Coronary artery lesion

冠状动脉病变
  • 文章类型: English Abstract
    OBJECTIVE: To investigate the changes in the serum levels of oxidized phospholipids (OxPLs) and endothelial nitric oxide synthase (eNOS) and their association with coronary artery disease (CAL) in children in the acute stage of Kawasaki disease (KD), as well as the clinical significance of OxPLs and eNOS.
    METHODS: A prospective study was conducted on 95 children in the acute stage of KD (KD group). According to the presence of absence of CAL, the KD group was further divided into a CAL subgroup and a non-CAL (NCAL) subgroup. Thirty children with fever due to lower respiratory tract infection were enrolled as the fever group. Thirty healthy children who underwent physical examination were enrolled as the healthy control group. The above groups were compared in terms of general information and serum levels of OxPLs, eNOS and other laboratory indexes, and the correlation between OxPLs level and eNOS level was analyzed.
    RESULTS: The KD group had a significantly higher level of OxPLs and a significantly lower level of eNOS compared with the fever group and the healthy control group (P<0.05). After treatment, the children with KD had a significantly decreased OxPLs level and a significantly increased eNOS level (P<0.05). Compared with the NCAL subgroup, the CAL subgroup had a significantly higher level of OxPLs and a significantly lower level of eNOS (P<0.05). Among the children of KD, the level of OxPLs was negatively correlated with that of eNOS (rs=-0.353, P<0.05).
    CONCLUSIONS: Serum OxPLs and eNOS in the acute stage of KD may be involved in the development of CAL in children with KD, and therefore, they may be used as the biomarkers to predict CAL in these children.
    目的: 探讨川崎病(Kawasaki disease, KD)急性期患儿的血清氧化磷脂(oxidized phospholipids, OxPLs)和内皮一氧化氮合酶(endothelial nitric oxide synthase, eNOS)水平的变化,分析血清OxPLs和eNOS水平与冠状动脉病变(coronary artery lesion, CAL)的相关性,并探讨其临床意义。方法: 前瞻性选择95例急性期KD患儿作为KD组,根据是否合并CAL分为CAL亚组和非冠状动脉病变(non-coronary artery lesion, NCAL)亚组;另外选取同期30例仅下呼吸道感染发热患儿作为发热组,30例健康体检儿童作为健康对照组。比较各组一般资料及血清OxPLs、eNOS等实验室指标的差异,分析血清OxPLs和eNOS的相关性。结果: KD组OxPLs水平高于发热组及健康对照组(P<0.05),eNOS水平低于发热组及健康对照组(P<0.05)。KD患儿治疗后较治疗前血清OxPLs下降,血清eNOS上升(P<0.05)。CAL亚组血清OxPLs高于NCAL亚组(P<0.05),血清eNOS水平低于NCAL亚组(P<0.05)。KD组患儿OxPLs与eNOS水平呈负相关(rs=-0.353, P<0.05)。结论: KD急性期血清OxPLs、eNOS参与了CAL发展,可成为预测KD患儿发生CAL的生物标志物。.
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  • 文章类型: Journal Article
    目的:探讨血清纤溶酶原激活物(PA)与D-二聚体的关系。儿童川崎病(KD)的严重程度,以及它们预测冠状动脉病变(CAL)的能力。
    方法:本回顾性研究分析了2020年1月至2023年9月在江南大学附属医院确诊的102例KD患儿的临床资料。该队列分为两组:CAL组中31名患有CAL的儿童,非CAL组中71名没有CAL的儿童。该研究评估了CAL的发生率,并调查了血清PA和D-二聚体水平与各种炎症标志物(白细胞(WBC)计数,血小板计数,和红细胞沉降率(ESR))。使用受试者工作特征(ROC)曲线来评估这些生物标志物对CAL的预测值。
    结果:CAL存在于30.04%的儿童中。Pearson相关分析显示血清PA水平与白细胞计数呈负相关(P=0.0187)。血小板计数(P=0.0116),和ESR(P=0.0041),而D-二聚体水平与这些标志物呈正相关(P<0.001)。PA和D-二聚体水平也呈负相关(P<0.001)。联合使用PA和D-二聚体水平来预测CAL的曲线下面积为0.871。
    结论:血清PA水平与KD的严重程度呈负相关,而D-二聚体水平呈正相关。一起,这些标记对CAL显示出显著的预测价值,强调其在评估KD儿童疾病严重程度和指导管理方面的效用。
    OBJECTIVE: To evaluate the relationships between serum plasminogen activator (PA) and D-dimer levels, the severity of Kawasaki disease (KD) in children, and their ability to predict coronary artery lesions (CAL).
