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Schrepf, A.

Publications and source records attributed to Schrepf, A..

2 recordsLinked to original sources

Concordance between the fast and efficient mixed-effects algorithm (FEMA) and conventional mixed-effects modeling for whole-brain connectivity in longitudinal chronic pain

Researchers increasingly have access to neuroimaging data with repeated measures within subjects. Linear mixed-effects modeling offers a valuable way to analyze such data, but its application remains limited in the neuroimaging literature due to high computational cost and a lack of mainstream analysis packages. Here we benchmark a recently published algorithm, the Fast and Efficient Mixed-Effects Algorithm (FEMA), against a conventional implementation (MATLAB's fitlme, restricted maximum likelihood) across 94,830 functional connectivity edges. In contrast to the Adolescent Brain Cognitive Development (ABCD) Study Dataset used in the development and testing of FEMA, the dataset used in the current analysis has a smaller sample size (n = 378) and comprises individuals with chronic pelvic pain scanned at up to four visits over three years. Despite these differences, the two implementations produced highly concordant results: fixed-effect estimates and test statistics correlated at r [≥] 0.999 (Lin's concordance correlation coefficient [≥] 0.999), and the two approaches reached the same statistical conclusion for 99.98% of edges. FEMA completed each analysis roughly 20 times faster. Agreement was weaker for the estimated variance components, where FEMA attributed systematically less variance to the participant random effect, yielding a slightly lower intraclass correlation in approximately 82% of edges. We further show that most residual disagreement reflected FEMA's default variance-grid resolution rather than the estimator itself, and could be eliminated at negligible computational cost. These findings support the use of FEMA for connectome-wide analysis of repeated-measures neuroimaging data.

neuroscience↗

Urobiome Analysis in Interstitial Cystitis/Bladder Pain Syndrome Reveals Nuanced Differences Associated with Localized Pain

PurposeInterstitial cystitis/bladder pain syndrome (IC/BPS) is a prevalent chronic pain syndrome associated with functional urinary disorders. IC/BPS symptoms can be localized to the pelvic-region or have co-occurring widespread pain. Importantly, response to treatment depends on pain localization phenotype. The etiology of IC/BPS remains elusive, and whether bacteria contribute to IC/BPS pathophysiology remains uncertain. Materials and MethodsWe used urine samples collected from a longitudinal randomized controlled trial of individuals with IC/BPS to study the association of the urobiome and IC/BPS symptoms over time. Individuals provided urine samples at baseline, post-treatment, and at five months. We performed a secondary analysis on urine samples applying 16S rRNA sequencing and assigned bacterial taxonomy to amplicon sequence variants (ASVs) to characterize the urobiome. We then compared urobiome bacterial diversity, stability, and its association with IC/BPS symptoms over time. We also assessed the relationship between pain localization and the urobiome. ResultsAs validation of this dataset, we noted a strong influence of menopausal status and recent urinary tract infection on the composition of the urobiome. We did not detect widespread differences in the urobiome that correlated with subjects pain localization or severity. Instead, we observed specific bacterial sequences that were altered in abundance in relation to symptomatology, such as reduced abundance of a Dialister ASV in persons with localized pelvic pain. ConclusionsTogether, this dataset advances our understanding of the urobiome in interstitial cystitis/bladder pain syndrome and sets the stage for future studies on the urobiome and interstitial cystitis/bladder pain syndrome symptoms.

microbiology↗