Does Celexa affect thyroid function? (3+ effects)

In this article, we will explore the potential effects of Celexa on thyroid function. We will also explore research studies on this topic and discuss the possible side effects and their management

Does Celexa affect thyroid function?

Yes, Celexa (Citalopram) does affect thyroid function and thyroid dysregulation is frequently observed with antidepressant medications, particularly selective serotonin receptor inhibitors (SSRIs). However, it is important to note that individual responses to these medications can vary, and not everyone using Celexa will necessarily experience thyroid dysregulation.

Although there is limited clinical evidence regarding Celexa’s effect on thyroid function, numerous studies have investigated potential interactions between SSRIs and thyroid hormones.

The thyroid gland plays a vital role in regulating metabolism and energy production through the production of thyroxine (T4) and triiodothyronine (T3) hormones. As an SSRI, Celexa does influence thyroid hormone levels, which could potentially lead to complications like hypothyroidism and hyperthyroidism (1,2,3).

What does research suggest?

As mentioned earlier, research studies have established a connection between SSRI medications and thyroid function.

A study that investigated SSRI-induced thyroid dysregulation in a group of 29 patients, reported SSRI medication, including Citalopram, potentially suppressed thyroid-stimulating hormone (TSH) secretion through antagonism of the dopamine-serotonergic pathway causing thyroid dysregulation (8).

Furthermore, another study reported the case of a 35-year-old woman undergoing treatment with Citalopram. This case indicated that prolonged use of this medication mimics hypothyroidism by displacing bound T4 (9).

Conversely, studies have hypothesized that thyroid hormones enhance antidepressant therapy in the management of mood disorders (2,3,7).

How does Citalopram affect thyroid function?

The mechanism of action of Citalopram involves elevating serotonin levels in the brain and peripheral system. Studies have hypothesized a direct link between Citalopram’s effects on the thyroid and the action of serotonin along the hypothalamus-pituitary-thyroid axis (HPT axis).

The HPT axis governs the production of thyroid hormones. The hypothalamus releases thyrotropin-releasing hormone (TRH), which signals the pituitary gland to produce thyroid-stimulating hormone (TSH). TSH, in turn, stimulates the thyroid gland to produce T4 and T3 (3).

Celexa-induced alterations of serotonin levels can influence the release of TRH and TSH, thus affecting thyroid hormone production and regulation. Moreover, serotonin receptors along the HPT axis may modulate the release of TRH and TSH, affecting thyroid hormone production (1).

Additionally, serotonin plays a role in the body’s response to stress. Stress often triggers the release of cortisol, a stress hormone, which may affect the HPT axis and thyroid function.

Through these mechanisms, dysregulation induced by Celexa may manifest as either hypothyroidism or hyperthyroidism.

Clinical manifestations of Celexa-induced thyroid dysregulation:

Celexa-induced thyroid dysregulation can manifest in two ways:

Hypothyroidism

Hypothyroidism is characterized by an underactive thyroid, resulting in insufficient thyroid hormone levels. This condition can be caused by factors such as iodine deficiency and medications like SSRIs, including Sertraline and Celexa. Similar to the side effects of Celexa, hypothyroidism can manifest as fatigue, dehydration, headaches, constipation, changes in appetite and more (5).

Hyperthyroidism

Hyperthyroidism, on the other hand, refers to an overactive thyroid, marked by increased thyroid hormone production and elevated thyroid radioactive iodine uptake. Much like the side effects of Celexa, it may lead to symptoms such as diarrhoea, insomnia, irritability, changes in sexual activity and more (6).

It is important to note that these conditions may influence Citalopram’s side effects in certain individuals, and conversely, this could exacerbate pre-existing conditions like depression and anxiety.

How to manage Celexa-induced thyroid dysregulation?

If you suspect that Celexa is causing thyroid dysregulation, it is crucial to discuss this with your healthcare provider. Your healthcare provider may consider adjusting the dosage to see if it can alleviate these concerns.

Furthermore, if undesirable effects related to thyroid dysregulation persist, your doctor may recommend discontinuing the medication under their guidance. They might also suggest transitioning to an alternative antidepressant with a lower likelihood of affecting the thyroid.

In managing thyroid dysregulation disorders, your doctor may also prescribe medications in the following ways:

  • For the management of hyperthyroidism – Carbamizole (20mg per day) or Propylthiouracil (300-450mg per day). Additionally, Beta-blockers like Propranolol can be used to alleviate symptoms such as rapid heart rate and tremors.
  • For the management of hypothyroidism – Levothyroxine 50-75mcg per day.

Additionally, lifestyle modifications such as maintaining a balanced diet, engaging in regular exercise, practising stress management and adopting good sleep hygiene practices can optimize thyroid health and reduce the risk of thyroid dysregulation.

Conclusion

This article has explored Celexa-induced thyroid dysregulation, its clinical manifestations, and provided helpful tips for managing these conditions.

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References

1.-

Eker SS, Akkaya C, Sarandol A, Cangur S, Sarandol E, Kirli S. Effects of various antidepressants on serum thyroid hormone levels in patients with major depressive disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry [Internet]. 2008 May [cited 2023 Oct 12];32(4):955–61. Available from: https://doi.org/10.1016/j.pnpbp.2007.12.029

 

2.-

de Carvalho GA, Bahls SC, Boeving A, Graf H. Effects of Selective Serotonin Reuptake Inhibitors on Thyroid Function in Depressed Patients with Primary Hypothyroidism or Normal Thyroid Function. Thyroid [Internet]. 2009 Jul [cited 2023 Oct 12];19(7):691–7. Available from: https://doi.org/10.1089/thy.2008.0261

3.-

Hage MP, Azar ST. The Link between Thyroid Function and Depression. Journal of Thyroid Research [Internet]. 2012 [cited 2023 Oct 12];2012(590648):1–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246784/

 

4.-

Liao H, Rosenthal DS, Salini Chellappan Kumar. Abnormal Thyroid Function Laboratory Results Caused by Selective Serotonin Reuptake Inhibitor (SSRI) Antidepressant Treatment. Case reports in psychiatry [Internet]. 2023 May 11 [cited 2023 Oct 12];2023:1–4. Available from:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195165/

 

5.-

Patil N, Rehman A, Jialal I. Hypothyroidism [Internet]. PubMed. Treasure Island (FL): StatPearls Publishing; 2023 [cited 2023 Oct 12]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK519536/#article-23304.s8

 

6.-

De Leo S, Lee SY, Braverman LE. Hyperthyroidism. The Lancet [Internet]. 2017 Aug [cited 2023 Oct 12];388(10047):906–18. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014602/

 

7.-

Abulseoud OA, Gitlin M, Altshuler L, Frye MA. Baseline thyroid indices and the subsequent response to citalopram treatment, a pilot study. Brain and Behavior [Internet]. 2013 Jan 18 [cited 2023 Oct 12];3(2):89–94. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607150/

 

8.-

Keen F, Chalishazar A, Mitchem K, Dodd A, Kalhan A. Central hypothyroidism related to antipsychotic and antidepressant medications: an observational study and literature review. European Thyroid Journal [Internet]. 2022 Apr 1 [cited 2023 Oct 12];11(2). Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963170/

 

9.-

Cohen BM, Sommer BR, Vuckovic A. Antidepressant-Resistant Depression in Patients With Comorbid Subclinical Hypothyroidism or High-Normal TSH Levels. American Journal of Psychiatry [Internet]. 2018 Jul [cited 2023 Oct 12];175(7):598–604. Available from: https://ajp.psychiatryonline.org/doi/10.1176/appi.ajp.2017.17080949

 

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