Health Benefits of Tennis Babette M Pluim (1), J Bart Staal (2), Bonita L Marks (3), Stuart Miller (4), Dave Miley (4) (1) Royal Netherlands Lawn Tennis Association (KNLTB), Amersfoort, The Netherlands
(2) Department of Epidemiology and Caphri Research Institute, Maastricht University, Maastricht, The
(3) Department of Exercise and Sport Science, University of North Carolina at Chapel Hil , Chapel Hil ,
(4) International Tennis Federation, London, UK
Corresponding Author:
Displayweg 4, 3821 BT Amersfoort, Netherlands
Objective: The aim of the study was to explore the role of tennis in the promotion of health and
prevention of disease. The focus of this study was on risk factors and diseases related to a sedentary
lifestyle, including low fitness levels, obesity, hyperlipidemia, hypertension, diabetes mel itus,
cardiovascular disease, and osteoporosis.
Methods: A literature search was undertaken to retrieve potential y relevant articles for the purpose of
this paper. Structured computer searches of PubMed, Embase, and Cumulative Index to Nursing and
Al ied Health Literature (CINAHL) were undertaken, along with hand-searching of key journals and
reference lists to locate relevant studies published up to March 2007. They had to be either cohort
studies (of either a cross-sectional or longitudinal design), case-control studies or experimental
Results: Twenty-four studies were identified that were related to physical fitness of tennis players,
including seventeen on intensity of play and sixteen on maximum oxygen uptake of tennis players.
Seventeen studies were found that investigated the relationship between tennis and (risk factors for)
cardiovascular disease. Twenty-two studies were retrieved that examined the effect of tennis on bone
Conclusions: It was concluded that 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, a reduced risk for developing cardiovascular disease, and improved bone health.
Key words: health, prevention, risk factors, tennis
The health benefits of exercise are wel established. Research has shown that regular moderate
physical activity has a beneficial effect on health[1] and is associated with a decreased risk of
diabetes[2-4] and cardiovascular disease[5-8]. Regular exercise has a beneficial effect on
cardiovascular risk factors through many mechanisms. It improves 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 function[16,17] and cardio-respiratory fitness.[16,17] In addition, exercise has a
Recommended exercise duration and intensity have changed over time. In the early nineties,
exercise recommendations exhorted vigorous intensity exercise (e.g. 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 (e.g. brisk walking, cycling, 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 that 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 wel -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 mil ions 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
stil unclear to what extent data are available indicating a direct relationship 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, i.e. low fitness levels, obesity, hypertension, hyperlipidemia, diabetes mel itus,
cardiovascular disease, and osteoporosis.
A literature search was undertaken to retrieve potential y relevant articles for the purpose of this paper.
The fol owing electronic databases were explored: PubMed (from 1966 up to March 2007), Embase
(from 1989 up to March 2007), and Cumulative Index to Nursing and Al ied 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 mel itus”, “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 performed to identify
To be included in this review, studies had to meet the fol owing criteria:
(1) They had to be cohort studies (of either a cross-sectional or longitudinal design), case-control
studies or experimental studies published in English or German; and
(2) They had to contain data on the relationship between playing tennis and physical fitness,
cardiovascular disease, obesity, hypertension, hyperlipidemia, diabetes mel itus, and
osteoporosis, or between playing tennis and the occurrence of health benefits in patients who
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
Our results in the PubMed, Embase and Cinahl databases resulted in, respectively, 191, 179, and 382
potential y 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
Twenty-four studies (25 articles) were identified that contained data on physical fitness of
tennis players[23-47]. Seventeen studies (18 articles) provided information on intensity of play[23-40]
and sixteen studies contained data on maximum oxygen uptake of tennis players[26-31,34,35,39,41-
47]. Seventeen studies[45,47-62] were found that investigated the relationship between tennis and risk
factors for cardiovascular disease and included eight cross-sectional studies on cardiac size and/or
function,[54-61] four cross-sectional studies on obesity,[45,47,50,51] two cross-sectional studies[47,
49] and one longitudinal study[48] on hyperlipidemia, two cross-sectional study on
hypertension,[47,52] one longitudinal study on diabetes,[53] and one longitudinal study on
cardiovascular morbidity and mortality.[62] Twenty-two studies (two of a longitudinal[63,64] and twenty
of a cross-sectional design[65-85]) were retrieved that examined the effect of tennis on bone health. Table 1. Intensity of match play (mean±SD) Reference* exercise Standard of during play
* First author and reference number; SD indicates standard deviation; ITN indicates International Tennis Number; m indicates male; f indicates female; N
indicates number of subjects; n.r. indicates not reported.
