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[Exercise Load Classification and Perceptual Difference Awareness Training Based on Exercise Load Entropy Theory in University Students]. [基于运动负荷熵理论的大学生运动负荷分类与知觉差异意识训练]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160207
Xin Li, Peina Yang, Luyao Wang, Haijun Han, Peng Bai, Jian Li, Xue Xiao

Objective: Based on exercise load entropy measurement theory, this study aimed to investigate patterns of change in exercise load classification, perceptual difference awareness, and Weber fraction among university students across different exercise load levels, thereby providing theoretical support for personalized exercise load assessment.

Methods: From January to April 2025, 138 college students completed six incrementally increasing load tests on a cycle ergometer. Based on self-perceived load staging and perceptual discrimination, discrimination thresholds and Weber fractions were calculated for each load level. Data were analyzed using univariate analysis, correlation analysis, and multiple linear regression analysis.

Results: With increasing exercise load levels, differential perception showed an overall downward trend, but the difference was not statistically significant (P = 0.156). The Weber fraction decreased progressively with increasing load level, from 0.49 at load level 2 to 0.11 at load level 6 (P = 0.034). Multiple linear regression analysis indicated that for each one-level increase in exercise load, the Weber fraction decreased by an average of 0.07 (95% CI: -0.12 to -0.02, P = 0.009). In addition, males had a lower Weber fraction than females (95% CI: -0.12 to -0.06, P < 0.001).

Conclusion: Among college students, the perception of exercise load changes nonlinearly as the load level increases, and the Weber fraction decreases as the load intensifies.

目的:基于运动负荷熵测量理论,探讨不同运动负荷水平下大学生运动负荷分类、感知差异意识和韦伯分数的变化规律,为个性化运动负荷评估提供理论支持。方法:从2025年1月至4月,138名大学生在自行车测力仪上完成了6次增量负荷试验。基于自感知负荷分期和感知判别,计算各负荷水平的判别阈值和韦伯分数。数据分析采用单因素分析、相关分析和多元线性回归分析。结果:随着运动负荷水平的增加,差异知觉整体呈下降趋势,但差异无统计学意义(P = 0.156)。随着负荷水平的增加,韦伯分数逐渐降低,从负荷水平2的0.49降至负荷水平6的0.11 (P = 0.034)。多元线性回归分析表明,运动负荷每增加一个水平,韦伯分数平均下降0.07 (95% CI: -0.12 ~ -0.02, P = 0.009)。此外,男性的韦伯分数低于女性(95% CI: -0.12至-0.06,P < 0.001)。结论:大学生对运动负荷的感知随负荷水平的增加呈非线性变化,韦伯分数随负荷的增加而降低。
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引用次数: 0
[Mendelian Randomization Analysis of Potential Molecular Targets for Type 2 Airway Inflammatory Diseases]. [孟德尔随机化分析2型气道炎性疾病的潜在分子靶点]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160102
Zihan Jiang, Juan Meng, Shixi Liu

Objective: To systematically identify potential pathological molecular and therapeutic targets for type 2 airway inflammatory diseases using Mendelian randomization (MR) and co-localization analysis.

Methods: This study analyzed 4,302 druggable plasma proteins as exposure factors and performed transcriptional MR analysis using their cis-expression quantitative trait loci (cis-eQTL) as instrumental variables. Disease outcome datasets from the UK Biobank and Finnish Cohortwere used for discovery and replication validation, respectively. For proteins successfully validated, cis-protein quantitative trait loci (cis-pQTL) were further used for protein-level MR analysis. By combining co-localization analysis, reverse MR analysis, and mediation analysis, we investigated the association of these plasma proteins with allergic rhinitis (AR), asthma (AS), and nasal polyps (NP).

Results: cis-eQTL MR analysis of 2528 proteins identified 10 proteins associated with AR (TLR10, ERBB3, PNMT, etc.), 7 associated with AS (ERBB3, SLC40A1, PRKCQ, etc.), and 3 associated with NP (IL18RAP, AXL, ERBB3). cis-pQTL MR analysis showed that IL18RAP was associated with lower NP disease risk, while ERBB3 was associated with lower risks of AR, AS, and NP. Co-localization analysis supported the association between ERBB3 and AR (pp.H4 = 0.910). Mediation analysis revealed that the associations between ERBB3 and AR/AS were mediated by eosinophils, with mediation effects accounting for 12.51% and 17.64% of the observed associations, respectively.

