首页 > 最新文献

Scientific Reports最新文献

英文 中文
Nature-based Solutions as Building Blocks for coastal flood risk reduction: a model-based ecosystem service assessment.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-09 DOI: 10.1038/s41598-025-95230-4
Massimiliano Marino, Martin J Baptist, Ahmad I K Alkharoubi, Sofia Nasca, Luca Cavallaro, Enrico Foti, Rosaria Ester Musumeci

Nature-based Solutions (NbS) are increasingly recognized as effective measures for mitigating flood risks and enhancing climate change adaptation. However, evaluating their efficacy in delivering flood risk reduction ecosystem service (FRR-ESS) is usually limited by reliance on qualitative, expert-based "quick-scan" scoring methods. While already challenging for present-day evaluations, this limitation becomes even more significant when addressing future climate scenarios, introducing deep uncertainties in the evaluation. The present study introduces a model-based framework to quantify FRR-ESS provided by coastal NbS, which integrates expert-based assessments with quantitative results from an eco-hydro-morphodynamic numerical model. The model enables a comparative evaluation of individual and combined effects of NbS following a Building Blocks approach. By integrating habitat map change prediction in the evaluation, NbS flood reduction response to present and future storm scenarios (i.e. wave climate and sea level rise) are investigated. The methodology is applied to a Mediterranean coastal lagoon in Sicily (Italy), and can be easily adapted to diverse coastal ecosystems. Our findings underscore the significant role of coastal habitats in reducing flood risk and highlight the importance of integrating physically-based modelling into FRR-ESS evaluation. This approach provides a robust and flexible tool for policymakers and stakeholders to make informed decisions that support both ecological sustainability and disaster risk reduction.

{"title":"Nature-based Solutions as Building Blocks for coastal flood risk reduction: a model-based ecosystem service assessment.","authors":"Massimiliano Marino, Martin J Baptist, Ahmad I K Alkharoubi, Sofia Nasca, Luca Cavallaro, Enrico Foti, Rosaria Ester Musumeci","doi":"10.1038/s41598-025-95230-4","DOIUrl":"https://doi.org/10.1038/s41598-025-95230-4","url":null,"abstract":"<p><p>Nature-based Solutions (NbS) are increasingly recognized as effective measures for mitigating flood risks and enhancing climate change adaptation. However, evaluating their efficacy in delivering flood risk reduction ecosystem service (FRR-ESS) is usually limited by reliance on qualitative, expert-based \"quick-scan\" scoring methods. While already challenging for present-day evaluations, this limitation becomes even more significant when addressing future climate scenarios, introducing deep uncertainties in the evaluation. The present study introduces a model-based framework to quantify FRR-ESS provided by coastal NbS, which integrates expert-based assessments with quantitative results from an eco-hydro-morphodynamic numerical model. The model enables a comparative evaluation of individual and combined effects of NbS following a Building Blocks approach. By integrating habitat map change prediction in the evaluation, NbS flood reduction response to present and future storm scenarios (i.e. wave climate and sea level rise) are investigated. The methodology is applied to a Mediterranean coastal lagoon in Sicily (Italy), and can be easily adapted to diverse coastal ecosystems. Our findings underscore the significant role of coastal habitats in reducing flood risk and highlight the importance of integrating physically-based modelling into FRR-ESS evaluation. This approach provides a robust and flexible tool for policymakers and stakeholders to make informed decisions that support both ecological sustainability and disaster risk reduction.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12070"},"PeriodicalIF":3.8,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neural insights on expert surgeons' mental workload during live robotic surgeries. 从神经角度洞察专家外科医生在实时机器人手术中的脑力劳动负荷。
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-09 DOI: 10.1038/s41598-025-96064-w
Chiho Lim, Marian Obuseh, Jackie Cha, James Steward, Chandru Sundaram, Denny Yu

Despite its adoption and benefits, robotic surgeries can impose additional mental workload on surgeons. Validated questionnaires mostly administered at the end of procedures may not accurately capture the dynamic nature of mental workload over an entire procedure. Hence, we sought to determine if electroencephalogram (EEG) based neural activities in different brain regions can measure variations in expert surgeons' mental workload intraoperatively. EEG data was collected from five different surgeons performing 13 robotic-assisted urological procedures. Data analysis focused on three surgery phases (before, critical, and after). After performing each phase, surgeons provided a rating of their perceived mental workload. A linear mixed effects model was applied to explore the impact of the study phases on the relative spectral band power of EEG signals. The relative theta band power in the frontal brain region was highest during the critical portions of the procedure (p < 0.05). As the subjective ratings increased, the relative frontal theta band power increased (p < 0.001) while the relative parietal alpha band power decreased across all phases. We show that EEG signals can distinguish intraoperative workload in robotic surgeries. This has several applications including predicting risk factors for increased case complexity and surgical education.

