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Measurement of Maximum Isometric Force Generated by Permeabilized Skeletal Muscle Fibers
Published on: June 16, 2015
Common genetic variation in the IGF1 associates with maximal force output
Antti Huuskonen1, Jani Lappalainen, Niku Oksala
1Institute of Biomedicine, Physiology, University of Eastern Finland, Kuopio, Finland.
Medicine and Science in Sports and Exercise
|May 10, 2011
Summary
Genetic variants in IGF1 and IGFBP3 influence maximal force production and body fat. These findings highlight the role of insulin-like growth factor-1 (IGF1) and IGF-binding protein-3 (IGFBP3) in muscle function and body composition.
Area of Science:
- Genetics and Sports Science
- Molecular Biology
- Human Physiology
Background:
- Single nucleotide polymorphisms (SNPs) can alter gene expression and protein function, impacting biological processes.
- Insulin-like growth factor-1 (IGF1) is crucial for skeletal muscle anabolic pathways.
- Interleukin-6 (IL6) plays a role in muscle energy homeostasis during exercise.
Purpose of the Study:
- To investigate the association between gene variants in IGF1, IGFBP3, IL6, and IL6R and physical performance.
- To examine the relationship between these gene variants and body composition.
- To determine the effect of these variants on circulating levels of IGF-1 and IL-6.
Main Methods:
- Genotyping of 841 healthy Finnish males for specific SNPs in IGF1, IGFBP3, IL6, and IL6R.
- Assessment of maximal force, maximal oxygen consumption, and body fat percentage.
- Measurement of circulating IGF-1 and IL-6 levels using ELISA and PCR assays.
Main Results:
- The IGF1 SNP rs7136446 (genotype CC) was associated with higher body fat and increased maximal force production.
- The IGFBP3 SNP rs2854744 (genotype CC) and IL6R SNP rs4537545 (genotype TT) were linked to higher IL-6 levels.
- No significant associations were found between the studied SNPs and aerobic performance.
Conclusions:
- Common variations in the IGF1 gene may influence maximal force production due to IGF1's role in muscle anabolism.
- Variations in IGF1 and IGFBP3 genes might contribute to higher body fat and altered IGF1-mediated tissue growth.
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