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Leroux, A.

Publications and source records attributed to Leroux, A..

4 recordsLinked to original sources

A Beta-Binomial Model for Estimating Zero- or One-inflated Pain Trajectories

Chronic pain is a widespread public health issue that imposes substantial health, emotional, and economic burdens on individuals and communities. Because pain is subjective and lacks objective biomarkers, it is typically measured using patient-reported scores, often on a numerical scale from zero to ten. Increasingly, pain studies use ecological momentary assessment, with multiple daily assessments over days and across study phases (e.g., a series of baseline and post-intervention assessments). These data frequently show many ratings at the extremes (i.e., at minimum or maximum pain scores), commonly referred to as zero- and one-inflation in the statistical literature, along with considerable within-person variability both within and across days. These phenomena present challenges for statistical analyses, as they violate assumptions of most commonly used statistical techniques (e.g., the normality assumption of linear mixed models). We propose a Bayesian beta-binomial mixed-effects model for modeling potential zero- or one-inflated pain scores while accounting for variability using random effects on the mean and variance parameters across subjects. A simulation study demonstrates that the method accurately estimates model parameters across realistic sample sizes, time points, and zero- and one-inflation levels. An application to data from two longitudinal pain studies demonstrates that the model fits the data better and, when correctly specified, yields accurate uncertainty intervals for longitudinal changes in pain compared to existing models, especially for zero- and one-inflated outcomes. Additionally, the model directly estimates the probability of clinically meaningful pain events. The proposed method provides a powerful statistical framework for studying the patient-reported pain trajectories.

bioinformatics↗

Exploring Links between Brain Image-Derived Phenotypes and Accelerometer-Measured Physical Activity in the UK Biobank

A broad range of neurodegenerative disorders are associated with altered functional connectivity (FC) patterns and atrophy of gray matter volume (GMV). Similarly, there are links between physical activity (PA) and a number of neurodegenerative disorders. However, studies investigating the link between brain image-derived phenotypes (IDPs) and PA remain limited. Using data from the UK Biobank, we investigated the multivariate association between two sets of brain IDPs (related to FC and GMV) and PA using canonical correlation analysis (CCA). We further quantified the importance of individual PA variables in modeling each set of IDPs using both supervised and unsupervised approaches, and assessed their predictive performance for individual brain phenotypes. Finally, we evaluated the predictive performance of brain IDPs and PA variables for diabetes, stroke, coronary heart disease (CHD), and cancer using nested logistic regression models, with their relative contributions to explained variation in disease status quantified using a coefficient of determination specifically designed for logistic regression. Our analyses identified a statistically robust but low-dimensional axis of shared variation between PA and FC (canonical correlation r = 0.50), whereas the corresponding association between PA and GMV was weaker (r = 0.19). Brain features contributing most strongly to these associations were located in motor- and attention-related networks. Across predictive models, a small set of correlated PA measures reflecting activity intensity and circadian rhythm consistently emerged as representative predictors of both FC and GMV variation. Finally, we found that PA variables demonstrated greater predictive utility than either FC or GMV alone, particularly for CHD and diabetes, as assessed by both the area under the receiver operating characteristic (ROC) curve (AUC) and the proportion of explained variation. Together, these findings indicate that objectively measured PA is strongly associated with a set of motor-related brain features and provides substantial predictive information for cardiometabolic disease risk, while cross-sectional neuroimaging measures offer more modest incremental explanatory value.

neuroscience↗

Equine piroplasmosis in different geographical areas in France: prevalence heterogeneity of asymptomatic carriers and low genetic diversity of Theileria equi and Babesia caballi