Conclusion: This study identified unique and shared molecular targets for type 2 airway inflammatory diseases, with ERBB3 potentially serving as a shared protective factor and biomarker for AR, AS, and NP.

目的:利用孟德尔随机化(MR)和共定位分析系统地识别2型气道炎症性疾病的潜在病理分子和治疗靶点。方法:本研究分析了4302种可用药血浆蛋白作为暴露因子,并以其顺式表达数量性状位点(cis-eQTL)作为工具变量进行转录MR分析。分别使用来自UK Biobank和Finnish cohort的疾病结局数据集进行发现和复制验证。对于成功验证的蛋白,进一步使用顺式蛋白数量性状位点(cis-pQTL)进行蛋白水平MR分析。通过结合共定位分析、反向MR分析和中介分析,我们研究了这些血浆蛋白与变应性鼻炎(AR)、哮喘(AS)和鼻息肉(NP)的关系。结果:对2528个蛋白进行顺式eqtl MR分析,鉴定出10个与AR相关的蛋白(TLR10、ERBB3、PNMT等),7个与AS相关的蛋白(ERBB3、SLC40A1、PRKCQ等),3个与NP相关的蛋白(IL18RAP、AXL、ERBB3)。顺式pqtl MR分析显示,IL18RAP与较低的NP疾病风险相关,而ERBB3与AR、AS和NP的较低风险相关。共定位分析支持ERBB3与AR之间的关联(pp.H4 = 0.910)。中介分析显示,ERBB3与AR/AS之间的关联是由嗜酸性粒细胞介导的,其中介作用分别占观察到的关联的12.51%和17.64%。结论:本研究确定了2型气道炎症疾病的独特和共享的分子靶点,其中ERBB3可能作为AR, as和NP的共享保护因子和生物标志物。
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引用次数: 0
[Research Progress on Quorum Sensing-Regulated Oral Microbial Interaction Networks in Periodontitis]. 牙周炎群体感应调节口腔微生物相互作用网络的研究进展
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160206
Lu Li, Zitong Yu, Yan Xu

Quorum sensing (QS) is a mechanism by which bacteria communicate and coordinate group behaviors through the secretion of signaling molecules, playing a critical role in oral microbial interactions and the pathogenesis of periodontitis. This review summarizes recent advances in QS-mediated regulation of oral microbial interaction networks in periodontitis, focusing on the molecular mechanisms that modulate biofilm formation, virulence factor expression, and pathogen community dynamics. In addition, novel QS-targeted therapeutic strategies are discussed. Although periodontitis is fundamentally a chronic inflammatory disease driven by oral dysbiosis, the precise mechanisms by which microbes trigger and amplify inflammatory damage through the "community dynamics-host interaction-microenvironment" axis remain unclear. Therefore, exploring novel therapeutic strategies targeting the QS system offers potential targets and innovative approaches for the clinical treatment of periodontitis.

群体感应(Quorum sensing, QS)是细菌通过分泌信号分子进行沟通和协调群体行为的一种机制,在口腔微生物相互作用和牙周炎发病中起着重要作用。本文综述了qs介导的牙周炎口腔微生物相互作用网络调控的最新进展,重点介绍了调节生物膜形成、毒力因子表达和病原体群落动态的分子机制。此外,本文还讨论了新的qs靶向治疗策略。虽然牙周炎从根本上是一种由口腔生态失调引起的慢性炎症性疾病,但微生物通过“群落动力学-宿主相互作用-微环境”轴触发和放大炎症损伤的确切机制尚不清楚。因此,探索针对QS系统的新治疗策略为牙周炎的临床治疗提供了潜在的靶点和创新的途径。
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引用次数: 0
[Retrospect and Prospect of Immune Caries Prevention Research in China]. [中国免疫预防龋齿研究回顾与展望]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160204
Qingan Xu, Mingwen Fan

Dental caries is one of the most prevalent oral diseases, significantly affecting public oral health. Current preventive measures, such as oral hygiene practices, fluoride application, and pit and fissure sealants, have not substantially reduced the incidence of dental caries in China. Immunological research on caries prevention in China has a history of over forty years, with considerable achievements and experience, and shows promise for advancing biological caries prevention. This paper reviews immunological research on caries prevention in China from multiple perspectives, including active immunity, passive immunity, and the relationship between steady-state medicine and caries vaccines. It also discusses future development prospects, suggesting that novel adjuvants and carriers are essential for breakthroughs in caries vaccine research.

