|Effect of urbanization on bone mineral density: a Thai epidemiological study.|
|Jump to Full Text|
|PMID: 15693996 Owner: NLM Status: MEDLINE|
|BACKGROUND: The incidence of fractures in rural populations is lower than in urban populations, although the reason for this difference is unclear. This cross-sectional study was designed to examine the difference in bone mineral density (BMD), a primary predictor of fracture risk, between urban and rural Thai populations. METHODS: Femoral neck and lumbar spine BMD was measured by dual-energy X-ray absorptiometry (GE Lunar, Madison, WI) in 411 urban and 436 rural subjects (340 men and 507 women), aged between 20 and 84 years. Body mass index (BMI) was calculated from weight and height. RESULTS: After adjusting for age and body weight in an analysis of covariance model, femoral neck BMD in rural men and women was significantly higher than those in urban men and women (P < 0.001), but the difference was not observed at the lumbar spine. After stratifying by sex, age group, and BMI category, the urban-rural difference in femoral neck BMD became more pronounced in men and women aged <50 years and with BMI > or = 25 kg/m2. CONCLUSIONS: These data suggest that femoral neck BMD in rural men and women was higher than their counterparts in urban areas. This difference could potentially explain part of the urban-rural difference in fracture incidence.|
|Chatlert Pongchaiyakul; Tuan V Nguyen; Vongsvat Kosulwat; Nipa Rojroongwasinkul; Somsri Charoenkiatkul; Rajata Rajatanavin|
Related Documents :
|12851746 - Role of parathyroid hormone in mediating age-related changes in bone resorption in men.
7891246 - Assessment of risk for periodontal disease. ii. risk indicators for alveolar bone loss.
15631376 - Presentation of osteomalacia in kohistani women.
17826496 - Predictors of skeletal complications in men with hormone-refractory metastatic prostate...
14671166 - Low vitamin d and high parathyroid hormone levels as determinants of loss of muscle str...
14739016 - Rapid screening method for schistosoma japonicum infection using questionnaires in floo...
|Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't Date: 2005-02-04|
|Title: BMC musculoskeletal disorders Volume: 6 ISSN: 1471-2474 ISO Abbreviation: BMC Musculoskelet Disord Publication Date: 2005|
|Created Date: 2005-02-21 Completed Date: 2006-01-31 Revised Date: 2009-11-18|
Medline Journal Info:
|Nlm Unique ID: 100968565 Medline TA: BMC Musculoskelet Disord Country: England|
|Languages: eng Pagination: 5 Citation Subset: IM|
|Division of Endocrinology, Department of Medicine, Faculty of Medicine, Khon Kaen University, Thailand. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Aged, 80 and over
Aging / metabolism
Femur Neck / radiography
Lumbar Vertebrae / radiography
Journal ID (nlm-ta): BMC Musculoskelet Disord
Publisher: BioMed Central, London
Copyright ? 2005 Pongchaiyakul et al; licensee BioMed Central Ltd.
open-access: This is an Open Access article distributed under the terms of the Creative Commons Attribution License (), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received Day: 6 Month: 7 Year: 2004
Accepted Day: 4 Month: 2 Year: 2005
collection publication date: Year: 2005
Electronic publication date: Day: 4 Month: 2 Year: 2005
Volume: 6First Page: 5 Last Page: 5
Publisher Id: 1471-2474-6-5
PubMed Id: 15693996
|Effect of urbanization on bone mineral density: A Thai epidemiological study|
|Chatlert Pongchaiyakul12||Email: firstname.lastname@example.org|
|Tuan V Nguyen2||Email: email@example.com|
|Vongsvat Kosulwat3||Email: firstname.lastname@example.org|
|Nipa Rojroongwasinkul3||Email: email@example.com|
|Somsri Charoenkiatkul3||Email: firstname.lastname@example.org|
|Rajata Rajatanavin4||Email: email@example.com|
1Division of Endocrinology, Department of Medicine, Faculty of Medicine, Khon Kaen University, Thailand
2Bone and Mineral Research Program, Garvan Institute of Medical Research, Sydney, Australia
3Institute of Nutrition, Salaya Campus, Mahidol University, Thailand
4Division of Endocrinology, Department of Medicine, Ramathibodi Hospital, Mahidol University, Thailand
Osteoporosis and its ultimate consequence of low traumatic fracture pose a major public health problem, because it incurs significant costs and increased risk of mortality [1-3]. Osteoporosis is sometimes considered a "consequence" of modernization, because the incidence of fractures in urban regions is often higher than in rural regions [4-10], although the underlying reason for this trend is largely unknown.
