首页 > 最新文献

BioMed Research International最新文献

英文 中文
Effect of Beetroot Extract Supplementation on Serum Fatty Acid Profiles and Oxidative Stress Markers in Chronic Coronary Artery Disease Patients: A Secondary Analysis of a Randomized Controlled Trial. 补充甜菜根提取物对慢性冠状动脉疾病患者血清脂肪酸谱和氧化应激标志物的影响:一项随机对照试验的二次分析
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-29 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/6654492
Amirhossein Mansouri-Baseri, Mohsen Moohebati, Leila Sadat Bahrami, Hamed Tabesh, Mitra Rezaie, Mohsen Nematy, Fatemeh Davoudi, Reza Rezvani

Background: Considering the role of a healthy diet in preventing atherogenesis, the use of beetroot as a functional food with anti-inflammatory, antioxidant, and anti-dyslipidemic effects due to its high nitrate content and bioactive compounds is one of the interesting approaches in coronary artery disease (CAD), a common worldwide chronic disease.

Methods: This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial that was conducted on 90 male (67.8%) and female (32.2%) chronic patients with CAD for 4 weeks. This secondary analysis investigated the effect of beetroot capsules within three groups on fatty acid profile, total antioxidant capacity, total oxidant status, malondialdehyde, and myeloperoxidase.

Results: In subjects with 4 weeks of beetroot consumption, significant changes in the level of SFAs/PUFAs (-130 μg/mL, p = 0.04), PA/OA (-250 μg/mL, p = 0.02), and MPO (-9.60 U/L, p < 0.01) were established. In beetroot-vitamin C group, docosahexaenoic acid (9.3 μg/mL, p < 0.01), omega 3 (31 μg/mL, p < 0.001), EPA + DHA (10 μg/mL, p < 0.01), SFAs/PUFAs (-370 μg/mL, p < 0.001), PA/OA (-360 μg/mL, p < 0.001), TOS (-1.42 μM, p < 0.01), and MPO (-12.42 U/L, p < 0.001) had notable changes.

Conclusion: Beetroot capsule consumption had favorable effects on serum omega 3 fatty acids as well as TOS and MPO, the oxidant and atherogenesis factors.

背景:考虑到健康饮食在预防动脉粥样硬化中的作用,甜菜根作为一种具有抗炎、抗氧化和抗血脂异常作用的功能性食品,由于其高硝酸盐含量和生物活性化合物,是治疗冠状动脉疾病(CAD)的有趣方法之一。方法:这是一项随机、双盲、安慰剂对照临床试验的二级分析,该试验对90名男性(67.8%)和女性(32.2%)慢性CAD患者进行了为期4周的研究。这项二级分析研究了三组甜菜根胶囊对脂肪酸分布、总抗氧化能力、总氧化状态、丙二醛和髓过氧化物酶的影响。结果:食用甜菜根4周后,SFAs/PUFAs (-130 μg/mL, p = 0.04)、PA/OA (-250 μg/mL, p = 0.02)、MPO (-9.60 U/L, p < 0.01)水平均有显著变化。甜菜根-维生素C组二十二碳六烯酸(9.3 μg/mL, p < 0.01)、欧米茄-3 (31 μg/mL, p < 0.001)、EPA + DHA (10 μg/mL, p < 0.01)、SFAs/PUFAs (-370 μg/mL, p < 0.001)、PA/OA (-360 μg/mL, p < 0.001)、TOS (-1.42 μM, p < 0.01)、MPO (-12.42 U/L, p < 0.001)变化显著。结论:食用甜菜根胶囊对血清omega - 3脂肪酸、TOS和MPO、氧化因子和动脉粥样硬化因子有良好的影响。
{"title":"Effect of Beetroot Extract Supplementation on Serum Fatty Acid Profiles and Oxidative Stress Markers in Chronic Coronary Artery Disease Patients: A Secondary Analysis of a Randomized Controlled Trial.","authors":"Amirhossein Mansouri-Baseri, Mohsen Moohebati, Leila Sadat Bahrami, Hamed Tabesh, Mitra Rezaie, Mohsen Nematy, Fatemeh Davoudi, Reza Rezvani","doi":"10.1155/bmri/6654492","DOIUrl":"10.1155/bmri/6654492","url":null,"abstract":"<p><strong>Background: </strong>Considering the role of a healthy diet in preventing atherogenesis, the use of beetroot as a functional food with anti-inflammatory, antioxidant, and anti-dyslipidemic effects due to its high nitrate content and bioactive compounds is one of the interesting approaches in coronary artery disease (CAD), a common worldwide chronic disease.</p><p><strong>Methods: </strong>This is a secondary analysis of a randomized, double-blind, placebo-controlled clinical trial that was conducted on 90 male (67.8%) and female (32.2%) chronic patients with CAD for 4 weeks. This secondary analysis investigated the effect of beetroot capsules within three groups on fatty acid profile, total antioxidant capacity, total oxidant status, malondialdehyde, and myeloperoxidase.</p><p><strong>Results: </strong>In subjects with 4 weeks of beetroot consumption, significant changes in the level of SFAs/PUFAs (-130 <i>μ</i>g/mL, <i>p</i> = 0.04), PA/OA (-250 <i>μ</i>g/mL, <i>p</i> = 0.02), and MPO (-9.60 U/L, <i>p</i> < 0.01) were established. In beetroot-vitamin C group, docosahexaenoic acid (9.3 <i>μ</i>g/mL, <i>p</i> < 0.01), omega 3 (31 <i>μ</i>g/mL, <i>p</i> < 0.001), EPA + DHA (10 <i>μ</i>g/mL, <i>p</i> < 0.01), SFAs/PUFAs (-370 <i>μ</i>g/mL, <i>p</i> < 0.001), PA/OA (-360 <i>μ</i>g/mL, <i>p</i> < 0.001), TOS (-1.42 <i>μ</i>M, <i>p</i> < 0.01), and MPO (-12.42 U/L, <i>p</i> < 0.001) had notable changes.</p><p><strong>Conclusion: </strong>Beetroot capsule consumption had favorable effects on serum omega 3 fatty acids as well as TOS and MPO, the oxidant and atherogenesis factors.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"6654492"},"PeriodicalIF":2.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12746008/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145861856","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exploring the Link Between Sleep Duration and Visual Impairment and Major Eye Diseases: National Health and Nutrition Examination Survey 2005-2008. 探讨睡眠时间与视力损害和主要眼病的关系:2005-2008年全国健康和营养调查。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-28 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/1229050
Jingyue Zhang, Tian Xia, Dongmei Zhang, Xi Yang

Objective: This study is aimed at investigating the association between sleep duration and visual impairment, as well as its relationship with major eye diseases, using data from a large-scale population-based survey.

Methods: This cross-sectional study investigated the prevalence of visual impairment and major eye conditions among 5231 individuals aged 40 and older, utilizing data from the NHANES 2005-2008 survey. Sleep duration was categorized as short (< 7 h), normal (7-9 h), and long (> 9 h). Visual impairment was defined as corrected visual acuity < 20/40, and major eye diseases included cataract surgery, diabetic retinopathy, age-related macular degeneration, glaucoma, any retinopathy, any ocular disease, and any objectively determined ocular disease. Univariate and multivariate logistic regression were used to assess associations between sleep duration, visual impairment, and major eye diseases. Stratified analyses were further conducted based on diabetes and hypertension status.

