TY - JOUR
T1 - Hypozincemia Is Associated With Increased Tyrosine Levels, Low Handgrip Strength, Increased Incidence of HCC, and Liver Disease Progression—A Cross-Sectional Study
AU - Kobayashi, Tomoo
AU - Inoue, Jun
AU - Tanaka, Yu
AU - Yamakawa, Mitsuru
AU - Kurihara, Makoto
AU - Handa, Tomoko
AU - Kondo, Yutaka
AU - Saitou, Akihiro
AU - Shiraki, Manabu
AU - Kojima, Yasuhiro
AU - Ohyauchi, Motoki
AU - Masamune, Atsushi
N1 - Publisher Copyright:
© 2025 The Author(s). JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.
PY - 2025/3
Y1 - 2025/3
N2 - Background: Serum zinc levels decrease in chronic liver disease (CLD), but their effects on liver reserve function, tyrosine, skeletal muscle mass, handgrip strength (HGS), and hepatocellular carcinoma (HCC) development remain poorly understood. Methods: A retrospective, cross-sectional study was conducted on 516 CLD cases. Patients were divided into a low zinc group (< 80 μg/dL) and a high zinc group (≥ 80 μg/dL). Serum zinc levels were analyzed with liver reserve function (assessed by modified albumin-bilirubin [mALBI] grade), tyrosine, branched-chain amino acid/tyrosine ratio (BTR), and HCC development. In 180 cases, the relationship between serum zinc levels and skeletal muscle characteristics, including sarcopenia and HGS, was investigated. Results: Tyrosine levels increased significantly with mALBI grade progression. Patients in the low zinc group had higher tyrosine levels (76.9 vs. 67.2 μmol/L, p < 0.001), a greater proportion of high tyrosine levels (5.3% vs. 1.7%, p < 0.001), and more HCC cases (10.5% vs. 3.7%, p < 0.005). Zinc levels were lower with more severe CLD (81 μg/dL [mALBI grade 1] vs. 35.2 μg/dL [grade 3], p < 0.001). Tyrosine levels were higher in HCC patients than in non-HCC patients (93.1 vs. 70.7 μmol/L, p < 0.001). Sarcopenia prevalence did not differ between groups (56.6% vs. 52.0%, p = 0.344), but low HGS was more frequent in low zinc patients (61.2% vs. 46.3%, p = 0.032). In a subset of patients with low zinc levels (n = 12), zinc supplementation reduced tyrosine levels after 3 months (86.3 vs. 73.3 μmol/L, p = 0.017). Conclusion: Hypozincemia is linked to elevated tyrosine levels, reduced HGS, increased HCC incidence, and CLD progression.
AB - Background: Serum zinc levels decrease in chronic liver disease (CLD), but their effects on liver reserve function, tyrosine, skeletal muscle mass, handgrip strength (HGS), and hepatocellular carcinoma (HCC) development remain poorly understood. Methods: A retrospective, cross-sectional study was conducted on 516 CLD cases. Patients were divided into a low zinc group (< 80 μg/dL) and a high zinc group (≥ 80 μg/dL). Serum zinc levels were analyzed with liver reserve function (assessed by modified albumin-bilirubin [mALBI] grade), tyrosine, branched-chain amino acid/tyrosine ratio (BTR), and HCC development. In 180 cases, the relationship between serum zinc levels and skeletal muscle characteristics, including sarcopenia and HGS, was investigated. Results: Tyrosine levels increased significantly with mALBI grade progression. Patients in the low zinc group had higher tyrosine levels (76.9 vs. 67.2 μmol/L, p < 0.001), a greater proportion of high tyrosine levels (5.3% vs. 1.7%, p < 0.001), and more HCC cases (10.5% vs. 3.7%, p < 0.005). Zinc levels were lower with more severe CLD (81 μg/dL [mALBI grade 1] vs. 35.2 μg/dL [grade 3], p < 0.001). Tyrosine levels were higher in HCC patients than in non-HCC patients (93.1 vs. 70.7 μmol/L, p < 0.001). Sarcopenia prevalence did not differ between groups (56.6% vs. 52.0%, p = 0.344), but low HGS was more frequent in low zinc patients (61.2% vs. 46.3%, p = 0.032). In a subset of patients with low zinc levels (n = 12), zinc supplementation reduced tyrosine levels after 3 months (86.3 vs. 73.3 μmol/L, p = 0.017). Conclusion: Hypozincemia is linked to elevated tyrosine levels, reduced HGS, increased HCC incidence, and CLD progression.
KW - chronic liver disease
KW - handgrip strength
KW - tyrosine
KW - zinc
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U2 - 10.1002/jgh3.70124
DO - 10.1002/jgh3.70124
M3 - Article
AN - SCOPUS:105000688392
SN - 2397-9070
VL - 9
JO - JGH Open
JF - JGH Open
IS - 3
M1 - e70124
ER -