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BP ; &COMO ANALIZAR LOS ALIMENTOSAntiguamente se analizaban con Kits caseros policlonales para investigar la presencia de gliadina En la actualidad se utiliza un kits comercial (R5 Ridascreen Gliadin) Es un Elisa en sandwich Su deteccin lmite es de 1.5 ppm gliadinas correspondientes a 0.0003% de gluten !!   ''RIDASCREEN - GLIADIN (R5)FDICIEMBRE DE 2007 EL INSTITUTO:  AOAC, RESERCH INSTITUTE CERTIFICATE OF PERFORMANCE TESTED STATUS O t o r g a e l c e r t i f i c a d o : N 1 2 0 6 0 1&f>( INFORMEr La determinacin de gluten se realiza mediante enzimoinmunoensayo(ELISA) Utilizando el Kit Ridascreen (R- Biofarm AG, Darmstadt, Germany) Lmite de deteccin de gluten 3.0 p.p.m (equivale a 1.5 p.m.m.de gliadina, indicando como libre de gluten hasta un mximo de 20 p.m.m. (equivale a 10 p.p.m. de gliadina):Z:0 %[)! AGRADECIDA POR LA ATENCIN|Z  / 0` 33` Sf3f` 33g` f` www3PP` ZXdbmo` \ғ3y`Ӣ` 3f3ff` 3f3FKf` hk]wwwfܹ` ff>>\`Y{ff` R>&- {p_/̴>?" dd@,|?" dd@   " @ ` n?" dd@   @@``PR    @ ` ` p>> `C(    6 " `}  :TITULO =  0 " `  kHaga clic para modificar el estilo de texto del patrn Segundo nivel Tercer nivel Cuarto nivel Quinto nivel7    lH  0޽h ? 3380___PPT10.p$! *Diseo predeterminado0 t#(  t t 04 P    P*   t 0,:     R*  d t c $ ?  / t 0l>  0  kHaga clic para modificar el estilo de texto del patrn Segundo nivel Tercer nivel Cuarto nivel Quinto nivel7    l t 6B _P   P*   t 6G _   R*  H t 0޽h ? 3380___PPT10.pv8 0% rMECANISMOS HUMORALES Y CELULARES DE LA ENFERMEDAD CELACA p$(  r  S s C   r  S x'g  <  c $ ? 33___PPT10i.K`rk+D=' # = @B +w0 4*(  4 4 c $ O[mI  [ DEFINICIN La Enfermedad Celaca EC es una enfermedad autoinmune que consiste en una intolerancia a las protenas del gluten (gliadinas, secalinas, hordenas y aveninas) que cursan con una atrofia severa de la mucosa del intestino delgado superior. Esta intolerancia es de carcter permanente, se mantiene a lo largo de toda la vida y se presenta en sujetos genticamente pre  dispuestos a padecerla. Es la enfermedad crnica ms prevalente del mundo y est sub  diagnosticada fZ qM<x V { |< 4 c $ ? 33___PPT10i.pZy+D=' # = @B +y20 11@F,1(  " d8   #">2 zd  F <4k[?@ 8  LHoffenberg, E.  Pediatrics, 2003 (13)&' &"  E <?z @ 8  G1:104& "  D <p[?d z 8  aDenver - Estados Unidos. &  $ C <,s[?@   ZHender, J.  Dtsh. Med. Wochenschr, 2002 (12)&. -"  .  B <x[?z @  G1:550& "  A <?d z  RAlemania.  &   @ <[?@ b   BCsizmadia, C.  Lancet, 1999 (11)&" !"  ? <4[?z b @  G1:198& "  > <[?db z  QNoruega. &   = <,[?@ b  |:Ertebin, V.  JPGN, 2005 (10)& "  < <X[?z @ b  G1:158& "  ; <[?d z b  QTurqua. &   : <t[?@ 0   z8Antunes, H.  JPGN, 2002 (9)& "  9 < [?z 0 @  G1:134& "  8 <4[?d0 z  RPortugal.  &   7 <[?@ 0  JCarlsson, A. K.  Pediatrics, 2001(8)&& %"  6 <h[?z @ 0  G1:100& "  5 <[?dz 0  PSuecia. &   4 <X[?@  RMaki, M.  