    METHODS: This retrospective study analyzed the clinical data of 102 children diagnosed with KD at the Affiliated Hospital of Jiangnan University from January 2020 to September 2023. The cohort was divided into two groups: 31 children with CAL in the CAL group and 71 without it in the non-CAL group. The study assessed the incidence of CAL and investigated the correlations between serum PA and D-dimer levels and various inflammatory markers (white blood cell (WBC) count, platelet count, and erythrocyte sedimentation rate (ESR)). Receiver operating characteristic (ROC) curves were used to evaluate the predictive value of these biomarkers for CAL.
    RESULTS: CAL was present in 30.04% of the children. Pearson correlation analysis revealed that serum PA levels were inversely correlated with WBC count (P = 0.0187), platelet count (P = 0.0116), and ESR (P = 0.0041), while D-dimer levels were positively correlated with these markers (P < 0.001). A negative correlation between PA and D-dimer levels was also observed (P < 0.001). The combined use of PA and D-dimer levels to predict CAL achieved an area under the curve of 0.871.
    CONCLUSIONS: Serum PA levels were negatively associated with the severity of KD, whereas D-dimer levels were positively associated. Together, these markers showed significant predictive value for CAL, highlighting their utility in assessing disease severity and guiding management in children with KD.
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  • 文章类型: Journal Article
    目的:维生素D状态与川崎病(KD)的关系,以及冠状动脉病变(CAL),尚未建立。
    方法:进行了荟萃分析,以评估维生素D状态与KD之间的相关性。以及维生素D状态对KD进展为CAL的影响。
    结果:荟萃分析显示,血清25(OH)D水平与KD发生之间存在一致且显著的关联(研究N=22;z=-3.51,P<0.001)。KD患者的维生素D水平明显低于健康对照组(SMD:-1.30ng/mL,95CI:-2.05至-0.55ng/mL)。
    结论:该研究提供了证据支持较低的血清维生素D水平与KD的发生之间存在显著关联。特别是在中国人口中。然而,研究结果未提示维生素D对KD患者CAL的发生有直接影响.
    OBJECTIVE: The relationship between vitamin D status and Kawasaki Disease (KD), as well as coronary artery lesion (CAL), has yet to be established.
    METHODS: A meta-analysis was conducted to assess the correlation between vitamin D status and KD, as well as the impact of vitamin D status on the progression of KD into CAL.
    RESULTS: The meta-analysis revealed a consistent and significant association between serum 25(OH)D level and the occurrence KD (studies N = 22; z = -3.51, P < 0.001). Patients with KD had markedly lower levels of vitamin D than healthy controls (SMD: -1.30 ng/mL, 95%CI: -2.05 to -0.55 ng/mL).
    CONCLUSIONS: The study provided evidence supporting a significant association between lower serum vitamin D levels and the occurrence of KD, particularly within the Chinese population. However, the findings did not suggest a direct impact of vitamin D on the development of CAL in KD patients.