尽管机器人手术被广泛采用并带来诸多益处,但它仍会给外科医生带来额外的脑力劳动负担。经过验证的调查问卷大多在手术结束时进行,可能无法准确捕捉整个手术过程中脑力劳动负荷的动态性质。因此,我们试图确定基于脑电图(EEG)的不同脑区神经活动是否能测量专家外科医生术中心理工作量的变化。我们收集了五位不同外科医生的脑电图数据,他们共进行了 13 例机器人辅助泌尿外科手术。数据分析集中在三个手术阶段(术前、关键和术后)。在完成每个阶段的手术后,外科医生对其感知到的心理工作量进行评分。研究人员采用线性混合效应模型来探讨研究阶段对脑电图信号相对频带功率的影响。在手术的关键部分,额叶脑区的相对θ波段功率最高(p
{"title":"Neural insights on expert surgeons' mental workload during live robotic surgeries.","authors":"Chiho Lim, Marian Obuseh, Jackie Cha, James Steward, Chandru Sundaram, Denny Yu","doi":"10.1038/s41598-025-96064-w","DOIUrl":"https://doi.org/10.1038/s41598-025-96064-w","url":null,"abstract":"<p><p>Despite its adoption and benefits, robotic surgeries can impose additional mental workload on surgeons. Validated questionnaires mostly administered at the end of procedures may not accurately capture the dynamic nature of mental workload over an entire procedure. Hence, we sought to determine if electroencephalogram (EEG) based neural activities in different brain regions can measure variations in expert surgeons' mental workload intraoperatively. EEG data was collected from five different surgeons performing 13 robotic-assisted urological procedures. Data analysis focused on three surgery phases (before, critical, and after). After performing each phase, surgeons provided a rating of their perceived mental workload. A linear mixed effects model was applied to explore the impact of the study phases on the relative spectral band power of EEG signals. The relative theta band power in the frontal brain region was highest during the critical portions of the procedure (p < 0.05). As the subjective ratings increased, the relative frontal theta band power increased (p < 0.001) while the relative parietal alpha band power decreased across all phases. We show that EEG signals can distinguish intraoperative workload in robotic surgeries. This has several applications including predicting risk factors for increased case complexity and surgical education.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12073"},"PeriodicalIF":3.8,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
RBM24 regulates apoptosis rates by modulating global transcriptome profile in CAL27 cells.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-09 DOI: 10.1038/s41598-025-96932-5
Jingjing Sun, Shuyuan Wang, Shumin Peng, Tingting Gao, Zhenjie Gao

RNA binding proteins (RBPs) are key factors regulating post-transcriptional events. Categorized as RBPs, RBM24 expression levels have been shown to be a prognosis-related pivotal gene in oral squamous cell carcinoma. We analyzed the binding targets and regulated post-transcriptional events of RBM24 in RBM24-overexpressing cell lines and controls using iRIP-seq and RNA-seq. RBM24-overexpressing cells showed significant changes in gene expression, which are involved in biological pathways related to apoptosis and immune inflammation. RBM24-regulated genes that undergo alternative splicing are primarily engaged in biological processes related to DNA damage repair and RNA metabolism. More notably, we found that RBM24 binds to lncRNAs in addition to pre-mRNAs. These results indicated that RBM24 could play a key role in cancer progression by finding clinical therapeutic targets for Oral squamous cell carcinoma.

