Department of Pediatrics, Section of Pediatric Neurology, Alberta Children's Hospital, Calgary, AB, Canada.
Dev Med Child Neurol. 2014 Jan;56(1):73-7. doi: 10.1111/dmcn.12263. Epub 2013 Sep 2.
To determine whether post-injury depressive symptoms, and pre-injury major life stressors and genetic factors (HTR1A C(-1019)G alleles; rs6295) are more common in children with mild traumatic brain injury (mTBI) who develop postconcussion syndrome (PCS) symptoms compared with children with asymptomatic mTBI.
This was a cross-sectional study of 47 symptomatic children (32 males, 15 females; mean age 14y [SD 3y 3mo]) who experienced post-concussive symptoms for 7 or more days and 42 asymptomatic children (26 males 16 females; mean age 13y 6mo [SD 3y 1mo]) after mTBI. Outcome measures were the Postconcussion Symptoms Inventory (PCSI), the Children's Depression Inventory (CDI), standard questionnaire of previous life events, and buccal DNA analysis to determine genotype and allele frequencies for the HTR1A C(-1019)G polymorphism.
Depressive symptoms were uncommon. CDI scores did not differ between groups. Allelic and genotypic frequencies for HTR1A C(-1019)G were similar in both groups. Symptomatic children continued to have elevated PCS scores compared with asymptomatic children 1.72 (SD 0.69) years later and had experienced significantly more life stressors (Wald (1)=8.51, p=0.004).
HTR1A polymorphisms do not differ in children with PCS. Children who have experienced more significant life stresses are more likely to develop PCS symptoms after mTBI.
确定创伤后抑郁症状以及创伤前主要生活应激源和遗传因素(5-羟色胺受体 1A 基因 C(-1019)G 等位基因;rs6295)是否更常见于发生脑震荡后综合征(PCS)症状的轻度创伤性脑损伤(mTBI)患儿,而非无症状 mTBI 患儿。
这是一项横断面研究,共纳入 47 例有症状患儿(32 名男性,15 名女性;平均年龄 14 岁[标准差 3 岁 3 个月]),他们在 mTBI 后出现 7 天以上的脑震荡后症状,以及 42 例无症状患儿(26 名男性,16 名女性;平均年龄 13 岁 6 个月[标准差 3 岁 1 个月])。结局指标为脑震荡后症状量表(PCSI)、儿童抑郁量表(CDI)、以往生活事件标准问卷和颊部 DNA 分析,以确定 5-羟色胺受体 1A 基因 C(-1019)G 多态性的基因型和等位基因频率。
抑郁症状并不常见。两组间 CDI 评分无差异。HTR1A C(-1019)G 等位基因和基因型频率在两组间相似。与无症状患儿相比,1.72 年后(标准差 0.69),有症状患儿的 PCSI 评分仍持续升高,且经历了更多的生活应激源(Wald(1)=8.51,p=0.004)。
5-羟色胺受体 1A 多态性在 PCS 患儿中无差异。经历过更严重生活应激源的患儿更有可能在 mTBI 后出现 PCS 症状。