Lifestyle Factors Related to Femoral and Spinal Bone Density in Young Saudi Adult Women
Article Information
Lina F Hammad1*, Nada Benajiba2, Layal K. Jambi1, Alhanouf F Alshedi1
1Radiological Sciences Department, College of Applied Medical Sciences, King Saud University, Riyadh, KSA
2Regional Designated Center of Nutrition AFRA/IAEA, (Ibn Tofail University-CNESTEN), Morocco
Corresponding Author: Lina Fahmi Hammad.
Received: 28 October 2024; Accepted: 31 October 2024; Published: 22 November 2024
Citation: Lina F Hammad, Nada Benajiba, Layal K. Jambi, Alhanouf F Alshedi. Lifestyle Factors Related to Femoral and Spinal Bone Density in Young Saudi Adult Women. Journal of Women’s Health and Development. 7 (2024): 155-162.
View / Download Pdf Share at FacebookAbstract
Introduction: Many lifestyle factors are contributors to osteoporosis; a major health problem worldwide that can be measured using Dual-energy X-ray Absorptiometry (DXA). Aim: To evaluate the correlation between some lifestyle factors and Bone Mineral Density (BMD) in young Saudi adult women. Methods: BMD (gm/cm2) measurements in the femoral neck area and the lumbar spine (L2-L4) were performed using DXA in 101 females aged 20–24.9 years. BMD, T-score and Z-score were evaluated. Lifestyle factors were assessed through a questionnaire. Results: Milk & dairy product consumption, sun exposure, calcium & vitamin D supplements and Exercise had a significant positive correlation with some BMD scores. Soft drink consumption was significantly negatively correlated with all DXA parameters. Multiple linear regression demonstrated that; the factor with the strongest significant association with Z-scoren..femur and T-scoren.femur was exercising, followed by calcium and vitamin D supplements in Z-scoren..femur and by BMI in T-scoren.femur. BMI and animal protein consumption were significantly associated with BMDn.femur. Conclusion: Dairy and milk consumption, physical activity and sun exposure were the factors that showed significant association with BMD parameters. Limited calcium and Vitamin D intake and high consumption of soft drinks are the major contributors to low bone density in young females.
Keywords
Lifestyle factors; Osteopenia; Osteoporosis; Saudi Arabia; Young women
Article Details
Introduction
Osteoporosis is a common disease that affects the global population, characterized by reduced bone mass with modification in microarchitecture which leads to bone fragility and increased risk of fracture [1]. In Saudi Arabia, the prevalence of osteoporosis is increasing [2]. Low bone quality was reported by Zeidan and colleagues in 9% of young healthy adult Saudi women [3]. The National Plan for Osteoporosis Prevention and Management recommendations of the Ministry of Health in the Kingdom of Saudi Arabia (KSA) include; education and health programs, early screening and intervention, regulation of post-fracture care to control secondary fractures, in addition to further research as contributors to reduce the onset of osteoporosis within Saudi Arabia [4]. Some risk factors have been implicated in the pathophysiology of osteoporosis. These factors could be categorized into, major non-changeable and modifiable risk factors. The non-changeable factors include age, gender, genetic history, race, menopause, hypogonadism and rheumatoid arthritis [5]. Modifiable risk factors that could be changed to manage the reduction in BMD and the increase in osteoporosis include; alcohol, smoking, high intake of glucocorticoid, vitamin D deficiency, mull nutrition, insufficient exercise, low dietary and calcium intake [6, 7]. In addition to that, Saudi adolescents demonstrate vitamin D deficiency, low dairy consumption, lack of physical activity, and avoidance of sun exposure [8] and inadequate knowledge about osteoporosis crucial for disease prevention were found in young Saudi female college students [9]. Previous studies recommended improving lifestyle factors that could maintain muscle and bone strength, including exercise, and sufficient vitamin D and calcium supplements [10]. Early in life, physical activity contributed to a higher peak bone mass [11]. Studies have suggested that calcium and protein intakes are important for bone mass gain during and after puberty [12]. Furthermore, milk and calcium-enriched foods affected bone accumulation positively and influenced total body bone mineral content [13]. Factors contributing to low bone mass include low calcium intake, limited dairy product consumption, insufficient fruit and vegetable intake, and an exaggerated intake of soft drinks [2]. A change in lifestyle patterns in young Saudis in recent years is well documented [14,15], which suggests the importance of studying their effects on bone health. This study aimed to examine the correlation between lifestyle factors including smoking, exercising, calcium and vitamin D supplements intake, sun exposure, soft drinks, animal protein, and dairy products intake and BMD in young Saudi females.
