Literature DB >> 32965605

Abnormal diastolic function and Global longitudinal strain in patients with Thalassemia Major on long term chelation therapy.

Sunil K Nadar1, Shahina Daar2,3, Wael A Abdelmottaleb4, Muhammad M Shaikh4, Hafsa Al Mahrouqi5, Majida Al-Raiisi5, Moez Hassan6, Badar Al Rawahi6, Sarah Al Rahbi6.   

Abstract

Cardiac complications are the major cause of mortality in patients with Thalassemia major (TM). Cardiac T2* MRI is currently the gold standard for assessing myocardial iron concentration. The aim of our study was to assess whether any echocardiographic parameter would correlate with these findings in patients well established on chelation therapy. This was a prospective study on patients with TM who are regularly followed in our clinic. Patients had a cardiac MRI and echocardiogram within 2 months of each other. Echo parameters included global longitudinal strain and diastolic function. We also compared these findings with those from a cohort of thalassemia intermedia (TI) and normal controls. A total of 84 patients (mean age 26.3 ± 6.1 years, 42.8% male) with TM were enrolled. All had normal left ventricular ejection fraction and only 8 patients had MRI T2* < 10. As compared to 17 patients with TI and 53 controls, these patients had significantly higher E/E' and lower pulmonary vein s/dd ratio suggesting early diastolic dysfunction. 28 patients fulfilled criteria for diastolic dysfunction even in the presence of normal MRI T2*. Global longitudinal strain (GLS) was significantly lower in the TM group as compared to the TI and controls. We found no correlation between any of the echo findings and the MRI T2*in TM patients. In patients with thalassemia and MRI T2* > 20 ms features of diastolic dysfunction persist even in the presence of normal LV function and normal GLS. This suggests that diastolic function remains abnormal even when myocardial iron concentrations are normal and follow up therefore is essential.

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Keywords:  Diastolic function; Echocardiogram; Global longitudinal strain; Thalassemia intermedia; Thalassemia major

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Year:  2020        PMID: 32965605     DOI: 10.1007/s10554-020-02036-8

Source DB:  PubMed          Journal:  Int J Cardiovasc Imaging        ISSN: 1569-5794            Impact factor:   2.357


  1 in total

1.  Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with beta thalassemia.

Authors:  Suchaya Silvilairat; Rekwan Sittiwangkul; Yupada Pongprot; Pimlak Charoenkwan; Charlie Phornphutkul
Journal:  Eur J Echocardiogr       Date:  2007-08-07
  1 in total
  2 in total

1.  Native cardiac magnetic resonance T1 mapping and cardiac mechanics as assessed by speckle tracking echocardiography in patients with beta-thalassaemia major.

Authors:  Wing-Shan See; Edwina Kam-Fung So; Gloria Yu-Yan Hwang; Leanne Chin; Lawrence Ip; Wendy Wai-Man Lam; Shau-Yin Ha; Yiu-Fai Cheung
Journal:  Int J Cardiol Heart Vasc       Date:  2021-12-31

2.  Global longitudinal strain for detection of cardiac iron overload in patients with thalassemia: a meta-analysis of observational studies with individual-level participant data.

Authors:  Armin Attar; Alireza Hosseinpour; Hamidreza Hosseinpour; Nahid Rezaeian; Firoozeh Abtahi; Fereshte Mehdizadeh; Mozhgan Parsaee; Nehzat Akiash; Mohaddeseh Behjati; Antonella Meloni; Alessia Pepe
Journal:  Cardiovasc Ultrasound       Date:  2022-08-12       Impact factor: 2.263

  2 in total

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