Available online at: https://doi.org/10.18778/1898-6773.86.4.04
Department of Anthropology, Wrocław University of Environmental and Life Sciences, Wrocław, Poland
Faculty of Biomedical Engineering, Department of Informatics and Medical Equipment, Silesian University of Technology, Gliwice, Poland
Department of Anthropology, Wrocław University of Environmental and Life Sciences, Wrocław, Poland
Faculty of Biomedical Engineering, Department of Biomechatronics, Silesian University of Technology, Gliwice, Poland
Faculty of Biomedical Engineering, Department of Biomechatronics, Silesian University of Technology, Gliwice, Poland
Faculty of Biomedical Engineering, Department of Biomechatronics, Silesian University of Technology, Gliwice, Poland
Faculty of Biomedical Engineering, Department of Biomechatronics, Silesian University of Technology, Gliwice, Poland
Faculty of Biomedical Engineering, Department of Informatics and Medical Equipment, Silesian University of Technology, Gliwice, Poland
ABSTRACT: Studies investigating the relationship between balance ability and body size, build and proportions tend to concentrate on body mass and height rather than breadth parameters or size of individual body segments. The purpose of this study was to determine a relationship between the ability to keep balance and the size, build and proportions, based on breadth and length dimensions of the body in healthy adult men and women during a position of free standing. This study also aimed to investigate how the lack of visual control affects the analyzed relationship. The study group consisted of 102 adults of both sexes. The investigations encompassed anthropometric measurements of the body and the ability to keep balance. The analysis covered a of series anthropometric parameters, 9 indices of body proportions, mean velocity of the COP movement (MV) and ellipse area (EA). A statistical analysis of the results was carried out taking into consideration the division into groups due to sexes. The results of the Pearson correlation have revealed that there is a statistically significant correlation (weak or moderate degree) between anthropometric parameters of the body and stabilographic values. Results differ between sexes and depend on whether Romberg’s test was performed with open or closed eyes. The obtained results showed that the surface area of ellipse significantly depends on the dimensions of these body elements which relate to the position of the centre of mass. The obtained results, which differ depending on sex, show that the values of the body sways in a position of free standing depend on breadth and length dimensions of the body, visual control and the analyzed parameter of balance.
KEY WORDS: anthropometry, body dimensions, stabilography, students, Romberg test.
Balance is defined as the ability to keep the centre of gravity of the body over the base of support, restricted by the outline of the feet. The sense of balance makes it possible to determine a position of the body and its individual parts in space, the movement of the body, a direction and velocity of changes. An efficient sense of balance enables keeping balance and stability in an automatic and continuous way in changing conditions (Hanes and McCollum 2006; Panankin 2018). The sense of balance is controlled by the organ of vision, the vestibular system of the ear as well as proprioceptors in muscles, joints and tendons (Peterka 2018). Ageing, disease or damage to any of the above-mentioned elements may result in balance disorders causing symptoms, such as difficulty keeping the right body posture, dizziness, disorders of vision and hearing, difficulty in concentration and memory (Loyd et al. 2021).
The primary sensory system is the organ of sight. It provides information on the surroundings and objects moving around the body, which gives a signal for the movement of the body (Peterka 2018). Central vision enables stabilization and control of spontaneous sways and rocking triggered by visual signals, on the other hand, peripheral vision makes it possible to control the body posture (Gaerlan et al. 2012).
Proprioceptive sensibility involves receptors, such as muscle and joint spindles, tactile and lamellated corpuscles, Ruffini corpuscles as well as Golgi tendon organs. These are specialized mechanoreceptors sensitive to stretching (extension) and changes in pressure within muscles, tendons and joints. A special role in keeping balance is played by signals from receptors located in the neck and ankles of lower limbs. The former informs about the direction in which the head is turning, the latter about the movement of the body, swaying, the surface area of standing including its features, such as hardness and adhesion (Peterka 2018).
The vestibular system of the ear consists of 3 semicircular canals, which transmit signals about the position of the head in three-dimensional space. The system also contains utricle and sacculus, which are responsible for vertical orientation and linear movement. Proper work of the receptors of both (right and left) vestibular systems consists in symmetrical and simultaneous transmission of signals to the brain (in the case of the head movements of different intensity on both sides) (Peterka 2018).
Information obtained through the visual channel provides details only about the surroundings. On the other hand, the vestibular system sends signals only about the head position. Balance can be kept thanks to simultaneous signals from these two sources supplemented with additional information from proprioceptors (Gaerlan et al. 2012). Nervous impulses are segregated in the brain, especially in the cerebellum, where they are integrated with previously learned pieces of information and habitual movements.
Because balance is a motor skill based on a very complex mechanism of nervous and muscular control, there are various factors which determine its diversity in the population. It can be intuitively divided into a group of internal factors, including measurable morphological parameters and possible pathologies occurring within the motor system and nervous system.
One of the best-studied factors affecting the postural stability is age. Healthy children reach an adult pattern of balance by the age of 10–12 years (Humphriss et al. 2011). An optimum control of body balance is achieved at late adolescence and maintained until around 60 years of age (Gaerlan et al. 2012). A similarly strong differentiating demographic factor is sex. It is believed that women are characterized by better stability due to lower location of the centre of mass in their bodies (Greve et al. 2013; Puszczałowska-Lisis et al. 2018). Further factors influencing balance keeping involve parameters connected with the location of the centre of pressure (COP). The above-mentioned parameters include the body build and shape. It is assumed that mainly body sway is related to height according to inverted pendulum model (McGrath et al. 2015). The taller the person, the greater body sways he/she features (Alonso et al. 2015). Studies show that the sway values are also affected by the body mass; the greater the body mass, the higher the amplitude of sways (Hue et al. 2007). It is the most noticeable in obese people (Ku et al. 2012). Due to ambiguity of the BMI index (Body Mass Index), an attempt was made to differentiate the muscle content and fat tissue content from the total body mass. The conducted analyses only ascertained the influence of the above-mentioned parameters on the velocity of sways. Fat content percentage correlates negatively with sway velocity, whereas fat-free mass percentage shows positive correlation.
