Skip to main content
BMC Musculoskeletal Disorders logoLink to BMC Musculoskeletal Disorders
. 2014 Jan 8;15:5. doi: 10.1186/1471-2474-15-5

Prevalence and factors associated with low bone mineral density in Saudi women: a community based survey

AlJohara M AlQuaiz 1,2, Ambreen Kazi 1,, Salwa Tayel 2, Shaffi Ahamed Shaikh 2, Abdullah Al-Sharif 3, Saleh Othman 4, Fawzia Habib 5, Mona Fouda 1,6, Riad Sulaimani 6
PMCID: PMC3893466  PMID: 24400907

Abstract

Background

Low bone mineral density (BMD) is a public health issue in Saudi Arabia. This study measured the prevalence and factors associated with low BMD in Saudi women in Riyadh, Saudi Arabia.

Methods

A cross sectional study using two stage cluster sampling technique was conducted in Riyadh, 2009. Thirty clusters, each comprising of 300 houses were randomly chosen and from each cluster 38–40 households were selected to identify 1150 women of >40 years. Women were invited to primary health care center for filling of self-administered questionnaire (n = 1069) comprising of sociodemographic, health, diet and physical activity variables. 1008 women underwent screening for low BMD using the quantitative ultrasound technique. 535 (53%) women with positive screening test were referred to King Khalid Hospital for Dual X-ray Energy absorptiometry (DXA).

Results

362 women underwent DXA and 212 (39.6%) were screened low BMD either at lumbar spine or femur neck. Mean age of women was 55.26(±8.84) years. Multivariate logistic analysis found; being aged 61 to 70 years (OR 2.75, 95% CI: 1.32-1.48), no literacy (OR 2.97, 95% CI:1.44 - 6.12) or primary education (OR 4.12, 95% CI:2.05-8.29), history of fractures (OR 2.20, 95% CI:1.03- 4.69) and not drinking laban(diluted yogurt) (OR 2.81, 95% CI:1.47- 5.37) significantly associated with low BMD.

Conclusions

Women with low level of education, who do not drink laban and had history of fractures were at high risk of low BMD.

Keywords: Low bone mineral density, Women, Dietary factors

Background

Low bone mineral density (BMD) manifesting as fragile bones mainly comprise of osteoporosis and osteopenia [1]. Prevalence of low BMD varies according to age, sex, ethnicity and type of skeletal bone [1]. According to global estimates, about 200 million women suffer from osteoporosis worldwide [2]. The American 2005–2008 National Health and Nutrition Examination Survey found 50% of women over 50 years of age suffering from low BMD [3]. Low BMD is a public health issue in Saudi Arabia and prevalence of lumbar and femur osteopenia ranges from 7% to 43.4% and osteoporosis from 2.5 to 46.7% [4-7].

National Osteoporotic foundation, USA and the National consensus group on osteoporosis for the Middle East and North Africa has indicated; menopause, low physical activity, family history of fractures, personal history of fracture as an adult, cigarette smoking, alcohol drinking, thin build, use of oral gluco-corticosteroid therapy for 3 months or more or having history of rheumatoid arthritis, thyroid disease, liver disease as major risk factors for low BMD [7-9]. In addition to above, Rouzi et al. in a prospective cohort study on healthy Saudi postmenopausal women found a combination of factors (age, physical activity, hand grip, bone mineral density, dietary calcium intake, serum 25 (OH)D levels and history of falls) to contribute significantly to osteoporosis-related fractures [10].

Low BMD leads to limitations in mobility along with high medical cost. To date, the gold standard technique for diagnosing low BMD is the dual energy x-ray absorptiometry (DXA) which has high predictive validity (sensitivity and specificity) [11]. Number of hospital based and few community based studies have measured risk factors for fractures and low BMD in Saudi Arabia; however, these studies have reported limitations in generalizability and quality [3-6]. In order to improve primary prevention against low BMD it is important to identify the few, most important risk factors through a community based study. The objective of this study was to measure the prevalence of low BMD using the DXA technique and identify the associated factors in Saudi women in Riyadh.

Methods

This was a community based household cross-sectional study conducted in Riyadh during April-May, 2009. Two stage cluster sampling technique was followed. Riyadh is divided into five administrative regions and one major primary health care center (PHCC) was selected from each region. The catchment population of PHCC served as a cluster. It is assumed that on an average there is one woman over forty years per Saudi family, therefore 230–240 households were randomly selected from each cluster to reach a sample size of 1150. Eligible women were invited to PHCC for filling of self-administered questionnaire and screening for low BMD using the Quantitative ultrasound (QUS) technique. Flow chart representing the enrollment and number of participants is given as Figure 1.

Figure 1.

