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KMID : 1040620220280010077
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Clinical and Molecular Hepatology
2022 Volume.28 No. 1 p.77 ~ p.90
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U-shaped relationship between urea level and hepatic decompensation in chronic liver diseases
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Lin Huapeng
Wong Grace Lai-Hung
Zhang Xinrong
Yip Terry Cheuk-Fung
Liu Ken
Tse Yee Kit
Hui Vicki Wing-Ki
Lai Jimmy Che-To
Chan Henry Lik-Yuen
Wong Vincent Wai-Sun
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Abstract
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Background/Aims: We aimed to determine the association between blood urea level and incident cirrhosis, hepatic decompensation, and hepatocellular carcinoma in chronic liver disease (CLD) patients.
Methods: The association between blood urea level and liver fibrosis/liver-related events were evaluated on continuous scale with restricted cubic spline curves based on generalized additive model or Cox proportional hazards models. Then, the above associations were evaluated by urea level within intervals.
Results: Among 4,282 patients who had undergone liver stiffness measurement (LSM) by transient elastography, baseline urea level had a U-shaped association with LSM and hepatic decompensation development after a median follow-up of 5.5 years. Compared to patients with urea of 3.6?9.9 mmol/L, those with urea ≤3.5 mmol/L (adjusted hazard ratio [aHR], 4.15; 95% confidence interval [CI], 1.68?10.24) and ≥10 mmol/L (aHR, 5.22; 95% CI, 1.86?14.67) had higher risk of hepatic decompensation. Patients with urea ≤3.5 mmol/L also had higher risk of incident cirrhosis (aHR, 3.24; 95% CI, 1.50?6.98). The association between low urea level and incident cirrhosis and hepatic decompensation was consistently observed in subgroups by age, gender, albumin level, and comorbidities. The U-shaped relationship between urea level and LSM was validated in another population screening study (n=917). Likewise, urea ≤3.5 mmol/L was associated with a higher risk of incident cirrhosis in a territory-wide cohort of 12,476 patients with nonalcoholic fatty liver disease at a median follow-up of 9.9 years (aHR, 1.27; 95% CI, 1.03?1.57).
Conclusions: We identified a U-shaped relationship between the urea level and liver fibrosis/incident cirrhosis/hepatic decompensation in patients with CLD.
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KEYWORD
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Urea, Liver cirrhosis, Fibrosis, Non-alcoholic fatty liver disease, Hepatitis B
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