Mg (Various Forms)
Regulates muscle contraction and relaxation, preventing cramps and spasms.
Supports GABA function and melatonin production, promoting relaxation and deeper sleep.
Modulates HPA axis and neurotransmitter balance, reducing stress response.
Required for ATP synthesis and mitochondrial function.
Magnesium-dependent enzymes convert vitamin D to its active form (calcitriol). Deficiency impairs D3 metabolism.
B6 enhances magnesium absorption and cellular uptake.
Start with lower doses to assess digestive tolerance. Magnesium glycinate is gentler on the gut; citrate has mild laxative effect. Take with meals to improve absorption.
Magnesium Fact Sheet for Health Professionals
Magnesium: Research Summary
Not all forms absorb equally — these are ordered best-absorbed first.
Chelated with glycine — well absorbed and gentle on the gut, with minimal laxative effect.
Good absorption, but mildly laxative at higher doses.
Well tolerated; often chosen for energy and muscle comfort.
Crosses into the brain, but carries little elemental magnesium per dose — see its own page.
Cheap and common but poorly absorbed (~4%); acts mostly as a laxative.
Absorption varies between people; informational only, not medical advice.
What the evidence says — with links to the original studies
Magnesium is an essential mineral with well-established biology, and there is strong, consistent evidence that supplement forms differ substantially in bioavailability: soluble organic salts (citrate, glycinate/bisglycinate, lactate, aspartate, chloride) are absorbed more completely than poorly soluble magnesium oxide, whose fractional absorption is only about 4%. Evidence that supplementation improves specific clinical outcomes is more mixed and condition-dependent (modest signals for migraine prevention, blood pressure, and type 2 diabetes risk; a well-conducted Cochrane review found no meaningful benefit for muscle cramps). Newer forms such as L-threonate show early human cognitive/sleep signals but the literature is small and largely industry-linked.
States roughly 30-40% of dietary magnesium is absorbed; that soluble aspartate, citrate, lactate and chloride forms are more bioavailable than oxide and sulfate; and that carbonate, chloride, gluconate and oxide most commonly cause diarrhea. Summarizes evidence for migraine, type 2 diabetes and blood pressure.
Open-access randomized cross-over trial showing magnesium citrate produced significantly higher 24-hour urinary magnesium excretion and higher serum magnesium at 2-6 hours than magnesium oxide after single-dose administration.
Classic source for the low absorption of magnesium oxide: reported fractional absorption of only ~4% for oxide, with chloride, lactate and aspartate showing significantly higher and equivalent bioavailability.
Open-access review plus in vitro/in vivo testing of 15 formulations; found in vivo bioavailability tracked solubility and bioaccessibility rather than elemental magnesium content, with organic salts outperforming inorganic oxide.
Open-access article concluding organic salts (bisglycinate, glycerophosphate) have higher bioavailability than inorganic salts such as oxide, but only when formulated as a highly soluble product - solubility is the key driver.
6-week, double-blind, placebo-controlled trial (n=100) reporting a small but statistically significant improvement in overall cognitive performance (p=0.043); a 2 g/day dose delivered only ~145 mg elemental magnesium, confirming its low elemental content per gram.
Concluded magnesium is unlikely to provide clinically meaningful reduction in muscle cramp frequency or severity in older adults, with inconclusive evidence in pregnancy - a common consumer use with weak support.
Notes supplementation only marginally lowers blood pressure (roughly 2-3 mmHg) and that osteoporosis and general cardiovascular benefits remain inconclusive and need further research.
Educational summary of published research — not medical advice. Consult a qualified professional before supplementing.
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