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Causal association of TSH with ischemic heart diseases and heart failure: A 2-sample Mendelian randomization study
Yuan Gao1, Tianwei Zhan2, Yingchun Xu1
1Department of Breast and Thyroid Surgery, Shaoxing People's Hospital, Shaoxing, China.
Insights
Thyroid-stimulating hormone (TSH) levels in euthyroid individuals may increase unstable angina risk but decrease heart failure risk in overweight patients. Careful TSH control is suggested for specific cardiovascular disease patients.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Genetics
Background:
- Thyroid dysfunction is linked to cardiovascular disease (CVD) risk.
- The impact of thyroid-stimulating hormone (TSH) levels within the euthyroid range on CVD risk remains uncertain.
- Investigating TSH's causal role in CVD is crucial for understanding disease mechanisms.
Purpose of the Study:
- To investigate the causal association between plasma TSH levels and cardiovascular diseases, specifically ischemic heart disease and heart failure (HF).
- To determine if genetically determined TSH levels influence the risk of specific cardiovascular events.
Main Methods:
- Two-sample Mendelian randomization analysis utilizing summary statistics from large genome-wide association studies (GWAS) datasets.
- Inverse-variance weighting was the primary analytical method.
- Sensitivity analyses, including MR Pleiotropy RESidual Sum and Outlier and leave-one-out methods, were employed to ensure result robustness.
Main Results:
- Genetically determined higher TSH levels showed a potential association with increased major coronary heart disease events and unstable angina pectoris.
- Conversely, higher TSH levels were potentially associated with a reduced risk of all-cause heart failure and HF with overweight.
- After Bonferroni correction, initial associations with major coronary heart disease and heart failure disappeared, highlighting the need for careful interpretation.
Conclusions:
- Elevated plasma TSH levels in euthyroid individuals may elevate the risk of unstable angina.
- Higher TSH levels might reduce heart failure risk specifically in overweight individuals.
- Plasma TSH levels warrant careful monitoring and management in specific patient populations at risk for cardiovascular events.
Abstract:
Thyroid dysfunction is associated with the risk of cardiovascular disease; however, whether plasma thyroid-stimulating hormone (TSH) levels in subjects with euthyroidism affect the risk of cardiovascular disease remains unclear. This study aimed to investigate the causal association between plasma TSH levels and cardiovascular diseases, particularly ischemic heart disease and heart failure (HF). Summary statistics from the Integrative Epidemiology Unit Open genome-wide association studies Project and FinnGen consortium were used to investigate the causal relationship between plasma TSH levels and the risk of cardiovascular diseases. Two-sample Mendelian randomization analysis using inverse-variance weighting as the primary method was performed. The MR Pleiotropy RESidual Sum and Outlier and leave-one-out methods were used to ensure the robustness of our findings. Genetically determined plasma TSH levels were associated with major coronary heart disease events (OR 1.0557, 95% CI 1.0141-1.0991), all-cause HF (OR 0.9587, 95% CI 0.9231-0.9956), and HF + non-ischemic cardiomyopathy (OR 0.9318, 95% CI 0.8786-0.9882). After the Bonferroni correction, the causation described above disappeared. In the secondary analysis, genetically determined higher TSH levels were associated with a higher risk for unstable angina pectoris (OR 1.0913, 95% CI 1.0350-1.1507), but were associated with a lower risk for HF + overweight (OR 0.9265, 95% CI 0.8821-0.9731). These results were further validated using sensitivity analysis. Our findings show that increased plasma TSH levels in patients with euthyroidism may increase the risk of unstable angina pectoris but reduce the risk of HF in overweight patients. This evidence indicates that plasma TSH levels may need to be carefully controlled in specific patients.
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