Original Article

Wessner B1, Stuparits P1, Fail C1, Pavic F1, Tschan H1, Bachl N1,2
1 Centre for Sport Science and University Sports, University of Vienna, Austria
2 Austrian Institute of Sports Medicine, Vienna, Austria


Background: During the last years many studies were conducted to investigate the contribution of various genetic variants to endurance and sprint/power performance of elite athletes. Data on team sport athletes are missing to a large extent. Therefore, the aim of the study was to investigate the frequency of selected polymorphisms on elite athlete status in Austrian team sport (handball, soccer), endurance and power athletes as well as in healthy control subjects.
Methods: Genotype and allele frequencies of ACTN3 R577X (rs1815739), ADRB1 Ser49Gly (rs1801252), ADRB2 Arg16Gly (rs1042713), ADRB2 Gln27Glu (rs1042714) and the ADRB3 Trp64Arg (rs4994) polymorphisms were determined in 56 Austrian sprint/power athletes, 86 endurance athletes, 143 team sport athletes and 216 healthy non-athletic controls. Genomic DNA was extracted from saliva and genotyping was performed by real time polymerase chain reaction using a standard protocol.
Results: Handball and soccer players had a higher frequency of the ACTN3 RR genotype and a lower frequency of RX + XX genotypes than the control group. Furthermore, the frequency of athletes being homozygous for the ADRB1 Ser49Ser genotype was significantly higher in team sport athletes in comparison to those competing in power/sprint sports. We did not detect any other differences in genotype distributions between the study groups.
Conclusion: This study provides some evidence that the ACTN3 R577X and the ADRB1 Ser49Gly polymorphisms are associated with team sport performance. Larger prospective studies focusing on the genetic influence of performance development are required for confirmation of these findings.


Hintergrund: In den letzten Jahren wurden zahlreiche Studien durchgeführt, um den Einfluss verschiedener genetischer Varianten auf die sportliche Leistungsfähigkeit von EliteathletInnen sowohl im Ausdauer- als auch im Sprint-/Kraftbereich zu untersuchen, der Bereich der Teamsportarten wurde dabei aber mit wenigen Ausnahmen ausser Acht gelassen. Das Ziel der vorliegenden Studie war es daher, die Häufigkeit ausgewählter Polymorphismen bei österreichischen AthletInnen aus den Bereichen Teamsport (Handball, Fussball), Ausdauersport und Kraftsport sowie in einer gesunden Kontrollgruppe zu erheben und miteinander zu vergleichen.
Methodik: Es wurden Genotyp- und Allelhäufigkeiten der ACTN3 R577X (rs1815739), ADRB1 Ser49Gly (rs1801252), ADRB2 Arg16Gly (rs1042713), ADRB2 Gln27Glu (rs1042714) und ADRB3 Trp64Arg (rs4994) Polymorphismen von 56 österreichischen Kraftsport-, 86 Ausdauer-, 143 TeamsportathletInnen sowie von 216 gesunden Kontrollpersonen erhoben. Genomische DNA wurde aus den Speichelproben isoliert und die genetischen Varianten mittels Polymerasekettenreaktion nach einem standardisierten Protokoll detektiert.
Resultate: Handball- und FussballspielerInnen hatten eine höhere Häufigkeit des ACTN3 RR Genotyps, wohingegen die RX + XX Genotypen seltener als in der Kontrollgruppe nachgewiesen wurden. Zusätzlich waren TeamsportlerInnen häufiger homozygot für den ADRB1 Ser49Ser Genotyp als KraftsportlerInnen. Darüber hinaus wurden keine weiteren Unterschiede zwischen den Gruppen beobachtet.
Conclusio: Diese Studie trägt zur Evidenz bei, dass die ACTN3 R577X und die ADRB1 Ser49Gly Polymorphismen mit der Teamsportperformance assoziiert sind. Es sind jedoch grössere prospektive Studien erforderlich, die den Einfluss der Genetik auf die Leistungsentwicklung untersuchen, um die vorliegenden Ergebnisse zu bestätigen.


