Liothyronine

Liothyronine sodium is the synthetic sodium salt of L-triiodothyronine (T3), the most active thyroid hormone. FDA-approved products are Cytomel and generic liothyronine sodium tablets for oral use, and Triostat and generic liothyronine sodium injection for intravenous use. Compounded preparations include oral capsules of liothyronine alone and combined with levothyroxine.

• Oral (Cytomel): replacement therapy for primary (thyroidal), secondary (pituitary) and tertiary (hypothalamic) congenital or acquired hypothyroidism in adults and pediatric patients.
• Oral (Cytomel): adjunct to surgery and radioiodine therapy for pituitary TSH suppression in well-differentiated thyroid cancer, and diagnostic agent in suppression tests for suspected mild hyperthyroidism or thyroid gland autonomy.
• Intravenous (Triostat): myxedema coma and precoma.
• Labeled oral dosing, as prescribed: Cytomel labeling describes usual adult maintenance doses of 25 to 75 mcg daily for hypothyroidism, given once daily, with lower starting doses in elderly patients and those with cardiovascular disease. Prescribers may divide daily doses.
• Prescribers also use liothyronine, alone or with levothyroxine, in selected patients with hypothyroidism outside these labeled regimens.

Liothyronine enters cells through membrane transporters such as MCT8 and binds nuclear thyroid hormone receptors (TR-alpha and TR-beta), which pair with retinoid X receptors on thyroid response elements to regulate gene transcription. Effects include increased basal metabolic rate, oxygen consumption and thermogenesis, increased heart rate and contractility, and changes in protein, lipid and carbohydrate metabolism. T3 binds the receptor with roughly 10-fold higher affinity than T4; most circulating T3 normally comes from peripheral deiodination of T4.

Liothyronine is rapidly absorbed after an oral dose. T3 is more than 99% protein bound but less tightly than T4, giving a faster onset and offset of effect. Liothyronine has a shorter half-life (about 2.5 days, per Cytomel labeling) than levothyroxine (about 6 to 7 days); it is shorter in hyperthyroidism and longer in hypothyroidism. Elimination is mainly by hepatic deiodination, with glucuronide and sulfate conjugation; metabolites are excreted in urine and bile.

• Uncorrected adrenal insufficiency.
• Hypersensitivity to liothyronine or to any component of the preparation.

• Cardiac adverse reactions in the elderly and in patients with cardiovascular disease: start at a lower dose. Over-treatment can cause arrhythmias, angina and myocardial infarction; monitor for arrhythmias during surgery in patients with coronary artery disease.
• Myxedema coma: oral thyroid hormone is not recommended because absorption is unpredictable; use intravenous products.
• Acute adrenal crisis: treat coexisting adrenal insufficiency with glucocorticoids before starting liothyronine.
• Narrow therapeutic index: over- or under-treatment can affect growth, cardiovascular function, bone metabolism, reproduction, cognition, mood and glucose and lipid metabolism. Doses are adjusted carefully by the prescriber with laboratory monitoring.
• Worsening of diabetic control: antidiabetic or insulin doses may need adjustment.
• Decreased bone mineral density with over-replacement, particularly in postmenopausal women.

• Calcium and iron preparations, antacids, bile acid sequestrants and ion-exchange resins can reduce absorption; separate by at least 4 hours.
• Warfarin and other oral anticoagulants: thyroid hormone increases catabolism of vitamin K-dependent clotting factors; monitor INR when starting or changing doses.
• Digitalis glycosides: serum digoxin levels and effect may fall.
• Insulin and oral antidiabetic agents: requirements may rise; monitor glucose.
• Sympathomimetics, tricyclic and tetracyclic antidepressants and ketamine: increased risk of tachycardia, hypertension and arrhythmia. T3 may enhance the effects of antidepressants; monitor.
• Estrogens, androgens, glucocorticoids, amiodarone, lithium, enzyme inducers such as rifampin and carbamazepine, and tyrosine kinase inhibitors can change thyroid hormone binding, levels or requirements. Biotin can interfere with thyroid immunoassays.

Adverse reactions are mainly those of over-replacement: palpitations, tachycardia, arrhythmias, angina, increased blood pressure, tremor, nervousness, anxiety, insomnia, headache, heat intolerance, sweating, fever, diarrhea, increased appetite, weight loss, menstrual irregularity, muscle weakness and decreased bone mineral density. Hypersensitivity to inactive ingredients can occur. Under-replacement leaves symptoms of hypothyroidism.

Pregnancy: thyroid hormone requirements often increase during pregnancy, and untreated maternal hypothyroidism carries risks for the mother and fetus. TSH is monitored and the dose adjusted. Fetal neurodevelopment depends on maternal T4, which T3 does not replace, so guidelines prefer levothyroxine monotherapy in pregnancy; T3 or combination therapy is generally continued only under specialist care.

Lactation: liothyronine is present in human milk in small amounts, and replacement doses are not expected to harm a breastfed infant. Dose requirements generally return to pre-pregnancy levels after delivery, with TSH monitoring.

• TSH in primary hypothyroidism, and serum T3 in secondary or tertiary disease; serum T4 is low during T3-only therapy, and T3 levels vary with time since the last dose.
• Heart rate, rhythm and blood pressure, especially in older patients and those with cardiovascular disease.
• Bone mineral density in at-risk patients on long-term therapy, glucose control in diabetes, and INR in patients on warfarin.
• Signs of over- or under-replacement, and growth and development in pediatric patients.

• Cytomel (liothyronine sodium tablets) Prescribing Information, Pfizer.
• Triostat (liothyronine sodium injection) Prescribing Information.
• Synthroid (levothyroxine sodium tablets) Prescribing Information, AbbVie.
• Jonklaas J, et al. Guidelines for the Treatment of Hypothyroidism, American Thyroid Association Task Force on Thyroid Hormone Replacement. Thyroid. 2014.
• Alexander EK, et al. 2017 Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and the Postpartum. Thyroid. 2017.