龋齿是最常见的口腔疾病之一,严重影响公众的口腔健康。目前的预防措施,如口腔卫生习惯、氟化物应用、牙窝和牙缝密封剂,并没有实质性地减少中国龋齿的发病率。中国对龋齿的免疫预防研究已有四十多年的历史,取得了相当大的成就和经验,有望推动龋齿的生物预防。本文从主动免疫、被动免疫、稳态医学与龋齿疫苗的关系等多个角度综述了国内预防龋齿的免疫学研究。本文还讨论了未来的发展前景,认为新型佐剂和载体对于龋疫苗研究的突破至关重要。
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引用次数: 0
[Research on Bacteriophage Resistance: Coevolutionary Arms Race Between Bacteria and Phages Drives Novel Antibacterial Therapies]. [噬菌体耐药性的研究:细菌和噬菌体之间的共同进化军备竞赛驱动新的抗菌疗法]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160205
Rou Li, Fang Wan, Jixia Wei, Yajin Wen, Panhong Jia, Ping Lin, Lin Liu, Min Wu

The growing threat of antimicrobial resistance requires the urgent development of new therapeutic strategies and agents. Bacteriophage therapy offers a promising alternative, utilizing phages' ability to specifically recognize and lyse bacterial cells. The ubiquity of bacteriophages subjects bacteria to constant evolutionary pressure, driving the emergence of diverse systems that defend against phage infection. The repertoire of phage defense genes includes a wide range of functions, such as nucleases, helicases, and ATPases. Host-phage interactions are complex and multifaceted. Bacterial defense mechanisms operate at various levels: initial innate defenses that inhibit phage adsorption, block nucleic acid injection, and interfere with virion assembly; early vesicle rupture targeting phage nucleic acids; systems that specifically target phage DNA and RNA; and abortive infection, which results in the degradation of bacterial nucleic acids, depletion of NAD+, and changes in cell membrane integrity. Notably, abortive infection prevents phage propagation, though at the cost of bacterial cell death. Although many defense systems have been predicted and identified through bioinformatics, the precise molecular mechanisms and detailed pathways of most systems remain poorly understood. Future research should focus on clarifying the exact molecular mechanisms, regulatory networks, distribution patterns, and roles in bacterial fitness for both newly discovered and established defense systems. Such insights are essential for developing innovative strategies to combat bacterial infections. This review examines the core mechanisms and application potential of bacterial antiphage defense. It systematically summarizes four key aspects of the bacterial antiphage defense system: early infection defense, phage nucleic acid-targeted defense, abortive infection defense, and transferable defense strategies. It also highlights current bottlenecks in the field, such as unclear defense mechanisms, insufficient clinical transformation technologies, and risks associated with the transferability of defense systems. Corresponding countermeasures and suggestions are proposed, including in-depth mechanistic research, construction of defense profiles for pathogenic bacteria, and development of engineered phages and synergistic therapies, to provide references for optimizing phage therapy and innovating bacterial infection treatment, thereby offering new perspectives for treating bacterial infections.

