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Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices
To the best of our knowledge, no available data with regard to changes in skeletal muscle mass for liver cirrhosis (LC) patients with esophageal varices (EVs) undergoing endoscopic therapy as a primary prophylaxis could exist. As endoscopic therapies, such as endoscopic injection sclerotherapy or en...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500087/ https://www.ncbi.nlm.nih.gov/pubmed/28658165 http://dx.doi.org/10.1097/MD.0000000000007377 |
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author | Sakai, Yoshiyuki Nishikawa, Hiroki Enomoto, Hirayuki Yoh, Kazunori Ishii, Akio Iwata, Yoshinori Miyamoto, Yuho Ishii, Noriko Yuri, Yukihisa Hasegawa, Kunihiro Nakano, Chikage Nishimura, Takashi Aizawa, Nobuhiro Ikeda, Naoto Takashima, Tomoyuki Takata, Ryo Iijima, Hiroko Nishiguchi, Shuhei |
author_facet | Sakai, Yoshiyuki Nishikawa, Hiroki Enomoto, Hirayuki Yoh, Kazunori Ishii, Akio Iwata, Yoshinori Miyamoto, Yuho Ishii, Noriko Yuri, Yukihisa Hasegawa, Kunihiro Nakano, Chikage Nishimura, Takashi Aizawa, Nobuhiro Ikeda, Naoto Takashima, Tomoyuki Takata, Ryo Iijima, Hiroko Nishiguchi, Shuhei |
author_sort | Sakai, Yoshiyuki |
collection | PubMed |
description | To the best of our knowledge, no available data with regard to changes in skeletal muscle mass for liver cirrhosis (LC) patients with esophageal varices (EVs) undergoing endoscopic therapy as a primary prophylaxis could exist. As endoscopic therapies, such as endoscopic injection sclerotherapy or endoscopic band ligation for EVs, accompany invasive procedure and patients with EVs receiving endoscopic therapies mostly rest in bed during hospitalization, clarifying these issues are clinically of importance. The purposes of this study were therefore to examine changes in skeletal muscle mass for LC patients with EVs undergoing endoscopic therapy as a primary prophylaxis and to identify pretreatment predictors which are associated with the amelioration in skeletal muscle mass. This is a subgroup analysis in our previous randomized controlled trial. A total of 51 LC patients with EVs were analyzed. Skeletal muscle mass was assessed using bioimpedance analysis (BIA). Skeletal muscle index (SMI) was defined as sum of skeletal muscle mass in body trunk and upper and lower extremities divided by height squared (cm(2)/m(2)) using data for BIA. We compared the changes in SMI at baseline and SMI at Day 50 after endoscopic treatment for EVs. Our study cohort included 33 males and 18 females with median (range) age of 62 (29–81) years. There were 31 patients with Child–Pugh A and 20 with Child–Pugh B. The median SMI for the entire cohort at baseline was 8.96 cm(2)/m(2) (range, 5.87–13.11 cm(2)/m(2)), while the median SMI for the entire cohort at Day 50 was 8.83 cm(2)/m(2) (range, 5.59–12.29 cm(2)/m(2)) (P = .9995). In baseline characteristics, prealbumin (P = .0477), branched-chain amino acid to tyrosine ratio (BTR) (P = .0056), and retinol-binding protein (P = .0296) in the increased SMI group (n = 15) were significantly higher than those in the nonincreased SMI group (n = 36). Multivariate analysis for the above 3 significant factors showed that only BTR was a significant prognostic pretreatment factor linked to the presence of increased SMI (P = .0235). In conclusion, pretreatment BTR level can be helpful for predicting increased SMI after endoscopic therapy as a primary prophylaxis for LC patients with EVs. |
format | Online Article Text |
id | pubmed-5500087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-55000872017-07-17 Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices Sakai, Yoshiyuki Nishikawa, Hiroki Enomoto, Hirayuki Yoh, Kazunori Ishii, Akio Iwata, Yoshinori Miyamoto, Yuho Ishii, Noriko Yuri, Yukihisa Hasegawa, Kunihiro Nakano, Chikage Nishimura, Takashi Aizawa, Nobuhiro Ikeda, Naoto Takashima, Tomoyuki Takata, Ryo Iijima, Hiroko Nishiguchi, Shuhei Medicine (Baltimore) 4500 To the best of our knowledge, no available data with regard to changes in skeletal muscle mass for liver cirrhosis (LC) patients with esophageal varices (EVs) undergoing endoscopic therapy as a primary prophylaxis could exist. As endoscopic therapies, such as endoscopic injection sclerotherapy or endoscopic band ligation for EVs, accompany invasive procedure and patients with EVs receiving endoscopic therapies mostly rest in bed during hospitalization, clarifying these issues are clinically of importance. The purposes of this study were therefore to examine changes in skeletal muscle mass for LC patients with EVs undergoing endoscopic therapy as a primary prophylaxis and to identify pretreatment predictors which are associated with the amelioration in skeletal muscle mass. This is a subgroup analysis in our previous randomized controlled trial. A total of 51 LC patients with EVs were analyzed. Skeletal muscle mass was assessed using bioimpedance analysis (BIA). Skeletal muscle index (SMI) was defined as sum of skeletal muscle mass in body trunk and upper and lower extremities divided by height squared (cm(2)/m(2)) using data for BIA. We compared the changes in SMI at baseline and SMI at Day 50 after endoscopic treatment for EVs. Our study cohort included 33 males and 18 females with median (range) age of 62 (29–81) years. There were 31 patients with Child–Pugh A and 20 with Child–Pugh B. The median SMI for the entire cohort at baseline was 8.96 cm(2)/m(2) (range, 5.87–13.11 cm(2)/m(2)), while the median SMI for the entire cohort at Day 50 was 8.83 cm(2)/m(2) (range, 5.59–12.29 cm(2)/m(2)) (P = .9995). In baseline characteristics, prealbumin (P = .0477), branched-chain amino acid to tyrosine ratio (BTR) (P = .0056), and retinol-binding protein (P = .0296) in the increased SMI group (n = 15) were significantly higher than those in the nonincreased SMI group (n = 36). Multivariate analysis for the above 3 significant factors showed that only BTR was a significant prognostic pretreatment factor linked to the presence of increased SMI (P = .0235). In conclusion, pretreatment BTR level can be helpful for predicting increased SMI after endoscopic therapy as a primary prophylaxis for LC patients with EVs. Wolters Kluwer Health 2017-06-30 /pmc/articles/PMC5500087/ /pubmed/28658165 http://dx.doi.org/10.1097/MD.0000000000007377 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 4500 Sakai, Yoshiyuki Nishikawa, Hiroki Enomoto, Hirayuki Yoh, Kazunori Ishii, Akio Iwata, Yoshinori Miyamoto, Yuho Ishii, Noriko Yuri, Yukihisa Hasegawa, Kunihiro Nakano, Chikage Nishimura, Takashi Aizawa, Nobuhiro Ikeda, Naoto Takashima, Tomoyuki Takata, Ryo Iijima, Hiroko Nishiguchi, Shuhei Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title | Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title_full | Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title_fullStr | Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title_full_unstemmed | Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title_short | Changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
title_sort | changes in skeletal muscle mass after endoscopic treatment in patients with esophageal varices |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500087/ https://www.ncbi.nlm.nih.gov/pubmed/28658165 http://dx.doi.org/10.1097/MD.0000000000007377 |
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