Figure 1

Enrollment flow chart of Saudi women (>40 years) in Riyadh, Saudi Arabia.

Questionnaire was designed based on previous identified factors and other biological plausible factors leading to low BMD. Information was collected on variables related to socio-demographic characteristics (age, education, occupation, marital status), sun exposure (time spent under the sun), present and past medical illnesses, obstetric & gynecological history (menstrual status, number of pregnancies and children, contraceptive use), personal history of fracture as an adult on trivial (minor) fall, family history of fractures, cigarette smoking, intake of dietary items; low fat milk, low fat cheese, low fat laban (diluted yogurt), meat, fish, vegetables, fruits, tea, coffee and physical activity (walking, climbing, swimming). All questions were phrased clearly for the participants to understand. Diet and physical activity was asked pertaining to last one week. Height and weight was measured through standard procedure. Those who had difficulty in reading or writing were interviewed by a trained research assistant.

Inclusion & exclusion criteria

Saudi females, >40 years of age and living in Riyadh city were included in the study. Women who self reported secondary causes of low BMD, such as hyperthyroidism, hyperparathyroidism or liver disease were excluded from the study.

Measurement of bone mineral density through quantitative ultrasound

QUS was done by scanning the calcaneum of the left foot using the Achilles machine (Lunar, General Electric, Madison, Wis.). The Achilles device is a water-based system, using fluid coupled through transmission in a temperature-controlled water bath (37 °C). The cutoff point for positive screened case was t score < −1 at the calcaneum heel bone [12]. Two QUS machines (from same manufacturer) were used and both machines were calibrated every morning according to the manufacturer’s instructions. Out of 1008 women who underwent QUS, 535 (53%) were screened positive. They were further referred to King Khalid University & Hospital (KKUH) for Dual energy x-ray absorptiometry (DXA) measurements.

A workshop was conducted to train the research assistants on the use of Achilles machine. Study protocol was approved by the Institutional Review Board (IRB) of the King Saud University.

Dual energy x-ray absorptiometry

Out of 535 referred women, 362 (68%) underwent DXA. BMD was measured at the anterio-posterior spine L1-4 and Dual Femur Total (using GE prodigy, Lunar GE, Wisconsin USA). The quality control procedure for the machine was carried out every morning according to manufacturer’s protocol. All patients had the test performed, processed and finalized for reporting on the same day. The automatic region of interest (ROI) was used in all procedures to calculate the BMD at lumbar spine and femoral neck. The manual adjustments in ROI were made for the lumbar spine when necessary, for example, in cases of severe scoliosis. In addition, women were asked to give their blood samples in the laboratory (KKUH) for measurement of serum calcium and 25(OH) vitamin D levels.

Statistical analysis

The stiffness index measured using the QUS was converted to corresponding t-scores with cut off of ≤ −1 as positive for LBMD. Similarly, low BMD measured using DXA was defined according to WHO cut off of t score ≤ −1[13] (includes both osteopenia and osteoporosis) present either at lumbar spine or femur neck to develop a dichotomous variable. Mean and standard deviation was calculated for continuous and proportions for categorical variables. All variables significant on univariate analyses and having biological plausibility were entered in multivariate logistic regression model using forward step modeling. Adjusted odds ratios and 95% confidence intervals were calculated. Significance was taken as α ≤ 0.05.

Results

The socio demographic characteristic of women undergoing screening using the QUS are presented in Table 1. Mean age of women was 55.64 (±8.84) with range from 41 to 85 years. Mean serum calcium and 25 (OH) vitamin D levels in low BMD and normal group were 2.22 (±0.16) vs 2.28 (±0.17)mmol/L and 42.20 (±28.43) vs 38.45 (±23.54)nmol/L respectively. Further division of vitamin D into ≥75, 74–50 and <50 nmo/L category found 30% vs 18%, 37% vs 20% and 136% vs 116% (p < 0.22) women in low BMD and normal BMD groups respectively.

Table 1.

Characteristic of Saudi women screened for low bone mineral density using quantitative ultrasound technique in Riyadh, Saudi Arabia

Characteristic Women screened as positive for low BMD using QUS (n%) Women screened as negative for low BMD using QUS (n%) P value
Age (in years)n = 1005
 
 
 
41 to 50
166 (31.1)
212 (45)
<0.01
51 to 60
228 (42.7)
185 (39.3)
61 to 70
103 (19.3)
55 (11.7)
70 and above
 
 
Marital Status n = 995
 
 
 
Single*
50 (9.5)
41 (8.8)
<0.01
Married
308 (58.2)
327 (70.2)
 
Widow
171 (32.3)
98 (21)
Education n = 1008
 
 
 
University and above
25 (4.7)
31 (6.6)
<0.01
Intermediate& secondary
30 (5.6)
48 (10.1)
 
