Figures
Abstract
This study aimed to investigate the epidemiology of low-energy lower-extremity fracture in Chinese men and women aged 50 years and above. This study was a part of Chinese National Fracture Survey (CNFS), which used the stratified multistage cluster random sampling method to recruit subjects between January and May 2015. A total of 512187 individuals participated in the CNFS and of them there were 154099 men and women aged 50 years and above included in this study for data analysis. Low-energy fracture was defined as a fracture caused by slip, trip or fall from standing height. Univariate analyses and gender-based multivariate logistic regression models were constructed to identify the independent risk factors. A total of 215 patients had sustained low-energy lower extremity fractures in 2014, indicating the overall incidence was 139.5 (120.9 to 158.2) per 100000 persons, with 127.8 (102.5 to 153.1) and 151.1 (123.8 to 178.5) per 100000 person-year in men and women. Over 80% of fractures occurred at home and on the common road. In men, alcohol consumption (OR, 2.00; 95%CI, 1.29 to 3.08), sleep duration<7h/d (OR, 2.60; 95%CI, 1.68 to 4.03) and history of past fracture (OR, 2.57; 95%CI, 1.33 to 4.95) were identified as significant risk factors associated with low-energy fractures. In women, advanced age (80+ years) (OR, 3.22; 95%CI, 1.80 to 5.75), alcohol consumption(OR, 1.72; 95%CI, 1.00 to 2.98), sleep duration <7h/d (OR, 2.11; 95%CI, 1.40 to 3.18), and history of past fracture (OR, 3.46; 95%CI, 1.97 to 6.09) were identified as significant risk factors and living in western region (OR, 0.60; 95%CI, 0.38 to 0.94) and current weight of 50 to 59.9 kg (OR, 0.17; 95%CI, 0.04 to 0.73) were identified as protective factors for fractures. Accordingly, awareness on the importance of sleep and alcohol consumption on fragility fracture should be improved, and health policies that focus on decreasing alcohol consumption and encouraging individuals to improve their sleep quality and duration should be considered. Maintaining a healthy bodyweight for women should be specifically emphasized to prevent low-energy fractures.
Citation: Zhu Y, Liu S, Chen W, Liu B, Zhang F, Lv H, et al. (2019) Epidemiology of low-energy lower extremity fracture in Chinese populations aged 50 years and above. PLoS ONE 14(1): e0209203. https://doi.org/10.1371/journal.pone.0209203
Editor: Cho Naing, International Medical University, MALAYSIA
Received: August 16, 2018; Accepted: December 1, 2018; Published: January 14, 2019
Copyright: © 2019 Zhu et al. 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 author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This study was funded by the Hebei Province Medical Science Special Major Projects Research Fund. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Osteoporosis-related fracture comprises a major part of public health care cost in the worldwide, and is associated high morbidity and mortality [1–3]. In 2001, the NIS Consensus Statement revised the definition of osteoporosis to include qualitative parameters related to low-energy fractures and set fracture prevention as the primary treatment goal for patients with osteoporosis [4]. In mid-aged and elderly individuals, approximately 70% of the osteoporosis-related fractures were lower extremity fractures, especially proximal femur and ankle fractures [5]. According to literature, the lifetime risk of lower extremity fractures caused by low-energy injury in Caucasian women was about 27%, and in men was about 10% [6, 7]. Moreover, elderly individuals who have osteoporosis-related lower or upper extremity fracture are at increased risk for secondary fall-related fractures and even death in the near future [8, 9].
By the end of 2016, there were over 280 million mid- and old-aged individuals aged 50 years and above in China (http://www.stats.gov.cn/tjsj/). Annually, approximately 1.4 million individuals had one low-energy lower extremity fracture in mid- and old-aged individuals [5]. It is predictable that this figure will increase dramatically in the next decade and accordingly, and the challenge from medical care costs is enormous for Chinese health policy-making institutions. Investigation of epidemiologic characteristics of these low-energy fractures is the fundamental task to develop public health programs. By use of these data on age- and gender specific incidence rates and the associated risk factors, we are able to adjust future policy, take preventive measures and optimize management in health care. Unfortunately, most epidemiologic reference data currently used by Chinese studies or policy-making institutions were from foreign researches. Data of such might not be applicable to our Chinese populations, due to the differences in ethnic origins, economic development and individual lifestyles between China and other countries. Additionally, most of previous studies focused on a single hospital, several hospitals in a region or populations of a certain subgroup [10–12], often reporting diverse incidence rates of low-energy fracture and controversial results for a certain risk factor.