Exercise intensity
In 17 studies the intensity of match play was examined using heart rate recordings [23-39] and/or
maximum oxygen uptake (VO2max)[23,26,27,39,40] during play (Table 1). Mean heart rate during
singles play ranged from 141±16 to 182±12 beats per minute (bpm), equating to 70 to 90% of
maximum heart rate. Mean oxygen consumption during play ranged from 23.1±3.1 ml⋅kg-1⋅min-1 to
40.3±5.7 ml⋅kg-1⋅min-1, reflecting 50% to 80% of VO2 max. Mean lactate levels during play were
general y 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
Table 2. Maximum oxygen uptake of tennis players of various levels of play (mean±SD) Reference* Level of play, country Aerobic capacity
One longitudinal and 15 cross-sectional studies on the VO2 max of tennis players were identified
(Table 2).[26-31,34,35,39,41-47] The mean VO2 max ranged from 35.5±5.8 ml⋅kg-1⋅min-1 to 65.9±6.3
ml⋅kg-1⋅min-1, depending on age, gender and training level, indicating that these tennis players had
high fitness levels, compared to norm values for normal y active controls of the same age and
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 to 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.
Obesity
Vodak et al.[45] found below average body fat in 25 male (42±6yrs) and 25 female (39±3yr) tennis
players, with mean values of 16.3% and 20.3% for males and females.
Schneider et al. (n = 7,248; 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 demonstrated 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 40-59) and the
older veterans (over 60) were on average 3% leaner than the non-tennis-playing moderately active
controls (17–20.5% vs. 21–25%, respectively).
Final y, LaForest et al.[51] 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 vs. 23.9%, p<0.05).
Hyperlipidemia
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 to
a sedentary group matched for age, sex and education. Mean plasma HDL-cholesterol levels were significantly higher in tennis players than in sedentary subjects (males 53.8±11.7 vs. 45.1±11.9
mg/100ml, [p<0.001], females 66.4±8.4 vs. 60.1±11.1 mg/100ml, [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 LDL-C concentrations
Ferrauti et al.[48] 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 males and 11 females, aged 43 to 47 years old) and compared these with 16 control
subjects, who continued their usual (tennis) habits. They found slight increases in HDL2-cholesterol as
wel as smal decreases in HDL3-cholesterol, LDL-cholesterol and triglycerides. Despite the overal
positive improvement of the lipid profile, the changes were not significantly different from the control
group, which may have been due to the limited number of subjects and the relatively short duration of
Final y, Swank et al.[47] studied 28 elite senior male tennis players (aged 40-60+ 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 40-59 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 (50±7 yr), using a portable
ambulatory blood pressure recorder.[52] Mean resting systolic blood pressure was 137±19 mmHg and
diastolic blood pressure was 88±13 mmHg, suggestive of pre-hypertension (blood pressure between
120/80 and 139/89 mm Hg).[88] Mean systolic blood pressure during play was 168±19 mmHg, with a
peak systolic blood pressure of 198±30 mmHg. Mean diastolic blood pressure during play decreased
Swank et al.[47] 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 (40-59 yrs: systolic blood pressure (SBP) = 121±10 vs.
124±14 mmHg, diastolic blood pressure (DBP) = 78±10 vs. 79±10 mmHg, 60+ yrs: SBP = 136±10
Diabetes Mellitus
Nessler[53] performed a longitudinal study of 12 patients (7 men, mean age 62±4yrs and 5 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 bal 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 smal but significant increases in insulin levels (10.3±3.8 µE/ml vs. 13.9±5.7 µE/ml, p=0.026) and c-peptide production
(3.5±1.0 vs. 4.7±1.4, p=0.001). The mean glucose concentration (mean of 12 participants measured
before and after 12 training sessions) dropped from 188.0±72.7 mg/dl before to 156.7±52.2 mg/dl after
Cardiovascular disease
Heart size
Eight studies examined the cardiac dimensions of elite tennis players.[54-61] Increased heart size and
increased performance capacity were noted regardless of gender.[54,55,59,60,61] Systolic and
diastolic function were within normal limits.[56,57,61]
Morbidity and mortality
Houston et al.[62] studied 1,019 male students between 1948 to 1964. After a standard physical
exam, the students were asked to rate their ability in tennis, golf, footbal , basebal and basketbal
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 higher 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]: 0.35-0.89) in the high-ability group and 0.67 (95% CI: 0.47-0.96) in the low-ability group,
compared with the no-ability group. A primary factor for this beneficial health profile may be due to the
fact that tennis was the sport that was played most frequently through midlife. Half of the tennis
players were stil participating in the sport in midlife, compared to only one quarter of those whom
reported playing golf, and none whom reported playing basebal , basketbal , or footbal .