Unlike the vast number of studies investigating the genetic contribution to endurance and sprint/power performance, the genetic contribution to success in team sport performance has received limited attention, and only a few studies have explicitly characterized genetic variants in elite team sport athletes, mainly soccer players [1–6]. While endurance and power athletes represent the physiological endpoints of the sporting continuum, handball and soccer players require a combination of anaerobic and aerobic qualities. As athletes engaged in handball and soccer have to repeatedly produce maximal efforts like sprints, interspersed with short (handball) or longer (soccer) recovery periods over an extended period of time, soccer and handball can be considered as mixed-energy system sports. In both sports, the ability to generate fast muscle actions during the short and highly intensive periods of critical game actions and a high endurance capacity during the periods in between can be considered as performance-limiting factors [7,8]. Having these physiological demands in mind, it seems to be necessary to investigate candidate genes known to influence both, power or sprinting capacity as well as endurance capacity.
The ACTN3 gene encodes for the sarcomeric α-actinin-3 (ACTN3) protein which is nearly exclusively expressed in fast, glycolytic type IIX fibres. Therefore, it plays an important role in the generation of explosive powerful contractions [9]. North et al. identified a common genetic variant (ACTN3 R577X) that results in either expressing a fully functional or a truncated version of ACTN3. Approximately 16% of the world population are predicted to have a congenital deficiency of α-actinin-3, suggesting that other factor(s) likely compensate for its absence at the Z lines of skeletal muscle fast fibres such as α-actinin-2, which is expressed in all muscle fibers [10,11]. Based on these findings, numerous studies have been conducted to investigate the influence of the ACTN3 R577X polymorphism on elite athletic performance and a recent meta-analysis strongly confirmed that ACTN3 deficiency is detrimental for power and sprint activities, but there seems to be no evidence that the X allele is advantageous for endurance sports [12].
Beta adrenergic receptors (ADRB) are members of the G protein-coupled receptor superfamily being targets for the endogenous catecholamines noradrenaline (norepinephrin) and adrenaline (epinephrine). In humans, three subtypes of beta adrenergic receptors are known (beta-1, beta-2 and beta-3). They are expressed in a large variety of cells and play a pivotal role in the regulation of the cardiac, pulmonary, vascular, endocrine and central nervous system [13]. As the cardiovascular response to exercise is highly individual, genetic variations in genes encoding for receptors involved in cardiovascular regulation are supposed to exert an influence on exercise performance [14]. Hence, ADRB genes are candidates of interest since B1-adrenergic receptors influence cardiac function like heart rate and stroke volume, while the B2-adrenergic receptors primarily affect vascular function as they are expressed through many cell types such as airway smooth muscle cells, airway epithelial cells and blood vessels [15]. On the contrary, B3-adrenergic receptors are primarily found in adipose tissue where they stimulate lipolysis and thermogenesis [16]. However, studies on ADRB polymorphisms and elite performance are scarce and in many cases solely endurance athletes are investigated [17–19].
Therefore, the aim of the study was to compare genotype and allele frequencies of the ACTN3 R577X (rs1815739), ADRB1 Ser49Gly (rs1801252), ADRB2 Arg16Gly (rs1042713), ADRB2 Gln27Glu (rs1042714) and the ADRB3 Trp64Arg (rs4994) polymorphisms between Austrian team sport athletes (handball, soccer) with Austrian endurance and power athletes as well as a healthy control group. We hypothesized that team sport athletes would have a higher frequency of the ACTN3 R577R (beneficial for power), ADRB1 Ser49Ser, ADRB2 Arg16Arg, ADRB2 Glu27Glu and ADRB3 Arg64Arg (beneficial for endurance capacity).


