Full length articleRelationships between walking speed, T-score and age with gait parameters in older post-menopausal women with low bone mineral density
Introduction
Osteoporosis is a systemic skeletal disease that is identified by decreased areal bone mineral density (BMD, g/cm2) and bone loss [1]. Osteoporosis can be a debilitating condition that predisposes primarily older women to an increased risk of fractures [1]. Every year, more than 8.9 million fractures worldwide are associated with osteoporosis, with 70% and 80% of these fractures occurring at the hip and forearm of women between 50–75 years of age, respectively [2]. The consequences of a fracture can be devastating with detrimental effects on a person’s well-being and independence, and high healthcare costs related to treatment and follow-up care.
Normal age-related changes in gait, such as reduced walking speed, decreased hip extension and reduced power generation at the ankle, have been well established in older adults [[3], [4], [5], [6]]. However the gait patterns of individuals with low BMD or osteoporosis have not been thoroughly investigated, and when examined, often studied in relation to falls and kyphosis [[7], [8], [9]] or temporal-spatial gait parameters only [10,11]. In one study, older women with low BMD exhibited increased gait variability in both step and stance time when compared to their peers with healthy BMD levels [10]. Increased gait variability has been associated with greater falls risk in older adults [12], but it has also been reported to improve local dynamic stability when walking slowly in young adults [13]. Temporal-spatial data do not examine the complex interactions between joint movements and mechanical power outputs by the muscles acting about the hip, knee and ankle joints during walking [14]. There is limited evidence of altered gait profiles for older women with low BMD including less hip extension, reduced power generation at the hip in early stance (termed H1 power burst [15]) and pre-swing (H3), less knee power absorption during terminal swing (K4) and smaller ankle power generation at push-off (A2) in comparison with women with normal BMD [16]. Nevertheless, there is a dearth of knowledge on the gait biomechanics of older women with low BMD and osteoporosis. This is important because walking is a recommended form of physical activity for the treatment of low BMD, particularly at the hip and femur [17] as the musculoskeletal loading can promote bone formation and attenuate further bone loss [18,19].
Previous studies investigated how much of the variance in BMD was explained by the peak hip joint moments in all three dimensions during level walking using multiple regression analysis [[19], [20], [21]]. In these studies, 40% to 93% of the femoral BMD variance was explained by hip joint moments [19,20]. However, the results from another study [21], which analysed the hip joint moments independent of body mass, did not fully corroborate with those previous studies [19,20] as the relationship between hip joint moment and BMD was reduced to essentially zero when scaled allometrically. Therefore, this relationship warrants further investigation. This information is important to enable the development of effective, safe and timely exercise-based interventions for older women.
To the authors’ knowledge, there has been only one study to date which has explored the three-dimensional gait kinematics and kinetics in women with osteopenia [16]. However, the participants’ gait speed was not reported [16] and yet the significant effects of speed on gait variables is well established [22]. Therefore, it is unclear how much of the explained variance could be attributed to speed alone in their study [16]. The aim of the current study was to investigate the relationships between gait parameters and self-selected, comfortable walking speed and BMD in older women with a broad range of T-scores (healthy to osteoporotic). It was hypothesised that walking speed would explain most of the variance in gait parameters but that adding T-score into the regression model would contribute to the explained variance for joint kinetic parameters about the hip and knee.
Section snippets
Participants
Forty-five women (13 women with healthy BMD levels, 26 with osteopenia and 6 with osteoporosis) were recruited from the local Centre for Metabolic Bone Disease. Inclusion criteria stipulated participants were women aged 65–70 years with a BMI of 18-30 kg/m2 (normal to overweight), who must have had a DXA scan within the previous 12 months, a T-score of 0 to −4, and without any cardiac problems. Participants were excluded if they had any known neurological disorder or obvious gait abnormalities,
Results
The participants’ mean (SD) walking gait speed was 1.40 (0.19) m·s−1 and explained (R2 = 12–68%) of the variance in temporal-spatial parameters (P ≤ 0.01) (Table 2). T-score alone accounted for R2 = 23% (P ≤ 0.001) and 6% (P ≤ 0.01) of the shared explained variance in stride width and double limb support time, respectively. However slope coefficients were smaller (B = 0.013 and B = 0.01, respectively) compared to those presented for speed alone (B = 0.039 and B = -0.155, respectively). When
Discussion
The aim of this study was to characterise the explained variance of the predictor variables (gait speed, T-score and age) on temporal-spatial parameters, lower limb joint kinematics, GRFs and joint kinetics during level walking in a sample of older women with T-scores ranging from healthy to osteoporotic. The regressive statistical procedures presented in this study allowed for the control of multiple predictors to be entered into the regression model progressively. The findings demonstrated
Conclusions
The results from this study suggest that older women across a wide range of T-scores can demonstrate level gait patterns similar to younger adults when walking at comfortable, but overall fast, self-selected speeds. Consistent with our hypothesis, speed was the most important predictor variable, not T-score and/or age. Our findings suggest walking speed should be taken into consideration when analysing the effects of BMD on gait parameters. Our findings also suggest the hip abductor, knee
Ethical approval
NHS Health Research Authority approved (REC Ref. 11/YH/0347). All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Conflicts of interest
The authors declare that there are no conflicts of interest.
Acknowledgments
This work would not have been possible without the invaluable contribution from Tom Chesters, who started the project, recruited and tested all the participants, hence providing all the raw data. Tom sadly passed away in 2013, but we would like to dedicate this paper to him.
The authors also gratefully acknowledge the funding from Osteoporosis Research in East Yorkshire (OSPREY), Charity Commission No 1013289, to undertake this research.
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