抗菌素耐药性的威胁日益严重,迫切需要开发新的治疗策略和药物。噬菌体疗法提供了一个很有前途的选择,利用噬菌体特异性识别和裂解细菌细胞的能力。无处不在的噬菌体使细菌承受着持续的进化压力,推动了各种防御噬菌体感染的系统的出现。噬菌体防御基因包括多种功能,如核酸酶、解旋酶和三磷酸腺苷酶。宿主-噬菌体相互作用是复杂和多方面的。细菌的防御机制在不同的水平上运作:最初的先天防御抑制噬菌体吸附,阻断核酸注射,干扰病毒粒子组装;靶向噬菌体核酸的早期囊泡破裂;专门针对噬菌体DNA和RNA的系统;流产感染,导致细菌核酸降解,NAD+耗竭,细胞膜完整性改变。值得注意的是,流产感染阻止了噬菌体的繁殖,尽管代价是细菌细胞死亡。虽然许多防御系统已经通过生物信息学预测和识别,但大多数系统的精确分子机制和详细途径仍然知之甚少。未来的研究应该集中在阐明确切的分子机制、调节网络、分布模式以及新发现和建立的防御系统在细菌适应性中的作用。这些见解对于开发对抗细菌感染的创新策略至关重要。本文就细菌抗噬菌体防御的核心机制及应用前景作一综述。系统总结了细菌抗噬菌体防御系统的四个关键方面:早期感染防御、噬菌体核酸靶向防御、流产感染防御和可转移防御策略。它还突出了该领域当前的瓶颈,例如防御机制不明确、临床转化技术不足以及与防御系统可转移性相关的风险。提出相应的对策和建议,包括深入机制研究、构建病原菌防御谱、开发工程噬菌体和协同疗法等,为优化噬菌体治疗和创新细菌感染治疗提供参考,从而为治疗细菌感染提供新的视角。
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引用次数: 0
[Recent Research Progress and Prospects on Periodontitis Affecting Systemic Comorbidities via the Oral-Gut Axis]. 牙周炎经口肠轴影响全身合并症的研究进展与展望
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160302
Shuwei Zhang, Yuchao Li, Ze Yang, Haifeng Huang, Yaping Pan

Periodontitis is a prevalent chronic infectious and inflammatory disease worldwide, which imposes harms extending far beyond the oral cavity. A large body of research has demonstrated that periodontitis is closely associated with various systemic diseases, such as diabetes mellitus, cardiovascular diseases, inflammatory bowel disease, and rheumatoid arthritis. Serving as a crucial pathway connecting the oral cavity to the entire body, the oral-gut axis becomes the core mechanism through which periodontitis affects systemic health, primarily via the ectopic colonization of salivary microbiota, intestinal dysbiosis, intestinal barrier disruption, and systemic inflammation. This review summarizes recent studies focusing on how periodontitis influences systemic comorbidities via the oral-gut axis, encompassing clinical studies, animal experimental and in vitro research. We summarize the research progress regarding how periodontitis perturbs intestinal homeostasis through ectopic colonization of oral pathogenic bacteria, immunoinflammation, host factor regulation, and metabolic disorders, and eventually affects systemic diseases via the oral-gut axis. This review aims to provide a new perspective for the prevention and treatment of periodontitis-related systemic comorbidities.

牙周炎是一种在世界范围内普遍存在的慢性感染性和炎症性疾病,其危害远远超出口腔。大量研究表明,牙周炎与多种全身性疾病密切相关,如糖尿病、心血管疾病、炎症性肠病和类风湿关节炎。作为连接口腔和整个身体的重要途径,口腔-肠道轴成为牙周炎影响全身健康的核心机制,主要通过唾液微生物群的异位定植、肠道生态失调、肠道屏障破坏和全身炎症。本文综述了牙周炎如何通过口腔-肠道轴影响全身合并症的最新研究,包括临床研究、动物实验和体外研究。本文综述了牙周炎如何通过口腔病原菌的异位定植、免疫炎症、宿主因子调节和代谢紊乱等途径扰乱肠道稳态,并最终通过口腔-肠道轴影响全身性疾病的研究进展。本文旨在为牙周炎相关的全身合并症的预防和治疗提供新的视角。
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引用次数: 0
[Research on the Construction of Aesthetic Education in Medical Universities Under the Background of New Medicine]. 新医学背景下医学院校美育建设研究
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160303
Yun Li, Linwei Yang, Xinhao Liu

In response to the demand for cultivating interdisciplinary medical talent under the "New Medical Science" initiative and to address challenges such as the marginalization of aesthetic education and its inadequate integration with specialized training in medical universities, this study aims to develop a systematic framework for implementing aesthetic education. Grounded in policy directives and theoretical analysis, this research proposes a tripartite aesthetic education model centered on "Life Aesthetics - Medical Humanities - Practical Innovation." This model is fundamentally guided by the spirit of Chinese aesthetic education, seeking to integrate the life aesthetics of "the beauty of vitality" with the medical ethical traditions of "benevolent heart and art" and "great virtue and sincerity," thereby enhancing its cultural identity and practical applicability. Through four practical pathways - curriculum restructuring, pedagogical innovation, cultural immersion, and institutional coordination - aesthetic education is integrated throughout the entire process of medical professional education. The goal is to foster the synergistic development of medical students' aesthetic cognition, humanistic sensibility, and innovative capabilities, ultimately providing a theoretical and practical framework for cultivating a new generation of medical professionals who are clinically competent, ethically grounded, culturally confident, and innovative.