{"title":"RBM24 regulates apoptosis rates by modulating global transcriptome profile in CAL27 cells.","authors":"Jingjing Sun, Shuyuan Wang, Shumin Peng, Tingting Gao, Zhenjie Gao","doi":"10.1038/s41598-025-96932-5","DOIUrl":"https://doi.org/10.1038/s41598-025-96932-5","url":null,"abstract":"<p><p>RNA binding proteins (RBPs) are key factors regulating post-transcriptional events. Categorized as RBPs, RBM24 expression levels have been shown to be a prognosis-related pivotal gene in oral squamous cell carcinoma. We analyzed the binding targets and regulated post-transcriptional events of RBM24 in RBM24-overexpressing cell lines and controls using iRIP-seq and RNA-seq. RBM24-overexpressing cells showed significant changes in gene expression, which are involved in biological pathways related to apoptosis and immune inflammation. RBM24-regulated genes that undergo alternative splicing are primarily engaged in biological processes related to DNA damage repair and RNA metabolism. More notably, we found that RBM24 binds to lncRNAs in addition to pre-mRNAs. These results indicated that RBM24 could play a key role in cancer progression by finding clinical therapeutic targets for Oral squamous cell carcinoma.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12069"},"PeriodicalIF":3.8,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812278","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Subclonal response heterogeneity to define cancer organoid therapeutic sensitivity.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-09 DOI: 10.1038/s41598-025-96204-2
Jeremy D Kratz, Shujah Rehman, Katherine A Johnson, Amani A Gillette, Aishwarya Sunil, Peter F Favreau, Cheri A Pasch, Devon Miller, Lucas C Zarling, Austin H Yeung, Linda Clipson, Samantha J Anderson, Alyssa K Steimle, Carley M Sprackling, Kayla K Lemmon, Daniel E Abbott, Mark E Burkard, Michael F Bassetti, Jens C Eickhoff, Eugene F Foley, Charles P Heise, Randall J Kimple, Elise H Lawson, Noelle K LoConte, Sam J Lubner, Daniel L Mulkerin, Kristina A Matkowskyj, Cristina B Sanger, Nataliya V Uboha, Sean J Mcilwain, Irene M Ong, Evie H Carchman, Melissa C Skala, Dustin A Deming

Tumor heterogeneity is predicted to confer inferior clinical outcomes with precision-based strategies, however, modeling heterogeneity in a manner that still represents the tumor of origin remains a formidable challenge. Sequencing technologies are limited in their ability to identify rare subclonal populations and predict response to treatments for patients. Patient-derived organotypic cultures have significantly improved the modeling of cancer biology by faithfully representing the molecular features of primary malignant tissues. Patient-derived cancer organoid (PCO) cultures contain subclonal populations with the potential to recapitulate heterogeneity, although treatment response assessments commonly ignore diversity in the molecular profile or treatment response. Here, we demonstrate the advantage of evaluating individual PCO heterogeneity to enhance the sensitivity of these assays for predicting clinical response. Additionally, organoid subcultures identify subclonal populations with altered treatment response. Finally, dose escalation studies of PCOs to targeted anti-EGFR therapy are utilized which reveal divergent pathway expression when compared to pretreatment cultures. Overall, these studies demonstrate the importance of population-based organoid response assessments, the use of PCOs to identify molecular heterogeneity not observed with bulk tumor sequencing, and PCO heterogeneity for understanding therapeutic resistance mechanisms.

{"title":"Subclonal response heterogeneity to define cancer organoid therapeutic sensitivity.","authors":"Jeremy D Kratz, Shujah Rehman, Katherine A Johnson, Amani A Gillette, Aishwarya Sunil, Peter F Favreau, Cheri A Pasch, Devon Miller, Lucas C Zarling, Austin H Yeung, Linda Clipson, Samantha J Anderson, Alyssa K Steimle, Carley M Sprackling, Kayla K Lemmon, Daniel E Abbott, Mark E Burkard, Michael F Bassetti, Jens C Eickhoff, Eugene F Foley, Charles P Heise, Randall J Kimple, Elise H Lawson, Noelle K LoConte, Sam J Lubner, Daniel L Mulkerin, Kristina A Matkowskyj, Cristina B Sanger, Nataliya V Uboha, Sean J Mcilwain, Irene M Ong, Evie H Carchman, Melissa C Skala, Dustin A Deming","doi":"10.1038/s41598-025-96204-2","DOIUrl":"https://doi.org/10.1038/s41598-025-96204-2","url":null,"abstract":"<p><p>Tumor heterogeneity is predicted to confer inferior clinical outcomes with precision-based strategies, however, modeling heterogeneity in a manner that still represents the tumor of origin remains a formidable challenge. Sequencing technologies are limited in their ability to identify rare subclonal populations and predict response to treatments for patients. Patient-derived organotypic cultures have significantly improved the modeling of cancer biology by faithfully representing the molecular features of primary malignant tissues. Patient-derived cancer organoid (PCO) cultures contain subclonal populations with the potential to recapitulate heterogeneity, although treatment response assessments commonly ignore diversity in the molecular profile or treatment response. Here, we demonstrate the advantage of evaluating individual PCO heterogeneity to enhance the sensitivity of these assays for predicting clinical response. Additionally, organoid subcultures identify subclonal populations with altered treatment response. Finally, dose escalation studies of PCOs to targeted anti-EGFR therapy are utilized which reveal divergent pathway expression when compared to pretreatment cultures. Overall, these studies demonstrate the importance of population-based organoid response assessments, the use of PCOs to identify molecular heterogeneity not observed with bulk tumor sequencing, and PCO heterogeneity for understanding therapeutic resistance mechanisms.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12072"},"PeriodicalIF":3.8,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The relationship between the triglyceride-glucose (TyG) index and all-cause mortality in ICU patients with primary hypertension: a retrospective study.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-09 DOI: 10.1038/s41598-025-96202-4
Jiacheng Ding, Jingqian Li, Xinyu Cai, Kai Zhang, Shi Yu, Keyan Liu, Maoxun Huang

