalities of magnetic resonance imaging of the central nervous system in patients with systemic lupus erythematosus correlate with disease severity. Clin Rheumatol 1994;13(4):615– 8. 65. Bodani M and Kopelman MD. A psychiatric perspective on the therapy of psychosis in systemic lupus erythematosus. Lupus 2003; 12(12):947-9. 66. Takada K, Illei GG, Boumpas DT. Cyclofosfamide for the treatment of systemic lupus erythematosus. Lupus 2001;10(3):154-61. 32 // EDITORIAL SCIENS

NOVEDADES Los polifenoles de la fruta: sus efectos en la señalización neuronal y en la conducta en la senescencia El advenimiento de enfermedades neurodegenerativas asociadas a la edad puede exacerbar los déficits cognitivos y motores que ocurren normalmente en el envejecimiento. Estudios epidemiológicos demostraron que el consumo de dietas ricas en compuestos antioxidantes y antiinflamatorios, como aquellos encontrados en las frutas y verduras, puede disminuir la probabilidad de contraer enfermedades como el Parkinson y la enfermedad de Alzheimer. Un investigador del USDA's Human Nutrition Research Center on Aging en la Tufts University de Boston, James Joseph, afirma que los compuestos polifenólicos que se encuentran en frutas tales como el arándano, las manzanas, la zarzamora, las frutillas, la espinaca y la nuez pueden exhibir efectos benéficos protegiendo de los efectos del stress oxidativo neuronal. Su mecanismo de acción se basa en la destrucción de los altamente tóxicos radicales libres que atacan a las células. En el estudio realizado se encontró que aquellos individuos que consumían 2-3 vasos de jugo de estas frutas por semana, tuvieron una menor incidencia de enfermedades neurodegenerativas. Joseph JA, Shukitt-Hale B, Lau FC. Fruit polyphenols and their effects on neuronal signaling and behavior in senescence.Ann N Y Acad Sci. 2007;1100:470-85. La terapia musical y del movimiento, tendría eficacia sobre los síntomas negativos de la Esquizofrenia; un tratamiento posible adjunto a la farmacoterapia Dra. D´Alessio Luciana La esquizofrenia afecta a una gran proporción de la población mundial, llegando a un valor de 24 millones de pacientes en todo el mundo. El descubrimiento de los fármacos antipsicóticos ha mejorado significativamente el pronóstico de la enfermedad, en especial con los nuevos antipsicoticos (atípicos), que logran una eficacia del 70% sobre los síntomas positivos, delirios y alucinaciones, con un mínimo de efectos adversos extrapiramidales. Si bien no hay dudas de la eficacia demostrada de los antipsicóticos sobre los síntomas positivos de la enfermedad, los síntomas negativos (abulia, aplanamiento afectivo y alogia) continúan siendo resistentes al tratamiento farmacológico, y afectan significativamente la calidad de vida y el funcionamiento social, laboral y familiar del paciente. El tratamiento integral del paciente esquizofrénico incluye el tratamiento de los síntomas negativos que permita la neurorehabilitación cognitiva y la rehabilitación social del paciente. La terapia musical y del movimiento, podría tener un efecto terapéutico sobre este tipo de sintomatología de acuerdo a un trabajo original, publicado recientemente. Los autores confeccionaron un estudio con un diseño randomizado y controlado, en donde administraron terapia musical y del movimiento durante un período corto de 5 semanas, adjunto al tratamiento antipsicótico en un grupo de pacientes esquizofrénicos (21 pacientes), y compararon la sintomatología negativa, con un grupo control que sólo recibió tratamiento antipsicótico (16 pacientes). Encontraron un efecto significativamente positivo sobre el puntaje de síntomas negativos en el grupo experimental que recibió el tratamiento con música y movimiento. Este trabajo nos demuestra como un ambiente enriquecido, que permita estimular funciones cognitivas, emocionales y motoras, permite mejorar la salud mental y el funcionamiento del SNC en una enfermedad crónica y discapacitante como la esquizofrenia The additional therapeutic effect of group music therapy for schizophrenic patients: a randomized study. Ulrich G, Houtmans T, Gold C. Acta Psychiatr Scand 2007: 116: 362–370 34 // EDITORIAL SCIENS

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