Skip to main content
British Journal of Sports Medicine logoLink to British Journal of Sports Medicine
. 2007 May 15;41(11):760–768. doi: 10.1136/bjsm.2006.034967

Health benefits of tennis

Babette M Pluim 1,2,3,4, J Bart Staal 1,2,3,4, Bonita L Marks 1,2,3,4, Stuart Miller 1,2,3,4, Dave Miley 1,2,3,4
PMCID: PMC2465255  PMID: 17504788

Abstract

The aim of the study was to explore the role of tennis in the promotion of health and prevention of disease. The focus was on risk factors and diseases related to a sedentary lifestyle, including low fitness levels, obesity, hyperlipidaemia, hypertension, diabetes mellitus, cardiovascular disease, and osteoporosis. A literature search was undertaken to retrieve relevant articles. Structured computer searches of PubMed, Embase, and CINAHL were undertaken, along with hand searching of key journals and reference lists to locate relevant studies published up to March 2007. These had to be cohort studies (of either cross sectional or longitudinal design), case–control studies, or experimental studies. Twenty four studies were identified that dealt with physical fitness of tennis players, including 17 on intensity of play and 16 on maximum oxygen uptake; 17 investigated the relation between tennis and (risk factors for) cardiovascular disease; and 22 examined the effect of tennis on bone health. People who choose to play tennis appear to have significant health benefits, including improved aerobic fitness, a lower body fat percentage, a more favourable lipid profile, reduced risk for developing cardiovascular disease, and improved bone health.

Keywords: health, prevention, risk factors, tennis


The health benefits of exercise are well established. Research has shown that regular moderate physical activity has a beneficial effect on health1 and is associated with a decreased risk of diabetes2,3,4 and cardiovascular disease.5,6,7,8 Regular exercise has a beneficial effect on cardiovascular risk factors through many mechanisms. It improves the plasma lipid profile,9,10 reduces body weight,11 lowers blood pressure,9,12 increases insulin sensitivity,13,14 and improves lung function,15 cardiac function16,17 and cardiorespiratory fitness.16,17 In addition, exercise has a positive effect on bone health.18

Recommended exercise duration and intensity have changed over time. In the early 1990s, exercise recommendations exhorted vigorous intensity exercise (for example, jogging) for at least 20 minutes continuously, three days a week, in order to reap the benefits.19,20 More recent recommendations prescribe the accumulation of at least 30 minutes of moderate intensity physical activity, almost daily, relative to the physical fitness of the individual (for example, brisk walking, cycling, or swimming).21,22 The requirement of continuous exercise has been dropped, because the benefits derived from the accumulation of shorter sessions have been shown to be equivalent to those of longer sessions as long as the total amount of energy expended is similar.6

The recommended type of exercise has also received attention. Jogging, cycling, and swimming are well known to have significant health benefits, but not everyone participates in these sports. Tennis is one of the most popular sports throughout the world and is played by millions of people. Furthermore, a large majority of the people who play tennis maintain the sport throughout life. Tennis would therefore be an ideal sport to improve physical activity levels of the general population.

Although many studies have been published on the health benefits of exercise in general, it is still unclear whether there is a direct relation between improved health and playing tennis. For that reason, we undertook a systematic review to explore the health benefits of tennis in the prevention of several risk factors and major diseases that have been related to a sedentary lifestyle—that is, low fitness levels, obesity, hypertension, hyperlipidaemia, diabetes mellitus, cardiovascular disease, and osteoporosis.

Methods

A literature search was undertaken to retrieve potentially relevant articles. The following electronic databases were explored: PubMed (from 1966 up to March 2007), Embase (from 1989 up to March 2007), and Cumulative Index to Nursing and Allied Health Literature (CINAHL) (from 1982 up to March 2007). A priori defined search terms (Medical subject heading (Mesh) and text words) used in this search were: “physical fitness”, “aerobic fitness”, “cardiovascular deconditioning”, “cardiovascular disease”, “heart disease”, “cardiac function”, “diabetes mellitus”, “hyperlipidemia”, “lipid profile”, “hypercholesterolemia”, “cholesterol level”, “hypertension”, “blood pressure”, “obesity”, “body mass index”, “BMI”, “osteoporosis”, and “bone health”. Each term was combined with “tennis”. Hand searching of key journals and citation tracking of the retrieved articles was also done to identify additional relevant articles.

To be included in this review, studies had to meet the following criteria:

  • they had to be cohort studies (of either cross sectional or longitudinal design), case–control studies, or experimental studies published in English or German;

  • they had to contain data on the relation between playing tennis and physical fitness, cardiovascular disease, obesity, hypertension, hyperlipidaemia, diabetes mellitus, and osteoporosis, or between playing tennis and the occurrence of health benefits in patients who suffer from these diseases.

The most important results of the identified studies were summarised and categorised according to the aforementioned categories. Studies on the prevention or treatment of sports injuries and literature reviews were excluded.

Results

Our results in the PubMed, Embase, and CINAHL databases resulted in, respectively, 191, 179, and 382 potentially relevant papers. Papers were included when the content was felt to be appropriate by two independent reviewers. In case of disagreement, further discussion was undertaken to achieve consensus.

Twenty four studies (25 articles) were identified that contained data on physical fitness of tennis players.23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47 Seventeen studies (18 articles) provided information on intensity of play,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40 and 16 studies contained data on maximum oxygen uptake of tennis players.26,27,28,29,30,31,34,35,39,41,42,43,44,45,46,47 Seventeen studies45,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62 were found that investigated the relation between tennis and risk factors for cardiovascular disease and included eight cross sectional studies on cardiac size or function,54,55,56,57,58,59,60,61 four cross sectional studies on obesity,45,47,50,51 two cross sectional studies47,49 and one longitudinal study48 on hyperlipidaemia, two cross sectional studies on hypertension,47,52 one longitudinal study on diabetes,53 and one longitudinal study on cardiovascular morbidity and mortality.62 Twenty two studies (two longitudinal63,64 and 20 cross sectional65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85) were retrieved that examined the effect of tennis on bone health.

Physical fitness levels

Exercise intensity

In 17 studies the intensity of match play was examined using heart rate recordings23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39 or maximum oxygen uptake (V̇o2max), or both23,26,27,39,40 during play (table 1). Mean (SD) heart rate during singles play ranged from 141 (16) to 182 (12) beats/minute, equating to 70–90% of maximum heart rate. Mean oxygen consumption during play ranged from 23.1 (3.1) to 40.3 (5.7) ml.kg−1.min−1, reflecting 50% to 80% of V̇o2max. Mean lactate levels during play were generally 2 to 3 mmol.l−1; however, one investigator reported levels as high as 6 mmol.l−1.28 The results of these studies indicate that singles tennis play can be categorised as vigorous intensity exercise (>6 Mets).

