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Evidence Based Longevity (EBL) Check what I take
Drug-Nutrient Depletion A fall in a nutrient's level caused by a medication, for example through reduced absorption or increased loss.

Corticosteroids (Oral Steroids)

Common brand names: Prednisone, Methylprednisolone, Dexamethasone

Evidence last reviewed July 2026

Four nutrients listed against this medication. The most severe is marked critical.

At a glance

Two of the four are marked well documented. The other two carry their own evidence levels.

At a glance

Corticosteroids (Oral Steroids)
  • Calcium + Vitamin D3Critical · Well documented
  • MagnesiumModerate · Mechanism only, no human trial
  • ZincModerate · Well documented
  • PotassiumModerate · Moderate evidence

Color shows how serious each listed effect is. The label beside it shows how strong the evidence is. The cards below explain each one and show its evidence.

Nutrients it can lower

Calcium + Vitamin D3
CriticalWell documented PMID 8495275

Mechanism, Corticosteroids reduce intestinal calcium absorption and increase renal calcium excretion. They also suppress osteoblast activity. Long-term use causes glucocorticoid-induced osteoporosis, the most common drug-induced osteoporosis.

Common signs, Bone density loss, fracture risk, osteoporosis, dental deterioration

Gennari (Br J Rheumatol, 1993; PMID PubMed ID: the permanent number the US National Library of Medicine gives a published paper. Each one links to that paper's record on PubMed. 8495275): glucocorticoids reduce intestinal calcium absorption, a driver of steroid-induced bone loss.

What the evidence shows

Calcium 1,000–1,200 mg daily from food first, with vitamin D3 1,500–2,000 IU, is the range in common use for steroid-induced bone loss. Gennari measured calcium absorption and bone mass on glucocorticoids and is not the source of this regimen; no guideline body is cited for it here.

Listed in the EBL dispensary: Vitamin D3 with K2, liquid
Magnesium
ModerateMechanistic · no human trial PMID 10612083

Mechanism, Corticosteroids increase renal magnesium excretion. Magnesium deficiency potentiates the bone loss caused by steroids.

Common signs, Muscle cramps, bone loss, fatigue, insulin resistance

Glucocorticoids can increase urinary magnesium excretion (mechanistic). The paper usually cited here, Rude (Magnes Res, 1999), is a rat study of magnesium-deficiency osteoporosis with no steroid exposure, a different question entirely. No human study measures steroid-caused magnesium depletion.

Common practice, not from a trial cited on this row

Magnesium 400 mg daily is a figure in common use, not from a trial cited on this row. The cited paper is a rat model of magnesium-deficiency osteoporosis with no steroid exposure, and no cited trial tested the bisglycinate form.

Zinc
ModerateWell documented PMID 4107980

Mechanism, Corticosteroids increase urinary zinc excretion and impair zinc utilization, relevant for immune function and wound healing.

Common signs, Impaired wound healing, immune suppression, increased infection risk

Flynn et al. (Lancet, 1971; PMID 4107980): rapid serum-zinc depletion during corticosteroid therapy.

What the evidence shows

Zinc 15–30 mg daily is a range in common use. Flynn reports serum zinc falling during corticosteroid therapy; that paper is not the source of this dose or form.

Listed in the EBL dispensary: Zinc picolinate 15 mg · view at Fullscript →
Potassium
ModerateModerate evidence PMID 19736807

Mechanism, Mineralocorticoid activity of corticosteroids increases renal potassium excretion.

Common signs, Muscle weakness, fatigue, cardiac arrhythmia

Glucocorticoids have mineralocorticoid activity that can lower potassium. In a cross-sectional study of 110 outpatients given 1 g of intravenous methylprednisolone daily for 3 days, 18% developed hypokalemia, nearly all of it mild (Tamez-Perez et al., Rev Invest Clin, 2009; PMID 19736807). That was high-dose pulse therapy; the rate on ordinary oral doses was not measured there.

What the evidence shows

Increased dietary potassium is described, with serum electrolytes monitored together with the prescriber.

For your next appointment

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Disclosure

Medical disclaimer

These statements have not been evaluated by the Food and Drug Administration. Any grade on this page describes the strength of published human trial evidence in the populations studied. It is not a recommendation for any individual and is not medical advice. Starting, stopping or changing any supplement or medication is a decision for your physician.

Grades move when new trials publish. A free monthly email lists every grade EBL moved, with the reason and the trial behind it: the sign-up is on the Evidence Log →