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Enhancing knowledge and practices toward Vitamin D deficiency through implementing awareness programs among medical science female students 通过在医学专业女生中开展宣传计划,提高她们对维生素 D 缺乏症的认识和实践能力
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-12-01 DOI: 10.1177/1721727x231223365
Hayaa M. Alhuthali, Hind A. Alzahrani, Eman F. Ataya, M. Almehmadi, A. Alsaiari, Amani A. Alrehaili, M. M. Bakhuraysah, F. Alsaeedi, Ohud Alsalmi, Wafaa Altalhi, Amal F. Gharib, Eman N. Ramadan
Vitamin D (VD) deficiency has widespread prevalence worldwide. In Saudi Arabia, it is the most common form of public health problem with regard to malnutrition. This is because there is insufficient knowledge about negative VD practices. The current study aimed to evaluate VD deficiency knowledge and practices before and after the implementation of an awareness programme. A quasi-experimental design was used for the study, which was conducted at the College of Applied Medical Science at Al-Baha University. A convenience sample encompassing all the female students in the Public Health Department was used ( n = 83 students). Two tools were used for data collection; the first was an intervention questionnaire to assess the students’ knowledge, and the second was a questionnaire concerned with students’ practices in preventing VD deficiency. The mean age of the students was 20.75 ± 7.85 years. Of the study’s subjects, 45.8% suffered from VD deficiency and 72.3% had a family history of VD deficiency. The study showed that there had been significant progress in students’ VD knowledge and behaviours following the programme. While 59% of the students had poor knowledge and 95.2% had unsatisfactory practices pre-intervention, 86.7% and 48.2% showed exemplary knowledge and a positive attitude towards VD, respectively, post-intervention. The scores achieved by the students had significantly changed ( p ≤ .01); compared to the knowledge and practice scores of 24.43 ± 7.21 out of 53 and 24.29 ± 5.23 out of 48, respectively, before the intervention, they were elevated to 46.89 ± 9.93 and 29.39 ± 14.23 following the awareness programme. This type of health education programme can raise VD deficiency knowledge and improve practices. This study highlights the importance of holding public health awareness campaigns and recommends the creation of specifically designed booklets and leaflets for medical students and patients/visitors to hospital and public places.
维生素 D(VD)缺乏症在全球普遍存在。在沙特阿拉伯,这是营养不良方面最常见的公共卫生问题。这是因为人们对缺乏维生素 D 的消极做法缺乏足够的了解。本研究旨在评估在实施提高认识计划前后人们对营养缺乏症的认识和做法。研究采用准实验设计,在巴哈大学应用医学院进行。研究采用了方便抽样(n = 83 名学生),涵盖了公共卫生系的所有女生。数据收集使用了两种工具:第一种是评估学生知识的干预问卷,第二种是关于学生预防性传播疾病的实践问卷。学生的平均年龄为(20.75 ± 7.85)岁。研究对象中,45.8%患有VD缺乏症,72.3%有VD缺乏症家族史。研究结果表明,在该计划实施后,学生们在缺乏维生素 D 的知识和行为方面有了显著的进步。干预前,59%的学生对性病的认识不足,95.2%的学生对性病的做法不满意,而干预后,86.7%和48.2%的学生对性病的认识和态度分别达到了模范水平和积极水平。学生们的得分有了明显的变化(P ≤ 0.01);与干预前的知识和实践得分(满分 53 分,分别为 24.43 ± 7.21 分和 24.29 ± 5.23 分)相比,干预后的得分(满分 48 分,分别为 46.89 ± 9.93 分和 29.39 ± 14.23 分)有所提高。这类健康教育计划可以提高人们对性传播疾病缺乏症的认识,并改善人们的做法。这项研究强调了开展公共卫生宣传活动的重要性,并建议为医科学生和医院及公共场所的病人/访客制作专门设计的小册子和传单。
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引用次数: 0
Alterations and predictive value of blood routine parameters in patients with lupus enteritis: A retrospective study 狼疮性肠炎患者血常规参数的变化和预测价值:一项回顾性研究
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-12-01 DOI: 10.1177/1721727x231220156
Wen-Xin Zhang, Jin-He Xiong
Lupus enteritis (LE) is prone to incorrect and missed diagnoses. LE primarily occurs during the active stage of systemic lupus erythematosus (SLE), which often manifests with alterations in peripheral blood cell that may serve as indicators of disease activity and organ damage. This study aims to investigate the alterations and predictive value of routine blood parameters for LE diagnosis. This exploratory study retrospectively analyzed the medical records of 36 patients with SLE who were admitted to Suining Central Hospital between January 2006 and April 2023. Additionally, a control group consisting of 72 SLE patients without LE, matched for sex and age, was enrolled. A comparison was made between the two groups regarding clinical characteristics and changes in routine blood parameters. Binary logistic regression and receiver operating characteristic (ROC) curve analyses were conducted to identify independent risk factors and evaluate their diagnostic performance for LE. The LE group exhibited significantly higher neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), along with a lower lymphocyte count (LYM), compared to the control group ( p < .05). Binary logistic regression analysis revealed that NLR independently predicted the onset of LE, with an odds ratio of 1.347 and a 95% confidence interval of 1.070–1.696 ( p < .01). ROC curve analysis demonstrated that NLR had an area under the curve of 0.68 for diagnosing LE ( p < .05). When the cutoff value was set at 2.44, the Youden Index was only 0.31. Significant differences were observed in several routine parameters between patients with LE and the control group, which can be attributed to the occurrence of LE during the active stage of SLE. However, only the NLR emerged as an independent risk factor for LE,and its predicting vulue for was insufficient; no blood routine parameter has been identified as an reliable predictor for LE.
