Abstract

Thyroid abnormalities, including mild forms of hypothyroidism and hyperthyroidism, are reported as risk factors for the development of a number of neuropsychiatric disorders, including schizophrenia. The diagnostic process still takes into account the extreme ranges of the accepted reference values for serum TSH since the concentration of free thyroxine in the serum does not change by definition. TSH mU/L cut-off values in psychiatric patients are currently clinically considered in the case of extremely high serum TSH levels (>4.0 mU/L). The results obtained in this study suggest that the clinically significant value has a lower TSH cut-off point with an upper limit of 2–2.5 mU/L. The criteria for the differential diagnosis of patients with schizophrenia, however, mainly take into account statutory reference ranges without a background related to the history of thyroid diseases in the family. The results indicate the need to lower the upper cut-off values for TSH among patients with early psychosis, which is related to the potential clinical significance of the obtained values both in the field of clinical evaluation and neuroimaging and laboratory evaluation parameters. The cut-off points obtained with the prior available knowledge coincided with the values established in the unsupervised clustering method, which further confirms the legitimacy of their use in the individualized diagnosis strategy of schizophrenia.

Highlights

  • Thyroid hormones (THs) play a key role in the development and proper functioning of the central nervous system (CNS) and influence the susceptibility to mental disorders.Taking into account the interaction between the endocrine and immune systems, THs influence the structure of neurons, microglia, astrocytes and oligodendrocytes, as well as the modulation of pro-inflammatory reactions [1]

  • According to a meta-analysis from 2021, an increased level of thyroidstimulating hormone (TSH) was observed in patients with multiple psychotic from 2021, an increased level of TSH was observed in patients with multiple psychotic episodes in relation to healthy people, while in patients in the first psychosis, a reduction episodes in relation to healthy people, while in patients in the first psychosis, a reduction in TSH and FT3 levels and an increase in FT4 levels compared to the control group were in TSH and FT3 levels and an increase in FT4 levels compared to the control group were observed [61]

  • We noted that the lower TSH cut-off levels, with an upper limit of 2–2.5 mU/L, were the most statistically significant in relation to severe depressive symptoms after three months of early psychosis therapy (BDI_12; ROC, AUC = 0.8)

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Summary

Introduction

Thyroid hormones (THs) play a key role in the development and proper functioning of the central nervous system (CNS) and influence the susceptibility to mental disorders. Taking into account the interaction between the endocrine and immune systems, THs influence the structure of neurons, microglia, astrocytes and oligodendrocytes, as well as the modulation of pro-inflammatory reactions [1]. Since brain development is strongly dependent on thyroid hormones, any impairment of the dynamics of their release causes 4.0/). The endocrine assessment of the functioning of the thyroid gland is an important element of the differential diagnosis of a patient with the first episode of psychosis or with exacerbation of symptoms [3]. Hypothyroidism is mainly associated with depressive symptoms. Clinical depression occurs in more than 40% of people suffering from hypothyroidism [6]

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