Table 1 Intensity of match play.
Reference* Standard of player ITN Sex n Age (years) Mean HR during play (beats/min) HRmax exercise test (beats/min) % HR max Lactate (mmol.l−1) Surface o2 mean during play (ml.kg−1.min−1) o2max exercise test (ml.kg−1.min−1)
Juniors
Girard et al23 Club 6 M 7 15 (2) 182 (12) 201 (9) 90 (5) 2.36 (0.47) Clay 40.3 (5.7) 50.3 (3.9)
M 7 15 (2) 173 (17) 201 (9) 86 (6) 3.08 (1.12) Hard court 35.9 (7.5) 50.3 (3.9)
Weber24 Competitive 4 M/F 18 12.6 (1.2) 172 (6) nr nr 1.41 (0.63) Carpet nr nr
18–35 years
Fernandez et al40 International 1–2 M 6 3.79 (2.03) Clay 26.6 (3.3) 58.2 (2.2)
Novas et al25 State, national 3 F 6 18.3 (2.5) 146 (20) Hard court
Smekal et al26 Top league 3–4 M 20 26 (4) 151 (19) 193 (9) 78 2.07 (0.88) Clay 29.1 (5.6) 57.3 (5.1)
Bernardi et al27 Intermediate 4–5 M 7 28.1 (3) 147 (9) 194 (5) 76 nr Clay 33 (3) 65 (6)
Christmass et al28 State 3 M 7 24 (2) nr 190 (3) 86 (1) 5.86 (1.33) Hard court nr 53.4 (1.8)
Christmass et al29 State 3 M 8 23 (1) 155 180 (3) 86 Hard court nr 54.3 (1.9)
Reilly et al30 Top club 4 M 8 23.4 (3.1) 146 (19) 191 (11) 76 nr Wood nr 53.2 (7.3)
Bergeron et al31 University 4 M 10 20.3 (2.5) 145 (13) 196 (6) 74 2.3 (1.2) Clay nr 58.5 (9.4)
Therminarias et al32,33 Intermediate 4–5 F 9 21.2 (1.9) 157 (3) 190 (3) 82 1.76 (0.3) Clay nr nr
Weber24 Competitive 4 M/F 18 23.8 (3.6) 148 (10) nr nr 2.11 (0.77) Carpet nr nr
Recreational 6–7 M/F 33 25.3 (2.5) 147 (11) nr nr 2.43 (1.28) Carpet nr nr
Beginners 9 M/F 16 25.8 (3.0) 135 (19) nr nr 1.92 (0.56) Carpet nr nr
Morgans et al34 Intermediate to advanced 2–4 M 17 31.4 (7.3) 154 (17) 188 (11) 82 nr Hard court nr 46.4 (6.2)
Eliott et al35 College 4 M 8 20.3 (1.3) 153 (3) 192 (11) 79 nr Hard court nr 65.9 (6.3)
Docherty 36 Low to high 4–9 M 42 25 (5) 150 (10) nr 70 nr Hard court nr nr
Kindermann et al37 Well trained 4–5 M 12 32.2 (8.5) 146 (20) nr nr 2.0 (0.5) Unknown nr nr
Seliger et al38 Top level 3 M 16 24.7 (3.7) 143 nr nr nr Indoor court 27.3 nr
35 years and over
Ferrauti et al39 National 2–3 M 6 47 (5.4) 142.5 (12.7) nr nr 1.24 (0.37) Clay 25.6 (2.8) 47.5 (4.3)
National 2–3 F 6 47.2 (6.6) 141.5 (18.9) nr nr 1.67 (0.49) Clay 23.1 (3.1) 41.4 (6.0)
Therminarias32, 33 Intermediate 4–5 F 10 46.5 (1.3) 156 (4) 175 (2) 89 1.79 (0.29) Clay nr nr
Weber24 Competitive 4 M/F 12 50.4 (4.9) 154 (15) nr nr 2.82 (0.92) Carpet nr nr
Recreational 6–7 M/F 18 54.3 (6.1) 141 (16) nr nr 2.67 (0.96) Carpet nr nr

Values are mean (SD).

*First author and reference number.

F, female; HR, heart rate; HRmax, maximum heart rate; ITN, international tennis number; M, male; n, number of subjects; nr, not reported.

Aerobic capacity

One longitudinal and 15 cross sectional studies on the V̇o2max of tennis players were identified (table 2).26,27,28,29,30,31,34,35,39,41,42,43,44,45,46,47 The mean V̇o2max ranged from 35.5 (5.8) to 65.9 (6.3) ml.kg−1.min−1, depending on age, sex, and training level, indicating that these tennis players had high fitness levels compared with the norm for normally active controls of the same age and sex.86,87

Table 2 Maximum oxygen uptake of tennis players of various levels of play.
Reference* Level of play, country ITN Sex n Age (years) o2max (ml.kg−1.min−1)
Juniors
Buti et al41 State squad, Australia 3 M 8 11.7 56.3 (6.5)
F 8 11.7 52.6 (8.2)
Carlson et al42 Elite junior, Australia 2–3 M 6 16.8 60.3 (6.4)
F 6 14.6 52.3 (7.5)
Powers, et al43 High school, USA 4–5 F 10 15.8 (0.4) 48 (2.1)
18–35 years
Smekal et al26 Top league, Austria 3–4 M 20 26 (4) 57.3 (5.1)
Bernardi et al27 Intermediate, Italy 4–5 M 7 28.1 (3) 65 (6)
Christmass et al28 State level, Australia 3 M 7 24 (2) 53.4 (1.8)
Kraemer et al44 College, Div I and III, USA 3–5 F 38 20 (2) 47.6 (4.4)
Christmass et al29 State level, Australia 3 M 8 23 (1) 54.3 (1.9)
Reilly et al30 Top club, UK 4 M 8 23.4 (3.1) 53.2 (7.3)
Bergeron et al31 University, Div I, USA 3–4 M 10 20.3 (2.5) 58.5 (9.4)
Morgans et al34 Intermediate to advanced, USA M 17 31.4 (7.3) 46.4 (6.2)
Elliott et al35 College level, Australia 3–4 M 8 20.3 (1.3) 65.9 (6.3)
Wilmore et al46 Beginners, USA 9–10 M 9 29 (6.6) 44.4 (7.5)
35 years and over
Ferrauti et al39 Nationally ranked, Germany 2–3 M 6 47 (5.4) 47.5 (4.3)
F 6 47.2 (6.6) 41.4 (6.0)
Vodak et al45 Recreational, USA 6–8 M 25 39 (3) 50.2 (5.7)
6–8 F 25 42 (6) 44.2 (5.4)
Swank et al47 Elite, USA 3–4 M 13 40–59 48.7 (11.7)
4–5 M 15 >60 35.3 (5.8)

Values are mean (SD).

*First author and reference number.

F, female; ITN, international tennis number; M, male; n, number of subjects; V̇o2max, maximum oxygen consumption.

In the one longitudinal study,46 38 sedentary, middle aged volunteers were randomly assigned into one of four groups: bicycling (9), tennis (10), jogging (9), and control (10). Each group exercised three times a week for 30 minutes per session for 20 weeks. Tennis produced modest increases in endurance capacity (5.7%), compared with cycling (14.8%) and jogging (13.3%). The control group did not change. However, it should be taken into account that the duration of each training session was only 30–50% of a typical time for playing tennis.

Cardiovascular risk factors

Obesity

Vodak et al45 found below average body fat in 25 male (age 42 (6) years) and 25 female (age 39 (3) years) tennis players, with mean values of 16.3% and 20.3% for men and women.

Schneider and Greenberg (n = 7248; 18–34 year old Americans),50 showed that runners/joggers/fast walkers and tennis players were less likely to be obese, smoke, consume large quantities of alcohol, or drive without seat belts than those who participate in team sports and an aggregate of other sports.

Further evidence of an association between below average body fat and tennis was provided by Swank et al,47 who found that elite male veteran tennis players had significantly less fat than an age matched active control group (p⩽0.05). Both the younger veterans (aged 40 to 59) and the older veterans (over 60) were on average 3% leaner than the non‐tennis‐playing moderately active controls (17–20.5% v 21–25%, respectively).

Finally, LaForest et al51 studied recreational tennis players who had played twice a week for the previous ten years. Mean body fat percentage of the tennis players (aged 23 to 69 years) was significantly lower than the body fat of the age matched controls (20.4% v 23.9%, p<0.05).

