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. 2018 Nov 29;18:1325. doi: 10.1186/s12889-018-6230-y

Associations of body mass index and diabetes with hip fracture risk: a nationwide cohort study

Hsiu-Ling Huang 1,2,#, Cheng-Chin Pan 3,#, Yu-Fen Hsiao 1, Ming-Chih Chen 4, Chuan-Yu Kung 5, Pei-Tseng Kung 6,7, Wen-Chen Tsai 2,
PMCID: PMC6267014  PMID: 30497430

Abstract

Background

The high prevalence of diabetes is associated with body mass index (BMI), and diabetes can cause many complications, such as hip fractures. This study investigated the effects of BMI and diabetes on the risk of hip fractures and related factors.

Methods

We retrospectively reviewed data from 22,048 subjects aged ≧ 40 years from the National Health Interview Survey in Taiwan (NHIST) in 2001, 2005, and 2009. We linked the NHIST data for individual participants with the National Health Insurance Research Database (NHIRD), which includes the incidence of hip fracture from 2000 to 2013. We defined five categories for BMI: low BMI (BMI < 18.5), normal BMI (18.5 ≦ BMI < 24), overweight (24 ≦ BMI < 27), mild obesity (27 ≦ BMI < 30), and moderate obesity (BMI ≧ 30). The Cox proportional hazards model was used to analyze the effects of BMI and diabetes on risk of hip fracture.

Results

The Cox proportional hazards model shows that hip fracture risk in participants with diabetes was 1.64 times that of non-diabetes patients (95% confidence interval [CI]:1.30–2.15). Participants with low BMIs showed a higher hip fracture risk (HR: 1.75) than those with normal BMI. Among the five BMI groups, compared with non-diabetes patients, only diabetes patients with a normal BMI showed a significantly higher risk on hip fracture (HR: 2.13, 95% CI: 1.48–3.06). In participants with diabetes, compared with those with normal BMI, those with overweight or obesity showed significantly lower hip fracture risks (HR: 0.49 or 0.42). The hip fracture risk in participants who expend ≧ 500 kcal/week in exercise was 0.67 times lower than in those who did not exercise.

Conclusions

Diabetes and low BMI separately are important risk factors for hip fracture. There was an interaction between diabetes and BMI in the relationship with hip fracture (p = 0.001). The addition of energy expenditure through exercise could effectively decrease hip fracture risk, regardless of whether the participants have diabetes or not. The results of this study could be used as a reference for health promotion measures for people with diabetes.

Keywords: BMI, Body mass index, Hip fracture, Diabetes, National Health Insurance

Background

The worldwide incidence of hip fracture is predicted to increase from 1.66 million as of 1990 to 6.26 million by 2050 [1]. The global population is ageing, and hip fractures significantly affect the mobility and mortality of the elderly. The associated medical costs should also not be overlooked [2, 3]. Both type 1 and type 2 diabetes can increase hip fracture risk and complications due to abnormal bone metabolism [4, 5]. Vestergaard found that compared with those without diabetes, the relative risk (RR) for hip fractures in patients with type 1 diabetes was 6.94, and that for hip fractures in patients with type 2 diabetes was 1.38 [6]. In other studies, patients with longer diabetes duration were associated with a higher hip fracture risk compared to patients without diabetes. When the diabetes duration was < 5 years, RR was 1.8, but when the diabetes duration was > 15 years, RR increased to 2.66 [7, 8]. According to previous studies, diabetes was positively associated with risk of hip fracture.

The high prevalence of diabetes is related to population ageing and body mass index (BMI, unit: kg/m2). The World Health Organization (WHO) recommends using BMI as an important indicator of obesity [9]; the higher the BMI, the higher a patient’s risk is for metabolic diseases [10]. Being either overweight or obese can increase the incidence of type 2 diabetes, and the incidence of diabetes in obese adults is approximately 3–7 times that of adults with normal weight. The incidence in those with a BMI of > 35 is 20 times that in those with BMIs of 18.5–24.9 [11, 12].

To understand, a higher BMI level was associated with a higher prevalence of type 2 diabetes, and diabetes is an important risk facture for hip fracture. In addition to BMI and diabetes, the study from Søgaard et al. found that risk of hip fracture decreased with increasing BMI [13]. De Laet et al. [14] also found that people with a BMI of 30 kg/m2 showed a lower hip fracture risk (RR: 0.83; 95% confidence interval [CI]: 0.69–0.99) than those with a BMI of 25 kg/m2. BMI is associated with the incidence of fracture. Aurégan et al. [15] suggest that low BMI independently increase the risk of fractures. Johansson et al. [16] also found that low BMI was a risk factor for hip and all osteoporotic fracture. However, another study found that among postmenopausal women, obese women showed a higher risk of ankle and upper leg fractures than nonobese women [17]. Thus, low BMI is an important risk factor for fractures, but the relation between high BMI and fractures is not clear [16, 17].