Twenty-two studies (23 articles) [63-85] were identified that examined the effects of tennis play on
bone health. General y, 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 compared to controls, and exercise
induced bone gain was greater in young than in old starters. Table 3 contains more specific
information regarding 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* Study design Study population Method Main results Ducher85
At the ultradistal radius, asymmetry in BMC in young and adult tennis
11.6±1.4yrs) and 47 adult tennis players
players was 16.35 and 13.8%, respectively (p<0.0001). At the mid- and
(23 men, 24 women, 22.3±2.7yrs), and 70
third-distal radius, asymmetry was much greater in adults than in
children (p<0.0001) for BMC (mid-distal radius, +6.6% versus +15.6%;
[12.2±1.6yrs] and 58 adults [23.3±3.2yrs]).
third-distal radius +6.9% versus +13.3%).
Fifty-two tennis players (24.2±5.8yrs),
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).
Twenty regional-level tennis players (10
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 sub-cortical 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 al bone variables (except volumetric
BMD) on both sides (r=0.48-0.86, P<0.05-0.0001) but the asymmetries
in muscle parameters did not correlate with those in bone parameters.
Fifty-seven regional-level tennis players
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% vs. 11.7±6.8%; third-distal
DXA Tennis players showed 8% greater BMC and 7% greater osseous area
players (60±5yrs) and 12 postmenopausal
in the dominant arm than in the non-dominant arm (p<0.05). There was a
controls (63±7yrs). Tennis players started
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).
Seventeen male tennis players (55 2yrs), 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 compared with
control subjects. Mean tennis participation
pQCT, The side-to-side differences in the young starters bone mineral content,
cortical area, total cross-sectional area of bone, and cortical wal
thickness were 8-22% higher than those of controls and 8-14% higher
(39±11yrs, mean starting age 26±8yrs),
Endocortical area (0.278±0.094 cm2 vs. 0.300±0.106 cm2), periosteal
(46±5yrs) who initiated training after bone
area (1.007±0.14 cm2 vs. 1.061±0.15 cm2), BMC (0.141±0.017 g vs.
had matured (mean starting age 36±3yrs).
0.147±0.017 g), moment of inertia (1598±413 mm4 vs. 1744±460 mm4),
section modulus (219±41 mm3 vs. 233±44 mm3), and SSI (352±66 mm3
vs. 376±71 mm3) of dominant midradius were significantly (p<0.01)
smal er compared to the non-dominant radius. BMD of trabecular bone
(0.383±0.060 g/cm3 vs. 0.363±0.070 g/cm3, p<0.05) and whole bone
(0.756±0.115 g/cm3 vs. 0.656±0.120 g/cm3, p<0.01) at the dominant
distal radius were significantly greater compared to the non-dominant
Bone gain was 1.3-2.2 times greater in favour of young starters: The
cohort study; players (22±8yrs, mean starting age
difference in BMC of humeral shaft in dominant vs. non-dominant arm
5-yr fol ow-up 11±2yrs), and 28 older female players
was 22±8.4% in young starters vs. 10±3.8% in old starters at fol ow-up.
(39±11yrs, mean starting age 26±8yrs),
starters reduced training from 4.7±2.7 to
1.4±1.3 times a week; old starters from
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
13 male former competitive tennis players DXA
Relative side-to-side BMC differences were significantly (p<0.001) larger
cohort study; (26±5yrs) who started their career at a
in players than in controls at al measured sites in both 1992 and 1996
4-yr fol ow-up mean age of 11yrs and 13 controls
for proximal humerus (1992 18.5% vs. 1.4% and 1996 18.4% vs. 0.5%),
(26±6yrs). The players had al retired from
humeral shaft (1992 25.2% vs. 4.7% and 1996 25.9% vs. 4.5%), radial
shaft (1992 13.9% vs. 1.8% and 1996 14.2% vs. 2.1%), and distal radius
(1992 13.2% vs. 2.0% and 1996 13.2% vs. 2.3%).
Forearms of 16 competitive tennis players pQCT
Players exhibited 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 compared with the
non-playing arm. In controls, side-to-side differences in these
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 that measured for the non-playing arm. In controls,
significant side-to-side differences were not found in any measured
Ninety-one 7- to 17-year-old female tennis DXA
In players, BMD inter-arm differences were significant (p<0.05 to <0.001)
in al Tanner stages, with mean differences ranging from 1.6% to 15.7%.
