Abstract
The aim of present study was to explore the relationships between osteopenia and dyslipidemia, glycemic levels or blood pressure in postmenopausal Chinese women. A total of 4080 women aged 42–85 years were enrolled in this cross-sectional study, which was nested in an ongoing longitudinal (REACTION) study. Calcaneus quantitative ultrasound (QUS) was performed and QUS T score was calculated to assess bone mineral density. Osteopenia was defined as a T score ≤−1.0. The relationship between osteopenia and dyslipidemia, glycemic levels or blood pressure was investigated. The prevalence of osteopenia was significantly lower in subjects with systolic blood pressure (SBP) ≥140 mmHg, fasting blood glucose (FBG) ≥8.0 mmol/L, postprandial blood glucose (PBG) ≥15.0 mmol/L, hemoglobin A1c (HbA1C) 6.5–7.5 %, HbA1C ≥7.5 %. These relationships remained significant after controlling for multiple factors. Moreover, significant trend between osteopenia and SBP, FBG, PBG and HbA1C was observed in women. In contrast, no significant associations between osteopenia and diastolic blood pressure (DBP), total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) were found, and no significant trend relationship between osteopenia and DBP, TC, TG, HDL-C, LDL-C was found in postmenopausal Chinese women. The present study showed a relationship between SBP, FBG, PBG, HbA1C and osteopenia in postmenopausal Chinese women, while no significant relationship was observed between dyslipidemia, DBP and osteopenia, even after controlling for multiple confounding factors.
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Introduction
Osteoporosis and its related fractures are one of the major factors of disability and death in elderly people [1]. The World Health Organization (WHO) estimates that 30 % of all postmenopausal women have osteoporosis [2]. Osteoporosis in women following menopause is a major health problem that affects up to 50 % of postmenopausal women [3]. It was found that, in postmenopausal women living in Beijing, there was an almost tenfold increase in vertebral fractures rates with age from 3.9 % at ages 50–59 years to 31.2 % (21.8–40.6 %) at age 80 years and older, and among them 42 % had two or more fractures [4]. The best way to deal with osteoporosis is to find osteopenia and treat it before the disease progresses. Osteopenia, cardiovascular diseases (CVD) and diabetes are very common age-related disorders in postmenopausal women and usually coexist in the same individual with aging. Blood pressure, dyslipidemia and diabetes are risk factors for CVD and diabetes. However, the relationship between these metabolic parameters and osteopenia is still unclear. The aim of this cross-sectional study in Beijing China was to determine whether independent relationships exist between osteopenia and dyslipidemia, glycemic levels or blood pressure. A better understanding of this relation may provide new opportunities for early intervention and may, ultimately, help prevent the bone loss in postmenopausal women.
Materials and methods
Participants and measures
The present QUS study was nested in an ongoing longitudinal (REACTION) study which was designed to investigate the association of T2DM and pre-diabetes with the risk of cancer in the Chinese population, described previously [5]. All permanent residents of Jinding communities of Beijing, China, aged 40 years and older, were invited to participate. Recruitment was performed by local resident associations and was conducted in the primary health care center located at this community. All investigators received extensive training relative to the study questionnaire and outcome measures before conducting the investigation. A total of 8400 individuals were registered between March and December, 2012. A total of 4080 postmenopausal women (age range 42–85 years) were enrolled in this study and signed the informed consents (Fig. 1). The study protocol was approved by the Committee on Human Research at Rui-Jin Hospital affiliated to School of Medicine, Shanghai Jiao Tong University.
Bone status data were obtained using the quantitative ultrasound (QUS) bone densitometer at the left calcaneus. QUS (Sahara, Hologic, USA) was used to measure the following indices: speed of sound (SOS, m/s); broadband ultrasound attenuation (BUA, dB/MHz); stiffness or the quantitative ultrasound index (QUI); and T score. The T score was produced by comparing the reference database through the built-in microprocessor. All the participants were checked by the same trained physician and same device. The QUS was calibrated in accordance with the manufacturer’s recommendations and before measurement each day.
