An epidemiological study on the factors including genetic polymorphism influencing ALT >30 U/L and liver fibrosis progression in metabolic dysfunction‐associated steatotic liver disease among the general population
2024

Factors Influencing ALT Levels and Liver Fibrosis in MASLD

Sample size: 228 publication Evidence: moderate

Author Information

Author(s): S Sato, Iino Chikara, Sasada Takafumi, Soma Go, Furusawa Keisuke, Yoshida Kenta, Sawada Kaori, Mikami Tatsuya, Fukuda Shinsaku, Nakaji Shigeyuki, Sakuraba Hirotake

Primary Institution: Hirosaki University Graduate School of Medicine

Hypothesis

This study aimed to investigate factors, including genetic polymorphisms, associated with elevated ALT levels and liver fibrosis in patients with metabolic dysfunction‐associated steatotic liver disease (MASLD).

Conclusion

An individualized treatment approach is warranted for patients with MASLD due to the influence of various factors on its progression, including genetic factors and lifestyle diseases.

Supporting Evidence

  • Male sex, younger age, and high triglyceride levels were significant risk factors for ALT levels >30 U/L.
  • GG genotypes of PNPLA3 rs738409 and rs2896019 were significant risk factors for elevated ALT levels.
  • The study included 228 patients diagnosed with MASLD.

Takeaway

This study found that being male, younger, having high triglycerides, and certain genetic factors can lead to higher liver enzyme levels in people with a specific liver disease.

Methodology

The study analyzed 228 participants diagnosed with MASLD from a health checkup project, measuring liver fat content and stiffness using FibroScan and assessing 13 SNPs related to NAFLD.

Limitations

The study used FibroScan instead of liver biopsy for diagnosis, which may not be as accurate, and the results may not be generalizable to other ethnicities.

Participant Demographics

Participants were adults aged 19–88 years, with a significant portion being male.

Statistical Information

P-Value

0.004 and 0.007 for SNPs

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1002/jgh3.70043

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