D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros

Autores:: Evren Haydardedeoğlu, Ali
Ural, Kerem
Orman, Abdulkadir
Aliç Ural, Deniz

Tipo de recurso:: Article of journal

Fecha de publicación:: 2018

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
dc.title.translated.eng.fl_str_mv	D-dimer levels as a procoagulative marker in association with disease progress during giardiasis in dogs
title	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
spellingShingle	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros D-dimer procoagulation inflammation biomarker giardiasis dogs D-dímero procoagulación inflamación biomarcador giardiasis perros
title_short	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
title_full	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
title_fullStr	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
title_full_unstemmed	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
title_sort	D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros
dc.creator.fl_str_mv	Evren Haydardedeoğlu, Ali Ural, Kerem Orman, Abdulkadir Aliç Ural, Deniz
dc.contributor.author.spa.fl_str_mv	Evren Haydardedeoğlu, Ali Ural, Kerem Orman, Abdulkadir Aliç Ural, Deniz
dc.subject.eng.fl_str_mv	D-dimer procoagulation inflammation biomarker giardiasis dogs
topic	D-dimer procoagulation inflammation biomarker giardiasis dogs D-dímero procoagulación inflamación biomarcador giardiasis perros
dc.subject.spa.fl_str_mv	D-dímero procoagulación inflamación biomarcador giardiasis perros
publishDate	2018
dc.date.accessioned.none.fl_str_mv	2018-05-01 00:00:00 2022-07-01T21:00:56Z
dc.date.available.none.fl_str_mv	2018-05-01 00:00:00 2022-07-01T21:00:56Z
dc.date.issued.none.fl_str_mv	2018-05-01
dc.type.spa.fl_str_mv	Artículo de revista
dc.type.eng.fl_str_mv	Journal article
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dc.relation.references.spa.fl_str_mv	Bartelt LA, Sartor RB. Advances in understanding Giardia: Determinants and mechanisms of chronic sequelae. F1000Prime Rep. 2015; 7:62. https://doi.org/10.12703/P7-62 Buret A, Amat C, Manko A, Beatty J, Halliez MM, Bhargava A, et al. Giardia duodenalis: New research developments in pathophysiology, pathogenesis, and virulence factors. Curr Trop Med Rep. 2015; 2(3):110–118. https://doi.org/10.1007/s40475-015-0049-8 Maizels RM. Parasite immunomodulation and polymorphisms of the immune system. J Biol. 2009; 8:62. https://doi.org/10.1186/jbiol166 McSorley HJ, Maizels RM. Helminth infections and host immune regulation. Clin Microbiol Rev. 2012; 25:585–608. https://doi.org/10.1128/CMR.05040-11 Kissoon-Singh V, Moreau F, Trusevych E, Chadee K. Entamoeba histolytica exacerbates epithelial tight junction permeability and proinflammatory responses in Muc2(−/−) mice. Am J Pathol. 2013; 182:852–865. https://doi.org/10.1016/j.ajpath.2012.11.035 Hanevik K, Hausken T, Morken MH, Strand EA, Mørch K, Coll P, Helgeland L, Langeland N. Persisting symptoms and duodenal inflammation related to Giardia duodenalis infection. J Infect. 2007; 55(6):524-530. https://doi.org/10.1016/j.jinf.2007.09.004 Sara D, Christine L, Kim N, Raymond D, Elaine H, Lars E. Novel model of colitis induced by a non-inflammatory small bowel infection. J Immunol 2011; 186: (1 Supplement) 166.10. Chen TL, Chen S, Wu HW, Lee TC, Lu YZ, Wu LL, et al.. Persistent gut barrier damage and commensal bacterial influx following eradication of Giardia infection in mice. Gut Pathog. 