Artık Abdülbaki, Öztelcan Gündüz Bahar, Mızrak Soycan, Işık Ümit
Faculty of Medicine, Child and Adolescent Mental Health Department, Uşak University, Ankara, Turkey.
Paediatric Department, Gülhane Training and Research Hospital, Ankara, Turkey.
Int J Dev Disabil. 2022 Nov 14;69(4):611-616. doi: 10.1080/20473869.2022.2143033. eCollection 2023.
A previous study has evaluated the association between serum tumour necrosis factor-like weak apoptosis inducer (TWEAK) levels and autism spectrum disorder (ASD). In line with this investigation, the present study aimed to measure serum TWEAK levels to determine whether their eventual alteration might have etiopathogenetic significance in children with ASD. A total of 40 treatment-naive children with ASD and 40 healthy children as controls were included in the present study. The Schedule for Affective Disorders and Schizophrenia for School-Aged Children-Present and Lifetime Version, DSM-5 was used by a psychiatrist to screen the healthy controls for psychiatric disorders after a physical examination by a paediatrician. The clinical severity of the ASD symptoms was assessed by the Childhood Autism Rating Scale. Venous blood samples were collected, and serum TWEAK levels were measured. This study included 80 children in total, with 40 (50.0%) in the patient group and 40 (50.0%) in the healthy control group. Thirty four (85.0%) of the participants in the patient group, and 31 (77.5%) in the healthy control group, were male, and the remainder were female. The distribution of the gender ratio was statistically similar between groups ( = 0.568). The volunteers were between 36 and 59 months old. The average age in the patient group was 46.0 ± 6.5, while that in the healthy control group was 45.2 ± 6.7. The ages were also statistically similar between groups ( = 0.615). The TWEAK values of the patient group were found to be statistically higher than those of the healthy control group ( < 0.001). This study examined whether serum TWEAK levels were related to ASD in childhood. Our findings indicate that children with ASD have higher TWEAK levels when compared to other children. The findings further indicate that serum TWEAK levels could be related to ASD etiopathogenesis independent of ASD symptom severity.
先前的一项研究评估了血清肿瘤坏死因子样弱凋亡诱导剂(TWEAK)水平与自闭症谱系障碍(ASD)之间的关联。与这项调查一致,本研究旨在测量血清TWEAK水平,以确定其最终变化是否可能对ASD儿童具有病因学意义。本研究共纳入40例未经治疗的ASD儿童和40例健康儿童作为对照。在儿科医生进行体格检查后,由精神科医生使用《学龄儿童情感障碍和精神分裂症量表(目前和终生版)》(DSM-5)对健康对照进行精神疾病筛查。ASD症状的临床严重程度通过儿童自闭症评定量表进行评估。采集静脉血样,测量血清TWEAK水平。本研究共纳入80名儿童,患者组40名(50.0%),健康对照组40名(50.0%)。患者组34名(85.0%)参与者和健康对照组31名(77.5%)参与者为男性,其余为女性。两组之间性别比例分布在统计学上相似(P = 0.568)。志愿者年龄在36至59个月之间。患者组的平均年龄为46.0±6.5岁,而健康对照组为45.2±6.7岁。两组之间的年龄在统计学上也相似(P = 0.615)。发现患者组的TWEAK值在统计学上高于健康对照组(P < 0.001)。本研究探讨了儿童血清TWEAK水平是否与ASD相关。我们的研究结果表明,与其他儿童相比,ASD儿童的TWEAK水平更高。研究结果进一步表明,血清TWEAK水平可能与ASD病因学相关,且与ASD症状严重程度无关。