Dong Gi Min1, Jae Hong Lee2, Han Seong Choe3, Eun Jung Kim4, So Hong Shin5, Jin Hwan Lee2. 1. Department of Rehabilitation Medicine, Keimyung University Dongsan Medicine Center, Republic of Korea. 2. Department of Physical Therapy, Daegu Health College, Republic of Korea. 3. Department of Physical Therapy, Catholic University of Daegu, Republic of Korea. 4. Department of Physical Therapy, Masan College, Republic of Korea. 5. Department of Nursing Science, Kyongbuk College of Science, Republic of Korea.
Abstract
[Purpose] This study evaluated differences between healthy elderly individuals and stroke patients by comparing their dominant and nondominant sides. [Subjects and Methods] Thirty-five elderly individuals participated in this study and divided into a stroke group and a control group. The outcome measures were general characteristics and bone mineral density. Bone mineral density was evaluated by using the osteoporosis index. OsteoPro, T score, and Z score were used for the calcaneus region of the dominant side, and OsteoPro was used for that of the nondominant side. Data were analyzed by using the SPSS 12.0 software, paired-samples t-test, and independent-samples t-test. [Results] The T and Z scores showed no significant differences between the dominant and recessive sides in the control group. However, the stroke group showed significant differences in osteoporosis index, T score, and Z score between the paretic and nonparetic sides. Changes in the scores between the recessive and dominant sides showed significant differences between the two groups. [Conclusion] A positive relationship was found between physical activity and bone mineral density in the stroke patients. Therefore, improved physical activity can be beneficial by reducing osteoporosis in stroke patients.
[Purpose] This study evaluated differences between healthy elderly individuals and strokepatients by comparing their dominant and nondominant sides. [Subjects and Methods] Thirty-five elderly individuals participated in this study and divided into a stroke group and a control group. The outcome measures were general characteristics and bone mineral density. Bone mineral density was evaluated by using the osteoporosis index. OsteoPro, T score, and Z score were used for the calcaneus region of the dominant side, and OsteoPro was used for that of the nondominant side. Data were analyzed by using the SPSS 12.0 software, paired-samples t-test, and independent-samples t-test. [Results] The T and Z scores showed no significant differences between the dominant and recessive sides in the control group. However, the stroke group showed significant differences in osteoporosis index, T score, and Z score between the paretic and nonparetic sides. Changes in the scores between the recessive and dominant sides showed significant differences between the two groups. [Conclusion] A positive relationship was found between physical activity and bone mineral density in the strokepatients. Therefore, improved physical activity can be beneficial by reducing osteoporosis in strokepatients.
Entities:
Keywords:
Bone mineral density; Osteoporosis; Stroke
Stroke impairs brain function via the obstruction of blood flow resulting from a blood clot
or ruptured blood vessels, and causes permanent disability in patients1). Hemiplegia is commonly associated with a decrease in
balance ability and postural control2).
Impaired balance and increased postural sway are known to be associated with abnormal weight
bearing on the lower extremities3). Gait
disability is a common symptom that is observed in 80% of patients with stroke4). The study was performed according to the
principles of the Declaration of Helsinki, and ethical approval was granted by the local
committee of the institutional review board of the university hospital. The management of
gait ability is an important goal in the process of therapy for stroke rehabilitation
because gait is a significant element in the achievement of functional independence5, 6).Restricted movement of patients with paretic stroke leads to a reduction in muscular
strength, load-bearing capacity on the nonparetic side, and physical activity. This in turn
causes osteoporosis due to bone loss7).
Many studies have been conducted to investigate the causes and characteristics of
osteoporosis after stroke. Sato et al.8)
reported that increased bone resorption as a result of decreased motion induces bone loss.
The incidence of osteoporosis and risk of fracture increase over time after a stroke9, 10).