Hyperlipidaemia

In a cross sectional study by Vodak et al,49 fasting plasma lipid and lipoprotein concentrations of 25 male and 25 female tennis players (mean age 42 years, nine years playing history) were compared with a sedentary group matched for age, sex, and education. Mean plasma high density lipoprotein (HDL) cholesterol was significantly higher in tennis players than in sedentary subjects (men, 1.39 (0.30) v 1.17 (0.31) mmol.l−1 (p<0.001); women, 1.72 (0.22) v 1.56 (0.29) mmol.l−1 (p = 0.02)). The increased plasma HDL cholesterol concentrations were independent of other factors known to alter these lipid concentrations. Very low density lipoprotein subfractions (VLDL‐C) and triglycerides were also significantly lower in the tennis players; however, total cholesterol (TC) and low density lipoprotein (LDL) cholesterol concentrations were similar to the controls.

Ferrauti et al48 investigated the short term effects of tennis training on lipid metabolism. They studied the effects of a six week running–intensive tennis training programme in 22 veteran players (11 men and 11 women aged 43 to 47 years) and compared these with 16 control subjects who continued their usual (tennis) habits. They found slight increases in HDL2 cholesterol as well as small decreases in HDL3 cholesterol, LDL cholesterol, and triglycerides. Despite the overall positive improvement of the lipid profile, the changes were not significantly different from the control group, possibly because of the limited number of subjects and the relatively short duration of the study.

Finally, Swank et al47 studied 28 elite senior male tennis players (aged 40 to 60+ years) who had participated in tennis for an average of 21 years, and 18 moderately active age matched controls. There were no significant differences between tennis players and the control group for total cholesterol, LDL cholesterol, HDL cholesterol, total cholesterol/HDL cholesterol ratio and triglycerides. However, the tennis players in the 40 to 59 year old age group had an average HDL cholesterol of 0.21 mmol greater than an age matched control group. Furthermore, tennis players in the 60+ year old age group had an average HDL cholesterol 0.06 mmol greater than their age matched control group.

Hypertension

Blood pressure was studied in 21 middle aged male tennis players (age 50 (7) years), using a portable ambulatory blood pressure recorder.52 Mean resting systolic blood pressure was 137 (19) mm Hg and diastolic blood pressure was 88 (13) mm Hg, suggestive of pre‐hypertension (blood pressure between 120/80 and 139/89 mm Hg).88 Mean systolic blood pressure during play was 168 (19) mm Hg, with a peak systolic pressure of 198 (30) mm Hg. Mean diastolic blood pressure during play decreased to 82 (16) mm Hg.

Swank et al47 studied 28 elite senior male tennis players (21 years of tennis play) and 18 moderately active age matched controls and found no significant difference between groups in either systolic or diastolic blood pressure values (40 to 59 years: systolic blood pressure (SBP) = 121 (10) v 124 (14) mm Hg, diastolic blood pressure (DBP) = 78 (10) v 79 (10) mm Hg; 60+ years: SBP = 136 (10) v 135 (14), DBP = 82 (7) v 81 (7) mm Hg).

Diabetes mellitus

Nessler53 undertook a longitudinal study of 12 patients (seven men, mean age 62 (4) years and five women, mean age 60 (4) years) with type II diabetes at the Sports University of Cologne. The untrained beginners played tennis twice a week with a modified ball for six weeks; training sessions lasted 90 minutes. No significant changes occurred in baseline glucose levels, HbA1c concentration, triglyceride levels, LDL, HDL, and total cholesterol levels, or free fatty acids. There were small but significant increases in plasma insulin (10.3 (3.8) v 13.9 (5.7) μE/ml, p = 0.026) and c‐peptide production (3.5 (1.0) v 4.7 (1.4 nmol.l−1), p = 0.001). The mean glucose concentration (mean of 12 participants measured before and after 12 training sessions) fell from 188.0 (72.7) mg/dl before to 156.7 (52.2) mg/dl after 90 minutes of training (p = 0.001).

Cardiovascular disease

Heart size

Eight studies examined the cardiac dimensions of elite tennis players.54,55,56,57,58,59,60,61 Increased heart size and increased performance capacity were noted regardless of sex.54,55,59,60,61 Systolic and diastolic function were within normal limits.56,57,61

Morbidity and mortality

Houston et al62 studied 1019 male students between 1948 and 1964. After a standard physical examination, the students were asked to rate their ability in tennis, golf, football, baseball, and basketball during medical school and earlier. The researchers assessed the participants' physical activities an average of 22 and 40 years later. Tennis was the only sport in which a greater ability during medical school was associated with a lower risk of cardiovascular disease. After adjustment for confounding variables, the relative risk of developing cardiovascular disease was 0.56 (95% confidence interval (CI), 0.35 to 0.89) in the high ability group and 0.67 (0.47 to 0.96) in the low ability group, compared with the no ability group. A primary factor for this beneficial health profile may be that tennis was the sport played most often through mid‐life. Half the tennis players were still participating in the sport in mid‐life, compared with only a quarter of those who reported playing golf and none who reported playing baseball, basketball, or football.

Osteoporosis

Twenty two studies (23 articles)63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85 were identified that examined the effects of tennis play on bone health. Generally, the bone mineral content (BMC) and bone density (BMD) were shown to be consistently greater in the dominant (playing) arm than in the non‐dominant arm. Also, BMC and BMD were greater in the hip and lumbar spine regions of tennis players than in controls, and exercise induced bone gain was greater in young than in old starters. Table 3 provides more specific information on the effect of tennis on bone health.

Table 3 Characteristics and results of included studies on the effect of playing tennis on indicators of bone health.

