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Mitochondrial DNA variation is associated with elite athletic status in the P olish population
There is mounting evidence that genetic factors located in mitochondrial and nuclear genomes influence sport performance. Certain mitochondrial haplogroups and polymorphisms were associated with the status of elite athlete, especially in endurance performance. The aim of our study was to assess whet...
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Published in: | Scandinavian journal of medicine & science in sports 2014-04, Vol.24 (2), p.311-318 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | There is mounting evidence that genetic factors located in mitochondrial and nuclear genomes influence sport performance. Certain mitochondrial haplogroups and polymorphisms were associated with the status of elite athlete, especially in endurance performance. The aim of our study was to assess whether selected mitochondrial
DNA (mtDNA)
and nuclear
DNA
variants are associated with elite athlete performance in a group of 395 elite
P
olish athletes (213 endurance athletes and 182 power athletes) and 413 sedentary controls. Our major finding was that the
mtDNA
haplogroup
H
and
HV
cluster influence endurance performance at the
O
lympic/
W
orld
C
lass level of performance (
P
= 0.018 and
P
= 0.0185, respectively). We showed that two polymorphisms located in the mtDNA control region were associated with achieving the elite performance level either in the total athlete's group as compared with controls (m.16362
C
, 3.8% vs 9.2%, respectively,
P
= 0.0025, odds ratio = 0.39, 95% confidence interval: 0.21–0.72), or in the endurance athletes as compared with controls (m.16080
G
, 2.35% vs 0%, respectively,
P
= 0.004). Our results indicate that
mtDNA
variability affects the endurance capacity rather than the power one. We also propose that
mtDNA
haplogroups and subhaplogroups, as well as individual
mtDNA
polymorphisms favoring endurance performance, could be population‐specific, reflecting complex cross‐talk between nuclear and mitochondrial genomes. |
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ISSN: | 0905-7188 1600-0838 |
DOI: | 10.1111/sms.12012 |