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de Assis, L. V. M.

Publications and source records attributed to de Assis, L. V. M..

2 recordsLinked to original sources

Circadian Oscillation Detection Analysis and Comparison (CODAC): a Multicriteria Method to Estimate and Compare Rhythmicity

Analysis of circadian patterns in time-series data requires computational methods that can accommodate several factors, including variable sampling resolution, replicate number, and missing values. Most existing tools simplify rhythmicity to a strict dichotomy based solely on a single p-value threshold. This leads to a level of uncertainty that affects many biological targets. We developed CODAC (Circadian Oscillation Detection Analysis and Comparison), a framework that integrates nonlinear constrained optimization with a multicriteria rhythmicity classification scheme to evaluate rhythmic patterns without relying on a single statistical cutoff. This approach allows CODAC to identify and exclude medium-confidence rhythms rather than force them into a rhythmic/arrhythmic dichotomy. CODAC comprises four modules: (i) CODAC_single estimates rhythmicity within a single group; (ii) CODAC_flex extends this to identify distinct waveform types within one group; (iii) CODAC_compare performs pairwise comparisons across two or more groups to detect rhythmic or arrhythmic changes; and (iv) CODAC_multi handles more complex designs involving multiple-group comparisons. Using in silico simulations and public transcriptomic datasets, we show that CODAC performs comparably to established methods while providing additional flexibility for rhythm classification and comparison. Taken together, CODAC provides a flexible and open-source package for circadian timeseries analysis with automated visualization tools.

systems biology↗

Hepatocyte Circadian Clocks Control Cholesterol Metabolism and Protect From Metabolic Dysfunction-Associated Steatohepatitis (MASH)

The circadian clock synchronizes physiological processes with the 24-hour light-dark cycle. Clock disruption contributes to metabolic disorders, including metabolic dysfunction-associated steatohepatitis (MASH). Here, we investigated the role of the hepatocyte clock in MASH using hepatocyte-specific Bmal1 deletion (Hep-Bmal1KO) mice. Hep-Bmal1KO mice showed faster MASH progression with increased hepatic cholesterol, inflammation, and fibrosis. Transcriptomic and lipidomic analyses revealed dysregulated cholesterol metabolism in Hep-Bmal1KO mice, marked by reduced expression and disrupted rhythmicity of key cholesterol-related genes. Bioinformatic analyses identified Chrebp as a potential co-regulator of these transcriptional changes. In an in vitro model with palmitate exposure and gene silencing, we found that Bmal1, but not Chrebp, regulated cholesterol accumulation, indicating Bmal1s specific role in hepatic cholesterol metabolism. Translating our findings to a human patient cohort revealed a significantly shifted circadian phase, despite no marked effect on hepatic cholesterol levels in the livers of patients with more advanced liver disease (i.e., MASH) compared to simple steatosis. Taken altogether, our findings offer a roadmap to understand the hepatocyte clocks role in MASH and its potential as a therapeutic target.

pathology↗