Reference* Design Study population Method Main results
Ducher et al85 XS 28 young (22 boys, 6 girls, 11.6 (1.4) y) and 47 adult tennis players (23 M, 24 F, 22.3 (2.7) y), and 70 age matched controls (12 children (12.2 (1.6) y) and 58 adults (23.3 (3.2) y)) DXA At the ultradistal radius, asymmetry in BMC in young and adult tennis players was 16.35% and 13.8%, respectively (p<0.0001). At the mid‐ and third‐distal radius, asymmetry was much greater in adults than in children (p<0.0001) for BMC (mid‐distal radius, +6.6% v +15.6%; third‐distal radius +6.9% v +13.3%).
Ducher et al82 XS 52 tennis players (24.2 (5.8) y), 16.2 (6.1) y of practice DXA Lean tissue mass, bone area, BMC, and BMD of the dominant forearm were significantly (p<0.0001) greater. Bone area and BMC correlated with grip strength on both sides (r = 0.81–0.84, p<0.0001).
Ducher et al83 XS 20 regional level tennis players (10 M; 10 F, mean age 23.1 (4.7) years, with 14.3 (3.4) years of playing) DXA Significant side‐to‐side differences (p<0.0001) were found in muscle volume (+9.7%), grip strength (+13.3%), BMC (+13.5%), total bone volume (+10.3%), and subcortical volume (+20.6%), but not in cortical volume (+2.6%, NS). The asymmetry in total bone volume explained 75% of the variance in BMC asymmetry (p<0.0001). Volumetric BMD was slightly higher on the dominant side (+3.3%, p<0.05). Grip strength and muscle volume correlated with all bone variables (except volumetric BMD) on both sides (r = 0.48–0.86, p<0.05–0.0001) but the asymmetries in muscle indices did not correlate with those in bone indices.
Ducher et al84 XS 57 regional level tennis players (33 M, 24 F). All had been practising tennis for at least 5 years DXA At the ultradistal radius, the side‐to‐side difference in BMD was larger than in bone area (8.4 (5.2)% and 4.9 (4.0)%, respectively, p<0.01). In he cortical sites, the asymmetry was lower (p<0.01) in BMD than in bone area (mid‐distal radius: 4.0 (4.3)% v 11.7 (6.8)%; third‐distal radius: 5.0 (4.8)% v 8.4 (6.2)%).
Sanchis‐Moysi et al66 XS 10 F postmenopausal tennis players (60 (5) y) and 12 postmenopausal controls (63 (7) y). Tennis players started at 31 (9) y and had been playing for 27 (7) y, at least 3 h/wk DXA Tennis players showed 8% greater BMC and 7% greater osseous area in the dominant arm than in the non‐dominant arm (p<0.05). There was a positive correlation between duration of tennis participation and inter‐arm asymmetry in BMC (r = 0.81, p<0.01) and bone area (r = 0.78, p<0.01).
Sanchis Moysi et al65 XS 17 M tennis players (55 (2) y), 9 F tennis players (61 (1) y), 15 M (56 (3) y) and 20 F (62 (2) y) control subjects. Mean tennis participation was 27 (7) y, 3 h/wk DXA Male tennis players had a 16% higher BMC and 10% BMD in legs than controls (p<0.05). 10–30% greater BMC and BMD were observed in the hip region and lumbar spine (L2–L4) of tennis players v controls (p<0.05).
Kontulainen et al80 XS 36 young F Finnish tennis/squash players (22 (8) y, mean starting age 11 (2) y), and 28 older F players (39 (11) y, mean starting age 26 (8) y), and 27 controls (29 (10) y) pQCT, DXA The side‐to‐side differences in the young starters bone mineral content, cortical area, total cross sectional area of bone, and cortical wall thickness were 8–22% higher than those of controls and 8–14% higher than those of old starters.
Nara‐Ashizawa et al68 XS 92 middle aged F tennis players (46 (5) y) who initiated training after bone had matured (mean starting age 36 (3) y) pQCT Endocortical area (0.278 (0.094) v 0.300 (0.106) cm2), periosteal area (1.007 (0.14) v 1.061 (0.15) cm2), BMC (0.141 (0.017) v 0.147 (0.017) g), moment of inertia (1598 (413) v 1744 (460) mm4), section modulus (219 (41) v 233 (44) mm3), and SSI (352 (66) v 376 (71) mm3) of dominant midradius were greater (p<0.01) than in the non‐dominant radius. BMD of trabecular bone (0.383 (0.060) v 0.363 (0.070) g/cm3, p<0.05) and whole bone (0.756 (0.115) v 0.656 (0.120) g/cm3, p<0.01) at the dominant distal radius were greater than in the non‐dominant radius.
Kontulainen et al64 PCS; 5‐y follow up 36 young F Finnish tennis/squash players (22 (8) y, mean starting age 11 (2) y), and 28 older female players (39 (11) y, mean starting age 26 (8) y), and 27 controls (29 (10) y). Young starters reduced training from 4.7 (2.7) to 1.4 (1.3) times/wk; old starters from 4.0 (1.4) to 2.0 (1.4) times/wk DXA Bone gain was 1.3–2.2 times greater in favour of young starters: The difference in BMC of humeral shaft in dominant v non‐dominant arm was 22 (8.4)% in young starters v 10 (3.8)% in old starters at follow up.
Haapasalo et al67 XS 12 M former Finnish national level tennis players (30 (5) y) and 12 age, height, and weight matched controls pQCT Among the players significant side‐to‐side differences (p<0.05) in favour of the dominant arm were found in BMC, total area, cortical area, and bone strength index at the proximal humerus, humeral shaft, distal humerus, radial shaft, and distal radius. Increased bone strength was mainly due to increased bone size and not to a change in volumetric bone density.
Kontulainen et al63 PCS; 4‐y follow up 13 M former competitive tennis players (26 (5) y) who started their career at a mean age of 11 y and 13 controls (26 (6) y). The players had all retired from top tennis before (mean 2.3 (0.6) y) follow up DXA Relative side‐to‐side BMC differences were significantly (p<0.001) larger in players than in controls at all measured sites in both 1992 and 1996 for proximal humerus (1992: 18.5% v 1.4%; 1996: 18.4% v 0.5%), humeral shaft (1992: 25.2% v 4.7%; 1996: 25.9% v 4.5%), radial shaft (1992: 13.9% v 1.8%; 1996: 14.2% v 2.1%), and distal radius (1992: 13.2% v 2.0%; 1996: 13.2% v 2.3%).
Ashizawa et al69 XS Forearms of 16 competitive tennis players (10 F) and 12 healthy controls (7 F) aged 18–24 y were scanned at mid and distal site of the radius pQCT Players had an increase in total BMC (13.3%, p<0.001), periosteal bone area (15.2%, p<0.001), cortical BMC (12.6%, p<0.001), and cortical bone area (13.5%, p<0.01) in the playing arm v the non‐playing arm. In controls, side‐to‐side differences in these variables were not significant.
In the distal radius, total BMC (13.8%, p<0.01), periosteal bone area (6.8%, p<0.05), total BMD (6.8, p<0.01), trabecular bone area (6.8%, p<0.05), and trabecular BMD (5.8%, p<0.05) of the playing arm were greater than in the non‐playing arm. In controls, significant side‐to‐side differences were not found in any measured variables.
Haapasalo et al70 XS 91 7–17 y F tennis players and 58 healthy F controls. In each Tanner stage, differences in BMD in playing and non‐playing arms and lumber spine were compared between the players and controls DXA In players, BMD inter‐arm differences were significant (p<0.05 to <0.001) in all Tanner stages, with mean differences ranging from 1.6% to 15.7%. Mean arm differences between players and controls did not become obvious until Tanner stage III (mean age 12.6 y). In the lumbar spine differences were not found until Tanner stage IV (mean age 13.5 y, 0.97 (0.13) v 0.89 (0.09) g/cm2, p<0.05) and Tanner stage V (mean age 15.5 y, 1.08 (0.105) v 0.96 (0.134) g/cm2, p<0.05).
Calbet et al71 XS 9 M professional tennis players (26 (6) y) and 17 non‐active M subjects (24 (3) y) DXA Total mass (4977 (908) v 4220 (632) g, lean mass (3772 (500) v 3246 (421) g, p<0.001, and BMC (229 (43.5) v 194 (33) g) were greater in the dominant arm of tennis players than in controls (all p<0.05). BMD was increased in tennis players v controls in the lumbar spine (1.25 (0.29) v 1.09 (0.12) g/cm2, p = 0.09) and in the trochanteric region (0.94 (0.11) v 0.80 (0.07) g/cm2, p<0.001).
Haapasalo et al72 XS 17 young competitive M tennis players (25 (5) y), 30 young F players (19 (3) y), 20 older F players (43 (5) y), 16 M controls (25 (5) y), 25 young F controls (21 (3) y), and 16 older F (39 (6) y). Starting age, M 10 (3) y, young F 9 (2) y, older F 29 (6) y DXA There were significant side‐to‐side humeral length differences in young M players (+1.4%), young F controls (+1.1%), and older F players (+0.7%). Relative side‐to‐side differences in BMC (range +7.6 to +25.2%), BMD (range +5.8% to +22.5%), cortical wall thickness (range +6.9% to +45.2%), cross sectional moment of inertia (range +7.8% to +26.4%), and section modulus (range +3.0% to +21.7%) were significantly larger in players than in controls at the proximal, mid, and distal part of the humerus. Relative side‐to‐side differences were significantly larger in young (range +11.7% to +45.2%) than in older players (range +3.0% to +12.4%).
Etherington et al73 XS 16 former tennis players (aged 40–65 y), 67 former middle and long distance runners and 585 age matched controls DXA Tennis players had greater BMD than runners (lumbar spine 12% (95% CI, 5.7 to 18.2), p = 0.0004, femoral neck 6.5% (–0.2 to 13.2), p = 0.066). Athletes had greater BMD than controls (lumbar spine 8.7% (5.4 to 12.0), p<0.001 and femoral neck 12.1% (9.0 to 15.3), p<0001). BMD of tennis players' forearms were greater than their non‐dominant forearms.
Tsuji et al74 XS 10 M college wrestlers (20 (1) y), 16 female college basketball players (20 (1) y), and 12 F college tennis players (21 (1) y) DXA A significant and positive relation was found between mid‐radial (0.48 (0.07) g/cm2) BMD and grip strength (31.2 (4.1) kg) in the dominant forearm of tennis players (r = 0.43, p<0.05). There was a significant difference between mid‐radial BMD in the dominant (range 0.63–0.87 g/cm2) and non‐dominant arm (range 0.52–0.57 g/cm2, p<0.05).
Kannus et al75 XS 105 F Finnish national level tennis/squash players (28 (11) y) and 50 controls (27 (9) y). Players were divided into starting groups according to the biological age (y before or after menarche) at which their playing careers began DXA The players had a larger (p<0.001) side‐to‐side difference in BMC for proximal humerus (1.42 (1.33) v 0.41 (1.08) g), humeral shaft (2.77 (2.20) v 0.57 (1.68) g), radial shaft (0.32 (0.47) v 0.12 (0.40) g), and distal radius (0.32 (0.38) v 0.11 (0.28) g). Differences were two to four times greater in players who started before or at menarche than 15 years after menarche.
Kannus et al76 XS 20 top level M Finnish tennis players (25 (5) y), and 20 controls (26 (5) y) DXA Relative side‐to‐side differences in BMD and BMC were significantly increased in players v controls for humeral shaft (BMD 0.29 (0.09) v 0.03 (0.10) g/cm2, BMC 6.41 (0.28) v 1.06 (0.33) g, p<0.001), and proximal humerus (BMD 0.12 (0.08) v 0.01 (0.10) g/cm2, BMC 2.38 (1.8) v 0.28 (1.7) g, p<0.001).
Krahl et al77, 78 XS 20 highly ranked professional tennis players (12 M, 8 F, 20.1 (4.5) y), and 12 controls (7 M, 5 F, 23.1 (4.7) y) x ray Relative side‐to‐side differences were significantly increased in tennis players v controls for ulnar diameter (2.1 v 0.02 mm, p<0.01), ulnar length (8 v 0.17 mm, p<0.01), second metacarpal diameter (0.9 v 0.0 mm, p<0.01), and second metacarpal length (2.7 v 0 mm, p<0.01).
Jacobson et al79 XS 11 college tennis players, 23 swimmers, and 86 older athletic F aged 23 to 75 y and age matched non‐athletic controls. Single and dual photon densitrometry Lumbar spine density was increased in tennis players v swimmers and controls (1.51 (37) v 1.39 (27) and 1.36 (49) g/cm2, p<0.02). Metatarsal density was increased in tennis players v swimmers and controls (626 (26) v 565 (14) and 512 (13) g/cm2, p<0.001). BMC of dominant arm of tennis players 16% higher than in non‐dominant arm; in controls ⩽3% (p<0.001). Differences between controls and athletic women were highest in oldest age groups.
Huddleston81 XS 35 active M tennis players were studied during the 1978 USTA's 70‐, 75‐, and 80‐y age group clay court championship (21 aged 70–74 y, 9 aged 75–79 y, 5 aged 80–84 y Transmission scanning with a low energy x‐ray beam Bone mass of the radius of the playing arm (mean, 1.37 g/cm) was greater than that of the non‐playing arm (mean, 1.23 g/cm) in all but one person. The quantity of BM present in the playing arms of the tennis population was greater than that of the dominant arm on non‐athletes.

