Serum cytokine, chemokine, and growth factor profiles and their modulation in inflammatory bowel disease
Ulcerative colitis (UC) and Crohn disease (CD) are the most common forms of inflammatory bowel disease (IBD). Because these subtypes of IBD are characterized by periods of activity and remission, an understanding of the modulation of biochemical markers with the clinical features of IBD or its treat...
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Published in: | Medicine (Baltimore) Vol. 98; no. 38; p. e17208 |
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Abstract | Ulcerative colitis (UC) and Crohn disease (CD) are the most common forms of inflammatory bowel disease (IBD). Because these subtypes of IBD are characterized by periods of activity and remission, an understanding of the modulation of biochemical markers with the clinical features of IBD or its treatment, may be useful for determining the correct treatment protocol.This study aimed to evaluate the serum levels of 27 protein biomarkers to determine their association with IBD, correlation with clinical findings of disease, and modulation according to the pharmacologic therapy.A case-control study was carried out in Zacatecas, Mexico. The 27 protein profiles of serum from 53 participants (23 UC, 11 CD, and 19 controls) were evaluated using the Pro Human Cytokine 27-Plex immunoassay (Bio-Rad).Considering the controls as a reference, the group with IBD endoscopic activity showed higher serum levels of granulocyte colony-stimulating factor (G-CSF), interleukin 1 receptor antagonist (IL-1Ra), and platelet-derived growth factor BB (PDGF-BB) (P < .05). Interferon-induced protein 10 (IP-10) was associated with extraintestinal symptoms of disease (P = .041). Both PDGF-BB and interleukin 6 (IL-6) showed the strongest correlations with clinical features of IBD. Levels of IL-6, IL-7, and monocyte chemoattractant protein 1 were higher with 5-aminosalicylic acid (5-ASA) + Azathioprine therapy than controls (P < .05). Combined therapy with 5-ASA + Adalimumab led to the strongest changes in marker modulation: IL-4, IL-5, IL-15, and PDGF-BB, were upregulated (P < .05).Elevated serum levels of G-CSF, IL-1Ra, and PDGF-BB were associated with IBD endoscopic activity, and of IP-10 with extraintestinal manifestations of IBD. Combined therapy of 5-ASA + Adalimumab produced significant upregulation of IL-4, IL-5, IL-15, and PDGF-BB. This information may be useful for deciding on the course of pharmacologic therapy for patients with IBD and for generating new therapy alternatives to improve the outcome of patients with IBD. |
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AbstractList | Ulcerative colitis (UC) and Crohn disease (CD) are the most common forms of inflammatory bowel disease (IBD). Because these subtypes of IBD are characterized by periods of activity and remission, an understanding of the modulation of biochemical markers with the clinical features of IBD or its treatment, may be useful for determining the correct treatment protocol.This study aimed to evaluate the serum levels of 27 protein biomarkers to determine their association with IBD, correlation with clinical findings of disease, and modulation according to the pharmacologic therapy.A case-control study was carried out in Zacatecas, Mexico. The 27 protein profiles of serum from 53 participants (23 UC, 11 CD, and 19 controls) were evaluated using the Pro Human Cytokine 27-Plex immunoassay (Bio-Rad).Considering the controls as a reference, the group with IBD endoscopic activity showed higher serum levels of granulocyte colony-stimulating factor (G-CSF), interleukin 1 receptor antagonist (IL-1Ra), and platelet-derived growth factor BB (PDGF-BB) (P < .05). Interferon-induced protein 10 (IP-10) was associated with extraintestinal symptoms of disease (P = .041). Both PDGF-BB and interleukin 6 (IL-6) showed the strongest correlations with clinical features of IBD. Levels of IL-6, IL-7, and monocyte chemoattractant protein 1 were higher with 5-aminosalicylic acid (5-ASA) + Azathioprine therapy than controls (P < .05). Combined therapy with 5-ASA + Adalimumab led to the strongest changes in marker modulation: IL-4, IL-5, IL-15, and PDGF-BB, were upregulated (P < .05).Elevated serum levels of G-CSF, IL-1Ra, and PDGF-BB were associated with IBD endoscopic activity, and of IP-10 with extraintestinal manifestations of IBD. Combined therapy of 5-ASA + Adalimumab produced significant upregulation of IL-4, IL-5, IL-15, and PDGF-BB. This information may be useful for deciding on the course of pharmacologic therapy for patients with IBD and for generating new therapy alternatives to improve the outcome of patients with IBD. Ulcerative colitis (UC) and Crohn disease (CD) are the most common forms of inflammatory bowel disease (IBD). Because these subtypes of IBD are characterized by periods of activity and remission, an understanding of the modulation of biochemical markers with the clinical features of IBD or its treatment, may be useful for determining the correct treatment protocol. This study aimed to evaluate the serum levels of 27 protein biomarkers to determine their association with IBD, correlation with clinical findings of disease, and modulation according to the pharmacologic therapy. A case–control study was carried out in Zacatecas, Mexico. The 27 protein profiles of serum from 53 participants (23 UC, 11 CD, and 19 controls) were evaluated using the Pro Human Cytokine 27-Plex immunoassay (Bio-Rad). Considering the controls as a reference, the group with IBD endoscopic activity showed higher serum levels of granulocyte colony-stimulating factor (G-CSF), interleukin 1 receptor antagonist (IL-1Ra), and platelet-derived growth factor BB (PDGF-BB) ( P < .05). Interferon-induced protein 10 (IP-10) was associated