The Influence of Reverse Triiodothyronine on Neuropsychiatric Disorders: A Narrative Review
Mark L. Gordon, Alison M. Gregg, Alicja B. Poleszak
Abstract
Introduction: Reverse triiodothyronine (rT3) is traditionally regarded as a biologically inactive isomer of triiodothyronine (T3), produced primarily via peripheral deiodination of thyroxine (T4). Although T3 binds to nuclear thyroid hormone receptors and regulates transcription of genes essential to neuronal development, synaptic plasticity, and myelination, rT3 lacks such agonist activity. Recent studies suggest rT3 may competitively inhibit T3 at receptor sites and influence thyroid hormone bioavailability by modulating deiodinase enzyme activity. These effects position rT3 as a potentially significant contributor to the pathophysiology of various neuropsychiatric conditions.
Materials and methods: A comprehensive literature review was conducted through 2024 using biomedical databases including PubMed, Scopus, and Google Scholar. Inclusion criteria targeted peer-reviewed studies investigating rT3 regulation, deiodinase enzyme function (particularly type 3 deiodinase, D3), and clinical correlations between altered thyroid hormone profiles and psychiatric illnesses. Key terms included “reverse T3,” “thyroid metabolism,” “deiodinase activity,” “functional hypothyroidism,” and various neuropsychiatric diagnoses. Articles emphasizing both molecular mechanisms and clinical outcomes were prioritized.
Results: Increased D3 activity during physiological stress, trauma, chronic inflammation, or psychiatric illness shifts T4 metabolism away from active T3 and toward inactive rT3. This leads to a biochemical state described as “functional hypothyroidism,” where serum T4 and thyroid-stimulating hormone (TSH) levels may appear normal, yet intracellular T3 action is diminished. Elevated rT3 and reduced T3/rT3 ratios have been identified in patients with depression, bipolar disorder, generalized anxiety, cognitive impairment, and schizophrenia. These alterations correlate with symptom severity and treatment resistance in some individuals. Additionally, rT3 has shown promise as a biomarker for disrupted thyroid signaling in neuropsychiatric contexts, potentially guiding more personalized treatment approaches.
Conclusions: Reverse T3, long viewed as a passive by-product, may play an active regulatory role in neuropsychiatric disorders by interfering with T3 signaling at the cellular level. Functional hypothyroidism driven by excess rT3 represents a distinct biochemical phenotype contributing to mood, cognition, and behavioral dysfunction. Recognition of this mechanism underscores the need for expanded thyroid assessment beyond standard TSH and T4 testing in psychiatric populations. Future research should focus on the therapeutic implications of correcting rT3 dominance and restoring optimal intracellular thyroid hormone activity.
PMID: 41168656
The Influence of Reverse Triiodothyronine on Neuropsychiatric Disorders: A Narrative Review – PubMed