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Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA

BACKGROUND: Adsorptive granulocyte and monocyte apheresis (GMA) with an Adacolumn in patients with ulcerative colitis (UC) has been applied as a non-pharmacological treatment strategy, but the efficacy has been encouraging as well as discouraging, depending on patients’ demography at entry. In this...

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Autores principales: Yokoyama, Yoko, Kawai, Mikio, Fukunaga, Ken, Kamikozuru, Koji, Nagase, Kazuko, Nogami, Koji, Kono, Tomoaki, Ohda, Yoshio, Iimuro, Masaki, Hida, Nobuyuki, Nakamura, Shiro, Miwa, Hiroto, Matsumoto, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583683/
https://www.ncbi.nlm.nih.gov/pubmed/23399416
http://dx.doi.org/10.1186/1471-230X-13-27
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author Yokoyama, Yoko
Kawai, Mikio
Fukunaga, Ken
Kamikozuru, Koji
Nagase, Kazuko
Nogami, Koji
Kono, Tomoaki
Ohda, Yoshio
Iimuro, Masaki
Hida, Nobuyuki
Nakamura, Shiro
Miwa, Hiroto
Matsumoto, Takayuki
author_facet Yokoyama, Yoko
Kawai, Mikio
Fukunaga, Ken
Kamikozuru, Koji
Nagase, Kazuko
Nogami, Koji
Kono, Tomoaki
Ohda, Yoshio
Iimuro, Masaki
Hida, Nobuyuki
Nakamura, Shiro
Miwa, Hiroto
Matsumoto, Takayuki
author_sort Yokoyama, Yoko
collection PubMed
description BACKGROUND: Adsorptive granulocyte and monocyte apheresis (GMA) with an Adacolumn in patients with ulcerative colitis (UC) has been applied as a non-pharmacological treatment strategy, but the efficacy has been encouraging as well as discouraging, depending on patients’ demography at entry. In this study, we looked for predictive factors for clinical response to GMA in patients with UC. METHODS: In a retrospective setting, 43 outpatients who had been treated with GMA for active UC were evaluated. Patients were divided into remission group and non-remission group based on Lichtiger’s clinical activity index (CAI) before and after 10, once a week GMA sessions. The efficacy was analysed in relation to patients’ demographic variables. To determine predictive factors that closely related to the response to GMA, receiver operating characteristic (ROC) curve, and multiple logistic regression analyses were applied. RESULTS: After 10 GMA sessions, the overall clinical remission rate (CAI < 4) was 53.5%. Multiple logistic regression and ROC analyses showed that the interval between relapse and the first GMA session was a significant and independent predictive factor for clinical response to GMA (P = 0.016); the clinical response was better in patients who received GMA immediately after a relapse and vice versa. Likewise, univariate analyses showed that, the duration of UC (P = 0.036) and the cumulative prednisolone (PSL) dose (P = 0.006) before the first GMA session were significantly greater in the GMA non-responder group as compared with the responder group. Additionally, a lower white blood cell (WBC) count at first GMA session was related to clinical response to GMA (P = 0.032). CONCLUSIONS: In this study, patients with a short duration of UC and low cumulative PSL dose seemed to respond well to GMA. However, we found that the best responders were patients who received GMA immediately after a clinical relapse. Additionally, GMA was effective in patients with low WBC count at the first GMA session. The findings of this study should spare medical cost and reduce morbidity time for many patients, relevant for decision making in clinical settings.
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spelling pubmed-35836832013-02-28 Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA Yokoyama, Yoko Kawai, Mikio Fukunaga, Ken Kamikozuru, Koji Nagase, Kazuko Nogami, Koji Kono, Tomoaki Ohda, Yoshio Iimuro, Masaki Hida, Nobuyuki Nakamura, Shiro Miwa, Hiroto Matsumoto, Takayuki BMC Gastroenterol Research Article BACKGROUND: Adsorptive granulocyte and monocyte apheresis (GMA) with an Adacolumn in patients with ulcerative colitis (UC) has been applied as a non-pharmacological treatment strategy, but the efficacy has been encouraging as well as discouraging, depending on patients’ demography at entry. In this study, we looked for predictive factors for clinical response to GMA in patients with UC. METHODS: In a retrospective setting, 43 outpatients who had been treated with GMA for active UC were evaluated. Patients were divided into remission group and non-remission group based on Lichtiger’s clinical activity index (CAI) before and after 10, once a week GMA sessions. The efficacy was analysed in relation to patients’ demographic variables. To determine predictive factors that closely related to the response to GMA, receiver operating characteristic (ROC) curve, and multiple logistic regression analyses were applied. RESULTS: After 10 GMA sessions, the overall clinical remission rate (CAI < 4) was 53.5%. Multiple logistic regression and ROC analyses showed that the interval between relapse and the first GMA session was a significant and independent predictive factor for clinical response to GMA (P = 0.016); the clinical response was better in patients who received GMA immediately after a relapse and vice versa. Likewise, univariate analyses showed that, the duration of UC (P = 0.036) and the cumulative prednisolone (PSL) dose (P = 0.006) before the first GMA session were significantly greater in the GMA non-responder group as compared with the responder group. Additionally, a lower white blood cell (WBC) count at first GMA session was related to clinical response to GMA (P = 0.032). CONCLUSIONS: In this study, patients with a short duration of UC and low cumulative PSL dose seemed to respond well to GMA. However, we found that the best responders were patients who received GMA immediately after a clinical relapse. Additionally, GMA was effective in patients with low WBC count at the first GMA session. The findings of this study should spare medical cost and reduce morbidity time for many patients, relevant for decision making in clinical settings. BioMed Central 2013-02-12 /pmc/articles/PMC3583683/ /pubmed/23399416 http://dx.doi.org/10.1186/1471-230X-13-27 Text en Copyright ©2013 Yokoyama et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yokoyama, Yoko
Kawai, Mikio
Fukunaga, Ken
Kamikozuru, Koji
Nagase, Kazuko
Nogami, Koji
Kono, Tomoaki
Ohda, Yoshio
Iimuro, Masaki
Hida, Nobuyuki
Nakamura, Shiro
Miwa, Hiroto
Matsumoto, Takayuki
Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title_full Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title_fullStr Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title_full_unstemmed Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title_short Looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to GMA
title_sort looking for predictive factors of clinical response to adsorptive granulocyte and monocyte apheresis in patients with ulcerative colitis: markers of response to gma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583683/
https://www.ncbi.nlm.nih.gov/pubmed/23399416
http://dx.doi.org/10.1186/1471-230X-13-27
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