Measurement of bone mineral density (BMD) is considered the primary predictor of fracture risk . Therefore, it could be hypothesized that the urban-rural difference in fracture incidence is partly explained by the urban-rural difference in BMD. However, such a difference has not been well documented due to limited data available [12-14]. Some previous studies reported that rural subjects had higher BMD or bone mineral content (BMC) than those urban subjects [12,13], but another study found no such difference .
The pace of urbanization in developing countries is more pronounced than in developed countries. Therefore, developing countries are ideal settings for studying the urban-rural difference in BMD. The aim of this study was to examine the difference in BMD between an urban population and a rural population in Thailand.
The present study was designed as a cross-sectional, population-based investigation. The setting was Bangkok city and Khon Kaen province in Thailand. Bangkok is the capital city with a population of 5.7 million and Khon Kaen is a rural province, located 445 km northeast of Bangkok with a population of 1.8 million and is largely an agricultural community. Further details of this study have been described elsewhere 
The study included 872 Thai men and women, aged between 20 and 84 years, of whom 422 subjects were from Bangkok and 450 subjects from Khon Kaen. In Khon Kaen, subjects were recruited from 2 villages in the Muang district. There were 14 hamlets in the two villages. In each hamlet, a full list of subjects was obtained, from which 40 subjects were randomly selected by the village's administrator. The selected subjects were then sent a letter of invitation to participating in the study. The response rate was 80.3%. In Bangkok, subjects were recruited via a media campaign, and the sampling technique was similar to the scheme used in Khon Kaen, where subjects were randomly selected from 5 districts within the city of Bangkok.
All Khon Kaen subjects were farmers, while Bangkok subjects were office workers, factory workers or house workers. Twenty-one subjects were excluded from analysis because of bone disorders, chronic diseases, history of taking medications that are deemed to affect calcium and bone metabolism, such as the use of steroids or thyroid hormone; and 4 women were excluded on the basis of pregnancy, lactation, delivery or abortion within the previous 3 months, previous history of oophorectomy and premature menopause. The study was conducted in accordance with the Helsinski Declaration in 1975 and as revised in 1983 and was approved by the Ethics Committee of Faculty of Medicine Ramathibodi Hospital Mahidol University (Bangkok) and Khon Kaen University (Khon Kaen), and written informed consent was obtained from all subjects.
BMD at the femoral neck and lumbar spine (L2-4) in g/cm2, was measured by dual-energy X-ray absorptiometry with a Lunar DXP-IQ densitometer (GE Lunar Radiation Corp, Madison, WI, USA). The two study sites (Bangkok and Khon Kaen) used the same model of the DXA machine and the same protocol of measurements. The radiation dose with this method is < 0.1 ?Gy. The coefficient of variation of BMD for normal subjects is 0.96 and 0.98 at proximal femur and lumbar spine, respectively.
Body weight (including light indoor clothing) was measured using an electronic balance (accuracy 0.1 kg) and standing height (without shoes) with a standiometer (nearest 0.1 cm). Body mass index (BMI) was calculated as ratio of weight (in kg) over height (in meter squared).