2013; 5:26. https://doi.org/10.1186/1757-4749-5-26 Benere E, Van Assche T, Van Ginneken C, Peulen O, Cos P, Maes L. Intestinal growth and pathology of Giardia duodenalis assemblage subtype a(i), a(ii), b and e in the gerbil model. Parasitol. 2012; 139:424–433. https://doi.org/10.1017/S0031182011002137 Dos Santos JI, Vituri Cde L. Some hematimetric findings in human Giardia lamblia infection. Rev Inst Med Trop. 1996; 38:91–95. https://doi.org/10.1590/S0036-46651996000200002 Koot BG, Kate FJ, Juffrie M, Rosalina I, Taminiau JJ, Benninga MA. Does Giardia lamblia cause villous atrophy in children?: A retrospective cohort study of the histological abnormalities in giardiasis. J Pediatr Gastroenterol Nutr. 2009; 49:304–308. https://doi.org/10.1097/MPG.0b013e31818de3c4 Aloisio F, Filippini G, Antenucci P, Lepri E, Pezzotti G, Caccio SM, Pozio E. Severe weight loss in lambs infected with Giardia duodenalis assemblage b. Parasitol. 2006; 142:154–158. https://doi.org/10.1016/j.vetpar.2006.06.023 Bartelt LA, Roche J, Kolling G, Bolick D, Noronha F, Naylor C, Hoffman P, Warren C, Singer S, Guerrant R. Persistent Giardia lamblia impairs growth in a murine malnutrition model. J Clin Investig. 2013; 123:2672–2684. https://doi.org/10.1172/JCI67294 Jimenez JC, Fontaine J, Grzych JM, Dei-Cas E, Capron M. Systemic and mucosal responsesto oral administration of excretory and secretory antigens from Giardia intestinalis. Clin Diagn Lab Immunol. 2004; 11:152-160. Turk V, Stoka V, Vasiljeva O, Renko M, Sun T, Turk B, Turk D. Cysteine cathepsins: From structure, function and regulation to new frontiers. Biochim Biophys Acta. 2012; 1824:68–88. https://doi.org/10.1016/j.bbapap.2011.10.002 Zareie M, McKay DM, Kovarik GG, Perdue MH. Monocyte/macrophages evoke epithelial dysfunction: Indirect role of tumor necrosis factor-alpha. Am J Physiol. 1998; 275:932-939. https://doi.org/10.1152/ajpcell.1998.275.4.C932 Davison AM, Thomson D, Robson JS. Intravascular coagulation complicating influenza A virus infection. Br Med J. 1973; 1:654-655. https://doi.org/10.1136/bmj.1.5854.654 Saibeni S, Cattaneo M, Vecchi M, Zighetti ML, Lecchi A, Lombardi R, et al. Low vitamin B6 plasma levels, a risk factor for thrombosis, in inflammatory bowel disease: role of inflammation and correlation with acute phase reactants. Am J Gastroenter. 2003; 98(1):112–117. https://doi.org/10.1111/j.1572-0241.2003.07160.x Saibeni S, Spina L, Vecchi M. Exploring the relationships between inflammatory response and coagulation cascade in inflammatory bowel disease. Eur Rev Med Pharmacol Sci. 2004; 8(5):205-208. Pastorelli L. Salvo CD, Mercado J R, Vecchi M, Pizarro TT. Central role of the gut epithelial barrier in the pathogenesis of chronic intestinal inflammation: lessons learned from animal models and human genetics. Front Immunol. 2013; 4:280. https://doi.org/10.3389/fimmu.2013.00280 Pastorelli L, Dozio E, Francesca LP, Anzoletti MB, Vianello E, Munizio N, et al. Procoagulatory state in inflammatory bowel diseases is promoted by impaired intestinal barrier function. Gastroenterol Res Pract. 2015; Article ID 189341. Ankarklev J, Jerlström-Hultqvist J, Ringqvist E, Troell K, Svärd SG. Behind the smile: cell biology and disease mechanisms of Giardia species. Nat Rev Microbiol. 2010; 8:413-422. https://doi.org/10.1038/nrmicro2317 Buret AG. Pathophysiology of enteric infections with Giardia duodenalis. Parasite. 