Materials and Methods
Study Design
The research work was designed as a cross-sectional study, implemented at the King Saud University campus. Of the young females (age range 20-24.9 years), all were of Saudi Arabic nationality. Exclusion criteria self-reported by the participant included using medication interacting with calcium metabolism before and during the study time, suffering from any health condition affecting bone metabolism, parathyroid diseases, having a history of any fracture or major systemic disorder; being pregnant or at any terminal illness stage. A total sample of 110 young females meeting the criteria were found suitable to be recruited for the study. Before taking measurements, the study protocol was explained to participants, and the informed consent was signed upon their agreement before inclusion in the study.
Bone Mineral Density (BMD) measurements
Measurements of BMD (gm/cm2) in the femoral neck area and the lumbar spine (L2-L4) were performed using DXA scans (Lunar IDXATM - GE Healthcare). The Middle East reference population was used to calculate the Z-score. A standard protocol supplied by the manufacturer was used, including a quality control test using a standard phantom provided by the manufacturer. The Z-score obtained is defined as the number of standard deviations a patient's BMD differs from the average BMD of their age, sex, and ethnicity [16]. Based on the criteria defined by the International Society for Clinical Densitometry (ISCD) guidelines [17].
Anthropometric measurements and lifestyle patterns of the studied population
An eye-level beam scale with a height rod from DetectoTM USA was used to measure height and weight. Body mass index (BMI) (kg/m2) was calculated after measuring the weight (Kg) and height (m) by the investigator. Classification of participants based on their BMI was done following the WHO guidelines. A participant was considered underweight if her BMI <18.50 kg/m2, normal if the BMI ranged between 18.50-24.99 kg/m2, overweight if the BMI ranged between 25.00-29.99 kg/m2 and obese if BMI was≥30.00 kg/m2 [18]. Lifestyle factors thought to influence bone health were assessed through a validated questionnaire by the authors. Participants were requested to answer questions related to smoking, exercising, sun exposure, calcium, and vitamin D supplement intake. Food-frequency questionnaire was used to assess the intake of main foods related to bone health (animal protein, soft drinks, and dairy products), which include food consumption per week, portion size and number of soft drink cans per day. The questionnaire was developed for the study and validated by the authors. The questions were taken from a previously published paper by Oommen & AlZahrani and similar to the questionnaire used by Lim and colleagues [19,20].
Statistical Analysis
All statistical analysis was performed using SPSS software (Version 24.0) (IBM Corporation, N.Y., USA). Results were expressed as percent, means ± standard deviation (SD). T-test and ANOVA tests were used to measure the difference between the groups. A significant difference was set at a cut-off p<0.05. A two-step multiple linear regression analysis was performed to assess lifestyle factors with a significant association with the three studied parameters BMD, T-score or Z-score in the neck of the femur and in the spine. Step 1 consisted of examining the presence of a significant correlation. In step 2, factors significantly correlated (p<0.05) were entered into multiple linear regression models to identify factors with the strongest association.
Results
Of the 110 subjects recruited, 9 subjects have withdrawn from the study citing unavailability of time. The general characteristics of the studied population are demonstrated in Table 1. The mean age was 21.3±0.8 years and the mean BMI was 22.2±3.7 kg/m2.
Parameter |
Mean ± SD |
Age (year) |
21.3±0.8 |
Height (m) |
1.6±0.1 |
Weight (kg) |
55.9±9.4 |
BMI (Kg/m2) |
22.2±3.7 |
BMI category |
N (%) |
Underweight |
14 (13.8) |
Normal |
69 (68.3) |
Overweight |
14 (13.8) |
Obese |
4 (3.9) |
BMI (kg/m2) = Body mass index. BMI categorization is based on the WHO guidelines: Underweight: <18.5 kg/m2, Normal: 18.5 - 24.9 kg/m2, Overweight ≥25.0 kg/m2 and obese ≥30.0 kg/m2 [18].
Table 1: General characteristics of the studied population (n=101)
The cut-off point is a Z-score of -2 or lower defined as “below the expected range for age” and a Z-score above -2.0 is “within the expected range [17].