Descriptive statistics were computed for each residential region and sex separately. In order to test for difference between urban and rural regions, an analysis of covariance (ANCOVA) model was performed. In this model, BMD was treated as outcome variables; age and weight (or BMI) were treated as covariates; and residence (urban or rural) was the factor. Interactions between age and BMI or age and residence variable were also considered in the model. Estimates of the model parameters were based on the least square method via the SPSS version 9.0 (SPSS, Inc, Chicago).
After excluding 25 subjects, data from 847 subjects (340 men and 507 women) were analysed. There was no significant difference between urban and rural subjects with respect to age or sex distribution. The mean age was 49 and 50 years old in men and women, respectively. However, urban men had higher weight and greater height than rural men (P < 0.001), whereas urban women had a greater height (P < 0.001) but equivalent weight (P = 0.72) compared with rural women (Table 1).
In the entire sample, higher weight was associated with higher BMD in men (r = 0.13, P = 0.017 for femoral neck, and r = 0.37, P < 0.001 for lumbar spine) and in women (r = 0.33, P < 0.001 for femoral neck, and r = 0.33, P < 0.001 for lumbar spine). On the other hand, advancing age was associated with a significant reduced BMD in men (r = -0.53, P < 0.001 for femoral neck, and r = -0.15, P = 0.007 for lumbar spine) and women (r = -0.63, P < 0.001 for femoral neck, and r = -0.60, P < 0.001 for lumbar spine).
However, the strength of relationship between age and BMD in urban subjects was less pronounced than in rural subjects, such that rural women had a higher cross-sectional "rate of bone loss" than urban women, particularly at the femoral neck. For example, in women, each 5-year increase in age was estimated to associate with a 2.1% and 1.2% decrease in femoral neck BMD for rural and urban group, respectively; in men, the respective rate of decrease was 1.3% and 0.8%. As a result, among those aged 50+ years, BMD in rural subjects tended to be lower than (or converged to) BMD in urban subjects (Figure).
In both sexes, after adjusting for age and weight, BMD in rural individuals was significantly higher than in urban individuals. For instance, femoral neck BMD in rural men and women was 0.22 and 0.23 g/cm2 significantly higher (P < 0.001) than in urban men and women, respectively; but the difference was lower for the lumbar spine BMD (0.12 g/cm2 in men, P = 0.017 and 0.05 g/cm2 in women, P = 0.293). The statistical significance of the age-by-residence interaction term in the ANCOVA model suggested that the urban-rural difference in BMD decreased with advancing age (Table 2).
Further analyses stratified by sex, age group, and BMI category indicated that the urban-rural difference in femoral neck BMD was more pronounced in the younger age group (< 50 years old) and higher BMI (? 25 kg/m2). This trend was consistent for men and women. However, for lumbar spine BMD, no significant urban-rural difference was observed in most subgroups, with the exception of women aged ? 50 years and BMI < 25 kg/m2 in whom BMD was lower in the rural group compared to the urban group (Table 3).
Osteoporosis has emerged as one of the most common diseases in the aged population, and represents one of the most significant public health problems in Asia [2,16,17]. A consistent trend in osteoporosis is that the incidence of fracture is higher in developed countries than in developing countries; and in any country, the incidence is higher in urban than in rural communities [5-11]. While many factors are hypothesized to be responsible for this trend, BMD is thought to be a primary determinant, because it is the most consistent and robust predictor of fracture risk [1,11].
In the present population-based study, we have shown that BMD in a rural Thai population was significantly higher than in urban population, particularly at femoral neck. The magnitude of difference was more than 1 standard deviation which is clinically relevant. It is difficult to compare the present study's results to previous studies' due to differences in methodology and study design. For instance, Sundberg et al  reported that lumbar spine BMD (measured by DXA) in rural adolescents was significantly higher than that in urban adolescents, but there was no significant difference in femoral neck BMD. Furthermore, a study from Southern Sweden suggested that bone mass at the forearm (measured by single-photon absorptiomety) in rural population was significantly higher than in urban population and the difference was more pronounced when comparing a true urban population who had lived their entire life in a city with a true rural population who had never lived in a city . A study from Eastern Poland found that the mean lumbar spine BMD values in every age range were higher in rural population than in urban population, but the difference was not statistically significant . Taken together, these results including ours, suggest that rural subjects tend to have higher BMD than in urban subjects.