Obesity is one of the major risk factors for type 2 diabetes, which may in turn also increase hip fracture risk. However, it is still uncertain whether BMI has an impact on hip fractures in diabetes patients. Thus, we investigated whether diabetes has same effects on risk of hip fracture in those with different BMI, and the effects of BMI on hip fracture risk in diabetes patients.

Methods

Data sources and participants

We retrospectively reviewed quadrennial data from the National Health Interview Survey in Taiwan (NHIST) for the years 2001, 2005, and 2009. The survey participants’ height and weight data were used to calculate the baseline BMI. We excluded pregnant women and participants younger than 40 years. We linked the NHIST participants’ individual data with the National Health Insurance Research Database (NHIRD), which includes nationwide data on all citizens in Taiwan. We extended the washout period to January 1st, 2000 for our participants in this study. All participants who had been diagnosed with hip fracture before NHIST survey were excluded from this study to make sure the temporal relationship between BMI/diabetes and hip fracture. We included a total of 22,048 participants and monitored hip fracture incidence for the period of 2000 to 2013.

The NHIST was conducted nationally and quadrennially by the Taiwan Health Promotion Administration. The information available from surveys include personal information, personal health status, knowledge about disease prevention, utilization of medical services, personal health behaviour, self-rated health status, and work and economic status, among others. The survey results provide a reference for developing and implementing healthcare policies in Taiwan [18].

This study was reviewed and approved by the research ethics committees of China Medical University (IRB No.: CMUH 103-REC3–109). We deleted all personal identification from the data analysed in this study to protect the patients’ personal identities. Taiwan’s National Health Insurance program was launched in March 1995, and as of 2013, the nationwide coverage rate was 99.68% [19]. This compulsory public health insurance program provides comprehensive information such as demographic data and data on all medical services, including prescription drugs, surgical treatments for outpatients, emergency care, and inpatient care. The NHIRD includes medical information on all citizens covered by insurance, including treatments for diabetes, hip fractures, and other conditions [20, 21]. The comprehensiveness and accuracy of the NHIRD have been confirmed by the Ministry of Health and Welfare, and the database has been used in numerous studies [22, 23].

Variable descriptions

The variables examined were BMI, personal basic characteristics (sex, age), environmental factors (urban or rural residential areas), socio-economic status (monthly salary), health status (Charlson Comorbidity Index [CCI] and diabetes complication severity index [DCSI]), health behaviour (weekly energy expenditure through exercise), and diabetes status. The WHO has developed a classification of BMI for international use, but the index for overweight Asian adults is lower than the world average. Thus, many Asian countries have developed their own criteria for overweight and obesity. We used the BMI classification criteria of the Taiwan Health Promotion Administration and divided the participants into five categories: low BMI (BMI < 18.5), normal BMI (18.5 ≦ BMI < 24), overweight (24 ≦ BMI < 27), mild obesity (27 ≦ BMI < 30), and moderate obesity (BMI ≧ 30) [24].

In healthcare, diagnosis codes are used as a tool to group and identify diseases, disorders, symptoms, poisonings, adverse effects of drugs and chemicals, injuries, and other reasons for patient encounters. In the NHIRD, diagnosis codes are collected using the ICD-9-CM code (The International Classification of Diseases, Ninth Revision, Clinical Modification). We defined diabetes patients as those who received a diagnosis of diabetes (ICD-9-CM: 250) and at least three outpatient treatments or one hospitalization during the year of the interview survey or within 365 days before or after the survey [25]. We excluded patients with type 1 diabetes, gestational diabetes, neonatal diabetes, or impaired glucose tolerance (ICD-9-CM: 6488, 7751, 7902, 6480). We defined hip fracture as a diagnosis of femoral neck fracture, intertrochanteric fracture, or subtrochanteric fracture (ICD-9-CM: 820.XX) and having received one of the following surgical treatments: partial hip replacement (ICD-9-CM: 81.52), open reduction of fracture with internal fixation of the femur (ICD-9-CM: 79.35), or closed reduction of fracture with internal fixation of the femur (ICD-9-CM: 79.15).

We divided residential areas into seven levels from most urban and to least urban [26]. We calculated the severity of comorbidities based on the CCI revised by Deyo et al. [27] and divided them into groups with scores of 0, 1–3, and  ≧ 4. We calculated the DCSI based on seven types of diabetes complications (retinopathy, nephropathy, neuropathy, cerebrovascular, cardiovascular, peripheral vascular disease, and metabolic) as classified by Young et al [28] and used different weight scores (0 or  ≧ 1) to represent different severities.