To address these questions, we conducted this study with data available from the China National Fracture Survey (CNFS) database. In this study, we aimed to report the national population-based incidence rate of low-energy lower extremity fracture for overall populations and for different subgroups stratified by age, gender and et al; and to investigate the independent risk factors, in term of demographics, socioeconomics, geographical locations and individual lifestyles.
Subjects and methods
CNFS was a population-based questionnaire survey, carried out in January to May of 2015, with aims to investigate the epidemiology of fractures in 2014. The survey was registered with the Chinese Clinical Trial Registry (ChiCTR-EPR-15005878). In our previous study [5], we described the details of the sampling methods (Supplementary Fig 1). Briefly, we used stratified multistage cluster random sampling method to recruit subjects. During the first phase, using stratified random sampling method we selected 8 provinces (municipalities) with 3 in eastern, 2 in central and 3 in western regions, based on geographic location, climate, population size and socioeconomic development. During the second phase, within each targeted province (municipalities), probability proportional to size method was used to complete the sampling separately in urban and rural areas. In each neighborhood or village, the households were calculated and selected. All members of eligible families living in their current residence at least 6 months were invited to participate in this study.
Our trained research team members were responsible for data collection, using the standardized questionnaires, and face-to-face interview with participants was conducted. Before data collection, informed consent was obtained from each participant. Data on demographics, geographical conditions, socioeconomics, and individual lifestyles were documented. Self-reported fractures between 1 January and December 2014 by participants and further confirmed by their clinical or radiographic data were confirmed. Eight quality control teams were responsible for check of random questionnaires (approximately 10% of all questionnaires) for potential omissions and errors. The CNFS was approved by the institutional review board of the third Hospital of Hebei Medical University.
Current study
Low-energy fracture was defined as a fracture that was caused by slip, trip or fall from standing height. Fractures caused by high-energy injuries (traffic trauma, fall from height, crushing injury, sharp trauma and others) were excluded. A total of 154099 women and men aged 50 years and older participated in this study and 937 participants had at least one fracture of any site caused by either low-or high-energy in 2014. 215 patients reporting 217 cases of low-energy fractures of femur and tibia (fibula) were identified as case group. The remaining 153162 participants without any fracture were defined as control group. The detailed flow chart was presented in Fig 1.
Variables of interest included age, height, weight and body mass index (BMI), residency category (rural or urban), regions, latitude zone (20°-29.9°, 30°-39.9° or 40°-49.9°), ethnic origins, occupation, educational level, frequency of drinking intake (tea, carbonate beverages, coffee), smoking status, alcohol consumption, dwelling place (ground floor, > 2nd floor with or without elevator), average sleep duration per day, history of past fracture, living situation (alone or with others), supplementation of calcium or Vitamin D or both for women and men; and age of menopause and number of births extra for women.
BMI was grouped on basis of the criteria suited to Chinese populations: underweight, <18.5 kg/m2; normal, 18.5–23.9 kg/m2; overweight, 24–27.9 kg/m2; obesity, > = 28 kg/m2 [5, 13]. Current smoking and alcohol consumption was defined as positive (yes), if participants smoked >1 time/week or drank > 1time/month during the 2014 year or the past year before fracture occurrence. Similarly within the time window, the average intake frequency of certain type of drinking was reported by participants; and supplementation of calcium or Vitamin D or both was defined as positive (yes) if participants acknowledged they take these medications for at least 1 month; otherwise, as negative (no).
Statistical analysis
Incidence rates of low-energy lower extremity fractures were estimated by the number of fractures divided by the total number of overall population and population in each subgroup by age (5-year interval), as well as by demographic factors such as ethnic origin, geographical region, education, occupation, and residency category (rural or urban), stratified by gender. Differences in incidence rate between categories of nominal variables, such as ethnic origin, regions, occupation, and residency category, were tested using the Chi-square test. Age and education as ordered categorical variables and trends in incidence rates by them were tested by univariate logistic regression models. We also assessed incidence rates of low-energy femur or tibia (fibula) fractures based on sites (proximal, shaft and distal), in men or women or combined.