As shown in Table 2 according to Z-score classification, 5% of the studied subjects had a femoral BMD below normal range at the neck of the femur. Moreover, in studying the BMD of the spine, about 8% of the participants had BMD below the normal range.
N=101(%) |
Mean ± SD (g/m2) |
||
BMD in the neck of femur |
|||
Normal range (>-2) |
96 (95.1) |
-0.42 ±0.81 |
p <0.001 |
Below normal range (£-2) |
5 (4.9) |
-2.20±0.11 |
|
Total |
101 (100) |
-0.51 ±0.80 |
|
BMD in the Spine |
|||
Normal range (>-2) |
93 (92.1) |
-0.39±0.92 |
p <0.001 |
Below normal range (£-2) |
8 (7.9) |
-2.31±0.30 |
|
Total |
101 (100) |
-0.55±1.03 |
Table 2: Distribution of the studied population-based on Z-score classification of BMD in the neck of femur and in the spine (n=101)
The effect of BMI and different lifestyle factors on the three parameters (Z-score, T-score and BMD of both neck of the femur and spine is tabulated in Table 3. A positive association was observed between BMI and the three above parameters, though only statistically significant in BMD and T-score in both neck of femur and spine. On the other hand, the high frequency of milk and dairy product consumption significantly increases the averages of the three studied parameters, except for BMDn.femur.
Lifestyle factors (n, %) |
Z-Score |
T-Score |
BMD |
|||
Spine |
Femur |
Spine |
Femur |
Spine |
Femur |
|
BMI category** Underweight (14, 13.8) Normal (69, 68.3) Overweight (14, 13.8) Obese (4, 3.9) |
-0.74±1.20 -0.61±1.01 -0.28±0.90 -0.28±1.08 p =0.24 |
-0.64±1.14 -0.63±0.81 -0.23±0.88 0.35±0.66 p =0.08 |
-1.04±1.31 -0.88±0.98 -0.32±0.86 0.58±0.81 p =0.01 |
-0.70±1.19 -0.77±0.77 -0.32±0.94 0.43±0.37 p =0.02 |
1.02±0.23 1.10±0.19 1.12±0.15 1.36±0.18 p =0.02 |
0.93±0.15 0.95±0.15 1.06±0.20 1.24±0.28 p < 0.01 |
Smoking* No (93, 92.0) Yes (8, 8.0) |
-0.53±1.04 -0.68±1.04 p = 0.30 |
-0.50±0.9 -0.50±0.9 p = 0.80 |
-0.75±1.07 -0.76±0.95 p =0.40 |
-0.6±0.9 -0.6±0.8 p =0.90 |
1.10±0.20 1.16±0.23 p =0.30 |
1.0±0.2 1.1±0.3 p =0.10 |
Dairy and milk consumption** Rare (<2 times/week) (46, 45.5) Moderate (2 times/week) (46, 45.5) Frequent (3-5times/week) (9, 8.9) |
-1.10±0.86 -0.13±0.91 0.08±1.17 p <0.01 |
-0.8±0.9 -0.3±0.8 0.2±0.8 p=0.03 |
-1.30±0.93 -0.38±0.94 -0.13±1.09 p < 0.01 |
-0.9±0.9 -0.4±0.8 -0.5±0.9 p = 0.01 |
1.02±0.18 1.18±0.19 1.15±0.20 p < 0.01 |
1.0±0.2 1.15±0.15 0.9±0.17 p = 0.20 |
Sun Exposure* No (60, 59.1) Yes (41, 40.8) |
-0.79±0.94 -0.15±1.06 p < 0.01 |
-0.62±0.87 -0.32±0.90 p =0.70 |
-1.03±1.11 -0.34±1.11 p < 0.01 |
-0.77±0.87 -0.45±0.88 p =0.08 |
1.06±1.07 1.17±0.22 p = 0.003 |
0.97±0.20 0.98±0.15 p = 0.09 |
Vit. D and Ca supplement* No (88, 86.8) Yes (13, 13.3) |
-0.64±0.98 0.06±1.23 p = 0.03 |
-0.6±0.8 -0.1±1.1 p = 0.01 |
-0.84±1.02 -0.28±1.18 p = 0.07 |
-0.7±0.8 -0.1±1.1 p = 0.01 |
1.09±0.20 1.17±0.21 p = 0.10 |
1.0±0.2 1.0±0.2 p = 0.90 |
Animal protein consumption** Rare (<2 times/week) (27, 27.0) Moderate (2-4 times/week) (41, 40.0) Frequent (daily) (33, 33.0) |
-0.66±0.87 -0.65±0.96 -0.28±1.20 p = 0.33 |
-0.62±0.7 -0.60±0.87 -0.25±0.98 p = 0.33 |
-0.92±0.93 -0.90±1.03 -0.45±1.13 p = 0.17 |
-0.84±0.74 -0.71±0.84 -0.37±0.98 p = 0.08 |
1.07±0.18 1.09±0.13 1.15±0.27 p = 0.20 |
0.93±0.14 0.94±0.18 1.05±0.18 p = 0.01 |
Soft drinks consumption** Rare (<1 can/day) (37, 37.0) Moderate (>2 cans/day) (47, 46.0) Frequent (>3 and large cans/day)(17, 17.0) |
-0.12±0.81 -0.70±1.06 -1.04±1.04 p = 0.05 |
-0.29±0.72 -0.53±0.92 -0.92±1.04 p = 0.05 |
-0.34±0.91 -0.87±1.16 -1.37±1.04 p = 0.01 |
-0.45±0.74 -0.66±0.92 -1.03±1.02 p = 0.07 |
1.15±0.15 1.10±0.22 1.01±0.20 p = 0.02 |
0.99±0.18 0.99±0.18 0.87±0.12 p = 0.02 |
Exercise* No (62, 61.3) Yes (39, 38,6) |
-0.66±1.05 -0.35±0.99 p = 0.06 |