狼疮肠炎(LE)容易误诊和漏诊。LE主要发生在系统性红斑狼疮(SLE)的活跃期,通常表现为外周血细胞的改变,可作为疾病活动性和器官损伤的指标。本研究旨在探讨血常规参数的变化及其对LE诊断的预测价值。本探索性研究回顾性分析了2006年1月至2023年4月绥宁市中心医院收治的36例SLE患者的病历。此外,还纳入了一个由72名性别和年龄相匹配的无LE的SLE患者组成的对照组。比较两组患者的临床特点及血常规指标的变化。采用二元logistic回归和受试者工作特征(ROC)曲线分析,确定独立危险因素并评价其对LE的诊断效果。与对照组相比,LE组中性粒细胞与淋巴细胞比率(NLR)和血小板与淋巴细胞比率(PLR)显著升高,淋巴细胞计数(LYM)显著降低(p < 0.05)。二元logistic回归分析显示,NLR独立预测LE的发生,比值比为1.347,95%可信区间为1.070 ~ 1.696 (p < 0.01)。ROC曲线分析显示,NLR诊断LE的曲线下面积为0.68 (p < 0.05)。当截断值为2.44时,约登指数仅为0.31。LE患者与对照组在几个常规参数上存在显著差异,这可能是由于LE发生在SLE的活动期。然而,只有NLR成为LE的独立危险因素,其预测价值不足;没有血常规参数被确定为LE的可靠预测指标。
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引用次数: 0
Effects of orthodontic treatment on porphyromonas gingivalis, gingipains and gingival inflammation 正畸治疗对牙龈卟啉菌、牙龈素和牙龈炎症的影响
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-12-01 DOI: 10.1177/1721727x231220237
Lin Wang, Zhigang Wang, Mei Zhang, Shuiqing Xiao, Qiushuang Gao
Purpose: To assess the effects of orthodontic treatment on the changes of Porphyromonas gingivalis ( P.g) and gingipains as well as gingival inflammation. Materials and methods: A total of 105 patients who had healthy gingivae and were treated as research subjects, the gingival crevicular fluid of whom was all collected before treatment and in the 1st, 2nd, 3rd, and 6th months after wearing an appliance. Then, the 16S ribosomal deoxyribonucleic acid (rDNA) polymerase chain reaction (PCR) technique was employed to detect the levels of P.g, Lys-gingipain (Kgp) and Arg-gingipain (Rgp) in the specimens. It was followed by a statistical analysis of the data via the SPSS 23.0 software package. Results: In P.g detection, the 16S rDNA PCR technique presented specific advantages and high sensitivity. The positive detection rate of P.g in the 1st, 2nd and 3rd month of treatment ( p < .05), that of Kgp in P.g-positive patients in the 2nd and 3rd months of treatment ( p < .05), and that of Rgp in P.g-positive patients in the 2nd and 3rd months of treatment ( p < .05) were higher than the pre-treatment results. Compared with gingival index (GI)-0 patients, GI-1 patients exhibited higher positive detection rates of P.g and Kgp and Rgp, which were further found to be positively correlated with the treatment duration and GI ( p < .05). Conclusion: In the early stage of orthodontic treatment, the levels of P.g, Kgp and Rgp rise after wearing the appliance, inducing gingival inflammation.