Results: The long sleep group demonstrated a significantly higher prevalence of vision impairment, cataract surgery, glaucoma, as well as any ocular disease and any objectively determined ocular disease compared to the normal and short sleep groups (all p < 0.05). After adjusting for confounders, long sleep duration was significantly associated with visual impairment (OR: 2.44, 95% CI: 1.09-5.49, p = 0.035), glaucoma (OR: 3.38, 95% CI: 1.06-10.8, p = 0.042), and any objectively determined ocular disease (OR: 2.24, 95% CI: 1.08-4.65, p = 0.035). No significant associations were found between short sleep duration and visual impairment or major eye diseases after controlling for confounders. In the nondiabetic population, long sleep was significantly related to glaucoma, any objectively determined ocular disease, and visual impairment. Among hypertensive patients, long sleep was associated with glaucoma.

Conclusion: Long sleep duration is independently associated with visual impairment, glaucoma, and any objectively determined ocular disease. Longitudinal studies are needed to validate current results and explore causal mechanisms.

目的:本研究旨在通过大规模人群调查数据,探讨睡眠时间与视力损害之间的关系,以及与主要眼病的关系。方法:本横断面研究调查了5231名年龄在40岁及以上的人的视力损害和主要眼病的患病率,利用了NHANES 2005-2008年调查的数据。睡眠时间为短(9小时)。结果:与正常睡眠组和短睡眠组相比,长睡眠组的视力损害、白内障手术、青光眼以及任何眼部疾病和任何客观确定的眼部疾病的患病率均显著高于正常睡眠组和短睡眠组(p < 0.05)。在调整混杂因素后,长时间睡眠与视力障碍(OR: 2.44, 95% CI: 1.09-5.49, p = 0.035)、青光眼(OR: 3.38, 95% CI: 1.06-10.8, p = 0.042)和任何客观确定的眼部疾病(OR: 2.24, 95% CI: 1.08-4.65, p = 0.035)显著相关。在控制混杂因素后,未发现短睡眠时间与视力损害或主要眼病之间存在显著关联。在非糖尿病人群中,长时间睡眠与青光眼、任何客观确定的眼部疾病和视力损害显著相关。在高血压患者中,长时间睡眠与青光眼有关。结论:长时间睡眠与视力损害、青光眼和任何客观确定的眼部疾病独立相关。需要纵向研究来验证当前的结果并探索因果机制。
{"title":"Exploring the Link Between Sleep Duration and Visual Impairment and Major Eye Diseases: National Health and Nutrition Examination Survey 2005-2008.","authors":"Jingyue Zhang, Tian Xia, Dongmei Zhang, Xi Yang","doi":"10.1155/bmri/1229050","DOIUrl":"10.1155/bmri/1229050","url":null,"abstract":"<p><strong>Objective: </strong>This study is aimed at investigating the association between sleep duration and visual impairment, as well as its relationship with major eye diseases, using data from a large-scale population-based survey.</p><p><strong>Methods: </strong>This cross-sectional study investigated the prevalence of visual impairment and major eye conditions among 5231 individuals aged 40 and older, utilizing data from the NHANES 2005-2008 survey. Sleep duration was categorized as short (< 7 h), normal (7-9 h), and long (> 9 h). Visual impairment was defined as corrected visual acuity < 20/40, and major eye diseases included cataract surgery, diabetic retinopathy, age-related macular degeneration, glaucoma, any retinopathy, any ocular disease, and any objectively determined ocular disease. Univariate and multivariate logistic regression were used to assess associations between sleep duration, visual impairment, and major eye diseases. Stratified analyses were further conducted based on diabetes and hypertension status.</p><p><strong>Results: </strong>The long sleep group demonstrated a significantly higher prevalence of vision impairment, cataract surgery, glaucoma, as well as any ocular disease and any objectively determined ocular disease compared to the normal and short sleep groups (all <i>p</i> < 0.05). After adjusting for confounders, long sleep duration was significantly associated with visual impairment (OR: 2.44, 95% CI: 1.09-5.49, <i>p</i> = 0.035), glaucoma (OR: 3.38, 95% CI: 1.06-10.8, <i>p</i> = 0.042), and any objectively determined ocular disease (OR: 2.24, 95% CI: 1.08-4.65, <i>p</i> = 0.035). No significant associations were found between short sleep duration and visual impairment or major eye diseases after controlling for confounders. In the nondiabetic population, long sleep was significantly related to glaucoma, any objectively determined ocular disease, and visual impairment. Among hypertensive patients, long sleep was associated with glaucoma.</p><p><strong>Conclusion: </strong>Long sleep duration is independently associated with visual impairment, glaucoma, and any objectively determined ocular disease. Longitudinal studies are needed to validate current results and explore causal mechanisms.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"1229050"},"PeriodicalIF":2.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12744952/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145854120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Functional and Structure Prediction of Hypothetical Proteins From Listeria aquatica FSL S10-1188: Bioinformatics Approaches. 水生李斯特菌FSL S10-1188假设蛋白的功能和结构预测:生物信息学方法。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-28 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/1235637
Mutaz Mohammed Abdallah, Ruaa Abdalla Ibrahim Suliman, Yousra Tagelsir Ahmed, Mawada Yahia

Background: Listeria aquatica FSL S10-1188 is a freshwater bacterium characterized by distinctive metabolic properties and a genome enriched in hypothetical proteins (HPs). Although it is not considered pathogenic, its genomic features and aquatic habitat raise concerns about potential involvement in horizontal antimicrobial resistance (AMR) gene transfer.

Methods: The genome of L. aquatica FSL S10-1188 (GenBank Accession: CP011539.1) contains 2789 predicted proteins that were initially screened. From these, 919 HPs were prioritized based on sequence length (> 50 amino acids), physicochemical stability assessed using ProtParam, and consistent subcellular localization predictions from CELLO, PSORTb, and PSLpred. Among these, two stable cytoplasmic, HPs EUJ18943.1 and EUJ18676.1, were selected for comprehensive characterization. Functional insights were explored through BLASTp, secondary structure prediction, and 3D structural modeling using AlphaFold3. Model quality was validated using multiple tools including SAVES v6.0 and QMEANDisCo. Virulence potential was predicted via VICMpred, VirulentPred, and DeepVF. Putative ligand-binding sites were identified using PrankWeb, and molecular docking analyses were conducted using ProBiS for ligand prediction and AutoDock to evaluate ligand-binding affinity.

Results: EUJ18943.1 (136 aa) and EUJ18676.1 (206 aa) are stable, hydrophilic proteins with acidic isoelectric points. BLASTp identified EUJ18943.1 as homologous to Imm48 immunity proteins and EUJ18676.1 as a GyrI-like detoxification protein. Both showed alpha-helix-rich secondary structures, with high-confidence AlphaFold3 models (pTM scores: 0.87 and 0.94). Structural validation confirmed the model quality. Virulence prediction tools classified both as potential virulence factors. Active sites were predicted by PrankWeb and ProBiS, identifying kanamycin A (score: 2.32) and streptomycin (score: 2.10) as top ligands. AutoDock v4.5.6 revealed strong binding affinities (Δ G = -7.17 and - 4.30 kcal/mol, respectively).