针对“新医学”建设对培养复合型医学人才的需求,以及医院校美育边缘化、与专业培养结合不足等问题,本研究旨在构建美育实施的系统框架。本研究以政策导向与理论分析为基础,提出以“生命美学-医学人文-实践创新”为核心的三位一体的美育模式。该模式从根本上以中国美育精神为指导,力求将“生机之美”的生命美学与“仁心仁术”、“大德诚”的医学伦理传统相结合,从而增强其文化认同和实用性。通过课程重组、教学创新、文化渗透和制度协调四个实践路径,将美育贯穿于医学专业教育的全过程。培养医学生的审美认知、人文情感和创新能力协同发展,为培养临床胜任、道德有基础、文化自信、创新能力强的新一代医学专业人才提供理论和实践框架。
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引用次数: 0
[Association Between Obesity and Dyslipidemia Among Adults in Three Counties (Cities) of Sichuan Province]. [四川省三县(市)成人肥胖与血脂异常的关系]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160208
Lihua Jiang, Ying Chen, Xinmao Xu, Li Zhao

Objective: To investigate the association between obesity and dyslipidemia among adult residents in three counties (cities) of Sichuan Province, and to reveal the potential non-linear dose-response relationship between body mass index (BMI) and waist circumference (WC) and the risk of dyslipidemia, providing an empirical basis for developing precise weight management strategies.

Methods: This study was conducted in Dujiangyan City, Pujiang County, and Jiange County of Sichuan Province. A multi-stage cluster random sampling method was used to select communities (townships), households, and participants within each county (city). The survey was conducted in 2023 and included 11561 permanent residents aged ≥18 years. A binary logistic regression model was used to analyze the association between different types of obesity and dyslipidemia. A restricted cubic spline (RCS) model was employed to explore the dose-response relationship between BMI, WC, and dyslipidemia, with the model's goodness of fit assessed by the AIC value.

Results: Among the study subjects, the prevalence of dyslipidemia was 29.07%, overweight was 33.50%, obesity was 11.95%, and abdominal obesity was 29.79%. Logistic regression analysis showed that, after adjusting for confounding factors, both obesity (odds ratio [OR] = 1.22, 95% CI: 1.05-1.42) and abdominal obesity (OR = 1.23, 95% CI: 1.11-1.36) were positively associated with dyslipidemia compared to individuals with normal weight. After stratification by gender, the association between abdominal obesity and dyslipidemia was more significant in females (OR = 1.36, 95% CI: 1.18-1.57). The RCS model further revealed that the relationship between BMI and dyslipidemia followed a J-shaped curve, with an inflection point at a BMI of 24.87 kg/m². The relationship between WC and dyslipidemia showed an S-shaped curve, with an inflection point at a WC of 86 cm. This indicates that the strength of the association changes non-linearly as the values of these indicators increase.

Conclusion: Among adult residents of three counties (or cities) in Sichuan Province, obesity and abdominal obesity are independently associated with dyslipidemia, and the association exhibits non-linearity and female specificity. Weight management strategies should focus on individuals with general and abdominal obesity, particularly females with abdominal obesity. The risk inflection points for BMI and WC should be used as key indicators for early intervention.