目的:探讨正畸治疗对牙龈卟啉单胞菌(Porphyromonas gingivalis, P.g)、牙龈疼痛及牙龈炎症的影响。材料与方法:选取健康牙龈患者105例作为研究对象,于治疗前及佩戴矫治器后1、2、3、6个月采集龈沟液。然后采用16S核糖体脱氧核糖核酸(rDNA)聚合酶链反应(PCR)技术检测标本中P.g、Lys-gingipain (Kgp)和Arg-gingipain (Rgp)的水平。采用SPSS 23.0软件包对数据进行统计分析。结果:在P.g检测中,16S rDNA PCR技术具有特异性优势和高灵敏度。治疗第1、2、3个月pg阳性检出率(p < 0.05),治疗第2、3个月pg阳性患者Kgp检出率(p < 0.05),治疗第2、3个月pg阳性患者Rgp检出率(p < 0.05)均高于治疗前。与牙龈指数(GI)-0患者相比,GI-1患者P.g、Kgp、Rgp的阳性检出率更高,且与治疗时间、GI呈正相关(p < 0.05)。结论:在正畸治疗早期,佩戴矫治器后P.g、Kgp、Rgp水平升高,诱发牙龈炎症。
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引用次数: 0
Experience in early diagnosis of pyoderma gangrenosum: A case report 早期诊断脓皮病的经验:病例报告
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-12-01 DOI: 10.1177/1721727x231214919
Cong mo Shen, Feng Li
The early clinical manifestations of pyoderma gangrenosum are not characteristic, it resembles other infectious skin lesions and is difficult to identify in the early stages. The exploratory surgery for direct observation of the superficial fascia of the suspected infection site for signs of infection, together with the collection of tissue samples for bacterial culture, combined with histopathological biopsy and clinical manifestations, was of significant value in the differential diagnosis of this disease and infectious skin lesions with similar manifestations. We introduce a patient who was admitted to hospital with redness and swelling of the left calf and foot for 7 days. The local appearance of the lesion resembled a carbuncle or early-stage necrotizing fasciitis. We performed surgical exploration for a definitive diagnosis but found no signs of infection, therefore, infection could be preliminarily ruled out. The disease was finally diagnosed as pyoderma gangrenosum, which was treated with hormone therapy and recovered after dressing change.
脓皮病的早期临床表现没有特征性,与其他感染性皮肤病相似,早期很难鉴别。通过探查性手术直接观察疑似感染部位的浅筋膜有无感染迹象,同时采集组织样本进行细菌培养,结合组织病理活检和临床表现,对本病和表现相似的感染性皮肤病的鉴别诊断具有重要价值。我们介绍了一名因左小腿和足部红肿 7 天而入院的患者。病变局部外观类似痈或早期坏死性筋膜炎。为了明确诊断,我们进行了手术探查,但没有发现感染迹象,因此可以初步排除感染。该病最终被诊断为脓皮病,经过激素治疗,换药后痊愈。
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引用次数: 0
Pulmonary tuberculosis in a case of acute myeloid leukemia during consolidation chemotherapy 急性髓系白血病巩固化疗期间肺结核1例
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-09-06 DOI: 10.1177/1721727x231184764
Jiakui Zhang, Dan Wu, Hong Zheng, Xiaojuan Ding, Xiujuan Ding, Yong Huang
Tuberculosis in acute myeloid leukemia (AML) has rarely been reported. Herein, we report the diagnosis and treatment of a patient with AML who was finally diagnosed with pulmonary tuberculosis following consolidation chemotherapy. In this case, chest CT showed space-occupying lesions near the right pulmonary hilum after the second cycle of consolidation chemotherapy. Initially, extramedullary infiltration of AML and lung cancer were considered. After consolidation chemotherapy, antibiotics were simultaneously administered, but persistent fever continued. Later, based on the positive acid-fast staining of the tissue puncture following tracheoscopy and the sputum, the patient was diagnosed to have pulmonary tuberculosis and immediately transferred to a dedicated tuberculosis hospital for anti-tuberculosis treatment. Unfortunately, the patient died of respiratory failure 3 months later. In conclusion, in cases wherein AML patients have persistent fever or pulmonary space-occupying lesions of unknown causes during chemotherapy, the possibility of tuberculosis should be considered. Early diagnosis and targeted anti-tuberculosis treatment may significantly improve the prognosis of patients.
急性髓性白血病(AML)中结核的报道很少。在此,我们报告了一位AML患者的诊断和治疗,他在巩固化疗后最终被诊断为肺结核。本例在第二周期巩固化疗后,胸部CT显示右肺门附近占位性病变。最初,髓外浸润被认为是AML和肺癌。巩固化疗后,同时给予抗生素治疗,但持续发热。随后,根据气管镜检查后组织穿刺及痰液抗酸染色阳性,诊断为肺结核,立即转至结核病专科医院接受抗结核治疗。不幸的是,患者3个月后死于呼吸衰竭。综上所述,AML患者在化疗期间出现持续发热或不明原因的肺部占位性病变时,应考虑结核病的可能性。早期诊断和靶向抗结核治疗可显著改善患者预后。
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引用次数: 0
Morin hydrate suppresses lipoteichoic acid-induced oxidative stress-mediated inflammatory events in macrophages via augmenting Nrf2/HO-1 and antioxidant defense molecules 水合桑里素通过增加Nrf2/HO-1和抗氧化防御分子抑制脂壁酸诱导的巨噬细胞氧化应激介导的炎症事件
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-09-01 DOI: 10.1177/1721727x231199414
Cheng-Ying Hsieh, T. Jayakumar, Kao-Chang Lin, T. Yen, Chih-Wei Hsia, Wei-Chieh Huang, J. Sheu, C. Hsia
Oxidative stress induces chronic inflammatory diseases in aerobic organisms, and antioxidants from plants represent an efficient strategy to prevent this condition. Morin hydrate (MH), a bioactive flavonoid, has a wide range of pharmacological properties, including anti-inflammatory and anti-oxidant. This study evaluated the protective effects of MH on lipoteichoic acid (LTA)-induced inflammation in RAW 264.7 macrophages by testing the main oxidative and inflammatory biomarkers and also investigating the molecular pathways involved. The antioxidant and anti-inflammatory effects of MH were evaluated in a cell-free system and RAW264.7 cells. Quantitative real-time PCR (RT-qPCR) and assay kits were used to measure the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase 1 (HO-1) mRNA, as well as the activity of antioxidant enzymes. The effects of MH on LTA-induced inducible nitric oxide synthase (iNOS), IL-1β, and TNF-α mRNA and protein expression were also evaluated by RT-qPCR and Western blotting. MH reduced DPPH and ABTS radicals in a cell-free system and LTA-induced ROS and NO production in RAW264.7 cells. MH upregulated Nrf2 and HO-1 mRNA expression and reversed LTA-mediated reduction of antioxidant enzymes, at a high concentration of 20 µM pretreated cells. MH also effectively attenuated LTA-induced iNOS, IL-1β, and TNF-α mRNA and protein expression, and these effects were reversed by ML385. The study found that the Nrf2/HO-1 played role in the inhibition of LTA-induced oxidative stress in macrophages by MH. This study may consider to be a promising induced macrophage-targeted strategy via regulating anti-oxidative defense to control inflammatory-related disease.