Conclusion: This study provides the first in silico structural and functional characterization of two HPs from L. aquatica FSL S10-1188, suggesting roles in stress response and virulence. These findings highlight their potential in AMR gene transfer and demonstrate the importance of computational annotation for guiding future experimental validation.

背景:水生李斯特菌FSL S10-1188是一种淡水细菌,具有独特的代谢特性和富含假想蛋白(HPs)的基因组。虽然它不被认为是致病性的,但它的基因组特征和水生栖息地引起了人们对可能参与水平抗微生物药物耐药性(AMR)基因转移的关注。方法:L. aquatica FSL S10-1188 (GenBank Accession: CP011539.1)基因组包含2789个初步筛选的预测蛋白。其中,根据序列长度(约50个氨基酸)、ProtParam评估的理化稳定性以及CELLO、PSORTb和PSLpred一致的亚细胞定位预测,对919个hp进行了优先排序。其中选择两个稳定的细胞质,EUJ18943.1和EUJ18676.1进行综合表征。通过BLASTp,二级结构预测和使用AlphaFold3的3D结构建模来探索功能见解。使用多种工具(包括SAVES v6.0和QMEANDisCo)验证模型质量。通过VICMpred、VirulentPred和DeepVF预测毒力潜力。利用PrankWeb确定可能的配体结合位点,并利用ProBiS进行配体预测和AutoDock进行分子对接分析,评估配体结合亲和力。结果:EUJ18943.1 (136 aa)和EUJ18676.1 (206 aa)是稳定的亲水蛋白,具有酸性等电点。BLASTp鉴定EUJ18943.1与Imm48免疫蛋白同源,EUJ18676.1为gyri样解毒蛋白。两者均显示富含α螺旋的二级结构,具有高置信度的AlphaFold3模型(pTM评分分别为0.87和0.94)。结构验证证实了模型的质量。毒力预测工具将两者归类为潜在的毒力因素。通过PrankWeb和ProBiS预测活性位点,确定卡那霉素A(得分:2.32)和链霉素(得分:2.10)为顶配体。AutoDock v4.5.6显示出较强的结合亲和力(Δ G分别= -7.17和- 4.30 kcal/mol)。结论:本研究首次从硅片上获得了水草FSL S10-1188中两个hp的结构和功能特征,提示其在逆境响应和毒力中发挥作用。这些发现突出了它们在AMR基因转移中的潜力,并证明了计算注释对指导未来实验验证的重要性。
{"title":"Functional and Structure Prediction of Hypothetical Proteins From <i>Listeria aquatica</i> FSL S10-1188: Bioinformatics Approaches.","authors":"Mutaz Mohammed Abdallah, Ruaa Abdalla Ibrahim Suliman, Yousra Tagelsir Ahmed, Mawada Yahia","doi":"10.1155/bmri/1235637","DOIUrl":"10.1155/bmri/1235637","url":null,"abstract":"<p><strong>Background: </strong><i>Listeria aquatica</i> FSL S10-1188 is a freshwater bacterium characterized by distinctive metabolic properties and a genome enriched in hypothetical proteins (HPs). Although it is not considered pathogenic, its genomic features and aquatic habitat raise concerns about potential involvement in horizontal antimicrobial resistance (AMR) gene transfer.</p><p><strong>Methods: </strong>The genome of <i>L. aquatica</i> FSL S10-1188 (GenBank Accession: CP011539.1) contains 2789 predicted proteins that were initially screened. From these, 919 HPs were prioritized based on sequence length (> 50 amino acids), physicochemical stability assessed using ProtParam, and consistent subcellular localization predictions from CELLO, PSORTb, and PSLpred. Among these, two stable cytoplasmic, HPs EUJ18943.1 and EUJ18676.1, were selected for comprehensive characterization. Functional insights were explored through BLASTp, secondary structure prediction, and 3D structural modeling using AlphaFold3. Model quality was validated using multiple tools including SAVES v6.0 and QMEANDisCo. Virulence potential was predicted via VICMpred, VirulentPred, and DeepVF. Putative ligand-binding sites were identified using PrankWeb, and molecular docking analyses were conducted using ProBiS for ligand prediction and AutoDock to evaluate ligand-binding affinity.</p><p><strong>Results: </strong>EUJ18943.1 (136 aa) and EUJ18676.1 (206 aa) are stable, hydrophilic proteins with acidic isoelectric points. BLASTp identified EUJ18943.1 as homologous to Imm48 immunity proteins and EUJ18676.1 as a GyrI-like detoxification protein. Both showed alpha-helix-rich secondary structures, with high-confidence AlphaFold3 models (pTM scores: 0.87 and 0.94). Structural validation confirmed the model quality. Virulence prediction tools classified both as potential virulence factors. Active sites were predicted by PrankWeb and ProBiS, identifying kanamycin A (score: 2.32) and streptomycin (score: 2.10) as top ligands. AutoDock v4.5.6 revealed strong binding affinities (<i>Δ</i> <i>G</i> = -7.17 and - 4.30 kcal/mol, respectively).</p><p><strong>Conclusion: </strong>This study provides the first in silico structural and functional characterization of two HPs from <i>L. aquatica</i> FSL S10-1188, suggesting roles in stress response and virulence. These findings highlight their potential in AMR gene transfer and demonstrate the importance of computational annotation for guiding future experimental validation.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"1235637"},"PeriodicalIF":2.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745843/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145861841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Digital Clinical Records Versus Paper Records in Dental Practice: A Comparative Study. 数字临床记录与纸质记录在牙科实践中的比较研究。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-28 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/5527391
Antonio Scarano, Francesco Inchingolo, Gianna Dipalma, Filiberto Mastrangelo

Background: Efficient analysis of patient histories is essential for dental treatment planning. Electronic health records (EHRs) facilitate the immediate identification of risk factors, such as medication allergies and sensitivities to dental materials, thereby reducing the risk of medical errors.

Objective: This study is aimed at comparing the effectiveness of an EHR interface with traditional paper medical records (PMRs) in evaluating the medical histories of dental patients.

Methods: Two hundred patient records were randomly assigned to either the PMR or EHR group. Twenty dental students reviewed the records and reported the planned dental procedure for each patient. Recording and reporting times, as well as the number of oversights, were measured for both groups.

Results: Students using EHRs identified critical systemic conditions more rapidly and with greater accuracy, with no oversights detected. In contrast, students using PMRs required more time and were more likely to overlook important health information. The mean number of oversights in the PMR group was significantly higher (9.3 ± 0.46, p ≤ 0.01).

Conclusion: The use of EHRs in dental practice significantly improves the identification of critical systemic conditions, enhances patient safety, and increases clinical efficiency. Despite the benefits, the high costs of software acquisition, staff training, and technical support may pose challenges to widespread adoption.

