Vitamin D for Prevention of Disease: Guidelines From the Endocrine Society

MaryAnn Dakkak, MD, MPH
Amy He, MD
Amy Min He, MD

American Family Physician. 2026;113(3):291-293.

Author disclosure: No relevant financial relationships.

This clinical content conforms to AAFP criteria for CME.

KEY POINTS FOR PRACTICE

• Avoid routine testing for vitamin D levels in healthy children and adults because there is no proven benefit, and no evidence-based target levels exist.
• Consider empiric vitamin D supplementation in children aged 1 to 18 years, pregnant adults, individuals with prediabetes, and adults 75 years and older for illness prevention without measuring or targeting vitamin D levels.
• Consider not recommending routine vitamin D supplementation for healthy adults aged 19 to 74 years because there are no proven health benefits.
From the AFP Editors

Although low levels of vitamin D are related to many common disorders, including musculoskeletal, metabolic, cardiovascular, malignant, autoimmune, and infectious diseases, the evidence for supplementation is mixed. Since 2000, the number of people in the United States taking vitamin D supplements at a dose of 1,000 IU or more increased from less than 1% to 18%. However, uncertainty regarding the optimal range of vitamin D serum levels has led to inconsistencies in clinical practice. The Endocrine Society has updated its guidelines on the evidence for vitamin D supplementation and testing for disease prevention.

VITAMIN D TESTING

In many reviews, testing for vitamin D (25-hydroxyvitamin D [25(OH)D]) levels has shown no proven benefit, and no evidence-based target levels exist. The Endocrine Society found evidence only for empiric supplementation without monitoring or targeting specific vitamin D levels.

Testing may be appropriate for specific indications, including patients with hypocalcemia; malabsorption syndromes such as short gut syndrome, gastric bypass, or inflammatory bowel disease; increased kidney losses of vitamin D (eg, nephrotic syndrome); and increased vitamin D catabolism (eg, caused by certain medications).

VITAMIN D SUPPLEMENTATION

Table 1 summarizes the populations in which vitamin D supplementation is suggested, and Table 2 lists the populations in which it is not recommended.

TABLE 1. Populations in Which Empiric Vitamin D Supplementation Is Suggested

PopulationSuggested intakeComments
Children aged 1–18 yearsDaily intake of fortified foods, vitamin D supplements (pill or drops), or multivitamins containing vitamin D; 300–2,000 IU/day
Average study dose: 1,200 IU/day
For prevention of nutritional rickets and to potentially lower the risk of respiratory tract infections
Healthy adults ≥ 75 yearsDaily intake of fortified foods, vitamin D supplements (pill or drops), or multivitamins containing vitamin D; 400–3,333 IU/day
Average study dose: 900 IU/day
Potential reduction in all-cause mortality
Daily, low-dose empiric vitamin D supplementation is recommended over nondaily, higher doses
PregnancyDaily intake of fortified foods, vitamin D supplements (pill or drops), or prenatal vitamins containing vitamin D; 600–5,000 IU/day or week
Average study dose: 2,500 IU/day
May reduce the risk of preeclampsia, intrauterine mortality, preterm birth, small-for-gestational-age infants, and neonatal mortality
High-risk prediabetes* Doses of 842–7,543 IU/day
Average study dose: 3,500 IU/day
In addition to lifestyle modification to lower the risk of progression to diabetes

*—Defined as meeting two of three American Diabetes Association criteria: fasting glucose level of 100–125 mg/dL (5.55–6.94 mmol/L), A1C level of 5.7% to 6.4%, and a 2-hour glucose level of 140–199 mg/dL (7.77–11.04 mmol/L) after a 75-g oral glucose challenge test.

MARYANN DAKKAK, MD, MPH; AMY HE, MD; and AMY MIN HE, MD, Boston Medical Center, Boston, Massachusetts

Address correspondence to MaryAnn Dakkak, MD, MPH, at maryann.dakkak@bmc.org.

Author disclosure: No relevant financial relationships.

Coverage of guidelines from other organizations does not imply endorsement by AFP or the AAFP.

This series is coordinated by Michael J. Arnold, MD, MHPE, AFP Assistant Medical Editor.

A collection of Practice Guidelines published in AFP is available at https://www.aafp.org/afp/practguide.

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