From Wikipedia, the free encyclopedia
  (Redirected from Liothyronine sodium)
Jump to navigation Jump to search
Liothyronine sodium
Liotironina sódica3D.png
Clinical data
Trade namesCytomel
  • US: A (No risk in human studies)
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding99.7%
Elimination half-life2.5 days
CAS Number
PubChem CID
PDB ligand
ECHA InfoCard100.000.203 Edit this at Wikidata
Chemical and physical data
Molar mass672.96 g/mol
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)

Liothyronine is a synthetic form of triiodothyronine (T3), a thyroid hormone used to treat hypothyroidism and myxedema coma. T3 is the metabolically active thyroid hormone, which causes feedback inhibition, and lowers elevated TSH levels. It increases metabolism in peripheral tissues and is indicated when there is an impaired conversion of T4 to T3 in peripheral tissues. It is also used as an augmentation strategy in treating major depressive disorder when used in combination with antidepressants.[1] It is marketed as the sodium salt under the brand name Cytomel (or Tertroxin in Australia).


Physicians may use liothyronine instead of or in addition to levothyroxine (T4) for patients undergoing thyroid hormone withdrawal. When a patient has thyroid cancer or Graves' disease, ablation therapy with radioactive iodine (131I) can be used to remove trace thyroid tissue that may remain after thyroidectomy (surgical excision of the gland). For 131I therapy to be effective, the trace thyroid tissue must be avid to iodine, which is achieved by elevating the patient's TSH levels.[2] For patients taking levothyroxine, TSH may be boosted by discontinuing levothyroxine for 3–6 weeks.[2] This long period of hormone withdrawal is required because of levothyroxine's relatively long biological half-life, and may result in symptoms of hypothyroidism in the patient. The shorter half-life of liothyronine permits a withdrawal period of two weeks, which may minimize hypothyroidism symptoms. One protocol is to discontinue levothyroxine, then prescribe liothyronine while the T4 levels are falling, and finally stop the liothyronine two weeks before the radioactive iodine treatment.[2]

Liothyronine may also be preferred for patients with myxedema coma because of its quicker onset of action when compared to levothyroxine.[3]

Low-dose liothyronine has been shown to improve depression symptoms in patients with normal thyroid function who do not have adequate relief from their depression after trying several different antidepressants. When added to existing medications, liothyronine helped achieve remission in 24% of patients participating in a subset of the large STAR*D depression trial.[4] According to a 2001 meta-analysis that analyzed the effectiveness of adding Liothyronine to tricyclic antidepressants, women in particular may benefit from Liothyronine.[5] The average effective dose for depression was 45 mcg of Liothyronine daily, which is lower than the doses used for treating hypothyroidism.[4] About 9% of patients stopped taking liothyronine due to side effects.[4] The difference in gender response may be due to differences in metabolism of thyroid precursors.[6]

An algorithm developed from the STAR*D trial recommends liothyronine as an option when patients have failed two antidepressant medications.[7][8]

Advantages in thyroid hormone replacement[edit]

See Hypothyroidism for an in-depth explanation of hormone replacement.

Liothyronine is an option for routine thyroid hormone replacement. It has a half-life of 24 hours.[9] (although the stated biological half-life is 2.5 days). This compares to a half life of 7 days with levothyroxine. The shorter half-life allows patients to know if they are taking too much (indicated by a heart rate>100 bpm for more than 24 hours or increased anxiety) or if they should take more (no increase in energy). It is recommended that labs be drawn monthly and the dose increased until the patients hypothyroid symptoms resolve.