-0.68±0.89 -0.23±0.82 p = 0.01 |
-0.91±1.03 -0.54±1.06 p = 0.04 |
-0.83±0.90 -0.36±0.78 p < 0.01 |
1.09±0.23 1.12±0.15 p = 0.20 |
0.95±0.18 1.01±0.17 p = 0.08 |
*t-test, **ANOVA tes
Table 3: Z-score, T-score, and BMD (Mean ± SD) of the spine and in the neck femur according to lifestyle factors. (P value obtained from t-test and ANOVA test)
The increased frequency of animal protein consumption was associated with an increase in the three parameters, though statistically significant in the BMDn.femur. Sun exposure affected the three evaluated parameters' mean values positively, though statistically significant in the spine area only.
In the present study, participants who do take vitamin D and Calcium supplements had significantly higher Z-scorespine, and Z-scoren.femur and T-scoren.femur values compared to the group who did not, in contrast to the above finding; soft drinks consumption had a statistically significant inverse relationship with all the parameters expect T-scoren.femur. The present study results revealed that participants who exercised showed significantly higher values of Z-scoren.femur, T-scoren.femur and T-scorespine than others who did not.
The present study evaluated the correlation coefficients (r2) of the studied parameters (BMD, T-score and Z-score) in the neck of the femur and the spine with the different lifestyle factors and results are represented in Table 4.
Z-Score |
T-Score |
BMD |
||||
Spine |
Femur |
Spine |
Femur |
Spine |
Femur |
|
BMI (Kg/m2) |
0.29** |
0.23* |
0.38*** |
0.31** |
0.36*** |
0.33** |
Smoking |
0.01 |
0.06 |
0.04 |
0.07 |
0.11 |
0.01 |
Milk and dairy products consumption |
0.44*** |
0.21* |
0.41*** |
0.21* |
0.33** |
0.01 |
Sun Exposure |
0.30** |
0.18* |
0.32** |
0.19* |
0.28** |
0.04 |
Calcium & Vitamin D supplements |
0.23* |
0.24** |
0.18* |
0.25** |
0.12 |
0.06 |
Animal protein consumption |
0.14 |
0.16 |
0.17* |
0.21* |
0.16 |
0.27** |
Soft drink consumption |
-0.30** |
-0.21* |
-0.31** |
-0.18* |
-0.22* |
-0.17* |
Exercise |
0.17 |
0.26** |
0.19* |
0.27** |
0.07 |
0.19* |
Table 4: Correlation coefficients r2 between Z-score, T-Score and BMD of the spine and in the neck femur and lifestyle factors. *p<0.05, **p<0.01, ***p<0.001
BMI showed a significant positive correlation with all the evaluated parameters, the highest correlation was obtained with T-scorespine (r2=0.38). However, the smoking lifestyle factor showed a non-significant correlation with all the examined parameters. Both factors; milk and dairy products consumption and sun exposure exhibited a significant positive correlation with all the evaluated parameters except with BMD femur. The highest correlation was found between Z-scorespine and milk and dairy products consumption (r2=-0.43) and T-scorespine with sun exposure (r2=-0.32). For Calcium & Vitamin D supplements, results revealed a significant positive correlation with only the T-score and Z-score at both neck of the femur and spine, the highest correlation was with T-score femur (r2=0.25). Nonetheless, there was a non-significant correlation with BMD. A significant positive correlation was found between animal protein consumption and only T-Score and BMD femur (r2=0.27) parameters. Additionally, there was a significant positive correlation between exercise and Z-score femur, T-score at both the neck of the femur and spine and BMD femur. A significant negative correlation was found between soft drink consumption and all investigated parameters. The models obtained from multiple linear regression were significant for the three parameters Z-score, T-score and BMD in both the neck of the femur and the spine (p <0.05) (Table 5).