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  • 文章类型: Journal Article
    本系统综述和荟萃分析旨在评估川崎病(KD)预后营养指数(PNI)和静脉免疫球蛋白(IVIG)抵抗与冠状动脉病变(CAL)之间的关系。
    在PubMed上搜索了相关文献,Embase,科克伦图书馆,WebofScience,和谷歌学者截至2023年8月5日。汇集的敏感性,特异性,正似然比(PLR),负似然比(NLR),诊断优势比(DOR),计算曲线下面积(AUC)以评估IVIG耐药和CAL的KD患者PNI的预测值。
    共纳入8篇文章,包含10项研究,涉及7,047名参与者。合并结果显示,合并灵敏度为0.44(0.25-0.65),合并特异性为0.87(0.73-0.94),合并PLR为3.4(2.0-5.9),合并的NLR为0.65(0.48-0.87),合并DOR为5.26(2.76-10.02),合并AUC为0.75(0.71-0.78),用于诊断KD和CAL。合并结果表明,合并灵敏度为0.69(0.60-0.77),特异性为0.76(0.69-0.82),PLR为2.9(2.1-4.1),NLR为0.40(0.29-0.56),DOR为7.27(3.89-13.59),诊断有IVIG耐药的KD的AUC为0.79(0.75-0.82)。综合结果显示,合并灵敏度为0.63(0.58-0.67),特异性为0.82(0.80-0.83),PLR为3.09(1.06-8.98),NLR为0.38(0.07-2.02),区分KD与发热患者的DOR为8.23(0.81-83.16)。这些发现表明PNI对KD的敏感性较低,特异性相对较高,KD-CAL,和抗IVIGKD。
    总而言之,本研究首次对PNI在合并IVIG耐药和CAL的KD中的诊断价值进行系统评价和荟萃分析。结果表明,PNI可作为区分KD的生物标志物,KD与CAL,和具有IVIG抗性的KD。
    UNASSIGNED: This systematic review and meta-analysis aimed to evaluate the relationship between the prognostic nutritional index (PNI) and intravenous immunoglobulin (IVIG) resistance and coronary artery lesion (CAL) in Kawasaki disease (KD).
    UNASSIGNED: The relevant literature was searched on PubMed, Embase, Cochrane Library, Web of Science, and Google Scholar up to August 5, 2023. A pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under curve (AUC) were calculated to assess the predicted values of PNI in KD patients with IVIG resistance and CAL.
    UNASSIGNED: A total of 8 articles containing 10 studies involving 7,047 participants were included. The pooled results revealed a pooled sensitivity of 0.44 (0.25-0.65), a pooled specificity of 0.87 (0.73-0.94), a pooled PLR of 3.4 (2.0-5.9), a pooled NLR of 0.65 (0.48-0.87), a pooled DOR of 5.26 (2.76-10.02), and a pooled AUC of 0.75 (0.71-0.78) in the diagnosis of KD with CAL. The pooled results suggested that a pooled sensitivity was 0.69 (0.60-0.77), specificity was 0.76 (0.69-0.82), PLR was 2.9 (2.1-4.1), NLR was 0.40 (0.29-0.56), DOR was 7.27 (3.89-13.59), and AUC was 0.79 (0.75-0.82) in the diagnosis of KD with IVIG resistance. The combined results revealed the pooled sensitivity was 0.63 (0.58-0.67), specificity was 0.82 (0.80-0.83), PLR was 3.09 (1.06-8.98), NLR was 0.38 (0.07-2.02), DOR was 8.23 (0.81-83.16) in differentiating KD from febrile patients. These findings demonstrated low sensitivity and relatively high specificity of PNI for KD, KD-CAL, and IVIG-resistant KD.
    UNASSIGNED: In conclusion, this study was the first systematic review and meta-analysis of the diagnostic value of PNI in KD with IVIG resistance and CAL. The results suggested that PNI could be used as biomarkers for distinguish KD, KD with CAL, and KD with IVIG resistance.
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  • 文章类型: Journal Article
    目的:了解主动脉瓣上狭窄修补术患者冠状动脉病变的发生率、解剖特征及其术后风险。
    方法:结构风险因素之间的关联,术后ST段改变,主要不良心脏事件采用logistic回归和Fisher精确检验。
    结果:在2000年至2017年期间的51例连续瓣上主动脉瓣狭窄患者中,27例患者(53%)共发现48个冠状动脉病变。口脊突出(I型)是最常见的冠状动脉病变,其次是小口(IIIb)或不(IIIa)弥漫性长段冠状动脉狭窄,冠状尖点粘连(Ⅱ型)。有54例伴随冠状动脉手术,包括43次主要更正和11次修订。33例患者接受了分叉补片的瓣上主动脉瓣狭窄修复术;13例(39.4%)患有右冠状动脉扭曲/扭结,需要补片折叠(n=8)和重新植入(n=5)。术后发生MACE9例(17.6%),包括三人死亡,四个需要机械循环支持,和六种室性心律失常.22例(43.1%)患者术后ST段改变,包括13个在24小时内解决的早期更改,和9个持续超过24小时的持续变化。III型病变患者与术后持续性ST段改变相关(p=0.04),并独立预测术后MACE(p=0.02)。预先存在冠状动脉病变的患者右冠状动脉扭曲/扭结的风险升高(p=0.045)。
    结论:主动脉瓣上狭窄修补术患者的ST段改变和MACE发生率较高。术前存在复杂冠状动脉病变是术后主要不良心脏事件的最重要预测因素。
    OBJECTIVE: The aim of this study was to identify the prevalence and anatomic characteristics of coronary artery lesions and their associated postoperative risk in patients undergoing supravalvular aortic stenosis repair.
