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Instituto Autnomo Hospital Universitario de los Andes. Mrida. Venezuela" g K   r0e0e?1 Ttulo> g 3 Espectroscopia Cerebral por Resonancia Magntica. 64 2g(g(H  0޽h ? I}OPM___PPT10i.C+D=' = @B +"= 0 D< (      rh_i0e0e?1 TtuloNe  g V Introduccin.  g((x   ci0e0e?02 Marcador de contenidov i N La espectroscopia por resonancia magntica (E-RM) realizada a travs de la determinacin del hidrgeno (H1), es una tcnica no invasiva que permite determinar "in vivo" los protones que se encuentran en el cerebro en condiciones normales y patolgicas permitiendo obtener un espectro metablico del cerebro. Se considera una tcnica promisoria para la evaluacin no invasiva del metabolismo cerebral, que no requiere sustancias radioactivas para su realizacin debido a la abundancia de los protones en forma 100% natural; requiere un tiempo no mayor de 6 minutos para su realizacin.$O OgH  0޽h ? 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I}OPM___PPT10i.0w^+D=' = @B +" 0 l(  #   rQ0e0e?1 Ttulo;h   Q ]Espectroscopia Cerebral* e    Q0e0e?02 Marcador de contenido"PK!Zf[Content_Types].xmlMO &2WR=cJ`F0iK`#̼vLw 9uSq:w`G ^i ½KI)c/ $oVjTMRc|}042ҥCƔM̏P~*ka/8^DkHbL8e i"K\XN\6rco4y@_;oPK!1_a _rels/.relsj0 ѽqCNo^K [ILcX&m߾0XFo;>0xM e`|X}đ I`߽N4aG2$RKIZ)4(M9`ctB{m:f@`3n|O,ܗr޾jxR0T ,0@}WBLǬ5vPK!=i[7Tdrs/shapexml.xmlXn6}/ Zd;NQIi Xbm(R%) )t l>4Xr.MZZW&w:3y۫I"'2Zɣt;PnZz:l%+rL-5xy ݠIcJ FGJ^/e*^ϭ(49H K/d3ʍ^27ɠf&wS-N/h!/0uiƋ+xId|rt<:9lerac4zkg45E!ғa"x4h*7^d?8<> x$F!yCѓZ= ?%?#|اD@]-^4*]lHߡΰN K=tu6ϼXGQ`K\,ȳ(ll% zv&!rͥY<=W؊,(C9%DԥVWT+jD[u Q<5Zd0i@fnAxCT2t{?c &M4l{"PS1VSǤ'S.IUr?5t^ZaURIP"J\JgTd]lp_J|P3- i> ܖtZ>S~!7S{XiE1LO'~0zD٪T4|/z_XdvcDv[cݐ=?q{r=1V 8140$jfý#Em﹉(u>'K藻}sq]vMa_;!Dx kd؞;x%o6r]ma?JutPK!drs/downrev.xmlDn0EHk*uNS(#V@%CCn4Z\PK-!Zf[Content_Types].xmlPK-!1_a /_rels/.relsPK-!=i[7T*drs/shapexml.xmlPK-!drs/downrev.xmlPK  Q i Mientras que la resonancia magntica convencional (RM) obtiene informacin anatmica basada en la seal del agua, la espectroscopia permite obtener un espectro metablico del cerebro basado en que la diferencia en la composicin qumica de sus metabolitos se refleja en una diferente frecuencia de resonancia, esto es lo que se conoce como chemical shift. Hj Zggg.V   z  RA??Picture 3F    LQ?5 CuadroTexto / r kEspectro normal del cerebro  e H  0޽h ? I}OPM___PPT10i.?U+D=' = @B +"@ 0 G?(  "   rh0e0e?1 TtuloN   \ Factores Fsicos . eaS   0e0e?02 Marcador de contenidoT /   i) Desde el punto de vista bioqumico los tomos de hidrgeno del agua, protenas o lpidos son los mismos. Sin embargo, las distintas molculas de acuerdo a su configuracin tridimensional generan por si mismas micro campos magnticos que se sobreponen al campo magntico generado por el resonador.$* *g   0e0e?07 Marcador de contenidop `  . Protones de hidrgeno en distintas molculas L/ g-gg  j= = cA??Picture 4@ ! H  0޽h ? I}OPM___PPT10i.  Lp+D=' = @B +" 0  (      rd"0e0e?1 Ttulo;{  g ZFactores Fsicos. ea+   "0e0e?02 Marcador de contenido;+  g A $ gL  L$g?5 CuadroTextosh  Esto condiciona que las molculas giren a una velocidad ligeramente diferente, la cual se mide en frecuencia de precesin, o ms frecuentemente en partes por milln (PPM). El espectro que se obtiene consta de unos picos estrechos, cuya rea es proporcional al nmero de ncleos detectados. Se usan adquisiciones en T2; mientras ms prolongado ms estrecho es el pico del espectro.  