The study population consisted of 56 power athletes (sprinters and jumpers (n=49), throwers (n=5), weightlifters (n=2)), 86 endurance athletes (middle and long distance runners (n=63), road cyclists (n=17), triathletes (n=5), biathletes (n=1), 143 team sport athletes (soccer players (n=82), handball players (n=61), and 216 healthy non-athletic controls. Participants included both genders, were of Caucasian descent and had an age between 18 and 83 years.
Athletes were included in the study sample only if they are currently active or had participated previously at the international or at least at the highest national level within the respective discipline. The physical activity level (PAL) of healthy controls was determined by dividing the total energy expenditure over a 24 hour period by the basal metabolic rate. While energy expenditure was estimated from the International Physical Activity Questionnaire (IPAQ) using metabolic equivalent (MET) values according to the 2011 compendium of physical activities [20], the basal metabolic rate was predicted as a function of sex, age, weight, and height as suggested previously [21]. Healthy controls were categorized into having a sedentary or light activity lifestyle (PAL 1.40-1.69), an active or moderately active lifestyle (PAL 1.70-1.99), a vigorous or vigorously active lifestyle (PAL 2.00-2.40) according to the cut points provided by the Food and Agriculture Organization of the United Nations [22]. Controls having a PAL above 2.40 were excluded from the study as they could be considered as having a PAL similar to athletes. Further exclusion criteria consisted of diagnosed cardiorespiratory disease (both groups) and the proven intake of performance-enhancing substances (athletes).
Written informed consent was obtained from all participants and the study was conducted according to the Declaration of Helsinki for Human Research of 1974 (last modified in 2000). The study protocol was approved by the ethics committee of the Medical University of Vienna, Austria (EK-Nr. 416/2008).

Genomic DNA was isolated from saliva using a mouthwash protocol as described previously [23]. The subjects were asked not to smoke, drink or eat one hour before sample collection. For saliva collection subjects had to rinse the mouth using 10 ml Listerine (Johnson & Johnson, Vienna, Austria) for at least 20 seconds and to spit the liquid into a 50 ml centrifuge tube. DNA was extracted from the saliva samples using the QIAamp DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. Quantity and quality of DNA was checked on a NanoDrop spectrophotometer (Peqlab, Erlangen, Germany). Isolated DNA was stored at –80°C until further analysis.
Genotyping was performed using real time PCR (7500 Real-Time PCR System, Applied Biosystems, Foster City, CA) and commercially available TaqMan SNP genotyping assays (ACTN3 R577X (rs1815739, C_590093_1), ADRB1 Ser49Gly (rs1801252, C_8898508_10), ADRB2 Arg16Gly (rs1042713, C_2084764_20), ADRB2 Gln27Glu (rs1042714, C_2084765_20), ADRB3 Trp64Arg (rs4994, C_2215549_20), Applied Biosystems). Each predesigned genotyping assay includes two allele-specific TaqMan MGB probes containing distinct fluorescent dyes (VIC, FAM) and a PCR primer pair to detect the specific SNP targets. Samples were analysed in duplicates and a non-template control was added on each 96 well plate to orient the VIC- and FAM dyes to an origin as well as to enable the detection of DNA contamination. Genotypes were analysed using the SDS 2.1 software (Applied Biosystems).

Statistical analysis
The SPSS statistical package version 21.0 was used to perform all statistical evaluations. Baseline differences between groups in continuous variables were calculated using ANOVA followed by Bonferroni-corrected post hoc analyses. Allele frequencies were determined by gene counting. The Chi-square test was used to prove whether the observed genotype frequencies were in Hardy-Weinberg equilibrium (HWE) and to compare the allele and genotype frequencies between the groups. The level of significance was set at p <0.05.

Table 1: Subject characteristics


Table 2: ACTN3 R577X (rs1815739) genotype and allele frequencies in Austrian controls (n=216), endurance athletes (n=86), team sport athletes (n=143) and power athletes (n=56)


