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• W2893632727 startingPage "1772" @default.
• W2893632727 abstract "Background Hereditary haemochromatosis ( HH ) is a common inherited disease. Abnormally increased intestinal iron absorption and accelerated recycling of iron by macrophages lead to progressive body iron accumulation and the generation of oxidative stress. In the late stages, iron overload can lead to dysfunction of the left ventricle ( LV ). It is believed that two‐dimensional speckle tracking echocardiography (2D STE ) can evaluate LV dysfunction more accurately than conventional echocardiography. This accurate evaluation seems to be clinically important in the early stages of HH before substantial damage of the LV . Evaluation of this assessment was the purpose of this paper. Methods We prospectively enrolled 24 patients with early diagnosed HH and without any history of cardiovascular diseases; 23 healthy age‐ and sex‐matched volunteers constituted the control group. Standard echocardiographic parameters and LV rotation and strain parameters were assessed and compared between the groups. Results All echocardiographic parameters were within normal ranges, and there were no differences between the groups. 2D STE revealed significantly worse basal and apical rotation, twist and torsion values in HH patients. The peak systolic longitudinal strain was decreased in HH patients, even though the LV ejection fraction ( LVEF ) was normal. There were weak correlations between the iron turnover and 2D STE parameters. Conclusions 2D STE seems to be more sensitive than traditional echocardiography for detecting LV abnormalities in HH patients who are diagnosed early. The results of this study may be clinically useful, but their relevance and therapeutic implications remain to be confirmed by further studies." @default.
• W2893632727 created "2018-10-05" @default.
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• W2893632727 date "2018-09-25" @default.
• W2893632727 modified "2023-10-18" @default.
• W2893632727 title "Can two-dimensional speckle tracking echocardiography be useful for left ventricular assessment in the early stages of hereditary haemochromatosis?" @default.
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• W2893632727 doi "https://doi.org/10.1111/echo.14141" @default.
• W2893632727 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30255609" @default.
• W2893632727 hasPublicationYear "2018" @default.
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