    METHODS: The association between structural risk factors, postoperative ST-segment changes, and major adverse cardiac events was explored using logistic regression and the Fisher\'s exact test.
    RESULTS: In 51 consecutive patients with supravalvular aortic stenosis treated between 2000 and 2017, a total of 48 coronary lesions were identified in 27 patients (53%). Prominent ostial ridge (type I) was the most common coronary lesion, followed by small ostium with (IIIb) or without (IIIa) diffuse long-segment coronary narrowing, and adhesion of the coronary cusp (type II). There were 54 concomitant coronary procedures, including 43 primary corrections and 11 revisions. Thirty-three patients underwent supravalvular aortic stenosis repair with a bifurcated patch, of which 13 (39.4%) had right coronary artery distortion/kinking requiring patch plication (n = 8) and reimplantation (n = 5). Postoperative major adverse cardiac events (MACE) occurred in 9 patients (17.6%), including 3 deaths, 4 needing mechanical circulatory support, and 6 experiencing ventricular arrhythmias. Twenty-two patients (43.1%) had postoperative ST-segment changes, including 13 early changes that resolved within 24 h and 9 persistent changes lasting >24 h. Patients with type III lesions were associated with postoperative persistent ST-segment change (P = 0.04) and these lesions independently predicted postoperative MACE (P = 0.02). Patients with pre-existing coronary lesions were at elevated risk of right coronary artery distortion/kinking (P = 0.045).
    CONCLUSIONS: The prevalence of ST-segment changes and MACE is high in patients undergoing supravalvular aortic stenosis repair. The preoperative presence of complex coronary lesions is the most important predictor for postoperative major adverse cardiac events.
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  • 文章类型: Journal Article
    冠状动脉病变(CAL)是川崎病(KD)的主要并发症,然而,关于复发性KD的CAL发生率和危险因素的数据有限.
    从2013年到2022年,对97例复发性KD儿童进行回顾性登记,并在入院时跟踪CAL发病率。放电,在后续行动中。
    最初,27.8%的人在入院和出院时患有CAL,出院后12个月下降至7.2%。大多数患者(97名患者中的66名,68.0%)在任何时间点都没有表现出CAL,在所有时间点出现7例CAL,表示持久的CAL。其余20例患者在入院时出现CAL,但在出院或随访期间恢复。值得注意的是,瞬态CAL在出院时出现,或者在后续行动中,但最终在出院后12个月得到解决。值得注意的是,先前的IVIG抵抗和凝血酶原时间增加似乎与复发性KD的CAL相关,表明他们可以帮助识别需要密切监测的患者。结论:该研究强调了随着时间的推移,复发性KD的CAL发病率下降,但模式不同,强调监测和进一步调查以确认这些发现的重要性。
    UNASSIGNED: Coronary artery lesions (CALs) are a major complication of Kawasaki disease (KD); however, data on CAL incidence and risk factors in recurrent KD are limited.
    UNASSIGNED: Ninety-seven children with recurrent KD were retrospectively enrolled from 2013 to 2022, and CAL incidence was tracked during admission, discharge, and during follow-up.
    UNASSIGNED: Initially, 27.8% had CAL at admission and discharge, declining to 7.2% at 12 months post-discharge. Most patients (66 of 97, 68.0%) did not exhibit CAL at any of the time points, 7 cases presented CAL at all time points, indicating a persistent CAL. The remaining 20 cases presented CAL at admission but recovered at discharge or during follow-up. Notably, transient CALs had presented at discharge, or during the follow-up, but finally resolved at 12 months after discharge. Notably, prior IVIG resistance and increased prothrombin time seemed associated with CAL in recurrent KD, suggesting they could help identify patients needing close monitoring.
    UNASSIGNED: The study highlights decreasing CAL incidence over time in recurrent KD but with diverse patterns, emphasizing the importance of monitoring and further investigations to confirm these findings.
