AI Article Synopsis

  • The relationship between thyroid dysfunction, metabolic syndrome (MetS), and cardiovascular (CV) risk creates a complex network that worsens health issues, showing that these conditions influence and contribute to one another.
  • Thyroid hormones significantly impact glucose and lipid metabolism, as well as blood flow regulation, while both MetS and thyroid dysfunction can lead to increased insulin resistance and lipid levels, along with endothelial dysfunction.
  • Given the association between MetS and thyroid issues along with their mutual inflammatory and oxidative stress factors, assessing and correcting thyroid function in MetS patients is crucial, yet more research is needed on treating subclinical thyroid problems in this group.

Article Abstract

The triad formed by thyroid dysfunction, metabolic syndrome (MetS), and cardiovascular (CV) risk forms a network with many connections that aggravates health outcomes. Thyroid hormones (THs) play an important role in glucose and lipid metabolism and hemodynamic regulation at the molecular level. It is noteworthy that a bidirectional association between THs and MetS and their components likely exists as MetS leads to thyroid dysfunction, whereas thyroid alterations may cause a higher incidence of MetS. Thyroid dysfunction increases insulin resistance, the circulating levels of lipids, in particular LDL-C, VLDL-C, and triglycerides, and induces endothelial dysfunction. Furthermore, THs are important regulators of both white and brown adipose tissue. Moreover, the pathophysiological relationship between MetS and TH dysfunction is made even tighter considering that these conditions are usually associated with inflammatory activation and increased oxidative stress. Therefore, the role of THs takes place starting from the molecular level, then manifesting itself at the clinical level, through an increased risk of CV events in the general population as well as in patients with heart failure or acute myocardial infarction. Thus, MetS is frequently associated with thyroid dysfunction, which supports the need to assess thyroid function in this group, and when clinically indicated, to correct it to maintain euthyroidism. However, there are still several critical points to be further investigated both at the molecular and clinical level, in particular considering the need to treat subclinical dysthyroidism in MetS patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477096PMC
http://dx.doi.org/10.3390/ijms251910628DOI Listing

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