Primary
24 (4.5)
41 (8.7)
 
Illiterate
456 (85.2)
353 (74.6)
Occupation n = 962
 
 
 
Doctor
1 (0.2)
5 (1.1)
0.08
Teacher/Administrator
45 (8.8)
51 (11.4)
 
Housewife
467 (91)
393 (87.5)
 
Husband Occupation n = 748
 
 
 
Doctors/teachers
32 (8.5)
26 (7)
0.36
Business man
98 (26)
104 (28)
 
Military
107 (28.4)
88 (23.7)
Administration
140 (37.1)
153 (41.2)
Type of House n = 965
 
 
 
Villa
390 (76.2)
342 (75.5)
0.95
Apartment
74 (14.5)
66 (14.6)
 
Small house
48 (9.4)
45 (9.9)
Body Mass Index n = 981
 
 
 
Normal
60 (11.5)
30 (6.6)
<0.01
Overweight
149 (28.5)
113 (24.7)
 
Obese
314 (60)
315 (68.8)
Exposure to sunlight per week n = 966
 
 
 
All the time
130 (25.4)
104 (22.9)
0.29
Twice-thrice per week
119 (23.2)
97 (21.4)
 
Occasionally
208 (40.6)
212 (46.7)
Not at all
55 (10.7)
41 (9)
 
Duration of exposure n = 785
 
 
 
Sixty minutes
7 (1.6)
4 (1.1)
0.13
Half an hour
103 (24.1)
66 (18.5)
 
Fifteen minutes
318 (74.3)
287 (80.4)
Obstetric history
Age at menarche n = 978
 
 
 
≤ than 11 years
141 (27.3)
119 (25.8)
0.82
12 to 14 years
303 (58.7)
274 (59.3)
 
≥15 years
72 (14)
69 (14.9)
 
Menstrual status n = 920
 
 
 
Regular
170 (36)
178 (39.7)
0.23
Peri-menopausal**
168 (35.6)
136 (30.4)
 
Menopause
134 (28.4)
134 (29.9)
 
Number of pregnancies n = 963
 
 
 
No pregnancy
10 (2)
20 (4.4)
0.08
Pregnant 1–4 times
66 (12.9)
62 (13.7)
 
Pregnant >5 times
436 (85.2)
369 (81.8)
 
History of breast feeding n = 956
 
 
 
Not at all***
16 (3.1)
20 (4.5)
<0.01
For <6 months
119 (23.4)
140 (31.3)
 
For >6 months
374 (73.5)
287 (64.2)
 
Use of Contraceptive pills
 
 
 
n = 947
 
 
 
Yes
272 (54)
208(47)
0.03
No
232 (46)
235(53)
 
Duration of contraceptive pill use n = 504
 
 
 
Less than 5 years
144 (57.8)
175 (68.6)
<0.01
5 to 10 years
78 (31.3)
47 (18.4)
 
More than 10 years
27 (10.8)
33 (12.9)
 
Past medical history
Diabetic on insulin n = 1008
 
 
 
No
337 (63)
283 (59.8)
0.30
Yes
198 (37)
190 (40.2)
 
Past history of fractures on trivial fall n = 954
 
 
 
No
442 (86.8)
398 (89.4)
0.13
Yes
67 (13.2)
47 (10.6)
 
Family History
History of Osteoporosis in the family n = 870
 
 
 
No
457 (98.3)
389 (96)
0.04
 
Yes
8 (1.7)
16 (4)
 
Family history of fracture on trivial fall n = 846
 
 
 
No
449 (98.5)
379 (97.2)
0.19
Yes
7 (1.5)
11 (2.8)
 
Physical Activity
Walking n = 1008
 
 
 
Yes
274 (51.2)
258 (54.5)
0.29
No
261 (48.8)
215 (45.5)
 
Climbing Stairs n = 1008
 
 
 
Yes
28 (5.2)
25 (5.3)
0.97
No
507 (94.8)
448 (94.7)
 
Swimming n = 1008
 
 
 
Yes
11 (2.1)
6 (1.3)
0.33
No
524 (97.9)
467 (98.7)
 
Dietary Habits
Milk (200 ml) n = 1008
 
 
 
Yes
420 (78.5)
397 (83.9)
0.03
No
115 (21.5)
76 (16.1)
 
Laban (200 ml) n = 1008
 
 
 
Yes
451 (84.3)
410 (86.7)
0.28
No
84 (15.7)
63 (13.3)
 
Cheese (slice = 100gms) n = 1008
 
 
 
Yes
421 (78.7)
399 (84.4)
0.02
No
114 (21.3)
74 (15.6)
 
Fish slice(any type) n = 1008
 
 
 