氧化应激在需氧生物中诱导慢性炎症性疾病,植物抗氧化剂是预防这种情况的有效策略。莫宁水合物(MH)是一种具有生物活性的类黄酮,具有广泛的药理作用,包括抗炎和抗氧化。本研究通过检测主要氧化和炎症生物标志物以及研究相关的分子途径,评估了MH对脂磷胆酸(LTA)诱导的RAW 264.7巨噬细胞炎症的保护作用。在无细胞系统和RAW264.7细胞中评价MH的抗氧化和抗炎作用。采用实时荧光定量PCR (RT-qPCR)和检测试剂盒检测核因子红细胞2相关因子2 (Nrf2)和血红素加氧酶1 (HO-1) mRNA表达及抗氧化酶活性。采用RT-qPCR和Western blotting检测MH对lta诱导的诱导型一氧化氮合酶(iNOS)、IL-1β和TNF-α mRNA和蛋白表达的影响。MH降低了无细胞系统中的DPPH和ABTS自由基,并降低了lta诱导的RAW264.7细胞中ROS和NO的产生。高浓度20µM的预处理细胞中,MH上调Nrf2和HO-1 mRNA的表达,逆转lta介导的抗氧化酶的减少。MH还能有效减弱lta诱导的iNOS、IL-1β和TNF-α mRNA和蛋白的表达,而ML385能逆转这些作用。本研究发现Nrf2/HO-1参与了MH对lta诱导的巨噬细胞氧化应激的抑制,本研究可以认为是一种有希望通过调节抗氧化防御来控制炎症相关疾病的诱导巨噬细胞靶向策略。
{"title":"Morin hydrate suppresses lipoteichoic acid-induced oxidative stress-mediated inflammatory events in macrophages via augmenting Nrf2/HO-1 and antioxidant defense molecules","authors":"Cheng-Ying Hsieh, T. Jayakumar, Kao-Chang Lin, T. Yen, Chih-Wei Hsia, Wei-Chieh Huang, J. Sheu, C. Hsia","doi":"10.1177/1721727x231199414","DOIUrl":"https://doi.org/10.1177/1721727x231199414","url":null,"abstract":"Oxidative stress induces chronic inflammatory diseases in aerobic organisms, and antioxidants from plants represent an efficient strategy to prevent this condition. Morin hydrate (MH), a bioactive flavonoid, has a wide range of pharmacological properties, including anti-inflammatory and anti-oxidant. This study evaluated the protective effects of MH on lipoteichoic acid (LTA)-induced inflammation in RAW 264.7 macrophages by testing the main oxidative and inflammatory biomarkers and also investigating the molecular pathways involved. The antioxidant and anti-inflammatory effects of MH were evaluated in a cell-free system and RAW264.7 cells. Quantitative real-time PCR (RT-qPCR) and assay kits were used to measure the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase 1 (HO-1) mRNA, as well as the activity of antioxidant enzymes. The effects of MH on LTA-induced inducible nitric oxide synthase (iNOS), IL-1β, and TNF-α mRNA and protein expression were also evaluated by RT-qPCR and Western blotting. MH reduced DPPH and ABTS radicals in a cell-free system and LTA-induced ROS and NO production in RAW264.7 cells. MH upregulated Nrf2 and HO-1 mRNA expression and reversed LTA-mediated reduction of antioxidant enzymes, at a high concentration of 20 µM pretreated cells. MH also effectively attenuated LTA-induced iNOS, IL-1β, and TNF-α mRNA and protein expression, and these effects were reversed by ML385. The study found that the Nrf2/HO-1 played role in the inhibition of LTA-induced oxidative stress in macrophages by MH. This study may consider to be a promising induced macrophage-targeted strategy via regulating anti-oxidative defense to control inflammatory-related disease.","PeriodicalId":55162,"journal":{"name":"European Journal of Inflammation","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47988916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A review of Janus kinase/signal transducer and activator of transcription signaling and cytokines in the pain mechanism of rheumatoid arthritis 类风湿性关节炎疼痛机制中Janus激酶/信号转导因子、转录信号激活因子及细胞因子的研究进展
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-09-01 DOI: 10.1177/1721727x231197498
Yue Xiong, Xiaohui Song, Xiangrui Sheng, Jian Wu, Xin Chang, Tian Ren, Jin Cao, T. Cheng, Mingjun Wang
Rheumatoid arthritis (RA) is a progressive autoimmune disease characterized by chronic synovitis and articular destruction. Pain is the earliest and most important symptom. The Janus kinase/stat signaling pathway not only participates in the physiological processes such as the growth and differentiation of normal cells, but also plays a significant role in the pathological mechanisms such as pain in RA patients. Pain in RA patients is mediated by both inflammatory and non-inflammatory factors, including central sensitization and peripheral sensitization. Cytokines can regulate the nociceptor threshold through the JAK pathway, which leads to sensitization. In this review, we provide an overview of the physiological basis of pain modulation, the underlying importance of cytokines and JAK/STAT pathway in pain modulation, and finally introduce the performance of JAK inhibitors in clinical research. Having a better understanding of the mechanism of pain in RA may provide new therapeutic ideas and directions for the clinical improvement of pain in RA patients.
