Evaluation of cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease using magnetic resonance imaging, echocardiography, and serum galectin-3

Background Myocardial fibrosis has recently been proposed as one of the contributing factors to the diverse pathogenicity of cardiomyopathy in sickle cell disease. Objective In this study, cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease were evaluated using card...

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Veröffentlicht in:Pediatric radiology 2023-11, Vol.53 (12), p.2515-2527
Hauptverfasser: Wagdy, Reham, Fathy, Alaa, Elnekidy, Abdelaziz, Salaheldin, Geylan, Nazir, Hanan, Fahmy, Rana, Elkafrawy, Hagar, Elkafrawy, Fatma
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container_end_page 2527
container_issue 12
container_start_page 2515
container_title Pediatric radiology
container_volume 53
creator Wagdy, Reham
Fathy, Alaa
Elnekidy, Abdelaziz
Salaheldin, Geylan
Nazir, Hanan
Fahmy, Rana
Elkafrawy, Hagar
Elkafrawy, Fatma
description Background Myocardial fibrosis has recently been proposed as one of the contributing factors to the diverse pathogenicity of cardiomyopathy in sickle cell disease. Objective In this study, cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease were evaluated using cardiac magnetic resonance imaging (MRI), tissue Doppler echocardiography and serum galectin-3. Materials and methods The study included 34 children with sickle cell disease who were compared with a similar number of healthy controls. Cardiac MRI was used to evaluate late gadolinium enhancement, native T1 mapping, extracellular volume, and T2* for estimation of iron load. Cardiac function and myocardial performance index (MPI, evaluated by tissue Doppler echocardiography) and serum galectin-3 were compared to controls. Results The mean age of the included patients was 13.3 ± 3.2 years. Myocardial iron load by T2* was normal. The mean level of extracellular volume (35.41 ± 5.02%) was significantly associated with the frequency of vaso-occlusive crises ( P  = 0.017) and negatively correlated with hemoglobin levels ( P  = 0.005). Galectin-3 levels were significantly higher among cases than controls ( P  =  0.00) , at a cutoff value on the receiver operating characteristic curve of 6.5 ng/ml, sensitivity of 82.5% and specificity of 72.8%. The extracellular volume was significantly higher in cases, with a MPI > 0.4. Conclusion Diffuse interstitial myocardial fibrosis can be detected early in children with sickle cell disease using T1 mapping and is associated with a high frequency of vaso-occlusive crisis. MPI of the left ventricle and serum galectin-3 are recommended screening tools for subclinical cardiac abnormalities. Graphical abstract
doi_str_mv 10.1007/s00247-023-05750-2
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Objective In this study, cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease were evaluated using cardiac magnetic resonance imaging (MRI), tissue Doppler echocardiography and serum galectin-3. Materials and methods The study included 34 children with sickle cell disease who were compared with a similar number of healthy controls. Cardiac MRI was used to evaluate late gadolinium enhancement, native T1 mapping, extracellular volume, and T2* for estimation of iron load. Cardiac function and myocardial performance index (MPI, evaluated by tissue Doppler echocardiography) and serum galectin-3 were compared to controls. Results The mean age of the included patients was 13.3 ± 3.2 years. Myocardial iron load by T2* was normal. The mean level of extracellular volume (35.41 ± 5.02%) was significantly associated with the frequency of vaso-occlusive crises ( P  = 0.017) and negatively correlated with hemoglobin levels ( P  = 0.005). Galectin-3 levels were significantly higher among cases than controls ( P  =  0.00) , at a cutoff value on the receiver operating characteristic curve of 6.5 ng/ml, sensitivity of 82.5% and specificity of 72.8%. The extracellular volume was significantly higher in cases, with a MPI &gt; 0.4. Conclusion Diffuse interstitial myocardial fibrosis can be detected early in children with sickle cell disease using T1 mapping and is associated with a high frequency of vaso-occlusive crisis. MPI of the left ventricle and serum galectin-3 are recommended screening tools for subclinical cardiac abnormalities. Graphical abstract</description><identifier>ISSN: 1432-1998</identifier><identifier>ISSN: 0301-0449</identifier><identifier>EISSN: 1432-1998</identifier><identifier>DOI: 10.1007/s00247-023-05750-2</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Abnormalities ; Cardiomyopathy ; Children ; Coronary artery disease ; Doppler effect ; Echocardiography ; Fibrosis ; Gadolinium ; Galectin-3 ; Heart diseases ; Hemoglobin ; Imaging ; Iron ; Magnetic resonance imaging ; Mapping ; Medical imaging ; Medicine ; Medicine &amp; Public Health ; Neuroradiology ; Nuclear Medicine ; Oncology ; Original Article ; Pathogenicity ; Pediatrics ; Performance evaluation ; Performance indices ; Radiology ; Sickle cell disease ; Ultrasound ; Ventricle</subject><ispartof>Pediatric