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  4. Increased risk of hepatocellular carcinoma in chronic hepatitis C patients with new onset diabetes: A nation-wide cohort study
 
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Increased risk of hepatocellular carcinoma in chronic hepatitis C patients with new onset diabetes: A nation-wide cohort study

Journal
Alimentary Pharmacology and Therapeutics
Journal Volume
42
Journal Issue
7
Pages
902-911
Date Issued
2015
Author(s)
YI-WEN HUANG  
Wang T.-C.
Yang S.-S.
Lin S.-Y.
Fu S.-C.
Hu J.-T.
CHUN-JEN LIU  
JIA-HORNG KAO  
DING-SHINN CHEN  
DOI
10.1111/apt.13341
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84940787488&doi=10.1111%2fapt.13341&partnerID=40&md5=ab2fbeb8d4ffb5e648289f7768fb49fe
https://scholars.lib.ntu.edu.tw/handle/123456789/581934
Abstract
Background The impact of diabetes for hepatocellular carcinoma (HCC) development in chronic hepatitis C (CHC) patients remains controversial. Aim To investigate the risk of HCC in CHC patients who develop new onset diabetes. Methods We conducted a nation-wide cohort study by using Taiwanese National Health Insurance Research Database, which comprised of data from >99% of entire population. Among randomly sampled one million enrollees, 6251 adult CHC patients were identified from 1997 to 2009. Diabetes was defined as new onset in the patient who was given the diagnosis in the years 1999-2009 but not in 1997-1998. The cohorts of CHC with new onset diabetes (n = 1100) and 1:1 ratio age-, gender-, and inception point (onset date of diabetes) matched nondiabetes (n = 1087) were followed up from the inception point until the development of HCC, withdrawal from insurance, or December 2009. Results After adjustment for competing mortality, patients with new onset diabetes had a significantly higher cumulative incidence of HCC (Relative Risk = 1.544, 95% CI = 1.000-2.387, modified log-rank test, P = 0.047) as compared to those without. After adjustment for age, gender, cirrhosis, hyperlipidaemia, CHC treatment, diabetes treatment, comorbidity index, obesity and statins therapy by Cox proportional hazard model, diabetes was still an independent predictor for HCC (hazard ratio (HR) = 1.906, 95% CI = 1.102-3.295, P = 0.021). The risk for HCC was increased in those who were 40-59 years old, independent of other variables (HR = 3.086, 95% CI = 1.045-9.112, P = 0.041), and after adjustment for competing mortality (modified log-rank test, P = 0.009). Conclusion Chronic hepatitis C patients who develop diabetes are at an increased risk of hepatocellular carcinoma over time. ? 2015 John Wiley & Sons Ltd.
SDGs

[SDGs]SDG3

Other Subjects
antidiabetic agent; hydroxymethylglutaryl coenzyme A reductase inhibitor; interferon; ribavirin; adult; aged; Article; cancer incidence; cancer risk; chronic hepatitis C; cohort analysis; comorbidity; controlled study; diabetes mellitus; diabetic patient; diagnostic test; disease association; female; gender; health insurance; high risk patient; human; hyperlipidemia; liver cell carcinoma; liver cirrhosis; major clinical study; male; middle aged; mortality; obesity; onset age; population research; prediction; priority journal; randomization; risk assessment; Taiwanese; very elderly; young adult; Carcinoma, Hepatocellular; case control study; complication; diabetes mellitus; Hepatitis C, Chronic; incidence; liver cirrhosis; Liver Neoplasms; risk factor; Taiwan; Adult; Aged; Carcinoma, Hepatocellular; Case-Control Studies; Cohort Studies; Diabetes Mellitus; Female; Hepatitis C, Chronic; Humans; Incidence; Liver Cirrhosis; Liver Neoplasms; Male; Middle Aged; Risk Factors; Taiwan
Publisher
Blackwell Publishing Ltd
Type
journal article

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