Peak bone mass is an important determinant of bone mass later in life, and an increase in peak bone mass should decrease the risk for osteoporotic fractures [1-3]. Therefore, exact identification of the determinants of peak bone mass could help clinicians devise strategies to prevent fractures. In healthy persons, suggested main determinants of peak bone mass are race, sex, heredity, hormonal status, nutrition, and physical activity [4]. Of these, genetic factors play a major part, accounting for 60% to 80% of the variance [1]. Still, 20% to 40% of the variance may be due to environmental factors, including nutrition and physical activity, and it is important to focus on these factors because both can be easily controlled in generally acceptable ways. The importance of physical activity in maintaining adult bone mass is widely recognized [1, 4-6]. However, the effects of physical activity on growing bone have received only scant and general attention [7-10], and, to our knowledge, no prospective, controlled follow-up studies have been done. Cross-sectional studies have provided preliminary evidence of the beneficial effect of exercise on the skeleton during growth, but they left many questions unanswered because of insufficient information about the type, intensity, frequency, and duration of the exercise and because of other limitations in the study design. Therefore, exact determination of the optimal age or level of exercise necessary to achieve maximal peak bone mass has not been possible [8]. Recent studies have shown unequivocally that bone mass increases dramatically and naturally during puberty and that bone mass reaches its peak before the end of the second decade of life, which is much earlier than was previously thought [11-15]. However, the extent to which physical activity can modify this development and the age at which the effects of exercise are most crucial are unknown. Our objective was to determine the effect of biological age at which unilateral loading was started (that is, the starting age of training relative to the age at menarche) on the difference in bone mass in playing and nonplaying arms of female racket-sport players. Using athletes with a known history of unilateral loading and a wide range of starting ages of playing (from early childhood to early middle age), adequately matched nonplaying controls, and a study design with side-to-side comparison, we could control many confounding factors encountered in earlier cross-sectional studies (intrinsic factors such as age, height, weight, and hormonal status and extrinsic factors such as nutrition, smoking, and alcohol consumption). Methods Participants We recruited 105 currently ranked national-level female tennis and squash players for our study through the Finnish tennis and squash federations. The ethical committee for clinical investigation at our institute approved the investigational protocol, and we obtained informed consent from all participants. Ninety-seven players were right-handed (played with the right, dominant hand), and the remaining eight were left-handed. The mean age of players was 27.7 11.4 years (SD). They were clinically healthy with no known diseases and were not receiving medications known to affect bone metabolism; none had previously had upper extremity fractures. The players' active training history had to be 5 years or more (mean, 10 6 years). The mean starting age of the playing career (that is, the age at which the athlete started to practice at least 2 sessions each week on a regular basis) was 16 9 years. They trained 4.4 times per week on average, and the average duration of each session was 80 minutes (range, 60 to 180 minutes). None of the participants performed or had performed activities, other than playing the racket sport, that affected only one extremity. For the control group, we recruited 50 healthy Finnish women from local schools and work places. All but 2 of them were right-handed (that is, the right hand was dominant). The mean age of this group was 27.2 9.2 years. All participants in this group were also clinically healthy and had had no previous upper extremity fractures. Although some of them did participate in casual recreational sports (such as jogging, biking, skiing, swimming, and aerobics), none was involved in intense physical training or activities or work affecting the dominant or nondominant arm only. Interview The participants received a mailed questionnaire, which they completed independently at home. At the session during which anthropometric and strength measurements were obtained, one of three investigators (PK, HH, or MS) quickly reviewed the questionnaire responses with participants. This review determined whether the participants had understood and answered all questions. The three procedures (anthropometric measurements, strength measurements, and questionnaire review) were done in random order and always after bone measurements were obtained. The investigator was blinded to the bone measurement