类风湿性关节炎(RA)是一种以慢性滑膜炎和关节破坏为特征的进行性自身免疫性疾病。疼痛是最早也是最重要的症状。Janus激酶/stat信号通路不仅参与正常细胞的生长和分化等生理过程,而且在RA患者的疼痛等病理机制中发挥着重要作用。RA患者的疼痛由炎症和非炎症因素介导,包括中枢致敏和外周致敏。细胞因子可以通过JAK途径调节伤害感受器阈值,从而导致致敏。在这篇综述中,我们概述了疼痛调节的生理基础、细胞因子和JAK/STAT通路在疼痛调节中的潜在重要性,并介绍了JAK抑制剂在临床研究中的作用。更好地了解RA疼痛的机制,可以为RA患者疼痛的临床改善提供新的治疗思路和方向。
{"title":"A review of Janus kinase/signal transducer and activator of transcription signaling and cytokines in the pain mechanism of rheumatoid arthritis","authors":"Yue Xiong, Xiaohui Song, Xiangrui Sheng, Jian Wu, Xin Chang, Tian Ren, Jin Cao, T. Cheng, Mingjun Wang","doi":"10.1177/1721727x231197498","DOIUrl":"https://doi.org/10.1177/1721727x231197498","url":null,"abstract":"Rheumatoid arthritis (RA) is a progressive autoimmune disease characterized by chronic synovitis and articular destruction. Pain is the earliest and most important symptom. The Janus kinase/stat signaling pathway not only participates in the physiological processes such as the growth and differentiation of normal cells, but also plays a significant role in the pathological mechanisms such as pain in RA patients. Pain in RA patients is mediated by both inflammatory and non-inflammatory factors, including central sensitization and peripheral sensitization. Cytokines can regulate the nociceptor threshold through the JAK pathway, which leads to sensitization. In this review, we provide an overview of the physiological basis of pain modulation, the underlying importance of cytokines and JAK/STAT pathway in pain modulation, and finally introduce the performance of JAK inhibitors in clinical research. Having a better understanding of the mechanism of pain in RA may provide new therapeutic ideas and directions for the clinical improvement of pain in RA patients.","PeriodicalId":55162,"journal":{"name":"European Journal of Inflammation","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41278989","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy of thymosin-α-1 in patients with COVID-19: A systematic review and meta-analysis 胸腺肽-α-1对新冠肺炎患者的疗效:系统回顾和荟萃分析
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-08-25 DOI: 10.1177/1721727x231197922
Pu Wang, Changhong Wang, Dawei Chen
To identify whether thymosin-α-1 (Tα1) is effective in patients with Coronavirus disease 2019 (COVID-19) and to determine a suitable population for Tα1 treatment. We included studies with ≥10 cases and adults (aged ≥18 years) with laboratory-confirmed SARS-CoV-2 infection, data on mortality or length of hospitalization, disease severity, and study location, while excluded pregnant and breastfeeding women and minors. Publications were searched from November 1, 2019, to July 5, 2023, in six databases, including PubMed, Web of Science, Embase, Cochrane Library, China Knowledge Resource Integrated Database, and Wanfang Database. We separately utilized Newcastle-Ottawa Scale and Cochrane handbook methodology to evaluate risk of bias and used Review Manager (version 5.4, Cochrane Collaboration, Copenhagen, Denmark) to present and synthesize results. Relative risks (RR) and Standardized Mean Difference (SMD) with 95% confidence intervals (CI) were analyzed for dichotomous variables and continuous variables, respectively. Nine studies (participants = 5417) were included. No significant differences were found in mortality (nine studies; n = 5417; RR = 0.95; 95% CI: 0.56, −1.60; p = .84; I2 = 90%) or length of hospitalization (four studies; n = 3688; SMD = 0.16; 95% CI: −0.38, −0.69; p = .57; I2 = 96%) between patients with COVID-19 who did and did not receive Tα1. Participants were divided by the severity of the disease (serious and non-serious) and study location. Among the serious group, the incidence of death among patients who received Tα1 treatment