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外周血补体因子C2和C3作为阿立哌唑治疗首发精神分裂症患者临床疗效的生物标志物。

Peripheral blood complement factors C2 and C3 as biomarkers of clinical efficacy in patients with first-episode schizophrenia after aripiprazole treatment.

作者信息

Cao Yin, Liang Jun, Dai Biao, Shan Feng, Xia Qingrong

机构信息

Affiliated Psychological Hospital of Anhui Medical University, Hefei, China.

Department of Pharmacy, Hefei Fourth People's Hospital, 316 Huangshan Road, Hefei, 230000, China.

出版信息

BMC Psychiatry. 2024 Dec 31;24(1):961. doi: 10.1186/s12888-024-06437-0.

Abstract

OBJECTIVE

The objective of this study was to identify serum complement factor-based biomarkers indicative of clinical efficacy in patients with first-episode schizophrenia (SCZ) following treatment with aripiprazole.

METHODS

The retrospective study cohort comprised 40 patients diagnosed with first-episode SCZ (SCZ group) and 40 healthy individuals (control group). Quantitative analyses were conducted on five complement factors, namely complement component 1 (C1), C2, C3, C4, and the 50% hemolytic complement (CH50). Baseline serum complement factor levels were compared between the SCZ and control groups. Patients diagnosed with SCZ underwent a 4-week treatment regimen with aripiprazole. The severity of psychiatric symptoms in these patients was assessed using the Positive and Negative Symptom Scale (PANSS) and the Brief Psychiatric Rating Scale-18 Item Version (BPRS). Comparative analyses were conducted on PANSS and BPRS scores, as well as serum complement factor levels, both prior to (pre-treatment group) and following aripiprazole administration (post-treatment group). Pearson's correlation test was employed to evaluate the relationships between changes in serum complement factor levels and the reduction rates of PANSS/BPRS scores.

RESULTS

At baseline, patients with SCZ exhibited significantly elevated levels of C1, C2, C3, C4, and CH50 compared to the control group (P < 0.05). Moreover, following treatment, there was a significant reduction in the PANSS total score, positive symptom score, negative symptom score, and BPRS score in the post-treatment group compared to the pre-treatment group (P < 0.05). Furthermore, patients in the post-treatment group exhibited a significant reduction in serum levels of C2, C3, and C4, alongside a significant increase in the serum level of CH50 compared to those in the pre-treatment group (P < 0.05). Additionally, the baseline serum C2 levels and the variations in serum C2 levels pre- and post-treatment exhibited a negative correlation with the reduction rate of PANSS/BPRS scores (P < 0.05). Similarly, both the baseline serum C3 levels and the changes in serum C3 levels pre- and post-treatment were negatively correlated with the reduction rate of PANSS/BPRS scores (P < 0.05).

CONCLUSION

Baseline serum levels of C2 and C3, as well as their variations pre- and post-treatment, may serve as biomarkers for predicting clinical efficacy in patients with first-episode SCZ undergoing treatment with aripiprazole.

摘要

目的

本研究的目的是确定基于血清补体因子的生物标志物,以指示首发精神分裂症(SCZ)患者接受阿立哌唑治疗后的临床疗效。

方法

回顾性研究队列包括40例诊断为首发SCZ的患者(SCZ组)和40名健康个体(对照组)。对五个补体因子进行定量分析,即补体成分1(C1)、C2、C3、C4和50%溶血补体(CH50)。比较SCZ组和对照组的基线血清补体因子水平。诊断为SCZ的患者接受了为期4周的阿立哌唑治疗方案。使用阳性和阴性症状量表(PANSS)和简明精神病评定量表18项版本(BPRS)评估这些患者的精神症状严重程度。对阿立哌唑给药前(治疗前组)和给药后(治疗后组)的PANSS和BPRS评分以及血清补体因子水平进行比较分析。采用Pearson相关检验评估血清补体因子水平变化与PANSS/BPRS评分降低率之间的关系。

结果

在基线时,与对照组相比,SCZ患者的C1、C2、C3、C4和CH50水平显著升高(P<0.05)。此外,治疗后,治疗后组的PANSS总分、阳性症状评分、阴性症状评分和BPRS评分与治疗前组相比显著降低(P<0.05)。此外,与治疗前组相比,治疗后组患者的血清C2、C3和C4水平显著降低,而血清CH50水平显著升高(P<0.05)。此外,基线血清C2水平以及治疗前后血清C2水平的变化与PANSS/BPRS评分降低率呈负相关(P<0.05)。同样,基线血清C3水平以及治疗前后血清C3水平的变化与PANSS/BPRS评分降低率呈负相关(P<0.05)。

结论

基线血清C2和C3水平及其治疗前后的变化,可作为预测接受阿立哌唑治疗的首发SCZ患者临床疗效的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/640a/11687148/0676ecc565a6/12888_2024_6437_Fig1_HTML.jpg

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