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Published on: October 6, 2023
Congenital Hypothyroidism and Brain Development: Association With Other Psychiatric Disorders
1Laboratory of Information Biology, Graduate School of Information Sciences, Tohoku University, Sendai, Japan.
Insights
Thyroid hormone insufficiency during development, known as congenital hypothyroidism, severely impacts brain development and is linked to psychiatric disorders. Early diagnosis and treatment are crucial to prevent lasting neurological damage.
Area of Science:
- Neuroendocrinology
- Developmental Neuroscience
- Psychiatry
Background:
- Thyroid hormones are essential for normal brain development.
- Perinatal thyroid hormone deficiency (congenital hypothyroidism) causes severe developmental delays.
- Congenital hypothyroidism arises from thyroid dysgenesis or low iodine intake.
Purpose of the Study:
- To review the disruption of brain function in congenital hypothyroidism.
- To connect basic and clinical research on thyroid dysfunction and psychiatric disorders.
Main Methods:
- Review of existing basic and clinical research.
- Analysis of animal models of hypothyroidism.
- Examination of neuropathological findings in affected patients.
Main Results:
- Thyroid hormone insufficiency perturbs neuronal architecture, affecting synapses, migration, and myelination.
- Reduced parvalbumin expression is a key molecular marker in congenital hypothyroidism.
- Animal studies confirm reproducible links between hypothyroidism, brain abnormalities, and altered molecular expression.
Conclusions:
- Congenital hypothyroidism leads to significant neuropathological changes.
- Thyroid dysfunction during development is relevant to psychiatric disorders.
- Further research integrating basic and clinical findings is warranted.
Abstract:
Thyroid hormones play an important role in brain development, and thyroid hormone insufficiency during the perinatal period results in severe developmental delays. Perinatal thyroid hormone deficiency is clinically known as congenital hypothyroidism, which is caused by dysgenesis of the thyroid gland or low iodine intake. If the disorder is not diagnosed or not treated early, the neuronal architecture is perturbed by thyroid hormone insufficiency, and neuropathological findings, such as abnormal synapse formation, defects in neuronal migration, and impairment of myelination, are observed in the brains of such patients. Furthermore, the expression of psychiatric disorder-related molecules, especially parvalbumin, is significantly decreased by thyroid hormone insufficiency during the perinatal period. Animal experiments using hypothyroidism models display decreased parvalbumin expression and abnormal brain architecture, and these experimental results show reproducibility and stability. These basic studies reinforce the results of epidemiological studies, suggesting the relevance of thyroid dysfunction in psychiatric disorders. In this review, we discuss the disruption of brain function associated with congenital hypothyroidism from the perspective of basic and clinical research.
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