red blood cell (RBC)

  • 文章类型: Journal Article
    良性前列腺增生(BPH)影响全球30%的男性,叶酸是生命所必需的。然而,很少有研究调查叶酸水平与BPH之间的关系。本研究旨在探讨红细胞(RBC)叶酸、长期叶酸摄入量的更好指标,和BPH在美国(美国)男性。
    我们使用了“国家健康和营养调查”(NHANES2001-2008)的四个周期的统计数据,RBC叶酸数据来自实验室数据,BPH数据来自问卷数据。使用多因素条件逻辑回归模型和亚组分析来评估红细胞叶酸和BPH之间的关联。
    在NHANES2001-2008年的四个调查周期中,647名男性,574名男性(88.7%)患有BPH。在调整了潜在的混杂因素后,在红细胞叶酸和BPH之间观察到相当大的相关性;以红细胞叶酸的前五分之一为参考,秒的多变量调整后的优势比(OR)和置信区间(95%CI),第三,第四,最高的五分位数为1.19(0.58~2.44),1.39(0.65~2.97),2.27(0.96~5.39),2.26(1.35~3.76)和5.37(1.85~15.59),分别。
    红细胞叶酸水平高的个体与美国男性自我报告的良性前列腺增生的风险增加相关。
    UNASSIGNED: Benign prostatic hyperplasia (BPH) affects 30% of men worldwide, folate is essential for life. However, few studies have investigated the relationship between folate levels and BPH. The present study aims to explore the relationship between red blood cell (RBC) folate, a better indicator of long-term folate intake, and BPH in United States (US) men.
    UNASSIGNED: We used statistics from four cycles of the \"National Health and Nutrition Examination Survey\" (NHANES2001-2008), RBC folate data come from laboratory data and BPH date come from questionnaire data. A multivariate conditional logistic regression model and subgroup analysis were using to assess the association between RBC folate and BPH.
    UNASSIGNED: 647 males from four survey cycles in the NHANES2001-2008, of which, 574 men (88.7%) had BPH. After adjusting for potential confounders, a considerable correlation was observed between RBC folate and BPH; With the first quintiles of RBC folate as the reference, multivariable-adjusted odds ratios (ORs) and confidence intervals (95% CIs) of the second, third, fourth, and the highest quintiles were 1.19 (0.58 ∼ 2.44), 1.39 (0.65 ∼ 2.97), 2.27 (0.96 ∼ 5.39), 2.26 (1.35 ∼ 3.76) and 5.37 (1.85 ∼ 15.59), respectively.
    UNASSIGNED: Individuals with high levels of RBC folate were associated with an increased risk of self-reported benign prostatic hyperplasia of US men.
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  • 文章类型: Journal Article
    由于癌症的高发病率和高死亡率,癌症已成为越来越重要的公共卫生问题。虽然传统的治疗方法相对有效,它们有局限性,例如高毒副作用,容易耐药,和高度的个体差异。同时,新兴疗法仍然有限,它们的实际抗肿瘤作用有待提高。纳米技术的发展和应用受到了广泛的关注。特别是,人造纳米载体已成为肿瘤治疗的重要方法。然而,某些缺陷仍然存在,包括免疫原性,渗透性,瞄准,和生物相容性。红细胞衍生材料的应用将有助于克服上述问题并提高治疗效果。通过应用物理和化学技术可以从天然红细胞膜中获得红细胞来源的材料,或通过使用细胞膜仿生技术将这些膜与合成内核材料整合。它们的天然特性,如生物相容性和长循环时间,使其成为药物输送或纳米颗粒生物涂层的理想选择。因此,红细胞衍生材料广泛应用于生物医学领域。然而,需要进一步的研究来评估它们的疗效,体内代谢,准备,设计,和临床翻译。根据最新的研究报告,这篇综述总结了生物学,合成,特点,和红细胞衍生物质的分布。此外,我们通过全面讨论红细胞衍生材料在恶性肿瘤治疗中的应用和面临的技术挑战,为进一步研究和临床转化提供参考。
    Cancer has become an increasingly important public health issue owing to its high morbidity and mortality rates. Although traditional treatment methods are relatively effective, they have limitations such as highly toxic side effects, easy drug resistance, and high individual variability. Meanwhile, emerging therapies remain limited, and their actual anti-tumor effects need to be improved. Nanotechnology has received considerable attention for its development and application. In particular, artificial nanocarriers have emerged as a crucial approach for tumor therapy. However, certain deficiencies persist, including immunogenicity, permeability, targeting, and biocompatibility. The application of erythrocyte-derived materials will help overcome the above problems and enhance therapeutic effects. Erythrocyte-derived materials can be acquired via the application of physical and chemical techniques from natural erythrocyte membranes, or through the integration of these membranes with synthetic inner core materials using cell membrane biomimetic technology. Their