Correlation of Trace Elements in Patients of Chronic Liver Disease with Respect to Child- Turcotte- Pugh Scoring System
Overview
Affiliations
Introduction: Zinc, copper, manganese and magnesium are essential trace elements whose role in chronic liver disease and its complications is not clear.
Aim: To study the concentration of these elements in patients with Chronic Liver Disease (CLD) with respect to Child-Torcotte-Pugh (CTP) scoring.
Materials And Methods: This was an observational study carried out in the Department of Medicine, JSS Hospital, Mysore, India, between October 2013 and October 2015. A total of 75 patients with cirrhosis were prospectively enrolled. Severity of liver disease was assessed based on CTP score and patients were grouped into Class A, B and C. Routine investigations were done and following trace elements were assessed in all-zinc, copper, manganese and magnesium.
Results: The serum concentrations of zinc decreased with severity of liver disease, and the mean difference between different severity classes was statistically significant (p<0.001). There was a significant negative correlation between zinc and CTP Score (r= -0.439; p<0.001). Copper concentration was increased in patients with more severe cirrhosis and mean level difference of copper among the CTP groups were statistically significant (p<0.001). Moreover, copper showed significant positive correlation with CTP Score (r=0.385; p<0.001). The serum levels of manganese were significantly higher in patients with CTP C class in comparison to patients with CTP A and B class (p<0.05); Manganese showed significant positive correlation with CTP Score (r=0.271; p= 0.019). The concentrations of magnesium did not differ significantly between CTP class with the mean level difference not statistically significant.
Conclusion: Increasing liver dysfunction alters the metabolism of trace elements towards excess of copper and deficiency of zinc.
Dewan S, Das A, Ahmed Z, Khan S, Nasim R, Sarwar M SAGE Open Med. 2024; 12:20503121241291977.
PMID: 39429543 PMC: 11489948. DOI: 10.1177/20503121241291977.
Nutritional Support for Liver Diseases.
Jamiol-Milc D, Gudan A, Kazmierczak-Siedlecka K, Holowko-Ziolek J, Maciejewska-Markiewicz D, Janda-Milczarek K Nutrients. 2023; 15(16).
PMID: 37630830 PMC: 10459677. DOI: 10.3390/nu15163640.
Trace Element Imbalances in Acquired Hepatocerebral Degeneration and Changes after Liver Transplant.
Nascimento H, Malaquias M, Pinto C, Sa Silva J, Rochate D, Fraga C Biology (Basel). 2023; 12(6).
PMID: 37372089 PMC: 10294919. DOI: 10.3390/biology12060804.
Baye M, Abay Z, Tesfaye T, Ahmed E, Arage G, Zewude E Heliyon. 2023; 9(4):e15133.
PMID: 37095908 PMC: 10121785. DOI: 10.1016/j.heliyon.2023.e15133.
The Study of the Aorta Metallomics in the Context of Atherosclerosis.
Kuzan A, Wujczyk M, Wiglusz R Biomolecules. 2021; 11(7).
PMID: 34202347 PMC: 8301911. DOI: 10.3390/biom11070946.