Women with a T score of ≤−1.0 were classified as osteopenia according to the WHO definition of osteoporosis [6]. Then participants were classified into two groups: the non-osteopenia group, defined as a T score of >−1.0; and the osteopenia group, defined as a T score of ≤−1.0.
All participants received comprehensive examinations that included a detailed questionnaire, anthropometric measurement, a standard 75 g oral glucose tolerance test and blood collection.
The self-administered questionnaire covered history of diabetes, hypertension, cardiovascular diseases (CVD, including myocardial infraction, stoke and coronary heart disease), alcohol intake, smoking habits, physical activity. Alcohol intake was classified as either consumption nearly/more than once a week currently or not; smoking habit was defined as either smoking more once a day or not. Physical activity was defined as engaging in sports more than once a week. BMI was calculated as body weight in kilograms divided by body height in meters squared (kg/m2).
Blood samples were collected by venipuncture. All participants received an oral glucose tolerance test and were told to fast for at least 10 h before the test. Plasma glucose, serum triglycerides (TG), total cholesterol (TC), HDL cholesterol (HDL-C) and LDL cholesterol (LDL-C) were measured using an autoanalyzer (Cobas 8000 modular analyzer series, Roche Diagnostics, Basel, Switzerland). Hemoglobin A1C (HbA1C) was determined by high-performance liquid chromatography using the VARIANT II Hemoglobin Testing System (Tosoh Corporation, Tokyo, Japan). HbA1C was measured together in the same device.
Statistical analysis
Statistical analysis was performed using SPSS software, version 19.0 (IBM, Chicago, IL). All continuous variables are presented as mean values and standard deviation (SD). The two-sample t test was used to compare the differences in baseline characteristics for all continuous variables. The differences in the proportions of the characteristics of the studied subjects were tested by Chi-square test. Then DBP was divided into <80, 80–89, ≥90 mmHg; SBP into <120, 120–140, ≥140 mmHg; TC into ≤4.14 mmol/L (160 mg/dL), 4.15–5.19 mmol/L (200 mg/dL), 5.19–6.22 mmol/L (240 mg/dL), >6.22 mmol/L; TG into <1.70 mmol/L (150 mg/dL), 1.70–2.83, ≥2.83 mmol/L (250 mg/dL); HDL-C into <1.03 mmol/L (40 mg/dL), 1.03–1.55 mmol/L, ≥1.55 mmol/L (60 mg/dL); LDL-C into <3.37 mmol/L (130 mg/dL), 3.37–4.14, ≥4.14 mmol/L (160 mg/dL); HbA1C into <6.50, 6.50–7.50, ≥7.50 mmol/L; FPG into <6.1, 6.1–7.0, 7.0–7.9, ≥8.0 mmol/L; PPG into <11.1, 11.1–13.0 mmol/L, 13.0–14.9, ≥15.0 mmol/L. The odds ratios (ORs) with 95 % confidence intervals (CIs) for low BMD were estimated by conducting logistic regression analyses to test the relationship between low BMD and TC, LDL-C, HDL-C, TG, HbA1C, FPG, PPG, SBP, DBP (all used as categorical variables). Multiple factors were considered, including age, physical activity, smoking, alcohol consumption, menopause age and BMI. The model was adjusted for these multiple confounding factors. Reported values were the multivariable-adjusted means and 95 % CIs. In all analyses, P < 0.05 was considered to be statistically significant.
Ethics statement
The study was nested in an ongoing longitudinal (REACTION) study, which is supported by the Chinese Society of Endocrinology and guided by Rui-Jin Hospital affiliated to School of Medicine, Shanghai Jiao Tong University. All procedures used in this study followed the institutional guidelines. The study protocol was approved by the Committee on Human Research at Rui-Jin Hospital affiliated to School of Medicine, Shanghai Jiao Tong University, and the informed consents were given by all study participants [5].
Results
Characteristics of the study subjects are shown in Table 1. A total of 4080 postmenopausal women (age range 42–85 years) were included in this study. The prevalence of osteopenia was 69.5 %. No significant differences between women with or without osteopenia were observed in regard to WC, TC, TG, LDL-C, SBP, FPG, PPG, HbA1C, physical activity, smoking status or alcohol consumption.