In total 501 subjects were enrolled in the study. The overall characteristics of these subjects are shown in Table 1. The frequency of female athletes was generally lower as compared to the healthy controls (χ2 = 60.2; p < 0.001). Furthermore, the age of team sport athletes was about 12 years lower than the mean age of all the other study groups. In addition, both male and female team sport athletes were taller than healthy controls and endurance athletes and had a higher body mass and BMI than endurance athletes. The mean PAL level of both male and female control subjects corresponded to an active lifestyle, whereby 13 (6.0%) people could be considered as inactive, 88 (17.6%) persons had a sedentary or lightly active lifestyle, 74 (40.7%) were categorized as moderately active and 41 (19.0%) as vigorously active.
Asking team-sport athletes (n = 142) to rate the importance of either endurance or strength for their respective discipline on a scale from 0 (= endurance) to 10 (= strength) the mean of all team sport athletes was 4.6 ± 1.5 with similar ratings in both groups (soccer players: 4.6 ± 1.6, handball players: 4.6 ± 1.4; p = 0.871) illustrating that team sport athletes consider endurance and strength equally important for achieving success.
Genotype distribution for the ACTN3 genotype was in Hardy-Weinberg equilibrium within each group. We did not observe any differences in either genotype or allele frequencies between groups (p > 0.05) as shown in table 2. However, when the dominant genetic model (RR vs. RX + XX) was applied, team sport athletes had a higher frequency of the RR genotype and a lower frequency of RX + XX than the control group (p = 0.029). A sub-group analysis between soccer and handball players did not reveal any differences.
Genotype distributions were in Hardy Weinberg equilibrium except for the ADRB1 Ser49Gly and ADRB2Gln27Glu variants in power athletes (ADRB1 Ser49Gly: controls: χ2 = 1.650; p = 0.199; endurance athletes: χ2 = 0.613; p = 0.688; team sport athletes: χ2 = 0.650; p = 0.420; power athletes: χ2 = 4.275;p = 0.039 and ADRB2 Gln27Glu: controls: χ2 = 1.560; p = 0.212; endurance athletes: χ2 = 0.8496; p = 0.357; team sport athletes: χ2 = 0.001; p = 0.973; power athletes: χ2 = 5.729; p = 0.017) and the ADRB3 Trp64Arg genotype in team sport athletes (controls: χ2 = 0.071; p = 0.789; endurance athletes: χ2 = 0.0108; p = 0.917; team sport athletes: χ2 = 11.012; p = 0.001; power athletes: χ2 = 0.966; p = 0.326).
With respect to the adrenergic receptors we did not observe significant overall differences in genotype and allele frequencies among the study groups, but having a closer look to pairwise comparisons between team sport athletes and the other groups, some trends could be detected as summarized in Table 3. In comparison to power athletes, the frequency of the ADRB1 Ser49Ser (GG) genotype was significantly higher in team sport athletes (7.1% versus 0.7%, p = 0.045). Furthermore, team sport athletes differed from controls as the proportion of subjects being heterozygote for the ADRB3 Trp64Arg genotype was significantly lower in team sport athletes than in controls (15.8% versus 9.1%, p = 0.037).

Table 3: ADRB genotype and allele frequencies in Austrian controls (n=216), endurance athletes (n=86), team sport athletes (n=143) and power athletes (n=56)


