Reuter-Rice Karin, Regier Michael, Bennett Ellen, Laskowitz Daniel
1 Division of Critical Care Medicine, Department of Pediatrics, School of Nursing, Duke University School of Medicine, Durham, NC, USA.
2 Department of Biostatistics, West Virginia University, Morgantown, WV, USA.
Biol Res Nurs. 2018 Oct;20(5):566-576. doi: 10.1177/1099800418785982. Epub 2018 Jul 11.
Pediatric traumatic brain injury (TBI) is a leading cause of death and disability. Polymorphisms in the apolipoprotein E ( APOE) gene have been linked to cerebral vasospasm (CV) and poor outcomes in adults with TBI, yet these associations remain poorly defined in children.
We examined the effect of the relationship between APOE polymorphisms and CV on functional outcomes in children with a TBI.
This prospective, descriptive study examined 60 children (aged 10 days to 15 years) with a TBI. Data included demographic information, genetic sampling for the APOE gene and single-nucleotide polymorphisms (SNPs; rs405509, rs429358, rs7412), and daily transcranial Doppler ultrasounds to evaluate for CV. We examined Glasgow Outcome Scale-Extended Pediatrics (GOS-E Peds) scores at the time of discharge and 4-6 weeks after discharge.
More than half (56.7%) of the 60 children ( M = 5.9 years) were male. Twenty-six participants (43.3%) experienced an occurrence of CV. There were significant differences in injury mechanism (unadjusted p = .048) and age (unadjusted p = .02) between those with and without CV. Also, the noncoding promoter SNP rs405509 T/T, when considered with injury severity, appeared to modify the relationship of APOE genotype to CV. The relationship between APOE and CV had no significant effect on GOS-E Peds scores.
Injury severity and the APOE noncoding promoter SNP rs405509 may modify the relationship between APOE and CV in children with TBI. More studies are needed to understand the role of APOE polymorphisms in outcomes in children with TBI.
小儿创伤性脑损伤(TBI)是死亡和残疾的主要原因。载脂蛋白E(APOE)基因多态性与成人TBI后的脑血管痉挛(CV)及不良预后有关,但这些关联在儿童中仍未明确。
我们研究了APOE基因多态性与CV之间的关系对TBI患儿功能预后的影响。
这项前瞻性描述性研究纳入了60例TBI患儿(年龄10天至15岁)。数据包括人口统计学信息、APOE基因和单核苷酸多态性(SNP;rs405509、rs429358、rs7412)的基因样本,以及每日经颅多普勒超声检查以评估CV。我们在出院时及出院后4 - 6周检查了格拉斯哥预后量表扩展版儿科(GOS - E Peds)评分。
60例患儿(平均年龄5.9岁)中超过一半(56.7%)为男性。26名参与者(43.3%)发生了CV。发生CV和未发生CV的患儿在损伤机制(未校正p = 0.048)和年龄(未校正p = 0.02)方面存在显著差异。此外,非编码启动子SNP rs405509 T/T与损伤严重程度相关时,似乎改变了APOE基因型与CV的关系。APOE与CV之间的关系对GOS - E Peds评分无显著影响。
损伤严重程度和APOE非编码启动子SNP rs405509可能改变TBI患儿中APOE与CV之间的关系。需要更多研究来了解APOE基因多态性在TBI患儿预后中的作用。