In each Tanner stage, differences in BMD
Mean arm-differences between players and controls did not became
obvious until Tanner stage III (mean age 12.6yrs). In the lumbar spine
differences were not found until Tanner stage IV (mean age 13.5yrs,
0.97±0.13 g/cm2 vs. 0.89±0.09 g/cm2, p<0.05) and Tanner stage V
(mean age 15.5yrs, 1.08±0.105 g/cm2 vs. 0.96±0.134 g/cm2, p<0.05).
Total mass (4977±908 g vs. 4220±632 g, lean mass (3772±500 g vs.
3246±421 g, p<0.001, and BMC (229±43.5 g vs. 194±33 g) were greater
in the dominant arm of tennis players than in controls (al p<0.05). BMD
was increased in tennis players compared to controls in the lumbar spine
(1.25±0.29 g/cm2 vs. 1.09 ±0.12 g/cm2, p=0.09) and in the trochanteric
region (0.94±0.11g/cm2 vs. 0.80±0.07 g/cm2, p<0.001).
Seventeen young competitive male tennis DXA
There were significant side-to-side humeral length differences in young
male players (+1.4%), young female controls (+1.1%) and older female
players (+0.7%). Relative side-to-side differences in BMC (range +7.6 to
+25.2%), BMD (range +5.8% to +22.5%), cortical wal thickness (range
+6.9% to +45.2%), cross-sectional moment of inertia (range +7.8% to
(21±3yrs) and 16 older women (39 6yrs).
+26.4%) and section modulus (range +3.0% to +21.7%) were
Starting age male players 10 3yrs, young
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
16 former tennis players (aged 40-65yrs), 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%, 95% CI –0.2 to 13.2,
p=0.066). Athletes had greater BMD than controls (lumbar spine 8.7%,
95% CI 5.4 to 12.0, p<0.001 and femoral neck 12.1%, 95% CI 9.0 to
15.3, p<0001). BMD of tennis players forearms were greater than their
10 male col ege wrestlers (20 1yrs), 16 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).
The players had a significantly (p<0.001) larger side-to-side difference in
BMC for proximal humerus (1.42±1.33 g vs. 0.41±1.08 g), humeral shaft
controls (27 9yrs). Players were divided
(2.77±2.20 g vs. 0.57±1.68 g), radial shaft (0.32±0.47 g vs. 0.12±0.40 g),
and distal radius (0.32±0.38 g vs. 0.11±0.28 g). Difference were two to
four times greater in players who started before or at menarche than 15
menarche) at which their playing careers
Relative side-to-side differences in BMD and BMC were significantly
increased in players compared to controls for humeral shaft (BMD
0.29±0.09 g/cm2 vs. 0.03±0.10 g/cm2, BMC 6.41±0.28 g vs. 1.06±0.33 g,
p<0.001) and proximal humerus (BMD 0.12±0.08 vs. 0.01±0.10 g/cm2,
BMC 2.38±1.8 vs. 0.28±1.7 g, p<0.001).
Relative side-to-side differences were significantly increased in tennis
players compared to controls for ulnar diameter (2.1 vs. 0.02 mm,
20.1±4.5yrs), and 12 controls (7 males, 5
p<0.01), ulnar length (8 vs. 0.17 mm, p<0.01), second metacarpal
diameter (0.9 vs. 0.0 mm, p<0.01) and second metacarpal length (2.7 vs.
Single Lumbar spine density was increased in tennis players compared to
photon swimmers and controls (1.51±37 g/cm2 vs. 1.39±27 g/cm2 and 1.36±49
densito g/cm2, p<0.02). Metatarsal density was increased in tennis players
compared to swimmers and controls (626±26 g/cm2 vs. 565±14 g/cm2
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
Thirty-five active male tennis players were
Bone mass of the radius of the playing arm (mean, 1.37 g/cm) was
studied during the 1978 USTA’s 70-,75-
greater than that of the non-playing arm (mean, 1.23 g/cm) in al but one
person. The quantity of BM present in the playing arms of the tennis
championship (21 were aged 70 to 74 yrs,
population was greater than that of the dominant arm on non-athletes.
*First author and year of publication. BMC indicates bone mineral content; BMD indicates bone mineral density; DXA indicates dual-energy x-ray
absorptiometry; pQTC indicates peripheral quantitative computer tomography; 95% CI indicates 95% confidence interval.
Discussion
The general findings of this review indicate that those who choose to play tennis appear to have
positive health benefits. Specifical y, lower body fat percentages, more favourable lipid profiles, and
enhanced aerobic fitness contributed to an overal 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 middle-adulthood.