Yes
330 (61.7)
323 (68.3)
0.03
No
205 (38.3)
150 (31.7)
 
Meat n = 1008
 
 
 
Yes
493 (92.1)
443 (93.7)
0.35
No
42 (7.9)
30 (6.3)
 
Green Tea (100 ml)n = 1008
 
 
 
Yes
488 (91.2)
431 (91.1)
0.95
No
47 (8.8)
42 (8.9)
 
Arabic coffee (100 ml)n = 1008
 
 
 
Yes
447 (83.6)
414 (87.5)
0.07
No
88 (16.4)
59 (12.5)
 
Beverages (250 ml)n = 1008
 
 
 
Yes
97 (18.1)
127 (26.8)
<0.01
No 438 (81.9) 346 (73.2)  

Total number of patients with low BMD either at the lumbar spine or femoral neck using the DXA was 212 (58.5%) out of 362. Univariate analysis found age 60–70 years, education, personal history of fractures as an adult, husband occupation as an administrator and intake of dietary items; low fat laban, green tea and Arabic coffee during last one week as significantly associated with low BMD (Table 2).

Table 2.

Univariate regression analysis between socio demographic, menstrual status, medical and dietary items and low bone mineral density in women (> 40 years) in Riyadh, Saudi Arabia

Characteristics Women with Low BMD
Women with normal BMD
OR
N = 212 N = 150 (95% CI)
Age (in years)n = 362
 
 
 
41 to 50
70 (33.2)
61 (41.2)
1.00
51 to 60
80 (37.9)
71 (48)
0.98 (0.61 - 1.56)
61 to 70
50 (23.7)
13 (8.8)
3.35 (1.66 - 6.75)
70 and above
11 (5.2)
3 (2)
3.19 (0.85 - 11.98)
Marital Status n = 357
 
 
 
Single2
12 (6.2)
12 (7.3)
1.00
Married
135 (64.6)
101 (67.8)
0.89 (0.14 - 5.43)
Widow
60 (28.7)
37 (24.8)
1.08 (0.17 –6.77)
Education n = 361
 
 
 
University and above
21 (9.9)
31 (20.8)
1.00
Intermediate& secondary
40 (18.9)
26 (17.4)
2.27 (1.08-4.77)
Primary
89 (42)
49 (32.9)
2.68 (1.39-5.15)
Illiterate
62 (29.2)
43 (28.9)
2.13 (1.08-4.18)
Occupation n = 341
 
 
 
Doctor
2 (1.4)
1 (0.5)
1.00
Teacher/Administrator
19 (9.5)
16 (11.4)
2.37 (0.19 - 28.67)
Housewife
181 (90)
122 (87.1)
2.96 (0.26 - 33.08)
Husbands Occupation n = 243
 
 
 
Doctors/teachers
11 (7.6)
17 (15.9)
1.00
Business man
47 (32.4)
33 (30.8)
2.20 (0.91 - 5.30)
Military
25 (17.2)
23 (210.5)
1.68 (0.65 - 4.32)
Administration
62 (42.8)
34 (31.8)
2.81 (1.18 - 6.70)
Type of House n = 339
 
 
 
Villa
169 (85.4)
120 (85.1)
1.00
Apartment
19 (9.6)
13 (9.2)
1.03 (0.49 - 2.18)
Small house
10 (5.1)
8 (5.7)
0.88 (0.34 - 2.31)
Body Mass Index n = 357
 
 
 
Normal
21 (10)
9 (6.1)
1.00
Overweight
61 (29)
36 (24.5)
0.72 (0.30 - 1.75)
Obese
128 (61)
102 (69.4)
0.53 (0.23 - 1.22)
Menstrual status n = 329
 
 
 
Regular
70 (36)
55 (41)
1.00
Perimenopausal
69 (35.4)
48 (35.8)
1.13 (0.67 – 1.88)
Menopause
56 (28.6)
31 (23.2)
1.42 (0.80-2.49)
Exposure to sunlight n = 341
 
 
 
All the time
45 (22.8)
39 (27)
1.00
Twice-thrice/week
49 (24.9)
34 (23.6)
1.24 (0.67 - 2.30)
Occasionally
83 (42)
58 (40.3)
1.24 (0.72 - 2.13)
Not at all
20 (10.2)
13 (9)
1.33 (0.58 - 3.02)
Renal disease n = 362
 
 
 
No
200 (94.3)
148 (98.7)
1.00
Yes
12 (5.7)
2 (1.3)
4.44 (1.01 - 20.13)
History of fractures as an adult on trivial fall n = 361
 
 
 
No
167 (84.3)
131 (92.3)
1.00
Yes
31 (15.7)
11 (7.7)
2.21 (1.07 - 4.56)
Family History of fracture on trivial fall n = 287
 