2008; 15:261-265. https://doi.org/10.1051/parasite/2008153261 Buret AG, Mitchell K, Muench DG, Scott KG. Giardia lamblia disrupts tight junctional ZO-1 and increases permeability in non-transformed human small intestinal epithelial monolayers: effects of epidermal growth factor. Parasitol. 2002; 125:11-19. https://doi.org/10.1017/S0031182002001853 Cotton JA, Beatty JK, Buret AG. Host parasite interactions and pathophysiology in Giardia infections. Int J Parasitol. 2011; 41:925-933. https://doi.org/10.1016/j.ijpara.2011.05.002 Teoh DA, Kamieniecki D, Pang G, Buret AG. Giardia lamblia rearranges F-actin and alpha-actinin in human colonic and duodenal monolayers and reduces transepithelial electrical resistance. J Parasitol. 2000; 86:800-806. Troeger H, Epple HJ, Schneider T, Wahnschaffe U, Ullrich R, Burchard GD, Jelinek T, Zeitz M, Fromm M, Schulzke JD. Effect of chronic Giardia lamblia infection on epithelial trans- port and barrier function in human duodenum. Gut. 2007; 56:328-335. https://doi.org/10.1136/gut.2006.100198 Scott KG, Meddings JB, Kirk DR, Lees-Miller SP, Buret AG. Intestinal infection with Giardia spp. reduces epithelial barrier function in a myosin light chain kinase-dependent fashion. Gastroenterol. 2002; 123:1179-1190. https://doi.org/10.1053/gast.2002.36002 Yuan SM, Shi YH, Wang JJ, Lü FQ, Gao S. Elevated plasma D-dimer and hypersensitive C-reactive protein levels may indicate aortic disorders. Rev Bras Cir Cardiovasc. 2011, 26(4):573-81. https://doi.org/10.5935/1678-9741.20110047 Ural DA, Ayan A, Aysul A, Balıkçı C, Ural K. Secnidazol treatment to improve milk yield in sheep with giardiasis. Atatürk Üniversitesi Vet Bil Derg. 2014, 9(2):74-82.
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dc.relation.citationedition.spa.fl_str_mv	Núm. 2 , Año 2018 : Revista MVZ Córdoba Volumen 23(2) Mayo-Agosto 2018
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spelling	Evren Haydardedeoğlu, Ali64dcdac2-7580-442f-8a09-f04bd70bd068-1Ural, Kerem95491f85-c6c0-4efb-a2a6-5405375603e9-1Orman, Abdulkadir90b923d8-4678-4ec7-88a7-26df48026bce-1Aliç Ural, Deniz0a1ac913-f01b-41f9-90ae-29cbeba1877f-12018-05-01 00:00:002022-07-01T21:00:56Z2018-05-01 00:00:002022-07-01T21:00:56Z2018-05-010122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/595110.21897/rmvz.1348https://doi.org/10.21897/rmvz.13481909-0544application/pdfapplication/epub+ziptext/htmlapplication/xmlspaUniversidad de Córdobahttps://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://revistamvz.unicordoba.edu.co/article/view/1348D-dimerprocoagulationinflammationbiomarkergiardiasisdogsD-dímeroprocoagulacióninflamaciónbiomarcadorgiardiasisperrosD dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perrosD-dimer levels as a procoagulative marker in association with disease progress during giardiasis in dogsArtículo de revistaJournal articleinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a85Bartelt LA, Sartor RB. Advances in understanding Giardia: Determinants and mechanisms of chronic sequelae. F1000Prime Rep. 2015; 7:62. https://doi.org/10.12703/P7-62Buret A, Amat C, Manko A, Beatty J, Halliez MM, Bhargava A, et al. Giardia duodenalis: New research developments in pathophysiology, pathogenesis, and virulence factors. Curr Trop Med Rep. 2015; 2(3):110–118. https://doi.org/10.1007/s40475-015-0049-8Maizels RM. Parasite immunomodulation and polymorphisms of the immune system. J Biol. 2009; 8:62. https://doi.org/10.1186/jbiol166McSorley HJ, Maizels RM. Helminth infections and host immune regulation. Clin Microbiol Rev. 2012; 25:585–608. https://doi.org/10.1128/CMR.05040-11Kissoon-Singh V, Moreau F, Trusevych E, Chadee K. Entamoeba histolytica exacerbates epithelial tight junction permeability and proinflammatory responses in Muc2(−/−) mice. Am J Pathol. 