Neurocognitive functioning in preschool children with sickle cell disease

被引:13
作者
Heitzer, Andrew M. [1 ]
Cohen, Diana L. [1 ]
Okhomina, Victoria I. [2 ]
Trpchevska, Ana [1 ]
Potter, Brian [1 ]
Longoria, Jennifer [1 ]
Porter, Jerlym S. [1 ]
Estepp, Jeremie H. [3 ]
King, Allison [4 ,5 ]
Henley, Misham [3 ]
Kang, Guolian [2 ]
Hankins, Jane S. [3 ]
机构
[1] St Jude Childrens Res Hosp, Dept Psychol, Memphis, TN USA
[2] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN USA
[3] St Jude Childrens Res Hosp, Dept Hematol, Memphis, TN USA
[4] Washington Univ, Program Occupat Therapy, St Louis, MO USA
[5] Washington Univ, Dept Pediat & Med, St Louis, MO USA
关键词
hydroxyurea; neurocognition; neurodevelopment; preschool; sickle cell disease; social determinants; socioeconomic status; SILENT CEREBRAL INFARCTS; YOUNG-CHILDREN; SOCIAL VULNERABILITY; SCHOOL READINESS; CONTROLLED-TRIAL; HEMOGLOBIN; ASSOCIATION; MULTICENTER; SEVERITY; TODDLERS;
D O I
10.1002/pbc.29531
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Children with sickle cell disease (SCD) experience neurodevelopmental delays; however, there is limited research with preschool-age children. This study examined neurocognitive risk and protective factors in preschoolers with SCD. Procedure Sixty-two patients with SCD (60% HbSS/HbS beta(0)-thalassemia; 40% HbSC/HbS beta(+)-thalassemia) between the ages of 3 and 6 years (mean = 4.77 years) received a neuropsychological evaluation as routine systematic surveillance. Patients were not selected for disease severity, prior central nervous system findings, or existing cognitive concerns. Thirty-four patients (82% HbSS/HbS beta(0)-thalassemia) were prescribed hydroxyurea (HU) at the time of their neuropsychological evaluation. On average, these patients had been prescribed HU at 2.15 (standard deviation = 1.45) years of age. The average dose was 28.8 mg/kg/day. Besides genotype, there were no group differences in medical or demographic factors based on HU treatment status. Results Patients with HbSS/HbS beta(0)-thalassemia scored below normative expectations on measures of intelligence, verbal comprehension, and school readiness (false discovery rate-adjusted p-value [p(FDR)] < .05). Age, sickle genotype, and HU treatment exposure were not associated with measured neurocognitive outcomes (p(FDR) > .05). Greater social vulnerability at the community level was associated with poorer performance on measures of intellectual functioning, verbal comprehension, visuomotor control, and school readiness, as well as parent report of executive dysfunction (p(FDR) < .05). Greater household socioeconomic status was positively associated with academic readiness. Conclusions Preschoolers with severe SCD (HbSS/HbS beta(0)-thalassemia) perform below age expectations on measures of intelligence and academic readiness. Sociodemographic factors were stronger drivers of neurocognitive performance than disease severity or disease-modifying treatment. Neurodevelopmental interventions targeting the home and broader community environment are needed.
引用
收藏
页数:11
相关论文
共 59 条
[1]  
Adams W., 1995, WIDE RANGE ASSESSMEN
[2]   Developmental Function in Toddlers With Sickle Cell Anemia [J].
Armstrong, F. Daniel ;
Elkin, T. David ;
Brown, R. Clark ;
Glass, Penny ;
Rana, Sohail ;
Casella, James F. ;
Kalpatthi, Ram V. ;
Pavlakis, Steven ;
Mi, Zhibao ;
Wang, Winfred C. .
PEDIATRICS, 2013, 131 (02) :E406-E414
[3]   Neurocognitive Screening With the Brigance Preschool Screen-II in 3-Year-Old Children With Sickle Cell Disease [J].
Aygun, Banu ;
Parker, Jennifer ;
Freeman, Molly B. ;
Stephens, Alexis L. ;
Smeltzer, Matthew P. ;
Wu, Song ;
Hankins, Jane S. ;
Wang, Winfred C. .
PEDIATRIC BLOOD & CANCER, 2011, 56 (04) :620-624
[4]  
Barratt W., 2006, The Barratt simplified measure of social status
[5]   Time to apply a social determinants of health lens to addressing sickle cell disorders in sub-Saharan Africa [J].
Berghs, Maria ;
Ola, Bola ;
Cronin De Chavez, Anna ;
Ebenso, Bassey .
BMJ GLOBAL HEALTH, 2020, 5 (07)
[6]   Multicenter prospective study of children with sickle cell disease:: Radiographic and psychometric correlation [J].
Bernaudin, F ;
Verlhac, S ;
Fréard, F ;
Roudot-Thoravel, F ;
Benkerrou, M ;
Thuret, I ;
Mardini, R ;
Vannier, JP ;
Ploix, E ;
Romero, M ;
Cassé-Perrot, C ;
Helly, M ;
Gillard, E ;
Sebag, G ;
Kchouk, H ;
Pracros, JP ;
Finck, B ;
Dacher, JN ;
Ickowicz, V ;
Raybaud, C ;
Poncet, M ;
Lesprit, E ;
Reinert, PH ;
Brugières, P .
JOURNAL OF CHILD NEUROLOGY, 2000, 15 (05) :333-343
[7]   Social-environmental factors and cognitive and behavioral functioning in pediatric sickle cell disease [J].
Bills, Sarah E. ;
Schatz, Jeffrey ;
Hardy, Steven J. ;
Reinman, Laura .
CHILD NEUROPSYCHOLOGY, 2020, 26 (01) :83-99
[8]  
Bracken B.A., 2006, BRACKEN BASIC CONCEP, Vthird
[9]   NEUROCOGNITIVE ASPECTS OF PEDIATRIC SICKLE-CELL DISEASE [J].
BROWN, RT ;
ARMSTRONG, FD ;
ECKMAN, JR .
JOURNAL OF LEARNING DISABILITIES, 1993, 26 (01) :33-45
[10]   Cognitive and fine motor deficits in a pediatric sickle cell disease cohort of mixed ethnic origin [J].
Burkhardt, Luise ;
Lobitz, Stephan ;
Koustenis, Elisabeth ;
Rueckriegel, Stefan Mark ;
Driever, Pablo Hernaiz .
ANNALS OF HEMATOLOGY, 2017, 96 (02) :199-213