背景:对患者病史进行有效的分析对于制定牙科治疗计划至关重要。电子健康记录(EHRs)有助于立即识别风险因素,例如药物过敏和对牙科材料的敏感性,从而降低医疗差错的风险。目的:本研究旨在比较EHR界面与传统纸质病历(pmr)在评估牙科患者病史方面的有效性。方法:200例患者病历随机分为PMR组和EHR组。20名牙科学生审阅了记录,并报告了每位患者的牙科手术计划。对两组的记录和报告时间以及疏忽次数进行了测量。结果:使用电子病历的学生更快速、更准确地识别出关键的系统状况,没有发现疏忽。相比之下,使用pmr的学生需要更多的时间,更有可能忽略重要的健康信息。PMR组的平均疏漏次数显著高于对照组(9.3±0.46,p≤0.01)。结论:在牙科医疗中使用电子病历可显著提高对全身危重疾病的识别,提高患者安全,提高临床效率。尽管有好处,但软件获取、员工培训和技术支持的高成本可能对广泛采用构成挑战。
{"title":"A Digital Clinical Records Versus Paper Records in Dental Practice: A Comparative Study.","authors":"Antonio Scarano, Francesco Inchingolo, Gianna Dipalma, Filiberto Mastrangelo","doi":"10.1155/bmri/5527391","DOIUrl":"10.1155/bmri/5527391","url":null,"abstract":"<p><strong>Background: </strong>Efficient analysis of patient histories is essential for dental treatment planning. Electronic health records (EHRs) facilitate the immediate identification of risk factors, such as medication allergies and sensitivities to dental materials, thereby reducing the risk of medical errors.</p><p><strong>Objective: </strong>This study is aimed at comparing the effectiveness of an EHR interface with traditional paper medical records (PMRs) in evaluating the medical histories of dental patients.</p><p><strong>Methods: </strong>Two hundred patient records were randomly assigned to either the PMR or EHR group. Twenty dental students reviewed the records and reported the planned dental procedure for each patient. Recording and reporting times, as well as the number of oversights, were measured for both groups.</p><p><strong>Results: </strong>Students using EHRs identified critical systemic conditions more rapidly and with greater accuracy, with no oversights detected. In contrast, students using PMRs required more time and were more likely to overlook important health information. The mean number of oversights in the PMR group was significantly higher (9.3 ± 0.46, <i>p</i> ≤ 0.01).</p><p><strong>Conclusion: </strong>The use of EHRs in dental practice significantly improves the identification of critical systemic conditions, enhances patient safety, and increases clinical efficiency. Despite the benefits, the high costs of software acquisition, staff training, and technical support may pose challenges to widespread adoption.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"5527391"},"PeriodicalIF":2.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745653/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145861801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Role of miR-138 in Cardiovascular Diseases. miR-138在心血管疾病中的作用
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-22 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/2356842
Taidou Jiang, Bijian Wang, Zhi Luo, Ying Xia, Yaoyu Qi, Sha Luo, Binyan Lang, Bolan Zhang, Shuzhan Zheng

Cardiovascular disease (CVD) represents the foremost cause of morbidity and mortality globally, posing a significant threat to human health. The regulatory mechanisms underlying CVD are still not fully elucidated. MicroRNA (miRNA), a class of noncoding short-chain RNA molecules, modulates individual genes or gene networks by binding to the complementary sequences of specific target genes, thereby influencing various biological processes including cell genesis, metabolism, proliferation, differentiation, and apoptosis. Among these, miR-138 plays a significant role in the onset and progression of CVDs. This article reviews the involvement of miR-138 in various cardiovascular conditions, including atherosclerosis (AS), myocardial ischemia-reperfusion injury (I/R), heart failure (HF), and pulmonary arterial hypertension (PAH), thereby offering novel insights for the prevention, diagnosis, and treatment of CVDs.

心血管疾病(CVD)是全球发病率和死亡率的首要原因,对人类健康构成重大威胁。CVD的调控机制仍未完全阐明。MicroRNA (miRNA)是一类非编码短链RNA分子,通过结合特定靶基因的互补序列来调节单个基因或基因网络,从而影响细胞发生、代谢、增殖、分化和凋亡等多种生物过程。其中,miR-138在cvd的发生和发展中起着重要作用。本文综述了miR-138在各种心血管疾病中的作用,包括动脉粥样硬化(AS)、心肌缺血再灌注损伤(I/R)、心力衰竭(HF)和肺动脉高压(PAH),从而为心血管疾病的预防、诊断和治疗提供了新的见解。
{"title":"The Role of miR-138 in Cardiovascular Diseases.","authors":"Taidou Jiang, Bijian Wang, Zhi Luo, Ying Xia, Yaoyu Qi, Sha Luo, Binyan Lang, Bolan Zhang, Shuzhan Zheng","doi":"10.1155/bmri/2356842","DOIUrl":"10.1155/bmri/2356842","url":null,"abstract":"<p><p>Cardiovascular disease (CVD) represents the foremost cause of morbidity and mortality globally, posing a significant threat to human health. The regulatory mechanisms underlying CVD are still not fully elucidated. MicroRNA (miRNA), a class of noncoding short-chain RNA molecules, modulates individual genes or gene networks by binding to the complementary sequences of specific target genes, thereby influencing various biological processes including cell genesis, metabolism, proliferation, differentiation, and apoptosis. Among these, miR-138 plays a significant role in the onset and progression of CVDs. This article reviews the involvement of miR-138 in various cardiovascular conditions, including atherosclerosis (AS), myocardial ischemia-reperfusion injury (I/R), heart failure (HF), and pulmonary arterial hypertension (PAH), thereby offering novel insights for the prevention, diagnosis, and treatment of CVDs.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"2356842"},"PeriodicalIF":2.3,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12723191/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145826791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Mechanism of Andrographis paniculata in the Treatment of Influenza Explored via Network Pharmacology and Molecular Docking. 网络药理学与分子对接探讨穿心莲治疗流行性感冒的作用机制。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-21 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/5752130
Lan-Ling Tian, Man-Lin Zhang, Cong Wang

Objective: The objective of this study is to investigate the potential mechanisms of Andrographis paniculata in treating influenza using network pharmacology and molecular docking approaches.

Methods: The active components of A. paniculata were identified through the traditional Chinese medicine systems pharmacology database (TCMSP), and potential targets were predicted using SwissTargetPrediction. Gene targets associated with influenza were obtained from the GeneCards and OMIM databases. Venny 2.1.0 was used to create a Venn diagram to determine overlapping targets between A. paniculata and influenza. A "drug-component-target" interaction network was constructed using Cytoscape 3.7.2. A protein-protein interaction (PPI) network was developed with STRING 12.0 and visualized using Cytoscape 3.9.1 to identify core genes. Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were conducted via the DAVID database, and the results were visualized using an online bioinformatics platform. Molecular docking was performed between major components and core targets using AutoDock 4.2.6 software.

Results: A total of 24 active components of A. paniculata were identified, yielding 646 predicted drug targets, 1876 influenza-associated gene targets, and 176 intersecting targets. GO enrichment analysis revealed 919 terms, primarily related to inflammatory responses and protein phosphorylation. KEGG analysis identified 173 enriched pathways, notably those related to lipid metabolism, atherosclerosis, and cancer. The principal active compounds demonstrated strong binding affinities with the core targets.

Conclusion: A. paniculata may exert therapeutic effects against influenza by acting on core targets, such as TNF, IL-6, AKT1, GAPDH, and STAT3. These findings provide a scientific foundation for the application of traditional Chinese medicine in the treatment of influenza.