2013; 182:852–865. https://doi.org/10.1016/j.ajpath.2012.11.035Hanevik K, Hausken T, Morken MH, Strand EA, Mørch K, Coll P, Helgeland L, Langeland N. Persisting symptoms and duodenal inflammation related to Giardia duodenalis infection. J Infect. 2007; 55(6):524-530. https://doi.org/10.1016/j.jinf.2007.09.004Sara D, Christine L, Kim N, Raymond D, Elaine H, Lars E. Novel model of colitis induced by a non-inflammatory small bowel infection. J Immunol 2011; 186: (1 Supplement) 166.10.Chen TL, Chen S, Wu HW, Lee TC, Lu YZ, Wu LL, et al.. Persistent gut barrier damage and commensal bacterial influx following eradication of Giardia infection in mice. Gut Pathog. 2013; 5:26. https://doi.org/10.1186/1757-4749-5-26Benere E, Van Assche T, Van Ginneken C, Peulen O, Cos P, Maes L. Intestinal growth and pathology of Giardia duodenalis assemblage subtype a(i), a(ii), b and e in the gerbil model. Parasitol. 2012; 139:424–433. https://doi.org/10.1017/S0031182011002137Dos Santos JI, Vituri Cde L. Some hematimetric findings in human Giardia lamblia infection. Rev Inst Med Trop. 1996; 38:91–95. https://doi.org/10.1590/S0036-46651996000200002Koot BG, Kate FJ, Juffrie M, Rosalina I, Taminiau JJ, Benninga MA. Does Giardia lamblia cause villous atrophy in children?: A retrospective cohort study of the histological abnormalities in giardiasis. J Pediatr Gastroenterol Nutr. 2009; 49:304–308. https://doi.org/10.1097/MPG.0b013e31818de3c4Aloisio F, Filippini G, Antenucci P, Lepri E, Pezzotti G, Caccio SM, Pozio E. Severe weight loss in lambs infected with Giardia duodenalis assemblage b. Parasitol. 2006; 142:154–158. https://doi.org/10.1016/j.vetpar.2006.06.023Bartelt LA, Roche J, Kolling G, Bolick D, Noronha F, Naylor C, Hoffman P, Warren C, Singer S, Guerrant R. Persistent Giardia lamblia impairs growth in a murine malnutrition model. J Clin Investig. 2013; 123:2672–2684. https://doi.org/10.1172/JCI67294Jimenez JC, Fontaine J, Grzych JM, Dei-Cas E, Capron M. Systemic and mucosal responsesto oral administration of excretory and secretory antigens from Giardia intestinalis. Clin Diagn Lab Immunol. 2004; 11:152-160.Turk V, Stoka V, Vasiljeva O, Renko M, Sun T, Turk B, Turk D. Cysteine cathepsins: From structure, function and regulation to new frontiers. Biochim Biophys Acta. 2012; 1824:68–88. https://doi.org/10.1016/j.bbapap.2011.10.002Zareie M, McKay DM, Kovarik GG, Perdue MH. Monocyte/macrophages evoke epithelial dysfunction: Indirect role of tumor necrosis factor-alpha. Am J Physiol. 1998; 275:932-939. https://doi.org/10.1152/ajpcell.1998.275.4.C932Davison AM, Thomson D, Robson JS. Intravascular coagulation complicating influenza A virus infection. Br Med J. 1973; 1:654-655. https://doi.org/10.1136/bmj.1.5854.654Saibeni S, Cattaneo M, Vecchi M, Zighetti ML, Lecchi A, Lombardi R, et al. Low vitamin B6 plasma levels, a risk factor for thrombosis, in inflammatory bowel disease: role of inflammation and correlation with acute phase reactants. Am J Gastroenter. 