RUHR-UNIVERSITY BOCHUM
“This puts our understanding of the interaction between the thyroid gland and the heart on a new footing and might pave the way to personalised preventive care,” says associate professor Dr. Johannes Dietrich from the Department of Medicine at St Josef Hospital, Clinic of Ruhr University Bochum, Germany (RUB). The researchers published their work in the journal Frontiers in Cardiovascular Medicine on 15 August 2022.
For the study, the heart and hormone researchers at RUB collaborated with a clinician scientist/hormone specialist affiliated with Tan Tock Seng Hospital, the Nanyang Technological University’s Lee Kong Chian School of Medicine and Duke-NUS Medical School in Singapore.
How should mild thyroid dysfunctions be treated?
Today, overt thyroid dysfunction is recognised as an established risk factor for major adverse cardiovascular events (MACE). However, the situation remained equivocal in mild thyroid dysfunction. “Whereas in some studies, minimal elevations of thyroid hormones and even high-normal concentrations within the reference range for healthy people predicted an increased risk for sudden cardiac death, other studies hadn’t shown such a correlation,” explains Johannes Dietrich. Until very recently, the jury was therefore still out on whether to treat those with subclinical forms of hyperthyroidism and hypothyroidism.
In order to gain a better understanding, a fresh systematic review by the international team analysed the results of 32 studies on this issue. In a pooled statistical evaluation with consecutive meta-analysis, the researchers found both subclinical hypothyroidism and subclinical hyperthyroidism to predict the risk for cardiovascular mortality. In particular, serum concentrations of the free thyroid hormone T4 (FT4) correlated directly with the probability of cardiac death and other adverse cardiovascular events.
Two different patterns
“The results suggest that cardiovascular risk increases continuously with the FT4 concentration, whereas a complex U-shaped risk relationship exists with the concentration of the controlling hormone thyrotropin, i.e. TSH,” elaborates Johannes Dietrich. This dualism may be explained by two different patterns of thyroid-mediated arrhythmia.
In one form (“dyshomeostatic type”), primary thyroid disease directly elevates the concentration of thyroid hormones and thereby increases the cardiovascular risk. In the other form (“allostatic type”), genetic factors, chronic stress and psychological strain increase the set point of the regulatory circuit between the pituitary gland and the thyroid gland, so that the indirectly increased FT4 concentration also promote arrhythmia.
Individual prevention and treatment
“The results of this study might pave the way to a personalised preventive strategy for heart outcomes,” conclude the authors. “Moreover, thyroid function might serve as a biomarker for the respective mechanism of origin in patients harbouring cardiac arrhythmia, helping to tailor individually optimised medication regimen.”
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