The group with osteopenia comprised 11.8 % patients with CVD, 43.8 % with hypertension, 21.9 % with type 2 diabetes mellitus and 11.3 % with a history of fracture. Women with osteopenia were older at enrollment (P < 0.001), had lower BMI (P < 0.001) and DBP (P < 0.001), had earlier menopause age (P < 0.001) and had higher HDL-C (P = 0.007) than those without osteopenia. In addition, women with osteopenia were more likely to have CVD (P = 0.014), hypertension (P = 0.034) and a fracture history (P < 0.001) than those without osteopenia.
We then examined which parameters relevant to CVD and diabetes are independently associated with osteopenia. Multiple logistic regression analysis with parameters relevant to CVD (including previous diagnosis of CVD, DBP, SBP, TC, TG, HDL-C and LDL-C), diabetes (including diagnosed T2DM, FPG, PPG and HbA1C) as independent categorical variables and corrected for confounding factors (Model 1 included age at enrollment for adjustment; Model 2 included the covariate in model 1 and also physical activity, smoking, alcohol consumption, age at menopause; Model 3 included the covariates in model 2 and also BMI for adjustment) was conducted.
Tables 2 and 3 show adjusted ORs for osteopenia according to the classification of parameters relevant to CVD or diabetes. The prevalence of osteopenia was significantly lower in subjects with SBP ≥ 140 mmHg (age-adjusted OR 0.719 [95 % CI 0.593, 0.871]); FBG 7.0–7.9 mmol/L (0.659 [0.473, 0.918]); FBG ≥ 8.0 mmol/L (0.720 [0.541, 0.958]); PBG ≥ 15.0 mmol/L (0.690 [0.513, 0.926]); HbA1C 6.5–7.5 % (0.638 [0.495, 0.824]); HbA1C ≥ 7.5 % (0.715 [0.533, 0.960]). These relationships remained significant even after controlling for multiple factors (SBP ≥ 140 mmHg: multivariable-adjusted OR 0.781 [95 % CI 0.636, 0.959]; FBG 7.0–7.9 mmol/L: 0.709 [0.506, 0.994]; FBG ≥ 8.0 mmol/L: 0.726 [0.544, 0.968]; PBG ≥ 15.0 mmol/L: 0.700 [0.520, 0.941]; HbA1C 6.5–7.5 %: 0.677 [0.523, 0.877] and HbA1C ≥ 7.5 %: 0.723 [0.538, 0.972]). Moreover, significant trend between osteopenia and SBP, FBG, PPG and HbA1C was observed in women. In contrast, no significant associations between osteopenia and DBP, TC, TG, HDL-C, LDL-C were found, and no significant trend relationship between osteopenia and DBP, TC, TG, HDL-C, LDL-C was found in postmenopausal Chinese women.
Discussion
In this study, we evaluated relationships between osteopenia and diabetes and cardiovascular risks in postmenopausal Chinese women. Decreasing prevalence of osteopenia was shown to be associated with rising SBP, FPG, PPG and HbA1C. However, no significant associations were found between osteopenia and DBP, TC, TG, HDL-C and LDL-C.
Researches on the relationship between blood pressures and BMD have generated controversial findings. In the present study, SBP and the prevalence of osteopenia have positive correlation which is difficult to explain. This finding was supported by Hanley et al. [7], who found a positive relation between hypertension and lumbar spine, femoral neck and trochanter BMD. Lidfeldt et al. [8] study also demonstrated that the wrist BMD was associated with systolic and diastolic blood pressure in postmenopausal women. However, one study reported higher blood pressure in elderly white women is associated with increased bone loss at the femoral neck [9]. Another study reported no relationship between proximal femoral BMD and hypertension, which was found in postmenopausal non-Hispanic white, non-Hispanic black and Mexican–American women [10]. Studies data have yielded conflicting results, perhaps because of the limited data available, the technological diversity of the BMD devices, the different populations studied, the various age ranges and the variety of sites measured. Taken together, the potential mechanisms are complex. None of these authors could offer a satisfactory physiopathological explanation for positive findings. On the contrary, in other studies an inverse relation between hypertension and BMD was explained via abnormal calcium metabolism, secondary parathyroid hormone secretion or sodium intake [11–13].