The present study's data and design can not elucidate any underlying factors that are responsible for the difference but some propositions could be put forward. The urban-rural difference in femoral neck BMD could be due to the difference in the peak of bone mass levels. In this study, both rural men and women aged between 20 and 30 years had significantly higher BMD than urban counterparts. For example, young rural men and women had significantly higher than urban subjects (1.17 vs. 1.03 g/cm2, [95% CI: 0.07?0.22] in men and 1.02 vs. 0.86 g/cm2, [95% CI: 0.10?0.22] in women). This finding was partially consistent with a previous study  and could be explain the fact that the urban-rural difference was mainly found in younger age groups.
This study also found that the urban-rural difference in femoral neck BMD decreased with advancing age. The difference may be attributed to the difference in physical activity between the two populations. Rural populations were generally more physically active than urban populations [18,19]. The rural population in this study was mainly farmers who spend most of their time in rice field long hours of physical activity.
However, the difference was sex- and site- dependent. The difference in femoral neck BMD was much more pronounced than that in lumbar spine and this was more transparent before the age of 50 in men and before the menopause in women. After this age the difference was no longer significant. The data suggested that the rate of bone loss in rural population may be more rapid than in urban population. However, this finding was not consistent with a previous study which demonstrated that the rate of bone loss was higher in urban population compared with rural population . The reason(s) for the higher rate of bone loss in rural population in this study is unknown, but low dietary calcium intake could be a contributory factor [20-22].
The present findings must be interpreted in the context of a number of potential strengths and weaknesses. The data were obtained from a large and well-defined rural vs. urban area, which allowed the rural and urban difference to be reliably delineated. The study subjects were Thai, among whom, cultural backgrounds and environmental living conditions are different from Western populations. Thus care should be taken when extrapolating these results to other populations.
These data have demonstrated that femoral neck BMD in rural men and women was higher than their counterparts in urban areas. This difference could potentially explain part of the urban-rural difference in fracture incidence.
All abbreviations are defined in the text.
The author(s) declare that they have no competing interests.
Chatlert Pongchaiyakul had an active role in the conduct of this study, obtained and analysed data, and drafted the manuscript. Tuan V Nguyen was involved in the conceptual discussion of this study, and had an active role in data analysis, drafting of the manuscript. Vongsvat Kosulwat, Nipa Rojroongwasinkul, and Somsri Charoenkiatkul had an active role in the study design, and was involved in the conceptual discussion. Rajata Rajatanavin conducted and established this study. All authors contributed to the last version of the manuscript.
The pre-publication history for this paper can be accessed here:
The study was supported by Thailand Research Fund. The first author would like to acknowledge the Faculty of Medicine, Khon Kaen University for grant to Garvan Institute of Medical Research. We also thank Mrs. Ratchanee Chotmongkol, RN and Mrs. Choowong Pongchaiyakul, RN for data collection. TVN is supported by a Australian National Health and Medical Research Council grant.