*First author and year of publication.

BMC, bone mineral content; BMD, bone mineral density; CI, confidence interval; DXA, dual energy x ray absorptiometry; F, female; M, male; PCS, prospective cohort study; pQTC, peripheral quantitative computer tomography; wk, week; XS, cross sectional study; y, years.

Discussion

The general findings of this review indicate that those who choose to play tennis appear to have positive health benefits. Specifically, lower body fat percentages, more favourable lipid profiles, and enhanced aerobic fitness contributed to an overall improved risk profile for cardiovascular morbidity. Furthermore, numerous studies have identified better bone health not only in tennis players with lifelong tennis participation histories, but also in those who take on the sport in mid‐adulthood.

A limitation of this review is the small number of studies with a longitudinal design. For example, of the 17 studies examining tennis and cardiovascular risk factors, only two had a longitudinal design (six week follow up). Similarly, of the 22 studies on bone health, only two had a longitudinal design. But to their credit, follow up was much longer (four and five years).

A second limitation, that of selection bias, may also have occurred in the studies reviewed, given that those who are healthy may be more inclined to play tennis (and continue lifelong participation) in comparison with others who may have health problems and deem tennis inappropriate for them. The type of person who is able to and does play tennis may self select for more positive health outcomes, as playing tennis is generally associated with a higher socioeconomic status.89 Furthermore, most of the studies included failed to adjust appropriately for confounding variables when studying the relation between tennis and health indices.

Despite these limitations, there remains an indication of positive health benefits associated with regular tennis participation. This conclusion concurs with those of other well designed studies investigating the general impact of exercise on various health indices.

The lower body fat percentage of tennis players compared with less active controls is an important finding because obesity has become a “global epidemic”, with more than one billion adults overweight (body mass index (BMI) >25) and at least 300 million of them clinically obese (BMI >30).90

What is already know on this topic

  • Regular moderate physical activity has a beneficial effect on health and is associated with a decreased risk of cardiovascular disease and diabetes and a positive effect on bone health.

  • Recommendations prescribe the accumulation of at least 30 minutes of moderate intensity physical activity, almost daily, relative to the physical fitness of the individual.

What this study adds

  • This study specifically focuses on the relation between tennis and risk factors and diseases related to a sedentary lifestyle.

  • There is a positive association between regular tennis participation and health benefits, including improved aerobic fitness, a leaner body, a more favourable lipid profile, improved bone health, and a reduced risk of cardiovascular morbidity and mortality.

This review shows that tennis is associated with increased plasma HDL cholesterol.47,48,49 Even though more than 200 risk factors for coronary heart disease have now been identified, the single most powerful predictor is hyperlipidaemia.91 It is also a significant one—more than half the cases of heart disease are attributable to lipid abnormalities. The higher HDL cholesterol concentrations associated with a lower risk of cardiovascular disease implies that playing tennis may be at reduced risk of cardiovascular events.92

The results of the study by Vodak et al49 indicate that blood pressure response during tennis play is comparable to the response to an acute bout of moderate intensity dynamic exercise.93 Unfortunately, no longitudinal studies on the long term effect of tennis on blood pressure were identified and further studies are warranted.

Studies retrieved in this review unanimously showed that tennis was related to healthier bone structure in both sexes and across the age spectrum.63,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85 The association depended on the duration of tennis participation and training frequency, being stronger in young starters than in old starters, but was maintained despite decreased tennis participation. This was most clearly present in load bearing bones such as the humerus of the dominant arm, lumbar spine, and femoral neck. These findings support the exercise recommendations described in the American College of Sports Medicine (ACSM) position stand on “Physical activity and bone health”, which recommends 20 to 40 minutes of weight bearing endurance activities, such as tennis, at least three times a week to augment bone mineral accretion in children and adolescents, and 30 to 60 minutes of these activities at least three times a week to preserve bone health during adulthood.94

Playing tennis on a regular basis (two to three times a week), either singles or doubles, meets the exercise recommendations of the ACSM and American Heart Association (AHA).20,21,22 Reported mean heart rates during singles tennis ranged from 70% to 90% of maximum heart rate, and mean oxygen consumption ranged from 50% to 80% of V̇o2max. Moderate intensity activities are those done at a relative intensity of 40% to 60% of V̇o2max (60–75% of maximum heart rate), whereas vigorous intensity activities are those done at a relative intensity of >60% of V̇o2max (>75% maximum heart rate). Thus exercise intensity during singles tennis play is high enough to categorise it as a moderate to vigorous intensity sport. This is supported by the findings that tennis players display an above average maximal oxygen uptake compared with normally active populations of the same age and sex.86,87

In doubles play, heart rate and V̇o2 tend to be lower than during singles play. However, it is not the absolute intensity of the exercise that is relevant, but rather the intensity relative to the physical capacity of the individual. This means that, while singles play may be necessary to result in health benefits for the younger player, doubles play may be sufficient for the middle aged or senior tennis player, because their maximum heart rate and V̇o2max are decreased. Doubles play is therefore particularly suitable for these categories. This has the added benefit that it increases the chance that those who play tennis are likely to maintain the sport when they grow older. Hence, the positive effects are maintained. In order for exercise to exert a positive effect, one has to embrace lifelong exercise patterns. The positive effects of sustained physical activity were demonstrated by Houston et al,62 who found that the association of high ability in tennis during college and a reduced risk of cardiovascular disease in later life was at least partly mediated through continued participation in tennis.