目的:利用网络药理学和分子对接方法,探讨穿心莲治疗流感的潜在机制。方法:通过中药系统药理学数据库(TCMSP)对金针藤的有效成分进行鉴定,并利用SwissTargetPrediction预测其潜在靶点。与流感相关的基因靶标从GeneCards和OMIM数据库中获得。利用Venny 2.1.0创建了一个Venn图,以确定甲蚜和流感之间的重叠目标。利用Cytoscape 3.7.2构建“药物-成分-靶点”相互作用网络。利用STRING 12.0构建蛋白相互作用(protein-protein interaction, PPI)网络,并利用Cytoscape 3.9.1进行可视化,鉴定核心基因。通过DAVID数据库进行基因本体(GO)富集和京都基因与基因组百科全书(KEGG)通路分析,并使用在线生物信息学平台将结果可视化。利用AutoDock 4.2.6软件对主要部件与核心靶点进行分子对接。结果:共鉴定出24种有效成分,预测药物靶点646个,流感相关基因靶点1876个,交叉靶点176个。氧化石墨烯富集分析揭示了919个术语,主要与炎症反应和蛋白磷酸化有关。KEGG分析确定了173条富集通路,特别是与脂质代谢、动脉粥样硬化和癌症相关的通路。主要活性化合物与核心靶点表现出较强的结合亲和力。结论:金针藤可能通过作用于TNF、IL-6、AKT1、GAPDH、STAT3等核心靶点发挥抗流感作用。这些发现为中医药治疗流行性感冒提供了科学依据。
{"title":"The Mechanism of <i>Andrographis paniculata</i> in the Treatment of Influenza Explored via Network Pharmacology and Molecular Docking.","authors":"Lan-Ling Tian, Man-Lin Zhang, Cong Wang","doi":"10.1155/bmri/5752130","DOIUrl":"10.1155/bmri/5752130","url":null,"abstract":"<p><strong>Objective: </strong>The objective of this study is to investigate the potential mechanisms of <i>Andrographis paniculata</i> in treating influenza using network pharmacology and molecular docking approaches.</p><p><strong>Methods: </strong>The active components of <i>A. paniculata</i> were identified through the traditional Chinese medicine systems pharmacology database (TCMSP), and potential targets were predicted using SwissTargetPrediction. Gene targets associated with influenza were obtained from the GeneCards and OMIM databases. Venny 2.1.0 was used to create a Venn diagram to determine overlapping targets between <i>A. paniculata</i> and influenza. A \"drug-component-target\" interaction network was constructed using Cytoscape 3.7.2. A protein-protein interaction (PPI) network was developed with STRING 12.0 and visualized using Cytoscape 3.9.1 to identify core genes. Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were conducted via the DAVID database, and the results were visualized using an online bioinformatics platform. Molecular docking was performed between major components and core targets using AutoDock 4.2.6 software.</p><p><strong>Results: </strong>A total of 24 active components of <i>A. paniculata</i> were identified, yielding 646 predicted drug targets, 1876 influenza-associated gene targets, and 176 intersecting targets. GO enrichment analysis revealed 919 terms, primarily related to inflammatory responses and protein phosphorylation. KEGG analysis identified 173 enriched pathways, notably those related to lipid metabolism, atherosclerosis, and cancer. The principal active compounds demonstrated strong binding affinities with the core targets.</p><p><strong>Conclusion: </strong><i>A. paniculata</i> may exert therapeutic effects against influenza by acting on core targets, such as TNF, IL-6, AKT1, GAPDH, and STAT3. These findings provide a scientific foundation for the application of traditional Chinese medicine in the treatment of influenza.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"5752130"},"PeriodicalIF":2.3,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719791/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145817757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sleep Quality and Its Determinants Among Patients With Chronic Diseases in Ethiopia: A Systematic Review With Meta-Analysis. 埃塞俄比亚慢性疾病患者的睡眠质量及其决定因素:荟萃分析的系统综述
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-21 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/6736381
Bekahegn Girma, Alemayehu Molla, Asresu Feleke, Takla Tamir, Ahmedin Sefa, Jemberu Nigussie

Background: Patients with chronic medical and mental illnesses are more vulnerable to poor sleep quality. However, there is little aggregated evidence about poor sleep quality among this population and its determinants in Ethiopia. This study was aimed at assessing the pooled prevalence of sleep quality and its determinants among patients with chronic diseases in Ethiopia.

Methods: We used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to write this review. Primary articles were retrieved from PubMed, PsycINFO, Hinari, ScienceDirect, African Journal Online (AJOL), and Google Scholar databases. A random-effects model was applied for analysis. I 2, Cochran's, and tau2 were checked to determine the degree of heterogeneity between the included studies. Egger's test and sensitivity analysis were conducted to check publication bias.

Results: The pooled prevalence of poor sleep quality among patients with chronic medical and mental illnesses was 53.12% (95% CI: 47.66, 58.58). Eight factors were associated with poor sleep quality: advanced age (POR = 1.04, 95% CI: 1.02, 1.07), female sex (POR = 2.95, 95% CI: 2.21, 3.93), social support (POR = 2.62, 95% CI: 1.90, 3.61), substance use (POR = 1.76, 95% CI: 1.51, 2.04), anxiety symptoms (POR = 2.92, 95% CI: 2.40, 3.56), comorbidity (POR: 2.47, 95% CI: 1.83, 3.33), sleep hygiene practice (POR: 2.86, 95% CI: 2.02, 4.04), and depression symptoms (POR = 3.73, 95% CI: 2.96, 4.69).

Conclusion and recommendation: More than half of patients with chronic diseases experienced poor sleep quality. Poor sleep quality was connected with advanced age, female sex, substance use, having comorbidity, inadequate social support and sleep hygiene practices, anxiety, and depression symptoms. Substance use should be restricted, and patients with chronic mental and medical illnesses should be counseled to avoid substance use. Moreover, special focus should be given to female patients, patients with other comorbid conditions, elderly individuals, and those who have poor sleep hygiene and social support. Lastly, patients with chronic medical and mental illnesses should be screened for anxiety and depression symptoms.