 
 
No
155 (96.9)
124 (97.6)
1.00
Yes
5 (3.1)
3 (2.4)
1.33 (0.31 - 5.68)
Eat Cheese (slice) 100 mg n = 362
 
 
 
Yes
178 (84)
125 (83.3)
1.00
No
34 (16)
25 (16.7)
0.95 (0.54 – 1.68)
Drink Milk (200 ml) n = 362
 
 
 
Yes
167 (78.8)
120 (80)
1.00
No
45 (21.2)
30 (20)
1.07 (0.64 – 1.81)
Drink Laban (200 ml) n = 362
 
 
 
Yes
163 (76.9)
135 (90)
1.00
No
49 (23.1)
15 (10)
2.70 (1.45 – 5.04)
Drink Green Tea n = 362
 
 
 
Yes
185 (87.3)
140 (93.3)
1.00
No
27 (12.7)
10 (6.7)
2.04 (0.95 - 4.36)
Drink Arabic coffee n = 362
 
 
 
Yes
177 (83.5)
137 (91.3)
1.00
No 35 (16.5) 13 (8.7) 2.08 (1.06 - 4.09)

Out of 535 women, 362 visited the hospital for DXA and 173 were missing. Women who did not get their DXA done reported transportation and male members’ unavailability as main factor for their absence. We compared the sociodemographic, health, dietary and physical activity data between those who got DXA done and not done. We found no significant difference (p > 0.05) among any of the variables except for husbands occupation (p < 0.01) between the two groups (results not shown).

In the final multivariate model, age 61 to 70 years (OR = 2.75 95%CI 1.32-1.48), no literacy (OR = 2.97, 95%CI 1.44-6.12), primary level of education (OR = 4.12 95%CI 2.05-8.29), history of personal fracture as an adult on trivial falls (OR = 2.20 95%CI 1.03-4.69) and not using laban in the diet (OR = 2.81 95%CI 1.47-5.37) were significantly associated with low BMD (Table 3). Physical activity was not associated with low BMD on univariate or multivariate analysis.

Table 3.

Multivariate logistic regression showing adjusted odds ratio between age, educational level, dietary and medical factors with low bone mineral density in Saudi women (> 40 years) in Riyadh, Saudi Arabia

Variables Adjusted Odds Ratio
P value
95% CI
Level of Education
University and above
1.00
 
Secondary& Intermediate
2.07 (1.06 - 4.55)
0.04
Primary
4.12 (2.05 - 8.29)
0.02
Illiterate
2.97 (1.44 - 6.12)
0.009
Use of low fat laban in diet
Yes
1.00
 
No
2.81 (1.47 - 5.37)
0.008
Age (in years)
41 to 50
1.00
 
51 to 60
0.88 (0.52-1.48)
0.42
61 to 70
2.75 (1.32-1.48)
0.01
70 and above
2.49 (0.63-9.89)
0.18
History of fractures as an adult on trivial fall
Yes
1.00
 
No 2.20 (1.03 - 4.69) 0.03

Discussion

Previous research findings on high prevalence of low BMD in Saudi women are supported by this community-based study [4-7,9,14]. Majority of studies, however, have focused on postmenopausal women, while we included women 40 years and above because symptoms for low BMD tend to appear earlier in Saudi women [14]. Analogous to high burden, factors associated with low BMD like age, education and dietary products are in support of earlier studies [3,7-9,13-15] . Pathophysiology of aging in women indicates disconnection of trabecular network leading to reduction in bone mineral, structural deterioration and decrease in bone strength [16] which may explain the increase in prevalence of low BMD by 5% for each ten-year period between 40 and 50 years and 50 to 60 years. Old age effects on bones are further aggravated by estrogen deficiency due to menopause. The National Health and Nutrition Examination Survey (NHANES) for 2005–2008 reported an increase after 50 years of age in low BMD with each decade of age [3], hence supporting our results. Similarly, finding that being aged 60 to 70 years had the highest odds of low BMD is supported by NHANES results which found prevalence to increase until age 70 years, after which it remained static [3]. The recommended age for screening Saudi women remains controversial, some recommending 55 years [14] and others 65 years [15]; however, based on our findings we propose screening of all Saudi women for low BMD at age of 60 years. Social determinants of health, such as low education have been associated with low BMD [17]. Low education may prevent women from getting information on healthy life style habits including physical activity and access to health care thus augmenting the risk of low BMD.

