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The prognostic impact of thyroid function in pulmonary hypertension
Manuel J Richter1, Natascha Sommer2, Ralph Schermuly2
1Department of Pneumology, Kerckhoff Heart and Thoracic Center, Bad Nauheim, Germany; Department of Internal Medicine, Justus Liebig University Giessen, and Universities of Giessen and Marburg Lung Center (UGMLC), member of the German Center for Lung Research (DZL), Germany, Giessen, Germany.
Thyroid hormone levels and replacement therapy impact survival in pulmonary hypertension (PH) patients, particularly those with idiopathic PAH. Abnormal thyroid function is a key predictor of mortality in PH subtypes.
Area of Science:
- Endocrinology
- Cardiology
- Pulmonology
Background:
- Thyroid disease is prevalent in pulmonary hypertension (PH) patients.
- The impact of thyroid function on long-term PH survival is not well understood.
Purpose of the Study:
- To investigate the prognostic significance of thyroid hormone levels (free triiodothyronine, free thyroxine, TSH) and thyroid hormone replacement (THR) therapy in PH patients.
- To identify thyroid function parameters associated with mortality in various PH subtypes.
Main Methods:
- Retrospective analysis of 1,756 patients from the Giessen PH Registry (1999-2013).
- Included patients with pulmonary arterial hypertension (PAH), idiopathic PAH (iPAH), PH due to left heart disease, PH due to lung diseases, and chronic thromboembolic PH (CTEPH).
- Utilized Cox regression and Kaplan-Meier analyses to assess mortality predictors.
Main Results:
- Absence of THR therapy independently predicted death in iPAH.
- Low or high TSH levels were associated with increased mortality in iPAH.
- Reduced free triiodothyronine (fT3) levels independently predicted death in PAH and CTEPH.
Conclusions:
- Thyroid hormone levels and THR therapy are significant prognostic factors in iPAH, PAH, and CTEPH.
- Further prospective studies are needed to confirm these findings and evaluate THR therapy's efficacy in PH.
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