Primary hypertension is the most common type of hypertension, with a complex and not fully understood pathogenesis. Insulin resistance (IR) is a metabolic abnormality that has been shown to be quite prevalent among patients with hypertension in existing literature. The triglyceride-glucose (TyG) index is a reliable indicator for assessing insulin resistance (IR). This study aims to evaluate the relationship between the TyG index at admission and all-cause mortality (ACM) in patients with severe primary hypertension, and to explore its role in predicting the future all-cause mortality risk in primary hypertension patients. This study employs a retrospective design to categorize all patients into four quartiles based on the TyG index. The Kaplan-Meier (K-M) method was utilized to estimate the survival curves for each group and to compare the survival outcomes across different quartiles. To assess the nonlinear relationship between the TyG index and prognosis, Cox proportional hazards regression models and restricted cubic splines (RCS) were applied, adjusting for potential confounders. Additionally, subgroup analyses were performed to conduct stratified analyses and interaction tests. Kaplan-Meier survival curve analysis showed that patients with higher TyG index levels had higher all-cause mortality rates at 30 days, 60 days, and 90 days post-admission. This indicates that a higher TyG index is associated with an increased risk of death in the short term. Additionally, multivariate Cox proportional hazards regression analysis revealed that an increased TyG index was significantly associated with all-cause mortality at 30 days, 60 days, and 90 days. Meanwhile, RCS analysis indicates that as the TyG index level increases, the hazard ratio (HR) shows a significant upward trend, suggesting a gradual increase in the risk of all-cause mortality. In summary, among patients with primary hypertension in the intensive care unit, elevated TyG levels are associated with an increased risk of short-term mortality.

{"title":"The relationship between the triglyceride-glucose (TyG) index and all-cause mortality in ICU patients with primary hypertension: a retrospective study.","authors":"Jiacheng Ding, Jingqian Li, Xinyu Cai, Kai Zhang, Shi Yu, Keyan Liu, Maoxun Huang","doi":"10.1038/s41598-025-96202-4","DOIUrl":"https://doi.org/10.1038/s41598-025-96202-4","url":null,"abstract":"<p><p>Primary hypertension is the most common type of hypertension, with a complex and not fully understood pathogenesis. Insulin resistance (IR) is a metabolic abnormality that has been shown to be quite prevalent among patients with hypertension in existing literature. The triglyceride-glucose (TyG) index is a reliable indicator for assessing insulin resistance (IR). This study aims to evaluate the relationship between the TyG index at admission and all-cause mortality (ACM) in patients with severe primary hypertension, and to explore its role in predicting the future all-cause mortality risk in primary hypertension patients. This study employs a retrospective design to categorize all patients into four quartiles based on the TyG index. The Kaplan-Meier (K-M) method was utilized to estimate the survival curves for each group and to compare the survival outcomes across different quartiles. To assess the nonlinear relationship between the TyG index and prognosis, Cox proportional hazards regression models and restricted cubic splines (RCS) were applied, adjusting for potential confounders. Additionally, subgroup analyses were performed to conduct stratified analyses and interaction tests. Kaplan-Meier survival curve analysis showed that patients with higher TyG index levels had higher all-cause mortality rates at 30 days, 60 days, and 90 days post-admission. This indicates that a higher TyG index is associated with an increased risk of death in the short term. Additionally, multivariate Cox proportional hazards regression analysis revealed that an increased TyG index was significantly associated with all-cause mortality at 30 days, 60 days, and 90 days. Meanwhile, RCS analysis indicates that as the TyG index level increases, the hazard ratio (HR) shows a significant upward trend, suggesting a gradual increase in the risk of all-cause mortality. In summary, among patients with primary hypertension in the intensive care unit, elevated TyG levels are associated with an increased risk of short-term mortality.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12071"},"PeriodicalIF":3.8,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of patients with decreased general condition and comparing HOTEL, WPS, and REMS for mortality prediction.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-08 DOI: 10.1038/s41598-025-97386-5
Emine Aykol, Mehmet Cihat Demir, Kudret Selki, Hasan Sultanoğlu