Two separate gender-based multiple logistic regression models were constructed to explore the independent risk factors associated with low-energy lower extremity fractures in women and men. Given the limited cases of fracture for each site (proximal, shaft and distal), we did not perform the subgroup analysis based on fracture site. The above-mentioned variables that were reported in previous literature to have positive or negative effects on bone mass density, or be associated with falls or low-energy fracture were all entered into the multivariate model. A stepwise backward elimination approach was used to exclude confounding covariates from the final model. Covariates were retained in the final model if the p value was ≤ 0.10. Odd ratio (OR) and 95% confidence interval (95% CI) were used to indicate the correlation magnitude between variables and the risk of low-energy fracture. The significance threshold was set at P < 0.05. The Hosmer–Lemeshow test was used to examine the goodness-of-ft of the final model, and a p value >0.05 indicated an acceptable fitness. All analyses were performed using SPSS 19.0 software (IBM Corporation, Armonk, NY)
Results
There were 76687 men and 77412 women, and their average age was 62.1 years (sd, 9.2). There were 70518, 30224 and 53357 participants from east, middle and west regions, respectively, and their average age was 62.5 (sd, 9.5), 62.2 (sd, 9.2) and 61.7 (sd, 9.0) years with significant difference (p<0.001). Of the 215 patients with 217 cases of fractures, there were 98 men and 117 women; and their average age at which fracture occurred was 65.1 years (sd, 10.2). Home (48.4%) was the most common place where lower extremity fracture occurred, followed by the common road (34.9%) (Fig 2). Totally, there were 87 patients with 88 cases of femur fracture and 128 patients with 129 cases of tibia (fibula) fracture.
The overall incidence rate of low-energy lower extremity fractures was 139.5 (120.9 to 158.2) per 100000 persons in 2014, with 127.8 (102.5 to 153.1) and 151.1 (123.8 to 178.5) per 100000 person-year in men and women, respectively (Table 1).
The results of trend test showed a significant increasing trend of incidence rate of low-energy lower extremity fracture with age both in men (p = 0.008) and women (p<0.001) (Table 1). In men, individuals aged 80+ years had the highest incidence rate (200.5/100000 person-year), followed by those of 65–69 years (193.2/100000 person-year) and 75–79 years (186.8/100000 person-year). Similarly, women of 80+ years had the highest incidence rate (398/100000 person-year), followed by 75–79 years (179.5/100000 person-year) and 65–59 years (161.3/100000 person-year). Women living in eastern region of China had the highest incidence rate of low-energy lower extremity fractures; the difference of incidences among populations in 3 regions was significant statistically for women (p = 0.024), but non-significant for men (p = 0.857). Regarding other variables, there was not significant difference, such as Ethnicity, residency category, education, and occupation. The detailed information was presented in Table 1.
Table 2 presented the incidence rates of femur and tibia (fibula) fractures, stratified by fracture site (proximal, shaft, distal). The overall incidence rate was 56.7 (44.6 to 68.8)/100000 person-years for femur fractures, and 83.0 (68.7 to 97.4)/10000 person-years for tibia (fibula) fractures. Proximal femur fractures accounted for approximately 80% of the total femur fractures, and their incidence was 45.0 (35.4 to 54.6) per 100000 person-years. Distal tibia and ankle fractures accounted for 74.3% of the total tibia (fibula) fractures, and their incidence rate was 61.7 (49.3 to 74.1) per 100000 person-years.
Multivariate analysis
After adjustment for confounding variables, alcohol consumption, sleep duration<7h/d and history of past fracture were identified as significant risk factors associated with low-energy lower extremity fractures in men (Table 3). The Hosmer–Lemeshow test demonstrated the adequate fitness (X2 = 7.105, p = 0.130).