Conclusions and recommendations

A positive association has been shown between regular tennis participation and positive health benefits, including improved aerobic fitness, a leaner body, a more favourable lipid profile, improved bone health, and a reduced risk of cardiovascular morbidity and mortality. Exercise intensity during tennis play meets the exercise recommendations of the ACSM and AHA, and playing tennis regularly will contribute to improved fitness levels. In addition, long term tennis play leads to increased bone mineral density and bone mineral content of the playing arm, lumbar spine, and legs. However, further longitudinal studies with appropriate adjustment for confounding variables and self selection are warranted, to determine whether the positive association between a leaner body, a more favourable lipid profile, and a reduced risk of cardiovascular morbidity and mortality and tennis is an indication of the health benefits of tennis, or the effect of self selection and a healthier lifestyle of tennis players.

Abbreviations

BMC - bone mineral content

BMD - bone mineral density

CINAHL - Cumulative Index to Nursing and Allied Health Literature

References

  • 1.Warburton D E R, Nicol C W, Bredin S S D. Health benefits of physical activity: the evidence. Can Med Assoc J 2006174801–809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Hu F B, Stampfer M J, Solomon C.et al Physical activity and risk for cardiovascular events in diabetic women. Ann Intern Med 200113496–105. [DOI] [PubMed] [Google Scholar]
  • 3.Wei M, Gibbons L W, Mitchell T L.et al The association between cardiorespiratory fitness and impaired fasting glucose and type 2 diabetes mellitus in men. Ann Intern Med 199913089–96. [DOI] [PubMed] [Google Scholar]
  • 4.Helmrich S, Ragland D R, Leung R W.et al Physical activity and reduced occurrence of non‐insulent‐dependent diabetes mellitus. N Engl J Med 1991325147–152. [DOI] [PubMed] [Google Scholar]
  • 5.Lee I‐M, Rexroe K M, Cook N R.et al Physical activity and coronary heart disease in women. JAMA 20012851447–1454. [DOI] [PubMed] [Google Scholar]
  • 6.Lee I‐M, Sesso H D, Paffenberger R S. Physical activity and coronary heart disease risk in men. Does the duration of exercise episodes predict risk? Circulation 2000102981–986. [DOI] [PubMed] [Google Scholar]
  • 7.Lee I‐M, Sesso H D, Oguma Y.et al Relative intensity of physical activity and risk of coronary heart disease. Circulation 20031071110–1116. [DOI] [PubMed] [Google Scholar]
  • 8.Yu S, Yarnell J W G, Sweetnam P M.et al What level of physical activity protects against premature cardiovascular death? The Caerphilly study. Heart 200389502–506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Williams P T. Relationships of heart disease risk factors to exercise quantity and intensity. Arch Intern Med 1998158237–245. [DOI] [PubMed] [Google Scholar]
  • 10.Kraus W E, Houmard J A, Duscha B D.et al Effects of the amount and intensity of exercise on plasma lipoproteins. N Engl J Med 20023471483–1492. [DOI] [PubMed] [Google Scholar]
  • 11.Slentz C A, Duscha B D, Johnson J L.et al Effects of the amount of exercise on body weight, body composition, and measures of central obesity: STRRIDE – a randomized controlled study. Arch Intern Med 200416431–39. [DOI] [PubMed] [Google Scholar]
  • 12.Barlow C E, LaMonte M J, Fitzgerald S J.et al Cardiorespiratory fitness is an independent predictor of hypertension incidence among initially normotensive healthy women. Am J Epidemiol 2006163142–150. [DOI] [PubMed] [Google Scholar]
  • 13.Houmard J A, Tanner C J, Slentz C A.et al Effect of the volume and intensity of exercise training on insulin sensitivity. J Appl Physiol 200496101–106. [DOI] [PubMed] [Google Scholar]
  • 14.DiPietro L, Dziura J, Yeckel C W.et al Exercise and improved insulin sensitivity in older women: evidence of the enduring benefits of higher intensity training. J Appl Physiol 2006100142–149. [DOI] [PubMed] [Google Scholar]
  • 15.Twisk J W, Staal B J, Brinkman M N.et al Tracking of lung function parameters and the longitudinal relationship with lifestyle. Eur Respir J 199812627–634. [DOI] [PubMed] [Google Scholar]
  • 16.Duncan G E, Anton S D, Sydeman S J.et al Prescribing exercise at varied levels of intensity and frequency: a randomized trial. Arch Intern Med 20051652362–2369. [DOI] [PubMed] [Google Scholar]
  • 17.Lemura L M, Von Duvillars S P, Mokerjee S. The effects of physical training of functional capacity in adults ages 46–90: a meta‐analysis. J Sports Med Phys Fitness 2000401–10. [PubMed] [Google Scholar]
  • 18.Borer K T. Physical activity in the prevention and amelioration of osteoporosis in women: interaction of mechanical, hormonal and dietary factors. Sports Med 200535779–830. [DOI] [PubMed] [Google Scholar]
  • 19.ACSM Position stand: The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory fitness and muscular fitness in healthy adults. Med Sci Sports Exerc 199022265–274. [PubMed] [Google Scholar]
  • 20.Pate R R, Pratt M, Blair S N.et al Physical activity and public health. A recommendation from the Centers for Disease Control and Prevention and the American College of Sports Medicine. JAMA 1995273402–407. [DOI] [PubMed] [Google Scholar]
  • 21.Thompson P D, Buchner D, Pina I L.et al AHA scientific statement: Exercise and physical activity in the prevention and treatment of atherosclerotic cardiovascular disease. Circulation 20031073109–3116. [DOI] [PubMed] [Google Scholar]
  • 22.ACSM Position stand: The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory fitness and muscular fitness, and flexibility in healthy adults. Med Sci Sports Exerc 199830975–991. [DOI] [PubMed] [Google Scholar]
  • 23.Girard O, Millet G P. Effects of the ground surface on the physiological and technical responses in young tennis players. In: Lees A, Kahn J‐F, Maynard IW, eds. Science and racket sports. London: Routledge, 200443–48.
  • 24.Weber K.Der Tennissport aus internistisch‐sportmedizinischer Sicht. Sankt Augustin: Verlag Hans Richarz, 1987
  • 25.Novas A M, Rowbottom D G, Jenkins D G. A practical method of estimating energy expenditure during tennis play. J Sports Sci 2003640–50. [DOI] [PubMed] [Google Scholar]
  • 26.Smekal G, von Duvillard S P, Pokan R.et al Changes in blood lactate and respiratory gas exchange measures in sports with discontinuous load profiles. Eur J Appl Physiol 200389489–495. [DOI] [PubMed] [Google Scholar]
  • 27.Bernardi M, De Vito G, Falvo M E, Lees A, Maynard L, Hughes M, Reilly T.et al Cardiorespiratory adjustment in middle‐level tennis players: are long term cardiovascular adjustments possible? In: eds. Science and racket sports II. London: E & FN Spon, 199820–26.
