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Published on: May 12, 2018
Pathophysiology of Drug-Induced Hypomagnesaemia
Periklis Katopodis1, Emmanouil Karteris2, Konstantinos P Katopodis3
1Department of Biosciences, College of Health and Life Sciences, Brunel University London, Uxbridge, London, UB8 3PH, UK. Katopodisper@gmail.com.
Magnesium (Mg2+) is vital for numerous cellular functions. This review details Mg2+ roles, kidney handling, and drugs like diuretics and PPIs causing hypomagnesaemia, aiding in prevention and treatment.
Area of Science:
- Biochemistry
- Human Physiology
- Nephrology
Background:
- Magnesium (Mg2+) is a critical intracellular and extracellular cation.
- It plays a key role in enzyme activity, nucleic acid stability, ion channel regulation, metabolism, and apoptosis.
Purpose of the Study:
- To review the physiological functions of Mg2+.
- To explain Mg2+ handling by the kidneys.
- To identify drugs causing hypomagnesaemia.
Main Methods:
- Literature review of Mg2+ physiology and drug-induced hypomagnesaemia.
- Analysis of mechanisms of Mg2+ imbalance.
- Discussion of clinical implications.
Main Results:
- Hypomagnesaemia stems from reduced intake, absorption, or increased renal excretion.
- Diuretics and proton-pump inhibitors (PPIs) are common drug culprits.
- Understanding these factors is crucial for managing Mg2+ homeostasis.
Conclusions:
- Mg2+ is essential for cellular health and physiological balance.
- Awareness of drug-induced hypomagnesaemia is vital for clinicians.
- This review provides insights for preventing and treating Mg2+ imbalances.
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