2003; 98(1):112–117. https://doi.org/10.1111/j.1572-0241.2003.07160.xSaibeni S, Spina L, Vecchi M. Exploring the relationships between inflammatory response and coagulation cascade in inflammatory bowel disease. Eur Rev Med Pharmacol Sci. 2004; 8(5):205-208.Pastorelli L. Salvo CD, Mercado J R, Vecchi M, Pizarro TT. Central role of the gut epithelial barrier in the pathogenesis of chronic intestinal inflammation: lessons learned from animal models and human genetics. Front Immunol. 2013; 4:280. https://doi.org/10.3389/fimmu.2013.00280Pastorelli L, Dozio E, Francesca LP, Anzoletti MB, Vianello E, Munizio N, et al. Procoagulatory state in inflammatory bowel diseases is promoted by impaired intestinal barrier function. Gastroenterol Res Pract. 2015; Article ID 189341.Ankarklev J, Jerlström-Hultqvist J, Ringqvist E, Troell K, Svärd SG. Behind the smile: cell biology and disease mechanisms of Giardia species. Nat Rev Microbiol. 2010; 8:413-422. https://doi.org/10.1038/nrmicro2317Buret AG. Pathophysiology of enteric infections with Giardia duodenalis. Parasite. 2008; 15:261-265. https://doi.org/10.1051/parasite/2008153261Buret AG, Mitchell K, Muench DG, Scott KG. Giardia lamblia disrupts tight junctional ZO-1 and increases permeability in non-transformed human small intestinal epithelial monolayers: effects of epidermal growth factor. Parasitol. 2002; 125:11-19. https://doi.org/10.1017/S0031182002001853Cotton JA, Beatty JK, Buret AG. Host parasite interactions and pathophysiology in Giardia infections. Int J Parasitol. 2011; 41:925-933. https://doi.org/10.1016/j.ijpara.2011.05.002Teoh DA, Kamieniecki D, Pang G, Buret AG. Giardia lamblia rearranges F-actin and alpha-actinin in human colonic and duodenal monolayers and reduces transepithelial electrical resistance. J Parasitol. 2000; 86:800-806.Troeger H, Epple HJ, Schneider T, Wahnschaffe U, Ullrich R, Burchard GD, Jelinek T, Zeitz M, Fromm M, Schulzke JD. Effect of chronic Giardia lamblia infection on epithelial trans- port and barrier function in human duodenum. Gut. 2007; 56:328-335. https://doi.org/10.1136/gut.2006.100198Scott KG, Meddings JB, Kirk DR, Lees-Miller SP, Buret AG. Intestinal infection with Giardia spp. reduces epithelial barrier function in a myosin light chain kinase-dependent fashion. Gastroenterol. 2002; 123:1179-1190. https://doi.org/10.1053/gast.2002.36002Yuan SM, Shi YH, Wang JJ, Lü FQ, Gao S. Elevated plasma D-dimer and hypersensitive C-reactive protein levels may indicate aortic disorders. Rev Bras Cir Cardiovasc. 2011, 26(4):573-81. https://doi.org/10.5935/1678-9741.20110047Ural DA, Ayan A, Aysul A, Balıkçı C, Ural K. Secnidazol treatment to improve milk yield in sheep with giardiasis. Atatürk Üniversitesi Vet Bil Derg. 2014, 9(2):74-82.https://revistamvz.unicordoba.edu.co/article/download/1348/pdfhttps://revistamvz.unicordoba.edu.co/article/download/1348/epubhttps://revistamvz.unicordoba.edu.co/article/download/1348/htmlhttps://revistamvz.unicordoba.edu.co/article/download/1348/2500Núm. 2 , Año 2018 : Revista MVZ Córdoba Volumen 23(2) Mayo-Agosto 201867362672623Revista MVZ CórdobaPublicationOREORE.xmltext/xml2737http://172.16.14.198/bitstreams/143730a6-32a6-447b-aa1b-55a01c872289/download52d0225632bd46774d0252509cfa233dMD51ucordoba/5951oai:172.16.14.198:ucordoba/59512023-10-06 00:45:23.432https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttp://172.16.14.198Repositorio Universidad de Córdobabdigital@metabiblioteca.com

D dímero como marcador procoagulante en asociación con el progreso de la enfermedad durante la giardiasis en perros

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