|Cummings SR,Melton LJ. Epidemiology and outcomes of osteoporotic fracturesLancet 2002;359:1761–1767. [pmid: 12049882] [doi: 10.1016/S0140-6736(02)08657-9]|
|Cooper C,Campion G,Melton LJ 3rd. Hip fractures in the elderly: a world-wide projectionOsteoporos Int 1992;2:285–289. [pmid: 1421796]|
|Center JR,Nguyen TV,Schneider D,Sambrook PN,Eisman JA. Mortality after all major types of osteoporotic fracture in men and women: an observational studyLancet 1999;353:878–882. [pmid: 10093980] [doi: 10.1016/S0140-6736(98)09075-8]|
|Sanders KM,Nicholson GC,Ugoni AM,Seeman E,Pasco JA,Kotowicz MA. Fracture rates lower in rural than urban communities: the Geelong Osteoporosis StudyJ Epidemiol Community Health 2002;56:466–470. [pmid: 12011207] [doi: 10.1136/jech.56.6.466]|
|Kaastad TS,Meyer HE,Falch JA. Incidence of hip fracture in Oslo, Norway: differences within the cityBone 1998;22:175–178. [pmid: 9477241] [doi: 10.1016/S8756-3282(97)00247-0]|
|Madhok R,Melton LJ 3rd,Atkinson EJ,O'Fallon WM,Lewallen DG. Urban vs. rural increase in hip fracture incidence. Age and sex of 901 cases 1980?89 in Olmsted County, U.S.AActa Orthop Scand 1993;64:543–548. [pmid: 8237321]|
|Falch JA,Kaastad TS,Bohler G,Espeland J,Sundsvold OJ. Secular increase and geographical differences in hip fracture incidence in NorwayBone 1993;14:643–645. [pmid: 8274307] [doi: 10.1016/8756-3282(93)90086-P]|
|Norton R,Yee T,Rodgers A,Gray H,MacMahon S. Regional variation in the incidence of hip fracture in New ZealandN Z Med J 1997;110:78–80. [pmid: 9137302]|
|Jonsson B,Gardsell P,Johnell O,Redlund-Johnell I,Sernbo I. Differences in fracture pattern between an urban and a rural population: a comparative population-based study in Southern SwedenOsteoporos Int 1992;2:269–73. [pmid: 1421793]|
|Mannius S,Mellstrom D,Oden A,Rundgren A,Zetterberg C. Incidence of hip fracture in Western Sweden 1974?1982. Comparison of rural and urban populationsActa Orthop Scand 1987;58:38–42. [pmid: 3577739]|
|Kanis JA. Diagnosis of osteoporosis and assessment of fracture riskLancet 2002;359:1929–1936. [pmid: 12057569] [doi: 10.1016/S0140-6736(02)08761-5]|
|Sundberg M,Duppe H,Gardsell P,Johnell O,Ornstein E,Sernbo I. Bone mineral density in adolescents. Higher values in a rural area ? a population-based study of 246 subjects in southern SwedenActa Orthop Scand 1997;68:456–460. [pmid: 9385246]|
|G?rdsell P,Johnell O,Nilsson BE,Sernbo I. Bone mass in an urban and a rural population: a comparative, population-based study in Southern SwedenJ Bone Miner Res 1991;6:67–75. [pmid: 1863289]|
|Filip RS,Zagorski J. Bone mineral density and osteoporosis in rural and urban women. Epidemiological study of the Lublin region (Eastern Poland)Ann Agric Environ Med 2001;8:221–226. [pmid: 11748880]|
|Pongchaiyakul C,Nguyen TV,Kosulwat V,Rojroongwasinkul N,Charoenkiatkul S,Eisman JA,Rajatanavin R. Effects of physical activity and dietary calcium intake on bone mineral density and osteoporosis risk in a rural Thai populationOsteoporos Int. 2004 Jun 3|
