4.5 Article

NAFLD polygenic risk score and risk of hepatocellular carcinoma in an East Asian population

Journal

HEPATOLOGY COMMUNICATIONS
Volume 6, Issue 9, Pages 2310-2321

Publisher

JOHN WILEY & SONS LTD
DOI: 10.1002/hep4.1976

Keywords

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Funding

  1. National Medical Research Council, Singapore [NMRC/CIRG/1456/2016]
  2. National Research Foundation, Singapore [370062002]
  3. U.S. National Institutes of Health (NIH) [R01 CA144034, UM1 CA182876]
  4. NIH [T32 CA186873]
  5. Cancer Center Support Grant from the National Cancer Institute [P30 CA047904]

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Using data from the Singapore Chinese Health Study (SCHS), researchers found a strong correlation between a polygenic risk score (PRS) for hepatic fat (HFC-PRS) and nonalcoholic fatty liver disease (NAFLD), as well as an increased risk of hepatocellular carcinoma (HCC).
It is difficult to identify people with nonalcoholic fatty liver disease (NAFLD) who are at high risk for developing hepatocellular carcinoma (HCC). A polygenic risk score (PRS) for hepatic fat (HFC-PRS) derived from non-Asians has been reported to be associated with HCC risk in European populations. However, population-level data of this risk in Asian populations are lacking. Utilizing resources from 24,333 participants of the Singapore Chinese Health Study (SCHS), we examined the relationship between the HFC-PRS and HCC risk. In addition, we constructed and evaluated a NAFLD-related PRS (NAFLD-PRS) with HCC risk in the SCHS. Cox proportional hazards models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) of HCC incidence with both HFC-PRS and NAFLD-PRS. The HFC-PRS and NAFLD-PRS were highly correlated (Spearman r = 0.79, p < 0.001). The highest quartiles of both the HFC-PRS and the NAFLD-PRS were associated with significantly increased risk of HCC with HR of 2.39 (95% CI 1.51, 3.78) and 1.77 (95% CI 1.15, 2.73), respectively, compared with their respective lowest quartile. Conclusion: The PRS for hepatic fat content or NAFLD may be useful for assessing HCC risk in both Asian and European populations. The findings of this and prior studies support a potential causal role of genetically determined NAFLD in HCC development.

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