Among anthropometric parameters and posture-metric parameters, researchers analyzed postural features related, among other things, to spinal curvatures and pelvic asymmetry. The values which showed a negative impact on balance are: severe inclination of the sacral bone, backward deflection of the body and increased thoracic kyphosis (Walicka-Cupryś et al. 2013). In addition, patients with idiopathic scoliosis achieved significantly worse results in stabilometric tests (Catan et al. 2020).
Since balance is an ability which is strongly conditioned by the development of the nervous system, a considerable number of persons with different degrees of mental disabilities was tested. Those investigations revealed that patients with autism spectrum, borderline and other disorders of moderate degree show a significant loss of balance ability (Gouleme et al. 2017), and the value of such a loss correlates with the disability degree (Bibrowicz et al. 2019; Lipowicz et al. 2019a). In addition, patients that have experienced stroke suffer a reduction of postural stability. However, some studies reported that mentally disabled persons and those with damaged central nervous system tissue exhibit improved balance skills as a result of training (Kang 2015; Lee et al. 2016).
There have been few studies investigating the relationship between balance ability and body size, build and proportions. Instead, researchers have been concentrated on investigating other anthropological aspects, such as body mass and height, often neglecting breadth parameters or size of individual body segments. Moreover, research on the relationship between balance and the build and shape of the body in children and adolescents revealed that regardless of age, boys and girls who are characterized by smaller morphological parameters sway more than individuals with stronger body build (Lipowicz et al. 2019b). The present work aimed to determine the relationship between the ability to keep balance and the body size, build and proportions in healthy adult men and women in a position of free standing. In addition, this study aimed to examine the extent to which a lack of sight control affects the relationship analysed herein.
The investigations encompassed 102 adults of both sexes being the students of the Academy of Physical Education in Katowice (Department of Physiotherapy) and the Silesian University of Technology, at the age 20–24 years (body mass: 73±15 kg, body height: 172.65±8.59 cm). The study group consisted of 47 men (body mass: 82±13 kg, body height: 179.5±5.61 cm) and 55 women (body mass: 65±11 kg, body height: 166.79±5.94 cm). The tests involved anthropometric measurements of the body and the ability to keep balance. Students at both universities did not differ significantly in body build and balance.
All the test participants agreed to take part in the tests. The study design was approved by the Bioethical Committee at the The Jerzy Kukuczka Academy of Physical Education in Katowice before commencement of the study (decision no. 3/2019).
Balance measurements were conducted using the Zebris FDM-S measuring platform (Zebris Medical GmbH, Isny, Germany). Each participant’s body was subjected to 26 measurements (Table 1). All measurements were carried out in accordance with the Martin technique. Mean values were adopted for the measurements done on both sides of the body. The measurements were conducted using an anthropometric equipment, such as anthropometer, callipers and centimetre tape measure. On the basis of the above-mentioned anthropometric measurements, 9 indexes of body proportions were calculated (Table 2).
Men | Women | ||||||
Mean | Min-max | SD | Mean | Min-max | SD | p | |
Age [years] | 20.6 | 18.8-24.7 | 1.5 | 20.7 | 18.8-30.6 | 1.9 | 0.5929 |
Body measurements | |||||||
Body weight [kg] | 81.9 | 55-117.5 | 13.9 | 65.4 | 48.0-106.0 | 10.7 | <0.0001 |
Stature [cm] | 179.5 | 168.5-194.4 | 5.6 | 166.7 | 154.3-179.0 | 6.0 | <0.0001 |
Suprasternale height [cm] | 145.7 | 136.5-159.1 | 5.1 | 135.7 | 127.0-146.0 | 5.1 | <0.0001 |
Acromial height (standing) [cm] | 146.6 | 135.5-161.0 | 5.2 | 136.0 | 127.8-147.5 | 5.5 | <0.0001 |
Elbow height (standing) [cm] | 113.2 | 100.5-127.9 | 5.0 | 105.4 | 98.5-114.8 | 4.2 | <0.0001 |
Wrist height [cm] | 87.6 | 76.0-98.8 | 4.4 | 82.1 | 71.4-89.6 | 3.9 | <0.0001 |
Waist height (Natural) [cm] | 113.6 | 102.0-123.8 | 4.4 | 106.6 | 98.6-115.1 | 4.7 | <0.0001 |
Tibiale height [cm] | 48.1 | 42.5-55.4 | 3.1 | 45.5 | 40.5-52.9 | 2.9 | <0.0001 |
Mean Iliospinale height [cm] | 101.1 | 91.8-11.8 | 4.3 | 94.0 | 56.9-103.2 | 4.2 | <0.0001 |
Sitting height [cm] | 94.5 | 89.8-102.3 | 3.1 | 89.2 | 81.4-96.7 | 3.2 | <0.0001 |
Trunk length [cm] | 54.5 | 48.3-65.9 | 4.1 | 51.1 | 45.3-57.5 | 2.9 | <0.0001 |
Mean length of the upper body segment [cm] | 90.3 | 81.5-99.7 | 4.6 | 82.1 | 74.1-90.9 | 3.8 | <0.0001 |
Upper extremity length [cm] | 77.7 | 61.5-85.7 | 4.3 | 70.7 | 47.3-85.6 | 6.5 | <0.0001 |
Acromion-Radiale length [cm] | 33.4 | 28.5-36.3 | 1.9 | 30.5 | 23.3-34.8 | 2.0 | <0.0001 |
Radiale-Dactylion III length [cm] | 44.3 | 26.9-49.9 | 4.2 | 40.1 | 20.8-53.1 | 5.6 | 0.0001 |
