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1.
Methods Mol Biol ; 2856: 157-176, 2025.
Article in English | MEDLINE | ID: mdl-39283451

ABSTRACT

Hi-C and 3C-seq are powerful tools to study the 3D genomes of bacteria and archaea, whose small cell sizes and growth conditions are often intractable to detailed microscopic analysis. However, the circularity of prokaryotic genomes requires a number of tricks for Hi-C/3C-seq data analysis. Here, I provide a practical guide to use the HiC-Pro pipeline for Hi-C/3C-seq data obtained from prokaryotes.


Subject(s)
Genome, Bacterial , Software , Genomics/methods , High-Throughput Nucleotide Sequencing/methods , Prokaryotic Cells/metabolism , Genome, Archaeal , Archaea/genetics , Bacteria/genetics , Computational Biology/methods , Data Analysis
2.
F1000Res ; 13: 490, 2024.
Article in English | MEDLINE | ID: mdl-39238832

ABSTRACT

This research explores the application of quadratic polynomials in Python for advanced data analysis. The study demonstrates how quadratic models can effectively capture nonlinear relationships in complex datasets by leveraging Python libraries such as NumPy, Matplotlib, scikit-learn, and Pandas. The methodology involves fitting quadratic polynomials to the data using least-squares regression and evaluating the model fit using the coefficient of determination (R-squared). The results highlight the strong performance of the quadratic polynomial fit, as evidenced by high R-squared values, indicating the model's ability to explain a substantial proportion of the data variability. Comparisons with linear and cubic models further underscore the quadratic model's balance between simplicity and precision for many practical applications. The study also acknowledges the limitations of quadratic polynomials and proposes future research directions to enhance their accuracy and efficiency for diverse data analysis tasks. This research bridges the gap between theoretical concepts and practical implementation, providing an accessible Python-based tool for leveraging quadratic polynomials in data analysis.


This study examines how quadratic polynomials, which are mathematical equations used to model and understand patterns in data, can be effectively applied using Python, a versatile programming language with libraries suited for mathematical and visual analysis. Researchers have focused on the adaptability of these polynomials in various fields, from software analytics to materials science, in order to provide practical Python code examples. They also discussed the predictive accuracy of the method, confirmed through a statistical measure called R-squared, and acknowledged the need for future research to integrate more complex models for richer data interpretation.


Subject(s)
Data Analysis , Algorithms , Software , Least-Squares Analysis , Models, Statistical
3.
Biom J ; 66(7): e202300363, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39330918

ABSTRACT

Functional data analysis (FDA) is a statistical framework that allows for the analysis of curves, images, or functions on higher dimensional domains. The goals of FDA, such as descriptive analyses, classification, and regression, are generally the same as for statistical analyses of scalar-valued or multivariate data, but FDA brings additional challenges due to the high- and infinite dimensionality of observations and parameters, respectively. This paper provides an introduction to FDA, including a description of the most common statistical analysis techniques, their respective software implementations, and some recent developments in the field. The paper covers fundamental concepts such as descriptives and outliers, smoothing, amplitude and phase variation, and functional principal component analysis. It also discusses functional regression, statistical inference with functional data, functional classification and clustering, and machine learning approaches for functional data analysis. The methods discussed in this paper are widely applicable in fields such as medicine, biophysics, neuroscience, and chemistry and are increasingly relevant due to the widespread use of technologies that allow for the collection of functional data. Sparse functional data methods are also relevant for longitudinal data analysis. All presented methods are demonstrated using available software in R by analyzing a dataset on human motion and motor control. To facilitate the understanding of the methods, their implementation, and hands-on application, the code for these practical examples is made available through a code and data supplement and on GitHub.