A limitation of this review is the low number of studies with a longitudinal design. For example,
of the seventeen studies examining tennis and cardiovascular risk factors, only two had a longitudinal
design (i.e. 6-week fol ow ups). Similarly, of the twenty-two studies on bone health, only two had a
longitudinal design. But to their credit, fol ow-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 to 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 general y associated with a higher socioeconomic status.[89]
Furthermore, most included studies failed to appropriately adjust for confounding variables when
studying the relationship between tennis and health parameters.
Despite these limitations, there remains an indication of positive health benefits associated
with regular tennis participation. This conclusion concurs with those of other wel -designed studies
investigating the general impact of exercise on various health parameters.
The lower body fat percentage of tennis players compared to less active controls is an
important finding because obesity has become a ‘global epidemic’, with more than 1 bil ion adults
overweight (BMI>25) and at least 300 mil ion of them clinical y obese (BMI>30).[90]
This review shows that tennis is associated with increased plasma HDL-cholesterol levels.[47-
49] Even though more than 200 risk factors for coronary heart disease have now been identified, the
single most powerful predictor of coronary heart diseases is hyperlipidemia.[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 reduced risk of cardiovascular disease implies that
playing tennis may reduce the risk of cardiovascular events.[92]
The results of the study by Vodak et al.[52] 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 genders and across the age spectrum.[63,65-85] The association depended on the
duration of tennis participation and training frequency, being stronger in young starters than in old
starters, but 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 ACSM Position Stand on “Physical
Activity and Bone Health”, who recommend 20-40 minutes of weight-bearing endurance activities,
such as tennis, at least three times per week to augment bone mineral accrual in children and
adolescents, and 30-60 minutes of these activities at least three times per week to preserve bone
Playing tennis on a regular basis (two to three times a week), either singles or doubles, meets
the exercise recommendations of the American Col ege of Sports Medicine (ACSM) and American
Heart Association (AHA).[20-22] Reported mean heart rates during singles tennis ranged from 70-90%
of maximum heart rate, and mean oxygen consumption ranged from 50-80% of VO2 max. Moderate
intensity activities are those performed at a relative intensity of 40-60% of VO2 max (60-75% of
maximum heart rate, whereas vigorous-intensity activities are those performed at a relative intensity of
>60% of VO2max (>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 to normal y
active populations of the same age and sex.[86,87]
In doubles play, heart rate and VO2 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 VO2max 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 shown by Houston et
al.[62], who demonstrated that the association of high ability in tennis during col ege and a reduced
risk of cardiovascular disease in later life was at least partly mediated through continued participation
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 wil 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 life-style of
References
1. Warburton DER, Nicol CW, Bredin SSD. Health benefits of physical activity: the evidence. CMAJ
2006;174:801-9.
2. Hu FB, Stampfer MJ, Solomon C, Liu S, Colditz G, Speizer FE, Wil ett WC, Manson JE. Physical
activity and risk for cardiovascular events in diabetic women. Ann Intern Med 2001;134:96-
3. Wei M, Gibbons LW, Mitchel TL, Kampert JB, Lee CD, Blair SN. The association between
cardiorespiratory fitness and impaired fasting glucose and type 2 diabetes mel itus in men.
Ann Intern Med 1999;130:89-96.
4. Helmrich S, Ragland DR, Leung RW, Paffenbarger RS Jr. Physical activity and reduced
occurrence of non-insulent-dependent diabetes mel itus. N Engl J Med 1991;325:147-52.
5. Lee I-M, Rexroe KM, Cook NR, Manson JE, Buring JE. Physical activity and coronary heart disease
in women. JAMA 2001;285:1447-54.
6. Lee I-M, Sesso HD, Paffenberger RS. Physical activity and coronary heart disease risk in men.
Does the duration of exercise episodes predict risk? Circulation 2000;102:981-6.
7. Lee I-M, Sesso HD, Oguma Y, Paffenberger RS. Relative intensity of physical activity and risk of
coronary heart disease. Circulation 2003;107:1110-6.
8. Yu S, Yarnel JWG, Sweetnam PM, Murray L. What level of physical activity protects against
premature cardiovascular death? The Caerphil y study. Heart 2003;89:502-6.
9. Williams PT. Relationships of heart disease risk factors to exercise quantity and intensity. Arch
10. Kraus WE, Houmard JA, Duscha BD et al. Effects of the amount and intensity of exercise on
plasma lipoproteins. N Engl J Med 2002;347:1483-92.
11. Slentz CA, Duscha BD, Johnson JL et al. Effects of the amount of exercise on body weight, body
composition, and measures of central obesity: STRRIDE--a randomized control ed study. Arch Intern Med 2004;164:31-9.