SPINE |
NECK OF FEMUR |
|||||
ß |
Partial R2 |
95.0% CI for B |
ß |
Partial R2 |
95.0% CI for B |
|
Z-SCORE |
||||||
BMI (Kg/m2) |
0.21 |
0.25* |
0.01, 0.11 |
0.15 |
0.16 |
-0.01, 0.08 |
Dairy and milk consumption |
0.38 |
0.41*** |
0.32, 0.89 |
0.18 |
0.12 |
-0.02, 0.52 |
Sun Exposure |
0.19 |
0.21* |
0.01, 0.78 |
0.01 |
0.01 |
-0.35, 0.39 |
Calcium & Vitamin D supplements |
0.14 |
0.16 |
-0.13, 0.95 |
0.23 |
0.24* |
0.01, 1.12 |
Soft drinks consumption |
-0.14 |
-0.16 |
-0.48, 0.06 |
-0.13 |
-0.12 |
-0.41, 0.11 |
Exercise |
--- |
--- |
--- |
0.26 |
0.27** |
0.12, 0.84 |
T-SCORE |
||||||
BMI (Kg/m2) |
0.30 |
0.36*** |
0.04, 0.13 |
0.25 |
0.28* |
0.02, 0.10 |
Dairy and milk consumption |
0.37 |
0.42*** |
0.32, 0.88 |
0.19 |
0.21* |
0.00, 0.52 |
Sun Exposure |
0.19 |
0.22* |
0.02, 0.80 |
0.02 |
0.02 |
-0.32, 0.39 |
Calcium & Vitamin D supplements |
0.07 |
0.1 |
-0.29, 0.75 |
0.21 |
0.23* |
0.05, 1.01 |
Animal protein consumption |
0.12 |
0.15 |
-0.07, 0.39 |
0.20 |
0.22* |
0.01, 0.44 |
Soft drinks consumption |
-0.09 |
-0.11 |
-0.40, 0.1 |
-0.03 |
-0.03 |
-0.28, 0.21 |
Exercise |
0.16 |
0.20 |
-0.02, 0.7 |
0.29 |
0.31** |
0.18, 0.88 |
BMD |
||||||
BMI (Kg/m2) |
0.30 |
0.33** |
0.01, 0.03 |
0.28 |
0.3* |
0.004, 0.02 |
Dairy and milk consumption |
0.30 |
0.33** |
0.04, 0.15 |
--- |
--- |
--- |
Sun Exposure |
0.23 |
0.25* |
0.02, 0.17 |
--- |
--- |
--- |
Soft drinks consumption |
-0.04 |
-0.05 |
-0.07, 0.04 |
-0.05 |
-0. |
-0.060, 0.03 |
Animal protein consumption |
--- |
--- |
--- |
0.28 |
0.30* |
0.022, 0.11 |
Exercise |
--- |
--- |
--- |
0.17 |
0.18 |
-0.007, 0.13 |
Model summaries:
In spine:
Z-score: F=9.59, p<0.01, R2= 0.35, SEE= 0.86
T-score: F=8.95, p<0.01, R2= 0.49, SEE= 0.83
BMD: F= 8.76, p<0.01, R2= 0.28, SEE= 0.17
In the neck of the femur:
Z-score: F= 4.21, p<0.01, R2= 0.22, SEE= 0.82
T-score: F=5.29, p<0.01, R2= 0.29, SEE= 0.77
BMD: F=6.21, p<0.01, R2= 0.25, SEE= 0.16
BMD: Bone mineral density. *p≤0.05, **p≤0.01, ***p≤0.001
Table 5: Multiple linear regression models.