Subject(s)
Biometry , Biometry/methods , Data Analysis , Machine Learning , Humans , Software , Principal Component Analysis
4.
Sci Rep ; 14(1): 21461, 2024 09 13.
Article in English | MEDLINE | ID: mdl-39271749

ABSTRACT

The analysis of eye movements has proven valuable for understanding brain function and the neuropathology of various disorders. This research aims to utilize eye movement data analysis as a screening tool for differentiation between eight different groups of pathologies, including scholar, neurologic, and postural disorders. Leveraging a dataset from 20 clinical centers, all employing AIDEAL and REMOBI eye movement technologies this study extends prior research by considering a multi-annotation setting, incorporating information from recordings from saccade and vergence eye movement tests, and using contextual information (e.g. target signals and latency of the eye movement relative to the target and confidence level of the quality of eye movement recording) to improve accuracy while reducing noise interference. Additionally, we introduce a novel hybrid architecture that combines the weight-sharing feature of convolution layers with the long-range capabilities of the transformer architecture to improve model efficiency and reduce the computation cost by a factor of 3.36, while still being competitive in terms of macro F1 score. Evaluated on two diverse datasets, our method demonstrates promising results, the most powerful discrimination being Attention & Neurologic; with a macro F1 score of up to 78.8%; disorder. The results indicate the effectiveness of our approach in classifying eye movement data from different pathologies and different clinical centers accurately, thus enabling the creation of an assistant tool in the future.


Subject(s)
Eye Movements , Humans , Eye Movements/physiology , Saccades/physiology , Data Analysis , Nervous System Diseases/diagnosis , Male
5.
Elife ; 132024 Sep 06.
Article in English | MEDLINE | ID: mdl-39240985

ABSTRACT

Mass cytometry is a cutting-edge high-dimensional technology for profiling marker expression at the single-cell level, advancing clinical research in immune monitoring. Nevertheless, the vast data generated by cytometry by time-of-flight (CyTOF) poses a significant analytical challenge. To address this, we describe ImmCellTyper (https://github.com/JingAnyaSun/ImmCellTyper), a novel toolkit for CyTOF data analysis. This framework incorporates BinaryClust, an in-house developed semi-supervised clustering tool that automatically identifies main cell types. BinaryClust outperforms existing clustering tools in accuracy and speed, as shown in benchmarks with two datasets of approximately 4 million cells, matching the precision of manual gating by human experts. Furthermore, ImmCellTyper offers various visualisation and analytical tools, spanning from quality control to differential analysis, tailored to users' specific needs for a comprehensive CyTOF data analysis solution. The workflow includes five key steps: (1) batch effect evaluation and correction, (2) data quality control and pre-processing, (3) main cell lineage characterisation and quantification, (4) in-depth investigation of specific cell types; and (5) differential analysis of cell abundance and functional marker expression across study groups. Overall, ImmCellTyper combines expert biological knowledge in a semi-supervised approach to accurately deconvolute well-defined main cell lineages, while maintaining the potential of unsupervised methods to discover novel cell subsets, thus facilitating high-dimensional immune profiling.


Subject(s)
Data Analysis , Flow Cytometry , Single-Cell Analysis , Humans , Flow Cytometry/methods , Single-Cell Analysis/methods , Software , Cluster Analysis
6.
Front Public Health ; 12: 1372320, 2024.
Article in English | MEDLINE | ID: mdl-39234094

ABSTRACT

Background: Air pollution is one of the biggest problems in societies today. The intensity of indoor and outdoor air pollutants and the urbanization rate can cause or trigger many different diseases, especially lung cancer. In this context, this study's aim is to reveal the effects of the indoor and outdoor air pollutants, and urbanization rate on the lung cancer cases. Methods: Panel data analysis method is applied in this study. The research includes the period between 1990 and 2019 as a time series and the data type of the variables is annual. The dependent variable in the research model is lung cancer cases per 100,000 people. The independent variables are the level of outdoor air pollution, air pollution level indoor environment and urbanization rate of countries. Results: In the modeling developed for the developed country group, it is seen that the variable with the highest level of effect on lung cancer is the outdoor air pollution level. Conclusions: In parallel with the development of countries, it has been determined that the increase in industrial production wastes, in other words, worsening the air quality, may potentially cause an increase in lung cancer cases. Indoor air quality is also essential for human health; negative changes in this variable may negatively impact individuals' health, especially lung cancer.


