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Updated: May 21, 2025

A Thrombotic Stroke Model Based On Transient Cerebral Hypoxia-ischemia
Published on: August 18, 2015
Associations of Free and Reverse Triiodothyronine with Long-Term All-Cause Mortality After Acute Ischemic Stroke and
Saulius Taroza1, Julius Burkauskas1, Aurelija Podlipskytė1
1Laboratory of Behavioral Medicine, Neuroscience Institute, Lithuanian University of Health Sciences, LT-00135 Palanga, Lithuania.
Insights
Lower free triiodothyronine (fT3) in acute ischemic stroke (aIS) and higher reverse T3 (rT3) in acute myocardial infarction (aMI) predict one-year mortality. These thyroid hormone associations with mortality did not persist over five years in arterial thrombosis patients.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Neurology
Background:
- Arterial thrombosis (AT), encompassing ischemic heart disease (IHD) and ischemic stroke (IS), is linked to altered thyroid hormone levels.
- Specifically, lowered free triiodothyronine (fT3) and elevated reverse T3 (rT3) have been observed in acute ischemic stroke (aIS) and acute myocardial infarction (aMI).
- Previous research indicated these hormonal changes correlate with worse one-year outcomes, but long-term associations and the role of rT3 in aIS remain unclear.
Purpose of the Study:
- To investigate the impact of fT3 and rT3 on all-cause mortality in patients with aIS and aMI over a five-year period.
- To determine if the one-year associations between fT3, rT3, and mortality persist beyond five years.
- To assess the prognostic value of rT3 in aIS outcomes over the extended follow-up.
Main Methods:
- A cohort study including 241 aIS and 289 aMI patients from Lithuania.
- Serum levels of fT3, rT3, free thyroxine, and thyroid-stimulating hormone were measured upon intensive care unit admission.
- All-cause mortality was tracked over one and five years post-event.
Main Results:
- Lower fT3 was independently associated with increased one-year all-cause mortality in aIS patients (OR = 0.41).
- Higher rT3 was independently associated with increased one-year all-cause mortality in aMI patients (OR = 1.69).
- No significant associations were found between fT3 or rT3 levels and all-cause mortality at the five-year follow-up for either aIS or aMI.
Conclusions:
- Reduced fT3 levels in aIS and elevated rT3 levels in aMI are significant predictors of one-year all-cause mortality.
- These thyroid hormone-mortality associations appear to be transient, diminishing by the five-year mark.
- Thyroid hormone status may serve as a short-term prognostic marker in acute arterial thrombotic events.
Abstract:
Background: Arterial thrombosis (AT), the main clinical manifestations of which are ischemic heart disease (IHD) and ischemic stroke (IS), is associated with lowered free triiodothyronine (fT3) in acute ischemic stroke (aIS) and acute myocardial infarction (aMI) but increased reverse T3 (rT3) in aMI, which are associated with worse outcomes at one year. Whether such associations remain independent over a longer follow-up period and the value of rT3 in aIS outcomes are largely unknown. This study was dedicated to examining the impact of fT3 and rT3 on aIS and aMI all-cause mortality over a longer 5-year period. Methods: Individuals from Lithuania who experienced aIS and aIM were included in this study. Serum fT3, rT3, free thyroxin and thyroid-stimulating hormone values were examined on admission to the intensive care department. Follow-up for all-cause mortality was divided into two time periods: 1 and 5 years. Results: The final study (aIS cohort age, 67.5 ± 9.6 years, 41.5% women and aMI cohort age, 61.8 ± 11.4 years, 28% women) consisted of 241 aIS and 289 aMI individuals, respectively. Lower fT3 was independently associated (OR = 0.41; 95% CI: 0.17-0.99, p = 0.049) with aIS, and higher rT3 (OR = 1.69; 95% CI: 1.06-2.67, p = 0.027) with aMI with increased all-cause mortality at 1 year. No associations were found between studied hormones and all-cause mortality at 5 years in both conditions. Conclusions: Lower fT3 in aIS and higher rT3 in aMI are associated with higher all-cause mortality at 1 year. No such associations were found at 5 years.
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