For the neck of the femur, they accounted for 21%, 29% and 25 % in Z-scoren.femur, T-scoren.femur and BMDn,.femur, respectively. For the spine, models explained a higher percent of the response data variability by 35% in Z-scorespine, 50% in T-scorespine and 28% in BMDspine. In the neck of the femur, multiple linear regression demonstrated that the factor with the strongest significant association with Z-scoren..femur and T-scoren.femur was exercising (ß=0.26 and ß=0.29, respectively), followed by calcium and vitamin D supplements in Z-scoren..femur and by BMI in T-scoren.femur. Concerning BMDn.femur, BMI and animal protein consumption were significantly associated with this parameter. The association was stronger for BMI than for animal and protein consumption (ß=0.346 versus ß=0.271, respectively). Different results were found in the spine. For the three parameters, BMI, dairy and milk consumption, and sun exposure were the factors that showed the strongest significant association. The highest ß was obtained for dairy and milk consumption (0.38 in Z-scorespine, 0.37 in T-scorespine and 0.30 in BMDspine).
Discussion
The present results showed that most of the participants had Z-score that matched their age, similar studies were reported by recently published findings by Al Nozha and colleagues [21]. The significant positive correlation between both milk and dairy product consumption and sun exposure with all the evaluated parameters except with BMD femur and the positive correlation between Calcium & Vitamin D supplements with T-score and Z-score at both neck of femur and spine are in agreement with previous studies [22, 23]. This is of importance as previous studies confirmed that women with vitamin D deficiency are known to be at high risk for bone loss, bone fractures and disability [24], in addition to that; calcium malabsorption with resultant secondary hyperparathyroidism was found to cause impairment of skeletal mineralization, rickets development and osteomalacia in children or osteomalacia and osteoporosis in adults [25].
Although the sun exposure duration was not measured in our study, a previous study in the Riyadh area found that sun exposure time for optimum vitamin D3 production is from 9:00 AM and before 10:30 AM and after 2:00 PM until 3:00 PM (local time) during summer time and from 10:00 AM until 2:00 PM (local time) during winter time. These timings are important from a public health perspective, as it’s a free and highly efficacious way for the management and the prevention of vitamin D deficiency [26], limited exposure to sunlight was reported as the main contributor to low serum 25(OH)D concentrations in the Saudi Arabian population as hot climate drives individuals to prefer air-conditioned comfort indoors that limit the endogenous production of vitamin D [27]. Other factors that would affect vitamin D production and might be of interest in future studies include; the effect of skin colour, season, altitude, time of the day, and amount of sun exposure within different areas of Saudi Arabia. The positive association between milk intake and BMDspine found in our study agrees with Yoshii and colleagues who suggested that milk consumption is beneficial for the bone health of adult women and high school females if accompanied by exercise [28]. The present study did not examine for the effect of the number of pregnancies nor the area of living on bone status as most of the sample studied were unmarried and lived within the same city (Riyadh) though earlier studies found that; factors like education level, number of pregnancies and area of living could influence the risk for osteopenia and osteoporosis [29]. Osteopenia was more common in unmarried urban women versus rural married ones, and college-educated females had considerable normal bone mass than females with lower than high school education. In the postmenopausal age (PMA) group, urban women were more Osteopenic than rural or industrial women and less than primary educated women were significantly more osteoporotic than college-educated women [29]. The present results reported a significant positive correlation between animal protein consumption and T-Score femur and BMD femur (r2=0.22 & 0.3 respectively, Table: 5), in contrast to our findings, other studies concluded that in healthy adults, little profits for bone health were found with increasing protein intake, though no detrimental effect was found [30].