natural properties such as biocompatibility and long circulation time make them an ideal choice for drug delivery or nanoparticle biocoating. Thus, red blood cell-derived materials are widely used in the field of biomedicine. However, further studies are required to evaluate their efficacy, in vivo metabolism, preparation, design, and clinical translation. Based on the latest research reports, this review summarizes the biology, synthesis, characteristics, and distribution of red blood cell-derived materials. Furthermore, we provide a reference for further research and clinical transformation by comprehensively discussing the applications and technical challenges faced by red blood cell-derived materials in the treatment of malignant tumors.
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  • 文章类型: Journal Article
    Hematuria is the most typical presentation of immunoglobulin A nephropathy (IgAN); however, its role in disease progression is still controversial. This study aimed to evaluate the association of hematuria and progression of IgAN.
    Retrospective cohort study.
    A cohort of 1,333 patients with IgAN treated at a Chinese referral hospital with a median follow-up of 45 months.
    Microhematuria was evaluated in fresh urine using a fully automated urine particle analyzer (automated method) and urine sediment examination by a skilled examiner (manual method). Hematuria was characterized as a time-varying attribute; namely, average hematuria level was calculated for every 6-month period for each patient during follow-up. Remission was defined as average red blood cell count ≤5/high-power field (manual method) or ≤28 red blood cells/μL (automated method) during the first 6 months of follow-up.
    Composite event of 50% decline in estimated glomerular filtration rate or development of kidney failure.
    Multivariable cause-specific hazards models to analyze the relationship between hematuria and the composite kidney disease progression event.
    Time-varying hematuria during follow-up was an independent risk factor for the composite kidney disease progression event (HR, 1.46; 95% CI, 1.13-1.87; P = 0.003). Hematuria remission during the 6 months after diagnosis was associated with a significantly lower rate of the composite kidney disease progression event (HR, 0.41; 95% CI, 0.28-0.61; P < 0.001). A significant interaction was detected between remission of proteinuria and remission of hematuria during the first 6 months (P < 0.001). The association between remission of hematuria and kidney disease progression was detectable (HR, 0.46; 95% CI, 0.32-0.68) within the subpopulation with persistent proteinuria (protein excretion > 1.0 g/d during the first 6 months), but not among patients whose proteinuria had remitted (HR, 0.64; 95% CI, 0.31-1.29; P = 0.2). The 2 techniques for hematuria evaluation were strongly and significantly linearly correlated (r = 0.948; P < 0.001), and results using these 2 methods were consistent.
    A single-center retrospective study. Proportional hazards regression incorporating time-varying covariates may create time-varying confounding. The predictive value of reductions in hematuria was not directly evaluated.
    Level of hematuria was independently associated with kidney disease progression, whereas hematuria remission was associated with improved kidney outcomes in IgAN among patients with persistent proteinuria. Additionally, to monitor IgAN progression, automated methods to evaluate hematuria hold promise as a replacement for manual evaluation of urinary sediment.