The emergency department (ED) plays a crucial role in evaluating patients with decreased general condition (DGC). Prompt diagnosis and precise risk stratification enhances clinical care outcomes. This study aimed to reveal which scoring system is better for predicting mortality in patients with DGC. This single-center prospective study was conducted between 1 March 2021 and 1 June 2021 in a tertiary university hospital's ED. All patients presented with DGC were included. The scores assessed upon ED admission for patients include the Hypotension, Oxygen saturation, low Temperature, ECG changes, and Loss of independence, abbreviated as HOTEL score, Rapid Emergency Medicine Score (REMS), and the Worthing Physiological Scoring (WPS). The study aimed to compare the scoring systems to identify which is the best mortality predictor. Independent risk factors for 30-day mortality were analyzed using binary logistic regression and ROC curves to assess the effectiveness of HOTEL, REMS, and WPS scores in predicting mortality. The study was conducted with 137 DGC patients. The median age of patients presented to the ED with DGC was 77 (66.5-87), and 50.4% were male. 52.6% of patients died within one month. Analysis of mortality risk factors revealed that gender, age, day of admission, visit type, home oxygen, urinary catheter use, and speech status were not independent risk factors. For one-month mortality prediction, AUCs were: HOTEL 0.644 (cut-off 1), REMS 0.635 (cut-off 8), WPS 0.547 (cut-off 5). For mechanical ventilation: HOTEL 0.689 (10), REMS 0.790 (10), WPS 0.777 (4). For ICU admission: HOTEL 0.697 (2), REMS 0.770 (9), WPS 0.728 (4). Both the HOTEL and REMS scoring systems have moderate prognostic value in predicting mortality in patients with a DGC. The REMS, and WPS scores are also more helpful in determining the need for intensive care unit admission and mechanical ventilation.

{"title":"Evaluation of patients with decreased general condition and comparing HOTEL, WPS, and REMS for mortality prediction.","authors":"Emine Aykol, Mehmet Cihat Demir, Kudret Selki, Hasan Sultanoğlu","doi":"10.1038/s41598-025-97386-5","DOIUrl":"https://doi.org/10.1038/s41598-025-97386-5","url":null,"abstract":"<p><p>The emergency department (ED) plays a crucial role in evaluating patients with decreased general condition (DGC). Prompt diagnosis and precise risk stratification enhances clinical care outcomes. This study aimed to reveal which scoring system is better for predicting mortality in patients with DGC. This single-center prospective study was conducted between 1 March 2021 and 1 June 2021 in a tertiary university hospital's ED. All patients presented with DGC were included. The scores assessed upon ED admission for patients include the Hypotension, Oxygen saturation, low Temperature, ECG changes, and Loss of independence, abbreviated as HOTEL score, Rapid Emergency Medicine Score (REMS), and the Worthing Physiological Scoring (WPS). The study aimed to compare the scoring systems to identify which is the best mortality predictor. Independent risk factors for 30-day mortality were analyzed using binary logistic regression and ROC curves to assess the effectiveness of HOTEL, REMS, and WPS scores in predicting mortality. The study was conducted with 137 DGC patients. The median age of patients presented to the ED with DGC was 77 (66.5-87), and 50.4% were male. 52.6% of patients died within one month. Analysis of mortality risk factors revealed that gender, age, day of admission, visit type, home oxygen, urinary catheter use, and speech status were not independent risk factors. For one-month mortality prediction, AUCs were: HOTEL 0.644 (cut-off 1), REMS 0.635 (cut-off 8), WPS 0.547 (cut-off 5). For mechanical ventilation: HOTEL 0.689 (10), REMS 0.790 (10), WPS 0.777 (4). For ICU admission: HOTEL 0.697 (2), REMS 0.770 (9), WPS 0.728 (4). Both the HOTEL and REMS scoring systems have moderate prognostic value in predicting mortality in patients with a DGC. The REMS, and WPS scores are also more helpful in determining the need for intensive care unit admission and mechanical ventilation.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"11956"},"PeriodicalIF":3.8,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812186","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A dynamic nonlinear flow algorithm to model patient flow.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-08 DOI: 10.1038/s41598-025-96536-z
Arsineh Boodaghian Asl, Jayanth Raghothama, Adam S Darwich, Sebastiaan Meijer