Per the liothyronine product insert, the starting dose may start at 5 mcg daily and increase by 5 mcg every two weeks. However, it should be noted that liothyronine should be taken with levothyroxine when liothyronine is taken long-term to avoid potential heart rate and rhythm abnormalities. Taking both levothyroxine and liothyronine separately allows for optimizing of reverse T3 and resolution of potential conversion problems of T4 to T3. Peripheral conversion problems are common when there is physiological stress (this will be felt as increased fatigue). Liothyronine can be compounded in a slow release form, however dangerous overdoses have been reported. [10]

Desiccated thyroid products have both the natural forms of T4 (thyroxine) and T3 (triiodothyronine) in one tablet in a ratio of 4 to 1 (T4 to T3). If the body does not metabolize thyroid hormones in this ratio (which is possible due to a thyroid problem) symptoms may worsen. This may be a reason to take synthetic forms of T4 and T3, levothyroxine and liothyronine, separately and target for upper range for fT3 and fT4, with rT3 in the bottom quartile. This is one therapeutic approach for patients who feel worse (HR>100bpm or profound fatigue or increased anxiety) after they start either levothyroxine or a desiccated thyroid product. These patients may benefit more from a customized ratio of T3/T4 such as reducing the ratio from 4:1 to 3:1 to 2:1 and so on until both symptomatic improvement and labs in ideal range as explained above. Patients who still have complications after obtaining normal labs may benefit from a slow-release formulation from a compounded pharmacy (no slow-release thyroid product is currently manufactured so it must be compounded).


Any person with a hypersensitivity to liothyronine sodium or any active ingredient of the formulation should not be on this medication. If there is uncorrected adrenal insufficiency or thyrotoxicosis, a different approach to therapy must be considered.[11]

Side effects[edit]

Liothyronine may cause a number of side effects, mostly similar to symptoms of hyperthyroidism, which include:[12]

  • weight loss
  • tremor
  • headache
  • upset stomach
  • vomiting
  • diarrhea
  • stomach cramps
  • nervousness
  • irritability
  • insomnia
  • excessive sweating
  • increased appetite
  • fever
  • changes in menstrual cycle
  • sensitivity to heat

Boxed warning[edit]

The package insert for Cytomel contains the following boxed warning, as do all thyroid hormones:[11]

Drugs with thyroid hormone activity, alone or together with other therapeutic agents, have been used for the treatment of obesity. In euthyroid patients, doses within the range of daily hormonal requirements are ineffective for weight reduction. Larger doses may produce serious or even life-threatening manifestations of toxicity, particularly when given in association with sympathomimetic amines such as those used for their anorectic effects.

Safety considerations[edit]


Per the U.S. FDA, liothyronine is categorized as Pregnancy Category A.[11] Thyroid hormone is minimally transferred to the fetus or placenta, however as of October 2014, studies have not shown any adverse effects to the fetus. Hypothyroid mothers should continue to take thyroid hormone replacement therapy throughout pregnancy to avoid adverse events.[13][14]


Breastmilk contains a low amount of thyroid hormone, so it is important to exercise caution when breastfeeding while taking liothyronine.[13]


Elderly patients should be started on lower doses of liothyronine.[11] Plasma (T3) concentrations in this population are decreased by 25% to 40%.[13] TSH must be routinely monitored since there is a risk of coronary artery disease, hyperthyroidism and excessive bone loss from inadequate or abnormal thyroid replacement.[13]


Liothyronine is the most potent form of thyroid hormone. As a salt of triiodothyronine (T3), it is chemically similar and pharmacologically equivalent to T3. As such, it acts on the body to increase the basal metabolic rate, affect protein synthesis and increase the body's sensitivity to catecholamines (such as adrenaline) by permissiveness. As monotherapy or in combination therapy with SSRIs, liothyronine may also enhance generation of new neurons in the central nervous system.[1] The thyroid hormones are essential to proper development and differentiation of all cells of the human body. These hormones also regulate protein, fat, and carbohydrate metabolism, affecting how human cells use energetic compounds.

In comparison to levothyroxine (T4), liothyronine has a faster onset of action as well as a shorter biological half-life, which may be due to less plasma protein binding to thyroxine-binding globulin and transthyretin.


