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Published on: December 2, 2014
Subclinical hypothyroidism, arterial stiffness, and myocardial reserve
P J D Owen1, C Rajiv, D Vinereanu
1Centre for Endocrine and Diabetes Sciences, Cardiff University, University Hospital of Wales, Cardiff CF14 4XN, Wales, United Kingdom.
Insights
Subclinical hypothyroidism (SCH) increases arterial stiffness, which improves with l-thyroxine treatment. However, myocardial functional reserve remains similar to controls and is unaffected by treatment.
Area of Science:
- Cardiology
- Endocrinology
- Vascular Medicine
Background:
- Subclinical hypothyroidism (SCH) is linked to cardiac disease risk, but its effects on arterial function are not well understood.
- Assessing arterial and cardiac function in SCH is crucial for understanding cardiovascular implications.
Purpose of the Study:
- To evaluate arterial and cardiac function in women with subclinical hypothyroidism.
- To determine the impact of l-thyroxine treatment on arterial stiffness and cardiac function in SCH patients.
Main Methods:
- A 6-month controlled observational study involving 19 female SCH patients and 10 female controls.
- Utilized pulse wave analysis and tissue Doppler dobutamine stress echocardiography to measure vascular stiffness and left ventricular function.
- Assessed changes following incremental doses of l-thyroxine in SCH patients.
Main Results:
- Subclinical hypothyroidism patients exhibited elevated baseline augmentation gradient and heart rate-corrected augmentation index compared to controls.
- L-thyroxine treatment significantly reduced arterial stiffness indices in SCH patients.
- No significant differences were observed in resting global or regional left ventricular function, or myocardial velocities during dobutamine stress between SCH patients and controls, or after treatment.
Conclusions:
- Arterial stiffness is increased in subclinical hypothyroidism and can be improved with l-thyroxine therapy.
- Myocardial functional reserve in SCH patients is comparable to healthy individuals and is not altered by l-thyroxine treatment.
Context:
Subclinical hypothyroidism (SCH) is associated with increased risk of cardiac disease; its impact on arterial function is less clear.
Objective:
The objective of the study was the assessment of arterial and cardiac function.
Design:
The study was a 6-month controlled observational study using pulse wave analysis and tissue Doppler dobutamine stress echocardiography.
Setting:
The study was conducted at a thyroid clinic.
Patients:
Nineteen female SCH patients with raised TSH, normal free T(4), and no cardiovascular disease [aged 49.2 +/- 3.8 yr; body mass index (BMI) 29.9 +/- 6.7 kg/m(2)] were recruited from the thyroid clinic, and 10 female controls (aged 50.2 +/- 3.4 yr; BMI 29.7 +/- 7.2 kg/m(2)) also participated in the study.
Interventions:
Incremental doses of l-thyroxine were used.
Main Outcome Measures:
Indices of vascular stiffness and left ventricular echocardiographic function were measured.
Results:
Baseline augmentation gradient was elevated in SCH, compared with controls [10.3 +/- 5.1 (sd) mm Hg vs. 8.0 +/- 4.2, P < 0.05]; when euthyroid (mean T(4) dose 114 mug/d), it fell to 8.8 +/- 5.3 mm Hg (P < 0.05). Heart rate-corrected augmentation index was 26.7 +/- 9.9 vs. 18.8 +/- 9.9% (P < 0.02), falling to 19.7 +/- 9.6% (P < 0.001) after treatment. Time of travel of the reflected wave was 139.3 +/- 11.7 msec, compared with 141.5 +/- 8.8 msec in controls (P < 0.05), increasing to 144.9 +/- 11.9 msec (P < 0.05). There were no differences in resting global, regional left ventricular function, or regional myocardial velocities during maximal dobutamine stress between SCH patients and controls, or in treated patients, compared with baseline.
Conclusions:
Arterial stiffness was increased in SCH and improved with l-thyroxine, which may be beneficial, whereas myocardial functional reserve was similar to controls and remained unaltered after treatment.
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