New England J. Med., 2003 (7)&* )"  *  3 <з[?z @  F1:99& "  2 <|[?dz  S Finlandia.  &   1 <p[?@ e z8Meloni, G.  Lancet, 1999(6)& "  0 <[?z e@  F1:95& "  / <[?dez  PItalia. &   . <$[?@ e @Korponay y Szabo  JPGN, 1999(5)&! "  - <[?z @ e F1:85& "  , < [?dz e QHungra. &   + <x[?@ 3 x6Catassi, C.  JPGN, 2005(4)& "  * < [?z 3@  G1:128& "  ) <[?d3z  \El Cairo - Egipto. &   ( <P[?@ 3 LCatassi, C.  Tissue Antigens, 2001(3)&' &"  ' <[?z @ 3 F1:18& "  & <,[?dz 3 YNorte de frica. &  HB G C dHB H C d8 8 HB I C dd8 HB J C 8 ZB L s *1 ?d33ZB M s *1 ?z z 8 ZB O s *1 ?@ @ 8 ZB R s *1 ?dZB ] s *1 ?deeZB h s *1 ?dZB s s *1 ?dZB ~ s *1 ?d0 0 ZB  s *1 ?d  ZB  s *1 ?db b ZB  s *1 ?d  ZB  s *1 ?d  2 l dc   #" dY Ӥ <[?@  @Mndez, V., Gonzlez, M.V., Velsquez, S., et al  Internacional Simposium on Coeliac Disease, 2004  Ireland, Belfast.(16).| {&  Ҥ <?z @  N1:66. &  Ѥ <?d z  QUruguay. &  n Ф <t?@   Gandolfi, L.,Prawtesi,R., Crdoba, JCM, et al  Am. J. Gastroenterol. 2000, 95: 689/692 (15)&] \"  Ϥ <?z @  G1:680& "  Τ <$?d z  PBrasil. &   ͤ <?@ c   NGomez, J.C., Selvaggio, G.S., Viola, M. y colaboradores  Presentado en Congreso de Gastroenterologa y Endoscopia Digestiva Argentina, Buenos Aires, octubre 2000.(14)& "  ̤ <?z c @  G1:168& "  ˤ <!?dc z  S Argentina.  &  HB Ԥ C dc c HB դ C dHB ֤ C dc dHB פ C c ZB ٤ s *1 ?d  ZB ڤ s *1 ?z c z ZB ܤ s *1 ?@ c @ ZB ߤ s *1 ?d    B\'d  A PREVALENCIA  <  c $ ? 33___PPT10i.Hr\L+D=' V= @B +0 `y(  A  0Cw FORMAS CLNICAS La EC es una enfermedad muy heterognea y se divide en: Formas Clsicas: Diarrea malabsortiva, cambios de carcter, falta de apetito, estacionamiento de la curva de peso, abdomen prominente, nalgas aplanadas, etc. Formas no Clsica: Estreimiento, edemas, anemia ferropnica, hipoplasia del esmalte dentario, epilepsia, calcificaciones intracraneales occipitales Formas Silentes: Asintomticos en familiares de primer grado. Formas Latentes: Consumiendo gluten tienen biopsia normal o aumento de LIE, en la evolucin presentarn atrofia con normalizacin anatmica tras la retirada del gluten y la re aparicin al re introducirlo. Formas Potenciales: Tienen la pre disposicin gentica, incremento de los linfocitos gama, delta, biopsia normal serologa negativa, asintomticos. I.<  c $ ? 33___PPT10i.IrĽ+D=' V= @B + 0  (  d  S .A?iceberg"`d <  c $ ? 33___PPT10i.p% +D=' V= @B +0 n(  6  090% sensibilidad, especificidad y se relaciona con el dao Anticuerpos antitransglutaminasas  tTG: Tcnica ELISA: Cambia la alta eficacia de los AAE con una sensibilidad y especificidad >90% y con las ventajas metodolgicas de los AAG (ELISA)"<  c $ ? 33___PPT10i.Kr0c+D=' V= @B +0 @I(  @ @ 0d gDIAGNSTICO No puede establecerse por datos clnicos ni serolgicos, es imprescindible la realizacin de al menos una biopsia de intestino delgado en la segunda porcin del duodeno y su estudio histolgico. 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