背景:患有慢性疾病和精神疾病的患者更容易出现睡眠质量差的情况。然而,关于埃塞俄比亚人口中睡眠质量差及其决定因素的综合证据很少。本研究旨在评估埃塞俄比亚慢性疾病患者睡眠质量的总体患病率及其决定因素。方法:我们使用系统评价和荟萃分析的首选报告项目(PRISMA)指南来撰写本综述。主要文章检索自PubMed、PsycINFO、Hinari、ScienceDirect、African Journal Online (AJOL)和谷歌Scholar数据库。采用随机效应模型进行分析。检查i2、Cochran’s和tau2以确定纳入研究之间的异质性程度。采用Egger检验和敏感性分析检查发表偏倚。结果:慢性内科和精神疾病患者中睡眠质量差的总患病率为53.12% (95% CI: 47.66, 58.58)。8个因素与睡眠质量差相关:高龄(POR = 1.04, 95% CI: 1.02, 1.07)、女性(POR = 2.95, 95% CI: 2.21, 3.93)、社会支持(POR = 2.62, 95% CI: 1.90, 3.61)、物质使用(POR = 1.76, 95% CI: 1.51, 2.04)、焦虑症状(POR = 2.92, 95% CI: 2.40, 3.56)、共病(POR: 2.47, 95% CI: 1.83, 3.33)、睡眠卫生习惯(POR: 2.86, 95% CI: 2.02, 4.04)和抑郁症状(POR = 3.73, 95% CI: 2.96, 4.69)。结论和建议:超过一半的慢性疾病患者睡眠质量较差。睡眠质量差与高龄、女性、药物使用、合并症、缺乏社会支持和睡眠卫生习惯、焦虑和抑郁症状有关。应限制物质使用,并应建议患有慢性精神疾病和医学疾病的患者避免使用物质。此外,应特别关注女性患者、其他合并症患者、老年人以及睡眠卫生和社会支持较差的患者。最后,患有慢性疾病和精神疾病的患者应该接受焦虑和抑郁症状的筛查。
{"title":"Sleep Quality and Its Determinants Among Patients With Chronic Diseases in Ethiopia: A Systematic Review With Meta-Analysis.","authors":"Bekahegn Girma, Alemayehu Molla, Asresu Feleke, Takla Tamir, Ahmedin Sefa, Jemberu Nigussie","doi":"10.1155/bmri/6736381","DOIUrl":"10.1155/bmri/6736381","url":null,"abstract":"<p><strong>Background: </strong>Patients with chronic medical and mental illnesses are more vulnerable to poor sleep quality. However, there is little aggregated evidence about poor sleep quality among this population and its determinants in Ethiopia. This study was aimed at assessing the pooled prevalence of sleep quality and its determinants among patients with chronic diseases in Ethiopia.</p><p><strong>Methods: </strong>We used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to write this review. Primary articles were retrieved from PubMed, PsycINFO, Hinari, ScienceDirect, African Journal Online (AJOL), and Google Scholar databases. A random-effects model was applied for analysis. <i>I</i> <sup>2</sup>, Cochran's, and tau<sup>2</sup> were checked to determine the degree of heterogeneity between the included studies. Egger's test and sensitivity analysis were conducted to check publication bias.</p><p><strong>Results: </strong>The pooled prevalence of poor sleep quality among patients with chronic medical and mental illnesses was 53.12% (95% CI: 47.66, 58.58). Eight factors were associated with poor sleep quality: advanced age (POR = 1.04, 95% CI: 1.02, 1.07), female sex (POR = 2.95, 95% CI: 2.21, 3.93), social support (POR = 2.62, 95% CI: 1.90, 3.61), substance use (POR = 1.76, 95% CI: 1.51, 2.04), anxiety symptoms (POR = 2.92, 95% CI: 2.40, 3.56), comorbidity (POR: 2.47, 95% CI: 1.83, 3.33), sleep hygiene practice (POR: 2.86, 95% CI: 2.02, 4.04), and depression symptoms (POR = 3.73, 95% CI: 2.96, 4.69).</p><p><strong>Conclusion and recommendation: </strong>More than half of patients with chronic diseases experienced poor sleep quality. Poor sleep quality was connected with advanced age, female sex, substance use, having comorbidity, inadequate social support and sleep hygiene practices, anxiety, and depression symptoms. Substance use should be restricted, and patients with chronic mental and medical illnesses should be counseled to avoid substance use. Moreover, special focus should be given to female patients, patients with other comorbid conditions, elderly individuals, and those who have poor sleep hygiene and social support. Lastly, patients with chronic medical and mental illnesses should be screened for anxiety and depression symptoms.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"6736381"},"PeriodicalIF":2.3,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719613/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145817790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Descriptive Epidemiology of Klebsiella spp. Urinary Tract Infections in Central Africa. 中非克雷伯氏菌尿路感染的描述流行病学。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-21 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/9558259
Evrard Mayombo Ngoussou, Franck Mounioko, Mambu Mundunge, Rolande Mabika Mabika, Ornella Zong Minko, Léonce Fauster Ondjiangui, Jean Fabrice Yala

Objective: Urinary tract infections are the most common bacterial infections encountered in clinical practice. Among the pathogens responsible, bacteria of the Klebsiella spp. are the second most frequently isolated uropathogenic agents worldwide. These bacteria are constantly evolving, both epidemiologically and in terms of the development of antimicrobial resistance. In Central Africa, available data on the spread of Klebsiella spp. are mainly derived from isolated studies, making it difficult to obtain an overview of their epidemiology in the subregion. Consequently, these systematic review and meta-analysis are aimed at estimating the pooled prevalence of urinary tract infections in Central Africa and to describe the epidemiology of the Klebsiella spp. strains responsible for these infections.

Methods: Relevant articles were searched in the SCOPUS, PubMed, and Google Scholar databases. The study selection process was conducted in accordance with the PRISMA flowchart recommendations. Systematic review and meta-analysis were used to summarize data on urinary tract infections. Prevalence was determined and visualized using a forest plot with R software Version 4.4.1. Also, finally, geographical mapping of the data distribution was carried out using QGIS software (Version 3.34.15-Prizren).

Result: Out of all the articles retrieved, 34 studies were deemed eligible for this analysis. The overall pooled prevalence of urinary tract infections in Central Africa was estimated at 28% (95% IC: 28, 29). The overall isolation rate of Klebsiella spp. responsible for urinary tract infections was 12% (95% IC: 11, 12). Analysis of the distribution of Klebsiella spp. isolation rates in urinary tract infections across Central Africa revealed variability by country, ranging from 10% to 25%. The species Klebsiella pneumoniae was the most frequently isolated, present in 96.15% of the studies. Furthermore, Klebsiella spp. strains responsible for urinary tract infections were predominantly identified in females, with an overall isolation rate of 82.23%, compared to 17.77% in males.

目的:尿路感染是临床最常见的细菌感染。在负责的病原体中,克雷伯氏菌是世界上第二大最常分离的泌尿系统病原体。这些细菌在流行病学和抗菌素耐药性方面都在不断发展。在中非,关于克雷伯氏菌传播的现有数据主要来自孤立的研究,因此很难获得该分区域的流行病学概况。因此,这些系统综述和荟萃分析旨在估计中非尿路感染的总流行率,并描述导致这些感染的克雷伯氏菌菌株的流行病学。方法:在SCOPUS、PubMed、谷歌Scholar数据库中检索相关文献。研究选择过程按照PRISMA流程图建议进行。系统回顾和荟萃分析用于总结尿路感染的数据。使用R软件4.4.1版本的森林图确定和可视化患病率。最后利用QGIS软件(Version 3.34.15-Prizren)对数据分布进行地理制图。结果:在所有检索到的文章中,34项研究被认为符合本分析。中部非洲尿路感染的总流行率估计为28% (95% IC: 28,29)。导致尿路感染的克雷伯氏菌总分离率为12% (95% IC: 11,12)。对中非尿路感染中克雷伯氏菌分离率分布的分析显示,各国存在差异,从10%到25%不等。肺炎克雷伯菌是最常见的分离种,占96.15%的研究。此外,克雷伯氏菌(Klebsiella spp.)在女性中以尿路感染为主,总分离率为82.23%,而在男性中则为17.77%。
{"title":"Descriptive Epidemiology of <i>Klebsiella</i> spp. Urinary Tract Infections in Central Africa.","authors":"Evrard Mayombo Ngoussou, Franck Mounioko, Mambu Mundunge, Rolande Mabika Mabika, Ornella Zong Minko, Léonce Fauster Ondjiangui, Jean Fabrice Yala","doi":"10.1155/bmri/9558259","DOIUrl":"10.1155/bmri/9558259","url":null,"abstract":"<p><strong>Objective: </strong>Urinary tract infections are the most common bacterial infections encountered in clinical practice. Among the pathogens responsible, bacteria of the <i>Klebsiella</i> spp. are the second most frequently isolated uropathogenic agents worldwide. These bacteria are constantly evolving, both epidemiologically and in terms of the development of antimicrobial resistance. In Central Africa, available data on the spread of <i>Klebsiella</i> spp. are mainly derived from isolated studies, making it difficult to obtain an overview of their epidemiology in the subregion. Consequently, these systematic review and meta-analysis are aimed at estimating the pooled prevalence of urinary tract infections in Central Africa and to describe the epidemiology of the <i>Klebsiella</i> spp. strains responsible for these infections.</p><p><strong>Methods: </strong>Relevant articles were searched in the SCOPUS, PubMed, and Google Scholar databases. The study selection process was conducted in accordance with the PRISMA flowchart recommendations. Systematic review and meta-analysis were used to summarize data on urinary tract infections. Prevalence was determined and visualized using a forest plot with R software Version 4.4.1. Also, finally, geographical mapping of the data distribution was carried out using QGIS software (Version 3.34.15-Prizren).</p><p><strong>Result: </strong>Out of all the articles retrieved, 34 studies were deemed eligible for this analysis. The overall pooled prevalence of urinary tract infections in Central Africa was estimated at 28% (95% IC: 28, 29). The overall isolation rate of <i>Klebsiella</i> spp. responsible for urinary tract infections was 12% (95% IC: 11, 12). Analysis of the distribution of <i>Klebsiella</i> spp. isolation rates in urinary tract infections across Central Africa revealed variability by country, ranging from 10% to 25%. The species <i>Klebsiella pneumoniae</i> was the most frequently isolated, present in 96.15% of the studies. Furthermore, <i>Klebsiella</i> spp. strains responsible for urinary tract infections were predominantly identified in females, with an overall isolation rate of 82.23%, compared to 17.77% in males.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"9558259"},"PeriodicalIF":2.3,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145817708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Systems Biology and Drug Repositioning Approach for the Analysis of Mutual Genes Between Celiac Disease and Irritable Bowel Syndrome. 乳糜泻与肠易激综合征相互基因分析的系统生物学和药物重新定位方法。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-21 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/8227229
Haitham Al-Madhagi