Related factors include the duration and extent of paralysis, patient age, serum calcium and
25-hydroxy vitamin D concentrations11),
diabetes mellitus, menopause, hyperthyroidism, and Cushing syndrome12). Osteoporosis is common in strokepatients and increases
the risk of fractures. Osteoporotic fractures are difficult to treat and prone to
complications; increase patient mortality10, 13); cause numerous socioeconomic problems,
including increased hospitalization duration and medical expenses; and lead to increased
difficulties for patients and their guardians. As changes in bone density of strokepatients
affect rehabilitation outcomes, they are a significant factor to be considered in the
treatment process14).Numerous studies have evaluated the influence of increased physical activity on strokepatients. However, only few studies have compared bone density between a healthy population
and strokepatients. This study aimed to compare bone density between the dominant and
nondominant sides of healthy elderly subjects aged >60 years and between the paretic and
nonparetic sides of hemiplegic strokepatients.
SUBJECTS AND METHODS
This study enrolled 15 strokepatients aged ≥60 years who had lived in a sanatorium in D
City for at least 6 months and 20 elderly individuals with no disease history as the control
group. The stroke group consisted of 9 male and 6 female subjects, and the control group
consisted of 4 male and 16 female subjects. The inclusion criteria were as follows: 1) could
follow instructions and answer questions; 2) capable of communication; 3) not taking any
drug or substance that could affect bone density, such as alcohol or smoking; and 4)
provided consent to participate in the study. The subjects’ mean age was 73.2 years; mean
height, 157 cm; mean weight, 56.2 kg; and mean body mass index, 22.5 kg/m2 (Table 1).
Table 1.
Demographic and clinical characteristics of the subjects (mean ± SD)
Variable
Stroke patients
Elderly
Age (years)
65.3 ± 8.5
61.4 ± 6.0
Height (cm)
156.5 ± 0.9
165.6 ± 6.0
Weight (kg)
58.2 ± 10.8
64.7 ± 7.5
BMI (kg/m2)
23.9 ± 4.8
23.5 ± 1.6
BMI: body mass index
BMI: body mass indexTo measure bone density, a quantitative ultrasonography device called OsteoPro (BM Tech,
Korea) was used. After entering data on age, height, weight, and foot size in the device and
performing zero-point calibration, bone density was measured at the right and left
calcaneus. The subject sat with a straight back, and the central axis of the footplate was
positioned between the second and third toes. During measurement, the subject was instructed
to sit still. Osteoporosis index (OI), T score, and Z
score were used to evaluate bone density.OI is an index that optimally combines all factors that affect bone density.
Z score was calculated by determining the difference between a certain
subject’s bone density and the mean bone density of an age- and gender-matched population,
and then dividing this by the standard deviation of that population. T
score was calculated by determining the difference between the bone density of a certain
subject and the maximum bone density in the general 20-year-old population, and then
dividing this by the standard deviation of that population. The World Health Organization
has used T scores to define clinical cutoff values for osteoporosis in
female adults. A T score of ≥−1.0 is defined as normal; a
T score between −1.0 and −2.5, as osteopenia; and a T
score of ≤−2.5, as osteoporosis15, 16). This study defined the change in bone
density as the difference in bone density between the paretic and nonparetic sides in the
stroke group, and between the dominant and nondominant sides in the control group.After dividing the subjects into a stroke group and a control group, paired-samples t-tests
were performed to analyze the OIs, T scores, and Z scores
of the paretic and nonparetic sides in the stroke group, and those of the dominant and
nondominant sides in the elderly group. Change in bone density was compared between the two
groups by using an independent-samples t-test. All results are shown as mean ± standard
deviation, and a p value of ≤0.05 was defined as statistically significant. All statistical
processing of data was performed by using SPSS 12.0.
RESULTS
No significant difference in bone density was found between the dominant and nondominant
sides in the control group in terms of OI, T score, or Z
score (p>0.05; Table 2). In the stroke group, the OI, T score, and
Z score for the nonparetic side were significantly higher than those for
the paretic side (p<0.05; Table 2). Change in
bone density was compared between the two groups based on the OIs, T
scores, and Z scores. A significant difference was found between the two
groups in terms of changes in OI, T score, and Z score
(p<0.05; Table 3). Between the two groups, the highest OI, T score, and
Z score values were obtained from the nonparetic side in the stroke group
(Table 2).
