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Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies.

Publication ,  Journal Article
Simon, TG; King, LY; Chong, DQ; Nguyen, LH; Ma, Y; VoPham, T; Giovannucci, EL; Fuchs, CS; Meyerhardt, JA; Corey, KE; Khalili, H; Chung, RT ...
Published in: Hepatology
May 2018

UNLABELLED: Type 2 diabetes (T2D) is a risk factor for hepatocellular carcinoma (HCC). However, it is unknown whether T2D duration or additional metabolic comorbidities further contribute to HCC risk. From the Nurses' Health Study (NHS), 120,826 women were enrolled in 1980, and from the Health Professionals Follow-up Study (HPFS), 50,284 men were enrolled in 1986 and followed through 2012. Physician-diagnosed T2D was ascertained at baseline and updated biennially. Cox proportional hazards regression models were used to calculate age- and multivariable-adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) for incident HCC. Over 32 years of follow-up (4,488,410 person-years), we documented 112 cases of HCC (69 women, 43 men). T2D was associated with an increased HCC risk (multivariable HR, 4.59; 95% CI, 2.98-7.07), as was an increasing T2D duration (Ptrend  < 0.001). Compared to nondiabetics, the multivariable HRs for HCC were 2.96 (95% CI, 1.57-5.60) for 0-<2 years; 6.08 (95% CI, 2.96-12.50) for 2-<10 years; and 7.52 (95% CI, 3.88-14.58) for ≥10 years. Increasing number of metabolic comorbidities (T2D, obesity, hypertension, and dyslipidemia) was associated with increased HCC risk (Ptrend  < 0.001); compared to individuals without metabolic comorbidity, those with four metabolic comorbidities had an 8.1-fold increased HCC risk (95% CI, 2.48-26.7). In T2D, neither insulin use nor oral hypoglycemic use was significantly associated with HCC risk (HR, 2.04 [95% CI, 0.69-6.09] and HR, 1.45 [95% CI, 0.69-3.07], respectively). CONCLUSION: T2D is independently associated with increased risk for HCC in two prospective cohorts of U.S. men and women. This risk is enhanced with prolonged diabetes duration and with comorbid metabolic conditions, suggesting the importance of insulin resistance in the pathogenesis of HCC. (Hepatology 2018;67:1797-1806).

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Published In

Hepatology

DOI

EISSN

1527-3350

Publication Date

May 2018

Volume

67

Issue

5

Start / End Page

1797 / 1806

Location

United States

Related Subject Headings

  • United States
  • Risk Factors
  • Prospective Studies
  • Middle Aged
  • Metabolic Syndrome
  • Male
  • Liver Neoplasms
  • Humans
  • Gastroenterology & Hepatology
  • Follow-Up Studies
 

Citation

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Simon, T. G., King, L. Y., Chong, D. Q., Nguyen, L. H., Ma, Y., VoPham, T., … Chan, A. T. (2018). Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies. Hepatology, 67(5), 1797–1806. https://doi.org/10.1002/hep.29660
Simon, Tracey G., Lindsay Y. King, Dawn Q. Chong, Long H. Nguyen, Yanan Ma, Trang VoPham, Edward L. Giovannucci, et al. “Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies.Hepatology 67, no. 5 (May 2018): 1797–1806. https://doi.org/10.1002/hep.29660.
Simon TG, King LY, Chong DQ, Nguyen LH, Ma Y, VoPham T, et al. Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies. Hepatology. 2018 May;67(5):1797–806.
Simon, Tracey G., et al. “Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies.Hepatology, vol. 67, no. 5, May 2018, pp. 1797–806. Pubmed, doi:10.1002/hep.29660.
Simon TG, King LY, Chong DQ, Nguyen LH, Ma Y, VoPham T, Giovannucci EL, Fuchs CS, Meyerhardt JA, Corey KE, Khalili H, Chung RT, Zhang X, Chan AT. Diabetes, metabolic comorbidities, and risk of hepatocellular carcinoma: Results from two prospective cohort studies. Hepatology. 2018 May;67(5):1797–1806.
Journal cover image

Published In

Hepatology

DOI

EISSN

1527-3350

Publication Date

May 2018

Volume

67

Issue

5

Start / End Page

1797 / 1806

Location

United States

Related Subject Headings

  • United States
  • Risk Factors
  • Prospective Studies
  • Middle Aged
  • Metabolic Syndrome
  • Male
  • Liver Neoplasms
  • Humans
  • Gastroenterology & Hepatology
  • Follow-Up Studies