12. Barlow CE, LaMonte MJ, Fitzgerald SJ et al. Cardiorespiratory fitness is an independent predictor
of hypertension incidence among initial y normotensive healthy women. Am J Epidemiol
2006;163:142-50.
13. Houmard JA, Tanner CJ, Slentz CA et al. Effect of the volume and intensity of exercise training on
insulin sensitivity. J Appl Physiol 2004;96:101-6.
14. DiPietro L, Dziura J, Yeckel CW et al. Exercise and improved insulin sensitivity in older women:
evidence of the enduring benefits of higher intensity training. J Appl Physiol 2006;100:142-9.
15. Twisk JW, Staal BJ, Brinkman MN et al. Tracking of lung function parameters and the longitudinal
relationship with lifestyle. Eur Respir J 1998;12:627-34.
16. Duncan GE, Anton SD, Sydeman SJ et al. Prescribing exercise at varied levels of intensity and
frequency: a randomized trial. Arch Intern Med 2005;165:2362-9.
17. Lemura LM, Von Duvil ars SP, Mokerjee S. The effects of physical training of functional capacity
in adults ages 46-90: a meta-analysis. J Sports Med Phys Fitness 2000;40:1-10.
18. Borer KT. Physical activity in the prevention and amelioration of osteoporosis in women:
interaction of mechanical, hormonal and dietary factors. Sports Med 2005;35:779-830.
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 1990;22:265-74.
20. Pate RR, Pratt M, Blair SN et al. Physical activity and public health. A recommendation from the
Centers for Disease Control and Prevention and the American Col ege of Sports Medicine.
JAMA 1995;273:402-7.
21. Thompson PD, Buchner D, Pina IL et al. AHA Scientific Statement: Exercise and physical activity
in the prevention and treatment of atherosclerotic cardiovascular disease. Circulation
2003;107:3109-16.
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 1998;30:975-91.
23. Girard O, Mil et GP. Effects of the ground surface on the physiological and technical responses in
young tennis players. In: Lees A, Kahn, J.-F., Maynard, I.W., editor. Science and Racket Sports. London: Routledge, 2004:43-8.
24. Weber K. Der Tennissport aus internistisch-sportmedizinischer Sicht. Sankt Augustin: Verlag Hans
25. Novas AM, Rowbottom DG, Jenkins DG. A practical method of estimating energy expenditure
during tennis play. J Sports Sci 2003;6:40-50.
26. Smekal G, von Duvil ard SP, Pokan R et al. Changes in blood lactate and respiratory gas
exchange measures in sports with discontinuous load profiles. Eur J Appl Physiol
2003;89:489-95.
27. Bernardi M, De Vito G, Falvo ME et al. Cardiorespiratory adjustment in middle-level tennis
players: are long term cardiovascular adjustments possible? In: Lees A, Maynard L, Hughes
M, Reil y T, eds. Science and Racket Sports II. London: E & FN Spon 1998:20-26.
28. Christmass MA, Richmond SE, Cable NT et al. Exercise intensity and metabolic response in
singles tennis. J Sports Sci 1998;16:739-47.
29. Christmass MA, Richmond SE, Cable NT et al. A metabolic characterisation of singles tennis. In:
Reil y T, Hughes M, Lees A, eds. Science and racket sports I. London: E & FN Spon, 1994:3-
30. Reilly T, Palmer, J. Investigation of exercise intensity in male singles lawn tennis. In: Reil y T,
Hughes M, Lees A, eds. Science and racket sports I. London: E&FN Spon, 1994:10-3.
31. Bergeron M, Maresh C, Kraemer WJ et al. Tennis: a physiological profile during match play Int J Sports Med 1991;12:474-9.
32. Therminarias A, Dansou P, Chirpaz-Oddou MF et al. Hormonal and metabolic changes during a
strenuous tennis match. Effect of ageing. Int J Sports Med 1991;12:10-6.
33. Therminarias A, Dansou P, Chirpaz-Oddou MF et al. Effects of age on heart rate response during
a strenuous match of tennis. J Sports Med Phys Fitness 1990;30:389-96.
34. Morgans LF, Jordan DL, Baeyens DA et al. Heart rate responses during singles and doubles
tennis competition. Physician Sportsmed 1987;15:67-74.
35. Elliott B, Dawson B, Pyke F. The energetics of singles tennis. J Human Mov Studies 1985;11:11-
36. Docherty D. A comparison of heart rate responses in racquet games Br J Sports Med 1982;16:96-
37. Kindermann W, Schnabel A, Schmitt WM et al. Verhalten von Herzfrequenz und Metabolismus
beim Tennis und Squash. Dtsch Z Sportmedizin 1981;9:229-37.
