What are the implications of hypozincemia?

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Last updated: October 29, 2025View editorial policy

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Implications of Hypozincemia (Plasma Zinc 45 μg/dL)

The low plasma zinc level of 45 μg/dL (normal range 56-134 μg/dL) indicates significant hypozincemia that requires treatment with zinc supplementation to prevent complications related to zinc deficiency.

Clinical Significance of Hypozincemia

  • Hypozincemia is associated with increased susceptibility to infections, as zinc plays a critical role in immune function 1
  • Low zinc levels can lead to dysgeusia (taste disturbances), which may be an early symptom of zinc deficiency 2
  • Hypozincemia is commonly observed in patients with chronic conditions such as chronic renal failure and chronic hepatitis C 3, 4
  • During acute infections, plasma zinc levels decrease as part of the acute phase response, which may not reflect true zinc deficiency 5

Potential Causes of Hypozincemia

  • Acute infections can cause transient hypozincemia due to the acute phase response 5
  • Chronic liver disease, particularly hepatitis C, is associated with hypozincemia due to decreased albumin production 4
  • Chronic kidney disease can lead to hypozincemia through increased urinary zinc excretion 3
  • Malnutrition or inadequate dietary zinc intake 2
  • Medications that chelate zinc or increase zinc excretion 5

Clinical Manifestations of Zinc Deficiency

  • Taste disturbances (dysgeusia) - often an early and reversible symptom 2
  • Impaired wound healing 5
  • Increased susceptibility to infections 1
  • Skin manifestations (dermatitis, hair loss) 2
  • Neurological symptoms (irritability, lethargy) 3

Diagnostic Considerations

  • Plasma zinc levels may be falsely low during acute infections due to the acute phase response 5
  • Albumin-corrected zinc levels may provide a more accurate assessment of zinc status in patients with acute infections 5
  • Serum albumin levels should be measured concurrently, as approximately 60% of serum zinc is bound to albumin 4
  • Consider measuring other markers of inflammation (CRP, ferritin) to assess for acute phase response 5

Treatment Recommendations

  • Oral zinc supplementation is the primary treatment for hypozincemia 2
  • Zinc acetate hydrate (50 mg/day of elemental zinc) has been shown to be effective in treating hypozincemia-induced dysgeusia 2
  • Treatment duration of at least 12-24 weeks may be necessary to normalize zinc levels and improve symptoms 2
  • Monitor serum zinc levels during treatment to ensure normalization 4
  • Monitor serum copper levels during zinc supplementation, as high-dose zinc can interfere with copper absorption 2

Monitoring and Follow-up

  • Recheck plasma zinc levels after 12 weeks of supplementation 2
  • Monitor for improvement in clinical symptoms, particularly taste disturbances 2
  • Assess for potential side effects of zinc supplementation (gastric irritation, copper deficiency with prolonged high-dose therapy) 2
  • Consider long-term supplementation in patients with chronic conditions that predispose to zinc deficiency 4

Special Considerations

  • In patients with acute infections, consider repeating zinc measurement after resolution of the infection 5
  • In patients with chronic liver disease, zinc supplementation may improve liver function parameters 4
  • In patients with chronic kidney disease, higher doses of zinc may be required due to increased urinary losses 3
  • Albumin-corrected zinc levels may provide a more accurate assessment of zinc status in patients with hypoalbuminemia 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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