Subject(s)
Air Pollution , Lung Neoplasms , Humans , Lung Neoplasms/etiology , Lung Neoplasms/epidemiology , Air Pollution/adverse effects , Air Pollution/analysis , Developed Countries/statistics & numerical data , Air Pollutants/analysis , Air Pollutants/adverse effects , Air Pollution, Indoor/adverse effects , Air Pollution, Indoor/analysis , Data Analysis , Urbanization , Income/statistics & numerical data , Environmental Exposure/adverse effects , Environmental Exposure/statistics & numerical data
7.
Sci Rep ; 14(1): 20646, 2024 09 04.
Article in English | MEDLINE | ID: mdl-39232120

ABSTRACT

The epidemiology of idiopathic inflammatory myopathies (IIMs) varies by country. Investigating the epidemiological profile among Thai IIMs could help to inform public health policy, potentially leading to cost-reducing strategies. We aimed to assess the prevalence and incidence of IIM in the Thai population between 2017 and 2020. A descriptive epidemiological study was conducted on patients 18 or older, using data from the Information and Communication Technology Center, Ministry of Public Health, with a primary diagnosis of dermatopolymyositis, as indicated by the ICD-10 codes M33. The prevalence and incidence of IIMs were analyzed with their 95% confidence intervals (CIs) and then categorized by sex and region. In 2017, the IIM cases numbered 9,074 among 65,204,797 Thais, resulting in a prevalence of 13.9 per 100,000 population (95% CI 13.6-14.2). IIMs were slightly more prevalent among women than men (16.8 vs 10.9 per 100,000). Between 2018 and 2020, the incidence of IIMs slightly declined from 5.09 (95% CI 4.92-5.27) in 2017 and 4.92 (95% CI 4.76-5.10) in 2019 to 4.43 (95% CI 4.27-4.60) per 100,000 person-years in 2020. The peak age group was 50-69 years. Between 2018 and 2020, the majority of cases occurred in southern Thailand, with incidence rates of 7.60, 8.34, and 8.74 per 100,000 person-years. IIMs are uncommon among Thais, with a peak incidence in individuals between 60 and 69, especially in southern Thailand. The incidence of IIMs decreased between 2019 and 2020, most likely due to the COVID-19 pandemic, which reduced reports and investigations.


Subject(s)
Myositis , Humans , Thailand/epidemiology , Male , Female , Incidence , Middle Aged , Prevalence , Adult , Aged , Myositis/epidemiology , Young Adult , Public Health , Adolescent , COVID-19/epidemiology , Aged, 80 and over , Data Analysis
8.
Article in English | MEDLINE | ID: mdl-39262318

ABSTRACT

Computerized adaptive testing (CAT) has become a widely adopted test design for high-stakes licensing and certification exams, particularly in the health professions in the United States, due to its ability to tailor test difficulty in real time, reducing testing time while providing precise ability estimates. A key component of CAT is item response theory (IRT), which facilitates the dynamic selection of items based on examinees' ability levels during a test. Accurate estimation of item and ability parameters is essential for successful CAT implementation, necessitating convenient and reliable software to ensure precise parameter estimation. This paper introduces the irtQ R package, which simplifies IRT-based analysis and item calibration under unidimensional IRT models. While it does not directly simulate CAT, it provides essential tools to support CAT development, including parameter estimation using marginal maximum likelihood estimation via the expectation-maximization algorithm, pretest item calibration through fixed item parameter calibration and fixed ability parameter calibration methods, and examinee ability estimation. The package also enables users to compute item and test characteristic curves and information functions necessary for evaluating the psychometric properties of a test. This paper illustrates the key features of the irtQ package through examples using simulated datasets, demonstrating its utility in IRT applications such as test data analysis and ability scoring. By providing a user-friendly environment for IRT analysis, irtQ significantly enhances the capacity for efficient adaptive testing research and operations. Finally, the paper highlights additional core functionalities of irtQ, emphasizing its broader applicability to the development and operation of IRT-based assessments.