In women, advanced age (80+ years), alcohol consumption, sleep duration <7h/d, and history of past fracture were identified to be associated with increased risk of lower extremity fractures. Living in west region (compared to eastern region) and weight of 50–59.9kg (compared to <40kg) were identified as protective factors for low-energy fracture. Supplementation of calcium or Vitamin D or both seemed to have positive effect on prevention of low-energy lower extremity fractures, but the significance did not approach to the statistical level (p = 0.074). The detailed statistical results were presented in Table 3. The Hosmer–Lemeshow test demonstrated the adequate fitness (X2 = 6.087, p = 0.638).
Discussion
To our knowledge, this is the most representative and comprehensive population-based study carried out in China, in which the incidence rates of low-energy lower extremity fractures by demographic and socioeconomic factors were estimated and various risk factors were identified. Over 80% of the fractures occurred at home and on the common road, which emphasized the importance of the primary preventive measures, especially home prevention. We also observed a significant trend towards increasing incidence of lower extremity fracture with age in women, but not in men. After adjustment for confounding variables, alcohol consumption, sleep duration<7h/d and history of past fracture were identified as significant risk factors for low-energy fractures, both in women and men. Additionally in women, weight of 50 to 59.9 kg and living in west region were identified as protective factors for low-energy fractures.
Comparison of incidences of low-energy fracture with studies
Knowledge of population-based incidence of low-energy fractures is fundamental to develop public health programs, but national epidemiologic surveys of such were very scarce. Currently, most researches selected a single hospital, a certain region or a subgroup of population as study object to obtain knowledge of epidemiologic situation [14–17]. In addition, geographical location, socioeconomic development, and individual lifestyles differ from each other among countries and or regions in the same country [18, 19]. Therefore, it might be explainable that the incidence rates of fractures in literature were greatly varied. In UK, Kaye et al [20] used the data from General Practice Research Database to report the incidence was 472 per 100000 person years for total lower extremity fracture, and 330/100000 person-years for femur and tibia (fibula) fractures, in individuals aged 50 years. In Finland, incidence of hip fracture was reported as 170 to 210 and 364 to 450 per 100000 person-years in men and women aged 50+ years [21, 22] and the incidence of low-energy ankle fracture was 114 and 174 per 100000 person-years for elderly men and women [23]. In USA, the adjusted annual incidence of hip fracture was 129 and 224 per 100000 person-years for men and women above 45 years [24]. Author also observed the declined trend of hip fracture incidence during the past 10 years before 2006, and suggested this result partially benefit from the active bone health intervention [24]. Compared to those western developed countries, the figures reported in this study was substantially lower, as 1/5to 1/3 of them. Even in Asian, the incidence of lower extremity fracture reported in this study was much lower than that of neighboring countries, as Japna [25] and South Korea [26]. The underlying mechanism might be related to relatively low prevalence of osteoporosis [27, 28]. Despite, low-energy lower extremity fracture caused undoubtedly constitutes a major public health issue in modern China, due to the huge base of mid-aged and elderly individuals (http://www.stats.gov.cn/tjsj/).
Risk factors associated with the low-energy fractures
Alcohol consumption, insufficient daily sleep duration (<7h/d) and history of past fracture were identified as significant risk factors for low-energy lower extremity fracture, both in men and women. Clark et al [29] suggested excess consumption of alcohol increase the risk of fractures through metabolic effects and alcohol-related falls. As was previously reported [30], men consuming >8 units and women consuming >6 units of alcohol on the heaviest drinking day in the past week had the 1.65 to 2.07-time increased risk of lifetime fractures. Stone et al [31] and Holmberg [32] reported the adverse effects of insufficient sleep on the risk of fracture in men or women and suggested frequent fall caused by insufficient sleep was the direct reason for fracture occurrence. History of past fracture as a risk factor for low-energy fracture was well-established in literature, and accelerated bone loss and the increased tendency to fall after the first fracture were suggested to contribute to the secondary fracture in a near future [33, 34]. Therefore, awareness on the importance of sleep and alcohol consumption on fragility fracture should be improved, and health policies that focus on decreasing alcohol consumption and encouraging individuals to improve their sleep quality and duration should be considered to reduce and prevent the low-energy fractures.