  • 28.Christmass M A, Richmond S E, Cable N T.et al Exercise intensity and metabolic response in singles tennis. J Sports Sci 199816739–747. [DOI] [PubMed] [Google Scholar]
  • 29.Christmass M A, Richmond S E, Cable N T.et al A metabolic characterisation of singles tennis. In: Reilly T, Hughes M, Lees A, eds. Science and racket sports I. London: E & FN Spon, 19943–9.
  • 30.Reilly T, Palmer J. Investigation of exercise intensity in male singles lawn tennis. In: Reilly T, Hughes M, Lees A, eds. Science and racket sports I. London: E&FN Spon, 199410–13.
  • 31.Bergeron M, Maresh C, Kraemer W J.et al Tennis: a physiological profile during match play. Int J Sports Med 199112474–479. [DOI] [PubMed] [Google Scholar]
  • 32.Therminarias A, Dansou P, Chirpaz‐Oddou M F.et al Hormonal and metabolic changes during a strenuous tennis match. Effect of ageing. Int J Sports Med 19911210–16. [DOI] [PubMed] [Google Scholar]
  • 33.Therminarias A, Dansou P, Chirpaz‐Oddou M F.et al Effects of age on heart rate response during a strenuous match of tennis. J Sports Med Phys Fitness 199030389–396. [PubMed] [Google Scholar]
  • 34.Morgans L F, Jordan D L, Baeyens D A.et al Heart rate responses during singles and doubles tennis competition. Physician Sportsmed 19871567–74. [Google Scholar]
  • 35.Elliott B, Dawson B, Pyke F. The energetics of singles tennis. J Human Mov Studies 19851111–20. [Google Scholar]
  • 36.Docherty D. A comparison of heart rate responses in racquet games. Br J Sports Med 19821696–100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Kindermann W, Schnabel A, Schmitt W M.et al Verhalten von Herzfrequenz und Metabolismus beim Tennis und Squash. Dtsch Z Sportmedizin 19819229–237. [Google Scholar]
  • 38.Seliger V, Ejem M, Pauer M.et al Energy metabolism in tennis. Int Z Angew Physiol 197331333–340. [DOI] [PubMed] [Google Scholar]
  • 39.Ferrauti A, Bergeron M F, Pluim B M.et al Physiological responses in tennis and running with similar oxygen uptake. Eur J Appl Physiol 20018527–33. [DOI] [PubMed] [Google Scholar]
  • 40.Fernandez J, Fernandez‐Garcia B, Mendez‐Villanueva A.et al Activity patterns, lactate profiles and ratings of perceived exertion (RPE) during a professional singles tennis tournament. In: Crespo M, McInerney P, Miley D, eds. Quality coaching for the future. 14th ITF Worldwide Coaches Workshop. London: ITF, 2005
  • 41.Buti T, Elliott B, Morton A. Physiological and anthropometric profiles of elite pre‐pubescent tennis players. Physician Sportsmed 198412111–116. [Google Scholar]
  • 42.Carlson J S, Cera M A. Cardiorespiratory, muscular strength and anthropometric characteristics of elite junior australian junior male and female tennis players. Aust J Sci Med Sport 1984167–13. [Google Scholar]
  • 43.Powers S K, Walker R. Physiological and anatomical characteristics of outstanding female junior tennis players. Res Q Exerc Sport 198253172–175. [DOI] [PubMed] [Google Scholar]
  • 44.Kraemer W, Triplett N, Fry A.et al An in‐depth sports medicine profile of women college tennis players. J Sport Rehabil 1995479–98. [Google Scholar]
  • 45.Vodak P A, Savin W M, Haskell W L.et al Physiological profile of middle‐aged male and female tennis players. Med Sci Sports Exerc 198012159–163. [PubMed] [Google Scholar]
  • 46.Wilmore J H, Davis J A, O'Brien R.et al Physiological alterations consequent to 20‐week conditioning programs of bicycling, tennis, and jogging. Med Sci Sports Exerc 1980121–8. [PubMed] [Google Scholar]
  • 47.Swank A M, Condra S, Yates J W. Effect of long term tennis participation on aerobic capacity, body composition, muscular strength and flexibility and serum lipids. Sports Med Training Rehab 1998899–112. [Google Scholar]
  • 48.Ferrauti A, Weber K, Struder H K. Effects of tennis training on lipid metabolism and lipoproteins in recreational players. Br J Sports Med 199731322–327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Vodak P A, Wood P D, Haskell W L.et al HDL‐cholesterol and other plasma lipid and lipoprotein concentrations in middle‐aged male and female tennis players. Metabolism 198029745–752. [DOI] [PubMed] [Google Scholar]
  • 50.Schneider D, Greenberg M R. Choice of exercise: a predictor of behavioral risks? Res Q Exerc Sport 199263231–237. [DOI] [PubMed] [Google Scholar]
  • 51.Laforest S, St‐Pierre D M M, Cyr J.et al Effects of age and regular exercise on muscle strength and endurance. Eur J Appl Physiol 199060104–111. [DOI] [PubMed] [Google Scholar]
  • 52.Jetté M, Landry F, Tiemann B.et al Ambulatory blood pressure and Holter monitoring during tennis play. Can J Sport Sci 19911640–44. [PubMed] [Google Scholar]
  • 53.Nessler A. Sportmedizinische Befunde und sportpraktische Erfahrungen zum Tennisunterricht in der Bewegungstherapie von Typ‐2‐Diabetikern. Thesis. Cologne: Deutsche Sporthochschule, 2001
  • 54.Brauer B M, Buttner K. Geisler H. Herz‐Kreislauf‐ und Stoffwechseluntersuchungen an Tennisspielern unter Labor‐, Trainings‐ und Wettkampfbedingungen. Theorie und Praxis der Köperkultur 1970191071–1084. [Google Scholar]
  • 55.Brauer B M, Büttner K. Herzgrösse und Leingstungsfähigkeit bei Tennisspielern. Theorie und Praxis der Köperkultur 197019350–359. [Google Scholar]
  • 56.Pelliccia A, Maron B J, Culasso F.et al Athlete's heart in women. Echocardiographic characterization of highly trained elite female athletes. JAMA 1996276211–215. [DOI] [PubMed] [Google Scholar]
  • 57.Pelliccia A, Maron B J, Spataro A.et al The upper limit of physiologic cardiac hypertrophy in highly trained elite athletes. N Engl J Med 1991324295–301. [DOI] [PubMed] [Google Scholar]
  • 58.Spirito P, Pelliccia A, Proschan M A.et al Morphology of the “athlete's heart” assessed by echocardiography in 947 elite athletes representing 27 sports. Am J Cardiol 199474802–806. [DOI] [PubMed] [Google Scholar]
  • 59.Keul J, Stockhausen W, Pokan R.et al [Metabolic and cardiovascular adaptation and performance of professional tennis players.] Dtsch Med Wochenschr 1991116761–767. [DOI] [PubMed] [Google Scholar]
  • 60.Keul J, Berg A, Huber G.et al [Kardiozirkulatorische und metabolische Anpassungsvorgänge bei Tennispielern.] Herz Kreislauf 19827373–381. [Google Scholar]
  • 61.Whyte G P, George K, Sharma S.et al The upper limit of physiological cardiac hypertrophy in elite male and female athletes: the British experience. Eur J Appl Physiol 200492592–597. [DOI] [PubMed] [Google Scholar]
  • 62.Houston T K, Meoni L A, Ford D E.et al Sports ability in young men and the incidence of cardiovascular disease. Am J Med 2002112689–695. [DOI] [PubMed] [Google Scholar]
  • 63.Kontulainen S, Kannus P, Haapasalo H.et al Changes in bone mineral content with decreased training in competitive young adult tennis players and controls: a prospective 4‐yr follow‐up. Med Sci Sports Exerc 199931645–652. [DOI] [PubMed] [Google Scholar]