目的:了解四川省3个县(市)成年居民肥胖与血脂异常的关系,揭示体重指数(BMI)、腰围(WC)与血脂异常风险之间潜在的非线性剂量-反应关系,为制定精准的体重管理策略提供经验依据。方法:本研究在四川省都江堰市、浦江县和江歌县进行。采用多阶段整群随机抽样的方法,在各县(市)内抽取社区(乡)、住户和参与者。该调查于2023年进行,包括11561名年龄≥18岁的常住居民。采用二元logistic回归模型分析不同类型肥胖与血脂异常之间的关系。采用限制性三次样条(restricted cubic spline, RCS)模型探讨BMI、WC与血脂异常之间的剂量-反应关系,以AIC值评价模型的拟合优度。结果:研究对象中,血脂异常患病率为29.07%,超重患病率为33.50%,肥胖患病率为11.95%,腹部肥胖患病率为29.79%。Logistic回归分析显示,在校正混杂因素后,与体重正常的个体相比,肥胖(比值比[OR] = 1.22, 95% CI: 1.05-1.42)和腹部肥胖(OR = 1.23, 95% CI: 1.11-1.36)与血脂异常呈正相关。按性别分层后,腹部肥胖和血脂异常之间的关联在女性中更为显著(OR = 1.36, 95% CI: 1.18-1.57)。RCS模型进一步揭示BMI与血脂异常之间的关系呈j型曲线,在BMI为24.87 kg/m²时出现拐点。腰围与血脂异常呈s型曲线关系,腰围在86 cm处出现拐点。这表明,随着这些指标值的增加,关联强度呈非线性变化。结论:在四川省3个县(市)的成年居民中,肥胖和腹部肥胖与血脂异常独立相关,且这种关联具有非线性和女性特异性。体重管理策略应侧重于一般肥胖和腹部肥胖的个体,特别是腹部肥胖的女性。BMI和WC的风险拐点应作为早期干预的关键指标。
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引用次数: 0
[Efficacy of Norvancomycin in the Treatment of Acute Hematogenous Osteomyelitis in Children and Its Effect on Inflammatory Indicators]. [去甲万古霉素治疗小儿急性血液性骨髓炎疗效及对炎症指标的影响]。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160604
Xueqin Zhang, Nan Zhang, Yuntao Pei, Yile Zhao
<p><strong>Objective: </strong>To evaluate the clinical efficacy of norvancomycin in pediatric patients with infection-related acute hematogenous osteomyelitis (AHO) and its impact on inflammatory markers.</p><p><strong>Methods: </strong>This study retrospectively analyzed children with infection-related AHO admitted to Hebei Children's Hospital from January 2016 to December 2024. Patients were divided into the vancomycin group (Group A, <i>n</i> = 103) and the norvancomycin group (Group B, <i>n</i> = 107) based on medication regimens. Baseline characteristics, including age, gender, weight, and lesion location, were adjusted for confounding factors using propensity score matching and multivariate regression analysis. Clinical efficacy and changes in inflammatory markers were compared between groups, including white blood cell (WBC) count, neutrophil (NE) count, C-reactive protein (CRP), and serum amyloid A (SAA) levels.</p><p><strong>Results: </strong>There was no statistically significant difference in clinical cure rates between the two groups (<i>P</i> > 0.05). At 1 and 3 weeks post-treatment, CRP and SAA levels showed statistically significant time effects (<i>F</i> <sub>time-point</sub> = 503.00 and 703.400, respectively, <i>P</i> < 0.05). Both WBC and NE levels showed statistically significant time effects and between-group effects (<i>F</i> <sub>time-point</sub> = 259.100 and 203.500, respectively; <i>F</i> <sub>between-group</sub> = 8.403 and 6.884, respectively; <i>P</i> < 0.05), WBC, NE, CRP, and SAA levels gradually declined at both 1 week and 3 weeks post-treatment (<i>P</i> < 0.05). Group A had higher WBC levels than Group B at 1 week post-treatment (<i>P</i> < 0.05) and higher NE levels at 3 weeks post-treatment (<i>P</i> < 0.05). The time required for WBC and NE to return to normal levels was longer in Group A than in Group B (<i>t</i> = 2.051, 2.001, <i>P</i> < 0.05), while the difference in recovery time for CRP and SAA between the two groups was not statistically significant (<i>P</i> > 0.05). Group A had a longer duration of fever resolution than Group B (<i>t</i> = 2.010, <i>P</i> < 0.05). No statistically significant intergroup difference was observed in the time to resolution of clinical symptoms such as pain and swelling (<i>P</i> > 0.05). The overall incidence of adverse reactions was 14.56% in Group A and 7.48% in Group B, with no statistically significant intergroup difference (<i>P</i> > 0.05). The per-patient treatment cost and cost-effectiveness ratio were higher in Group A than in Group B (<i>t</i> = 14.385, <i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>Norexvancomycin achieved clinical cure rates comparable to those of vancomycin in treating infection-associated AHO. Furthermore, it demonstrated advantages in accelerating the recovery of WBC and NE counts and the resolution of fever. These clinical benefits were coupled with lower per-patient costs and more favorable cost-effectiveness ratios compared to van
目的:评价去甲万古霉素治疗小儿感染相关性急性血流变性骨髓炎的临床疗效及对炎症指标的影响。方法:回顾性分析2016年1月至2024年12月河北省儿童医院收治的感染相关who患儿。根据用药方案将患者分为万古霉素组(A组,n = 103)和去甲万古霉素组(B组,n = 107)。基线特征,包括年龄、性别、体重和病变位置,使用倾向评分匹配和多变量回归分析来调整混杂因素。比较两组患者的临床疗效及炎症标志物的变化,包括白细胞(WBC)计数、中性粒细胞(NE)计数、c反应蛋白(CRP)、血清淀粉样蛋白A (SAA)水平。结果:两组患者临床治愈率比较,差异无统计学意义(P < 0.05)。治疗后1周和3周,CRP和SAA水平的时间效应有统计学意义(F时间点分别为503.00和703.400,P < 0.05)。WBC、NE水平的时间效应和组间效应均有统计学意义(F时间点分别为259.100、203.500;F组间值分别为8.403、6.884,P < 0.05), WBC、NE、CRP、SAA水平在治疗后1周、3周逐渐下降(P < 0.05)。治疗后1周,A组WBC水平高于B组(P < 0.05),治疗后3周,NE水平高于B组(P < 0.05)。A组WBC、NE恢复正常所需时间较B组长(t = 2.051、2.001,P < 0.05), CRP、SAA恢复时间两组比较差异无统计学意义(P < 0.05)。A组发热消退时间较B组长(t = 2.010, P < 0.05)。两组间疼痛、肿胀等临床症状缓解时间差异无统计学意义(P < 0.05)。A组总不良反应发生率为14.56%,B组总不良反应发生率为7.48%,组间差异无统计学意义(P < 0.05)。A组患者人均治疗费用和成本-效果比高于B组(t = 14.385, P < 0.05)。结论:去甲万古霉素治疗感染相关性who的临床治愈率与万古霉素相当。此外,它在加速WBC和NE计数的恢复以及发烧的解决方面显示出优势。与万古霉素相比,这些临床益处与较低的每位患者成本和更有利的成本-效果比相结合。
