Elsevier

Bone

Volume 39, Issue 4, October 2006, Pages 880-885
Bone

Low lumbar spine bone mineral density in both male and female endurance runners

https://doi.org/10.1016/j.bone.2006.03.012Get rights and content

Abstract

There have been many reports of low bone mineral density (BMD) in female endurance runners. Although there have been several reports of low BMD in male runners, it is unclear how comparable the problem is to that in females. We compared BMD between male and female endurance runners and with a reference population. One hundred and nine endurance runners (65 females, 44 males) aged 19–50 years participated and had been training regularly for at least 3 years (32–187.2 km week−1) in events from 3 km to the marathon. BMD was measured at the lumbar spine (L2–L4) and hip by DXA. A questionnaire assessed training and menstrual status. Lumbar spine T scores were similar in male and female runners (−0.8 (0.8) versus −0.8 (0.7); f = 0.015; P = 0.904) as were total hip T scores (0.6 (7.9) versus 0.5 (9.2); f = 0.192; P = 0.662). The proportion of male runners with low lumbar spine BMD (<−1.0) (n = 16 from 44) compared to that of females (n = 27 from 65) (P = 0.675). Males had lower spine T scores than eumenorrhoeic females (−0.8 (0.7) versus −0.4 (0.7); f = 5.169; P = 0.03). There were moderate negative correlations between weekly running distance and lumbar spine BMD in males and females (r2 = 0.267; 0.189; P < 0.001), independent of menstrual status in females (r2 = 0.192; P < 0.001). Lumbar spine but not hip T scores were greater in runners who participated in resistance training at least twice-a-week (male: −0.4 versus −1.1; female: −0.5 versus −1.1; P < 0.01). Using multiple regression, running distance (−) and BMI (+) together best predicted lumbar spine T scores (r2 = 0.402; P < 0.01) in females. Although weak, BMI (+) best predicted hip T scores (r2 = 0.167; P < 0.05). In males, running distance and training years (−) together best predicted lumbar spine T scores (r2 = 0.400; P < 0.01). Training years (−) best predicted hip T scores (r2 = 0.361; P < 0.01). To conclude, our findings suggest that male runners face the same bone threat at the spine, as female runners. Further research in male athletes is required. Incorporation of regular resistance training into an athlete's training programme may be a useful preventative strategy.

Introduction

Since the early 1980s, many studies have confirmed the problem of low bone mineral density (BMD) in highly trained female athletes, particularly in endurance runners, and this evidence continues to accumulate. Cross-sectional studies report between 3 and 24% lower BMD in highly trained female runners compared to age-matched controls [1], [2], [3], [4] and longitudinal studies report significant bone loss over 2 to 10 years in female runners [5], [6]. There is some evidence for low BMD in male runners [7], [8], [9], [10], [11], although this has received relatively little attention, despite the recognition that 1 in 5 men will suffer from osteoporosis in their lifetime [12].

Suggested risk factors for low BMD in female athletes include exercise-induced amenorrhea (absence of menses), disordered eating and low body weight. Although estrogen deficiency was once presumed the underlying cause [1], [2], [3], [4], [5], [6], [13], it is now established that energy deficiency (arising from disordered eating or simply an insufficient energy intake to match expenditure [14], [15]), is the driving factor for bone loss and low BMD in this population [16]. Of interest, animal studies indicate that exercise-induced menstrual irregularity and the associated estrogen deficiency are secondary to energy deficit [17]. In male runners, low BMD appears to be unrelated to levels of sex hormones [8], [9], [10], but short-term energy deficiency has been shown to suppress bone formation in male athletes [18].

To date, no studies have compared BMD in male and female runners; thus, the hypothesis that low BMD in athletes should only be of significant concern for females has not yet been tested. In light of this, we aimed to compare BMD between male and female runners and with a reference population. This would seem an important starting point from which further studies can investigate potential factors associated with BMD in athletes, which may or may not be sex-specific.

Section snippets

Materials and methods

All eligible subjects provided signed informed consent and participated in the study conducted in accordance to the principles in the Declaration of Helsinki and with approval from the Leeds (West) Research Ethics Committee.