Lower extremity length (Trochanterion) [cm] | 89.2 | 80.4-100.8 | 4.4 | 84.5 | 73.4-93.9 | 4.3 | <0.0001 |
Mean Thigh length [cm] | 53.0 | 46.3-60.0 | 3.0 | 48.6 | 40.6-56.0 | 3.4 | 0.0023 |
Head and neck height [cm] | 33.8 | 30.6-38.2 | 1.5 | 31.0 | 27.1-34.5 | 1.6 | <0.0001 |
Biacromial breadth [cm] | 40.2 | 33.2-44.1 | 2.3 | 36.4 | 33.0-39.7 | 1.6 | <0.0001 |
Bideltoid breadth [cm] | 47.3 | 40.4-55.2 | 3.3 | 41.8 | 35.5-50.7 | 2.8 | <0.0001 |
Chest breadth [cm] | 28.9 | 24.5-33.5 | 1.9 | 24.8 | 22.4-29.0 | 1.8 | <0.0001 |
Chest depth[cm] | 19.5 | 16.4-23.0 | 1.5 | 18.1 | 14.6-23.0 | 1.9 | 0.0003 |
Biiliocristale breadth [cm] | 28.8 | 22.6-33.5 | 1.9/2 | 27.9 | 25.1-32.0 | 1.7 | 0.0239 |
Chest circumference (below bust) –rest [cm] | 87.6 | 75.7-102.5 | 6.2 | 75.4 | 67.0-89.0 | 5.5 | <0.0001 |
Chest circumference (below bust)- inhalation [cm] | 93.1 | 83.0-109.0 | 6.0 | 79.8 | 71.5-92.0 | 5.2 | <0.0001 |
Waist circumference [cm] | 79.1 | 66.0-101.0 | 6.7 | 72.1 | 62.0-93.0 | 7.2 | <0.0001 |
Buttock (hip) circumference [cm] | 98.9 | 82.7-115.0 | 6.7 | 98.1 | 83.0-123.0 | 7.4 | 0.5558 |
Thigh circumference [cm] | 57.6 | 47.8-68.5 | 4.8 | 56.8 | 45.0-77.0 | 5.5 | 0.4881 |
Indices | |||||||
BMI [kg/cm2] | 25.4 | 18.0-35.3 | 3.9 | 2.5 | 17.8-36.7 | 3.6 | 0.0154 |
Sitting Height Ratio (SHR) | 52.4 | 41.4-55.1 | 2.0 | 53.3 | 40.8-56.1 | 2.1 | 0.0004 |
Skelic index | 91.1 | 81.6-141.5 | 8.6 | 88.0 | 78.1-145.3 | 9.1 | 0.0003 |
Upper extremity length to stature index | 43.3 | 32.7-47.2 | 2.5 | 42.4 | 29.4-51.5 | 3.4 | 0.1219 |
Arm length to height index | 18.6 | 15.4-20.8 | 1.1 | 18.3 | 16.6-20.2 | 1.0 | 0.1373 |
Arm to forearm index | 76.9 | 61.3-97.2 | 7.8 | 76.9 | 62.1-112.9 | 8.3 | 0.3126 |
Lower extremity length to stature index | 56.3 | 54.0-59.8 | 1.3 | 56.4 | 53.7-59.3 | 1.4 | 0.5640 |
Width- breadth chest index | 67.7 | 56.6-84.2 | 6.4 | 73.4 | 58.3-84.4 | 7.1 | <0.0001 |
WHR waist to hip ratio | 0.81 | 0.73-0.90 | 0.03 | 0.73 | 0.66-0.85 | 0.04 | <0.0001 |
WTR waist to high ratio | 138.6 | 123.4-157.8 | 6.5 | 127.0 | 110.5-157.4 | 9.2 | <0.0001 |
Body balance parameters | |||||||
Sway path (SP) EO [mm] | 326.3 | 183.5-592.9 | 81.8 | 345.4 | 179.7-563.4 | 70.0 | 0.2126 |
Sway path (SP) EC [mm] | 380.0 | 217.9-716.2 | 101.9 | 395.913 | 272.3-606.0 | 83.8 | 0.3948 |
Elipse area (EA) EO [mm2] | 95.1 | 12.4-264.4 | 59.6 | 96.0 | 20.4-331.6 | 67.6 | 0.9451 |
Elipse area (EA) EC [mm2] | 127.1 | 21.6-458.8 | 101.0 | 113.0 | 26.4-285.2 | 68.1 | 0.4122 |
Mean velocity EO [mm/s] | 5.4 | 3.1-9.9 | 1.4 | 5.8 | 3.0-9.4 | 1.2 | 0.2126 |
Mean velocity EC [mm/s] | 6.3 | 3.6-11.9 | 1.7 | 6.6 | 4.5-10.1 | 1.4 | 0.3948 |
Indices | Calculation method |
SHR sitting height ratio | ([BS-v]/[B-v])*100 SHR, sitting height/Stature ×100 |
Skelic index | ([B-v]-[BS-v]/[BS-v])*100 (limb length / body length with head) * 100 (length of the legs / length of the trunk with head) x 100 |
Upper extremity length to stature index | ([a-daIII]/[B-v])*100 (Upper extremity and palm length / Stature) * 100 |
Arm length to height index | ([a-r]/[B-v])*100 (Acromion-Radiale Length / Stature) *100 |
Arm to forearm index | ([r-sty]/[a-r])*100 (forearm length / Acromion-Radiale Length) *100 |
Lower extremity length to stature index | ([B-is]/[B-v])*100 (length of the lower limb / Stature) *100 |
Width-breadth chest index | ([xi-ths]/[thl-thl])*100 (Chest depth / Chest breadth) * 100 |
WHR waist to hip ratio | Waist circumference / Buttock (hip) circumference |
WTR waist to high ratio | Waist circumference / Thigh circumference |
BMI body mass index | Body weight / (Stature in m)2 |
The balance test (the analysis of the position of the resultant of ground reaction forces) was based on the Romberg test. During that test, a study participant was standing on their lower limbs, which were positioned as wide apart as the width of their pelvis, and their arms were hanging freely alongside their body. Romberg’s test was conducted twice: with eyes open (EO) and eyes closed (EC). The time of each test equalled 60 seconds.
The analysis involved 2 parameters:
• mean velocity of the COP movement (MV) [mm/s] – total length of the path covered by the COP (the path covered by the centre of pressure of ground reaction force during the measurement) divided by the time of the test duration,
• ellipse area (EA) [mm2] in which the COP was located during the test (the surface area of ellipse created by 95% of the COP positions during the test).
Analyzed values were obtained from a 30-second measurement (i.e., from 15. to 45. second).
Descriptive statistics, which are presented in Table 3, include mean, standard deviation and range values. Analyses were performed for each sex separately. Because of non-normal distribution of stabilographic parameters, MV and EA were logarithmically transformed. Furthermore, correlation between stabilographic and anthropometric parameters were studied, using Pearson’s coefficients. Computations were made for the values obtained during tests with eyes open and closed. Next, for each obtained correlation coefficient a significance test was carried out. The test values at *p<0.05; **p<0.01; ***p<0.001 were considered statistically significant.