{"title":"[Efficacy of Norvancomycin in the Treatment of Acute Hematogenous Osteomyelitis in Children and Its Effect on Inflammatory Indicators].","authors":"Xueqin Zhang, Nan Zhang, Yuntao Pei, Yile Zhao","doi":"10.12182/20260160604","DOIUrl":"10.12182/20260160604","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To evaluate the clinical efficacy of norvancomycin in pediatric patients with infection-related acute hematogenous osteomyelitis (AHO) and its impact on inflammatory markers.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;This study retrospectively analyzed children with infection-related AHO admitted to Hebei Children's Hospital from January 2016 to December 2024. Patients were divided into the vancomycin group (Group A, &lt;i&gt;n&lt;/i&gt; = 103) and the norvancomycin group (Group B, &lt;i&gt;n&lt;/i&gt; = 107) based on medication regimens. Baseline characteristics, including age, gender, weight, and lesion location, were adjusted for confounding factors using propensity score matching and multivariate regression analysis. Clinical efficacy and changes in inflammatory markers were compared between groups, including white blood cell (WBC) count, neutrophil (NE) count, C-reactive protein (CRP), and serum amyloid A (SAA) levels.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;There was no statistically significant difference in clinical cure rates between the two groups (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). At 1 and 3 weeks post-treatment, CRP and SAA levels showed statistically significant time effects (&lt;i&gt;F&lt;/i&gt; &lt;sub&gt;time-point&lt;/sub&gt; = 503.00 and 703.400, respectively, &lt;i&gt;P&lt;/i&gt; &lt; 0.05). Both WBC and NE levels showed statistically significant time effects and between-group effects (&lt;i&gt;F&lt;/i&gt; &lt;sub&gt;time-point&lt;/sub&gt; = 259.100 and 203.500, respectively; &lt;i&gt;F&lt;/i&gt; &lt;sub&gt;between-group&lt;/sub&gt; = 8.403 and 6.884, respectively; &lt;i&gt;P&lt;/i&gt; &lt; 0.05), WBC, NE, CRP, and SAA levels gradually declined at both 1 week and 3 weeks post-treatment (&lt;i&gt;P&lt;/i&gt; &lt; 0.05). Group A had higher WBC levels than Group B at 1 week post-treatment (&lt;i&gt;P&lt;/i&gt; &lt; 0.05) and higher NE levels at 3 weeks post-treatment (&lt;i&gt;P&lt;/i&gt; &lt; 0.05). The time required for WBC and NE to return to normal levels was longer in Group A than in Group B (&lt;i&gt;t&lt;/i&gt; = 2.051, 2.001, &lt;i&gt;P&lt;/i&gt; &lt; 0.05), while the difference in recovery time for CRP and SAA between the two groups was not statistically significant (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). Group A had a longer duration of fever resolution than Group B (&lt;i&gt;t&lt;/i&gt; = 2.010, &lt;i&gt;P&lt;/i&gt; &lt; 0.05). No statistically significant intergroup difference was observed in the time to resolution of clinical symptoms such as pain and swelling (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). The overall incidence of adverse reactions was 14.56% in Group A and 7.48% in Group B, with no statistically significant intergroup difference (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). The per-patient treatment cost and cost-effectiveness ratio were higher in Group A than in Group B (&lt;i&gt;t&lt;/i&gt; = 14.385, &lt;i&gt;P&lt;/i&gt; &lt; 0.05).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Norexvancomycin achieved clinical cure rates comparable to those of vancomycin in treating infection-associated AHO. Furthermore, it demonstrated advantages in accelerating the recovery of WBC and NE counts and the resolution of fever. These clinical benefits were coupled with lower per-patient costs and more favorable cost-effectiveness ratios compared to van","PeriodicalId":39321,"journal":{"name":"四川大学学报(医学版)","volume":"57 1","pages":"230-235"},"PeriodicalIF":0.0,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12980010/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147463966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Aging-Associated Oral Microbiota Dysbiosis and Hypofunction: Their Role in Alzheimer's Disease Pathogenesis]. 衰老相关的口腔微生物群失调和功能减退:它们在阿尔茨海默病发病机制中的作用。
Q3 Medicine Pub Date : 2026-01-20 DOI: 10.12182/20260160510
Yazhuo Li, Yuqing Chen, Shuai Chen, Xiaojing Huang