Subject(s)
Educational Measurement , Psychometrics , Software , Humans , Educational Measurement/methods , Educational Measurement/standards , Calibration , Algorithms , United States , Data Analysis , Health Occupations/education
10.
JMIR Public Health Surveill ; 10: e59237, 2024 Sep 09.
Article in English | MEDLINE | ID: mdl-39250185

ABSTRACT

Background: Hand, foot, and mouth disease (HFMD) is a notable infectious disease predominantly affecting infants and children worldwide. Previous studies on HFMD have primarily focused on natural patterns, such as seasonality, but research on the influence of important social time points is lacking. Several studies have indicated correlations between birthdays and certain disease outcomes. Objective: This study aimed to explore the association between birthdays and HFMD. Methods: Surveillance data on HFMD from 2008 to 2022 in Yunnan Province, China, were collected. We defined the period from 6 days before the birthday to the exact birthday as the "birthday week." The effect of the birthday week was measured by the proportion of cases occurring during this period, termed the "birthday week proportion." We conducted subgroup analyses to present the birthday week proportions across sexes, age groups, months of birth, and reporting years. Additionally, we used a modified Poisson regression model to identify conditional subgroups more likely to contract HFMD during the birthday week. Results: Among the 973,410 cases in total, 116,976 (12.02%) occurred during the birthday week, which is 6.27 times the average weekly proportion (7/365, 1.92%). While the birthday week proportions were similar between male and female individuals (68,849/564,725, 12.19% vs 48,127/408,685, 11.78%; χ21=153.25, P<.001), significant differences were observed among different age groups (χ23=47,145, P<.001) and months of birth (χ211=16,942, P<.001). Compared to other age groups, infants aged 0-1 year had the highest birthday week proportion (30,539/90,709, 33.67%), which is 17.57 times the average weekly proportion. Compared to other months, patients born from April to July and from October to December, the peak months of the HFMD epidemic, had higher birthday week proportions. Additionally, a decreasing trend in birthday week proportions from 2008 to 2022 was observed, dropping from 33.74% (3914/11,600) to 2.77% (2254/81,372; Cochran-Armitage trend test: Z=-102.53, P<.001). The results of the modified Poisson regression model further supported the subgroup analyses findings. Compared with children aged >7 years, infants aged 0-1 year were more likely to contract HFMD during the birthday week (relative risk 1.182, 95% CI 1.177-1.185; P<.001). Those born during peak epidemic months exhibited a higher propensity for contracting HFMD during their birthday week. Compared with January, the highest relative risk was observed in May (1.087, 95% CI 1.084-1.090; P<.001). Conclusions: This study identified a novel "birthday week effect" of HFMD, particularly notable for infants approaching their first birthday and those born during peak epidemic months. Improvements in surveillance quality may explain the declining trend of the birthday week effect over the years. Higher exposure risk during the birthday period and potential biological mechanisms might also account for this phenomenon. Raising public awareness of the heightened risk during the birthday week could benefit HFMD prevention and control.