Male and female endurance runners aged 19 to 50 years were recruited by a national athletics magazine advertisement, word of mouth and posters at athletic clubs, universities and competition venues throughout the UK. The majority of peak bone density accrual has occurred by

Results

Table 1 gives the results data for all variables and differences in measurements between male and female runners. Male subjects ran further distances per week than females (P < 0.05), ranging from 32 to 187.2 km in males and 32 to 152 km in females.

Sex-specific T scores for BMD were comparable in male and female runners (lumbar spine f = 0.015; P = 0.904; total hip f = 0.192; P = 0.662; femoral neck f = 0.205; P = 0.651). In both sexes, lumbar spine T scores were statistically lower than zero (P

Discussion

While it is established that female runners with menstrual irregularity face a bone threat [1], [2], [3], [4], [5], [6], there is less of a consensus that male runners are also at risk. We found significantly lower lumbar spine BMD in male runners compared to reference values, with over one third of the group having low BMD. Interestingly, we also found lower lumbar spine T scores in male runners compared to female eumenorrhoeic runners, to a level indifferent to that of oligoamenorrhoeic

Acknowledgments

This study was supported by a University of Leeds PhD scholarship.

References (42)

  • M.L. Hetland et al.

    Low bone mass and high bone turnover in male long distance runners

    J. Clin. Endocrinol. Metab.

    (1993)
  • K.L. Bennell et al.

    Effect of altered reproductive function and lowered testosterone levels on bone density in male endurance athletes

    Br. J. Sports Med.

    (1996)
  • K.J. MacKelvie et al.

    Bone mineral density and serum testosterone in chronically trained, high mileage 40–55 year old male runners

    Br. J. Sports Med.

    (2000)
  • Osteoporosis in men

    National Osteoporosis Society publication

    (2004)
  • R. Pacifici

    Estrogen, cytokines and pathogenesis of osteoporosis

    J. Bone Miner. Res.

    (1996)
  • C.L. Zanker et al.

    Relation between bone turnover, oestradiol and energy balance in women distance runners

    Br. J. Sports Med.

    (1998)
  • K.K. Miller et al.

    Preservation of neuroendocrine control of reproductive function despite severe undernutrition

    Clin. Endocrinol. Metab.

    (2004)
  • C.L. Zanker et al.

    Energy balance, bone turnover and skeletal health in physically active individuals

    Med. Sci. Sports Exercise

    (2004)
  • N.I. Williams et al.

    Evidence for a causal role of low energy availability in the induction of menstrual cycle disturbances during strenuous exercise training

    J. Clin. Endocrinol. Metab.

    (2001)
  • C.L. Zanker et al.

    Responses of bone turnover markers to repeated endurance running in humans under conditions of energy balance or energy restriction

    Eur. J. Appl. Physiol.

    (2000)
  • J.P. Bonjour et al.

    Critical years and stages of puberty for spinal and femoral bone mass accumulation during adolescence

    J. Clin. Endocrinol. Metab.

    (1991)
  • Cited by (110)

    • Relative energy deficiency in sport in the youth athlete

      2023, The Youth Athlete: A Practitioner's Guide to Providing Comprehensive Sports Medicine Care
    • Bone mineral density and hip structure changes over one-year in collegiate distance runners and non-athlete controls

      2021, Bone Reports
      Citation Excerpt :

      Our findings are similar to other cross-sectional studies reporting higher aBMD in male runners in comparison to non-athletic controls (Tam et al., 2018; McCormack et al., 2019; Kemmler et al., 2006). As with previous research (Fredericson et al., 2007), we also report advantages in aBMD at bone sites loaded during running like the FN, TH, and WB but not at relatively unloaded sites, such as the PA or lateral spine (Hind et al., 2006). The significantly greater aBMD in the male runners at the TH and WB over the male controls are likely the result of impact forces achieved through running (Kohrt et al., 2004; Bennell et al., 1997).

    View all citing articles on Scopus
    View full text