Skip to main content
Article thumbnail
Location of Repository

Relative telomere length: a novel non-invasive biomarker for the risk of non-cirrhotic hepatocellular carcinoma in patients with chronic hepatitis B infection.

By Xiaoying Fu, Shaogui Wan, Hie-Won MD Hann, Ronald E PhD Myers, Richard S Hann, Jennifer Au, Bicui Chen, Jinliang Xing and Hushan Yang

Abstract

BACKGROUND AND AIMS: Telomere length has emerged as a promising risk predictor of various cancers including hepatocellular carcinoma (HCC). However, the majority of studies in this area measured telomere length in hepatocytes and one in lymphocytes with conflicting results. Moreover, no studies have been reported on using circulating DNA telomere length as a non-invasive HCC biomarker. METHODS: We conducted a nested case-control study to determine the relative telomere length (RTL) in serum DNA from 140 hepatitis B virus (HBV)-related HCC cases and 280 frequency-matched cancer-free HBV controls. RESULTS: Cases had a significantly longer RTL (median, 0.31; range, 0.02-2.31) than controls (median, 0.20; range, 0.01-1.60) (P = 0.003). Consistently, longer RTLs conferred a significantly increased HCC risk compared to short RTLs in a univariate logistic regression analysis (odds ratio [OR] = 1.55, 95% confidence interval [CI] = 1.02-2.33, P = 0.038). This association attenuated after multivariate adjustment (OR = 1.40, 95% CI = 0.90-2.19, P = 0.132). In a quartile analysis, a significant dose-response relationship was noted in univariate analysis (P(trend) = 0.017) which was again attenuated in multivariate analysis (P(trend) = 0.079). Further analyses revealed that the significant association between serum RTL and HCC risk was evident in non-cirrhotic (OR = 3.54, 95% CI 1.58-7.93 P = 0.002), but not cirrhotic (OR = 0.95, 95% CI 0.55-1.64, P = 0.860) HBV patients. Moreover, the significantly increased HCC risk conferred by cirrhosis was modulated by RTL with a significant interaction effect (P(interaction) = 0.013). CONCLUSIONS: RTL in circulating cell-free serum DNA could potentially be used as a novel non-invasive biomarker for non-cirrhotic HCC. Prospective cohort studies are warranted to validate this finding and assess its clinical significance in HCC prevention

Topics: Biological Markers, Carcinoma, Hepatocellular, Case-Control Studies, Female, Hepatitis B, Chronic, Humans, Liver Neoplasms, Male, Middle Aged, Risk Factors, Serum, Telomere Homeostasis, Carcinoma, Hepatocellular, Hepatitis B, Chronic, Gastroenterology, Hepatology
Publisher: Jefferson Digital Commons
Year: 2012
OAI identifier: oai:jdc.jefferson.edu:gastro_hepfp-1011

Suggested articles


To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.