In terms of health behaviour, we calculated the weekly energy expenditure through exercise according to the method proposed by Wen et al. [29] using the NHIST. Each type of exercise corresponds to a different Metabolic Equivalent of Task (MET, a unit of exercise intensity) according to the breathing status during exercise. One MET is defined as the oxygen uptake in ml/kg/min when sitting quietly (3.5 ml/kg/min). The weekly energy expended in exercise is calculated as follows: MET * frequency of exercises over the past 2 weeks (times) * each exercise duration (hours) * body weight (kg) * 7/14. We used the MET to collect and validate the weekly energy expenditure in kilocalories (kcal) for specific exercises, based on which participants were divided into three groups according to the expenditure per week: no exercise, < 500 kcal/week, and  ≧ 500 kcal/week.

Statistical analysis

SAS statistical analysis software version 9.3 (SAS Institute, Cary, NC, U.S.A.) was used for the analysis, and p-values < 0.05 were considered statistically significant. In descriptive statistics, the participants’ variables were analysed, including BMI, diabetes status, basic personal characteristics (sex and age), environmental factors (urbanization degree of residential areas), social and economic status (monthly salary), health status (CCI and DCSI), and health behaviour (weekly energy expenditure through exercise). Our aim was to compare the numbers of subjects with hip fractures and percentage distributions. A chi-square test was used to perform analysis to determine the relationship between the variables and incidence of diabetes and level of BMI. A log-rank test was used to determine the relationship with hip fracture incidence.

For the inferential statistical analysis, a Cox proportional hazard model was used to investigate the effects of BMI and diabetes on hip fracture risk after controlling for variables such as personal basic characteristics, environmental factors, social and economic status, health status, and health behaviour. Further, in order to examine whether diabetes has a same effect on risk of hip fracture in those with different BMI, we also examined the interaction relationship between diabetes status and level of BMI on the risk of hip fracture. A stratified analysis was further performed to investigate the effects of diabetes on hip fracture risk in those with different BMI if there was an interaction relationship between diabetes status and level of BMI. Finally, the Cox proportional hazard model was used to investigate the effects of BMI on hip fracture incidence in participants with diabetes.

Results

Participant demographics and cox proportional hazard model analysis

A total of 22,048 subjects were eligible for inclusion in this study (Table 1), of which 3508 had diabetes and 315 had hip fractures. Among the different level of BMI groups, we found that the higher of the BMI, the higher prevalence of diabetes. When the participants had moderate obesity (BMI ≧ 30), diabetes risk was as high as 33.33%. There was significant difference between diabetes and non-diabetes patients in risk of hip fracture (p < 0.05). Additionally, participants with low BMI (BMI < 18.5) showed a higher hip fracture rate (3.56%) than other BMI subgroups. There were significant differences between participants with diabetes and those without diabetes in BMI, hip fracture, sex, age, urbanization of residence area, monthly salary, CCI, DCSI and weekly energy expenditure through exercise (P < 0 .05). In Table 2, there were significant differences in hip fracture incidence between the participants in terms of variables, including BMI, diabetes status, age, monthly salary, CCI, and DCSI (p < 0.05).

Table 1.