Equine piroplasmosis is a worldwide tick-borne disease caused by the protozoan parasites Theileria equi and Babesia caballi, with significant economic and sanitary consequences. It can also limit the export of infected horses to piroplasmosis-free countries. These two parasites are genetically variable, with greater diversity observed in T. equi. This variability can potentially impact diagnostic accuracy. Our study aimed to evaluate the frequency of asymptomatic carriers of these parasites in France and describe the circulating genotypes. We used a species-specific nested PCR protocol targeting the 18S small subunit (SSU) rRNA gene and subsequent amplicon sequencing on blood samples collected from 566 asymptomatic horses across four National Veterinary Schools. The carrier frequency varied considerably, ranging from 18.7% around Paris (central-north) to 56.1% around Lyon (southeast), with an overall prevalence of 38.3%. T. equi carriers were ten times more frequent (91.7%, 209/228 isolates) compared to B. caballi carriers (8.8%, 19/228 isolates). Notably, T. equi carrier frequency was significantly lower in the northern region (Ile de France) compared to the southeastern regions. Interestingly, a strong correlation was observed between the frequencies of asymptomatic carriers and reported cases of acute piroplasmosis across all four geographic areas. Neither gender (female, gelding, or stallion) nor horse age showed a significant effect on the frequency of asymptomatic carriers. In areas with the highest carrier frequency, a substantial proportion of horses (22.2% to 37.5%) carried T. equi before the age of three, indicating high infection pressure. Genotyping of 201 T. equi isolates revealed a predominance of genotype E (98%), with only a few isolates belonging to genotype A (2%). Notably, two of the four genotype A isolates were detected in horses originating from Spain. All 19 B. caballi isolates belonged to the most common genotype A of this species. The discussion section explores the link between these results, the tick distribution and abundance, and the frequency of detection of T. equi and B. caballi in febrile cases attributed to piroplasmosis.

microbiology↗

Patterns of sedentary and active time accumulation are associated with mortality in US adults: The NHANES study

PurposeSedentary behavior has become a public health pandemic and has been associated with a variety of comorbidities including cardiovascular disease, type 2 diabetes, and some cancers. Previous studies have also shown that excessive amount of sedentary behavior is associated with all-cause mortality. However, no studies investigated whether patterns of sedentary and active time accumulation are associated with mortality independently of total sedentary and total active times. This study addresses this question by i) comparing several analytical ways to quantify patterns of both sedentary and active time accumulation through metrics of fragmentation of objectively-measured physical activity and ii) exploring the association of these metrics with all-cause mortality in a nationally representative US sample of elderly adults.\n\nMethodsThe accelerometry data of 3400 participants aged 50 to 84 in the National Health and Nutrition Examination Survey 2003-2006 cohorts were analyzed. Ten fragmentation metrics were calculated to quantify the duration of sedentary and active bouts: average bout duration, Gini index, average hazard, between-state transition probability, and the parameter of power law distribution. The association of these fragmentation metrics with all-cause mortality followed through December 31, 2011 was assessed with survey-weighted Cox proportional hazard models.\n\nResultsIn models adjusted for age, sex, race/ethnicity, education, body mass index, common comorbidities, and total sedentary/active time, four fragmentation metrics were associated with lower mortality risk: average active bout duration (HR=0.72 for 1SD increase, 95% CI = 0.590.88), Gini index for active bouts (HR = 0.75, 95% CI = 0.64-0.86), the parameter of power law distribution for sedentary bouts (HR = 0.75, 95% CI = 0.63-0.90), and sedentary-to-active transition probability (HR = 0.77, 95% CI = 0.61-0.96), and four fragmentation metrics were associated with higher mortality risk: the active-to-sedentary transition probability (HR = 1.40, 95% CI=1.23-1.58), the parameter of power law distribution for active bouts (HR = 1.33, 95% CI = 1.16-1.52), average hazard for durations of active bouts (HR = 1.32, 95% CI = 1.18-1.48), and average sedentary bout duration (HR =1.07, 95% CI = 1.01-1.13). After sensitivity analysis, average sedentary bout duration and sedentary-to-active transition probability became insignificant.\n\nConclusionLonger average duration of active bouts, a lower probability of transitioning from active to sedentary behavior, and a higher normalized variability of active bout durations were strongly negatively associated with all-cause mortality independently of total active time. A larger proportion of longer sedentary bouts were positively associated with all-cause mortality independently of total sedentary time. The results also suggested a nonlinear association of average active bout duration with mortality that corresponded to the largest risk increase in subjects with average active bout duration less than 3 minutes.

epidemiology↗