|Lau EM,Lee JK,Suriwongpaisal P,Saw SM,Das De S,Khir A,Torralba T,Sham A,Sambrook P. The incidence of hip fracture in four Asian countries: the Asian Osteoporosis Study (AOS)Osteoporos Int 2001;12:239–243. [pmid: 11315243] [doi: 10.1007/s001980170135]|
|Lau EM. Epidemiology of osteoporosisBest Pract Res Clin Rheumatol 2001;15:335–344. [pmid: 11485333] [doi: 10.1053/berh.2001.0153]|
|Jonsson B,Gardsell P,Johnell O,Sernbo I,Gullberg B. Life-style and different fracture prevalence: a cross-sectional comparative population-based studyCalcif Tissue Int 1993;52:425–433. [pmid: 8369989] [doi: 10.1007/BF00571331]|
|Ringsberg KA,Gardsell P,Johnell O,Josefsson PO,Obrant KJ. The impact of long-term moderate physical activity on functional performance, bone mineral density and fracture incidence in elderly womenGerontology 2001;47:15–20. [pmid: 11244287] [doi: 10.1159/000052765]|
|Marshall TA,Stumbo PJ,Warren JJ,Xie XJ. Inadequate nutrient intakes are common and are associated with low diet variety in rural, community-dwelling elderlyJ Nutr 2001;131:2192–2196. [pmid: 11481416]|
|Gaddi A,Cicero AF,Wani FO,Dormi A,Pasquarelli V,D'Addato S. The realization of a project aimed at reducing the plasmatic lipid level in a large Italian population improves the mean calcium daily intake: the Brisighella StudyEur J Clin Nutr 2001;55:97–106. [pmid: 11305632] [doi: 10.1038/sj.ejcn.1601123]|
|Pettifor JM,Moodley GP. Appendicular bone mass in children with a high prevalence of low dietary calcium intakesJ Bone Miner Res 1997;12:1824–1832. [pmid: 9383687]|
[Figure ID: F1]
Interaction effects of age and residence variable on bone mineral density at the femoral neck in men (A) and women (C), and at the lumbar spine in men (B) and women (D).
Characteristics of study subjects
|Urban (Bangkok)||Rural (Khon Kean)||Mean Difference (95% CI)||P value|
|Number of Subjects||159||181|
|Age (years)||49.6 ? 17.5||49.1 ? 17.1||0.5 (-3.2, 4.2)||0.800|
|Body weight (kg)||64.3 ? 11.1||58.2 ? 8.8||6.1 (3.0, 8.1)||<0.001|
|Height (cm)||165.5 ? 6.3||161.2 ? 5.9||4.3 (3.0, 5.6)||<0.001|
|Body Mass Index (kg/m2)||23.4 ? 3.6||22.4 ? 2.8||1.0 (0.3, 1.7)||0.003|
|Bone Mineral Density (g/cm2)|
|?Femoral neck||0.87 ? 0.16||0.96 ? 0.18||-0.09 (-0.13, 0.05)||<0.001|
|?Lumbar spine||1.12 ? 0.17||1.11 ? 0.16||0.01 (-0.03, 0.04)||0.64|
|Number of Subjects||252||255|
|Age (years)||50.4 ? 15.1||50.6 ? 15.9||-0.2 (-2.9, 2.4)||0.853|
|Body weight (kg)||55.5 ? 8.9||55.9 ? 10.5||-0.4 (-2.0, 1.4)||0.718|
|Height (cm)||154.7 ? 5.4||152.1 ? 5.2||2.6 (1.6, 3.5)||<0.001|
|Body Mass Index (kg/m2)||23.2 ? 3.8||24.1 ? 4.0||-0.9 (-1.5, -0.1)||0.017|
|Bone Mineral Density (g/cm2)|
|?Femoral neck||0.79 ? 0.13||0.87 ? 0.19||-0.08 (-0.11, -0.05)||<0.001|
|?Lumbar spine||1.05 ? 0.18||1.01 ? 0.21||0.04 (-0.11, 0.08)||0.16|
All values are shown in mean ? standard deviation (SD).