Participant demographics with descriptive statistics

Variable Total % Non-diabetes Diabetes p-value BMI < 18.5 18.5≦BMI < 24 24 ≦ BMI < 27 27 ≦ BMI < 30 BMI≧30 p-value
N % N % N % N % N % N % N %
Total 22,048 100.00 18,540 84.09 3508 15.91 786 3.56 10,858 49.25 6474 29.36 2742 12.44 1188 5.39
BMI < 0.001
 BMI < 18.5 786 3.56 711 3.83 75 2.14
 18.5 ≦ BMI < 24 10,858 49.25 9581 51.68 1277 36.40
 24 ≦ BMI < 27 6474 29.36 5358 28.90 1116 31.81
 27 ≦ BMI < 30 2742 12.44 2098 11.32 644 18.36
 BMI≧30 1188 5.39 792 4.27 396 11.29
Diabetes < 0.001
 No 18,540 84.09 711 90.46 9581 88.24 5358 82.76 2098 76.51 792 66.67
 Yes 3508 15.91 75 9.54 1277 11.76 1116 17.24 644 23.49 396 33.33
Hip Fracture < 0.001 < 0.001
 No 21,733 98.57 18,308 98.75 3425 97.63 758 96.44 10,689 98.44 6396 98.80 2712 98.91 1178 99.16
 Yes 315 1.43 232 1.25 83 2.37 28 3.56 169 1.56 78 1.20 30 1.09 10 0.84
Sex 0.036 < 0.001
 Male 10,908 49.47 9230 49.78 1678 47.83 312 39.69 4944 45.53 3607 55.72 1474 53.76 571 48.06
 Female 11,140 50.53 9310 50.22 1830 52.17 474 60.31 5914 54.47 2867 44.28 1268 46.24 617 51.94
Age < 0.001 < 0.001
 40–49 9015 40.89 8287 44.70 728 20.75 301 38.30 4728 43.54 2503 38.66 1039 37.89 444 37.37
 50–59 6347 28.79 5177 27.92 1170 33.35 176 22.39 2877 26.50 2031 31.37 871 31.77 392 33.00
 60–69 3616 16.40 2715 14.64 901 25.68 108 13.74 1652 15.21 1138 17.58 509 18.56 209 17.59
 70–79 2274 10.31 1740 9.39 534 15.22 119 15.14 1149 10.58 632 9.76 259 9.45 115 9.68
 ≧80 796 3.61 621 3.35 175 4.99 82 10.43 452 4.16 170 2.63 64 2.33 28 2.36
Urbanization of residence area < 0.001 0.297
 1 & 2 10,027 45.48 8524 45.98 1503 42.84 356 45.29 5016 46.20 2947 45.52 1180 43.03 528 44.44
 3 & 4 7234 32.81 6096 32.88 1138 32.44 255 32.44 3521 32.43 2122 32.78 940 34.28 396 33.33
 5–7 4787 21.71 3920 21.14 867 24.71 175 22.26 2321 21.38 1405 21.70 622 22.68 264 22.22
Monthly salary (NTD) < 0.001 < 0.001
 ≦ 17,280 2578 11.69 2373 12.80 205 5.84 136 17.30 1343 12.37 680 10.50 280 10.21 139 11.70
 17,281–22,800 9925 45.02 8149 43.95 1776 50.63 329 41.86 4864 44.80 2935 45.34 1254 45.73 543 45.71
 22,801–36,300 5121 23.23 4255 22.95 866 24.68 197 25.06 2459 22.65 1499 23.15 667 24.33 299 25.17
 > 36,300 4424 20.07 3763 20.30 661 18.84 124 15.78 2192 20.19 1360 21.01 541 19.73 207 17.42
CCI < 0.001 < 0.001
 0 16,988 77.05 14,507 78.25 2481 70.72 550 69.97 8439 77.72 5042 77.88 2110 76.95 847 71.30
 1–3 4303 19.52 3376 18.21 927 26.43 189 24.05 2017 18.58 1240 19.15 563 20.53 294 24.75
 ≧ 4 757 3.43 657 3.54 100 2.85 47 5.98 402 3.70 192 2.97 69 2.52 47 3.96
DCSI < 0.001 < 0.001
 0 20,784 94.27 17,703 95.49 3081 87.83 737 93.77 10,300 94.86 6096 94.11 2565 93.54 1089 91.67
 ≧ 1 1264 5.73 837 4.51 427 12.17 49 6.23 558 5.14 381 5.89 177 6.46 99 8.33
Weekly energy expended of calories in exercise < 0.001 < 0.001
 No exercise 12,001 54.43 10,216 57.02 1785 51.49 464 64.27 5881 55.96 3434 54.25 1522 57.00 700 60.66
 < 500 kcal/week 3630 16.46 3045 16.99 585 16.87 142 19.67 1980 18.84 1029 16.26 345 12.92 134 11.61
 ≧ 500 kcal/week 5755 26.10 4658 25.99 1097 31.64 116 16.07 2649 25.20 1867 29.49 803 30.07 320 27.73
 Missing 662 3.00

BMI body mass index, CCI Charlson Comorbidity Index, DCSI diabetes complication severity index

NTD New Taiwan Dollar, 32 NTD = 1 US dollar

Urbanization of residence area (Level 1 was the most urbanized)

p-value: chi-square test

Table 2.