In women, another modifiable factor was the weight, and in this study weight of 50 to 59.9kg was shown to have significantly positive effect on the lower extremity fracture, compared to the weight of <40kg. And this result was consistent with that of a previous meta-analysis [35], which showed being underweight increased the risk of lower extremity fractures, while being overweight increased the risk of upper arm fractures, in elderly women. Therefore, maintaining a healthy bodyweight with a normal BMI is of clear significance on prevention of low-energy fractures, for both upper and lower extremity fractures. Other several non-modifiable risk factors have also been identified to be associated with lower extremity fracture in women, including advanced age (80+ years) and geographic position. And the latter this might be related to intense pace of life and more frequent exposure to the hazardous lifestyles for individuals living in east region. However, this result this result should be treated cautiously and dialectically. On the hand, individuals in west region had a relatively shortened life span (72.3 years), (http://bbs1.people.com.cn/post/2/0/0/166947095.html), and it was a possibility that death came prior to the incident fracture, especially hip fracture. On the other hand, western region like Xinjiang province had a highest amount of solar radiation annually, which objectively facilitated the synthesis of vitamin D and calcium absorption to benefit bone health, especially in elderly individuals [36–38]. In addition, inhibition of alcohol due to religious reason among Muslim population in western part of China (Xinjiang area) and economy of that region being still centered on agriculture (higher physical activities) might be also the contributing factors [39].
Strengths and limitations
The main strengths of the current study included the stratified multistage cluster random sampling method used for recruiting subjects, largest sample size, face-to-face interview for data collection and adjustment for numerous important covariates. “Double” identification of fracture case via patients' self-reports and clinical or radiographic data increased the accuracy and precision of diagnosis.
Despite, there are some potential limitations that should be mentioned. Firstly, there was some recall bias due to its nature of retrospective design. Secondly, there remain residual confounding effects, because data on clinical chronic disease status, medication use and other socioeconomic factors that may have affected BMD or propensity to fall could not be available for adjustment in the multivariate analysis model. Thirdly, the study could not capture information about fracture cases in which the patients died. Overall, the incidence rate of low-energy lower extremity fracture was underestimated.
Conclusions
This study provided the distribution of low-energy lower extremity fractures, including population-based incidence, occurrence place, and the associated risk factors. These data could be used as updated clinical evidence base for healthcare planning and preventive efforts in China, as elsewhere. On the basis of these findings, awareness on the importance of sleep and alcohol consumption on fragility fracture should be improved, and health policies that focus on decreasing alcohol consumption and encouraging individuals to improve their sleep quality and duration should be considered. Specifically for women, maintaining a healthy bodyweight should be emphasized to prevent the lower extremity fractures.
Acknowledgments
We are grateful to B. Wang and B. Zhang of the Department of Orthopedics, and to Q. Zhang of the Department of Statistics and Applications for their kind assistance.
References
- 1. Lübbeke A, Stern R, Grab B, Herrmann F, Michel JP, Hoffmeyer P. Upper extremity fractures in the elderly: consequences on utilization of rehabilitation care. Aging Clin Exp Res. 2005; 17: 276–280. pmid:16285192
- 2. Foote JE, Rozental TD. Osteoporosis and upper extremity fragility fractures. J Hand Surg. 2012; 37: 165–167.
- 3. Ikpeze TC, Smith HC, Lee DJ, Elfar JC. Distal Radius Fracture Outcomes and Rehabilitation. Geriatr Orthop Surg Rehabil. 2016; 7: 202–205. pmid:27847680
- 4. Statement NC. Osteoporosis prevention, diagnosis, and therapy. Nih Consensus Statement. 2001; 17: 1–45.
- 5. Chen W, Lv H, Liu S, Liu B, Zhu Y, Chen X, et al. National incidence of traumatic fractures in China: a retrospective survey of 512 187 individuals. Lancet Glob Health. 2017; 5: e807–e817. pmid:28666814
- 6. Johnell O, Kanis J. Epidemiology of osteoporotic fractures. Osteoporosis & the Osteoporosis of Rheumatic Diseases. 2006; 16: 1–13.