  1. ^ a b Rosenthal, Lisa J.; Goldner, Whitney S.; O’Reardon, John P. (October 2011). "T3 augmentation in major depressive disorder: safety considerations". Am. J. Psychiatry. 168 (10): 1035–1040. doi:10.1176/appi.ajp.2011.10030402. PMID 21969047.
  2. ^ a b c "Thyroid Cancer (Papillary and Follicular)". American Thyroid Association. Retrieved 2016-12-25.
  3. ^ Klubo-Gwiezdzinska, J; Wartofsky, L (March 2012). "Thyroid emergencies". Medical Clinics of North America. 96 (2): 385–403. doi:10.1016/j.mcna.2012.01.015. PMID 22443982.
  4. ^ a b c Nierenberg, AA; Fava, M; Trivedi, MH; Wisniewski, SR; Thase, ME; McGrath, PJ; Alpert, JE; Warden, D; Luther, JF; Niederehe, G; Lebowitz, B; Shores-Wilson, K; Rush, AJ (September 2006). "A comparison of lithium and T(3) augmentation following two failed medication treatments for depression: a STAR*D report". The American Journal of Psychiatry. 163 (9): 1519–30, quiz 1665. doi:10.1176/appi.ajp.163.9.1519. PMID 16946176.
  5. ^ Altshuler, LL; Bauer, M; Frye, MA; Gitlin, MJ; Mintz, J; Szuba, MP; Leight, KL; Whybrow, PC (October 2001). "Does thyroid supplementation accelerate tricyclic antidepressant response? A review and meta-analysis of the literature". The American Journal of Psychiatry. 158 (10): 1617–22. doi:10.1176/appi.ajp.158.10.1617. PMID 11578993.
  6. ^ Berent, Dominika; Zboralski, Krzysztof; Orzechowska, Agata; Gałecki, Piotr (18 January 2014). "Thyroid hormones association with depression severity and clinical outcome in patients with major depressive disorder". Molecular Biology Reports. 41 (4): 2419–2425. doi:10.1007/s11033-014-3097-6. PMC 3968440.
  7. ^ Cooper-Kazaz, R; Cohen, R; Karagichev, L; Muhammed-Moussa, S; Grupper, D; Drori, T; Newman, ME; Sackeim, HA; Glaser, B; Lerer, B (2007). "Combined treatment with sertraline and liothyronine in major depression: a randomized, double-blind, placebo-controlled trial". Arch Gen Psychiatry. 64: 679–688. doi:10.1001/archpsyc.64.6.679. PMID 17548749.
  8. ^ G, Bradley; Rush, J; Trivedi, M; Wisniewski, S; Spencer, D; Fava, M (2008). "The STAR*D Study: Treating Depression in the Real World". Cleveland Clinic Journal of Medicine. 75.1: 57–66. doi:10.3949/ccjm.75.1.57.
  9. ^ Koda-Kimble, MA; Alldredge, BK (2012). Applied therapeutics: the clinical use of drugs (10th ed.). Baltimore: Wolters Kluwer Health/Lippincott Williams & Wilkins. ISBN 978-1609137137.
  10. ^ (Bains, Ajay, Ami-Joseph Brosseau, and David Harrison. “Iatrogenic Thyrotoxicosis Secondary to Compounded Liothyronine.” The Canadian Journal of Hospital Pharmacy 68.1 (2015): 57–59. Print.)
  11. ^ a b c d Cytomel (Liothyronine Sodium) Drug Information: Warnings and Precautions - Prescribing Information at RxList, retrieved on 29-October-2014
  12. ^ MedlinePlus. "Liothyronine." Last accessed July 14, 2007.
  13. ^ a b c d "Liothyronine (Lexi-Drugs)". LexiComp. Retrieved 29 October 2014.
  14. ^ Montalvo, JM; Wahner, HW; Mayberry, WE; Lum, RK (Aug 1973). "Serum triiodothyronine, total thyroxine, and thyroxine to triiodothyronine ratios in paired maternal-cord sera and at one week and one month of age". Pediatr Res. 7: 706–711. doi:10.1203/00006450-197308000-00006. PMID 4200034.