Beer Yaakov - Ness-Ziona Mental Health Center, Beer Yaakov, Israel.
Neuropsychobiology. 2013;68(2):124-7. doi: 10.1159/000353267. Epub 2013 Jul 19.
It has been suggested that the etiology of schizophrenia, in a distinct group of patients, originates from an autoimmune reaction against platelets. Previous studies have demonstrated significantly higher blood titers of platelet-associated autoantibodies (PAA) in adult schizophrenia patients as compared to normal healthy subjects. In addition, young adult schizophrenia patients at their early stages of the disorder displayed higher PAA titers than older patients with longer duration of the disorder.
To assess the blood titers of PAA in children with schizophrenia as compared to matched control subjects without psychotic disorders, as a possible diagnostic parameter.
Twenty-nine children with DSM-IV schizophrenia in the active psychotic state, with an age range of 6-12 years (mean ± SD: 9.6 ± 1.5 years), with average Positive and Negative Syndrome Scale scores of 108 ± 19.2, were assessed. The control group consisted of 25 children with DSM-IV conduct disorder in a similar age range of 5-12 years (mean ± SD: 9.5 ± 1.6 years). The blood titers of PAA were evaluated using an optimized ELISA test, expressed by a linear optical density (OD) scale. The blood samples of all participants were tested anonymously and were scored under a code number. A test recording above 1.4 OD units was predefined as positive.
The titers of PAA of children with schizophrenia (1.9 ± 0.5 OD units, range: 0.7-2.44 units) were significantly (p < 0.00001) higher than those of the control group (1.0 ± 0.4 OD units, range: 0.45-2.28 units). In 83% of the children with schizophrenia (24 out of the 29 patients) a positive test, i.e. OD >1.4, was detected. In contrast, in the control group, only 12% (3 of the 25 subjects) displayed a positive test, p < 0.00001.
High titers of PAA in children with schizophrenia as compared with nonpsychotic controls may indicate an active autoimmune process in the early onset of schizophrenia. The PAA level may therefore provide a supportive diagnostic biomarker for childhood schizophrenia.
有人提出,在特定患者群体中,精神分裂症的病因源于针对血小板的自身免疫反应。先前的研究表明,成年精神分裂症患者的血小板相关自身抗体 (PAA) 血液滴度明显高于正常健康受试者。此外,处于疾病早期阶段的年轻成年精神分裂症患者的 PAA 滴度高于病程较长的老年患者。
评估精神分裂症儿童与无精神病障碍的匹配对照组之间的 PAA 血液滴度,作为可能的诊断参数。
评估了 29 名处于活跃精神病状态的 DSM-IV 精神分裂症儿童(年龄 6-12 岁,平均年龄±标准差:9.6±1.5 岁),阳性和阴性综合征量表评分范围为 108±19.2。对照组由 25 名年龄在 5-12 岁(平均年龄±标准差:9.5±1.6 岁)之间的 DSM-IV 品行障碍儿童组成。使用优化的 ELISA 试验评估 PAA 的血液滴度,以线性光密度 (OD) 表示。所有参与者的血液样本均匿名检测,并在代码编号下评分。预设 OD 记录值超过 1.4 单位为阳性。
精神分裂症儿童的 PAA 滴度(1.9±0.5 OD 单位,范围:0.7-2.44 单位)明显高于对照组(1.0±0.4 OD 单位,范围:0.45-2.28 单位),p<0.00001。29 名精神分裂症儿童中有 83%(24 名患者)检测出阳性试验,即 OD>1.4,而对照组中只有 12%(3 名受试者),p<0.00001。
与非精神病对照组相比,精神分裂症儿童的 PAA 滴度较高可能表明精神分裂症早期存在活跃的自身免疫过程。因此,PAA 水平可能为儿童精神分裂症提供支持性诊断生物标志物。