with extraintestinal symptoms of disease ( P = .041). Both PDGF-BB and interleukin 6 (IL-6) showed the strongest correlations with clinical features of IBD. Levels of IL-6, IL-7, and monocyte chemoattractant protein 1 were higher with 5-aminosalicylic acid (5-ASA) + Azathioprine therapy than controls ( P < .05). Combined therapy with 5-ASA + Adalimumab led to the strongest changes in marker modulation: IL-4, IL-5, IL-15, and PDGF-BB, were upregulated ( P < .05). Elevated serum levels of G-CSF, IL-1Ra, and PDGF-BB were associated with IBD endoscopic activity, and of IP-10 with extraintestinal manifestations of IBD. Combined therapy of 5-ASA + Adalimumab produced significant upregulation of IL-4, IL-5, IL-15, and PDGF-BB. This information may be useful for deciding on the course of pharmacologic therapy for patients with IBD and for generating new therapy alternatives to improve the outcome of patients with IBD. |
Author | Rocha-Pizaña, Maria R. Ortiz-Castro, Yolanda Rodriguez-Sanchez, Iram P. Trejo-Vazquez, Fabiola Villela-Ramirez, Gabriela A. Martinez-Fierro, Margarita L. Garza-Veloz, Idalia Flores-Morales, Virginia Cid-Baez, Miguel A. Delgado-Enciso, Ivan Cardenas-Vargas, Edith |
AuthorAffiliation | Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS Laboratorio de Sintesis Asimetrica y Bioenergetica (LSAyB), Ingenieria Quimica, Universidad Autonoma de Zacatecas, Zacatecas Tecnologico de Monterrey, Escuela de Ingenieria y Ciencias, Puebla School of Medicine, University of Colima, and Cancerology State Institute, Colima State Health Services, Colima Laboratorio de Fisiologia Molecular y Estructural, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, Monterrey Nuevo Leon, Mexico |
AuthorAffiliation_xml | – name: Laboratorio de Fisiologia Molecular y Estructural, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, Monterrey Nuevo Leon, Mexico – name: Laboratorio de Sintesis Asimetrica y Bioenergetica (LSAyB), Ingenieria Quimica, Universidad Autonoma de Zacatecas, Zacatecas – name: School of Medicine, University of Colima, and Cancerology State Institute, Colima State Health Services, Colima – name: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – name: Tecnologico de Monterrey, Escuela de Ingenieria y Ciencias, Puebla – name: c Tecnologico de Monterrey, Escuela de Ingenieria y Ciencias, Puebla – name: d Hospital General Zacatecas “Luz González Cosío”, Servicios de Salud de Zacatecas – name: g School of Medicine, University of Colima, and Cancerology State Institute, Colima State Health Services, Colima – name: e Hospital General de Zacatecas, Instituto de Seguridad y Servicios Sociales para los Trabajadores del Estado (ISSSTE) – name: h Laboratorio de Fisiologia Molecular y Estructural, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, Monterrey Nuevo Leon, Mexico – name: f Laboratorio de Sintesis Asimetrica y Bioenergetica (LSAyB), Ingenieria Quimica, Universidad Autonoma de Zacatecas, Zacatecas – name: a Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – name: b Posgrado en Ingenieria y Tecnologia Aplicada, Unidad Academica de Ingenieria Electrica, Universidad Autonoma de Zacatecas, Zacatecas |
Author_xml | – sequence: 1 givenname: Margarita L. surname: Martinez-Fierro fullname: Martinez-Fierro, Margarita L. organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 2 givenname: Idalia surname: Garza-Veloz fullname: Garza-Veloz, Idalia organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 3 givenname: Maria R. surname: Rocha-Pizaña fullname: Rocha-Pizaña, Maria R. organization: Tecnologico de Monterrey, Escuela de Ingenieria y Ciencias, Puebla – sequence: 4 givenname: Edith surname: Cardenas-Vargas fullname: Cardenas-Vargas, Edith organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 5 givenname: Miguel A. surname: Cid-Baez fullname: Cid-Baez, Miguel A. organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 6 givenname: Fabiola surname: Trejo-Vazquez fullname: Trejo-Vazquez, Fabiola organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 7 givenname: Virginia surname: Flores-Morales fullname: Flores-Morales, Virginia organization: Laboratorio de Sintesis Asimetrica y Bioenergetica (LSAyB), Ingenieria Quimica, Universidad Autonoma de Zacatecas, Zacatecas – sequence: 8 givenname: Gabriela A. surname: Villela-Ramirez fullname: Villela-Ramirez, Gabriela A. organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS – sequence: 9 givenname: Ivan surname: Delgado-Enciso fullname: Delgado-Enciso, Ivan organization: School of Medicine, University of Colima, and Cancerology State Institute, Colima State Health Services, Colima – sequence: 10 givenname: Iram P. surname: Rodriguez-Sanchez fullname: Rodriguez-Sanchez, Iram P. organization: Laboratorio de Fisiologia Molecular y Estructural, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, Monterrey Nuevo Leon, Mexico – sequence: 11 givenname: Yolanda surname: Ortiz-Castro fullname: Ortiz-Castro, Yolanda organization: Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS |
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SubjectTerms | Adalimumab - therapeutic use Adult Aged Anti-Inflammatory Agents - therapeutic use Azathioprine - therapeutic use Becaplermin - blood Biomarkers - blood Case-Control Studies Chemokine CXCL10 - blood Chemokines - blood Cytokines - blood Female Granulocyte Colony-Stimulating Factor - blood Humans Inflammatory Bowel Diseases - blood Inflammatory Bowel Diseases - drug therapy Intercellular Signaling Peptides and Proteins - blood Interleukin-6 - blood Male Mesalamine - therapeutic use Middle Aged Observational Study Receptors, Interleukin-1 - blood |
Title | Serum cytokine, chemokine, and growth factor profiles and their modulation in inflammatory bowel disease |
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