Celiac disease (CD) and irritable bowel syndrome (IBS) are two disorders that share common features, such as similar symptoms and autoimmune involvement. However, the molecular genetic mechanisms underlying their pathogenesis remain unclear. An in silico systems biology approach was performed to analyze the RNA-seq (GSE146190 and GSE166869) and microarray data (GSE164883 and GSE63379) of both diseases. Gene ontology was first identified, followed by transcriptional factors and miRNAs that regulate the mutual genes by Enrichr platform. Moreover, a protein-protein interaction network of the shared genes was constructed, and the hub genes were identified using Network Analyst and Cytoscape. Finally, the tertiary structure of the most significant hub gene product was downloaded and screened against approved drugs using DrupRep server for drug repurposing. Four hundred thirty-nine shared genes between CD and IBS were revealed, which were mainly involved in response to stimulus, proliferation regulation, metabolism of small molecules, and apoptosis. RARG, NFE2L2, VDR, NCOA1, and RXRA were the top five transcription factors that regulated these genes, whereas hsa-miR-4632-3p, hsa-miR-598-5p, hsa-miR-7108-3p, and hsa-miR-29b-3p were the top five miRNAs. SRC, STAT1, CCNB1, CDK1, CD44, RRM2, ERBB2, BUB1B, KIF11, and TOP2A were ranked as the Top 10 hub genes by the PPI network analysis. Temoporfin, rimegepant, and eltrombopag were suggested as the top three lead candidates by the virtual screening against SRC with binding affinities of -11.1, 10.9, and -10.8 kcal/mol, respectively. These drugs are potential SRC inhibitors that warrant further experimental validation. Novel insights into the molecular genetic mechanisms of CD and IBS and new therapeutic avenues for these disorders were provided by this study.

乳糜泻(CD)和肠易激综合征(IBS)是两种具有共同特征的疾病,例如相似的症状和自身免疫性疾病。然而,其发病机制的分子遗传机制尚不清楚。采用计算机系统生物学方法分析两种疾病的RNA-seq (GSE146190和GSE166869)和微阵列数据(GSE164883和GSE63379)。首先确定基因本体,然后通过enrichment平台确定转录因子和调控相互基因的mirna。此外,构建了共享基因的蛋白-蛋白相互作用网络,并利用network Analyst和Cytoscape对中心基因进行了鉴定。最后,下载最重要的枢纽基因产物的三级结构,并使用DrupRep服务器对已批准的药物进行筛选,以进行药物再利用。共发现439个CD和IBS共有基因,主要涉及刺激反应、增殖调控、小分子代谢和细胞凋亡等。RARG、NFE2L2、VDR、NCOA1和RXRA是调节这些基因的前五大转录因子,而hsa-miR-4632-3p、hsa-miR-598-5p、hsa- mir - 7101 -3p和hsa-miR-29b-3p是前五大miRNAs。通过PPI网络分析,SRC、STAT1、CCNB1、CDK1、CD44、RRM2、ERBB2、BUB1B、KIF11、TOP2A被评为Top 10枢纽基因。通过对SRC的虚拟筛选,Temoporfin、rimegepant和eltrombopag的结合亲和力分别为-11.1、10.9和-10.8 kcal/mol,被推荐为前三名候选药物。这些药物是潜在的SRC抑制剂,需要进一步的实验验证。本研究为乳糜泻和肠易激综合征的分子遗传机制提供了新的见解,为这些疾病的治疗提供了新的途径。
{"title":"A Systems Biology and Drug Repositioning Approach for the Analysis of Mutual Genes Between Celiac Disease and Irritable Bowel Syndrome.","authors":"Haitham Al-Madhagi","doi":"10.1155/bmri/8227229","DOIUrl":"10.1155/bmri/8227229","url":null,"abstract":"<p><p>Celiac disease (CD) and irritable bowel syndrome (IBS) are two disorders that share common features, such as similar symptoms and autoimmune involvement. However, the molecular genetic mechanisms underlying their pathogenesis remain unclear. An in silico systems biology approach was performed to analyze the RNA-seq (GSE146190 and GSE166869) and microarray data (GSE164883 and GSE63379) of both diseases. Gene ontology was first identified, followed by transcriptional factors and miRNAs that regulate the mutual genes by Enrichr platform. Moreover, a protein-protein interaction network of the shared genes was constructed, and the hub genes were identified using Network Analyst and Cytoscape. Finally, the tertiary structure of the most significant hub gene product was downloaded and screened against approved drugs using DrupRep server for drug repurposing. Four hundred thirty-nine shared genes between CD and IBS were revealed, which were mainly involved in response to stimulus, proliferation regulation, metabolism of small molecules, and apoptosis. RARG, NFE2L2, VDR, NCOA1, and RXRA were the top five transcription factors that regulated these genes, whereas hsa-miR-4632-3p, hsa-miR-598-5p, hsa-miR-7108-3p, and hsa-miR-29b-3p were the top five miRNAs. SRC, STAT1, CCNB1, CDK1, CD44, RRM2, ERBB2, BUB1B, KIF11, and TOP2A were ranked as the Top 10 hub genes by the PPI network analysis. Temoporfin, rimegepant, and eltrombopag were suggested as the top three lead candidates by the virtual screening against SRC with binding affinities of -11.1, 10.9, and -10.8 kcal/mol, respectively. These drugs are potential SRC inhibitors that warrant further experimental validation. Novel insights into the molecular genetic mechanisms of CD and IBS and new therapeutic avenues for these disorders were provided by this study.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"8227229"},"PeriodicalIF":2.3,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719798/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145817743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epidemiology of Human and Animal Anthrax in India, 1990-2022: A Comprehensive Analysis of Literature and National Surveillance Data. 印度人类和动物炭疽流行病学,1990-2022:文献和国家监测数据的综合分析。
IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-12-21 eCollection Date: 2025-01-01 DOI: 10.1155/bmri/5633425
Suresh K Puttahonnappa, Jessica Radzio-Basu, Hindol Maity, Ramya K Rao, Robab Katani, Divakar Hemadri, Sharanagouda Patil, Jayashree Anand, Samer Singh, Divya Kandari, Rajinder Kaur, Rani Prameela, Shivraj Murag, Niranjana Sahoo, Vivek Kapur, Shah Hossain, Mohan Papanna