radiology, 2023-11, Vol.53 (12), p.2515-2527</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c347t-27ec56d23cbefd235aedf589862c9c92515a0647c319a268980d5ef04da55b583</cites><orcidid>0000-0002-3607-9107 ; 0009-0009-0063-5405 ; 0000-0001-6258-9576 ; 0000-0003-0738-9306</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00247-023-05750-2$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00247-023-05750-2$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids></links><search><creatorcontrib>Wagdy, Reham</creatorcontrib><creatorcontrib>Fathy, Alaa</creatorcontrib><creatorcontrib>Elnekidy, Abdelaziz</creatorcontrib><creatorcontrib>Salaheldin, Geylan</creatorcontrib><creatorcontrib>Nazir, Hanan</creatorcontrib><creatorcontrib>Fahmy, Rana</creatorcontrib><creatorcontrib>Elkafrawy, Hagar</creatorcontrib><creatorcontrib>Elkafrawy, Fatma</creatorcontrib><title>Evaluation of cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease using magnetic resonance imaging, echocardiography, and serum galectin-3</title><title>Pediatric radiology</title><addtitle>Pediatr Radiol</addtitle><description>Background Myocardial fibrosis has recently been proposed as one of the contributing factors to the diverse pathogenicity of cardiomyopathy in sickle cell disease. Objective In this study, cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease were evaluated using cardiac magnetic resonance imaging (MRI), tissue Doppler echocardiography and serum galectin-3. Materials and methods The study included 34 children with sickle cell disease who were compared with a similar number of healthy controls. Cardiac MRI was used to evaluate late gadolinium enhancement, native T1 mapping, extracellular volume, and T2* for estimation of iron load. Cardiac function and myocardial performance index (MPI, evaluated by tissue Doppler echocardiography) and serum galectin-3 were compared to controls. Results The mean age of the included patients was 13.3 ± 3.2 years. Myocardial iron load by T2* was normal. The mean level of extracellular volume (35.41 ± 5.02%) was significantly associated with the frequency of vaso-occlusive crises ( P  = 0.017) and negatively correlated with hemoglobin levels ( P  = 0.005). Galectin-3 levels were significantly higher among cases than controls ( P  =  0.00) , at a cutoff value on the receiver operating characteristic curve of 6.5 ng/ml, sensitivity of 82.5% and specificity of 72.8%. The extracellular volume was significantly higher in cases, with a MPI &gt; 0.4. Conclusion Diffuse interstitial myocardial fibrosis can be detected early in children with sickle cell disease using T1 mapping and is associated with a high frequency of vaso-occlusive crisis. MPI of the left ventricle and serum galectin-3 are recommended screening tools for subclinical cardiac abnormalities. 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Objective In this study, cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease were evaluated using cardiac magnetic resonance imaging (MRI), tissue Doppler echocardiography and serum galectin-3. Materials and methods The study included 34 children with sickle cell disease who were compared with a similar number of healthy controls. Cardiac MRI was used to evaluate late gadolinium enhancement, native T1 mapping, extracellular volume, and T2* for estimation of iron load. Cardiac function and myocardial performance index (MPI, evaluated by tissue Doppler echocardiography) and serum galectin-3 were compared to controls. Results The mean age of the included patients was 13.3 ± 3.2 years. Myocardial iron load by T2* was normal. The mean level of extracellular volume (35.41 ± 5.02%) was significantly associated with the frequency of vaso-occlusive crises ( P  = 0.017) and negatively correlated with hemoglobin levels ( P  = 0.005). Galectin-3 levels were significantly higher among cases than controls ( P  =  0.00) , at a cutoff value on the receiver operating characteristic curve of 6.5 ng/ml, sensitivity of 82.5% and specificity of 72.8%. The extracellular volume was significantly higher in cases, with a MPI &gt; 0.4. Conclusion Diffuse interstitial myocardial fibrosis can be detected early in children with sickle cell disease using T1 mapping and is associated with a high frequency of vaso-occlusive crisis. MPI of the left ventricle and serum galectin-3 are recommended screening tools for subclinical cardiac abnormalities. 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subjects Abnormalities
Cardiomyopathy
Children
Coronary artery disease
Doppler effect
Echocardiography
Fibrosis
Gadolinium
Galectin-3
Heart diseases
Hemoglobin
Imaging
Iron
Magnetic resonance imaging
Mapping
Medical imaging
Medicine
Medicine & Public Health
Neuroradiology
Nuclear Medicine
Oncology
Original Article
Pathogenicity
Pediatrics
Performance evaluation
Performance indices
Radiology
Sickle cell disease
Ultrasound
Ventricle
title Evaluation of cardiac fibrosis and subclinical cardiac changes in children with sickle cell disease using magnetic resonance imaging, echocardiography, and serum galectin-3
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