Descriptive statistics of participants with or without hip fractures

Variable Total % Without hip fractures With hip fractures p -value
N % N %
Total 22,048 100.00 21,733 98.57 315 1.43
BMI < 0.001
 BMI < 18.5 786 3.56 758 3.49 28 8.89
 18.5 ≦ BMI < 24 10,858 49.25 10,689 49.18 169 53.65
 24 ≦ BMI < 27 6474 29.36 6396 29.43 78 24.76
 27 ≦ BMI < 30 2742 12.44 2712 12.48 30 9.52
 ≧ 30 1188 5.39 1178 5.42 10 3.17
Diabetes < 0.001
 No 18,540 84.09 18,308 84.24 232 73.65
 Yes 3508 15.91 3425 15.76 83 26.35
Sex 0.205
 Male 10,908 49.47 10,762 49.52 146 46.35
 Female 11,140 50.53 10,971 50.48 169 53.65
Age < 0.001
 40–49 9015 40.89 8993 41.38 22 6.98
 50–59 6347 28.79 6310 29.03 37 11.75
 60–69 3616 16.40 3547 16.32 69 21.90
 70–79 2274 10.31 2161 9.94 113 35.87
 ≧ 80 796 3.61 722 3.32 74 23.49
Urbanization of residence area 0.099
 1 & 2 10,027 45.48 9903 45.57 124 39.37
 3 & 4 7234 32.81 7140 32.85 94 29.84
 5–7 4787 21.71 4690 21.58 97 30.79
Monthly salary (NTD) < 0.001
 ≦ 17,280 2578 11.69 2489 11.45 89 28.25
 17,281-22,800 9925 45.02 9793 45.06 132 41.90
 22,801-36,300 5121 23.23 5069 23.32 52 16.52
 > 36,300 4424 20.07 4382 20.16 42 13.33
CCI < 0.001
 0 16,988 77.05 16,808 77.34 180 57.14
 1–3 4303 19.52 4197 19.32 105 33.33
 ≧ 4 757 3.43 727 3.35 30 9.53
DCSI < 0.001
 0 20,784 94.27 20,504 94.35 280 88.89
 ≧ 1 1264 5.73 1229 5.65 35 11.11
Weekly amount of calories burned in exercise 0.831
 No exercise 12,001 54.43 11,845 56.09 156 57.99
 < 500 kcal 3630 16.46 3585 16.98 45 16.73
 ≧ 500 kcal 5755 26.10 5687 26.93 68 25.28
 Missing 662 3.00

BMI body mass index, CCI Charlson Comorbidity Index, DCSI diabetes complication severity index

NTD New Taiwan Dollar; 32 NTD = 1 US dollar

Urbanization of residence area (Level 1 was the most urbanized)

p-value: log-rank test

We also used the Cox proportional hazard model to analyze the effects of BMI and diabetes on hip fracture risk. The results of four models of are shown in Table 3. The first model is the univariate analysis of diabetes and hip fracture with unadjusted results, the second is for diabetes without BMI, the third is for BMI without the diabetes variable, and the final model is for both variables together. In the final model, we found that hip fracture risk in diabetes patients was 1.64 times the risk in non-diabetes patients (95% CI: 1.30–2.15, p < 0.05). Patients with low BMI showed a higher hip fracture risk (Adjusted hazards ratio [Adj. HR]: 1.75, 95% CI: 1.17–2.61) than those with normal BMI (reference). Additionally, patients who were overweight, mildly obese, or moderately obese had lower hip fracture risk than patients with normal BMI, but the differences were not statistically significant (p > 0.05). Hip fracture risk in female patients was 1.29 times that in male patients (95% CI: 1.03–1.62, p = 0.027). Compared with a reference group (aged 40–49 years), older patients showed a higher hip fracture risk (p < 0.05): among subjects  ≧ 80 years old, hip fracture risk was as high as 52.16 times the baseline risk. Separately, participants with higher CCI scores showed a higher hip fracture risk than the reference group (CCI = 0), and hip fracture risk in those who expended  ≧ 500 kcal/week in exercise was 0.67 times lower than in those who did not exercise (95% CI: 0.50–0.89).

Table 3.