MV eo | EA eo | MV ec | EA ec | |
Men | ||||
MV eo | - | 0.45** | 0.76*** | 0.45** |
EA eo | 0.44** | - | 0.44** | 0.68*** |
MV ec | 0.50*** | 0.28* | - | 0.59*** |
EA ec | 0.18 | 0.62*** | 0.40** | - |
Women |
Legend: MV – mean velocity of the COP movement [mm/s]; EA – ellipse area [mm2]; eo – eyes open; ec – eyes closed; level of significance: ** p<0.01, *** p<0.001
Table 3 presents the correlation values for the stabilographic parameters obtained in tests with open and closed eyes. In women, the correlation values were within the 0.18 to 0.62 range, whereas in men the values ranged between 0.44 and 0.76. The above-mentioned values indicated the lack of full dependence between the path length and ellipse area, which suggests a different impact of various factors on the balance parameters in both sexes in different conditions.
Men | Women | |||||||
eyes open (eo) | eyes closed (ec) | >eyes open (eo) | eyes closed (ec) | |||||
MV | EA | MV | EA | MV | EA | MV | EA | |
Body measurements | ||||||||
Body weight [kg] | -0.33* | ns | ns | ns | -0.45** | ns | ns | ns |
BMI | ns | ns | ns | ns | -0.51*** | ns | ns | ns |
Stature [cm] | ns | ns | ns | ns | ns | 0.31* | 0.30* | 0.36** |
Suprasternale height [cm] | ns | ns | ns | ns | ns | ns | ns | 0.36** |
Acromial height (standing) [cm] | ns | ns | ns | ns | ns | 0.32* | ns | 0.39** |
Elbow height (standing) [cm] | ns | ns | ns | ns | ns | ns | ns | 0.30* |
Wrist height [cm] | ns | ns | ns | ns | ns | ns | ns | ns |
Waist Height (Natural) [cm] | ns | ns | ns | ns | ns | ns | ns | 0.33* |
Tibiale height [cm] | ns | ns | ns | ns | ns | 0.33* | ns | 0.34* |
Mean Iliospinale height [cm] | ns | ns | ns | ns | ns | ns | ns | 0.29* |
Sitting height [cm] | ns | ns | ns | ns | ns | ns | 0.42** | 0.33* |
Trunk length [cm] | -0.29* | ns | ns | ns | ns | ns | 0.35* | ns |
Mean length of the upper body segment [cm] | -0.30* | ns | ns | ns | ns | ns | 0.42** | ns |
Upper extremity length [cm] | ns | ns | ns | ns | 0.31* | 0.28* | 0.39** | |
Acromion-Radiale length [cm] | -0.38** | ns | ns | ns | ns | 0.36** | 0.40** | |
Radiale-Dactylion III length [cm] | ns | ns | ns | ns | 0.29* | 0.32* | ||
Lower extremity length (Trochanterion) [cm] | ns | ns | ns | ns | ns | ns | 0.33* | |
Mean Thigh length [cm] | -0.31* | ns | ns | ns | ns | ns | ns | ns |
Head and neck height [cm] | ns | ns | ns | .35* | 0.28* | 0.34* | ns | |
Biacromial breadth [cm] | ns | ns | ns | ns | ns | ns | ns | |
Bideltoid breadth [cm] | -0.29* | ns | ns | ns | ns | ns | ns | ns |
Chest breadth [cm] | ns | ns | ns | ns | ns | ns | ns | |
Chest depth[cm] | -0.35* | -0.37* | ns | ns | -0.30* | ns | ns | ns |
Biiliocristale breadth [cm] | -0.35* | ns | ns | ns | ns | ns | ns | |
Chest circumference (below bust) - rest [cm] | -0.34* | ns | ns | ns | -0.30* | ns | ns | ns |
Chest circumference (below bust) - inhalation [cm] | -0.36* | ns | ns | ns | ns | ns | ns | ns |
Waist circumference [cm] | -0.36* | ns | ns | ns | -0.44** | ns | ns | ns |
Buttock (hip) circumference [cm] | ns | ns | ns | ns | -0.50*** | ns | ns | ns |
Thigh circumference[cm] | ns | ns | ns | ns | -0.51*** | ns | ns | ns |
Indices | ||||||||
Sitting height ratio (SHR) | ns | ns | ns | ns | ns | ns | ns | ns |
Skelic index | ns | ns | ns | ns | ns | ns | ns | ns |
Upper extremity length to stature index | ns | ns | ns | ns | ns | ns | ns | 0.29* |
Arm length to height index | ns | ns | ns | ns | ns | ns | ns | ns |
Arm to forearm index | ns | ns | ns | ns | ns | ns | ns | ns |
Lower extremity length to stature index | ns | ns | ns | ns | -0.30* | ns | -0.37** | ns |
Width-breadth chest index | ns | ns | ns | ns | ns | ns | ns | ns |
WHR waist to hip ratio | ns | ns | ns | ns | ns | ns | ns | ns |
WTR waist to thigh ratio | -0.31* | ns | ns | ns | ns | ns | ns | ns |
Legend: MV – mean velocity of the COP movement [mm/s]; EA – ellipse area [mm2]. Level of significance: * p<0.05; ** p<0.01; *** p<0.001; ns – not significant.
The tests of Pearson’s correlation r (Table 4) revealed that correlation between body parameters and features connected with stability is statistically significant, in a small or moderate degree. Correlations of the highest level of statistical significance were observed only in women, in tests with open eyes. Such correlations were related to the association between sway velocity (MV) and factors such as: body mass (r = -0.45, p<0.001), BMI (r = -0.51, p<0.0001), hip circumference (r = -0.50, p<0.0001), the largest circumference of the thigh (r = -0.51, p<0.0001) and waist circumference (r = -0,44; p<0.001). Negative values of the correlation coefficients revealed that higher velocity was shown by women having smaller body mass as well as smaller circumferences of waist, hips and thighs. Moreover, women who swayed more quickly had significantly smaller circumference of the chest and smaller depth of the chest as well as a longer head with the neck. In addition, the MV EO significantly depended on the proportions of the length of the lower limb in relation to the body height (women with relatively short legs were prone to swaying more quickly). After the closure of the eyes, the correlation values decreased and became statistically insignificant. None of the breadth dimensions and body circumferences showed any considerable influence on the velocity of sways. After the elimination of the sight control, the sway velocity path was affected by the length dimensions of female bodies. Taller women having longer spine and longer upper limbs were characterized by considerably higher velocity. Moreover, the MV EC significantly depended on the proportions of the length of the lower limb in relation to the body height, which means that women with shorter legs in relation to the body height were prone to swaying more quickly).
