Abstract

The existence of a phase of prolonged suppression of TSH despite normalization of serum thyroid hormones over a variable period of time during the recovery of thyrotoxicosis has been documented in literature. Conversely, a temporary elevation of TSH despite attainment of euthyroid levels of serum thyroid hormones following extreme hypothyroidism has also been observed. This rate-independent lag time in TSH recovery is an evidence of a “persistent memory” of the history of dysthyroid states the hypothalamus–pituitary–thyroid (HPT) axis has encountered after the thyroid hormone perturbations have faded out, a phenomenon termed “hysteresis.” Notwithstanding its perplexing nature, hysteresis impacts upon the interpretation of thyroid function tests with sufficient regularity that clinicians risk misdiagnosing and implementing erroneous treatment out of ignorance of this aspect of thyrotropic biology. Mathematical modeling of this phenomenon is complicated but may allow the euthyroid set point to be predicted from thyroid function data exhibiting strong hysteresis effects. Such model predictions are potentially useful for clinical management. Although the molecular mechanisms mediating hysteresis remain elusive, epigenetics, such as histone modifications, are probably involved. However, attempts to reverse the process to hasten the resolution of the hysteretic process may not necessarily translate into improved physiology or optimal health benefits. This is not unexpected from teleological considerations, since hysteresis probably represents an adaptive endocrinological response with survival advantages evolutionarily conserved among vertebrates with a HPT system.

Highlights

  • Given the exquisite potency of thyroid hormones on the body, the hypothalamus–pituitary–thyroid (HPT) axis is under extremely delicate homeostatic control to ensure that the circulating thyroid hormone levels are finely adjusted to physiological concentrations critical for normal cellular, tissue, and organ development, function as well as the overall survival of the organism [1,2,3]

  • Thyroid function test (TFT) data have revealed that mild departure of free T4 (FT4) and TSH away from their respective normal ranges often led to the recovery of FT4 and TSH to their expected baseline levels in a coupled fashion fairly rapidly

  • Hyperthyroidism and hypothyroidism lead to temporary suppression and overexpression of TSH out of the normal reference range

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Summary

INTRODUCTION

Given the exquisite potency of thyroid hormones on the body, the hypothalamus–pituitary–thyroid (HPT) axis is under extremely delicate homeostatic control to ensure that the circulating thyroid hormone levels are finely adjusted to physiological concentrations critical for normal cellular, tissue, and organ development, function as well as the overall survival of the organism [1,2,3]. The HPT axis is naturally regulated by a negative feedback loop in order to keep FT3 and FT4 from swinging off the normal limits In this system, excessive FT4 (when deiodinated to FT3 intracellularly) and FT3 suppresses the expression of TRH and TSH. During thyroid hormone excess when FT3 and FT4 are rising and have exceeded their upper limits, serum TSH will decline and even become suppressed below the lower limit of normal. A strange observation has been noticed by clinicians treating patients with thyroid hormone disorders This pertains to elevated serum TSH for a variable period despite restoration of euthyroid levels of FT3/FT4, following treatment of severe hypothyroidism [13, 14]. The following review is devoted to the discussion of hysteresis of the HPT axis and its clinical implications

BRIEF HISTORICAL PERSPECTIVES OF HYSTERESIS
CLINICAL SCENARIOS
EXPERIMENTAL EVIDENCE OF HYSTERESIS IN LOWER VERTEBRATES
HHyysstteerreessiiss aanndd tthhee TThhyyrrooiidd AAxxiiss
OF HYSTERESIS
CLINICALLY RELEVANT CONSIDERATIONS AND APPLICATIONS
CONCLUSION
Findings
AUTHOR CONTRIBUTIONS
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