Cox proportional hazard model analysis of hip fracture risk in all participants

Variables Unadjusted HR p-value Diabetes without BMI BMI without diabetes Diabetes and BMI together
Adjusted HR 95% CI Adjusted HR 95% CI Adjusted HR 95% CI p-value
Diabetes
 No (ref.)
 Yes 2.04 < 0.001 1.54 1.18 2.00 1.64 1.30 2.15 < 0.001
BMI
 18.5 ≦ BMI < 24 (ref.)
 BMI < 18.5 2.58 < 0.001 1.71 1.14 2.56 1.75 1.17 2.61 0.007
 24 ≦ BMI < 27 0.78 0.072 0.86 0.66 1.13 0.84 0.64 1.10 0.205
 27 ≦ BMI < 30 0.72 0.098 0.75 0.51 1.11 0.70 0.48 1.04 0.076
 BMI ≧ 30 0.60 0.111 0.61 0.32 1.16 0.55 0.29 1.05 0.072
Sex
 Male (ref.)
 Female 1.15 0.206 1.28 1.02 1.60 1.30 1.04 1.63 1.29 1.03 1.62 0.027
Age
 40–49 (ref.)
 50–59 2.66 0.000 2.47 1.45 4.19 2.63 1.55 4.46 2.50 1.47 4.25 0.001
 60–69 9.12 < 0.001 7.81 4.79 12.72 8.62 5.31 14.01 7.87 4.83 12.83 < 0.001
 70–79 27.67 < 0.001 23.19 14.41 37.33 24.86 15.47 39.94 22.68 14.08 36.52 < 0.001
 ≧ 80 75.60 < 0.001 56.01 33.99 92.29 58.24 35.39 95.87 52.16 31.60 86.09 < 0.001
Urbanization of residence area
 1 & 2 (ref.)
 3 & 4 0.96 0.787 0.97 0.74 1.28 0.96 0.73 1.26 0.96 0.73 1.26 0.768
 5–7 1.28 0.073 1.21 0.91 1.60 1.17 0.88 1.56 1.18 0.89 1.57 0.251
Monthly salary (NTD)
  ≦ 17,280 (ref.)
 17,281–22,800 0.36 < 0.001 0.71 0.52 0.97 0.78 0.57 1.05 0.70 0.52 0.96 0.025
 22,801–36,300 0.34 < 0.001 0.85 0.58 1.23 0.93 0.64 1.35 0.84 0.58 1.22 0.349
 > 36,300 0.27 < 0.001 0.87 0.58 1.31 0.98 0.66 1.45 0.86 0.58 1.29 0.471
CCI
 0 (ref.)
 1–3 2.55 < 0.001 1.58 1.23 2.04 1.56 1.22 2.01 1.58 1.23 2.04 0.000
  ≧ 4 5.44 < 0.001 2.58 1.73 3.86 2.46 1.65 3.66 2.64 1.77 3.95 < 0.001
DCSI
 0 (ref.)
 ≧ 1 2.55 < 0.001 1.34 0.93 1.93 1.43 0.99 2.07 1.35 0.93 1.95 0.112
Weekly energy expended of calories in exercise
 No exercise (ref.)
 < 500 kcal/week 0.78 0.129 0.80 0.57 1.11 0.81 0.58 1.13 0.80 0.57 1.11 0.181
 ≧ 500 kcal/week 0.75 0.038 0.65 0.49 0.86 0.68 0.51 0.91 0.67 0.50 0.89 0.006

BMI body mass index, CCI Charlson Comorbidity Index, DCSI diabetes complication severity index, HR hazard ratio, CI confidence interval

NTD New Taiwan Dollar; 32 NTD = 1 US dollar

Urbanization of residence area (overall 7 levels; Level 1 was the most urbanized)

We also tested the interaction relationship between diabetes status and level of BMI in risk of hip fracture. The result revealed that there was a significant interaction effect between diabetes status and level of BMI in hip fracture risk (p = 0.001).

Stratified analysis of the effects of BMI and relative factors on hip fracture risk in diabetes patients

We used stratified analysis to examine the relative risk of hip fracture between diabetes and non-diabetes patients at different level of BMI (Table 4). After relevant variables were controlled in Cox proportional hazard model, hip fracture risk in diabetes patients was greater than that in non-diabetes patients regardless of BMI. Among the five BMI groups, compared with non-diabetes patients, only diabetes patients with a normal BMI (18.5 ≦ BMI < 24) showed a statistically significant difference in hip fracture risk (Adj. HR: 2.13, 95% CI: 1.48–3.06, P < 0.05). It means that diabetes increases risk of hip fracture but the magnitude of risk varies with the BMI level.

Table 4.

Stratified analysis of the relative risk of hip fracture between diabetes and non-diabetes patients in terms of BMI

Variables Diabetes patients Non-diabetes patients Adj. HR (diabetes vs. non-diabetic) 95% CI p -value
N Hip fractures N Hip fractures (N) (%)
(N) (%) (N) (%)
Sum 3508 83 2.37 18,540 232 1.25 1.64 1.30 2.15 < 0.001
BMI
 BMI < 18.5 75 6 8.00 711 22 3.09 2.47 0.90 6.74 0.079
 18.5 ≦ BMI < 24 1277 46 3.60 9581 123 1.28 2.13 1.48 3.06 < 0.001
 24 ≦ BMI < 27 1116 17 1.52 5358 61 1.14 1.01 0.57 1.75 0.996
 27 ≦ BMI < 30 644 9 1.40 2098 21 1.00 1.24 0.54 2.86 0.618
 BMI ≧ 30 396 5 1.26 792 5 0.63 2.37 0.57 9.84 0.236

Note: Cox proportional hazards model was used and controlled for sex, age, urbanization of residence area, monthly salary, CCI, DCSI and weekly energy expenditure through exercise

Analysis of the effects of relative factors on hip fracture risk in diabetes patients

A Cox proportional hazard model was used to analyze diabetes patients (Table 5 & Fig. 1). Compared with a reference group (normal BMI, 18.5 ≦ BMI < 24), those with overweight (24 ≦ BMI < 27) or obesity (BMI ≧ 27) showed a lower hip fracture risk (Adj. HR: 0.49 vs. 0.42, p < 0.05). Compared with the reference group (aged 40–49 years), older patients showed a higher hip fracture risk, but statistically significant differences were only observed in patients  ≧ 60 years old (p < 0.05). Among diabetes patients, those with higher CCI or DCSI scores were associated with a higher hip fracture risk. As the weekly energy expended in exercise increased in diabetes patients, hip fracture risk decreased compared with diabetes patients without exercise. In particular, when the weekly energy expenditure was  ≧ 500 kcal/week, hip fracture risk in diabetes patients was significantly decreased to 0.54 times (95% CI: 0.31–0.94, p < 0.05).