Hospitals are complex systems, and the flow of patients is dynamic and nonlinear in such systems. Network representation allows flow algorithms to observe bottlenecks as candidates for optimisation. To model the dynamic behaviour of the patient flow, we need to consider the variability in arrival rates and service times (length of stay). Previously proposed dynamic flow algorithms mainly focused on arrival and departure rates, inflow and outflow, edges' and vertices' capacity, and routing, with applications mainly in transportation and telecommunication. In hospitals, bottlenecks that emerge from the patients' flow are a result of the vertices (wards) behaviour defined by capacity (beds), number of servers (staff), service time variability, and edges (care pathways) distribution probability. We offer a modified flow algorithm that takes a hospital network, iterates over the patients' arrival rates, and measures the flow with respect to vertices' capacities, servers, service time variability, edge capacity, and distribution probability. The result is a dynamic residual graph to measure the bottlenecks' persistency and severity, identify the root causes of bottlenecks, and wards' dynamic nonlinear behaviour. The algorithm provides a quick holistic view of hospital performance and the analysis of the edges and vertices' behaviour over time.

{"title":"A dynamic nonlinear flow algorithm to model patient flow.","authors":"Arsineh Boodaghian Asl, Jayanth Raghothama, Adam S Darwich, Sebastiaan Meijer","doi":"10.1038/s41598-025-96536-z","DOIUrl":"https://doi.org/10.1038/s41598-025-96536-z","url":null,"abstract":"<p><p>Hospitals are complex systems, and the flow of patients is dynamic and nonlinear in such systems. Network representation allows flow algorithms to observe bottlenecks as candidates for optimisation. To model the dynamic behaviour of the patient flow, we need to consider the variability in arrival rates and service times (length of stay). Previously proposed dynamic flow algorithms mainly focused on arrival and departure rates, inflow and outflow, edges' and vertices' capacity, and routing, with applications mainly in transportation and telecommunication. In hospitals, bottlenecks that emerge from the patients' flow are a result of the vertices (wards) behaviour defined by capacity (beds), number of servers (staff), service time variability, and edges (care pathways) distribution probability. We offer a modified flow algorithm that takes a hospital network, iterates over the patients' arrival rates, and measures the flow with respect to vertices' capacities, servers, service time variability, edge capacity, and distribution probability. The result is a dynamic residual graph to measure the bottlenecks' persistency and severity, identify the root causes of bottlenecks, and wards' dynamic nonlinear behaviour. The algorithm provides a quick holistic view of hospital performance and the analysis of the edges and vertices' behaviour over time.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12052"},"PeriodicalIF":3.8,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Entanglement detection with quantum support vector machine (QSVM) on near-term quantum devices.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-08 DOI: 10.1038/s41598-025-95897-9
Mahmoud Mahdian, Zahra Mousavi

Detecting and quantifying quantum entanglement remain significant challenges in the noisy intermediate-scale quantum (NISQ) era. This study presents the implementation of quantum support vector machines (QSVMs) on IBM quantum devices to identify and classify entangled states. By employing quantum variational circuits, the proposed framework achieves a runtime complexity of [Formula: see text], where N is the number of qubits, t is the number of iterations, and ε is the acceptable error margin. We investigate various quantum circuits with multiple blocks and obtain the accuracy of QSVM as measures of expressibility and entangling capability. Our results demonstrate that the QSVM framework achieves over 90% accuracy in distinguishing entangled states, despite hardware noise such as decoherence and gate errors. Benchmarks across superconducting qubit platforms (e.g., IBM Perth, Lagos, and Nairobi) highlight the robustness of the model. Furthermore, the QSVM framework effectively classifies two-qubit states and extends its predictive capabilities to three-qubit entangled states. This work marks a significant advancement in quantum machine learning for entanglement detection.