- 7. Adachi JD, Ioannidis G, Pickard L, Berger C, Prior JC, Joseph L, et al. The association between osteoporotic fractures and health-related quality of life as measured by the Health Utilities Index in the Canadian Multicentre Osteoporosis Study (CaMos). Osteoporos Int. 2003; 14: 895–904. pmid:12920507
- 8. Chen CW, Huang TL, Su LT, Kuo YC, Wu SC, Li CY, et al. Incidence of subsequent hip fractures is significantly increased within the first month after distal radius fracture in patients older than 60 years. J Trauma Acute Care Surg. 2013; 74: 317–321. pmid:23505668
- 9. Jpw B, Bell JE, Cantu RV, Wang Q, Mcdonough CM, Carmichael D, et al. Second fractures among older adults in the year following hip, shoulder, or wrist fracture. Osteoporos Int. 2016; 27: 1–9.
- 10. Weiss RJ, Montgomery SM, Al DZ, Jansson KA. National data of 6409 Swedish inpatients with femoral shaft fractures: stable incidence between 1998 and 2004. Injury. 2009; 40: 304–308. pmid:19171340
- 11. Maharlouei N, Khodayari M, Forouzan F, Rezaianzadeh A, Lankarani KB. The incidence rate of hip fracture in Shiraz, Iran during 2008–2010. Arch Osteoporos. 2014; 9: 1–6.
- 12. Mann E, Icks A, Haastert B, Meyer G. Hip fracture incidence in the elderly in Austria: an epidemiological study covering the years 1994 to 2006. Bmc Geriatrics. 2008; 8: 35–39. pmid:19105814
- 13. Zhu Y, Liu S, Zhang X, Chen W, Zhang Y. Incidence and risks for surgical site infection after adult tibial plateau fractures treated by ORIF: a prospective multicentre study. Int Wound J. 2017; 14:982–988. pmid:28303656
- 14. Löfman O, Berglund K, Larsson L, Toss G. Changes in Hip Fracture Epidemiology: Redistribution Between Ages, Genders and Fracture Types. Osteoporos Int. 2002; 13: 18–25. pmid:11878451
- 15. Piirtola M, Vahlberg T, Isoaho R, Aarnio P, Kivelä SL. Incidence of fractures and changes over time among the aged in a Finnish municipality: a population-based 12-year follow-up. Aging Clin Exp Res. 2007; 19: 269–276. pmid:17726356
- 16. Chevalley T, Guilley E, Herrmann FR, Hoffmeyer P, Rapin CH, Rizzoli R. Incidence of hip fracture over a 10-year period (1991–2000): reversal of a secular trend. Bone. 2007; 40: 1284–1289. pmid:17292683
- 17. Horii M, Fujiwara H, Ikeda T, Ueshima K, Ikoma K, Shirai T, et al. Urban versus rural differences in the occurrence of hip fractures in Japan’s Kyoto prefecture during 2008–2010: a comparison of femoral neck and trochanteric fractures. BMC Musculoskelet Disord. 2013; 14: 304–311. pmid:24156244
- 18. Cooper C. Epidemiology of osteoporotic fracture: looking to the future. Rheumatology. 2005; 44: iv36. pmid:16306481
- 19. Curtis EM, Van dVR, Moon RJ, Jp VDB, Geusens P, De VF, et al. Epidemiology of fractures in the United Kingdom 1988–2012: Variation with age, sex, geography, ethnicity and socioeconomic status. Bone. 2016; 87: 19–26. pmid:26968752
- 20. Kaye JA, Jick H. Epidemiology of lower limb fractures in general practice in the United Kingdom. Inj Prev. 2004; 10: 368–374. pmid:15583259
- 21. Lonnroos E, Kautiainen H, Karppi P, Huusko T, Hartikainen S, Kiviranta I, et al. Increased incidence of hip fractures. A population based-study in Finland. Bone. 2006; 39: 623–627. pmid:16603427
- 22. Koski AM, Patala A, Patala E, Sund R. Incidence of osteoporotic fractures in elderly women and men in Finland during 2005–2006: a population-based study. Scand J Surg. 2014; 103: 215–221. pmid:24759377
- 23. Kannus P, Palvanen M, Niemi S, Parkkari J, Jrvinen M. Increasing number and incidence of low-trauma ankle fractures in elderly people: finnish statistics during 1970–2000 and projections for the future. Bone. 2002; 31: 430–433. pmid:12231418
- 24. Adams AL, Shi J, Takayanagi M, Dell RM, Funahashi TT, Jacobsen SJ. Ten-year hip fracture incidence rate trends in a large California population, 1997–2006. Osteoporos Int. 2013; 24: 373–376. pmid:22349963
- 25. Arakaki H, Owan I, Kudoh H, Horizono H, Arakaki K, Ikema Y, et al. Epidemiology of hip fractures in Okinawa, Japan. J Bone Miner Metab. 2011; 29: 309–314. pmid:20814705
- 26. Yoon BH, Lee YK, Kim SC, Kim SH, Ha YC, Koo KH. Epidemiology of proximal femoral fractures in South Korea. Arch Osteoporos. 2013; 8: 157–159. pmid:24150727
- 27. Xu L, Lu A, Zhao X, Chen X, Cummings SR. Very low rates of hip fracture in Beijing, People's Republic of China the Beijing Osteoporosis Project. Am J Epidemiol. 1996; 144: 901–907. pmid:8890668
- 28. Shen RG, Zhang SW, Wang JH. The epidemiological study of perimenopausal women with osteoporosis in Beijing. Maternal & Child Health Care of China. 2004.