The association between other dietary patterns such as high consumption of fish and olive oil and low red meat intake was not investigated in this study, other studies suggested the potential bone-preserving properties of this eating pattern throughout adult life [31]. The significant positive correlation between exercise and both Z-score femur, T-score femur in this study is in agreement with findings from a review paper that suggested that walking as an exercise program for postmenopausal women can improve the femoral BMD [32]. Although previous meta-analysis found that bone strength improvements ranged from 0.5% to 2.5% with high exercise compliance in premenopausal women [33], the significantly higher T-scorespine in participants who exercised (Table3) suggests the importance of studying the effect of different exercise programs (resistance, aerobic and impact) on both bone and muscle strength. As low bone mineral density is a risk factor for the low quality of life in old age [34], the above findings suggest further research into different lifestyle factors that may affect bone strength. It could provide an approach to health education intervention to improve lifestyle and bone health in the Saudi population. In terms of limitation, the study design was cross-sectional meaning that causality between the different lifestyle factors and BMD could not be determined. In addition, the interpretation of the current findings could not be generalized because of the sample size, however, it could serve as a direction to develop larger research studies among this critical age group and set adequate public health policies in this regard.
Conclusion
Some lifestyle factors were found to be significantly correlated with low BMD in young Saudi females. Significant negative effects of soft drink consumption were found, whereas, milk and dairy products consumption, sun exposure, calcium & Vitamin D supplements and exercising exhibited significant positive effects on some BMD parameters. Understanding lifestyle factors that increase the occurrence of osteopenia and osteoporosis should help in planning preventive measures. Further studies are required to provide in-depth knowledge of the effect of each factor on the development of bones and later the prevention of osteoporosis.
Acknowledgments
This research was supported by a grant from the “Research Center of the Female Scientific and Medical Colleges”, Deanship of Scientific Research. The funding body had no role in the design of the study and collection, analysis, and interpretation of data or in writing the manuscript.
Conflicts of interest
The authors declare that they have no competing interests
Ethical approval
The study was approved by the Research Ethics Committee of the University (Ethics No. CAMS18/3S36), and was performed according to the principles of the Helsinki Declaration.
Authors contributions
LFH: Conceived and designed the study; collected data; wrote the initial draft and contributed to the final draft.
NB: Performed data analysis tools; contributed to the final draft.
LKJ: contributed to the final draft
AFA: contributed to the final draft
References
- Curtis EM, Moon RJ, Harvey NC, et al. Reprint of: the impact of fragility fracture and approaches to osteoporosis risk assessment worldwide. International journal of orthopaedic and trauma nursing 26 (2017): 7-17.
- Al-Saleh Y, Sulimani R, Sabico S, et al. Guidelines for Osteoporosis in Saudi Arabia: Recommendations from the Saudi Osteoporosis Society. Annals of Saudi medicine 35 (2015): 1-12.
- Zeidan ZA, Sultan IE, Guraya SS, et al. Low bone mineral density among young healthy adult Saudi women: Prevalence and associated factors in the age group of 20 to 36 years. Saudi medical journal 37 (2016): 1225.
- Ministry of Health. National Plan for Osteoporosis Prevention and Management in the Kingdom of Saudi Arabia (2018).
- Pouresmaeili F, Kamalidehghan B, Kamarehei M, et al. A comprehensive overview on osteoporosis and its risk factors. Therapeutics and clinical risk management (2018): 2029-2049.
- Kanis JA, Johnell O, Odén A, et al. Smoking and fracture risk: a meta-analysis. Osteoporosis international 16 (2005): 155-162.
- Kanis JA, Johansson H, Johnell O, et al. Alcohol intake as a risk factor for fracture. Osteoporosis international 16 (2005): 737-742.
- Al-Raddadi R, Bahijri S, Borai A, et al. Prevalence of lifestyle practices that might affect bone health in relation to vitamin D status among female Saudi adolescents. Nutrition 45 (2018): 108-113.
- Alshareef SH, Alwehaibi A, Alzahrani A, et al. Knowledge and awareness about risk factors of osteoporosis among young college women at a university in Riyadh, KSA. J Bone Res 6 (2018): 2.
- Hammad LF, Benajiba N. Lifestyle factors influencing bone health in young adult women in Saudi Arabia. African health sciences 17 (2017): 524-531.
- Strope MA, Nigh P, Carter MI, et al. Physical activity-associated bone loading during adolescence and young adulthood is positively associated with adult bone mineral density in men. American journal of men's health 9 (2015): 442-450.
- Rizzoli R. Nutrition: its role in bone health. Best practice & research Clinical endocrinology & metabolism 22 (2008): 813-829.
- Rizzoli R, Bianchi ML, Garabédian M, et al. Maximizing bone mineral mass gain during growth for the prevention of fractures in the adolescents and the elderly. Bone 46 (2010): 294-305.