{"title":"Entanglement detection with quantum support vector machine (QSVM) on near-term quantum devices.","authors":"Mahmoud Mahdian, Zahra Mousavi","doi":"10.1038/s41598-025-95897-9","DOIUrl":"https://doi.org/10.1038/s41598-025-95897-9","url":null,"abstract":"<p><p>Detecting and quantifying quantum entanglement remain significant challenges in the noisy intermediate-scale quantum (NISQ) era. This study presents the implementation of quantum support vector machines (QSVMs) on IBM quantum devices to identify and classify entangled states. By employing quantum variational circuits, the proposed framework achieves a runtime complexity of [Formula: see text], where N is the number of qubits, t is the number of iterations, and ε is the acceptable error margin. We investigate various quantum circuits with multiple blocks and obtain the accuracy of QSVM as measures of expressibility and entangling capability. Our results demonstrate that the QSVM framework achieves over 90% accuracy in distinguishing entangled states, despite hardware noise such as decoherence and gate errors. Benchmarks across superconducting qubit platforms (e.g., IBM Perth, Lagos, and Nairobi) highlight the robustness of the model. Furthermore, the QSVM framework effectively classifies two-qubit states and extends its predictive capabilities to three-qubit entangled states. This work marks a significant advancement in quantum machine learning for entanglement detection.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"11931"},"PeriodicalIF":3.8,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812198","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Femtosecond laser microfabrication of a fully-integrated optofluidic device for 3D imaging flow cytometry.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-08 DOI: 10.1038/s41598-025-93118-x
Federico Sala, Petra Paiè, Alessia Candeo, Francesco Ceccarelli, Roberto Osellame, Andrea Bassi, Francesca Bragheri

In recent years imaging flow cytometry (IFC) is gaining increasing attention as it combines the characteristics of conventional flow cytometry with optical microscopy techniques, allowing for high-throughput, multi-parameter screening of single cell populations. In the field of biology, the always increasing demand for high content morphological and spatial information led to the development of systems for volumetric imaging. However, current 3D IFC systems are often limited by the incompatibility with available microfluidic devices or by instrumental complexity that might lead to optical misalignment or mechanical instabilities in day-by-day operation. To this end, here we demonstrate the importance of advancing the laser fabrication technique by reporting on a fully integrated optofluidic platform composed of a borosilicate glass chip encompassing reconfigurable integrated photonic circuits for patterned light generation, bonded to a fused silica glass chip incorporating cylindrical hollow lenses, for light-sheet illumination, perfectly aligned to a microchannel where the sample under investigation flows. The system is capable of high-resolution imaging flow cytometry by implementing structured light sheet microscopy in a heterogeneously integrated platform with unprecedented stability. All the components are realized by femtosecond laser irradiation followed by chemical etching. The extreme level of integration permitted by the advanced optimization of the laser fabrication technique allowed the reduction of the assembled components and the absence of moving parts, thus ensuring durable alignment as well as mechanical and thermal stability both in short and long-term operation of the device, for the automated fluorescence signal acquisition during the sample flow.