  • 64.Kontulainen S, Kannus P, Haapasalo H.et al Good maintenance of exercise‐induced bone gain with decreased training of female tennis and squash players: a prospective 5‐year follow‐up study of young and old starters and controls. J Bone Miner Res 200116195–201. [DOI] [PubMed] [Google Scholar]
  • 65.Sanchis Moysi J, Dorado C, Vicente‐Rodriguez G.et al Inter‐arm asymmetry in bone mineral content and bone area in postmenopausal recreational tennis players. Maturitas 200448289–298. [DOI] [PubMed] [Google Scholar]
  • 66.Sanchis Moysi J, Vicente‐Rodriguez G, Serrano J A.et al The effect of tennis participation on bone mass is better retained in male than female master tennis players. In: Lees A, Kahn J‐F, Maynard IW, eds. Science and racket sports III. London: Routledge, 2003
  • 67.Haapasalo H, Kontulainen S, Sievanen H.et al Exercise‐induced bone gain is due to enlargement in bone size without a change in volumetric bone density: a peripheral quantitative computed tomography study of the upper arms of male tennis players. Bone 200027351–357. [DOI] [PubMed] [Google Scholar]
  • 68.Nara‐Ashizawa N, Liu L J, Higuchi T.et al Paradoxical adaptation of mature radius to unilateral use in tennis playing. Bone 200230619–623. [DOI] [PubMed] [Google Scholar]
  • 69.Ashizawa N, Nonaka K, Michikami S.et al Tomographical description of tennis‐loaded radius: reciprocal relation between bone size and volumetric BMD. J Appl Physiol 1999861347–1351. [DOI] [PubMed] [Google Scholar]
  • 70.Haapasalo H, Kannus P, Sievanen H.et al Effect of long‐term unilateral activity on bone mineral density of female junior tennis players. J Bone Miner Res 199813310–319. [DOI] [PubMed] [Google Scholar]
  • 71.Calbet J A, Moysi J S, Dorado C.et al Bone mineral content and density in professional tennis players. Calcif Tissue Int 199862491–496. [DOI] [PubMed] [Google Scholar]
  • 72.Haapasalo H, Sievanen H, Kannus P.et al Dimensions and estimated mechanical characteristics of the humerus after long‐term tennis loading. J Bone Miner Res 199611864–872. [DOI] [PubMed] [Google Scholar]
  • 73.Etherington J, Harris P A, Nandra D.et al The effect of weight‐bearing exercise on bone mineral density: a study of female ex‐elite athletes and the general population. J Bone Miner Res 1996111333–1338. [DOI] [PubMed] [Google Scholar]
  • 74.Tsuji S, Tsunoda N, Yata H.et al Relation between grip strength and radial bone mineral density in young athletes. Arch Phys Med Rehabil 199576234–238. [DOI] [PubMed] [Google Scholar]
  • 75.Kannus P, Haapasalo H, Sankelo M.et al Effect of starting age of physical activity on bone mass in the dominant arm of tennis and squash players. Ann Intern Med 199512327–31. [DOI] [PubMed] [Google Scholar]
  • 76.Kannus P, Haapasalo H, Sievanen H.et al The site‐specific effects of long‐term unilateral activity on bone mineral density and content. Bone 199415279–284. [DOI] [PubMed] [Google Scholar]
  • 77.Krahl H, Pieper H G, Quack G. [Bone hypertrophy as a results of training.] Orthopade 199524441–445. [PubMed] [Google Scholar]
  • 78.Krahl H, Michaelis U, Pieper H G.et al Stimulation of bone growth through sports. A radiologic investigation of the upper extremities in professional tennis players. Am J Sports Med 199422751–757. [DOI] [PubMed] [Google Scholar]
  • 79.Jacobson P C, Beaver W, Grubb S A.et al Bone density in women: college athletes and older athletic women. J Orthop Res 19842328–332. [DOI] [PubMed] [Google Scholar]
  • 80.Kontulainen S, Sievanen H, Kannus P.et al Effect of long‐term impact‐loading on mass, size, and estimated strength of humerus and radius of female racquet‐sports players: a peripheral quantitative computed tomography study between young and old starters and controls. J Bone Miner Res 200318352–359. [DOI] [PubMed] [Google Scholar]
  • 81.Huddleston A L, Rockwell D, Kulund D N.et al Bone mass in lifetime tennis athletes. JAMA 19802441107–1109. [PubMed] [Google Scholar]
  • 82.Ducher G, Jaffre C, Arlettaz A.et al Effects of long‐term tennis playing on the muscle‐bone relationship in the dominant and nondominant forearms. Can J Appl Physiol 2005303–17. [DOI] [PubMed] [Google Scholar]
  • 83.Ducher G, Courteix D, Meme S.et al Bone geometry in response to long‐term tennis playing and its relationship with muscle volume: a quantitative magnetic resonance imaging study in tennis players. Bone 200537457–466. [DOI] [PubMed] [Google Scholar]
  • 84.Ducher G, Prouteau S, Courteix D.et al Cortical and trabecular bone at the forearm show different adaptation patterns in response to tennis playing. J Clin Densitom 20047399–405. [DOI] [PubMed] [Google Scholar]
  • 85.Ducher G, Tournaire N, Meddahi‐Pelle A.et al Short‐term and long‐term site‐specific effects of tennis playing on trabecular and cortical bone at the distal radius. J Bone Miner Metab 200624484–490. [DOI] [PubMed] [Google Scholar]
  • 86.Jackson A S, Beard E F, Wier L T.et al Changes in aerobic power of men, ages 25–70 yr. Med Sci Sports Exerc 199527113–120. [PubMed] [Google Scholar]
  • 87.Jackson A S, Beard E F, Wier L T.et al Changes in aerobic power of women, ages 20–64 yr. Med Sci Sports Exerc . 1996;28884–891. [DOI] [PubMed]
  • 88.Chobanian A V B G, Black H R, Cushman W C.et al Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension 2003421206–1252. [DOI] [PubMed] [Google Scholar]
  • 89.Breedveld K, Tiessen‐Raaphorst A. Rapportage Sport 2006. The Hague: Sociaal Cultureel Planbureau, 2006
  • 90. 2006: http://www.who.int/dietphysicalactivity/publications/facts/obesity/en/ Accessed 29 October 2006
  • 91.Hobbs F D. Cardiovascular disease and lipids. Issues and evidence for the management of dyslipidaemia in primary care. Eur J Gen Pract 2003916–24. [DOI] [PubMed] [Google Scholar]
  • 92.Rubins H B, Robins S J, Collins D.et al Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high density lipoprotein cholesterol. Veterans Affairs High‐Density Lipoprotein Cholesterol Intervention Trial Study Group. N Engl J Med 1999341410–418. [DOI] [PubMed] [Google Scholar]
  • 93.Guidry M A, Blanchard B E, Thompson P D.et al The influence of short and long duration on the blood pressure response to an acute bout of dynamic exercise. Am Heart J 20061511322, e512. [DOI] [PubMed] [Google Scholar]
  • 94.ACSM Position Stand: Physical activity and bone health. Med Sci Sports Exerc 2004361985–1996. [DOI] [PubMed] [Google Scholar]
  • 95.Kemper H C, Verschuur R. Longitudinal study of maximal aerobic power in teenagers. Ann Hum Biol 198714435–444. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Sports Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES