# Hypomagnesemia: A Clinical and Nutritional Update

**Authors:** Anastasia Papagiannidou, Maria Mitropoulou, Konstantinos Papantzikos, Dimitra Petropoulou, Dimitrios Tsilingiris, Faidon Magkos, Maria Dalamaga

PMC · DOI: 10.1007/s13668-026-00745-5 · 2026-03-24

## TL;DR

This review discusses hypomagnesemia, a common but overlooked condition linked to various diseases, and highlights dietary and medical factors contributing to magnesium deficiency.

## Contribution

The paper synthesizes recent evidence on magnesium's role in disease and emphasizes the need for improved diagnosis and management strategies.

## Key findings

- Low magnesium is linked to cardiometabolic, neuropsychiatric, and immune disorders.
- Modern diets and medications contribute to widespread magnesium deficiency.
- Supplementation shows modest benefits in blood pressure and metabolic health.

## Abstract

Hypomagnesemia, defined as low serum/plasma magnesium concentration, is a highly prevalent yet underrecognized electrolyte disorder with extensive clinical, metabolic, and nutritional implications. This review provides an updated synthesis of magnesium physiology, dietary determinants, homeostatic regulation, diagnostic challenges, and therapeutic strategies, with particular emphasis on recent meta-analyses and large-scale epidemiological evidence linking hypomagnesemia to multisystem disease.

Accumulating evidence has shown consistent associations between low serum or dietary magnesium and increased risk of cardiometabolic disorders (hypertension, type 2 diabetes mellitus, metabolic syndrome, and cardiovascular disease), neuropsychiatric conditions (migraine, depression, cognitive impairment, and dementia), osteoporosis, immune dysregulation, and adverse outcomes in hospitalized, critically ill, and chronic kidney disease patients. Mechanistic studies have clarified the roles of TRPM6/7 channels, tight junction claudins, and basolateral magnesium transporters in intestinal and renal magnesium handling, elucidating pathways underlying both inherited and acquired deficiencies. Research has also highlighted the contribution of modern dietary patterns, food processing, mineral-depleted drinking water, medication use (notably proton pump inhibitors, diuretics and chemotherapeutic agents), and gut microbiome alterations to widespread subclinical deficiency. Meta-analyses of RCTs indicate that magnesium supplementation confers modest but clinically relevant improvements in blood pressure, glycemic control, inflammatory markers, endothelial function, migraine frequency, and depressive symptoms, particularly in individuals with baseline hypomagnesemia. However, serum magnesium remains an insensitive biomarker of total body magnesium status, and consensus on optimal diagnostic thresholds and replacement strategies is lacking.

Magnesium deficiency contributes to a wide spectrum of multisystem disorders, and is driven by dietary insufficiency, gastrointestinal and renal losses, medication use, chronic disease, and altered microbiome function. Meta-analytic evidence supports its role as a modifiable risk factor across cardiovascular, metabolic, neurological, skeletal, and immune disorders. Dietary modification, optimized supplementation, and correction of underlying causes of deficiency remain central to management. Future research should focus on improved diagnostic tools, personalized dosing approaches and long-term outcomes of magnesium repletion. Enhancing clinical awareness and integrating magnesium evaluation into routine care may reduce the growing burden of hypomagnesemia.

## Linked entities

- **Genes:** TRPM6 (transient receptor potential cation channel subfamily M member 6) [NCBI Gene 140803], TRPM7 (transient receptor potential cation channel subfamily M member 7) [NCBI Gene 54822]
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), metabolic syndrome (MONDO:0000816), cardiovascular disease (MONDO:0004995), migraine (MONDO:0005277), depression (MONDO:0002050), dementia (MONDO:0001627), osteoporosis (MONDO:0005298), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, DCT (dopachrome tautomerase) [NCBI Gene 1638] {aka OCA8, TRP-2, TYRP2}, CLDN16 (claudin 16) [NCBI Gene 10686] {aka HOMG3, PCLN1}, SLC8A1 (solute carrier family 8 member A1) [NCBI Gene 6546] {aka NCX1}, TAC1 (tachykinin precursor 1) [NCBI Gene 6863] {aka Hs.2563, NK2, NKNA, NPK, TAC2}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GABARAP (GABA type A receptor-associated protein) [NCBI Gene 11337] {aka ATG8A, GABARAP-a, MM46}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, DNAH8 (dynein axonemal heavy chain 8) [NCBI Gene 1769] {aka ATPase, SPGF46, hdhc9}, TRPM6 (transient receptor potential cation channel subfamily M member 6) [NCBI Gene 140803] {aka CHAK2, HMGX, HOMG, HOMG1, HSH}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, G6PC1 (glucose-6-phosphatase catalytic subunit 1) [NCBI Gene 2538] {aka G6PC, G6PT, G6Pase, GSD1, GSD1a}, CLDN19 (claudin 19) [NCBI Gene 149461] {aka HOMG5}, SLC41A3 (solute carrier family 41 member 3) [NCBI Gene 54946] {aka SLC41A1-L2}, CYP24A1 (cytochrome P450 family 24 subfamily A member 1) [NCBI Gene 1591] {aka CP24, CYP24, HCAI, HCINF1, P450-CC24}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, KNG1 (kininogen 1) [NCBI Gene 3827] {aka BDK, BK, HAE6, HK, HMWK, KNG}, CLCNKB (chloride voltage-gated channel Kb) [NCBI Gene 1188] {aka CLCKB, ClC-K2, ClC-Kb}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC12A1 (solute carrier family 12 member 1) [NCBI Gene 6557] {aka BSC, BSC-1, BSC1, CCC2, NKCC2}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, POLB (DNA polymerase beta) [NCBI Gene 5423], CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, KCNJ1 (potassium inwardly rectifying channel subfamily J member 1) [NCBI Gene 3758] {aka KIR1.1, ROMK, ROMK1}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, SLC12A3 (solute carrier family 12 member 3) [NCBI Gene 6559] {aka NCC, NCCT, TSC}, HK1 (hexokinase 1) [NCBI Gene 3098] {aka CNSHA5, HK, HK1-ta, HK1-tb, HK1-tc, HKD}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CASR (calcium sensing receptor) [NCBI Gene 846] {aka CAR, EIG8, FHH, FIH, GPRC2A, HHC}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** dementia (MESH:D003704), AI (MESH:D000080146), electrocardiographic abnormalities (MESH:C566733), steatorrhea (MESH:D045602), refeeding syndrome (MESH:D055677), autosomal recessive condition (MESH:D020763), Hemolysis (MESH:D006461), myocardial infarction (MESH:D009203), musculoskeletal symptoms (MESH:D009140), hyperlipidemia (MESH:D006949), atrial fibrillation (MESH:D001281), gastrointestinal symptoms (MESH:D012817), coronary vasospasm (MESH:D003329), AKI (MESH:D058186), circulatory system disorders (MESH:D012769), preeclampsia (MESH:D011225), viral infections (MESH:D014777), HSH (MESH:C566593), Neuromuscular irritability (MESH:D009468), intracellular (MESH:D015270), Cancer (MESH:D009369), polyuria (MESH:D011141), coronary heart disease (MESH:D003327), migraine (MESH:D008881), overweight (MESH:D050177), chronic disease (MESH:D002908), renal wasting (MESH:D019282), autosomal recessive tubulopathy (MESH:C536350), Gitelman or Bartter syndromes (MESH:D053579), cardiometabolic disease (MESH:D024821), autosomal dominant hypocalcemia (MESH:C562783), AD (MESH:D000544), respiratory alkalosis (MESH:D000472), necrosis (MESH:D009336), long COVID (MESH:D000094024), Electrolyte disorders (MESH:D014883), loss of appetite (MESH:D001068), Immune dysregulation (OMIM:614878), Hypertension (MESH:D006973), chronic diarrhea (MESH:D003967), osteoporosis (MESH:D010024), icterus (MESH:D007565), calcium deficiency (MESH:D002128), heart failure (MESH:D006333), starvation (MESH:D013217), cluster headaches (MESH:D003027), convulsions (MESH:D012640), thrombosis (MESH:D013927), celiac disease (MESH:D002446), inflammation (MESH:D007249), Hypomagnesemia (OMIM:613882), Hypercalcemia (MESH:D006934), fractures (MESH:D050723), Inherited disorders (MESH:D030342), FEMg (MESH:D008275), vomiting (MESH:D014839), renal failure (MESH:D051437), arrhythmias (MESH:D001145), tremor (MESH:D014202), impaired fasting glucose (MESH:D007003)
- **Chemicals:** creatinine (MESH:D003404), phosphate (MESH:D010710), proton (MESH:D011522), 1,25-dihydroxyvitamin D (MESH:C097949), Na (MESH:D012964), colchicine (MESH:D003078), serotonin (MESH:D012701), cetuximab (MESH:D000068818), Magnesium (MESH:D008274), aminoglycosides (MESH:D000617), amino acids (MESH:D000596), gluconate (MESH:C030691), panitumumab (MESH:D000077544), carbohydrates (MESH:D002241), carboplatin (MESH:D016190), vitamin D (MESH:D014807), ATP (MESH:D000255), bicarbonate (MESH:D001639), calmagite (MESH:C006876), aspartate (MESH:D001224), phytates (MESH:D010833), thiazides (MESH:D049971), Butyrate (MESH:D002087), oxalate (MESH:D010070), glucose (MESH:D005947), chlorophyll (MESH:D002734), SCFA (MESH:D005232), phosphorus (MESH:D010758), Water (MESH:D014867), MgSO4 (MESH:D008278), GABA (MESH:D005680), sulfate (MESH:D013431), thiocyanate (MESH:C031760), NO (MESH:D009569), Ca2+ (-), bisphosphonates (MESH:D004164), citrate (MESH:D019343), Ca (MESH:D002118), hydrogen (MESH:D006859), silicones (MESH:D012828), Amiloride (MESH:D000584), chloride (MESH:D002712), ethanol (MESH:D000431), lactate (MESH:D019344), magnesium citrate (MESH:C110422), zalutumumab (MESH:C546618), omeprazole (MESH:D009853), PGI2 (MESH:D011464), Cl- (MESH:D002713), oxaliplatin (MESH:D000077150), platinum (MESH:D010984), Magnesium chloride (MESH:D015636), hydroxyapatite (MESH:D017886), alcohol (MESH:D000438), N-methyl-D-aspartate (MESH:D016202), Cisplatin (MESH:D002945), lipid (MESH:D008055), PGE1 (MESH:D000527), zinc (MESH:D015032), EDTA (MESH:D004492)
- **Species:** Bifidobacterium (genus) [taxon 1678], Enterobacteriaceae (enterobacteria, family) [taxon 543], Rattus norvegicus (brown rat, species) [taxon 10116], Lactobacillus (genus) [taxon 1578], Spinacia oleracea (spinach, species) [taxon 3562], Akkermansia muciniphila (species) [taxon 239935], Mus musculus (house mouse, species) [taxon 10090], Romboutsia ilealis (species) [taxon 1115758], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606], Turicibacter sanguinis (species) [taxon 154288]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13009017/full.md

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Source: https://tomesphere.com/paper/PMC13009017