Table 2.
Comparison of OI, T score, and Z score between
the healthy elderly and the stroke patients (mean ± SD)
BMD
Elderly
Stroke patients
Right foot
Left foot
Nonparetic side
Paretic side
OI
36.3 ± 5.3
35.7 ± 5.7
41.4 ± 5.1
38.1 ± 4.8
**
T score
−2.9 ± 0.98
−2.98 ± 1.0
−2.3 ± 1.0
−2.97 ± 0.96
**
Z score
−0.1 ± −0.98
−0.3 ± 0.9
−0.6 ± 1.2
−1.3 ± 1.2
**
BMD: bone mineral density. **p<0.01
Table 3.
Comparison of the changes in scores between the healthy elderly and stroke
patients (mean ± SD)
BMD
Elderly
Stroke patients
OI
0.59 ± 3.60
3.37 ± 3.74
**
T score
0.12 ± 0.71
0.67 ± 0.74
**
Z score
0.20 ± 0.94
0.67 ± 0.74
**
BMD: bone mineral density. **p<0.01
BMD: bone mineral density. **p<0.01BMD: bone mineral density. **p<0.01
DISCUSSION
In their study that focused on the correlation between asymmetric weight bearing and bone
density, Shin and Kim17) reported that
bone density increased with greater weight bearing load, as the T score of
the nonparetic side was higher than that of the paretic side in strokepatients with chronic
hemiplegia. Liu et al.18) measured bone
density in the radius, femur, calcaneus, and lumbar vertebrae on the paretic and nonparetic
sides of hemiplegic strokepatients at the time of hospital admission and discharge. A
comparison of the results showed higher values on the nonparetic side. Many other studies
have shown evidence of higher bone density on the nonparetic side than on the paretic
side19, 20). Jorgensen et al.21) measured patients’ bone density regularly for a year after stroke
to observe changes in bone density as the patients gradually recovered their motor
abilities. Patients who recovered their walking ability within 2 months after stroke showed
less bone loss than those who did not. Kohrt et al.22) and Unsi et al.23) asserted that appropriate weight bearing would significantly
increase bone density because suitable physical activity helps maintain or improve bone
density. However, studies conducted by Young et al.24) and Bauer et al.25) showed conflicting results.Studies that compared bone density in the upper and lower limbs between the dominant and
nondominant sides revealed that the dominant hand showed better bone density than the
nondominant hand, but the lower limb showed no difference or the opposite result26,27,28).In the present study, significant differences were found between the paretic and nonparetic
sides of the strokepatients in terms OI, T score, and Z
score, and the change in bone density was significant. Moreover, among the whole study
population, the strokepatients showed the highest bone density values for the nonparetic
side. The nonparetic side of strokepatients is exposed to greater weight bearing input and
to excessive physical activity, causing it to gain greater bone density than that of the
healthy population16, 17). Increased physical activity through functional recovery of
hemiplegic patients can be considered important in preventing decreased bone density
throughout the whole body.The limitations to this study are as follows: First, as bone density could not be measured
in patients before stroke, the actual extent of bone loss on the affected side could not be
determined. Second, physical stimulation, including weight bearing, was the only factor
taken into consideration, and other influencing factors such as changes in the sympathetic
nerve system, smoking, and drinking were not considered. Third, the small number of subjects
makes it difficult to generalize the results. Last, the criteria used for selecting subjects
were age of ≥60 years and having lived in a sanatorium for at least 6 months. The number of
subjects in the two groups differed because the subjects were compared under an identical
environment. Therefore, future studies on reduced bone density due to decreased physical
activity should completely exclude influences from changes in the sympathetic nerve system,
smoking, drinking, and other risk factors, and examine a larger pool of subjects with an
equal number of subjects in each group. In addition, measurement methods other than
quantitative measurement should be used to observe the qualitative changes in bones, such as
structural changes, bone replacement, and bone composition, in order to accurately evaluate
the influence of reduced physical activity due to hemiplegia on bone density and to prevent
osteoporosis in strokepatients.