In women, ellipse area EA, contrary to MV, showed a significant correlation solely with length parameters, and not with breadth parameters of the body. A bigger surface area of ellipse in tests with open eyes was typical of taller women with a higher position of their shoulder, knee, and longer upper limbs. After the closure of the eyes, different measurements describing the height of the body and length of its individual segments gained on statistical significance in their relation to the ellipse area confirming greater sways in taller women with longer upper and lower limbs.
In tests with open eyes, greater velocity of sways was characteristic of men with smaller body mass (r = -0.33; p<0.05), shorter trunk, shorter upper limbs and shorter thighs. Moreover, those who swayed more quickly were characterized by smaller breadth dimensions of the body, such as: upper breadth of the body (r = -0.29, p<0.05), hip breadth (r = -0.35, p<0.05), chest depth (r = -0.35, p<0.05) and smaller circumferences of the body, such as: chest at rest (r = -0.34, p<0.05) and chest while breathing in (r = -0.36, p<0.05) as well as waist (r = -0,36, p<0.05). Quicker sways were characteristic of men with lower WTR values, i.e., a smaller circumference of the thigh in relation to the waist circumference. After the closure of eyes, none of the parameters of the body build and shape in men significantly influenced the velocity of sways. This fact suggests that in such a situation the men’s body build lost its significance for the stability of the body and men with various types of body build swayed in a similar way with their eyes closed.
Among all analyzed dimensions of male bodies, such as length, circumference and breadth, none showed any significant relationship with the ellipse area in tests with open eyes. The only dimension that revealed some relationship was the depth of the chest. Men with more oval chests had a significantly larger ellipse area describing the sways. After the closure of eyes, the men’s body build and shape did not considerably affect the size of the ellipse area.
Moreover, it was observed that men revealed a significant relationship between sway velocity in tests with eyes opened (EO) and mainly the build of the upper part of their body, namely the length of trunk and upper segment of the body, the breadth of the upper part of the body, the circumference of thorax and waist as well as chest depth. On the other hand, in women, a significant relationship occurred both in the case of upper body dimensions (e.g., thorax and waist circumferences) and lower body dimensions (e.g., hip and thigh circumferences).
Balance in terms of biomechanics is defined as ability to keep the centre of gravity of the body over the base of support. However, the borderline of stability does not coincide with the outline of the feet. Postural stability is one of the most important indexes of correct body posture and involves ability to regain balance. The size of sways is described by parameters connected with the stabilometric path, most often with the path length (or the velocity of sways – the value obtained from the division of the path length by the test time) and the size of the ellipse area describing maximum sways occurring in a position of standing (Jurkojć 2018). Velocity of sways and the ellipse area showed a moderate correlation (from 0.4 for women with eyes closed to 0.59 for men with eyes closed), which means that, for instance, study participants making quicker movements around the centre of mass (with a longer path of stabilogram) may achieve both large and small values of the ellipse area. The correlation values suggest that postural stability depends on various and not always the same factors. Literature mentions age and sex, efficiency of body functioning, proper posture, muscle strength as well as body build and shape (Wang et al. 2022).
The present study describes the ability to keep balance by means of the velocity of sways MV and the area of ellipse EA. The above-mentioned are indicated as the most informative parameter when body sway is assessed (Raymakers et al. 2005; Błaszczyk and Beck 2023). The obtained results showed a different influence of the body build on MV, and different on EA.
In general, the velocity of sways significantly depended on the dimensions describing the breadth of the body, for instance the breadth of the upper body (in men), hip breadth (in men), chest circumference (in both sexes), waist circumference (in both sexes), hip circumference and thigh circumference (in women). The smaller breadth dimensions in a tested person, the higher sway velocity (and the longer path of stabilogram) they showed. Similar results were obtained by Lipowicz et al. (2019a; 2019b) in the case of children and adolescence. Regardless of age, children and youth characterized by lower body circumferences (thorax, waist, hips, arms) swayed more, especially in medio-lateral plane. Also, Alonso et al. (2015) suggested that the fat mass concentration in the chest and abdomen (android shape) increases the load on the hips, explaining the larger stabilographic medio-lateral path. Smaller breadth dimensions may indicate weaker muscularity of the body, lower mass of muscles and more delicate skeleton structure (Xiao et al. 2005; Malakar et al. 2022). The dependence between the sway control and a relatively low muscle component was observed in the investigations of girl gymnasts, where ectomorphic subjects showed 72% of more body sway than endomorphic girls (Allard et al. 2001). It was also reported that there was a certain relationship between a degree of muscularity of lower extremity and sways (Muehlbauer et al. 2015). Weaker muscles of lower limbs are responsible for relatively greater sways, whereas strength training improves the postural stability of the body (Youssef et al. 2018). In addition, the results of Alonso et al. (2015) suggest that lower lean body mass can be a risk factor for the postural control. In addition, what cannot be excluded is greater tiredness of muscles in slimmer, less muscular subjects (Sterkowicz et al. 2016). This fact may cause greater difficulty in keeping motionless body posture and result in higher velocity of sways.
