Bettina Schuppelius

Postdoctoral Researcher

DIfE

The projects of

Bettina Schuppelius

B01

Targeting

Circadian rhythms and chronotherapy in multiple sclerosis

Multiple sclerosis features disturbances in sleep, metabolism, and immune activity across the circadian cycle, which may actively contribute to disease activity. This project investigates how these rhythms influence disease progression and whether strengthening them can be therapeutically beneficial.

Circadian rhythms and chronotherapy in multiple sclerosis

Multiple sclerosis features disturbances in sleep, metabolism, and immune activity across the circadian cycle, which may actively contribute to disease activity. This project investigates how these rhythms influence disease progression and whether strengthening them can be therapeutically beneficial.

The publications of

Bettina Schuppelius

Targeting

Impact of Intended Isocaloric Early versus Late Time-Restricted Eating on Plasma Lipidome in Women with Overweight or Obesity: Secondary Analysis of the ChronoFast Trial

November 4, 2025

Time-restricted eating (TRE) is a promising strategy against metabolic disorders, but its effects on lipid metabolism remain controversial. The present research assesses and compares the impact of early (eTRE) versus late (lTRE) TRE on the plasma lipidomic profile. This is an exploratory outcome of the previously published randomized crossover trial, which examines 31 women with overweight or obesity who follow a two-week eTRE and a two-week lTRE in an intended isocaloric setting. Blood plasma and subcutaneous adipose tissue biopsies are analyzed using shotgun lipidomics and transcriptomics, respectively. Between interventions and within the lTRE, lipid species and classes, as well as enzyme activity indices, are not substantially changed. Within the eTRE, changes are observed for 103 lipid species, including a reduction of ceramide and phosphatidylcholine classes, and for the desaturation indices D5D, D6D, and D9D, as well as the elongation index ELOVL6. Combined analysis of plasma lipidome and adipose tissue reveals alterations in the glycerophospholipid pathway and in the expression of phospholipase enzymes PLB1, PLA2G6, and PLAG4B, dependent on TRE timing. These results suggest that eating timing during TRE may be crucial for remodeling the plasma lipidome and adipose tissue transcriptome and highlight the need of future lipidomic research in TRE.