Effect of Selenium Deficiency on the Development of Overt Hepatic Encephalopathy in Patients with Chronic Liver Disease

Author:

Nakahata Yuki12ORCID,Hanai Tatsunori13,Miwa Takao14ORCID,Maeda Toshihide1,Imai Kenji1,Suetsugu Atsushi1,Takai Koji15,Shimizu Masahito1ORCID

Affiliation:

1. Department of Gastroenterology/Internal Medicine, Gifu University Graduate School of Medicine, Gifu 5011194, Japan

2. Department of Gastroenterology, Asahi University Hospital, Gifu 5008523, Japan

3. Center for Nutrition Support & Infection Control, Gifu University Hospital, Gifu 5011194, Japan

4. Health Administration Center, Gifu University, Gifu 5011193, Japan

5. Division for Regional Cancer Control, Gifu University Graduate School of Medicine, Gifu 5011194, Japan

Abstract

Selenium is an essential trace element to maintain good health. This retrospective study investigated the prevalence of selenium deficiency and its effect on overt hepatic encephalopathy (OHE) in patients with chronic liver disease (CLD). Patients who underwent serum selenium level measurement between January 2021 and April 2022 were enrolled. The factors associated with selenium deficiency (≤10 µg/dL) and the association between selenium deficiency and OHE were analyzed. Among 98 eligible patients, 24% were observed to have selenium deficiency, with a median serum selenium level of 11.8 µg/dL. The serum selenium levels were significantly lower in patients with cirrhosis than in those with chronic hepatitis (10.9 µg/dL vs. 12.4 µg/dL; p = 0.03). The serum selenium levels were negatively correlated with mac-2 binding protein glycan isomer, the FIB-4 index, albumin-bilirubin (ALBI) score, and Child–Pugh score. The ALBI score remained significantly associated with selenium deficiency (odds ratio, 3.23; 95% confidence interval [CI], 1.56–6.67). During a median follow-up period of 2.9 months, nine patients experienced OHE. Selenium deficiency was associated with OHE (hazard ratio, 12.75; 95% CI, 2.54–70.22). Selenium deficiency is highly prevalent in patients with CLD and is associated with an increased risk of OHE development.

Funder

Japan Agency for Medical Research and Development

MHLW Policy Research for Hepatitis Measures Program

Publisher

MDPI AG

Subject

General Medicine

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