Subject(s)
Hand, Foot and Mouth Disease , Hand, Foot and Mouth Disease/epidemiology , China/epidemiology , Humans , Female , Male , Infant , Child, Preschool , Child , Adolescent , Infant, Newborn , Anniversaries and Special Events , Data Analysis
11.
BMC Public Health ; 24(1): 2581, 2024 Sep 27.
Article in English | MEDLINE | ID: mdl-39334184

ABSTRACT

BACKGROUND: Early in the pandemic, the United States population experienced a sharp rise in the prevalence rates of opioid use, social isolation, and pain interference. Given the high rates of pain reported by patients on medication for opioid use disorder (MOUD), the pandemic presented a unique opportunity to disentangle the relationship between opioid use, pain, and social isolation in this high-risk population. We tested the hypothesis that pandemic-induced isolation would partially mediate change in pain interference levels experienced by patients on MOUD, even when controlling for baseline opioid use. Such work can inform the development of targeted interventions for a vulnerable, underserved population. METHODS: Analyses used data from a cluster randomized trial (N = 188) of patients on MOUD across eight opioid treatment programs. As part of the parent trial, participants provided pre-pandemic data on pain interference, opioid use, and socio-demographic variables. Research staff re-contacted participants between May and June 2020 and 133 participants (71% response rate) consented to complete a supplemental survey that assessed pandemic-induced isolation. Participants then completed a follow-up interview during the pandemic that again assessed pain interference and opioid use. A path model assessed whether pre-pandemic pain interference had an indirect effect on pain interference during the pandemic via pandemic-induced isolation. RESULTS: Consistent with hypotheses, we found evidence that pandemic-induced isolation partially mediated change in pain interference levels among MOUD patients during the pandemic. Higher levels of pre-pandemic pain interference and opioid use were both significantly associated with higher levels of pandemic-induced isolation. In addition, pre-pandemic pain interference was significantly related to levels of pain interference during the pandemic, and these pain levels were partially explained by the level of pandemic-induced isolation reported. CONCLUSIONS: Patients on MOUD with higher use of opioids and higher rates of pain pre-pandemic were more likely to report feeling isolated during COVID-related social distancing and this, in turn, partially explained changes in levels of pain interference. These results highlight social isolation as a key risk factor for patients on MOUD and suggest that interventions promoting social connection could be associated with reduced pain interference, which in turn could improve patient quality of life. TRIAL REGISTRATION: NCT03931174 (Registered 04/30/2019).


Subject(s)
COVID-19 , Opioid-Related Disorders , Social Isolation , Humans , Male , Female , COVID-19/epidemiology , Opioid-Related Disorders/epidemiology , Adult , Social Isolation/psychology , Middle Aged , United States/epidemiology , Analgesics, Opioid/therapeutic use , Pain/drug therapy , Pain/epidemiology , Pandemics , Data Analysis , Secondary Data Analysis
12.
Nat Commun ; 15(1): 7136, 2024 Aug 20.
Article in English | MEDLINE | ID: mdl-39164279

ABSTRACT

Untargeted metabolomic analysis using mass spectrometry provides comprehensive metabolic profiling, but its medical application faces challenges of complex data processing, high inter-batch variability, and unidentified metabolites. Here, we present DeepMSProfiler, an explainable deep-learning-based method, enabling end-to-end analysis on raw metabolic signals with output of high accuracy and reliability. Using cross-hospital 859 human serum samples from lung adenocarcinoma, benign lung nodules, and healthy individuals, DeepMSProfiler successfully differentiates the metabolomic profiles of different groups (AUC 0.99) and detects early-stage lung adenocarcinoma (accuracy 0.961). Model flow and ablation experiments demonstrate that DeepMSProfiler overcomes inter-hospital variability and effects of unknown metabolites signals. Our ensemble strategy removes background-category phenomena in multi-classification deep-learning models, and the novel interpretability enables direct access to disease-related metabolite-protein networks. Further applying to lipid metabolomic data unveils correlations of important metabolites and proteins. Overall, DeepMSProfiler offers a straightforward and reliable method for disease diagnosis and mechanism discovery, enhancing its broad applicability.


