Triiodothyronine (T3)
Code:9003|CPT:84480|LOINC:3053-6
| Includes | Triiodothyronine (T3) |
|---|
Analysis details
Methodology
- Electrochemiluminescence immunoassay (ECLIA)
Expected Turnaround Time
1 day
Special Instructions
- Avoid high‑dose biotin for at least 72 hours before the blood draw; document biotin use prior to testing.
- For infants younger than 1 year, withhold feeding for 30–40 minutes before collection.
- Do not eat for 2–3 hours before collection; water is allowed.
- With clinician approval, hold steroid and thyroid hormone medications for 48 hours before testing.
- Refrain from strenuous physical activity and significant emotional stress during the 24 hours before testing.
- Do not smoke for 3 hours before collection.
How to use
The Triiodothyronine (T3), Total test (also known as total triiodothyronine or TT3) is used to assess thyroid function when thyrotoxicosis is suspected, with special utility in T3 thyrotoxicosis where T3 is elevated and T4 remains normal. It supports the diagnostic evaluation of hyperthyroidism across causes, including Graves disease and toxic nodules, and is informative when TSH is suppressed but the standard thyroid profile is normal or borderline. The assay may be used to monitor patients receiving T3 (liothyronine) therapy. In selected presentations—unexplained weight loss, tachyarrhythmias, or proximal myopathy with a non‑elevated T4—total T3 can provide additional diagnostic context.
Limitations
T3 is the more potent thyroid hormone at the tissue level and is generated predominantly by peripheral deiodination of T4. In circulation, the majority of T3 is bound to thyroxine‑binding globulin, transthyretin, and albumin, with less than 1% present as the free, biologically active fraction. Because total T3 reflects both bound and free hormone, changes in binding proteins influence measured concentrations. Total T3 increases during pregnancy and with oral contraceptive use, and other binding‑protein abnormalities can also shift results. T3 concentrations may be reduced in nonthyroidal illness and during fasting, and serum T3 may remain normal in thyroxine‑mediated thyrotoxicosis. Interpretation requires correlation with the clinical setting and awareness of conditions and therapies that alter binding protein levels.
| Unit | ng/dL | ||||||
|---|---|---|---|---|---|---|---|
| Reference interval |
| ||||||
| Indications | Low (suppressed) TSH with a normal free T4, raising concern for T3 thyrotoxicosis., Symptoms and signs suggestive of thyrotoxicosis despite a normal free T4 (eg, tachycardia, weight loss, tremor, insomnia, ophthalmopathy)., Clinical features consistent with hypothyroidism (eg, weight gain, xerosis, constipation, cold intolerance, edema, alopecia, menstrual irregularity)., Isolated high total T4 in a clinically euthyroid individual, suggesting altered thyroxine‑binding globulin concentration. |
Possible Causes of Abnormal Results
Increased levels
- amiodarone
- antithyroid drugs
- clofibrate
- estrogens
- lithium
- methadone
- multiple myeloma
- oral contraceptives
- phenothiazines
- pregnancy
- rifampin
- severe liver disease
- tamoxifen
- terbutaline
- valproic acid
Decreased levels
- amiodarone
- anabolic steroids
- androgens
- antithyroid drugs
- atenolol
- carbamazepine
- cimetidine
- coumarin derivatives
- dexamethasone
- fasting
- furosemide
- lithium
- nonthyroidal illness
- propranolol
- salicylates
- theophylline
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Volume | 1 mL (min 0.7 mL) |
| Storage Instructions | Room temperature, Refrigerated, Frozen |
References
Greenspan FS, Rapoport B. Thyroid gland. In: Greenspan FS, Forsham PH, eds. Basic and Clinical Endocrinology. Los Altos, Calif: Lange Medical Publications;1983:153.
Ingbar SH. Diseases of the thyroid. In: Braunwald E, Isselbacher KJ, Petersdorf RG, et al, eds. Harrison's Principles of Internal Medicine. 11th ed. New York, NY: McGraw-Hill; 1987:1732-1752.
Takamatsu J, Kuma K, Mozai T. Serum tri-iodothyronine to thyroxine ratio: A newly recognized predictor of the outcome of hyperthyroidism due to Graves' disease. J Clin Endocrinol Metab. 1986 May; 62(5):980-983. PubMed 3754263
Watts NB, Keffer JH. Practical Endocrine Diagnosis. 4th ed. Philadelphia, Pa: Lea & Febiger;1989.
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