38. Seliger V, Ejem M, Pauer M et al. Energy metabolism in tennis. Int Z Angew Physiol 1973;31:333-
39. Ferrauti A, Bergeron MF, Pluim BM et al. Physiological responses in tennis and running with
similar oxygen uptake. Eur J Appl Physiol 2001;85:27-33.
40. Fernandez J, Fernandez-Garcia B, Mendez-Vil anueva 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, El iott B, Morton A. Physiological and anthropometric profiles of elite pre-pubescent tennis
players. Physician Sportsmed 1984;12:111-6.
42. Carlson JS, Cera MA. Cardiorespiratory, muscular strength and anthropometric characteristics of
elite junior australian junior male and female tennis players. Aust J Sci Med Sport 1984;16:7-
43. Powers SK, Walker R. Physiological and anatomical characteristics of outstanding female junior
tennis players Res Q Exerc Sport 1982;53:172-5.
44. Kraemer W, Triplett N, Fry A et al. An in-depth sports medicine profile of women col ege tennis
players. J Sport Rehabil 1995;4:79-98.
45. Vodak PA, Savin WM, Haskel WL et al. Physiological profile of middle-aged male and female
tennis players. Med Sci Sports Exerc 1980;12:159-63.
46. Wilmore JH, Davis JA, O'Brien RS et al. Physiological alterations consequent to 20-week
conditioning programs of bicycling, tennis, and jogging. Med Sci Sports Exerc 1980;12:1-8.
47. Swank AM, Condra S, Yates JW. Effect of long term tennis participation on aerobic capacity, body
composition, muscular strength and flexibility and serum lipids. Sports Med Training Rehab
1998;8:99-112.
48. Ferrauti A, Weber K, Struder HK. Effects of tennis training on lipid metabolism and lipoproteins in
recreational players. Br J Sports Med 1997;31:322-27.
49. Vodak PA, Wood PD, Haskel WL et al. HDL-cholesterol and other plasma lipid and lipoprotein
concentrations in middle-aged male and female tennis players. Metabolism 1980;29:745-52.
50. Schneider D, Greenberg MR. Choice of exercise: a predictor of behavioral risks? Res Q Exerc Sport 1992;63:231-7.
51. Laforest S, St-Pierre DMM, Cyr J et al. Effects of age and regular exercise on muscle strength
and endurance. Eur J Appl Physiol 1990;60:104-11.
52. Jetté M, Landry F, Tiemann B et al. Ambulatory blood pressure and Holter monitoring during
tennis play. Can J Sport Sci 1991;16:40-4.
53. Nessler A. Sportmedizinische Befunde und sportpraktische Erfahrungen zum Tennisunterricht in
der Bewegungstherapie von Typ-2-Diabetikern. Thesis. Cologne: Deutsche Sporthochschule,
54. Brauer BM, Buttner, K., Geisler, H. Herz-Kreislauf- und Stoffwechseluntersuchungen an
Tennisspielern unter Labor-, Trainings- und Wettkampfbedingungen. Theorie und Praxis der Köperkultur 1970;19:1071-84.
55. Brauer BM, Büttner K. Herzgröße und Leingstungsfähigkeit bei Tennisspielern Theorie und Praxis der Köperkultur 1970;19:350-9.
56. Pelliccia A, Maron BJ, Culasso F et al. Athlete's heart in women. Echocardiographic
characterization of highly trained elite female athletes. JAMA 1996;276:211-5.
57. Pelliccia A, Maron BJ, Spataro A et al. The upper limit of physiologic cardiac hypertrophy in highly
trained elite athletes. N Engl J Med 1991;324:295-301.
58. Spirito P, Pel iccia A, Proschan MA et al. Morphology of the "athlete's heart" assessed by
echocardiography in 947 elite athletes representing 27 sports. Am J Cardiol 1994;74:802-6.
59. Keul J, Stockhausen W, Pokan R et al. [Metabolic and cardiovascular adaptation and
performance of professional tennis players] Dtsch Med Wochenschr 1991;116:761-7.
60. Keul J, Berg A, Huber G et al. Kardiozirkulatorische und metabolische Anpassungsvorgänge bei
Tennispielern. Herz Kreislauf 1982;7:373-81.
61. Whyte GP, George K, Sharma S, Firoozi S, Stephens N, Senior R, et al. The upper limit of
physiological cardiac hypertrophy in elite male and female athletes: the British experience. Eur
62. Houston TK, Meoni LA, Ford DE et al. Sports ability in young men and the incidence of
cardiovascular disease. Am J Med 2002;112:689-95.
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 fol ow-up.