Sedat et al. found incidence of vertebral fractures in Saudi Arabia between 20% and 24% [14]. One of the risk factors mentioned by National Osteoporosis Foundation in its guidelines for MENA region (Middle East and North Africa) is having personal history of fractures as an adult [8]. Fractures occurring during adulthood on exposure to some exercise, weight lifting or falls indicate weak bones and low bone mass density [18] and are a concern for future risk of osteoporosis [19]. Hence fractures and low bone density follow a viscous cycle; one leading to other and aggravating the condition further. Early screening of all such cases should be made mandatory as managing fractures in elderly is tedious and require support from family as well as health personal. In addition, the mortality, morbidity, disability and financial cost associated with management of fractures make screening for low BMD imperative [20,21].

Bone health is associated with diet rich in calcium and vitamin D, such as milk, cheese and laban (diluted yogurt) [22]. Milk and cheese, though consumed by majority after adjustment were not significantly associated with low BMD. However, “laban” also commonly known as “lasi” a dairy product manufactured by thermophilic fermented milk cultured with lactobacillus, bulgaricus and streptococcus thermophiles was significantly associated with low BMD. Several therapeutic benefits have been associated with fermented milk, [23,24] including decrease in bone deterioration, geriatric osteoporosis, skin ulcers, gastrointestinal symptoms and aging [24-27]. Quasi-experimental studies conducted on animal models have found fermented milk to reduce osteoporotic changes in mice [26,27]. Laban increases calcium assimilation [28]. Laban is a traditional drink of Saudi Arabia; however, its use seems to decrease with the introduction of new beverages. In view of present findings, we recommend regular use of laban as one of the preventive strategies against low BMD. As one cup (200 ml) of laban contains 238 mg of calcium and 80 IU of vitamin D, each women needs to take on an average 4–5 cups of laban per day in order to meet the recommended amount of calcium and vitamin D (daily recommended amount of Calcium 1000-1200 mg and vitamin D 600 IU) [29], therefore we conclude laban is an important and significant factor and even if taken alone in recommended amount can prevent low BMD. There may be other dietary sources contributing to blood vitamin D and calcium levels (for eg milk and cheese) and preventing low BMD but were not significant in our final model, for example, recently, use of green tea is proven to be protective against LBMD [30]. Future studies can recommend a dietary plan based on local food items to prevent women from developing low BMD.

This study is novel as it has used QUS as baseline screening test to identify “at risk” women before referring them for a much costlier and radiation exposed investigation, DXA. Recent studies found QUS to be a reliable screening instrument for low BMD/fractures and recommended its use in primary care settings [12,31,32]. Unnecessary exposure and cost related to DXA was reduced as 47% (473 women out of 1008) were normal on baseline screening and did not require undergoing DXA.

Vitamin D deficiency is supposed to identify at risk population for low BMD [33] but our results conclude that vitamin D may not be a reliable indicator for women in Saudi Arabia as majority were suffering from vitamin D deficiency, in fact low BMD women had higher values as compared to normal group.

Limitations

Study had some limitations. 173 (32%) women did not undergo DXA testing. The main reason identified was limited mobility due to cultural factors. Although comparison of the characteristics of those tested and not tested with DXA revealed no significant difference except for husbands occupation, however, the groups may have differed on some characteristics that we did not ascertain. Several studies have taken cutoff point for QUS as t < −1; however, Sedat et al. recommended a different cut off [32] based on population differences, difference in results could be expected due to difference in cutoff. Women were labeled as menopausal and perimenopausal according to their responses and no laboratory investigation (FSH levels) was done to support their responses. Sun exposure was asked for current months only and type of clothing and seasonal variation was not taken into consideration. In addition, frequency of dietary items and physical activity may have been subjected to information bias. Thus, it is possible that residual uncontrolled confounding may have played a role in our findings.

Conclusions

In conclusion, low BMD poses a high public health burden in Saudi Arabia which can be identified through screening and risk factors assessment at primary care level. Health education, regular screening and use of dietary products like laban (diluted yogurt) can help prevent low BMD in women.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

Dr. JAQ was involved in conceptualization and write of proposal, conduction of the study and write up of the manuscript. Drs. AK, ST, SS, AAS and FH were involved in data collection, data cleaning, analysis and write up phase. Dr SO facilitated the conduction of study in King Khalid Hospital and was involved in the manuscript write up. Drs MF and RS monitored and facilitated the data collection process and reviewed the manuscript. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2474/15/5/prepub

Contributor Information

AlJohara M AlQuaiz, Email: jalquaiz@yahoo.com.

Ambreen Kazi, Email: akamran@ksu.edu.sa.

Salwa Tayel, Email: salwatayel123@gmail.com.

Shaffi Ahamed Shaikh, Email: shaffi786@yahoo.com.

Abdullah Al-Sharif, Email: asharif@cchi.gov.sa.

Saleh Othman, Email: sothman@KSU.EDU.SA.

Fawzia Habib, Email: dr_fawziah_h@hotmail.com.