was 0.67 times that of patients who did not receive Tα1 treatment (four studies; n = 1230; RR: 0.67; 95% CI: 0.58, −0.77; p < .00,001; I2 = 0%). There was no significant difference in length of hospitalization between the groups (two studies; n = 410; SMD = 0.66; 95% CI: −0.06, −1.38; p = .07; I2 = 87%). Among the non-serious group, compared to not having Tα1 treatment, receiving Tα1 treatment reduced hospitalization length (two studies; n = 3670; SMD = −0.28; 95% CI: −0.41, −0.14; p < .0001; I2 = 51%), while no significant difference in mortality (three studies; n = 3775; RR = 1.06; 95% CI: 0.22, −5.03; p = .94; I2 = 89%). Moreover, there was no significant difference between subgroups when divided by study locations (Studies within China: seven studies; n = 5263; RR = 1.14; 95% CI: 0.64, −2.04; p = .65; I2=92%; Studies outside of China: two studies; n = 154; RR = 0.41; 95% CI: 0.14, −1.24; p = .11; I2 = 51%). For patients with serious types of COVID-19, Tα1 significantly decreased mortality, which supports the utilization of Tα1 in patients with severe and critical types of COVID-19. Moreover, regarding hospitalization length, patients with non-serious COVID-19 who used Tα1 reduced their hospitalization length compared to those that did not use Tα1. However, these results have high heterogeneity and limited generalizability.
确定胸腺肽-α-1(Tα1)对2019冠状病毒病(新冠肺炎)患者是否有效,并确定适合治疗Tα1的人群。我们纳入了对≥10例病例和实验室确诊感染严重急性呼吸系统综合征冠状病毒2型的成年人(年龄≥18岁)的研究,包括死亡率或住院时间、疾病严重程度和研究地点的数据,同时排除了孕妇、哺乳期妇女和未成年人。从2019年11月1日至2023年7月5日,在PubMed、Web of Science、Embase、Cochrane Library、中国知识资源综合数据库和万方数据库等六个数据库中检索出版物。我们分别使用Newcastle Ottawa量表和Cochrane手册方法来评估偏倚风险,并使用Review Manager(5.4版,Cochrane Collaboration,Copenhagen,Denmark)来呈现和综合结果。分别分析了二分变量和连续变量的相对风险(RR)和95%置信区间的标准化平均差(SMD)。包括9项研究(参与者=5417人)。在接受和未接受Tα1治疗的新冠肺炎患者的死亡率(9项研究;n=5417;RR=0.95;95%CI:0.56,−1.60;p=.84;I2=90%)或住院时间(4项研究;n=3688;SMD=0.16;95%CI:−0.38,−0.69;p=.57;I2=96%)方面未发现显著差异。参与者根据疾病的严重程度(严重和非严重)和研究地点进行划分。在严重组中,接受Tα1治疗的患者的死亡发生率是未接受Tα1治疗患者的0.67倍(四项研究;n=1230;RR:0.67;95%CI:0.58,-0.77;p<.00001;I2=0%)。两组之间的住院时间没有显著差异(两项研究;n=410;SMD=0.66;95%CI:−0.06,−1.38;p=.07;I2=87%)。在非严重组中,与未接受Tα1治疗相比,接受Tα-1治疗缩短了住院时间(两项研究;n=3670;SMD=−0.28;95%CI:−0.41,−0.14;p<.0001;I2=51%),而死亡率没有显著差异(三项研究;n=3775;RR=1.06;95%CI:0.22,−5.03;p=.94;I2=89%)。此外,按研究地点划分的亚组之间没有显著差异(中国境内研究:7项研究;n=5263;RR=1.14;95%CI:0.64,−2.04;p=.65;I2=92%;中国境外研究:2项研究;n=154;RR=0.41;95%CI:0.14,−1.24;p=.11;I2=51%)。对于严重型新冠肺炎患者,Tα1显著降低死亡率,这支持了Tα1在严重型和危重型新冠肺炎患者中的应用。此外,关于住院时间,使用Tα1的非严重新冠肺炎患者与未使用Tα2的患者相比,缩短了住院时间。然而,这些结果具有高度的异质性和有限的可推广性。
{"title":"Efficacy of thymosin-α-1 in patients with COVID-19: A systematic review and meta-analysis","authors":"Pu Wang, Changhong Wang, Dawei Chen","doi":"10.1177/1721727x231197922","DOIUrl":"https://doi.org/10.1177/1721727x231197922","url":null,"abstract":"To identify whether thymosin-α-1 (Tα1) is effective in patients with Coronavirus disease 2019 (COVID-19) and to determine a suitable population for Tα1 treatment. We included studies with ≥10 cases and adults (aged ≥18 years) with laboratory-confirmed SARS-CoV-2 infection, data on mortality or length of hospitalization, disease severity, and study location, while excluded pregnant and breastfeeding women and minors. Publications were searched from November 1, 2019, to July 5, 2023, in six databases, including PubMed, Web of Science, Embase, Cochrane Library, China Knowledge Resource Integrated Database, and Wanfang Database. We separately utilized Newcastle-Ottawa Scale and Cochrane handbook methodology to evaluate risk of bias and used Review Manager (version 5.4, Cochrane Collaboration, Copenhagen, Denmark) to present and synthesize results. Relative risks (RR) and Standardized Mean Difference (SMD) with 95% confidence intervals (CI) were