Serum lipids and lipoproteins are also argued to be associated with BMD. Serum lipid levels have a prominent role in the pathogenesis of CVD. Some [14, 15] observational studies found that treatment of CVD with statins, lipid-lowering drugs, was associated with a significantly reduced fracture risk and increased BMD. Therefore, the question arises whether lipids are associated with the pathogenesis of low BMD. One study reported that BMD was inversely correlated with low HDL-C and elevated TG levels in South Korean men [16]. However, an absent [17, 18] or even a positive [19] relationship has also been reported. In the present study, no significant associations were found to be related to low BMD.
Regarding the relationships between low BMD and parameters relevant to type 2 diabetes mellitus (T2DM), despite a high incidence of fragility fracture in T2DM patients, data on bone change in T2DM were conflicting, ranging from decrease, no change or increase in BMD [20–22]. In the present study, decreasing prevalence of osteopenia was shown to be associated with rising FPG, PPG and HbA1C. The result suggests that bone change in diabetic women may be more complicated and need alternative marker to predict the fracture risk.
There are several limitations in the present study. First, the causal relationship between SBP, FPG, PPG, HbA1C and osteopenia cannot be established based on the nature of our cross-sectional study. Second, we used calcaneal quantitative ultrasound (QUS) as a measurement rather than dual X-ray absorptiometry (DXA) to assess BMD, although meta-analysis of prospective studies shows that QUS using validated devices predicts risk of different types of fracture with similar performance across different devices and in elderly men and women. Finally, we did not exclude subjects who underwent pharmaceutical therapies for CVD, hypertension and T2DM, which might affect bone metabolism. Further studies are needed to fully ascertain the mechanisms underlying the association between osteopenia and diabetes.
In conclusion, the present study showed a relationship between SBP, FBG, PPG, HbA1C and osteopenia in postmenopausal Chinese women, while no significant relationship was observed between dyslipidemia, DBP and osteopenia, even after controlling for multiple confounding factors. Bone change in diabetic women may be more complicated and need alternative marker to predict the osteopenia.
Abbreviations
- QUS:
-
Calcaneus quantitative ultrasound
- BMI:
-
Body mass index
- CVD:
-
Cardiovascular disease
- SBP:
-
Systolic blood pressure
- DBP:
-
Diastolic blood pressure
- FBG:
-
Fasting blood glucose
- PBG:
-
Postprandial blood glucose
- HbA1c:
-
Hemoglobin A1c
- SBP:
-
Systolic blood pressure
- SOS:
-
Speed of sound
- BUA:
-
Broadband ultrasound attenuation
- QUI:
-
Quantitative ultrasound index
- HDL-C:
-
High-density lipoprotein cholesterol
- LDL-C:
-
Low-density lipoprotein cholesterol
- OR:
-
Odds ratio
- CI:
-
Confidence interval
- TC:
-
Total cholesterol
- TG:
-
Triglycerides
References
Marshall D, Johnell O, Wedel H. Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures. BMJ. 1996;312:1254–9.
Kanis JA. Assessment of fracture risk and its application to screening for postmenopausal osteoporosis: synopsis of a WHO report. WHO Study Group. Osteoporos Int. 1994;4:368–81.
Sambrook P, Cooper C. Osteoporosis. Lancet. 2006;367:2010–8.
Ling X, Cummings SR, Mingwei Q, et al. Vertebral fractures in Beijing, China: the Beijing Osteoporosis Project. J Bone Miner Res. 2000;15:2019–25.
Ning G. Risk evaluation of cAncers in Chinese diabeTic individuals: a lONgitudinal (REACTION) study. J Diabetes. 2012;4:172–3.