Mona Fouda, Email: monafoudaneel@yahoo.com.

Riad Sulaimani, Email: sulimanirs@gmail.com.

Acknowledgements

We shall like to acknowledge Dr. Mohammad Desouki for his support and guidance. We also thank the staff of PHCC and all females who participated in the study for their time and co-operation.

Funding source

This study was funded by Princess Nora Bent Abdallah Women Health Research Chair and the Center for Medical Research, College of Medicine, King Saud University.

References

  1. NIH. Consensus development panel on osteoporosis, prevention, diagnosis and therapy. JAMA. 2001;285:785–795. doi: 10.1001/jama.285.6.785. [DOI] [PubMed] [Google Scholar]
  2. Cooper C, Campion G, Melton LJ 3rd. Hip fractures in the elderly: a world-wide projection. Osteoporos Int. 1999;22:285–289. doi: 10.1007/BF01623184. [DOI] [PubMed] [Google Scholar]
  3. Ghannam NN, Hammami MM, Bakheet SM, Khan BA. Bone mineral density of the spine and femur in healthy Saudi females: relation to vitamin D status, pregnancy and lactation. Calcif Tissue Int. 1999;65:23–28. doi: 10.1007/s002239900652. [DOI] [PubMed] [Google Scholar]
  4. El-Desouki MI. Osteoporosis in postmenopausal Saudi women using dual X-Ray bone densitometry. Saudi Med J. 2003;24:953–956. [PubMed] [Google Scholar]
  5. Sadat-Ali M, Al-Habdan IM, Al–Mulhim FA, El-Hassan AY. Bone mineral density among postmenopausal Saudi women. Saudi Med J. 2004;25:1623–1625. [PubMed] [Google Scholar]
  6. Ardawi MS, Maimany AA, Bahksh TM, Nasrat HA, Millaat WA, Al-Raddadi RM. Bone mineral density of the spine and femur in healthy Saudi Arabs. Osteoporos Int. 2005;16:43–55. doi: 10.1007/s00198-004-1639-9. [DOI] [PubMed] [Google Scholar]
  7. Maalouf G, Gannagé-Yared MH, Ezzedine J. et al. Lebanese osteoporosis prevention society, Shariati hospital, Iran. Middle East and North Africa consensus on osteoporosis. J Musculoskelet Neuronal Interact. 2007;7:131–143. [PubMed] [Google Scholar]
  8. National Osteoporosis Foundation. Clinician’s Guide to prevention and treatment of osteoporosis. Washington, DC: National Osteoporosis Foundation; 2010. Accessed from : http://www.nof.org/files/nof/public/content/file/344/upload/159.pdf. [Google Scholar]
  9. Rouzi AA, Al Sibiani SA, Al Senani NS, Radaddi RM, Aradawi MS. Independent predictors of all osteoporosis related fractures among healthy Saudi postmenopausal women :the CEOR study. Bone. 2012;50:713–722. doi: 10.1016/j.bone.2011.11.024. [DOI] [PubMed] [Google Scholar]
  10. Cummings SR, Bales D, Black DM. Clinical use of bone densitometry. Scientific review. JAMA. 2002;288:1889–1897. doi: 10.1001/jama.288.15.1889. [DOI] [PubMed] [Google Scholar]
  11. Moayyeri A, Adams JE, Adler RA. et al. Quantitative ultrasound of the heel and fracture risk assessment: an updated meta-analysis. Osteoporos Int. 2012;23:143–153. doi: 10.1007/s00198-011-1817-5. [DOI] [PubMed] [Google Scholar]
  12. World Health Organization. Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. Report of a WHO Study Group. World Health Organ Tech Rep Series. 1994;843:1–129. [PubMed] [Google Scholar]
  13. Sadat-Ali M, Al-Habdan IM, Al-Turki HA, Azam MQ. An epidemiological analysis of the incidence of osteoporosis and osteoporosis-related fractures among the Saudi Arabian population. Ann Saudi Med. 2012;32:637–641. doi: 10.5144/0256-4947.2012.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Looker CA, Borrud GL, Dawson-Hughes B, Shepherd AJ, Wright CN. Osteoporosis or Low bone mineral at the femur neck or lumbar spine in older adults: United States, 2005–2008. 2012. NCHS Data Brief. No. 93. Accessed from http://www.cdc.gov/nchs/data/databriefs/db93.pdf. [PubMed]