The ellipse area is a parameter describing the range of maximum sways which can be achieved by a person in a position of free standing. The obtained results show that the size of the ellipse area depends on the body elements connected with the location of the COP, namely the dimensions of the body height measured, for instance from the ground to the top of the head, shoulder, elbow, waist, knee, and correlated length of upper extremities. The higher the centre of mass is located, the greater ellipse area the body sways in free standing. Among the tested adults the ellipse area EA changed along with the length dimensions, such as the height of body, shoulder, knee, head with the neck as well as the length of upper extremity. In the test performed without eyesight control, the above-mentioned relationship only grew in importance. Generally speaking, the higher the measurement point was located in a tested person (e.g., the top of the head, jugular notch, iliac spine), the greater the ellipse area became in a standing position. These associations were statistically significant only in women. Similarly significant positive correlations of length dimensions (height and trunk-cephalic length), and not waist-hip ratio (WHR) with the COP area, were reported among adult men and women from Brazil in tests with open eyes (Alonso et al. 2015). From a biomechanical perspective, greater sways in tall and slim women result from a higher location of the centre of mass (COM) of the body. Such a postural sway can be explained by the inverted pendulum model, which is based on the relation between the motion of a pendulum and its length, mass, and stiffness. According to this model, in a position of free standing the body sways mostly around the ankle joint. It may be supposed that the fact that taller women are prone to greater sways results from behaviour. Shorter women far more often wear high-heeled shoes and thus most probably train the postural stability and cope with greater sways (Wan et al. 2019). However, whether foot shape and more flexible longitudinal arch observed in taller and heavier women leads to a greater postural sway (Aurichio et al. 2011; De Blasiis et al. 2023) is an area for further investigation.
Body mass and BMI are anthropometric variables which, next to body height, are the most often analyzed factors influencing the ability to keep balance. However, the results of investigations are not uniform. In the current work, the BMI turned out to be a vital factor affecting only the velocity of sways in women in the tests with open eyes (r = -0.51, p <0.0001). The higher the BMI in women, the lower velocity of sways was achieved by women. Among young men no significant relationship was revealed, either with MV or EA. Among Brazilian adults aged over 60, the BMI and fat mass did not seem to influence the balance during a one-leg stance task (Pereira et al. 2018). A different study ascertained that the body mass was an independent factor and accounted for as much as 52-54% of the variance of balance stability in group of men with a wide BMI spectrum (17.4–63.8 kg/m2; Hue et al. 2007), in whom the decline of balance stability was strongly correlated with an increase in body weight. Moreover, Mainenti et al. (2011) showed that elderly women with more fat mass had larger balance sway. In addition, Neri et al. (2021) found that there is no differences between women with gynoid and android obesity. Winters and Snow (2000) reported that 31% of postural sway variability in premenopausal women was caused by the fat mass. Conversely, Farenc et al. (2003) analysing the influence of body characteristics of 20-60 years-old individuals on their upright stance, showed that thinner subjects have larger horizontal displacements of the centre of gravity (COG) than normal or corpulent subjects. Smaller sways in subjects with larger BMI, which were observed in the present work, may relate to a low variability of this feature in the studied population (young healthy persons, without overweight or obesity) and specificity of the BMI index measuring rather muscularity than fat content in young people.
Our study confirmed the conclusion drawn by Alonso et al. (2015) reporting that for the young adults, without major diseases or other abnormalities, the anthropometric variables had different relations to postural sway according to sex. For instance, men showed a statistically significant correlation between the velocity of sways and the dimensions of the upper parts of the body, whereas women revealed such correlation for both upper and lower parts of the body. The reasons for such dimorphic differences can be found in diverse distribution of fat tissue (android and gynoid type of the adipose tissue distribution) and muscle tissue as well as different proportions of the body in both sexes (broader shoulders in men, broader hips in women).
After closing their eyes, both men and women showed an increase in sway velocity and ellipse area. This fact confirms significance of the visual stimulus for the body stability. However, the elimination of vision had a different impact on the analysed relationship in both sexes. In men with closed eyes, the value of sways ceased to depend on their body build, while in the case of women with closed eyes, their body build began to play a greater role for their stability. This fact can be observed particularly in the ellipse surface area. Similarly, Chiari et al. (2002) showed that the postural sway parameters increase while in a position of standing with eyes closed, and further, that body size and body composition are strongly related to postural sway in conditions with eyes closed. However, Alonso et al. (2015), in their multi-factor analysis encompassing both men and women, stated the significance of trunk-cephalic length for sway velocity and the COP area in tests with eyes closed, whereas the tests with eyes open showed the importance of only body height. This phenomenon can be explained by the possibility of two diverse strategies (ankle and hip strategies) applied by both sexes to both testing conditions (which can be seen in the differences in the degree of muscularity and muscle training, body shape and the point of the body mass weight, differences in the risk of falling at an elderly age between sexes). The literature reports some contrary observations showing that after the closure of eyes the stiffness decreases in the tarsal joint, which increases sways (Rothwell 2012), or vice versa, that the stiffness increases after the closures of eyes to reduce the risk of falling (Alonso et al. 2015). Regardless of the observations related to the change in body stiffness, it is clearly visible that when the visual information is omitted, signals from the somato-sensory and vestibular systems have a greater importance for the postural control, especially in women. An increased sensitivity to sensory information from proprioceptive and vestibular systems, activation of receptors placed in the muscles and joints, together with vestibular cues, provide the brain with information about where the body and its parts are located with respect to the gravitational environment (Tanaka et al. 2000). In addition, Alonso et al. (2015) suggested that ankle and hip strategies have opposite behaviours in relation to vision and the inverted pendulum.
From the perspective of postural correction therapy and the prevention of falls in persons with different types of disorders, investigating the relationship between body build and balance keeping is of considerable interest. Few studies investigating this issue have focused mainly on the relationships between sway values and body height, body mass and the BMI. Study participants of such studies tended to be characterized by specific features, for instance exhibiting obesity (Greve et al. 2007), disability (Lipowicz et al. 2019a), or focus on a specific age class, e.g., children (Lipowicz et al. 2019b; Plandowska et al. 2019) or the elderly (Jochymczyk-Woźniak et al. 2018).
This work, on the other hand, presents a relationship between balance parameters and a big number of measurements which precisely describe the body build of young adults, men and women, without balance disorders and with diverse body structure. The obtained results showed that the smaller breadth dimensions in a tested person, the higher velocity of sways (and the longer path of stabilogram) was observed. On the other hand, the ellipse area was substantially dependent on these body elements which is related to the location of the COP. The higher the position of the COP, the larger the ellipse area made by the body sway in a position of free standing. The pattern of dependence of sway values in adults was different in both sexes. It also depended on the visual control (eyes opened / closed) and the analysed balance parameter (sway velocity / ellipse area). These relations were often statistically significant although low; in general, they achieved higher values in women than in men.
