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Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma

BACKGROUND: The impact of obesity on the prognosis of hepatocellular carcinoma (HCC) has not been well characterized in a Chinese population. Therefore, the aim of this study was to examine the influence of BMI on the clinicopathological characteristics and mortality of patients with HCC. METHODS: T...

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Autores principales: Li, Qinggang, Xing, Hui, Liu, Dan, Li, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596284/
https://www.ncbi.nlm.nih.gov/pubmed/26444667
http://dx.doi.org/10.1186/s12957-015-0713-4
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author Li, Qinggang
Xing, Hui
Liu, Dan
Li, Hui
author_facet Li, Qinggang
Xing, Hui
Liu, Dan
Li, Hui
author_sort Li, Qinggang
collection PubMed
description BACKGROUND: The impact of obesity on the prognosis of hepatocellular carcinoma (HCC) has not been well characterized in a Chinese population. Therefore, the aim of this study was to examine the influence of BMI on the clinicopathological characteristics and mortality of patients with HCC. METHODS: The study cohort consisted of 379 patients who were diagnosed with HCC at the First Affiliated Hospital of Harbin Medical University between June 2012 and August 2014. Study subjects were divided into two body mass index (BMI) categories: normal weight (BMI <23 kg/m(2)) and overweight (BMI ≥23 kg/m(2)). RESULTS: Of the 379 patients, 44 (11.6 %) were underweight (<18.5 kg/m(2)), 172 (45.4 %) had a normal weight (18.5 ≤ BMI < 23.0), 133 (35.1 %) were overweight (23.0 ≤ BMI < 27.5), and 30 (7.9 %) were obese (BMI ≥27.5). After a median follow-up time of 296 (range, 15–720) days, 168 (44.3 %) patients died with median survival time of 159 (range, 15–690) days. Patients with lower BMIs also exhibited a higher liver-related mortality rate (60.6 vs. 22.7 %; p = 1.8 × 10(−13)) and a shorter survival time (353 days vs. 571 days; p = 6.2 × 10(−6)) than patients with higher BMIs. In multivariate analysis, the BMI class was also found to be a significant independent impact factor for overall survival (p = 2.2 × 10(−8)), age, alpha-fetoprotein level, Child–Pugh score, treatment strategy, antiviral treatment, extrahepatic metastasis, and tumor infiltration of the portal vein. CONCLUSIONS: Our data suggest that lower BMI has a significant impact regarding poor outcomes in patients with HCC. To better understand the impact of BMI on the prognosis of HCC patients, more large-scale cohort studies will be necessary.
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spelling pubmed-45962842015-10-08 Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma Li, Qinggang Xing, Hui Liu, Dan Li, Hui World J Surg Oncol Research BACKGROUND: The impact of obesity on the prognosis of hepatocellular carcinoma (HCC) has not been well characterized in a Chinese population. Therefore, the aim of this study was to examine the influence of BMI on the clinicopathological characteristics and mortality of patients with HCC. METHODS: The study cohort consisted of 379 patients who were diagnosed with HCC at the First Affiliated Hospital of Harbin Medical University between June 2012 and August 2014. Study subjects were divided into two body mass index (BMI) categories: normal weight (BMI <23 kg/m(2)) and overweight (BMI ≥23 kg/m(2)). RESULTS: Of the 379 patients, 44 (11.6 %) were underweight (<18.5 kg/m(2)), 172 (45.4 %) had a normal weight (18.5 ≤ BMI < 23.0), 133 (35.1 %) were overweight (23.0 ≤ BMI < 27.5), and 30 (7.9 %) were obese (BMI ≥27.5). After a median follow-up time of 296 (range, 15–720) days, 168 (44.3 %) patients died with median survival time of 159 (range, 15–690) days. Patients with lower BMIs also exhibited a higher liver-related mortality rate (60.6 vs. 22.7 %; p = 1.8 × 10(−13)) and a shorter survival time (353 days vs. 571 days; p = 6.2 × 10(−6)) than patients with higher BMIs. In multivariate analysis, the BMI class was also found to be a significant independent impact factor for overall survival (p = 2.2 × 10(−8)), age, alpha-fetoprotein level, Child–Pugh score, treatment strategy, antiviral treatment, extrahepatic metastasis, and tumor infiltration of the portal vein. CONCLUSIONS: Our data suggest that lower BMI has a significant impact regarding poor outcomes in patients with HCC. To better understand the impact of BMI on the prognosis of HCC patients, more large-scale cohort studies will be necessary. BioMed Central 2015-10-06 /pmc/articles/PMC4596284/ /pubmed/26444667 http://dx.doi.org/10.1186/s12957-015-0713-4 Text en © Li et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Qinggang
Xing, Hui
Liu, Dan
Li, Hui
Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title_full Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title_fullStr Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title_full_unstemmed Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title_short Negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
title_sort negative impact of low body mass index on liver cirrhosis patients with hepatocellular carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596284/
https://www.ncbi.nlm.nih.gov/pubmed/26444667
http://dx.doi.org/10.1186/s12957-015-0713-4
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