Effects of age, weight and residence on bone mineral density: estimates of parameters of the analysis of covariance stratified by sex and BMD site
|Effect||Estimate ? SE||P value|
|Femoral neck BMD|
|?Age (+5 yr)||-0.020 ? 0.003||<0.001|
|?Weight (+5 kg)||0.015 ? 0.004||<0.001|
|?Residence (Rural)||0.222 ? 0.046||<0.001|
|?Age ? Residence (Rural)||-0.012 ? 0.004||0.008|
|Lumbar spine BMD|
|?Age (+5 yr)||-0.001 ? 0.003||0.874|
|?Weight (+5 kg)||0.030 ? 0.004||<0.001|
|?Residence (Rural)||0.122 ? 0.051||0.017|
|?Age ? Residence (Rural)||-0.010 ? 0.004||0.048|
|Femoral neck BMD|
|?Age (+5 yr)||-0.026 ? 0.002||<0.001|
|?Weight (+5 kg)||0.026 ? 0.003||<0.001|
|?Residence (Rural)||0.233 ? 0.034||<0.001|
|?Age ? Residence (Rural)||-0.015 ? 0.003||<0.001|
|Lumbar spine BMD|
|?Age (+5 yr)||-0.033 ? 0.003||<0.001|
|?Weight (+5 kg)||0.031 ? 0.003||<0.001|
|?Residence (Rural)||0.047 ? 0.045||0.293|
|?Age ? Residence (Rural)||-0.009 ? 0.004||0.036|
SE, Standard Error.
Notes: Since height was not a significant factor in the analysis of covariance model, it was removed from the final model with no significant change of the results.
Bone mineral density in urban and rural men and women by age group and body mass index
|(a) Lumbar spine BMD|
|Sex||Age (years)||BMI (kg/m2)||Bone mineral density (g/cm2)|
|Urban||Rural||Mean difference and 95% CI|
|Men||< 50||< 25||0.94 ? 0.16||1.05 ? 0.16||-0.11a (-0.16, -0.06)|
|? 25||0.89 ? 0.12||1.04 ? 0.17||-0.15b (-0.26, -0.03)|
|? 50||<25||0.80 ? 0.15||0.86 ? 0.15||-0.06b (-0.12, -0.01)|
|? 25||0.83 ? 0.11||0.92 ? 0.15||-0.09b (-0.17, -0.01)|
|Women||< 50||< 25||0.85 ? 0.11||0.97 ? 0.13||-0.12a (-0.16, -0.09)|
|? 25||0.92 ? 0.11||1.04 ? 0.13||-0.12b (-0.20, -0.05)|
|? 50||<25||0.70 ? 0.11||0.71 ? 0.15||-0.01 (-0.05, 0.03)|
|? 25||0.76 ? 0.11||0.82 ? 0.15||-0.06b (-0.11, -0.01)|
|(b) Femoral neck BMD|
|Sex||Age (years)||BMI (kg/m2)||Bone mineral density (g/cm2)|
|Urban||Rural||Mean difference and 95% CI|
|Men||< 50||< 25||1.12 ? 0.14||1.13 ? 0.15||-0.01 (-0.06, 0.04)|
|? 25||1.11 ? 0.09||1.14 ? 0.16||-0.03 (-0.13, 0.08)|
|? 50||< 25||1.05 ? 0.18||1.06 ? 0.16||-0.01 (-0.07, 0.05)|
|? 25||1.21 ? 0.19||1.19 ? 0.20||0.02 (-0.11, 0.14)|
|Women||< 50||< 25||1.14 ? 0.13||1.13 ? 0.14||0.01 (-0.04, 0.04)|
|? 25||1.21 ? 0.15||1.15 ? 0.13||0.06 (-0.02, 0.15)|
|? 50||< 25||0.92 ? 0.14||0.83 ? 0.19||0.09b (0.03, 0.14)|
|? 25||1.02 ? 0.17||0.97 ? 0.21||0.05 (-0.01, 0.13)|
Statistical significance at aP < 0.001 and bP < 0.05. Statistical significance is indicated by bold-faced letters.
Previous Document: Parental educational level and cardiovascular disease risk factors in schoolchildren in large urban ...
Next Document: Simplicity within complexity: seasonality and predictability of hospital admissions in the province ...