Subject(s)
Deep Learning , Lung Neoplasms , Mass Spectrometry , Metabolome , Metabolomics , Humans , Metabolomics/methods , Mass Spectrometry/methods , Lung Neoplasms/metabolism , Lung Neoplasms/blood , Lung Neoplasms/diagnosis , Adenocarcinoma of Lung/metabolism , Adenocarcinoma of Lung/blood , Adenocarcinoma of Lung/diagnosis , Male , Female , Data Analysis , Reproducibility of Results , Middle Aged
14.
STAR Protoc ; 5(3): 103181, 2024 Sep 20.
Article in English | MEDLINE | ID: mdl-39178110

ABSTRACT

Here, we present a protocol to comprehensively quantify autophagy initiation using the readout of the microtubule associated protein 1 light chain 3 beta (LC3B) Förster's resonance energy transfer (FRET) biosensor. We describe steps for cell seeding, transfection, FRET/FLIM (fluorescence lifetime imaging microscopy) imaging, and image analysis. This protocol can be useful in any physiology- or disease-related paradigm where the LC3B biosensor can be expressed to determine whether autophagy has been initiated or is stalled. The analysis pipeline presented here can be applied to any other genetically encoded FRET sensor imaged using FRET/FLIM. For complete details on the use and execution of this protocol, please refer to Gökerküçük et al.1.


Subject(s)
Autophagy , Biosensing Techniques , Fluorescence Resonance Energy Transfer , Microtubule-Associated Proteins , Fluorescence Resonance Energy Transfer/methods , Biosensing Techniques/methods , Humans , Microtubule-Associated Proteins/metabolism , Microtubule-Associated Proteins/analysis , Autophagy/physiology , Microscopy, Fluorescence/methods , Data Analysis
15.
Methods Mol Biol ; 2846: 47-62, 2024.
Article in English | MEDLINE | ID: mdl-39141229

ABSTRACT

Chromatin immunoprecipitation (ChIP) followed by next-generation sequencing (-seq) has been the most common genomics method for studying DNA-protein interactions in the last decade. ChIP-seq technology became standard both experimentally and computationally. This chapter presents a core workflow that covers data processing and initial analytical steps of ChIP-seq data. We provide a step-by-step protocol of the commands as well as a fully assembled Snakemake workflow. Along the protocol, we discuss key tool parameters, quality control, output reports, and preliminary results.


Subject(s)
Chromatin Immunoprecipitation Sequencing , Computational Biology , Software , Workflow , Chromatin Immunoprecipitation Sequencing/methods , Computational Biology/methods , High-Throughput Nucleotide Sequencing/methods , Data Analysis , Chromatin Immunoprecipitation/methods , Humans
16.
Sci Rep ; 14(1): 17782, 2024 08 01.
Article in English | MEDLINE | ID: mdl-39090143

ABSTRACT

Previous correlative and modeling approaches indicate influences of environmental factors on COVID-19 spread through atmospheric conditions' impact on virus survival and transmission or host susceptibility. However, causal connections from environmental factors to the pandemic, mediated by human mobility, received less attention. We use the technique of Convergent Cross Mapping to identify the causal connections, beyond correlation at the country level, between pairs of variables associated with weather conditions, human mobility, and the number of COVID-19 cases for 32 European states. Here, we present data-based evidence that the relatively reduced number of cases registered in Northern Europe is related to the causal impact of precipitation on people's decision to spend more time at home and that the relatively large number of cases observed in Southern Europe is linked to people's choice to spend time outdoors during warm days. We also emphasize the channels of the significant impact of the pandemic on human mobility. The weather-human mobility connections inferred here are relevant not only for COVID-19 spread but also for any other virus transmitted through human interactions. These results may help authorities and public health experts contain possible future waves of the COVID-19 pandemic or limit the threats of similar human-to-human transmitted viruses.


