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血清抗 DIDO1、抗 CPSF2 和抗 FOXJ2 抗体作为急性缺血性脑卒中的预测风险标志物。

Serum anti-DIDO1, anti-CPSF2, and anti-FOXJ2 antibodies as predictive risk markers for acute ischemic stroke.

机构信息

Department of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.

Department of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.

出版信息

BMC Med. 2021 Jun 9;19(1):131. doi: 10.1186/s12916-021-02001-9.

Abstract

BACKGROUND

Acute ischemic stroke (AIS) is a serious cause of mortality and disability. AIS is a serious cause of mortality and disability. Early diagnosis of atherosclerosis, which is the major cause of AIS, allows therapeutic intervention before the onset, leading to prevention of AIS.

METHODS

Serological identification by cDNA expression cDNA libraries and the protein array method were used for the screening of antigens recognized by serum IgG antibodies in patients with atherosclerosis. Recombinant proteins or synthetic peptides derived from candidate antigens were used as antigens to compare serum IgG levels between healthy donors (HDs) and patients with atherosclerosis-related disease using the amplified luminescent proximity homogeneous assay-linked immunosorbent assay.

RESULTS

The first screening using the protein array method identified death-inducer obliterator 1 (DIDO1), forkhead box J2 (FOXJ2), and cleavage and polyadenylation specificity factor (CPSF2) as the target antigens of serum IgG antibodies in patients with AIS. Then, we prepared various antigens including glutathione S-transferase-fused DIDO1 protein as well as peptides of the amino acids 297-311 of DIDO1, 426-440 of FOXJ2, and 607-621 of CPSF2 to examine serum antibody levels. Compared with HDs, a significant increase in antibody levels of the DIDO1 protein and peptide in patients with AIS, transient ischemic attack (TIA), and chronic kidney disease (CKD) but not in those with acute myocardial infarction and diabetes mellitus (DM). Serum anti-FOXJ2 antibody levels were elevated in most patients with atherosclerosis-related diseases, whereas serum anti-CPSF2 antibody levels were associated with AIS, TIA, and DM. Receiver operating characteristic curves showed that serum DIDO1 antibody levels were highly associated with CKD, and correlation analysis revealed that serum anti-FOXJ2 antibody levels were associated with hypertension. A prospective case-control study on ischemic stroke verified that the serum antibody levels of the DIDO1 protein and DIDO1, FOXJ2, and CPSF2 peptides showed significantly higher odds ratios with a risk of AIS in patients with the highest quartile than in those with the lowest quartile, indicating that these antibody markers are useful as risk factors for AIS.

CONCLUSIONS

Serum antibody levels of DIDO1, FOXJ2, and CPSF2 are useful in predicting the onset of atherosclerosis-related AIS caused by kidney failure, hypertension, and DM, respectively.

摘要

背景

急性缺血性脑卒中(AIS)是死亡和残疾的主要原因。AIS 是死亡和残疾的主要原因。早期诊断动脉粥样硬化,这是 AIS 的主要原因,可以在发病前进行治疗干预,从而预防 AIS。

方法

通过 cDNA 表达 cDNA 文库和蛋白质阵列方法进行血清 IgG 抗体识别的抗原的血清学鉴定。从候选抗原中获得重组蛋白或合成肽作为抗原,使用扩增发光近同相测定 - 酶联免疫吸附测定法比较健康供体(HDs)和与动脉粥样硬化相关疾病患者的血清 IgG 水平。

结果

使用蛋白质阵列方法的初次筛选鉴定出凋亡诱导抑制剂 1(DIDO1)、叉头框 J2(FOXJ2)和剪接和多聚腺苷酸化特异性因子(CPSF2)为 AIS 患者血清 IgG 抗体的靶抗原。然后,我们制备了各种抗原,包括谷胱甘肽 S-转移酶融合 DIDO1 蛋白以及 DIDO1 的氨基酸 297-311、FOXJ2 的 426-440 和 CPSF2 的 607-621 的肽,以检查血清抗体水平。与 HDs 相比,AIS、短暂性脑缺血发作(TIA)和慢性肾脏病(CKD)患者的 DIDO1 蛋白和肽的抗体水平显著升高,但急性心肌梗死和糖尿病(DM)患者的抗体水平没有升高。大多数与动脉粥样硬化相关疾病的患者的血清抗 FOXJ2 抗体水平升高,而血清抗 CPSF2 抗体水平与 AIS、TIA 和 DM 相关。受试者工作特征曲线显示,血清 DIDO1 抗体水平与 CKD 高度相关,相关性分析表明,血清抗 FOXJ2 抗体水平与高血压相关。缺血性脑卒中的前瞻性病例对照研究证实,DIDO1 蛋白和 DIDO1、FOXJ2 和 CPSF2 肽的血清抗体水平在最高四分位数的患者中与 AIS 风险的比值明显更高,表明这些抗体标志物可用作 AIS 的危险因素。

结论

DIDO1、FOXJ2 和 CPSF2 的血清抗体水平分别可用于预测由肾衰竭、高血压和 DM 引起的动脉粥样硬化相关 AIS 的发病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/384c/8188684/52554e7c8f54/12916_2021_2001_Fig1_HTML.jpg

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