In this study we aimed to investigate whether genetic variants in the ACTN3, ADRB1, ADRB2 and ADRB3 genes would differ between Austrian team sport, endurance and power athletes as well as healthy controls. Our data revealed that handball and soccer players had a higher frequency of the ACTN3 RR genotype and a lower frequency of RX + XX genotypes than observed in the control group. Furthermore, the frequency of athletes being homozygous for the ADRB1 Ser49Ser genotype was significantly higher in team sport athletes in comparison to those competing in power/sprint sports. We did not detect any other differences in genotype distributions between the study groups.
Our results for the ACTN3 genotype are in line with a study from Santiago et al. showing a higher proportion of the “fast” RR genotype in professional soccer players than in sedentary controls [24]. However, when considering differences between team sport, endurance and power athletes, team sport athletes are less likely to harbour the RR genotype when compared to power athletes, but the R577X genotype distribution was similar in team sport athletes and endurance athletes [25]. From the mechanistic point of view it is assumed that the RR genotype would correspond to higher speed and strength, whereas the ACTN3 deficiency (XX geno­type) would result in higher endurance capacity. A study with 200 professional soccer players of Brazilian first division teams showed that ACTN3/RR individuals spent less time to run 10, 20 and 30 m, presented a higher jump potential, but had a lower VO2max than ACTN3/XX individuals [5]. A very recent study from the same group, where the athletes were first ranked in ascending order according to their performance in each test and then divided into performance quartiles, did not reveal any significant differences in genotypic or allelic frequencies between different performance ratings in adult, professional, U-20 and U-17 years Brazilian first-division soccer players [3].
However, Massida et al. [26] demonstrated the importance of the ACTN3 R577X polymorphism in soccer performance by constructing a new genetic model based on genotype scores proposed by Williams and Folland [27]. By analysing the relationship between six genetic polymorphisms (ACE, ACTN3, BDKRB2, VDR-ApaI, VDR-BsmI, and VDR-FokI) and jumping performance, they came to the conclusion that the ACTN3 R577X polymorphism was the most important genetic variation in predicting vertical jump height, even though no significant differences in the total genotype score between athletes and the control group were detected. In summary, it seems to be evident that the ACTN3 R577X genotype is associated with power and/or speed, but it has to be confirmed in further studies whether this association is relevant for success in team sports such as handball or soccer.
This is the first study investigating the allelic and genotype frequencies of four main variants of adrenoceptor beta genes (ADRB1 Ser49Gly, ADRB2 Arg16Gly, ADRB2 Gln27Glu and ADRB3 Trp64Arg) in endurance, sprint/power and team sport athletes competing in Austria and our data revealed that team sport athletes differed in their ADRB1 Ser49Gly genotype distribution from sprint/power athletes as well as in their ADRB3 Trp64Arg genetic profile from controls. Studies on the association of the ADRB1 Ser49Gly polymorphism and sports performance are scarce and are mainly performed in patients with cardiological problems. Hence, a study in patients with heart failure has shown that subjects homozygous for Gly49 had a better physical endurance and a lower resting hearth rate than those homozygous for Ser49 [28]. Furthermore, a study in Polish athletes observed that the frequency of the 49Gly allele was significantly higher in endurance athletes than in the controls (11% versus 6.4%) [29]. Although the frequency of the Gly49Gly genotype is generally somewhat lower in our study group, we detected the highest proportion of this genotype in the group of team sport athletes (7.1%) which could point to a possible favourable effect of the Ser49 variant for team sports performance.
The ADRB2 Gly16Arg polymorphism was previously associated with endurance capacity with the Arg (A) allele exerting a favourable effect [18]. For the ADRB2 Gln27Glu polymorphism it has been shown that maximal oxygen consumption is lower in women homozygous for ADRB2 Glu27Glu implying a favourable effect of the Gln (C) allele for endurance performance [30]. However, similar to some other studies we could not confirm any association with athletic status and ADRB2 polymorphisms [17,31].
The ADRB3 Arg (C) allele has been shown to be overrepresented in Spanish world-class endurance athletes [17]. Furthermore, a study among Korean controls and athletes from different disciplines revealed that the highest proportion of the subject carrying the Arg allele was detected for volleyball and gymnastics [32]. This corresponds well to our data indicating the highest frequency of the Arg allele in team sport athletes.
Summarising our study results from the genetic point of view, it can be assumed that sprint/power as well as endurance performance seems to be equally important for success in team sport athletes as both the “power” variant of ACTN3 as well as the “endurance” variant of ADBR1 and ADBR3 were slightly overrepresented. This assumption is further supported by the fact that the team sport athletes themselves rated both strength and endurance as being equally for achieving success. However, this study results have to be treated with some cautions as several limitations might have impacted the results.
First of all we have to consider that there is a limited number of elite athletes worldwide and especially in Austria when it comes to summer sports. Hence, we were unable to find a suitable high number of “world class” athletes as defined previously [33]. However, the included athletes are amongst the best within their discipline in Austria and the data obtained could be very useful on the national level. Furthermore, the number of females is clearly underrepresented in our study population, which indicates that the results of this study may be applicable for male athletes rather than for athletes of both sexes. Finally, the cross-sectional design of our study does not allow drawing cause-effect relationships for the assessment of team sport performance. It is obvious that there are other genetic variants and epigenetic mechanisms that influence athletic performance in complex sports such as handball or soccer. Thus, additional large-scale prospective studies should be envisioned eliminating the above mentioned limitations.


In summary, this study provides preliminary evidence that the ACTN3 R577X as well as the ADRB1 Ser49Gly polymorphisms are associated with team sport performance. Larger prospective studies involving performance tests and including world class elite team sport athletes of both genders are required for confirmation of these findings.