results. The questionnaire included data on years of active playing, starting age of playing, number of training sessions per week, training intensity, average duration of each session, physical activities other than tennis or squash playing, injuries, medication, known diseases, diet, possible vitamin or mineral supplementation, consumption of alcohol, and use of cigarettes. We assessed the daily dietary calcium intake using a prospective 7-day questionnaire on consumed food, and we analyzed the results using Micro-nutrica software (Social Insurance Institution, Helsinki, Finland). We also asked all participants about the age at onset of menses. We determined the menstrual status and divided the participants into three categories: 1) normal cycle of 23 to 35 days, with or without use of low-dose oral contraceptives, 2) any irregularity in menstrual pattern [such as short or long period, anovulatory cycles, short luteal phase, or oligomenorrhea], and 3) amenorrhea (no menstruation during the previous 6 months). We also asked the participants whether they had ever had disturbances in menstruation and the duration (in years) of such disturbances. To test our hypothesis that the biological age at which the playing career was started was important for the development of the side-to-side difference in bone mass, we divided the players into six groups according to the starting age of playing relative to the age at menarche: more than 5 years before menarche, 3 to 5 years before menarche, 2 to 0 years before menarche, 1 to 5 years after menarche, 6 to 15 years after menarche, and more than 15 years after menarche. This division was based on the general knowledge of the pubertal and growth development of healthy Finnish and other white girls [11-16]: Puberty, once begun, is generally complete within 3 years; growth spurts and accelerated natural bone accumulation begin at the onset of Tanner stage 2, reach a peak at stages 3 to 4, and end at stage 5; menarche usually occurs during stage 4; and the longitudinal growth and natural bone accumulation rates markedly decrease soon after menarche, so that increases are only minimal in Tanner stage 5. Thus, the women in the six groups could be named as players who had started their playing careers at childhood [mean starting age, 7.4 1.4] years) prepuberty (10.1 1.2 years), puberty (12.0 1.4 years), postpuberty (15.2 2.4 years), early adulthood (24.0 3.0 years), and adulthood (33.7 3.8 years). Anthropometric Measurements We measured the height and weight of each participant. Using a measuring tape, we determined the circumference of upper extremities. We measured upper arm circumference just below the lateral part of the triceps brachii muscle and measured forearm circumference at the middle of the medial epicondyle of the humerus and the styloid process of the ulna. Strength Measurements We determined the maximal isometric strength of upper extremities using an arm flexion-extension dynamometer (Digitest, Inc., Muurame, Finland). We measured grip strength using a standard grip strength meter. Bone Mineral Measurements Using a Norland XR-26 DXA scanner (Norland, Inc., Fort Atkinson, Wisconsin), a technician determined bone mineral content (expressed in grams) from four sites in the upper extremity (proximal humerus, humeral shaft, radial shaft, and distal radius) and from the right calcaneus. The same experienced laboratory technician did all measurements. Her day-to-day coefficient of variation for repeated bone mineral content measurements of the same participants was low, ranging from 0.5% to 1.2% depending on the site measured [17, 18]. Statistical Analyses We made intra-individual side-to-side comparisons using the matched, paired t-test. We used the Student nonpaired t-test to compare the continuous-type background variables, arm and calcaneus bone mineral content, and percentage of side-to-side differences among the players and controls. To compare the noncontinuous background variables of players and controls, we used the chi-square or Fisher exact test. We tested the players' side-to-side bone mineral content differences across the six groups of players using analysis of variance, analysis of covariance, and a test for linear trend for adjusted group means. According to the previously noted hypothesis that puberty is critical in natural bone accumulation and that menarche is the first sign of cessation of bone development, the analysis of covariance was designed to include 5 (6 1) orthogonal or pairwise uncorrelated contrasts: 1) starting playing no later than at menarche (the first three groups) compared with starting thereafter (the remaining three groups); 2) starting no later than 3 years before menarche (the first two groups) compared with starting at menarche (the third group); 3) starting more than 5 years before menarche (the first group) compared with starting 3 to 5 years before menarche (the second group); 4) starting 1 to
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