e C   "0e0e?08 Marcador de contenidop ` g Y Espectro de metabolitos$ gz  RA??Picture 4` hH  0޽h ? I}OPM___PPT10i.  Lp+D=' = @B +"# 0 *"0 (   $   r0e0e?1 TtuloNe   ^Consideraciones Tcnicas* eV   X0e0e?02 Marcador de contenidosg   l Los metabolitos en el cerebro se encuentran en concentraciones milimolares, por lo tanto, las seales del agua, grasa del cerebro y las estructuras vecinas pueden sobrepasar y distorsionar las seales de los metabolitos de inters. Para superar esto, se emplean tcnicas para impedirles resonar. La cuantificacin del espectro es compleja, se usa la comparacin y relaciones entre los diferentes metabolitos, usando a la creatina como control por considerarse el pico ms estable. 2  g.@   H  0޽h ? I}OPM___PPT10i. P"$+D=' = @B +"  0 @ $(  $$ $  r0e0e?1 Ttulo;N    ^Consideraciones Tcnicas* e! $  0e0e?02 Marcador de contenido   7; Se realizan tres tipos de muestreo: Single voxel: volumen seleccionado de 2x2x2 cm dimetro. Multi-voxel: corte total del cerebro, obteniendo anlisis de varias regiones en forma simultnea. Chemical shift imaging: representa metabolitos en escala de colores sobrepuesta a imagen convencional referencial. z %   7gog^ ,3Wo  $ j2 b'A??Picture 4eVQ  $ jB:BA??Picture 6Q V4 $ L/?8 CuadroTextod KA   $ Lx9?9 CuadroTexto d  KB  ' $ N\B?10 CuadroTextoj r? #Multi voxel (A), Chemical shift (B)"$ $g,  H  $ 0޽h ? I}OPM___PPT10i. P"$+D=' = @B +"M 0 TLP((  (" (  rQ0e0e?1 TtuloN   \Metabolitos Cerebrales* e (  Z0e0e?02 Marcador de contenido*  N-acetil aspartato (NAA, pico 2.0ppm): es un marcador neuronal y sus concentraciones disminuyen en diferentes tipos de insultos cerebrales. Colina (Co, pico 3.2 ppm): forma parte de la membrana celular, su incremento refleja el aumento del nmero de clulas. Creatina ( Cr 3.03 ppm y 3.94 ppm): es utilizado como reserva de los fosfatos de alta energa y adems acta como buffer en los reservorios de ATP-ADP. Lactato (Lac, pico 1.32): lo podemos encontrar en lesiones necrticas o qusticas. 2  gPsIH ( 0޽h ? I}OPM___PPT10i.>ā+D=' = @B +" 0 `,(  ," ,  rJ0e0e?1 Ttulo;{   \Metabolitos Cerebrales* e ,  0e0e?02 Marcador de contenido*=  Mioinositol (MI, pico 3.56 ppm): acta en la neurorrecepcin hormona-sensitiva. La combinacin de MI elevado con disminucin da NAA se ha observado en la Enfermedad de Alzheimer. Glutamato (Glu, pico 2.1-2.5 ppm): neurotransmisor que acta en el metabolismo de las mitocondrias. Alanina (pico 1.3-1.4 ppm): funcin incierta. Se puede incrementar en tumores intracraneales como los meningiomas. r    OgCgl  EN H , 0޽h ? I}OPM___PPT10i.>ā+D=' = @B +" 0 ~p0(  0  0  r(0e0e?1 Ttulo;{e   D Conclusin e 0  Ġ0e0e?02 Marcador de contenido8[   La espectroscopia por resonancia magntica, es una tcnica no invasiva, con capacidad para detectar y cuantificar "in vivo un conjunto de metabolitos de un volumen cerebral. Permite as analizar las variaciones de estos metabolitos en las diversas alteraciones patolgicas. La informacin es independiente de las posibles alteraciones estructurales; de esta manera aporta informacin complementaria a la imagen por resonancia magntica y constituye en ocasiones el nico marcador de la patologa, ya que es capaz de detectar alteraciones que cursan con un estudio estructural normal. "SSgH 0 0޽h ? I}OPM___PPT10i.