Table 5.

Analysis of the effect of BMI on hip fracture risk in diabetes patients

Variables Unadjusted HR p-value Adjusted HR 95% CI p-value
BMI
 18.5 ≦ BMI < 24 (ref.)
 BMI < 18.5 2.54 0.032 1.78 0.75 4.26 0.193
 24 ≦ BMI < 27 0.42 0.002 0.49 0.28 0.85 0.012
 BMI  ≧  27 0.38 0.001 0.42 0.23 0.78 0.006
Sex
 Male (ref.)
 Female 1.34 0.189 1.33 0.85 2.08 0.215
Age
 40–49 (ref.)
 50–59 1.81 0.258 1.73 0.62 4.88 0.298
 60–69 5.16 0.001 4.67 1.78 12.25 0.002
 70–79 11.32 < 0.001 10.20 3.82 27.27 < 0.001
  ≧  80 23.02 < 0.001 16.97 5.94 48.43 < 0.001
Urbanization of residence area
 1 & 2 (ref.)
 3 & 4 0.76 0.289 0.79 0.46 1.36 0.402
 5–7 0.81 0.425 0.84 0.47 1.47 0.535
Monthly salary (NTD)
 ≦ 17,280 (ref.)
 17,281–22,800 0.55 0.122 0.74 0.34 1.63 0.457
 22,801–36,300 0.78 0.548 1.09 0.47 2.51 0.837
 > 36,300 0.42 0.058 0.63 0.25 1.61 0.338
CCI
 0 (ref.)
 1–3 2.17 0.001 1.51 0.92 2.47 0.106
 ≧  4 5.63 < 0.001 3.51 1.43 8.59 0.006
DCSI
 0 (ref.)
  ≧  1 2.70 < 0.001 1.68 0.94 3.03 0.082
Weekly energy expended of calories in exercise
 No exercise (ref.)
 < 500 kcal/week 0.73 0.314 0.65 0.35 1.22 0.178
 ≧  500 kcal/week 0.59 0.050 0.54 0.31 0.94 0.029

BMI body mass index, CCI Charlson Comorbidity Index, DCSI diabetes complication severity index;

HR hazard ratio, CI confidence interval

NTD New Taiwan Dollar, 32 NTD = 1 US dollar

Urbanization of residence area (overall 7 levels; Level 1 was the most urbanized)

Fig. 1.

Fig. 1

Comparisons of hip fracture risk among different BMI groups in patients with diabetes (After controlling for sex, age, urbanization of residence area, monthly salary, CCI, DCSI and weekly energy expenditure through exercise)

Discussion

This study is the first to use nationwide survey data in combination with data from the NHIRD to investigate the effects of BMI, diabetes, and relative factors on hip fracture risk. According to findings from previous studies, multiple complex factors in diabetes patients may cause abnormal bone metabolism and increase fracture incidence and subsequent complications [5, 6]. After controlling for other variables (including BMI), we also found that hip fracture risk in patients with type 2 diabetes was 1.64 times that in non-diabetes patients (Table 3), which was consistent with previous studies [4, 5, 30].

The analysis results in Table 3 show that all participants with low BMI (< 18.5) had a higher hip fracture risk (Adj. HR: 1.75, 95% CI: 1.17–2.61, p = 0.007) than those with normal BMI (18.5 ≦ BMI < 24). De Laet et al. [14] used a meta-analysis approach to study nearly 60,000 men and women from 12 cohorts of both Asian and Western participants. They found that low BMI conferred a significant risk for all types of fractures in both Asian and Western populations. They found that low BMI is an important risk factor for hip fractures. There were similar findings in the diabetes patients group (Table 5), but the result was not significant (Adj. HR: 1.78, 95% CI: 0.75–4.26, p = 0.193). After further analysis, only 83 diabetes patients had hip fractures. In addition, it was found that only six individuals had hip fractures among 75 diabetes patients with low BMI (BMI < 18.5). We believe that if the number of subjects was increased or if the subjects were observed for a longer period of time, the statistical results in variables could perhaps become significant.

