Toward Automated Detection of Silent Cerebral Infarcts in Children and Young Adults With Sickle Cell Anemia

被引:1
|
作者
Chen, Yasheng [1 ]
Wang, Yan [1 ]
Phuah, Chia-Ling [1 ]
Fields, Melanie E. [2 ]
Guilliams, Kristin P. [3 ]
Fellah, Slim [1 ]
Reis, Martin N. [4 ]
Binkley, Michael M. [1 ]
An, Hongyu [1 ,4 ]
Lee, Jin-Moo [1 ,4 ]
McKinstry, Robert C. [4 ]
Jordan, Lori C. [5 ]
DeBaun, Michael R. [6 ]
Ford, Andria L. [1 ,4 ,7 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol, St Louis, MO USA
[2] Washington Univ, Sch Med, Div Pediat Hematol Oncol, St Louis, MO USA
[3] Washington Univ, Sch Med, Div Pediat Neurol, St Louis, MO USA
[4] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, St Louis, MO USA
[5] Vanderbilt Univ Med, Dept Pediat, Div Pediat Neurol, Nashville, TN USA
[6] Vanderbilt Univ, Vanderbilt Meharry Ctr Excellence Sickle Cell Dis, Dept Pediat, Div Hematol & Oncol,Med Ctr, Nashville, TN USA
[7] Washington Univ, Sch Med, Dept Neurol, 660 S Euclid Ave,Campus Box 8111, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
cerebral infarct; deep learning; diagnostic imaging; sickle cell anemia; white matter diseases; PREVALENT; DISEASE; INJURY; TRIAL;
D O I
10.1161/STROKEAHA.123.042683
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND:Silent cerebral infarcts (SCI) in sickle cell anemia (SCA) are associated with future strokes and cognitive impairment, warranting early diagnosis and treatment. Detection of SCI, however, is limited by their small size, especially when neuroradiologists are unavailable. We hypothesized that deep learning may permit automated SCI detection in children and young adults with SCA as a tool to identify the presence and extent of SCI in clinical and research settings. METHODS:We utilized UNet-a deep learning model-for fully automated SCI segmentation. We trained and optimized UNet using brain magnetic resonance imaging from the SIT trial (Silent Infarct Transfusion). Neuroradiologists provided the ground truth for SCI diagnosis, while a vascular neurologist manually delineated SCI on fluid-attenuated inversion recovery and provided the ground truth for SCI segmentation. UNet was optimized for the highest spatial overlap between automatic and manual delineation (dice similarity coefficient). The optimized UNet was externally validated using an independent single-center prospective cohort of SCA participants. Model performance was evaluated through sensitivity and accuracy (%correct cases) for SCI diagnosis, dice similarity coefficient, intraclass correlation coefficient (metric of volumetric agreement), and Spearman correlation. RESULTS:The SIT trial (n=926; 31% with SCI; median age, 8.9 years) and external validation (n=80; 50% with SCI; age, 11.5 years) cohorts had small median lesion volumes of 0.40 and 0.25 mL, respectively. Compared with the neuroradiology diagnosis, UNet predicted SCI presence with 100% sensitivity and 74% accuracy. In magnetic resonance imaging with SCI, UNet reached a moderate spatial agreement (dice similarity coefficient, 0.48) and high volumetric agreement (intraclass correlation coefficient, 0.76; & rho;=0.72; P<0.001) between automatic and manual segmentations. CONCLUSIONS:UNet, trained using a large pediatric SCA magnetic resonance imaging data set, sensitively detected small SCI in children and young adults with SCA. While additional training is needed, UNet may be integrated into the clinical workflow as a screening tool, aiding in SCI diagnosis.
引用
收藏
页码:2096 / 2104
页数:9
相关论文
共 50 条
  • [41] Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarction
    Tewari, Sanjay
    Renney, George
    Brewin, John
    Gardner, Kate
    Kirkham, Fenella
    Inusa, Baba
    Barrett, James E.
    Menzel, Stephan
    Thein, Swee Lay
    Ward, Malcolm
    Reese, David C.
    HAEMATOLOGICA, 2018, 103 (07) : 1136 - 1142
  • [42] Silent Cerebral Infarct Pathophysiology Study in Sickle Cell Anemia Children By a Multimodal Approach
    Brousse, Valentine
    Grevent, David
    Arnaud, Cecile
    Kamden, Annie
    Kossorotoff, Manoelle
    De Montalembert, Mariane
    Boutonnat-Faucher, Benedicte
    Allali, Slimane
    Charlot, Keyne
    Connes, Philippe
    Da Costa, Lydie
    Pondarre, Corinne
    Verlhac, Suzanne
    BLOOD, 2017, 130
  • [43] Acute silent infarction in children with sickle cell anemia
    Dowling, Michael M.
    Quinn, Charles T.
    Rogers, Zora R.
    Buchanan, George R.
    NEUROLOGY, 2007, 68 (12) : A357 - A357
  • [44] The Progression and Development of Silent Infarcts in Children with Sickle Cell Anemia Is Prevented by Chronic Transfusions and Is Unrelated to Level of Hemolysis
    Abboud, Miguel R.
    Yim, Eunsil
    Adams, Robert J.
    BLOOD, 2008, 112 (11) : 264 - 265
  • [45] Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease
    Schatz, J
    Brown, RT
    Pascual, JM
    Hsu, L
    DeBaun, MR
    NEUROLOGY, 2001, 56 (08) : 1109 - 1111
  • [46] Silent Infarcts, White Matter Integrity, and Oxygen Metabolic Stress in Young Adults With and Without Sickle Cell Trait
    Wang, Yan
    Guilliams, Kristin P.
    Fields, Melanie E.
    Fellah, Slim
    Binkley, Michael M.
    Reis, Martin
    Vo, Katie D.
    Chen, Yasheng
    Ying, Chunwei
    Blinder, Morey
    King, Allison A.
    Hulbert, Monica L.
    An, Hongyu
    Lee, Jin-Moo
    Ford, Andria L.
    STROKE, 2022, 53 (09) : 2887 - 2895
  • [47] Association of silent infarcts in sickle cell anemia with decreased annexin A5 resistance
    Morrone, Kerry A.
    Pecker, Lydia H.
    Rand, Jacob
    Davila, Jennifer
    Oyeku, Suzette
    Little, Jane A.
    Xue Xiaonan
    Manwani, Deepa
    BLOOD CELLS MOLECULES AND DISEASES, 2018, 69 : 53 - 56
  • [48] Silent Cerebral Infarcts Are Not Associated with Magnetic Resonance Imaging-Defined Intracranial Vasculopathy or with Elevated Transcranial Doppler Measurements in Children with Sickle Cell Anemia
    Thangarajh, Mathula
    Fuchs, Dana
    McKinstry, Robert C.
    Noetzel, Michael J.
    Casella, James F.
    Vendt, Bruce A.
    Barton, Bruce
    DeBaun, Michael R.
    NEUROLOGY, 2009, 72 (11) : A268 - A269
  • [49] Cerebral vasculopathy in children with sickle cell anemia
    Fasano, Ross M.
    Meier, Emily R.
    Hulbert, Monica L.
    BLOOD CELLS MOLECULES AND DISEASES, 2015, 54 (01) : 17 - 25
  • [50] Blood transfusion therapy is feasible in a clinical trial setting in children with sickle cell disease and silent cerebral infarcts
    King, Allison A.
    Noetzel, Michael
    White, Desiree A.
    McKinstry, Robert C.
    DeBaun, Michael R.
    PEDIATRIC BLOOD & CANCER, 2008, 50 (03) : 599 - 602