Background: Anthrax, a neglected zoonotic disease caused by Bacillus anthracis, exerts considerable health consequences in resource-limited regions and is notably prevalent in India, causing persistent outbreaks that pose major animal and public health challenges. This study reviews the spatiotemporal patterns of human and animal anthrax outbreaks in India to identify high-risk areas and assess the correlation with environmental factors.

Methods: A comprehensive literature search covering the period from 1990 to 2022 was conducted across various databases including CAB Direct, PubMed, Scopus, and Web of Science, alongside Indian government databases like the Integrated Disease Surveillance Programme (IDSP) and the National Animal Disease Referral Expert System (NADRES). We extracted data from studies published in English, using predefined keywords, and evaluated them using the Joanna Briggs Institute checklists. Data analysis was carried out using Microsoft Excel and EpiInfo, with spatial mapping in ArcGIS Pro.

Results: Out of the 423 studies reviewed, 44 fulfilled our inclusion criteria, providing data on 174 human outbreaks (1778 cases, 130 fatalities) and 1775 animal outbreaks (7818 deaths). We identified key hotspots for human anthrax in West Bengal, Odisha, and Andhra Pradesh, and significant hotspots for animal anthrax in Karnataka, Andhra Pradesh, Tamil Nadu, and West Bengal. Majority of human outbreaks were reported between March and June, whereas the majority of animal outbreaks were reported between June and September. A strong correlation was observed between rainfall and animal outbreaks in the eastern region (correlation coefficient of 0.94).

Conclusion: The study highlights key hotspots for human and animal anthrax and discrepancies in human and animal anthrax reporting and gaps in surveillance. There is a critical need for enhanced One Health surveillance and animal anthrax vaccination programs for effective management and mitigate the disease. These strategies are essential not only for public health and livestock welfare in India but also for global health security.

背景:炭疽是由炭疽芽孢杆菌引起的一种被忽视的人畜共患疾病,在资源有限的地区造成相当大的健康后果,在印度尤为普遍,造成持续爆发,对动物和公共卫生构成重大挑战。本研究回顾了印度人类和动物炭疽疫情的时空格局,以确定高风险地区并评估其与环境因素的相关性。方法:对涵盖1990年至2022年期间的各种数据库进行了全面的文献检索,包括CAB Direct、PubMed、Scopus和Web of Science,以及印度政府数据库,如综合疾病监测计划(IDSP)和国家动物疾病转诊专家系统(NADRES)。我们从用英语发表的研究中提取数据,使用预定义的关键词,并使用乔安娜布里格斯研究所的核对表对它们进行评估。数据分析采用Microsoft Excel和EpiInfo软件,空间制图采用ArcGIS Pro软件。结果:在审查的423项研究中,44项符合我们的纳入标准,提供了174例人类疫情(1778例,130例死亡)和1775例动物疫情(7818例死亡)的数据。我们确定了西孟加拉邦、奥里萨邦和安得拉邦人类炭疽热的主要热点地区,以及卡纳塔克邦、安得拉邦、泰米尔纳德邦和西孟加拉邦动物炭疽热的重要热点地区。大多数人间疫情报告发生在3月至6月期间,而大多数动物疫情报告发生在6月至9月期间。在东部地区,降雨与动物暴发有很强的相关性(相关系数为0.94)。结论:本研究突出了人畜炭疽的重点热点,人畜炭疽报告的差异和监测的空白。迫切需要加强“同一个卫生”监测和动物炭疽疫苗接种规划,以有效管理和减轻疾病。这些战略不仅对印度的公共卫生和牲畜福利至关重要,而且对全球卫生安全也至关重要。
{"title":"Epidemiology of Human and Animal Anthrax in India, 1990-2022: A Comprehensive Analysis of Literature and National Surveillance Data.","authors":"Suresh K Puttahonnappa, Jessica Radzio-Basu, Hindol Maity, Ramya K Rao, Robab Katani, Divakar Hemadri, Sharanagouda Patil, Jayashree Anand, Samer Singh, Divya Kandari, Rajinder Kaur, Rani Prameela, Shivraj Murag, Niranjana Sahoo, Vivek Kapur, Shah Hossain, Mohan Papanna","doi":"10.1155/bmri/5633425","DOIUrl":"10.1155/bmri/5633425","url":null,"abstract":"<p><strong>Background: </strong>Anthrax, a neglected zoonotic disease caused by <i>Bacillus anthracis</i>, exerts considerable health consequences in resource-limited regions and is notably prevalent in India, causing persistent outbreaks that pose major animal and public health challenges. This study reviews the spatiotemporal patterns of human and animal anthrax outbreaks in India to identify high-risk areas and assess the correlation with environmental factors.</p><p><strong>Methods: </strong>A comprehensive literature search covering the period from 1990 to 2022 was conducted across various databases including CAB Direct, PubMed, Scopus, and Web of Science, alongside Indian government databases like the Integrated Disease Surveillance Programme (IDSP) and the National Animal Disease Referral Expert System (NADRES). We extracted data from studies published in English, using predefined keywords, and evaluated them using the Joanna Briggs Institute checklists. Data analysis was carried out using Microsoft Excel and EpiInfo, with spatial mapping in ArcGIS Pro.</p><p><strong>Results: </strong>Out of the 423 studies reviewed, 44 fulfilled our inclusion criteria, providing data on 174 human outbreaks (1778 cases, 130 fatalities) and 1775 animal outbreaks (7818 deaths). We identified key hotspots for human anthrax in West Bengal, Odisha, and Andhra Pradesh, and significant hotspots for animal anthrax in Karnataka, Andhra Pradesh, Tamil Nadu, and West Bengal. Majority of human outbreaks were reported between March and June, whereas the majority of animal outbreaks were reported between June and September. A strong correlation was observed between rainfall and animal outbreaks in the eastern region (correlation coefficient of 0.94).</p><p><strong>Conclusion: </strong>The study highlights key hotspots for human and animal anthrax and discrepancies in human and animal anthrax reporting and gaps in surveillance. There is a critical need for enhanced One Health surveillance and animal anthrax vaccination programs for effective management and mitigate the disease. These strategies are essential not only for public health and livestock welfare in India but also for global health security.</p>","PeriodicalId":9007,"journal":{"name":"BioMed Research International","volume":"2025 ","pages":"5633425"},"PeriodicalIF":2.3,"publicationDate":"2025-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719797/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145817770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
BioMed Research International
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1