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Selenium, Whole Blood

Code:8057|CPT:84255|LOINC:5722-4

Synonyms
Selenium (Se), blood
IncludesSelenium, Blood

Analysis details

Methodology

  • Inductively coupled plasma mass spectrometry (ICP-MS)

Expected Turnaround Time

3–5 days

Special Instructions

  • Infants younger than 1 year: withhold feeding for 30–40 minutes before collection.
  • Avoid food for 2–3 hours prior to the draw; plain, noncarbonated water is allowed.
  • Do not smoke during the 30 minutes preceding specimen collection.

How to use

The Selenium, Whole Blood test (also referred to as Selenium [Se], blood) is used to assess selenium deficiency and to monitor exposure or toxicity. It supports evaluation of people living in low-selenium regions, patients with malabsorption, individuals on long-term parenteral nutrition, and those following bariatric surgery. The measurement is additionally applicable in selected metabolic conditions such as propionic acidemia, in which trace element assessment may be part of longitudinal care. Because whole blood includes the erythrocyte compartment, it integrates short- and intermediate-term status and is suitable for follow-up when supplementation or exposure has changed.

Limitations

Selenium is an essential micronutrient required for the biosynthesis of selenoproteins such as glutathione peroxidases and thioredoxin reductases, which limit oxidative damage and maintain cellular redox balance. It also supports thyroid hormone metabolism through the iodothyronine deiodinases and contributes to normal immune and reproductive function. Insufficient selenium intake or absorption can blunt antioxidant defense and immune responses and has been linked to cardiomyopathy characteristic of Keshan disease. Deficiency may also contribute to hypothyroidism with myxedema—particularly when iodine deficiency co-occurs—impair linear growth and neurocognitive development, and is implicated in the endemic osteoarthropathy Kashin–Beck disease. In contrast, excess exposure leads to selenosis, which can present with a garlic-like breath odor from dimethyl selenide, gastrointestinal complaints, hair loss, brittle nails, dermatitis, and peripheral neuropathy. Dietary intake is the primary source for most individuals and typically suffices with mixed diets. Risk for deficiency increases with poor intake, malabsorption, or extended parenteral nutrition lacking selenium supplementation. Whole-blood measurement reflects selenium within both erythrocytes and plasma, providing an integrated view of selenium status and recent exposure.

Unitmcg/L
Reference interval
MinMax
10160
IndicationsEvaluation of suspected Keshan disease (endemic cardiomyopathy) where selenium deficiency is a concern, Assessment for Kashin–Beck disease (endemic osteoarthropathy) in at‑risk settings, Workup in areas with endemic cretinism, Hypothyroidism with myxedema, particularly when iodine deficiency coexists, Residence in locales known for low environmental selenium availability, Malabsorption syndromes with potential micronutrient deficits, Prolonged parenteral nutrition without adequate selenium supplementation, Post–bariatric surgery status with risk for trace element deficiency, Clinical suspicion of selenium toxicity (selenosis), Monitoring in occupational settings with selenium exposure

Possible Causes of Abnormal Results

Increased levels

  • recent high dietary selenium intake
  • selenium supplements

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume2 mL (min 0.6 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen

References

Lalonde L, Jean Y, Roberts KD, et al. Fluorometry of selenium in serum or urine. Clin Chem. 1982;28(1):172-174. PMID: 7055906.

Jacobs DS, DeMott WR, Oxley DK, et al. Laboratory Test Handbook With Key Word Index. 5th ed. Hudson, OH: Lexi-Comp Inc; 2001.

Tutelyan VA, Mazo VK, Shirina LI. The significance of selenium in adequate human nutrition. Consilium Medicum. Gynecology. 2002;4(2).