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  • 文章类型: English Abstract
    Kawasaki disease (KD) is a systemic inflammatory vascular disorder that predominantly affects children and is the leading cause of acquired heart disease in children. Although the etiology of this disease remains unclear, genome-wide association and genome-wide linkage studies have shown that some susceptible genes and chromosomal regions are associated with the development and progression of KD. With the advancement of high-throughput DNA sequencing techniques, more and more genomic information related to KD is being discovered. Understanding the genes involved in the pathogenesis of KD may provide novel insights into the diagnosis and treatment of KD. By analyzing related articles and summarizing related research advances, this article mainly discusses the T cell activation-enhancing genes that have been confirmed to be closely associated with the development and progression of KD and reveals their association with the pathogenesis of KD and coronary artery lesions.
    川崎病(Kawasaki disease, KD)是一种好发于儿童的全身性血管炎症疾病,是儿童后天性心脏病的主要原因。虽然该病病因尚不清楚,但通过全基因组关联和全基因组连锁研究发现,一些易感基因和染色体区域与KD的发生发展相关。随着高通量DNA测序技术的发展,越来越多与KD相关的基因组信息被发现。了解KD发病机制中涉及的基因可能为该病的诊断和治疗提供新思路。该文通过分析相关文献,总结研究进展,主要讨论目前已证实与KD发生发展密切相关的增强T细胞活化类基因,揭示其与KD发病及冠状动脉损伤的相关性。.
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  • 文章类型: English Abstract
    OBJECTIVE: To explore the role and potential mechanisms of chitinase-3-like protein 1 (CHI3L1) in coronary artery lesions in a mouse model of Kawasaki disease (KD)-like vasculitis.
    METHODS: Four-week-old male SPF-grade C57BL/6 mice were randomly divided into a control group and a model group, with 10 mice in each group. The model group mice were intraperitoneally injected with 0.5 mL of lactobacillus casei cell wall extract (LCWE) to establish a mouse model of KD-like vasculitis, while the control group mice were injected with an equal volume of normal saline. The general conditions of the mice were observed on the 3rd, 7th, and 14th day after injection. Changes in coronary artery tissue pathology were observed using hematoxylin-eosin staining. The level of CHI3L1 in mouse serum was measured by enzyme-linked immunosorbent assay. Immunofluorescence staining was used to detect the expression and localization of CHI3L1, von Willebrand factor (vWF), and α-smooth muscle actin (α-SMA) in coronary artery tissue. Western blot analysis was used to detect the expression of CHI3L1, vWF, vascular endothelial cadherin (VE cadherin), Caspase-3, B cell lymphoma-2 (Bcl-2), Bcl-2 associated X protein (Bax), nuclear factor κB (NF-κB), and phosphorylated NF-κB (p-NF-κB) in coronary artery tissue.
    RESULTS: The serum level of CHI3L1 in the model group was significantly higher than that in the control group (P<0.05). Compared to the control group, the expression of CHI3L1 in the coronary artery tissue was higher, while the expression of vWF was lower in the model group. The relative expression levels of CHI3L1, Bax, Caspase-3, NF-κB, and p-NF-κB were significantly higher in the model group than in the control group (P<0.05). The relative expression levels of vWF, VE cadherin, and Bcl-2 were lower in the model group than in the control group (P<0.05).
    CONCLUSIONS: In the LCWE-induced mouse model of KD-like vasculitis, the expression levels of CHI3L1 in serum and coronary arteries increase, and it may play a role in coronary artery lesions through endothelial cell apoptosis mediated by inflammatory reactions.
