2017
DOI: 10.1159/000484574
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Digoxin and Hypermagnesuria

Abstract: In a recent issue of Nephron, Abu-Amer et al.[1] reported the presence of hypermagnesuria in patients following acute intravenous administration of digoxin and suggested that the Na+/K+-ATPase γ-subunit, which is the pharmacological target of digoxin, can play a role in this process. Hypermagnesuria induced by digoxin may have important clinical consequences, particularly in the presence of inherited and acquired conditions associated with hypermagn… Show more

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Cited by 6 publications
(3 citation statements)
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“…83 However, several drugs currently used in patients with CKD, such as proton pump inhibitors, loop diuretics, and cyclosporine, can lead to hypomagnesaemia. 84 The risk of hypomagnesaemia increases when these drugs are used in combination. Magnesium supplementation and the shift from proton pump inhibitors to H 2 antagonists is sufficient to restore magnesium levels in most patients with CKD.…”
Section: Destiffening Strategiesmentioning
confidence: 99%
“…83 However, several drugs currently used in patients with CKD, such as proton pump inhibitors, loop diuretics, and cyclosporine, can lead to hypomagnesaemia. 84 The risk of hypomagnesaemia increases when these drugs are used in combination. Magnesium supplementation and the shift from proton pump inhibitors to H 2 antagonists is sufficient to restore magnesium levels in most patients with CKD.…”
Section: Destiffening Strategiesmentioning
confidence: 99%
“…Digoxin reduces serum Mg concentration via increased urinary Mg excretion. It has been proposed that a missense mutation in the γ subunit (FXYD2) of Na + /K + ‐ATPase, which is the pharmacological target of digoxin, might be involved in this process 130 . It appears that FXYD2 is a positive regulator of Na,K‐ATPase in the DCT 131 …”
Section: Drugs Associated With Hypomagnesemiamentioning
confidence: 99%
“…Lastly, intracellular magnesium deficiency may not only be related to MVD ( 43 ) but also an important risk factor for AF ( 44 ). cDGX may continuously inhibit the Na + -K + -ATPase pump, deplete intracellular magnesium ions ( 45 ), further lead to CMD, and eventually induce AF.…”
Section: Discussionmentioning
confidence: 99%