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Updated: Jul 11, 2026

Induction and Assessment of Exertional Skeletal Muscle Damage in Humans
Published on: December 11, 2016
ACE ID genotype affects blood creatine kinase response to eccentric exercise
Chen Yamin1, Offer Amir, Moran Sagiv
1Department of Genetics and Molecular Biology, The Zinman College of Physical Education and Sport Sciences at the Wingate Institute, Netanya, Israel.
The ACE ID genotype is linked to higher creatine kinase (CK) levels after strenuous exercise, indicating increased muscle damage risk. The DD genotype may offer protective effects against exercise-induced muscle injury.
Area of Science:
- Exercise Physiology
- Genetics
- Molecular Biology
Background:
- Unaccustomed exercise can lead to muscle breakdown, evidenced by elevated serum creatine kinase (CK) levels.
- The skeletal muscle renin-angiotensin system (RAS) is implicated in exercise metabolism and muscle tissue injury.
- A common polymorphism in the angiotensin I-converting enzyme (ACE) gene (rs4646994), known as the I/D variant, influences ACE activity.
Purpose of the Study:
- To investigate the association between the ACE I/D genotype and the variability in creatine kinase (CK) response to unaccustomed eccentric exercise.
- To determine if the ACE genotype is an independent predictor of post-exercise muscle damage.
Main Methods:
- Young individuals performed maximal eccentric contractions of elbow flexor muscles.
- Serum CK activity was measured before and after exercise.
- ACE gene polymorphism (I/D) was determined and correlated with CK levels and changes.
Main Results:
- ACE genotype significantly correlated with post-exercise CK increase and peak CK activity.
- Individuals with the II genotype exhibited higher peak CK values compared to those with ID and DD genotypes.
- The ACE genotype was identified as a powerful independent determinant of peak CK activity, with the I allele associated with greater muscle damage.
Conclusions:
- The ACE I/D genotype is positively associated with the CK response to strenuous exercise.
- The II genotype may increase the risk of muscle damage from exercise, while the DD genotype might offer protective benefits.
- These findings highlight the role of the local RAS in regulating exercise-induced muscle injury.
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