Subject(s)
COVID-19 , SARS-CoV-2 , Weather , COVID-19/epidemiology , COVID-19/transmission , COVID-19/virology , Humans , Europe/epidemiology , SARS-CoV-2/isolation & purification , SARS-CoV-2/pathogenicity , Pandemics , Data Analysis
17.
Sci Rep ; 14(1): 18843, 2024 08 14.
Article in English | MEDLINE | ID: mdl-39138264

ABSTRACT

Application of stable isotopically labelled (SIL) molecules in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging (MALDI-MSI) over a series of time points allows the temporal and spatial dynamics of biochemical reactions to be tracked in a biological system. However, these large kinetic MSI datasets and the inherent variability of biological replicates presents significant challenges to the rapid analysis of the data. In addition, manual annotation of downstream SIL metabolites involves human input to carefully analyse the data based on prior knowledge and personal expertise. To overcome these challenges to the analysis of spatiotemporal MALDI-MSI data and improve the efficiency of SIL metabolite identification, a bioinformatics pipeline has been developed and demonstrated by analysing normal bovine lens glucose metabolism as a model system. The pipeline consists of spatial alignment to mitigate the impact of sample variability and ensure spatial comparability of the temporal data, dimensionality reduction to rapidly map regional metabolic distinctions within the tissue, and metabolite annotation coupled with pathway enrichment modules to summarise and display the metabolic pathways induced by the treatment. This pipeline will be valuable for the spatial metabolomics community to analyse kinetic MALDI-MSI datasets, enabling rapid characterisation of spatio-temporal metabolic patterns from tissues of interest.


Subject(s)
Glucose , Lens, Crystalline , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Animals , Cattle , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Lens, Crystalline/metabolism , Glucose/metabolism , Isotope Labeling/methods , Workflow , Metabolomics/methods , Data Analysis , Metabolic Networks and Pathways
18.
Sci Rep ; 14(1): 19035, 2024 08 16.
Article in English | MEDLINE | ID: mdl-39152163

ABSTRACT

Glial scar formation represents a fundamental response to central nervous system (CNS) injuries. It is mainly characterized by a well-defined spatial rearrangement of reactive astrocytes and microglia. The mechanisms underlying glial scar formation have been extensively studied, yet quantitative descriptors of the spatial arrangement of reactive glial cells remain limited. Here, we present a novel approach using point pattern analysis (PPA) and topological data analysis (TDA) to quantify spatial patterns of reactive glial cells after experimental ischemic stroke in mice. We provide open and reproducible tools using R and Julia to quantify spatial intensity, cell covariance and conditional distribution, cell-to-cell interactions, and short/long-scale arrangement, which collectively disentangle the arrangement patterns of the glial scar. This approach unravels a substantial divergence in the distribution of GFAP+ and IBA1+ cells after injury that conventional analysis methods cannot fully characterize. PPA and TDA are valuable tools for studying the complex spatial arrangement of reactive glia and other nervous cells following CNS injuries and have potential applications for evaluating glial-targeted restorative therapies.


Subject(s)
Astrocytes , Cicatrix , Neuroglia , Animals , Mice , Cicatrix/pathology , Neuroglia/pathology , Astrocytes/pathology , Microglia/pathology , Ischemic Stroke/pathology , Data Analysis , Disease Models, Animal , Male , Glial Fibrillary Acidic Protein/metabolism , Mice, Inbred C57BL
19.
Aging Clin Exp Res ; 36(1): 165, 2024 Aug 09.
Article in English | MEDLINE | ID: mdl-39120630

