Author ORCID Identifier
N/A
https://orcid.org/0000-0002-2330-5427
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https://orcid.org/0000-0002-7224-0754
https://orcid.org/0009-0003-7977-4577
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N/A
N/A
N/A
https://orcid.org/0000-0003-2021-4033
https://orcid.org/0000-0002-0365-2149
https://orcid.org/0000-0002-9812-3505
N/A
N/A
https://orcid.org/0000-0003-1061-8528
https://orcid.org/0000-0002-5841-798X
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N/A
Document Type
Article
Publication Date
2007
College/Unit
Eberly College of Arts and Sciences
Department/Program/Center
Exercise Physiology
Abstract
Background
Of the five sub-phenotypes defining metabolic syndrome, all are known to have strong genetic components (typically 50–80% of population variation). Studies defining genetic predispositions have typically focused on older populations with metabolic syndrome and/or type 2 diabetes. We hypothesized that the study of younger populations would mitigate many confounding variables, and allow us to better define genetic predisposition loci for metabolic syndrome.
Methods
We studied 610 young adult volunteers (average age 24 yrs) for metabolic syndrome markers, and volumetric MRI of upper arm muscle, bone, and fat pre- and post-unilateral resistance training.
Results
We found the PPARα L162V polymorphism to be a strong determinant of serum triglyceride levels in young White males, where carriers of the V allele showed 78% increase in triglycerides relative to L homozygotes (LL = 116 ± 11 mg/dL, LV = 208 ± 30 mg/dL; p = 0.004). Men with the V allele showed lower HDL (LL = 42 ± 1 mg/dL, LV = 34 ± 2 mg/dL; p = 0.001), but women did not. Subcutaneous fat volume was higher in males carrying the V allele, however, exercise training increased fat volume of the untrained arm in V carriers, while LL genotypes significantly decreased in fat volume (LL = -1,707 ± 21 mm3, LV = 17,617 ± 58 mm3 p = 0.002), indicating a systemic effect of the V allele on adiposity after unilateral training. Our study suggests that the primary effect of PPARα L162V is on serum triglycerides, with downstream effects on adiposity and response to training.
Conclusion
Our results on association of PPARα and triglycerides in males showed a much larger effect of the V allele than previously reported in older and less healthy populations. Specifically, we showed the V allele to increase triglycerides by 78% (p = 0.004), and this single polymorphism accounted for 3.8% of all variation in serum triglycerides in males (p = 0.0037).
Digital Commons Citation
Uthurralt, Julieta; Gordish-Dressman, Heather; Bradbury, Meg; Tesi-Rocha, Carolina; Devaney, Joseph; Harmon, Brennan; Reeves, Erica K.; Brandoli, Cinzia; Hansen, Barbara C.; Seip, Richard L.; Thompson, Paul D.; Price, Thomas B.; Angelopoulos, Theodore J.; Clarkson, Priscilla M.; Moyna, Niall M.; Pescatello, Linda S.; Visich, Paul S.; Zoeller, Robert F.; Gordon, Paul M.; and Hoffman, Eric P., "PPARα L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males" (2007). Faculty & Staff Scholarship. 2842.
https://researchrepository.wvu.edu/faculty_publications/2842
Source Citation
Uthurralt, J., Gordish-Dressman, H., Bradbury, M. et al. PPARα L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males. BMC Med Genet 8, 55 (2007). https://doi.org/10.1186/1471-2350-8-55
Comments
© 2007 Uthurralt et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.