Alzheimer's disease (AD), a multifactorial neurodegenerative condition, imposes a major burden on societies with aging populations. Recent research indicates that oral cavity health is a critical factor influencing AD pathology, making proactive investigation of this modifiable risk factor essential. This review proposes that aging-related oral microecological dysbiosis and oral hypofunction may promote AD progression by inducing or exacerbating systemic inflammation and disrupting the homeostasis of the "oral-gut-brain" axis. Moreover, each factor may worsen damage through distinct biological pathways: oral microbiota dysbiosis allows direct invasion of the central nervous system by oral pathogens, promoting amyloid β-protein (Aβ) deposition and Tau hyperphosphorylation, while chronic sensory deprivation from oral dysfunction triggers neuronal degeneration and adverse remodeling in key cognitive brain regions. This review aims to systematically elucidate the roles of oral microbiota dysbiosis and oral hypofunction in AD pathogenesis in the context of aging, clarify their underlying biological mechanisms, and explore the potential value of integrating oral cavity health management into comprehensive AD prevention and treatment strategies.

阿尔茨海默病(AD)是一种多因素神经退行性疾病,对人口老龄化的社会造成了重大负担。最近的研究表明,口腔健康是影响AD病理的关键因素,因此主动调查这一可改变的危险因素至关重要。这篇综述提出,与年龄相关的口腔微生态失调和口腔功能减退可能通过诱导或加剧全身炎症和破坏“口腔-肠-脑”轴的稳态来促进AD的进展。此外,每种因素都可能通过不同的生物学途径加重损伤:口腔微生物群失调允许口腔病原体直接侵入中枢神经系统,促进淀粉样β蛋白(Aβ)沉积和Tau蛋白过度磷酸化,而口腔功能障碍引起的慢性感觉剥夺会引发关键认知脑区域的神经元变性和不良重塑。本文旨在系统阐述衰老背景下口腔菌群失调和口腔功能减退在AD发病中的作用,阐明其潜在的生物学机制,探讨将口腔健康管理纳入AD综合防治策略的潜在价值。
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引用次数: 0
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四川大学学报(医学版)
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