Practical implications

  • These study shows that sports performance in team sports is affected by genetics (similar to sheer endurance or power sports).
  • Genetic testing of team sport athletes may have limited value without considering the physiological demands of the respective discipline.
  •  Ethical issues have to be considered (especially when testing young athletes or when personal data are available for third parties).

Corresponding author

Assoc. Prof. DI Dr. Barbara Wessner
Centre for Sport Science and University Sports
University of Vienna
Auf der Schmelz 6
A-1150 Vienna, Austria
Mail: barbara.wessner@univie.ac.at
Phone: +43-1-4277-48875


  1. Eynon N, Banting LK, Ruiz JR, Cieszczyk P, Dyatlov DA, Maciejewska-Karlowska A, et al. ACTN3 R577X polymorphism and team-sport performance: a study involving three European cohorts. J Sci Med Sport. 2014;17(1):102-6.
  2. Alvarez R, Terrados N, Ortolano R, Iglesias-Cubero G, Reguero JR, Batalla A, et al. Genetic variation in the renin-angiotensin system and athletic performance. Eur J Appl Physiol. 2000;82(1-2):117-20.
  3. Coelho DB, Pimenta E, Rosse IC, Veneroso C, Becker LK, Carvalho MR, et al. The alpha-actinin-3 r577x polymorphism and physical performance in soccer players. J Sports Med Phys Fitness. 2016;56(3):
  4. Egorova ES, Borisova AV, Mustafina LJ, Arkhipova AA, Gabbasov RT, Druzhevskaya AM, et al. The polygenic profile of Russian football players. J Sports Sci. 2014;32(13):1286-93.
  5. Pimenta EM, Coelho DB, Veneroso CE, Barros Coelho EJ, Cruz IR, Morandi RF, et al. Effect of ACTN3 gene on strength and endurance in soccer players. J Strength Cond Res. 2013;27(12):3286-92.
  6. Juffer P, Furrer R, Gonzalez-Freire M, Santiago C, Verde Z, Serratosa L, et al. Genotype distributions in top-level soccer players: a role for ACE? Int J Sports Med. 2009;30(5):387-92.
  7. Haugen T, Tonnessen E, Hisdal J, Seiler S. The Role and Development of Sprinting Speed in Soccer. Int J Sports Physiol Perform. 2013.
  8. Stolen T, Chamari K, Castagna C, Wisloff U. Physiology of soccer: an update. Sports Med. 2005;35(6):501-36.
  9. Adamo KB, Tesson F. Genotype-specific weight loss treatment advice: how close are we? Appl Physiol Nutr Metab. 2007;32(3):351-66.
  10. North KN, Yang N, Wattanasirichaigoon D, Mills M, Easteal S, Beggs AH. A common nonsense mutation results in alpha-actinin-3 deficiency in the general population. Nat Genet. 1999;21(4):353-4.
  11. MacArthur DG, North KN. ACTN3: A genetic influence on muscle function and athletic performance. Exerc Sport Sci Rev. 2007;35(1):
  12. Alfred T, Ben-Shlomo Y, Cooper R, Hardy R, Cooper C, Deary IJ, et al. ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies. Hum Mutat. 2011;32(9):1008-18.
  13. Bylund DB, Eikenberg DC, Hieble JP, Langer SZ, Lefkowitz RJ, Minneman KP, et al. International Union of Pharmacology nomenclature of adrenoceptors. Pharmacological reviews. 1994;46(2):121-36.
  14. Snyder EM, Beck KC, Dietz NM, Eisenach JH, Joyner MJ, Turner ST, et al. Arg16Gly polymorphism of the beta2-adrenergic receptor is associated with differences in cardiovascular function at rest and during exercise in humans. J Physiol. 2006;571(Pt 1):121-30.
  15. Snyder EM, Johnson BD, Joyner MJ. Genetics of beta2-adrenergic receptors and the cardiopulmonary response to exercise. Exerc Sport Sci Rev. 2008;36(2):98-105.