Acknowledgement
The study was realized within the project “DISC4SPINE dynamic individual stimulation and control for spine and posture interactive rehabilitation” (grant no. POIR.04.01.02-00-0082/17-00) co-founded by the European Regional Development Found within Operational Program Smart Growth Action 4.1.2.
Ethics statement
The study design was approved by the Bioethical Committee at the The Jerzy Kukuczka Academy of Physical Education in Katowice before commencement of the study (decision no. 3/2019). All the test participants agreed to take part in the tests.
Authors’ contributions
AL – is the initiator of the work, participated in the collection of material; she is a co-author of the paper’s draft and final versions; MNB – performed the statistical analyses; KG – took part in collecting material and writing the text; KN-L – participated in collecting material and writing the text; KJ-W – participated in collecting material and writing the text; DF – participated in collecting material and writing the text; RM – participated in the interpretation of the results; AWM – participated in the interpretation of the results.
Allard P, Nault ML, Hinse S, LeBlanc R, Labelle H. 2001. Relationship between morphologic somatotypes and standing posture equilibrium. Ann Hum Biol 28:624–633. https://doi.org/10.1080/03014460110047946
Alonso AC, Mochizuki L, Luna NMS, Ayama S, Canonica AC, Greve JMDA. 2015. Relation between the sensory and anthropometric variables in the quiet standing postural control: is the inverted pendulum important for the static balance control? Biomed Res Int 2015:985312. https://doi.org/10.1155/2015/985312
Aurichio TR, Rebelatto JR, de Castro AP. 2011. The relationship between the body mass index (BMI) and foot posture in elderly people. Arch Gerontol Geriatr 52:e89–e92. https://doi.org/10.1016/j.archger.2010.06.014
Bibrowicz K, Szurmik T, Wodarski P, Michnik R, Myśliwiec A, Barszcz J, Mikołajowski G, Mitas A. 2019. Quality of body posture and postural stability in people with intellectual disability playing volleyball. Acta Bioeng Biomech 21:23–30. https://doi.org/10.5277/ABB-01264-2018-02
Błaszczyk JW, Beck M. 2023. Posturographic standards for optimal control of human standing posture. J Hum Kinet. 86:7–15. https://doi.org/10.5114/jhk/159452
Cațan L, Cerbu S, Amaricai E, Suciu O, Horhat DI, Popoiu CM, Adam O, Boia E. 2020. Assessment of static plantar pressure, stabilometry, vitamin D and bone mineral density in female adolescents with moderate idiopathic scoliosis. Int J Environ Res Public Health. 17(6):2167. https://doi.org/10.3390/ijerph17062167
Chiari L, Rocchi L, Cappello A. 2002. Stabilometric parameters are affected by anthropometry and foot placement. Clin Biomech (Bristol, Avon) 17:666–677. https://doi.org/10.1016/s0268-0033(02)00107-9
De Blasiis P, Caravaggi P, Fullin A, Leardini A, Lucariello A, Perna A, Guerra G, De Luca A. 2023. Postural stability and plantar pressure parameters in healthy subjects: variability, correlation analysis and differences under open and closed eye conditions. Front Bioeng Biotechnol. 11:1198120. https://doi.org/10.3389/fbioe.2023.1198120
Farenc I, Rougier P, Berger L. 2003. The influence of gender and body characteristics on upright stance. Ann Hum Biol 30:279–294. https://doi.org/10.1080/0301446031000068842
Gaerlan M, Alpert PT, Cross C, Louis M, Kowalski S. 2012. Postural balance in young adults: the role of visual, vestibular and somatosensory systems. J Am Assoc Nurse Pract 24:375–381. https://doi.org/10.1111/j.1745-7599.2012.00699.x
Gouleme N, Scheid I, Peyre H, Seassau M, Maruani A, Clarke J, Delorme R, Bucci MP. 2017. Postural control and emotion in children with autism spectrum dsorders. Transl Neurosci 8:158–166. https://doi.org/10.1515/tnsci-2017-0022
Greve J, Alonso A, Bordini AC, Camanho GL. 2007. Correlation between body mass index and postural balance. Clinics (Sao Paulo, Brazil) 62:717–720. https://doi.org/10.1590/s1807-59322007000600010
Greve JM, Cuğ M, Dülgeroğlu D, Brech GC, Alonso AC. 2013. Relationship between anthropometric factors, gender, and balance under unstable conditions in young adults. BioMed Res Int 850424. https://doi.org/10.1155/2013/850424
Hanes DA, McCollum G. 2006. Cognitive-vestibular interactions: a review of patient difficulties and possible mechanisms. J Vestib Res: Equilib Orientat 16:75–91. https://doi.org/10.3233/VES-2006-16301
Hue O, Simoneau M, Marcotte J, Berrigan F, Doré J, Marceau P, Marceau S, Tremblay A, Teasdale N. 2007. Body weight is a strong predictor of postural stability. Gait Posture 26:32–38. https://doi.org/10.1016/j.gaitpost.2006.07.005
Humphriss R, Hall A, May M, Macleod J. 2011. Balance ability of 7 and 10 year old children in the population: results from a large UK birth cohort study. Int J Pediatr Otorhinolaryngol 75:106–113. https://doi.org/10.1016/j.ijporl.2010.10.019
Jochymczyk-Woźniak K, Nowakowska K, Michnik R, Nawrat-Szołtysik A, Górka W. 2018. Assessment of balance of older people living at a social welfare home. In: M Gzik, E Tkacz, Z Paszenda, E Piętka, editors. Innovation in Biomedical Engineering, Cham: Springer International Publishing, Advances in Intelligent System and Computing, 623, 217–224. http://doi.org/10.1007/978-3-319-70063-2_23
Jurkojć J. 2018. Balance disturbances coefficient as a new value to assess ability to maintain balance on the basis of FFT curves. Acta Bioeng Biomech 20:143–151. http://doi.org/10.5277/ABB-01082-2018-02
Kang KY. 2015. Effects of core muscle stability training on the weight distribution and stability of the elderly. J Phys Ther Sci 27:3163–3165. http://doi.org/10.1589/jpts.27.3163
