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Thyroxine, Free (FT4)


Definition


  • Both free and bound forms of T4 and T3 are present in the blood. More than 99% of the T4 and T3 circulates in the blood bound to carrier proteins, leaving <1% unbound. It is this level of unbound or free hormone that correlates with the functional thyroid state in most individuals. FT4 is usually 0.02 " “0.04% of total T4 (see Table 16.76).
  • Normal range (adults): 0.58 " “1.64 ng/dL.
    • Pregnant women:
      • First trimester: 0.73 " “1.13 ng/dL
      • Second trimester: 0.54 " “1.18 ng/dL
      • Third trimester: 0.56 " “1.09 ng/dL

Use


  • FT4 gives corrected values in patients in whom the total T4 is altered on account of changes in serum proteins or in binding sites (e.g., pregnancy, drugs [such as androgens, estrogens, birth control pills, phenytoin], altered levels of serum proteins [e.g., nephrosis]).
  • Monitoring restoration to normal range is the only laboratory criterion to estimate appropriate replacement dose of levothyroxine because 6 " “8 weeks are required before TSH reflects these changes.
  • Not generally helpful unless pituitary/hypothalamic disease is suspected.

Interpretation


Increased In


  • Hyperthyroidism.
  • Hypothyroidism treated with thyroxine.
  • Euthyroid sick syndrome.
  • Occasional patients with hydatidiform mole or choriocarcinoma with marked hCG elevations may show increased FT4, suppressed TSH, and blunted TSH response to TRH stimulation; returns to normal with effective treatment of trophoblastic disease; severe dehydration (may be >6.0 ng/dL).

Decreased In


  • Hypothyroidism
  • Hypothyroidism treated with triiodothyronine
  • Euthyroid sick syndrome

Limitations


  • FT4 assays based on direct equilibrium dialysis are considered reference methods.
  • FT4 assays are prone to inaccurate readings in pregnant women. The studies have shown that FT4 index measurement is more reliable than free T4 immunoassays in pregnant women.
  • Anticonvulsant drug therapy (particularly phenytoin) may result in decreased FT4 levels due to an increased hepatic metabolism and secondarily to displacement of hormone from binding sites.
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