Dextrothyroxine sodium

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Dextrothyroxine Sodium is a synthetic thyroid hormone analogue, specifically a form of thyroxine (T4) where the chirality of the molecule is reversed. It was investigated for use in reducing cholesterol levels and managing hyperlipidemia, but its use has been largely discontinued due to a lack of significant benefit and the emergence of more effective treatments.

Overview[edit | edit source]

Dextrothyroxine Sodium, also known as d-thyroxine, was once considered for the treatment of hypercholesterolemia (high cholesterol levels) and as an adjunct therapy in the management of hyperlipidemia (high levels of lipids in the blood). It operates by mimicking the natural thyroid hormone, thyroxine, which is critical in regulating metabolism, including the metabolism of lipids. However, unlike the naturally occurring L-thyroxine, dextrothyroxine sodium has a different spatial configuration, making it a mirror image of the natural form.

Pharmacology[edit | edit source]

The pharmacological action of Dextrothyroxine Sodium involves the acceleration of the body's metabolism, leading to an increased rate of lipid metabolism. This theoretically could help in reducing cholesterol levels in the bloodstream. However, clinical trials and studies have shown that the efficacy of dextrothyroxine in significantly impacting cholesterol levels is minimal. Moreover, concerns regarding its safety profile, particularly its effects on the heart, led to a reevaluation of its use in clinical practice.

Clinical Use and Discontinuation[edit | edit source]

Initially, Dextrothyroxine Sodium was explored as a potential treatment option for patients with high cholesterol levels, especially those who were at risk of cardiovascular diseases. However, during the 1970s, studies began to reveal that the benefits of dextrothyroxine might not outweigh its risks, particularly concerning cardiac side effects. The most notable study that led to the discontinuation of its use was the Coronary Drug Project, which found that dextrothyroxine did not significantly reduce the risk of coronary heart disease and might even increase mortality in certain groups of patients.

Conclusion[edit | edit source]

As a result of these findings, the use of Dextrothyroxine Sodium in clinical practice was largely abandoned, and it is no longer considered a viable treatment option for hypercholesterolemia or hyperlipidemia. The focus of treatment for these conditions has since shifted to other classes of drugs, such as statins, which have proven to be more effective and safer for patients.


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Contributors: Prab R. Tumpati, MD