ABSTRACT

BACKGROUND: We aimed to explore the association of sleep duration with depressive symptoms among rural-dwelling older adults in China, and to estimate the impact of substituting sleep with sedentary behavior (SB) and physical activity (PA) on the association with depressive symptoms. METHODS: This population-based cross-sectional study included 2001 rural-dwelling older adults (age ≥ 60 years, 59.2% female). Sleep duration was assessed using the Pittsburgh Sleep Quality Index. We used accelerometers to assess SB and PA, and the 15-item Geriatric Depression Scale to assess depressive symptoms. Data were analyzed using restricted cubic splines, compositional logistic regression, and isotemporal substitution models. RESULTS: Restricted cubic spline curves showed a U-shaped association between daily sleep duration and the likelihood of depressive symptoms (P-nonlinear < 0.001). Among older adults with sleep duration < 7 h/day, reallocating 60 min/day spent on SB and PA to sleep were associated with multivariable-adjusted odds ratio (OR) of 0.81 (95% confidence interval [CI] = 0.78-0.84) and 0.79 (0.76-0.82), respectively, for depressive symptoms. Among older adults with sleep duration ≥ 7 h/day, reallocating 60 min/day spent in sleep to SB and PA, and reallocating 60 min/day spent on SB to PA were associated with multivariable-adjusted OR of 0.78 (0.74-0.84), 0.73 (0.69-0.78), and 0.94 (0.92-0.96), respectively, for depressive symptoms. CONCLUSIONS: Our study reveals a U-shaped association of sleep duration with depressive symptoms in rural older adults and further shows that replacing SB and PA with sleep or vice versa is associated with reduced likelihoods of depressive symptoms depending on sleep duration.


Subject(s)
Depression , Exercise , Rural Population , Sedentary Behavior , Sleep , Humans , Female , Male , Aged , Depression/epidemiology , Cross-Sectional Studies , Exercise/physiology , Middle Aged , Sleep/physiology , China/epidemiology , Aged, 80 and over , Data Analysis
20.
Discov Med ; 36(187): 1610-1615, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39190376

ABSTRACT

BACKGROUND: Atrial fibrillation (AF) is the most common type of arrhythmia. Heart rate variability (HRV) may be associated with AF risk. The aim of this study was to test HRV indices and arrhythmias as predictors of paroxysmal AF based on 24-hour dynamic electrocardiogram recordings of patients. METHODS: A total of 199 patients with paroxysmal AF (AF group) and 204 elderly volunteers over 60 years old (Control group) who underwent a 24-hour dynamic electrocardiogram from August 2022 to March 2023 were included. Time-domain indices, frequency-domain indices, and arrhythmia data of the two groups were classified and measured. Binary logistic regression analysis was performed on variables with significant differences to identify independent risk factors. A nomogram prediction model was established, and the sum of individual scores of each variable was calculated. RESULTS: Gender, age, body mass index and low-density lipoprotein (LDL) did not differ significantly between AF and Control groups (p > 0.05), whereas significant group differences were found for smoking, hypertension, diabetes, and high-density lipoprotein (HDL) (p < 0.05). The standard deviation of all normal to normal (NN) R-R intervals (SDNN), standard deviation of 5-minute average NN intervals (SDANN), root mean square of successive NN interval differences (rMSSD), 50 ms from the preceding interval (pNN50), low-frequency/high-frequency (LF/HF), LF, premature atrial contractions (PACs), atrial tachycardia (AT), T-wave index, and ST-segment index differed significantly between the two groups. Logistic regression analysis identified rMSSD, PACs, and AT as independent predictors of AF. For each unit increase in rMSSD and PACs, the odds of developing AF increased by 1.0357 and 1.0005 times, respectively. For each unit increase in AT, the odds of developing AF decreased by 0.9976 times. The total score of the nomogram prediction model ranged from 0 to 110. CONCLUSION: The autonomic nervous system (ANS) plays a pivotal role in the occurrence and development of AF. The individualized nomogram prediction model of AF occurrence contributes to the early identification of high-risk patients with AF.


Subject(s)
Atrial Fibrillation , Heart Rate , Humans , Atrial Fibrillation/physiopathology , Atrial Fibrillation/diagnosis , Atrial Fibrillation/epidemiology , Heart Rate/physiology , Male , Female , Middle Aged , Aged , Risk Factors , Electrocardiography/methods , Nomograms , Electrocardiography, Ambulatory/methods , Data Analysis , Arrhythmias, Cardiac/physiopathology , Arrhythmias, Cardiac/diagnosis , Arrhythmias, Cardiac/epidemiology , Arrhythmias, Cardiac/etiology
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