Tract specific analysis in patients with sickle cell disease

被引:6
|
作者
Chai, Yaqiong [1 ,2 ,3 ]
Coloigner, Julie [1 ,2 ]
Qu, Xiaoping [1 ,3 ]
Choi, Soyoung [2 ]
Bush, Adam [2 ,3 ]
Borzage, Matt [5 ]
Vu, Chau [2 ]
Lepore, Natasha [1 ,3 ,4 ]
Wood, John [2 ]
机构
[1] Childrens Hosp Los Angeles, Dept Radiol, CIBORG Lab, Los Angeles, CA 90027 USA
[2] Childrens Hosp Los Angeles, Div Cardiol, Los Angeles, CA USA
[3] Univ So Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
[4] Univ So Calif, Dept Radiol, Los Angeles, CA 90089 USA
[5] Childrens Hosp Los Angeles, Dept Neonatol, Los Angeles, CA USA
关键词
sickle cell disease; white matter; statistical analysis; CHILDREN;
D O I
10.1117/12.2213617
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Sickle cell disease (SCD) is a hereditary blood disorder in which the oxygen-carrying hemoglobin molecule in red blood cells is abnormal. It affects numerous people in the world and leads to a shorter life span, pain, anemia, serious infections and neurocognitive decline. Tract-Specific Analysis (TSA) is a statistical method to evaluate white matter alterations due to neurocognitive diseases, using diffusion tensor magnetic resonance images. Here, for the first time, TSA is used to compare 11 major brain white matter (WM) tracts between SCD patients and age-matched healthy subjects. Alterations are found in the corpus callosum (CC), the cortico-spinal tract (CST), inferior fronto-occipital fasciculus (IFO), inferior longitudinal fasciculus (ILF), superior longitudinal fasciculus (SLF), and uncinated fasciculus (UNC). Based on previous studies on the neurocognitive functions of these tracts, the significant areas found in this paper might be related to several cognitive impairments and depression, both of which are observed in SCD patients.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] Cancer specific survival in patients with sickle cell disease
    Brunson, Ann
    Keegan, Theresa H. M.
    Mahajan, Anjlee
    Paulukonis, Susan
    Wun, Ted
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2019, 185 (01) : 128 - 132
  • [2] Tract-specific analysis and neurocognitive functioning in sickle cell patients without history of overt stroke
    Chai, Yaqiong
    Ji, Chaoran
    Coloigner, Julie
    Choi, Soyoung
    Balderrama, Melissa
    Vu, Chau
    Tamrazi, Benita
    Coates, Thomas
    Wood, John C.
    O'Neil, Sharon H.
    Lepore, Natasha
    [J]. BRAIN AND BEHAVIOR, 2021, 11 (03):
  • [3] Comparison of Strokes in Adult Hospitalized Patients with Sickle Cell Disease and Patients without Sickle Cell Disease: A Nationwide Analysis
    Atodaria, Kuldeepsinh
    Eisenstaedt, Richard S.
    Fidler, Christian Joseph
    Atam, Sarin
    [J]. BLOOD, 2022, 140 : 8268 - 8269
  • [4] Semen analysis in patients with sickle cell disease on hydroxyurea
    Wolf, S.
    Barroso, F.
    Kaya, B.
    Telfer, P.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2018, 181 : 125 - 125
  • [5] Longitudinal Analysis of Patient Specific Predictors for Mortality in Sickle Cell Disease
    Curtis, Susanna A.
    Danda, Neeraja
    Etzion, Zipora
    Cohen, Hillel W.
    Billett, Henny H.
    [J]. PLOS ONE, 2016, 11 (10):
  • [6] FREQUENCY OF URINARY TRACT ABNORMALITIES IN SICKLE CELL DISEASE
    FRICKER, GA
    [J]. CALIFORNIA MEDICINE, 1970, 112 (05): : 64 - &
  • [7] SICKLE CELL ANEMIA, A RACE SPECIFIC DISEASE
    不详
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1947, 133 (01): : 33 - 34
  • [8] ELECTROCARDIOGRAM ANALYSIS IN ADULT PATIENTS WITH SICKLE-CELL DISEASE
    HOLLOMAN, KL
    JOHNSON, CS
    HAYWOOD, LJ
    [J]. JOURNAL OF THE NATIONAL MEDICAL ASSOCIATION, 1987, 79 (08) : 809 - 814
  • [9] SICKLE CELL DISEASE INPATIENT DATA ANALYSIS OF MEDICARE PATIENTS
    Saunders, W.
    Ruban, C.
    [J]. VALUE IN HEALTH, 2017, 20 (05) : A361 - A362
  • [10] Craniofacial morphology in patients with sickle cell disease: a cephalometric analysis
    Licciardello, Valeria
    Bertuna, Gregoria
    Samperi, Piera
    [J]. EUROPEAN JOURNAL OF ORTHODONTICS, 2007, 29 (03) : 238 - 242