Lin · Frontiers in endocrinology 2022 · controlled parallel-group interventional trial · n=20

The Effect of Sleep Restriction, With or Without Exercise, on Skeletal Muscle Transcriptomic Profiles in Healthy Young Males.

Cited 12 times in the scientific literature.

Level 2 - randomized trial

Controlled human interventional trial with parallel allocation and pre/post tissue sampling

PubMed 35937838 · doi:10.3389/fendo.2022.863224 · record verified 2026-08-26

What was done

Twenty healthy young males were allocated to one of three five-night protocols: Normal Sleep (8 hours time in bed per night, 11 pm - 7 am), Sleep Restriction (4 hours time in bed per night, 3 am - 7 am), or Sleep Restriction and Exercise (4 hours time in bed plus three sessions of high-intensity interval exercise). Skeletal muscle samples were collected pre- and post-intervention for RNA sequencing. Gene set enrichment analysis was performed and compared against existing transcriptomic datasets from 24-hour sleep deprivation.

What was found

Gene set enrichment analysis indicated increased enrichment of inflammatory and immune response pathways in the sleep restriction group post-intervention, whereas the sleep restriction plus exercise group showed enrichment in the opposite direction. No significant differential expression was observed at the individual gene level from pre- to post-intervention. A set of genes previously shown to decrease with 24-hour sleep deprivation also decreased with sleep restriction, but increased in the sleep restriction plus exercise group. The abstract reports no numerical p-values, fold changes, or effect sizes.

Why it matters

This study shows that moderate short-term sleep restriction induces subtle pathway-level inflammatory shifts in human skeletal muscle rather than gross individual gene expression changes. High-intensity interval exercise appears capable of offsetting these specific transcriptional alterations.

Limits

The sample size was small (n=20 divided across three arms). The cohort was restricted to healthy young males, limiting generalizability to females, older populations, or individuals with metabolic disease. The abstract does not report whether allocation was randomized, nor does it provide protein-level validation or functional metabolic measurements.

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