Abstract
Magnesium (Mg) is the second most abundant intracellular cation and the fourth most abundant cation of the human body. Magnesium plays an essential role as a cofactor for a variety of enzymes, including those involved in several key steps of intermediary metabolism and phosphorylation. In addition, Mg is required for protein and nucleic acid synthesis, the cell cycle progression, cytoskeletal and mitochondrial integrity, and the binding of substances to the plasma membrane. Disorders of Mg homeostasis may lead to profound changes in the function and well being of the organism. Serum Mg concentration is normal in patients with early renal failure, but hypermagnesemia usually occurs in the advanced stage of renal failure due to the reduced urinary Mg excretion. Following the introduction of chronic hemodialysis or continuous ambulatory peritoneal dialysis (CAPD) treatment, the major factor to determine Mg balance is Mg levels in the dialysate. Patients with end-stage renal disease (ESRD) who are receiving dialysis may develop various complications including hypertension, atherosclerosis, dyslipidemia, and renal osteodystrophy. The disturbance of Mg balance in those patients maintained on dialysis may affect the development of these complications.
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Okuno, S., Inaba, M. (2007). Magesium in Hemodialysis Patients. In: Nishizawa, Y., Morii, H., Durlach, J. (eds) New Perspectives in Magnesium Research. Springer, London. https://doi.org/10.1007/978-1-84628-483-0_26
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DOI: https://doi.org/10.1007/978-1-84628-483-0_26
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