A Deeper Understanding of the Causal Relationships Between Thyroid Function and Atrial Fibrillation

Abstract

Thyroid hormones are highly pleiotropic and even minor variations in thyroid function have been associated with various adverse clinical outcomes in observational studies. This has opened up discussions whether mild (subclinical) thyroid dysfunction should be treated and whether reference ranges for thyroid function tests should be adapted. However, observational studies are prone to various sources of bias, including residual confounding, reverse causality, and selection bias, which can affect their results and disrupt their interpretation. It is therefore key to first assess whether the reported associations are causal or not. While most of the reported associations have not been verified by randomized controlled trials or experimental studies, Mendelian randomization (MR) is a well-established and widely used method to investigate causality. Its fundamental principle is that genetic variants which alter an exposure that is causal for the outcome of interest should also be associated with this outcome to the extent corresponding to their effects on the exposure (1). In this way, genetic variants are used as proxies to evaluate the causal effect of an exposure (eg, thyroid function) on the outcome of interest. They draw from the fact that genetic variants segregate randomly from parents to offspring, which can be compared with the randomization applied in clinical trials and allows potential confounding to be overcome. However, this approach requires several assumptions: the genetic variants used as instruments in MR analyses have to be associated with the exposure, they have to be independent of confounders of the exposure–outcome relationship, and their effects on the outcome of interest have to be mediated solely by the exposure under study. Consequently, any so-called horizontal pleiotropic variants should be excluded as they can bias the results of a MR analysis (1). Up to 65% of the interindividual variation in thyroid function is determined by genetic factors (2, 3). Recent large-scale meta-analyses of genome-wide association studies on thyroid function significantly increased the number of genetic variants associated with normal-range thyrotropin (TSH) and free thyroxine levels, which paved the way for well-powered MR studies (3, 4). Indeed, various MR studies on thyroid function provided evidence for causal effects on several classical thyroid hormone dependent outcomes, such as atrial fibrillation (AF), blood pressure, and serum cholesterol levels, which confirms that this method is truly effective in detecting causality (5, 6). Besides providing evidence for causality, multivariable MR (MVMR) analyses can also elucidate the pathophysiological mechanisms behind the observed association by simultaneously testing the effects of multiple factors on the outcome of interest. In brief, factors that attenuate the effect of the analyzed exposure on the tested outcome in a MVMR analysis are considered as mediators for the causal relationship between these 2 traits. Using this approach, AF was identified as a mediator for the causal association between variation in normal-range thyroid function and stroke (7). In the current study, Shi et al. (8) used the MVMR approach to discover mediators for the causal relationship between variation in normal-range thyroid function and AF risk, next to the direct effects of thyroid hormone on the heart. For this, several physiologically plausible mediators were assessed in their study (eg, blood pressure, heart rate, and various cardiac structure parameters). Correction for height attenuated the effect of genetically predicted TSH levels on AF risk from –0.12 (±0.02) to –0.06 (±0.02) change in log-transformed odds ratio (±standard error) per a standard deviation increase in TSH. In this way, height was identified as the major independent mediator in the causal association between variation in normal-range thyroid function and AF risk (8). This finding is in line with well-documented effects of thyroid function on childhood growth as well as with previous observational studies showing that height positively correlates with AF risk. Importantly, the authors subsequently showed that height was not a mediator in the relation between thyroid function and AF when analyses were restricted to only those TSH-associated genetic variants which are also related to autoimmune thyroid disease. This supports the biological plausibility of their findings, since autoimmune thyroid disease usually presents in adulthood far after the completion of growth (8). The fact that the effects of genetically determined thyroid function on AF risk are partly mediated by height is not only interesting from a pathophysiological point of view, but also from a clinical perspective: as height is determined in early life, it is likely that correction of thyroid function in later life will not fully reverse the effects of variation in thyroid function on AF risk described in observational studies. This sh