- 29. Clark MK, Sowers MF, Dekordi F, Nichols S. Bone mineral density and fractures among alcohol-dependent women in treatment and in recovery. Osteoporos Int. 2003; 14: 396–403. pmid:12730765
- 30. Scholes S, Panesar S, Shelton NJ, Francis RM, Mirza S, Mindell JS, et al. Epidemiology of lifetime fracture prevalence in England: a population study of adults aged 55 years and over. Age Ageing. 2014; 43: 234–240. pmid:24231585
- 31. Stone KL, Ancoli-Israel S, Blackwell T, Ensrud KE, Cauley JA, Redline S, et al. Actigraphy-measured sleep characteristics and risk of falls in older women. Arch Intern Med. 2008; 168: 1768–1775. pmid:18779464
- 32. Holmberg AH, Johnell O, Nilsson PM, Nilsson J, Berglund G, Akesson K. Risk factors for fragility fracture in middle age. A prospective population-based study of 33,000 men and women. Osteoporos Int. 2006; 17: 1065–1077. pmid:16758143
- 33. Klotzbuecher CM, Ross PD, Landsman PB, Abbott TA 3rd, Berger M. Patients with prior fractures have an increased risk of future fractures: a summary of the literature and statistical synthesis. J Bone Miner Res. 2000; 15: 721–739. pmid:10780864
- 34. Kanis JA, Johnell O, De Laet C, Johansson H, Oden A, Delmas P, et al. A meta-analysis of previous fracture and subsequent fracture risk. Bone. 2004; 35: 375–382. pmid:15268886
- 35. Johansson H, Kanis JA, Oden A, McCloskey E, Chapurlat RD, Christiansen C, et al. A meta-analysis of the association of fracture risk and body mass index in women. J Bone Miner Res. 2014; 29: 223–233. pmid:23775829
- 36. Durvasula S, Gies P, Mason RS, Chen JS, Henderson S, Seibel MJ, et al. Vitamin D response of older people in residential aged care to sunlight-derived ultraviolet radiation. Arch Osteoporos. 2014; 9: 197. pmid:25311734
- 37. Saraiva GL, Cendoroglo MS, Ramos LR, Araujo LM, Vieira JG, Kunii I, et al. Influence of ultraviolet radiation on the production of 25 hydroxyvitamin D in the elderly population in the city of Sao Paulo (23 degrees 34'S), Brazil. Osteoporos Int. 2005; 16: 1649–1654. pmid:15947862
- 38. Rice SA, Carpenter M, Fityan A, Vearncombe LM, Ardern-Jones M, Jackson AA, et al. Limited exposure to ambient ultraviolet radiation and 25-hydroxyvitamin D levels: a systematic review. Br J Dermatol. 2015; 172: 652–661. pmid:25646772
- 39. Qanta AA, Ziad AM, Benedetta A, Didier P. Muslim health-care workers and alcohol-based handrubs. The Lancet. 2006; 367: 1025–1027.