  15. Raef H, Al-Bugami M, Balharith S. et al. Recommendations for the diagnosis and management of osteoporosis: a local perspective. Ann Saudi Med. 2011;3:111–128. doi: 10.4103/0256-4947.77502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mantila RSM, Hurd AL, Xu H, Fuchs RK, Warden SJ. Age related changes in proximal humerus bone health in healthy, white males. Osteoporos Int. 2012;23:2775–2783. doi: 10.1007/s00198-012-1893-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Luong ML, Cleveland RJ, Nyrop KA, Callahan LF. Social determinants and osteoarthritis outcomes. Aging health. 2012;8:413–437. doi: 10.2217/ahe.12.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Svejme O, Ahlborg HG, Nilsson JÅ, Karlsson MK. Low BMD is an independent predictor of fracture and early menopause of mortality in post-menopausal women–a 34-year prospective study. Maturitas. 2013;74:341–345. doi: 10.1016/j.maturitas.2013.01.002. [DOI] [PubMed] [Google Scholar]
  19. Barcenilla-Wong AL, Chen JS, March LM. Concern and risk perception of osteoporosis and fracture among post-menopausal Australian women: results from the global longitudinal study of osteoporosis in women (GLOW) cohort. Arch Osteoporos. 2013;8:155. doi: 10.1007/s11657-013-0155-y. [DOI] [PubMed] [Google Scholar]
  20. Browner WS, Pressman AR, Nevitt MC, Cummings SR. Mortality following fractures in older women. The study of osteoporotic fractures. Arch Inter Med. 1996;156:1521–1525. doi: 10.1001/archinte.1996.00440130053006. [DOI] [PubMed] [Google Scholar]
  21. Dalal BD, Sadat-Ali M. Economic implications of osteoporosis-related femoral fractures in Saudi Arabian society. Calcif Tissue Int. 2007;81:455–458. doi: 10.1007/s00223-007-9090-5. [DOI] [PubMed] [Google Scholar]
  22. Hui YH, Evranuz EÖ. Handbook of animal-based fermented food and beverage technology. Second. CRC Press; 2012. p. 814. [Google Scholar]
  23. Hitchins DA, McDonough EF. Prophylactic and therapeutic aspects of fermented milk. Am J Nutr. 1989;49:675–684. doi: 10.1093/ajcn/49.4.675. [DOI] [PubMed] [Google Scholar]
  24. Seneca H, Gaymont S. Clinical uses of yogurt. J Am Geriatr Soc. l957;5:932–935. doi: 10.1111/j.1532-5415.1957.tb00492.x. [DOI] [PubMed] [Google Scholar]
  25. Savaiano DA, Levitt MD. Nutritional and therapeutic aspects of fermented dairy products. J Dent Child. l984;1:305–308. [PubMed] [Google Scholar]
  26. Kimoto-Nira H, Suzuki C, Kobayashi M, Sasaki K, Kurisaki J, Mizumachi K. Anti-ageing effect of a lactococcal strain: analysis using senescence-accelerated mice. Br J Nutr. 2007;98:1178–1186. doi: 10.1017/S0007114507787469. [DOI] [PubMed] [Google Scholar]
  27. Cheong SH, Chang KJ. The preventive effect of fermented milk supplement containing tomato (lycopersionesculentum) and taurine on bone loss in ovariectomizedrats. Adv Exp Med Biol. 2009;643:333–340. doi: 10.1007/978-0-387-75681-3_34. [DOI] [PubMed] [Google Scholar]
  28. Calcium and vitamin D important at every age. http://www.niams.nih.gov/health_info/bone/bone_health/nutrition/
  29. Office of dietary supplements. National institute of health. Accessed at: http://ods.od.nih.gov/
  30. Shen CL, Yeh JK, Cao JJ, Wang JS. Green tea and bone metabolism. Nutr Res. 2009;29:437–456. doi: 10.1016/j.nutres.2009.06.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Al-Habdan IM, Sadat-Ali M, Al-Muhanna FA, Al-Elq AH, Al-Mulhim AA. Bone mass measurement using quantitative ultrasound in healthy Saudi women. A cross-sectional screening. Saudi Med J. 2009;30:1426–1431. [PubMed] [Google Scholar]
  32. Sadat–Ali M, Al-Elq A, Al-Habdan I. et al. Quantitative ultrasound (QUS) of the oscalcis in Saudi women: defining Saudi reference value for the diagnosis of low bone mass. Arch Osteoporos. 2010;5:139–144. doi: 10.1007/s11657-010-0047-3. [DOI] [Google Scholar]
  33. Ardawi MS, Qari MH, Rouzi AA, Maimani AA, Raddadi RM. Vitamin D status in relation to obesity, bone mineral density, bone turnover markers and vitamin D receptor genotypes in healthy Saudi pre- and postmenopausal women. Osteoporos Int. 2011;22:463–475. doi: 10.1007/s00198-010-1249-7. [DOI] [PubMed] [Google Scholar]

Articles from BMC Musculoskeletal Disorders are provided here courtesy of BMC

RESOURCES