#0+D=' = @B +" 0  4(  4  4  r,0e0e?1 TtuloN   F Bibliografa eP  4  0e0e?02 Marcador de contenido* `l H@___PPT9"  4 Onofre J, Martinez H, Arteaga M, Gmez A, Mauregui S. Resonancia magntica en el cerebro humano.Principios bsicos. Rev Mex Neuroci 2002,3(4):207-210. Myung K, Chang H, Systemic lupus erithematosus: brain MR imaging and single voxel hydrogen 1 MR spectroscopy. Radiology 2000:217:43-49. Barker P. Magnetic resonance spectroscopy in cerebral ischemia and infarction. Seminars Cerebrovasc Dis Stroke 2001;1:331-342. Poptani H, Gupta R, Roy R, Pandey R, Jain V, Chhabra D. Characterization of intracranial mass lesions with in vivo proton MR spectroscopy. AJNR Am J Neuroradiol 1995;16:1593 603. Rand SD, Prost R, Haughton V, Mark L, Strainer J, Johansen J et al. Accuracy of single-voxel proton MR spectroscopy in distinguishing neoplastic from nonneoplastic brain lesions. AJNR Am J Neuroradiol 1997;18:1695 704. Filippi M, Grossman RI. MRI techniques to monitor MS evolution: The present and the future. Neurology 2002;58:1147 53. Moriarty M, Belinda S, Li Y, Regal B, He J,Markowitz C, Grossman R, Gonen O. Espectroscopa por Resonancia Magntica de N-Acetilaspartato Cerebral Total Un Marcador Potencial para la Toma de Decisiones en la EM Recurrente-Remitente. Davie C, Hawkins C, Barker G. Serial proton magnetic resonance spectroscopy in acute multiple sclerosis lesions. Brain 1994;117:49-58. :" gY-      6 X          ~ W  *      8    H 4 0޽h ? I}OPM___PPT10i.&@B1E+D=' = @B +"r<W-$y Oh+'0 `h    $,4 Espectroscopia Cerebral por Resonancia Magntica. ramonDr. Ricardo Videla 37Microsoft Office PowerPoint@H(@@qC@@%hG g  F  yI}--$xx--'@Times New Roman-. 2 I! Caren Gonz."Systemv-@Times New Roman-.  2 I7.-@Times New Roman-. @2 I:&lez, Cesar Villamizar, Gustavo Rojas, .-@Times New Roman-. .2 N!Franklin Moreno, Mercedes .-@Times New Roman-.  2 NW.-@Times New Roman-. (2 NZvila, Carlos Parales. .-@Times New Roman-. 2 U Instituto Aut.-@Times New Roman-.  2 U3.-@Times New Roman-. F2 U5*nomo Hospital Universitario de los Andes. .-@Times New Roman-.  2 Z?M.-@Times New Roman-.  2 ZC.-@Times New Roman-. 2 ZErida. Venezuela.-@Times New Roman-. 12 0Espectroscopia Cerebral por .-@Times New Roman-. 2 ;$Resonancia Magn.-@Times New Roman-.  2 ;i.-@Times New Roman-. 2 ;mtica. .-՜.+,0    Presentacin en pantalla personalSR  ArialCalibriTimes New RomanTema de Office4 Espectroscopia Cerebral por Resonancia Magntica. Introduccin ObjetivosEspectroscopia Cerebral Factores Fsicos Factores FsicosConsideraciones TcnicasConsideraciones TcnicasMetabolitos CerebralesMetabolitos Cerebrales Conclusin Bibliografa Fuentes usadasPlantilla de diseoTtulos de diapositiva +_0Dr. Ricardo Videla Dr. Ricardo Videla   !"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwxyz{|}~      !"#$%&'()*,-./012456789:<=>?@ABGRoot EntrydO)PicturesUCurrent User;SummaryInformation(+PowerPoint Document(DocumentSummaryInformation83Root EntrydO)p,qKPicturesUCurrent UserbSummaryInformation(+      !"#$%&'()*,-./012456789:G._Maria Elena CastrillonMaria Elena Castrillon