  16. Skeberdis VA, Gendviliene V, Zablockaite D, Treinys R, Macianskiene R, Bogdelis A, et al. beta3-adrenergic receptor activation increases human atrial tissue contractility and stimulates the L-type Ca2+ current. J Clin Invest. 2008;118(9):3219-27.
  17. Santiago C, Ruiz JR, Buxens A, Artieda M, Arteta D, Gonzalez-Freire M, et al. Trp64Arg polymorphism in ADRB3 gene is associated with elite endurance performance. Br J Sports Med. 2011;45(2):147-9.
  18. Wolfarth B, Rankinen T, Muhlbauer S, Scherr J, Boulay MR, Perusse L, et al. Association between a beta2-adrenergic receptor poly­morphism and elite endurance performance. Metabolism. 2007;56(12):1649-51.
  19. Tsianos GI, Evangelou E, Boot A, Zillikens MC, van Meurs JB, Uitterlinden AG, et al. Associations of polymorphisms of eight muscle- or metabolism-related genes with performance in Mount Olympus marathon runners. J Appl Physiol. 2010;108(3):567-74.
  20. Ainsworth BE, Haskell WL, Herrmann SD, Meckes N, Bassett DR, Jr., Tudor-Locke C, et al. 2011 Compendium of Physical Activities: a second update of codes and MET values. Med Sci Sports Exerc. 2011;43(8):1575-81.
  21. WHO. Energy and protein requirements. Report of a Joint FAO/WHO/UNU Expert Consultation. Geneva: World Health Organization; 1985 [Available from: http://www.fao.org/docrep/003/aa040e/AA040E15.htm#notea18.
  22. FAO. Food and Nutrition Technical Report Series 1. Human energy requirements. Report of a Joint FAO/WHO/UNU Expert Consultation. Rome: Food and Agriculture Organization of the United Nations (FAO); 2004 [Available from: http://www.fao.org/docrep/007/y5686e/y5686e00.htm.
  23. Lum A, Le Marchand L. A simple mouthwash method for obtaining genomic DNA in molecular epidemiological studies. Cancer Epidemiol Biomarkers Prev. 1998;7(8):719-24.
  24. Santiago C, Gonzalez-Freire M, Serratosa L, Morate FJ, Meyer T, Gomez-Gallego F, et al. ACTN3 genotype in professional soccer players. Br J Sports Med. 2008;42(1):71-3.
  25. Eynon N, Banting LK, Ruiz JR, Cieszczyk P, Dyatlov DA, Maciejewska-Karlowska A, et al. ACTN3 R577X polymorphism and team-sport performance: A study involving three European cohorts. J Sci Med Sport. 2013.
  26. Massidda M, Scorcu M, Calo CM. New Genetic Model for Predicting Phenotype Traits in Sports. Int J Sports Physiol Perform. 2013.
  27. Williams AG, Folland JP. Similarity of polygenic profiles limits the potential for elite human physical performance. J Physiol-London. 2008;586(1):113-21.
  28. Scharin Tang M, Lindberg E, Gruner Svealv B, Magnusson Y, Andersson B. Cardiac reserve in the transplanted heart: effect of a graft polymorphism in the beta1-adrenoceptor. J Heart Lung Transplant. 2007;26(9):915-20.
  29. Sawczuk M, Maciejewska-Karlowska A, Cieszczyk P, Zarebska A. Ser49Gly and Arg389Gly polymorphisms of the ADRB1 gene and endurance performance. Central European Journal of Biology. 2012;7(5):794-800.
  30. Moore GE, Shuldiner AR, Zmuda JM, Ferrell RE, McCole SD, Hagberg JM. Obesity gene variant and elite endurance performance. Metab-Clin Exp. 2001;50(12):1391-2.
  31. Sarpeshkar V, Bentley DJ. Adrenergic-beta(2) receptor polymorphism and athletic performance. J Hum Genet. 2010;55(8):479-85.
  32. Kim SM, Oh SD, Jung IG, Lee J, Sim YJ, Lee JK, et al. Distribution of the Trp64Arg polymorphism the beta(3)-adrenergic receptor gene in athletes and its influence on cardiovascular function. Kardiol Pol. 2010;68(8):920-6.
  33. Eynon N, Hanson ED, Lucia A, Houweling PJ, Garton F, North KN, et al. Genes for Elite Power and Sprint Performance: ACTN3 Leads the Way. Sports Med. 2013;43(9):803-17.

Comments are closed.