Ku PX, Abu Osman NA, Yusof A, Wan Abas WA. 2012. Biomechanical evaluation of the relationship between postural control and body mass index. J Biomech 45:1638–1642. http://doi.org/10.1016/j.jbiomech.2012.03.029
Lee K, Lee M, Son C. 2016. Balance training improves postural balance, gait, and functional strength in adolescents with intellectual disabilities: Single-blinded, randomized clinical trial. Disabil Health J 9:416–422. https://doi.org/10.1016/j.dhjo.2016.01.010
Lipowicz A, Bugdol MN, Szurmik T, Bibrowicz K, Kurzeja P, Mitas AW. 2019. Body balance analysis of children and youth with intellectual disabilities. J Intellect Disabil Res 63:1312–1323. https://doi.org/10.1111/jir.12671
Lipowicz A, Szurmik T, Bugdol MN, Graja K, Kurzeja P, Mitas AW. 2019. Relationship between body sway and body building in girls and boys in developmental age. In: E Piętka, P Badura, J Kawa, W Wieclawek, editors. Information Technologies in Biomedicine 7th International Conference. ITIB 2019. Kamień Śląski, Cham: Springer. Advances in Intelligent System and Computing, 1011:361–370. https://doi.org/10.1007/978-3-030-23762-2_32
Loyd BJ, Agnew L, Fangman A, Thackeray A, Peterson DS, Schubert MC, Dibble L. 2021. Characterizing gaze and postural stability deficits in people with multiple sclerosis. Mult Scler Relat Disord. 2021 Oct;55:103205. https://doi.org/10.1016/j.msard.2021.103205
Malakar B, Roy SK, Pal B. 2022. Relationship between physical strength measurements and anthropometric variables: multivariate analysis. J Public Hlth Dev. 20(1):132–145. https://doi.org/10.55131/jphd/2022/200111
McGrath M, Howard D, Baker R. 2015. The strengths and weaknesses of inverted pendulum models of human walking. Gait Posture. 41(2):389–94. https://doi.org/10.1016/j.gaitpost.2014.10.023
Mainenti MR, Rodrigues E, Oliveira JF, Ferreira A, Dias CM, Silva AL. 2011. Adiposity and postural balance control: correlations between bioelectrical impedance and stabilometric signals in elderly Brazilian women. Clinics (Sao Paulo, Brazil) 66:1513–1518. https://doi.org/10.1590/s1807-59322011000900001
Muehlbauer T, Gollhofer A, Granacher U. 2015. Associations between measures of balance and lower-extremity muscle strength/power in healthy individuals across the lifespan: a systematic review and meta-analysis. Sports Med (Auckland, N.Z.) 45:1671–1692. https://doi.org/10.1007/s40279-015-0390-z
Neri SGR, Pereira JC, de David AC, Lima RM. 2021. The influence of body fat distribution on postural balance and muscle quality in women aged 60 years and over. J Appl Biomech. 37(3):182–187. https://doi.org/10.1123/jab.2020-0277
Pankanin E. 2018. The importance of visual control in the process of maintaining the balance of the body. J Edu Health and Sport. 8(8):381–387.
Pereira C, Silva R, de Oliveira MR, Souza R, Borges RJ, Vieira ER. 2018. Effect of body mass index and fat mass on balance force platform measurements during a one-legged stance in older adults. Aging Clin Exp Res 30:441–447. https://doi.org/10.1007/s40520-017-0796-6
Peterka RJ. Sensory integration for human balance control. Handb Clin Neurol. 2018;159:27-42. https://doi.org/10.1016/B978-0-444-63916-5.00002-1. PMID: 30482320.
Plandowska M, Lichota M, Górniak K. 2019. Postural stability of 5-year-old girls and boys with different body heights. PloS one 14:e0227119. https://doi.org/10.1371/journal.pone.0227119
Puszczalowska-Lizis E, Bujas P, Jandzis S, Omorczyk J, Zak M. 2018. Inter-gender differences of balance indicators in persons 60–90 years of age. Clin Interv Aging. 13:903–912. https://doi.org/10.2147/CIA.S157182
Raymakers JA, Samson MM, Verhaar HJ. 2005. The assessment of body sway and the choice of the stability parameter(s). Gait Posture 21:48–58. https://doi.org/10.1016/j.gaitpost.2003.11.006
Rothwell JC. 2012. Control of human voluntary movement. Springer Science & Business Media.
Sterkowicz S, Jaworski J, Lech G, Pałka T, Sterkowicz-Przybycień K, Bujas P, Pięta P, Mościński Z. 2016. Effect of acute effort on isometric strength and body balance: trained vs. untrained paradigm. PloS one, 11:e0155985. https://doi.org/10.1371/journal.pone.0155985
Tanaka H, Nakashizuka M, Uetake T, Itoh T. 2000. The effects of visual input on postural control mechanisms: an analysis of center-of-pressure trajectories using the auto-regressive model. J Hum Ergol, 29:15–25. http://www.humanergology.com/old/2000/Tanaka.pdf
Walicka-Cupryś K, Skalska-Izdebska R, Drzał-Grabiec J, Sołek A. 2013. Correlation between body posture and postural stability of school children. Adv Rehab 27:47–54. https://doi.org/10.2478/rehab-2014-0026
Wan F, Yick KL, Yu W. 2019. Effects of heel height and high-heel experience on foot stability during quiet standing. Gait Posture 68:252–257. https://doi.org/10.1016/j.gaitpost.2018.12.004
Wang Q, Li L, Mao M, Sun W, Zhang C, Mao D, Song Q. 2022. The relationships of postural stability with muscle strength and proprioception are different among older adults over and under 75 years of age. J Exerc Sci Fit. 20(4):328–334. https://doi.org/10.1016/j.jesf.2022.07.004
Winters KM, Snow CM. 2000. Body composition predicts bone mineral density and balance in premenopausal women. J Women’s Halth Gend-based Med. 9:865–872. https://doi.org/10.1089/152460900750020892
Xiao G, Lei L, Dempsey PG, Lu B, Liang Y. 2005. Isometric muscle strength and anthropometric characteristics of a Chinese sample. Int J Ind Ergon 35:674–679. https://doi.org/10.1016/j.ergon.2005.02.003
Youssef NM, Abdelmohsen AM, Ashour AA, Elhafez NM, Elhafez SM. 2018. Effect of different balance training programs on postural control in chronic ankle instability: a randomized controlled trial. Acta Bioeng Biomech 20(2):159–169. PMID: 30220726