analyzed for dichotomous variables and continuous variables, respectively. Nine studies (participants = 5417) were included. No significant differences were found in mortality (nine studies; n = 5417; RR = 0.95; 95% CI: 0.56, −1.60; p = .84; I2 = 90%) or length of hospitalization (four studies; n = 3688; SMD = 0.16; 95% CI: −0.38, −0.69; p = .57; I2 = 96%) between patients with COVID-19 who did and did not receive Tα1. Participants were divided by the severity of the disease (serious and non-serious) and study location. Among the serious group, the incidence of death among patients who received Tα1 treatment was 0.67 times that of patients who did not receive Tα1 treatment (four studies; n = 1230; RR: 0.67; 95% CI: 0.58, −0.77; p < .00,001; I2 = 0%). There was no significant difference in length of hospitalization between the groups (two studies; n = 410; SMD = 0.66; 95% CI: −0.06, −1.38; p = .07; I2 = 87%). Among the non-serious group, compared to not having Tα1 treatment, receiving Tα1 treatment reduced hospitalization length (two studies; n = 3670; SMD = −0.28; 95% CI: −0.41, −0.14; p < .0001; I2 = 51%), while no significant difference in mortality (three studies; n = 3775; RR = 1.06; 95% CI: 0.22, −5.03; p = .94; I2 = 89%). Moreover, there was no significant difference between subgroups when divided by study locations (Studies within China: seven studies; n = 5263; RR = 1.14; 95% CI: 0.64, −2.04; p = .65; I2=92%; Studies outside of China: two studies; n = 154; RR = 0.41; 95% CI: 0.14, −1.24; p = .11; I2 = 51%). For patients with serious types of COVID-19, Tα1 significantly decreased mortality, which supports the utilization of Tα1 in patients with severe and critical types of COVID-19. Moreover, regarding hospitalization length, patients with non-serious COVID-19 who used Tα1 reduced their hospitalization length compared to those that did not use Tα1. However, these results have high heterogeneity and limited generalizability.","PeriodicalId":55162,"journal":{"name":"European Journal of Inflammation","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2023-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46883743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mannose binding lectin deficiency and COVID-19 rates of thrombosis and mortality: Partial protection by immunodeficiency 甘露聚糖结合凝集素缺乏与新冠肺炎血栓形成率和死亡率:免疫缺陷的部分保护
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-08-10 DOI: 10.1177/1721727x231195205
Breanne Hayes, Brian P. Peppers
Objective: The purpose of this study is to determine the effects of COVID-19 infection on individuals with mannose binding lectin deficiency. Methods: An electronic medical records search was conducted for MBL deficiency and COVID-19 positive tests from March 2020-August 2022. Individualized chart analysis was conducted and statistical analysis was performed. Results: Thirty-three people in WVU medicine health system carry a diagnosis of mannose binding lectin deficiency and were diagnosed with COVID-19. The mean age of this cohort was 41 years. Seven individuals had severe enough symptoms to lead to an emergency department visit. One person was hospitalized. MBL deficient individuals had 7 times the odds of hospitalization ( p = .1506, OR 7.06 (CI 1.117-44.52)) compared to the general public. There was zero mortality among the MBL deficient population. None of the patients reported thrombosis or blood clots. Conclusion: This retrospective cross-sectional analysis of those with known MBL deficiency and COVID-19 infection suggest a lower risk of fatalities and thrombotic events in this cohort. There was however a higher odds ratio of hospitalization compared to the general public, although this was not statistically significant.
