Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; The Child and Adolescent Psychiatry Division, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Laboratory of Biological Psychiatry, Felsenstein Medical Research Center, Petah Tikva, Israel; Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
Schizophr Res. 2021 May;231:164-169. doi: 10.1016/j.schres.2021.03.023. Epub 2021 Apr 16.
Individuals with 22q11.2 deletion syndrome (22q11.2DS) are at risk for having both psychotic and immune disorders, thus, implying a possible link between the two. The aim of the current study was to evaluate the usefulness of the neutrophiles to leukocytes ratio (NLR), an inflammatory marker, as a bio-marker for overt and prodromal psychotic symptoms in 22q11.2DS.
Forty-nine individuals with 22q11.2DS (13 with psychotic disorders and 36 without psychotic disorders) and 30 age- and sex-matched healthy controls underwent psychiatric evaluation using a structured psychiatric interview, the Scale of Prodromal Symptoms (SOPS) and the Global Assessment of Functioning (GAF) scale. Blood samples were collected from all participants on the day of assessment. NLR was calculated, compared among the study groups and correlated with SOPS and GAF scores. The non-psychotic 22q11.2DS group was further divided into high- and low-inflammation groups by NLR values and the analyses were done again.
NLR was higher in the psychotic- and the high-inflammation non-psychotic 22q11.2DS groups compared to the low-inflammation non-psychotic 22q11.2DS group and controls. In the high-inflammation non-psychotic 22q11.2DS group NLR increase was associated with an increase of total negative symptoms scores on SOPS and a decrease in GAF scores.
Our results suggest the potential utility of NLR as a bio-marker for psychotic disorders and subthreshold prodromal symptoms in 22q11.2DS. Furthermore, they imply that a disequilibrium between the innate and adaptive arms of the immune system facilitates the progression of psychosis in at risk populations. Further longitudinal studies are warranted to validate our findings, as this was a cross sectional observation.
患有 22q11.2 缺失综合征(22q11.2DS)的个体存在精神和免疫紊乱的风险,这表明两者之间可能存在关联。本研究的目的是评估中性粒细胞与白细胞比值(NLR)作为 22q11.2DS 显性和前驱精神病症状生物标志物的有用性。
49 名 22q11.2DS 患者(13 名患有精神病,36 名未患有精神病)和 30 名年龄和性别匹配的健康对照者接受了结构化精神病学访谈、前驱症状量表(SOPS)和总体功能评估(GAF)量表的精神病评估。所有参与者在评估当天采集血样。计算 NLR,并在研究组之间进行比较,与 SOPS 和 GAF 评分相关。根据 NLR 值将非精神病性 22q11.2DS 组进一步分为高炎症和低炎症组,并再次进行分析。
精神病性和高炎症非精神病性 22q11.2DS 组的 NLR 高于低炎症非精神病性 22q11.2DS 组和对照组。在高炎症非精神病性 22q11.2DS 组中,NLR 的增加与 SOPS 总阴性症状评分的增加和 GAF 评分的降低相关。
我们的结果表明,NLR 作为 22q11.2DS 精神病和前驱症状的生物标志物具有潜在的应用价值。此外,它们表明,先天和适应性免疫系统之间的失衡促进了高危人群精神病的发展。需要进一步的纵向研究来验证我们的发现,因为这是一项横断面观察。