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Distinct diurnal temperature rhythm patterns in critical illness myopathy: secondary analysis of two prospective trials

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Item Type:Article
Title:Distinct diurnal temperature rhythm patterns in critical illness myopathy: secondary analysis of two prospective trials
Creators Name:Mewes, D., Weber-Carstens, S., Rubarth, K., Boie, S.D., Spies, C., Kramer, A., Fielitz, J., Wollersheim, T., Ananthasubramaniam, B., Braune, F., Hancke, L., Spies, L., Balzer, F. and Engelhardt, L.J.
Abstract:BACKGROUND: Critical illness myopathy (CIM) increases mortality and causes long-term disabilities. CIM is characterized by reduced muscle excitability, muscle atrophy, weakness, and impaired glucose metabolism. Functional circadian rhythms are important for skeletal muscle homeostasis. Circadian rhythms are often disrupted during critical illness in the Intensive Care Unit (ICU). This analysis investigates whether diurnal temperature rhythms differ in critically ill CIM compared to no-CIM patients. METHODS: This is a secondary analysis of two prospective trials including critically ill patients with CIM (n = 32) or no-CIM (n = 30) based on electrophysiological tests. Diurnal body temperature rhythms were compared between CIM and no-CIM groups in reference to n = 16 participants included in a bed rest study. Cosinor analysis was performed to determine the rhythm parameters and classify into rhythm classes. Aggregated and longitudinal data were compared between groups using non-parametric tests. Rhythm parameters were correlated with muscle atrophy, weakness and insulin sensitivity. RESULTS: CIM and no-CIM patients had severe multiorgan failure (median SOFA score 12 in both groups, p = 0.39). The temperature rhythm nadir timepoint was shifted in CIM patients (10:43 [09:21, 12:22]) and no-CIM (11:12 [09:43, 13:30]) compared to the healthy bed rest group (5:03 [3:22, 6:36]) p < 0.001. CIM patients showed lower temperature rhythm mesors than no-CIM patients (p = 0.041). The temperature rhythm amplitude was lower in both CIM and no-CIM patients compared to the healthy bed rest group (CIM: 0.3 °C [0.2, 0.4]; no-CIM: 0.2 °C [0.2, 0.3]; healthy bed rest: 0.5 °C [0.2, 0.6]; p < 0.01). Compared to no-CIM patients, CIM patients had higher temperature rhythm amplitudes (p = 0.021) and showed a less pronounced reduction in temperature rhythm amplitudes during ICU stay (p = 0.017). A higher temperature rhythm amplitude correlated negatively with M. vastus lateralis myocyte cross-sectional area. CONCLUSIONS: Heterogeneous phase shifts of diurnal temperature rhythms in CIM and no-CIM groups compared to healthy bed rest volunteers may indicate ICU-related circadian disruption. Suppression of temperature rhythm amplitude during ICU stay could represent an adaptive response to this disruption. Blunted amplitude suppression observed in CIM compared to no-CIM patients might reflect reduced adaptation, potentially contributing to muscle catabolism. This hypothesis-generating analysis underlines the need for mechanistic studies exploring circadian regulation in skeletal muscle during critical illness.
Keywords:Circadian Rhythms, Diurnal Rhythms, Circadian Rhythm Disruption, Body Temperature, Temperature Rhythm, Critical Illness, Skeletal Muscle Atrophy, Critical Illness Myopathy, Muscle Weakness
Source:Annals of Intensive Care
ISSN:2110-5820
Publisher:SpringerOpen
Volume:15
Number:1
Page Range:171
Date:27 October 2025
Official Publication:https://doi.org/10.1186/s13613-025-01582-5
PubMed:View item in PubMed

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