{"title":"Femtosecond laser microfabrication of a fully-integrated optofluidic device for 3D imaging flow cytometry.","authors":"Federico Sala, Petra Paiè, Alessia Candeo, Francesco Ceccarelli, Roberto Osellame, Andrea Bassi, Francesca Bragheri","doi":"10.1038/s41598-025-93118-x","DOIUrl":"https://doi.org/10.1038/s41598-025-93118-x","url":null,"abstract":"<p><p>In recent years imaging flow cytometry (IFC) is gaining increasing attention as it combines the characteristics of conventional flow cytometry with optical microscopy techniques, allowing for high-throughput, multi-parameter screening of single cell populations. In the field of biology, the always increasing demand for high content morphological and spatial information led to the development of systems for volumetric imaging. However, current 3D IFC systems are often limited by the incompatibility with available microfluidic devices or by instrumental complexity that might lead to optical misalignment or mechanical instabilities in day-by-day operation. To this end, here we demonstrate the importance of advancing the laser fabrication technique by reporting on a fully integrated optofluidic platform composed of a borosilicate glass chip encompassing reconfigurable integrated photonic circuits for patterned light generation, bonded to a fused silica glass chip incorporating cylindrical hollow lenses, for light-sheet illumination, perfectly aligned to a microchannel where the sample under investigation flows. The system is capable of high-resolution imaging flow cytometry by implementing structured light sheet microscopy in a heterogeneously integrated platform with unprecedented stability. All the components are realized by femtosecond laser irradiation followed by chemical etching. The extreme level of integration permitted by the advanced optimization of the laser fabrication technique allowed the reduction of the assembled components and the absence of moving parts, thus ensuring durable alignment as well as mechanical and thermal stability both in short and long-term operation of the device, for the automated fluorescence signal acquisition during the sample flow.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"11950"},"PeriodicalIF":3.8,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genetic association between glucocorticoid receptor gene Bcl1 rs41423247 and rs6198 polymorphisms and risk of obesity in Egyptian children : By.
IF 3.8 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Pub Date : 2025-04-08 DOI: 10.1038/s41598-025-94447-7
Nanees A Salem, Angi A Alwakeel, Mayada Abdel-Latif, Shaimaa R Hendawy, Mai S Korkor

Obesity represents a major global public-health problem during childhood and adolescence. The genetic contribution to obesity and its consequences is well-established. Variation in glucocorticoid (GC)-sensitivity can be partly explained by polymorphisms in GC receptor (GR) gene where NR3C1; Bcl1 rs41423247 and NR3C1 rs6198 single nucleotide polymorphisms (SNPs) have been linked to higher and lower GC sensitivity, respectively. We aimed to explore the potential association between the GR gene SNPs and risk of obesity in a cohort of Egyptian children. We included 100 pre-pubertal children; 60 obese children and 40 age-and sex-matched normal-weight controls. Bcl1 rs41423247 SNP was genotyped using PCR-restriction fragment length polymorphism technique and NR3C1 rs6198 SNP was genotyped using Real-time-PCR.In Bcl1 rs41423247, obese children had more frequent CG, GG genotypes and G allele compared to healthy controls (P = 0.039, 0.019 and 0.007 respectively). Moreover, insulin resistance was significantly higher in combined CG + GG group compared to CC group. On the contrary, no significant differences were found in genotypes, alleles frequencies or insulin resistance between obese and non-obese children in NR3C1 rs6198. GR Bcl1 rs41423247 gene polymorphism may play a role in genetic susceptibility to obesity that can be a future targeted therapy for obesity.

{"title":"Genetic association between glucocorticoid receptor gene Bcl1 rs41423247 and rs6198 polymorphisms and risk of obesity in Egyptian children : By.","authors":"Nanees A Salem, Angi A Alwakeel, Mayada Abdel-Latif, Shaimaa R Hendawy, Mai S Korkor","doi":"10.1038/s41598-025-94447-7","DOIUrl":"https://doi.org/10.1038/s41598-025-94447-7","url":null,"abstract":"<p><p>Obesity represents a major global public-health problem during childhood and adolescence. The genetic contribution to obesity and its consequences is well-established. Variation in glucocorticoid (GC)-sensitivity can be partly explained by polymorphisms in GC receptor (GR) gene where NR3C1; Bcl1 rs41423247 and NR3C1 rs6198 single nucleotide polymorphisms (SNPs) have been linked to higher and lower GC sensitivity, respectively. We aimed to explore the potential association between the GR gene SNPs and risk of obesity in a cohort of Egyptian children. We included 100 pre-pubertal children; 60 obese children and 40 age-and sex-matched normal-weight controls. Bcl1 rs41423247 SNP was genotyped using PCR-restriction fragment length polymorphism technique and NR3C1 rs6198 SNP was genotyped using Real-time-PCR.In Bcl1 rs41423247, obese children had more frequent CG, GG genotypes and G allele compared to healthy controls (P = 0.039, 0.019 and 0.007 respectively). Moreover, insulin resistance was significantly higher in combined CG + GG group compared to CC group. On the contrary, no significant differences were found in genotypes, alleles frequencies or insulin resistance between obese and non-obese children in NR3C1 rs6198. GR Bcl1 rs41423247 gene polymorphism may play a role in genetic susceptibility to obesity that can be a future targeted therapy for obesity.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"12012"},"PeriodicalIF":3.8,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143812268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Scientific Reports
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:481959085
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