Kanis JA, Melton LJ 3rd, Christiansen C, Johnston CC, Khaltaev N. The diagnosis of osteoporosis. J Bone Miner Res. 1994;9:1137–41.
Hanley DA, Brown JP, Tenenhouse A, et al. Associations among disease conditions, bone mineral density, and prevalent vertebral deformities in men and women 50 years of age and older: cross-sectional results from the Canadian Multicentre Osteoporosis Study. J Bone Miner Res. 2003;18:784–90.
Lidfeldt J, Holmdahl L, Samsioe G, et al. The influence of hormonal status and features of the metabolic syndrome on bone density: a population-based study of Swedish women aged 50 to 59 years. The women’s health in the Lund area study. Metabolism. 2002;51:267–70.
Cappuccio FP, Meilahn E, Zmuda JM, Cauley JA. High blood pressure and bone-mineral loss in elderly white women: a prospective study. Study of Osteoporotic Fractures Research Group. Lancet. 1999;354:971–5.
Mussolino ME, Gillum RF. Bone mineral density and hypertension prevalence in postmenopausal women: results from the Third National Health and Nutrition Examination Survey. Ann Epidemiol. 2006;16:395–9.
Orwoll ES, Bevan L, Phipps KR. Determinants of bone mineral density in older men. Osteoporos Int. 2000;11:815–21.
Woo J, Kwok T, Leung J, Tang N. Dietary intake, blood pressure and osteoporosis. J Hum Hypertens. 2009;23:451–5.
Jeon YK, Lee JG, Kim SS, et al. Association between bone mineral density and metabolic syndrome in pre- and postmenopausal women. Endocr J. 2011;58:87–93.
Chan KA, Andrade SE, Boles M, et al. Inhibitors of hydroxymethylglutaryl-coenzyme A reductase and risk of fracture among older women. Lancet. 2000;355:2185–8.
Rejnmark L, Vestergaard P, Mosekilde L. Statin but not non-statin lipid-lowering drugs decrease fracture risk: a nation-wide case-control study. Calcif Tissue Int. 2006;79:27–36.
Kim YH, Nam GE, Cho KH, et al. Low bone mineral density is associated with dyslipidemia in South Korean men: the 2008–2010 Korean National Health and Nutrition Examination Survey. Endocr J. 2013;60:1179–89.
Hernández JL, Olmos JM, Pariente E, et al. Metabolic syndrome and bone metabolism: the Camargo Cohort study. Menopause. 2010;17:955–61.
Kim YH, Cho KH, Choi YS, et al. Low bone mineral density is associated with metabolic syndrome in South Korean men but not in women: the 2008–2010 Korean National Health and Nutrition Examination Survey. Arch Osteoporos. 2013;8:142. doi:10.1007/s11657-013-0142-3.
Arikan DC, Coskun A, Ozer A, Kilinc M, Atalay F, Arikan T. Plasma selenium, zinc, copper and lipid levels in postmenopausal Turkish women and their relation with osteoporosis. Biol Trace Elem Res. 2011;144:407–17.
Yaturu S, Humphrey S, Landry C, Jain SK. Decreased bone mineral density in men with metabolic syndrome alone and with type 2 diabetes. Med Sci Monit. 2009;15:CR5–9.
Petit MA, Paudel ML, Taylor BC, et al. Bone mass and strength in older men with type 2 diabetes: the Osteoporotic Fractures in Men Study. J Bone Miner Res. 2010;25:285–91.
Yamaguchi T, Kanazawa I, Yamamoto M, et al. Associations between components of the metabolic syndrome versus bone mineral density and vertebral fractures in patients with type 2 diabetes. Bone. 2009;45:174–9.
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This work was supported in part by National Science and Technology Major Project [2011ZX09307-001-08].
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Sun, Q., Zheng, Y., Chen, K. et al. Osteopenia is associated with glycemic levels and blood pressure in Chinese postmenopausal women: a cross-sectional study. Clin Exp Med 17, 85–91 (2017). https://doi.org/10.1007/s10238-015-0397-7
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DOI: https://doi.org/10.1007/s10238-015-0397-7