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Correlation Between Serum Albumin and Serum Zinc in Malignant Lymphoma

Abstract

Objectives: Zinc (Zn) is a cofactor for more than 200 enzymes within the human body. Zn deficiency can result in cell-mediated immune dysfunction. Furthermore, serum Zn levels have been reported to be associated with nutritional status, but this association has not been clarified in malignant lymphoma. This study aimed to examine the deficiency of serum Zn levels and clarify the factors that are correlated with serum Zn in malignant lymphoma.

Methods: Initial malignant lymphoma was diagnosed in patients at Fujita Health University Hospital between April 2011 and March 2019. Based on the serum Zn levels, the study population was divided into "deficient" and "low or normal". For the serum Zn levels of patients undergoing pre-chemotherapy, laboratory parameters and nutritional factors were included. We compared these factors between the abovementioned two groups, and the serum Zn levels with its correlation factors were investigated.

Results: A total of 77 patients (Deficient group, n=20 and Low or Normal group, n=57) were enrolled. Histology, hemoglobin, serum albumin levels, Glasgow Prognostic Score (GPS), neutrophile-lymphocyte ratio (NLR), prognostic nutrition index (PNI) and Controlling Nutritional Status (CONUT) were significantly different between the two groups. Of these parameters, only serum albumin level was significantly associated with serum Zn level (p=0.0024; estimated regression coefficient, 9.51; adjusted coefficient of determination, 0.28).

Conclusions: Poor nutritional status at the initial diagnosis may have affected Zn deficiency in initial malignant lymphoma.

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References
1.
Fukushima T, Horike H, Fujiki S, Kitada S, Sasaki T, Kashihara N . Zinc deficiency anemia and effects of zinc therapy in maintenance hemodialysis patients. Ther Apher Dial. 2009; 13(3):213-9. DOI: 10.1111/j.1744-9987.2009.00656.x. View

2.
Kambe T, Yamaguchi-Iwai Y, Sasaki R, Nagao M . Overview of mammalian zinc transporters. Cell Mol Life Sci. 2004; 61(1):49-68. PMC: 11138893. DOI: 10.1007/s00018-003-3148-y. View

3.
Whitehouse R, Prasad A, Rabbani P, Cossack Z . Zinc in plasma, neutrophils, lymphocytes, and erythrocytes as determined by flameless atomic absorption spectrophotometry. Clin Chem. 1982; 28(3):475-80. View

4.
Sangthawan D, Phungrassami T, Sinkitjarurnchai W . Effects of zinc sulfate supplementation on cell-mediated immune response in head and neck cancer patients treated with radiation therapy. Nutr Cancer. 2015; 67(3):449-56. DOI: 10.1080/01635581.2015.1004735. View

5.
Lesourd B . Nutrition and immunity in the elderly: modification of immune responses with nutritional treatments. Am J Clin Nutr. 1997; 66(2):478S-484S. DOI: 10.1093/ajcn/66.2.478S. View