# Identifying Chronotype for the Preservation of Muscle Mass, Quality and Strength

**Authors:** Roberto Barrientos-Salinas, Norma Dahdah, Jorge Alvarez-Luis, Nuria Vilarrasa, Pablo M. Garcia-Roves

PMC · DOI: 10.3390/nu18020221 · 2026-01-10

## TL;DR

This review explains how a person's natural sleep and activity patterns affect muscle health and offers lifestyle strategies to preserve muscle mass and strength.

## Contribution

The paper introduces a framework for aligning chrono-nutrition, sleep, and exercise with circadian rhythms to improve muscle health.

## Key findings

- Evening chronotypes are linked to worse sleep, eating habits, and muscle health compared to morning types.
- Disruptions in circadian genes like BMAL1 and PER2 affect protein synthesis and energy metabolism.
- Aligning lifestyle behaviors with circadian rhythms can preserve muscle mass and metabolic health.

## Abstract

Chronotype, an individual’s preferred timing of sleep and activity within a 24 h cycle, significantly influences metabolic health, muscle function, and body composition. This review explores the interplay between circadian rhythms, hormonal fluctuations, and behavioral patterns—such as nutrition timing, physical activity and sleep quality—and their impact on muscle mass, strength, and quality. Evening chronotypes (ETs) are consistently associated with poorer sleep, irregular eating habits, reduced physical activity, and increased risk of obesity, sarcopenia and metabolic disorders compared to morning types (MTs). At the molecular level, disruptions in circadian clock gene expression (e.g., BMAL1, PER2, CRY1) affect protein synthesis, insulin sensitivity, and energy metabolism, contributing to muscle degradation and impaired recovery. The review highlights critical components—targeting chrono-nutrition, sleep quality, and exercise timing—to align lifestyle behaviors with circadian biology, thereby preserving muscle health and improving overall metabolic outcomes.

## Linked entities

- **Genes:** BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406], PER2 (period circadian regulator 2) [NCBI Gene 8864], CRY1 (cryptochrome circadian regulator 1) [NCBI Gene 1407]
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406] {aka ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3}, PER2 (period circadian regulator 2) [NCBI Gene 8864] {aka FASPS, FASPS1}, CRY1 (cryptochrome circadian regulator 1) [NCBI Gene 1407] {aka DSPD, PHLL1}
- **Diseases:** metabolic disorders (MESH:D008659), sarcopenia (MESH:D055948), obesity (MESH:D009765)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844850/full.md

---
Source: https://tomesphere.com/paper/PMC12844850