To understand whether hip fracture risk of diabetes was the same in patients with different BMI, stratified analysis was performed (Table 4). Analysis results showed that diabetes patients had a higher hip fracture risk than non-diabetes patients in all MBI subgroups, but only those with a normal BMI showed significant differences (Adj. HR: 2.13, 95% CI: 1.48–3.06). It reflected the impact of diabetes on risk of hip fracture were not constant in people with different BMIs. The effect of diabetes on increasing hip fracture risk was more significant in those with lower BMI. The results indicated that diabetes as a risk factor for hip fracture was not independent of BMI, which was a novel finding.

Many studies have pointed out that overweight and obesity can increase the incidence of metabolic diseases [11, 12]. The similar result was also found in Table 1. Participant with a higher BMI had higher risks in type 2 diabetes. However, as shown in Table 5 and Fig. 1, we found that diabetes patients with high BMI (24 ≦ BMI < 27) or obesity (BMI ≧ 27) showed a lower hip fracture risk (Adj. HR: 0.49 vs. 0.42, p < 0.05) compared with the reference group (normal BMI). This is consistent with the report by Johansson et al [16], who analysed > 300,000 women from more than 25 countries and found that 87% of hip fractures occurred in those without obesity (defined as BMI ≧ 30 kg/m2). Furthermore, a relatively high BMI decreased the fracture risk in these women. The same result was found in all participants in which high BMI was protective against hip fracture, but there was no significant difference from the reference group (normal BMI, Table 3).However, high BMI is hardly a public health strategy that should be advocated, given concerns about cardiovascular disease in this population.

Limitations

There were several limitations to our analyses. Data from the NHIRD were used for the analysis, so not all health behaviours and other factors were included in the analysis, such as eating habits, body composition/muscle mass, muscle function/sarcopenia, and history of falls history. Moreover, the duration of diabetes in all subjects and their blood glucose control status were not known.

Conclusion

In this study, we found that diabetes increased hip fracture risk (HR: 1.64), and both diabetes and BMI had an interaction on risk of hip fracture (P = 0.001). The findings from this study revealed the following: (1) those with diabetes sustain more hip fractures, (2) low BMI was a risk factor for hip fracture, (3) The effect of diabetes on increasing hip fracture risk was more significant in those with lower BMI, and (4) physical exercise was important in preventing hip fractures, including among patients with diabetes.

It was not even clear whether any exercise was a significant protective factor in individuals with diabetes alone, or whether the result was driven by the general population. However, we found that energy expenditure through exercise  ≧ 500 kcal/week per week could effectively decrease hip fracture risk in the general population and in those with diabetes. Regardless of BMI or diabetes status, exercise helps prevent falls and hip fractures and was therefore especially important for diabetes patients. Hence, health education for diabetes on managing body weight and increasing the amount of exercise could effectively prevent hip fractures. The results of this study could be used as a reference for health education and health promotion measures for diabetes patients.

Acknowledgments

This study was supported by the grants (CMU104-S-27, DOH10541) from China Medical University as well as Ministry of Health and Welfare, Taiwan. We are grateful for use of the National Health Insurance Research Database and the National Health Interview Survey in Taiwan. R.O.C.

Funding

This study was supported by the grants (CMU104-S-27, DOH10541) from China Medical University as well as Ministry of Health and Welfare, Taiwan.

Abbreviations

Adj. HR

Adjusted hazards ratio

BMI

Body mass index

CCI

Charlson Comorbidity Index

CI

Confidence interval

DCSI

Diabetes complication severity index

ICD-9-CM

The International Classification of Diseases, Ninth Revision, Clinical Modification

MET

Metabolic Equivalent of Task

NHIRD

National Health Insurance Research Database

NHIST

National Health Interview Survey in Taiwan

NTD

New Taiwan Dollar

RR

Relative risk

US

United States

WHO

World Health Organization

Authors’ contributions

HLH and WCT drafted the manuscript. WCT, YFH and PTK designed the study. CCP, LTC, MCC and CYK collected data. HLH, PTK and WCT were responsible for study conceptualization and developing the analytical plan. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Data are available from the Science Center, the Ministry of Health and Welfare (MOHW), Taiwan. This study obtained the databases published and managed by the MOHW. All researchers are allowed to use the databases for their interested studies. Before using the databases for research, all studies should get the IRB permission. The institutional review board of China Medical University approved this study (IRB No.: CMUH 103-REC3–109).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Hsiu-Ling Huang, Email: hmling88@gmail.com.

Cheng-Chin Pan, Email: scorpius051@gmail.com.

Yu-Fen Hsiao, Email: elisa8897@gmail.com.

Ming-Chih Chen, Email: hendry97@gmail.com.

Chuan-Yu Kung, Email: kama@pnhb.mohw.gov.tw.

Pei-Tseng Kung, Email: ptkung@asia.edu.tw.

Wen-Chen Tsai, Phone: +886-422073070, Email: wtsai@mail.cmu.edu.tw.

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