    目的: 探究壳多糖酶3样蛋白1(chitinase-3-like protein 1, CHI3L1)在川崎病(Kawasaki disease, KD)样血管炎小鼠模型冠状动脉损伤中的作用及其潜在机制。方法: 将4周龄雄性SPF级C57BL/6小鼠随机分为正常对照组和模型组,每组10只。模型组小鼠通过腹腔注射干酪乳杆菌细胞壁提取物(lactobacillus casei cell wall extract, LCWE)0.5 mL构建KD样血管炎小鼠模型,对照组腹腔注射等量的生理盐水。注射后第3天、第7天和第14天观察小鼠的一般情况。采用苏木精-伊红染色法观察冠状动脉组织病理学变化。采用酶联免疫吸附法检测小鼠血清中CHI3L1水平。采用免疫荧光染色法检测CHI3L1、血管性血友病因子(von Willebrand factor, vWF)、α-平滑肌肌动蛋白(α-smooth muscle actin, α-SMA)在冠状动脉组织中的表达及定位。采用Western blot法检测冠状动脉组织中CHI3L1、vWF、血管内皮钙黏蛋白(vascular endothelial cadherin, VE cadherin)、半胱天冬酶-3(Caspase-3)、B细胞淋巴瘤-2(B cell lymphoma-2, Bcl-2)、Bcl-2相关X蛋白(Bcl-2 associated X protein, Bax)、核转录因子κB(nuclear factor-κB, NF-κB)及磷酸化NF-κB(p-NF-κB)表达情况。结果: 模型组小鼠血清中CHI3L1含量较对照组明显升高(P<0.05)。与对照组相比,模型组小鼠冠状动脉组织中CHI3L1表达高于对照组,vWF表达低于对照组。模型组小鼠CHI3L1、Bax、Caspase-3、NF-κB及p-NF-κB蛋白相对表达量明显高于对照组(P<0.05)。模型组vWF、VE cadherin和Bcl-2蛋白相对表达量低于对照组(P<0.05)。结论: LCWE诱导的KD样血管炎小鼠模型中,血清及冠状动脉CHI3L1的表达水平升高,可能通过炎性反应介导血管内皮细胞凋亡在冠状动脉损伤中发挥作用。.
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  • 文章类型: Meta-Analysis
    OBJECTIVE: To systematically evaluate the value of the platelet-to-lymphocyte ratio (PLR) in predicting coronary artery lesions (CAL) in Chinese children with Kawasaki Disease (KD).
    METHODS: A comprehensive search was conducted in databases including PubMed, Embase, Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang Data, China Biomedical Literature Database, and China Science and Technology Journal Database from inception to December 2022. The quality of the included literature was assessed using the Newcastle-Ottawa Scale, and a Meta analysis was performed using Stata 15.1.
    RESULTS: A total of ten published reports, involving 3 664 Chinese children with KD, were included in this Meta analysis, of whom 1 328 developed CAL. The Meta analysis revealed a sensitivity of 0.78 (95%CI: 0.71-0.83), specificity of 0.71 (95%CI: 0.61-0.80), overall diagnostic odds ratio of 8.69 (95%CI: 5.02-15.06), and an area under the curve of the summary receiver operating characteristic of 0.82 (95%CI: 0.78-0.85) for PLR in predicting CAL in the children with KD. The sensitivity, specificity, and area under the curve of summary receiver operating characteristic were lower for PLR alone compared to PLR in combination with other indicators. Sensitivity analysis demonstrated the stability of the Meta analysis results with no significant changes upon excluding individual studies. However, a significant publication bias was observed (P<0.001).
    CONCLUSIONS: PLR demonstrates certain predictive value for CAL in Chinese children with KD.
    目的: 系统评价血小板与淋巴细胞比值(platelet-to-lymphocyte ratio, PLR)对川崎病(Kawasaki disease, KD)患儿冠状动脉病变(coronary artery lesion, CAL)的预测价值。方法: 检索PubMed、Embase、Cochrane Library、Web of Science、中国知网、万方数据、中国生物医学文献检索数据库、维普数据库等数据库自建库至2022年12月PLR预测中国KD患儿发生CAL的相关研究。采用纽卡斯尔-渥太华量表(Newcastle-Ottawa Scale)评价纳入文献的质量,采用Stata 15.1进行Meta分析。结果: 共纳入10项研究,包括3 664例中国KD儿童,其中1 328例发生了CAL。Meta分析显示:PLR预测KD患儿发生CAL的灵敏度为0.78(95%CI:0.71~0.83),特异度为0.71(95%CI:0.61~0.80),总诊断比值比为8.69(95%CI:5.02~15.06),拟合受试者操作特征的曲线下面积为0.82(95%CI:0.78~0.85)。亚组分析显示,单独使用PLR预测KD患儿发生CAL的灵敏度、特异度和曲线下面积低于PLR联合其他指标。敏感性分析显示,逐一排除纳入研究后结果无显著变化,提示Meta分析结果稳健。发表偏倚结果显示,纳入的研究存在显著的发表偏倚(P<0.001)。结论: PLR对中国KD患儿CAL的发生有一定的预测价值。.