目的:本研究旨在确定新冠肺炎感染对甘露糖结合凝集素缺乏症患者的影响。方法:从2020年3月至2022年8月,对MBL缺乏和新冠肺炎阳性检测进行电子病历搜索。进行个性化图表分析,并进行统计分析。结果:WVU医疗卫生系统中有33人被诊断为甘露糖结合凝集素缺乏,并被诊断为新冠肺炎。该队列的平均年龄为41岁。七个人的症状严重到需要去急诊室就诊。一人住院治疗。MBL缺乏者的住院几率是普通人群的7倍(p=.1506,OR 7.06(CI 1.117-44.52))。MBL缺乏人群的死亡率为零。没有一名患者报告血栓或血栓。结论:这项对已知MBL缺乏和新冠肺炎感染者的回顾性横断面分析表明,该队列中死亡和血栓事件的风险较低。然而,与普通公众相比,住院的几率更高,尽管这在统计上并不显著。
{"title":"Mannose binding lectin deficiency and COVID-19 rates of thrombosis and mortality: Partial protection by immunodeficiency","authors":"Breanne Hayes, Brian P. Peppers","doi":"10.1177/1721727x231195205","DOIUrl":"https://doi.org/10.1177/1721727x231195205","url":null,"abstract":"Objective: The purpose of this study is to determine the effects of COVID-19 infection on individuals with mannose binding lectin deficiency. Methods: An electronic medical records search was conducted for MBL deficiency and COVID-19 positive tests from March 2020-August 2022. Individualized chart analysis was conducted and statistical analysis was performed. Results: Thirty-three people in WVU medicine health system carry a diagnosis of mannose binding lectin deficiency and were diagnosed with COVID-19. The mean age of this cohort was 41 years. Seven individuals had severe enough symptoms to lead to an emergency department visit. One person was hospitalized. MBL deficient individuals had 7 times the odds of hospitalization ( p = .1506, OR 7.06 (CI 1.117-44.52)) compared to the general public. There was zero mortality among the MBL deficient population. None of the patients reported thrombosis or blood clots. Conclusion: This retrospective cross-sectional analysis of those with known MBL deficiency and COVID-19 infection suggest a lower risk of fatalities and thrombotic events in this cohort. There was however a higher odds ratio of hospitalization compared to the general public, although this was not statistically significant.","PeriodicalId":55162,"journal":{"name":"European Journal of Inflammation","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48811790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Magnesium sulfate enhances lipopolysaccharide tolerance 硫酸镁增强脂多糖耐受性
IF 0.7 4区 医学 Q4 Medicine Pub Date : 2023-08-09 DOI: 10.1177/1721727x231195719
Ya-Ying Chang, Wei-Horng Jean, Cheng-Wei Lu, Tzu-Yu Lin
Lipopolysaccharide (LPS) tolerance is the downregulation of LPS signaling after pre-exposure to LPS, and it provides protection against hyperactive inflammation. Cytokine production decreases during LPS tolerance, and the phenotype of LPS-tolerant monocytes shifts toward M2 (anti-inflammatory) type. Magnesium sulfate (MgSO4) is a widely used anti-inflammatory agent. Although MgSO4 inhibits LPS signaling, the effect of MgSO4 on LPS tolerance is unknown. In the present study, we investigated the in vitro effects of MgSO4 on LPS tolerance. To induce LPS tolerance, THP-1 cells were stimulated with LPS (200 ng/mL, 2 h) after pre-exposure to LPS (200 ng/mL, 24 h) with or without pre-treatment of MgSO4 (20 mM, 24 h). Our results revealed that MgSO4 enhanced LPS tolerance by downregulating nuclear factor-κB (NF-κB)-induced tumor necrosis factor-α or interleukin-6, and upregulating cluster of differentiation 163 (a M2-associated marker). Furthermore, the LPS-triggered upregulation of phosphoinositide 3-kinase (PI3K) was significantly increased during LPS tolerance. MgSO4 activated PI3K, but inhibited NF-κB in LPS-stimulated cells. Notably, MgSO4 mitigated the signaling of both PI3K and NF-κB in LPS-tolerant cells, suggesting the effect of MgSO4 on LPS tolerance relies on the modulation of the crosstalk between PI3K and NF-κB. MgSO4 enhanced LSP tolerance, thus providing evidence for a novel underlying mechanism of the anti-inflammatory effects of MgSO4.
脂多糖(LPS)耐受是预先暴露于LPS后LPS信号的下调,它提供对过度活跃炎症的保护。细胞因子的产生在LPS耐受期间减少,并且LPS耐受的单核细胞的表型向M2(抗炎)型转变。硫酸镁(MgSO4)是一种广泛使用的抗炎剂。尽管MgSO4抑制LPS信号传导,但MgSO4对LPS耐受性的影响尚不清楚。在本研究中,我们研究了MgSO4对LPS耐受性的体外影响。为了诱导LPS耐受性,在预暴露于LPS(200 ng/mL,24小时)后,用LPS(200 mg/mL,2小时)刺激THP-1细胞,同时或不预处理MgSO4(20 mM,24 h)。我们的结果显示,MgSO4通过下调核因子-κB(NF-κB)诱导的肿瘤坏死因子-α或白细胞介素-6,并上调分化簇163(一种M2相关标志物)来增强LPS耐受性。此外,LPS诱导的磷酸肌醇3-激酶(PI3K)的上调在LPS耐受过程中显著增加。MgSO4激活LPS刺激的细胞中的PI3K,但抑制NF-κB。值得注意的是,MgSO4减轻了LPS耐受细胞中PI3K和NF-κB的信号传导,表明MgSO4对LPS耐受的影响依赖于PI3K与NF-κB之间串扰的调节。MgSO4增强了LSP耐受性,从而为MgSO4抗炎作用的新的潜在机制提供了证据。
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引用次数: 1
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European Journal of Inflammation
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