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  • 文章类型: Journal Article
    Cognitive impairment can occur after aneurysmal subarachnoid hemorrhage (aSAH) though it commonly tends to be neglected. Red blood cell (RBC) indices are associated with long-term functional outcomes, while it is unclear whether RBC indices could be a potential predictor of cognitive decline after aSAH. We aimed to investigate the association between RBC indices and post-aSAH cognitive impairment at 1 year.
    Patients with aSAH received neuropsychological test by the Montreal Cognitive Assessment (MoCA) and underwent serum and cerebrospinal fluid (CSF) samples test. To determine the association between RBC indices and cognitive impairment after acute aSAH, we adjusted for demographic and vascular risk factors using multivariate logistic regression analysis.
    Of the 126 patients included in this study, 33% (42/126) of them were diagnosed with cognitive impairment (MoCA<26). After adjustment for potential confounders, increased mean corpuscular volume (MCV) (OR: 1.36, 95%CI: 1.19-1.55) and mean corpuscular hemoglobin (MCH) (OR: 1.61, 95%CI: 1.25-2.08), reflecting systemic iron status, are more likely to be associated with cognitive impairment after aSAH.
    In this aSAH population, our data shows the positive association between MCH and MCV and cognitive impairment at 1 year.
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  • 文章类型: Journal Article
    目的:在本研究中,我们旨在测量全髋关节置换手术后红细胞(RBC)免疫和细胞因子水平的变化.
    方法:通过测量术前和术后RBC自然肿瘤红细胞花环率(NTERR),对20例接受全髋关节置换术的患者进行了调查。红细胞C3b受体花环率(RC3bRR),红细胞膜CD35、CD58和CD59表达及细胞因子水平[包括肿瘤坏死因子α(TNF-α),白细胞介素2(IL-2),干扰素γ(IFN-γ),白细胞介素10(IL-10)和前列腺素E2(PGE2)]。在手术前一天和髋关节置换术后的第一天收集血液样品。
    结果:术后NTERR和RC3bRR明显低于术前水平(p<0.05)。术后RBC膜CD35、CD58和CD59的表达较术前水平明显降低。重要的是,RBC促淋巴细胞增殖率术后显著降低。此外,术后TNF-α,红细胞和淋巴细胞培养液中IL-2和IFN-γ水平低于术前,而IL-10和PGE2与术前水平相比显着增加(p<0.05)。
    结论:红细胞免疫功能的改变可能参与髋关节置换术后感染的发生和发展。这表明了一种预防这种感染的新策略。
    OBJECTIVE: In this study, we aimed to measure changes in red blood cell (RBC) immunity and cytokine levels after performing total hip replacement surgery.
    METHODS: Twenty patients receiving total hip arthroplasty were investigated by measuring presurgical and postoperative RBC natural tumor erythrocyte rosette rate (NTERR), RBC C3b receptor rosette rate (RC3bRR), RBC membrane CD35, CD58 and CD59 expression and cytokine levels [including tumor necrosis factor α (TNF-α), interleukin 2 (IL-2), interferon γ (IFN-γ), interleukin 10 (IL-10) and prostaglandin E2 (PGE2)]. Blood samples were collected on the day before surgery and on the first day after hip arthroplasty.
    RESULTS: Postoperative NTERR and RC3bRR were significantly lower than presurgical levels (p < 0.05). The RBC membrane CD35, CD58 and CD59 expressions were significantly decreased in the postoperative phase compared to pre-operative levels. Importantly, RBC promoting lymphocyte proliferation rates were significantly reduced after surgery. In addition, postoperative TNF-α, IL-2 and IFN-γ levels in RBC and lymphocyte culture fluid were lower than those pre-operation, whereas IL-10 and PGE2 were significantly increased compared to presurgical levels (p < 0.05).
    CONCLUSIONS: The modification of RBC immune function may be involved in the occurrence and development of the infection following hip arthroplasty, and this suggests a novel strategy to prevent such infection.
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