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  • 文章类型: Journal Article
    探讨FGA基因多态性与川崎病冠状动脉病变的相关性。
    230名川崎病患儿(KD组),纳入200例健康儿童(正常组)和208例非KD发热儿童(发热组)。一般临床指标,血清MMPs的浓度,TIMP-1,FG-α,纤维蛋白原水平,分子功能(FMPV/ODmax)和FGAThr312Ala多态性在早晨禁食后通过检测外周静脉血单独检测。
    三组之间的平均年龄没有显着差异,3.03±1.22年,3.17±1.30年,3.21±1.31年,分别。与发热组相比,白细胞计数(WBC)的水平,血小板计数(PLT),降钙素原(PCT),C反应蛋白(CRP),红细胞沉降率(ESR),白细胞介素-6(IL-6),单核细胞趋化蛋白-1(MCP-1),KD组纤维蛋白原(Fg)水平明显升高。红细胞计数(RBC)和血红卵白(Hb)程度显著下降(p<0.05)。血清MMPs的浓度,KD组和发热组TIMP-1、FG-α明显高于正常组(p<0.05)。KD组MMP-2、MMP-3、MMP-9、MMP-13、TIMP-1、FG-α浓度明显高于发热组(p<0.05)。KD组分为两个亚组,55例合并CAL的患者和179例未合并CAL的患者。联合CAL组血浆纤维蛋白原浓度明显高于非联合CAL组和正常组(p<0.01)。三组间FMPV/ODmax差异无统计学意义(p>0.05)。与正常组相比,FGAGG,GA,AA基因型和G,FGA基因多态性的A等位基因频率在KD组中无显著差别(p>0.05)。在KD组,CAL儿童中最常见的类型是GA,而无CAL儿童中最常见的类型是GG。
    在KD患者中MMPs和FG-α显著上调。CAL患儿FGA基因型的比例明显高于无CAL患儿,提示FGA基因多态性影响KD患儿冠状动脉病变。
    UNASSIGNED: To investigate the correlation between FGA gene polymorphisms and coronary artery lesion in Kawasaki disease.
    UNASSIGNED: Two hundred and thirty four children with Kawasaki disease (KD group), 200 healthy children (normal group) and 208 children with non-KD fever (fever group) were enrolled. General clinical indicators, the concentration of serum MMPs, TIMP-1, FG-α,fibrinogen level, molecular function (FMPV/ODmax) and FGA Thr312Ala polymorphism were detected individually by testing peripheral venous blood after fasting in the morning.
    UNASSIGNED: There was no significant difference in average age among the three groups, which were 3.03 ± 1.22 years, 3.17 ± 1.30 years, and 3.21 ± 1.31 years, respectively. Compared with those in the fever group, the levels of white blood cell count (WBC), platelet count (PLT), procalcitonin (PCT), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), and fibrinogen (Fg) levels were significantly increased in the KD group. Red blood cell count (RBC) and hemoglobin (Hb) levels were significantly decreased (p < 0.05).The concentration of serum MMPs, TIMP-1, and FG-α in the KD and fever groups were significantly higher than those in the normal group (p < 0.05). The concentration of MMP-2, MMP-3, MMP-9, MMP-13, TIMP-1, and FG-α in the KD group were significantly higher than those in the fever group (p < 0.05).The KD group was divided into two subgroups,55 patients with combined CAL and 179 patients without combined CAL. The plasma fibrinogen concentration in the combined CAL group was significantly higher than that in the non-combined CAL and normal groups (p < 0.01). There was no statistically significant difference in FMPV/ODmax among the three groups (p > 0.05). Compared with normal group, the FGA GG, GA, and AA genotype and G, A allele frequency of the FGA gene polymorphism in the KD group showed no significant difference (p > 0.05). In the KD group, the most common type in children with CAL was GA, while the most common type in children without CAL was GG.
    UNASSIGNED: MMPs and FG-α were significantly upregulated in KD patients. The proportion of FGA genotype GA in children with CAL was significantly higher than that in children without CAL, suggesting that FGA gene polymorphisms affect coronary artery lesion in children with KD.
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