- Alkhateeb SA, Alkhameesi NF, Lamfon GN, et al. Pattern of physical exercise practice among university students in the Kingdom of Saudi Arabia (before beginning and during college): a cross-sectional study. BMC public health 19 (2019): 1716.
- Al-Hazzaa HM, Abahussain NA, Al-Sobayel HI, et al. Lifestyle factors associated with overweight and obesity among Saudi adolescents. BMC public health 12 (2012): 354.
- Ward RJ, Roberts CC, Bencardino JT, et al. ACR appropriateness criteria® osteoporosis and bone mineral density. Journal of the American College of Radiology 14 (2017): S189-S202.
- Schousboe JT, Shepherd JA, Bilezikian JP, et al. Executive summary of the 2013 international society for clinical densitometry position development conference on bone densitometry. Journal of clinical densitometry 16 (2013): 455-66.
- Organization WH. Obesity: preventing and managing the global epidemic: report of a WHO consultation (2000).
- Oommen A, AlZahrani I. Prevalence of osteoporosis and factors associated with osteoporosis in women above 40 years in the Northern Part of Saudi Arabia. Int J Res Med Sci 2 (2014): 274.
- Lim H-S, Ji S-I, Hwang H, et al. Relationship between bone density, eating habit, and nutritional intake in college students. Journal of bone metabolism 25 (2018): 181-186.
- Al Nozha OM, El Tarhouny S, Taha I, et al. Association Between Vitamin D Level and Z-Score Changes of Bone Density in College-Age Saudi Girls: A Cross-Sectional Study. International Journal of General Medicine (2023): 865-874.
- Sadat-Ali M, Al Elq AH, Al-Turki HA, et al. Influence of vitamin D levels on bone mineral density and osteoporosis. Annals of Saudi medicine 31 (2011): 602-608.
- John Cecily HS. Early Detection and Prevention of osteoporosis among pre-and Postmenopausal Women in Saudi Arabia. Clinical Nursing Research 29 (2020): 48-55.
- Yousef FM. Associations Factors Affecting on Osteoporosis in Postmenopausal Women in Saudi Arabian, Jeddah. International Journal of Pharmaceutical Research & Allied Sciences 6 (2017).
- Khoja S, Khan J, Maimani A, et al. Influence of diet on bone health in Saudi Arabian women. International Congress Series 1297 (2007): 296-302.
- Alshahrani FM, Almalki MH, Aljohani N, et al. Vitamin D: Light side and best time of sunshine in Riyadh, Saudi Arabia. Dermato-endocrinology 5 (2013): 177-180.
- Zareef TA, Jackson RT. Knowledge and attitudes about vitamin D and sunlight exposure in premenopausal women living in Jeddah, and their relationship with serum vitamin D levels. Journal of Health, Population and Nutrition 40 (2021): 38.
- Yoshii S, Kamimotono S, Sawai S, et al. Cross-sectional survey on the relationship between dairy product intake and bone density among adult women and high school students. Nutrition research 27 (2007): 618-624.
- Al-Habdan IM, Sadat-Ali M, Al-Muhanna FA, et al. Bone mass measurement using quantitative ultrasound in healthy Saudi women. A cross-sectional screening. Saudi medical journal 30 (2009): 1426-1431.
- Darling AL, Manders RJ, Sahni S, et al. Dietary protein and bone health across the life-course: an updated systematic review and meta-analysis over 40 years. Osteoporosis International 30 (2019): 741-761.
- Kontogianni MD, Melistas L, Yannakoulia M, et al. Association between dietary patterns and indices of bone mass in a sample of Mediterranean women. Nutrition 25 (2009): 165-171.
- Moreira LDF, Oliveira MLd, Lirani-Galvão AP, et al. Physical exercise and osteoporosis: effects of different types of exercises on bone and physical function of postmenopausal women. Arquivos Brasileiros de Endocrinologia & Metabologia 58 (2014): 514-522.
- Nikander R, Sievänen H, Heinonen A, et al. Targeted exercise against osteoporosis: A systematic review and meta-analysis for optimising bone strength throughout life. BMC Medicine 8 (2010): 47.
- Sànchez-Riera L, Carnahan E, Vos T, et al. The global burden attributable to low bone mineral density. Annals of the Rheumatic Diseases 73 (2014): 1635-1645.