Med Sci Sports Exerc 1999;31:645-52.
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 fol ow-up
study of young and old starters and controls. J Bone Miner Res 2001;16:195-201.
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 2004;48:289-
66. Sanchis Moysi J, Vicente-Rodriguez G, Serrano JA 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 2000;27:351-7.
68. Nara-Ashizawa N, Liu LJ, Higuchi T et al. Paradoxical adaptation of mature radius to unilateral
use in tennis playing. Bone 2002;30:619-23.
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 1999;86:1347-51.
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 1998;13:310-9.
71. Calbet JA, Moysi JS, Dorado C et al. Bone mineral content and density in professional tennis
players. Calcif Tissue Int 1998;62:491-6.
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 1996;11:864-72.
73. Etherington J, Harris PA, 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
1996;11:1333-8.
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 1995;76:234-8.
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 1995;123:27-31.
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 1994;15:279-84.
77. Krahl H, Pieper HG, Quack G. [Bone hypertrophy as a results of training]. Orthopade
1995;24:441-5.
78. Krahl H, Michaelis U, Pieper HG et al. Stimulation of bone growth through sports. A radiologic
investigation of the upper extremities in professional tennis players. Am J Sports Med
1994;22:751-7.
79. Jacobson PC, Beaver W, Grubb SA et al. Bone density in women: col ege athletes and older
athletic women. J Orthop Res 1984;2:328-32.
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 2003;18:352-9.
81. Huddleston AL, Rockwel D, Kulund DN, Harrison RB. Bone mass in lifetime tennis athletes. JAMA 1980;244:1107-9.
82. Ducher G, Jaffre C, Arlettaz A, Benhamou CL, Courteix D. Effects of long-term tennis playing on
the muscle-bone relationship in the dominant and nondominant forearms. Can J Appl Physiol
2005;30:3-17.
83. Ducher G, Courteix D, Meme S, Magni C, Viala JF, Benhamou CL. 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 2005;37:457-66.
84. Ducher G, Prouteau S, Courteix D, Benhamou CL. Cortical and trabecular bone at the forearm
show different adaptation patterns in response to tennis playing. J Clin Densitom 2004;7:399-
85. Ducher G, Tournaire N, Meddahi-Pel e A, Benhamou CL, Courteix D. Short-term and long-term
site-specific effects of tennis playing on trabecular and cortical bone at the distal radius. J Bone Miner Metab 2006;24:484-90.
86. Jackson AS, Beard EF, Wier LT et al. Changes in aerobic power of men, ages 25-70 yr. Med Sci Sports Exerc 1995;27:113-20.
87. Jackson AS, Beard EF, Wier LT et al. Changes in aerobic power of women, ages 20-64 yr. Med
88. Chobanian AVBG, Black HR, Cushman WC et al. Seventh report of the Joint National Committee
on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension
2003;42:1206-52.
89. Breedveld K, Tiessen-Raaphorst A. Rapportage Sport 2006. The Hague: Sociaal Cultureel
90. 2006:http://www.who.int/dietphysicalactivity/publications/facts/obesity/en/. Accessed 29 October
91. Hobbs FD. Cardiovascular disease and lipids. Issues and evidence for the management of
dyslipidaemia in primary care. Eur J Gen Pract 2003;9:16-24.
92. Rubins HB, Robins SJ, Col ins 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 1999;341:410-
93. Guidry MA, Blanchard BE, Thompson PD et al. The influence of short and long duration on the
blood pressure response to an acute bout of dynamic exercise. Am Heart J 2006;151:1322,
94. ACSM. Position Stand: Physical activity and bone health. Med Sci Sports Exerc 2004:36:1985-96.
95. Kemper HC, Verschuur R. Longitudinal study of maximal aerobic power in teenagers. Ann Hum Biol 1987;14:435-44.
What is already known 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 specifical y focuses on the relationship between tennis and risk factors and diseases
• There is a positive association 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.
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by the American Association for Laboratory Animal Science Animal Well-Being III. An Overview of Assessment J. Derrell Clark,1,2 Dawn R. Rager,3* and Janet P. Calpin2† Abstract Assessment of animal well-being is a complex matter. It is difficult to establish a causal link between stimuli and internal state because of numerous variables and the time interval between cause and effect
For reprint orders, please contact:reprints@futuremedicine.com Effects of dopamine D2 receptor gene polymorphisms on smoking cessation: abstinence and withdrawal symptoms Marcus R Munafò & Evaluation of: Robinson JD, Lam CY, Minnix JA et al. : The DRD2 TaqI-B Elaine C Johnstone polymorphism and its relationship to smoking abstinence and withdrawal symptoms.