Download as pdf or txt
Download as pdf or txt
You are on page 1of 6

J Nutr Health Aging.

2018;22(2):216-221
© Serdi and Springer-Verlag International SAS, part of Springer Nature

TEA CONSUMPTION IS ASSOCIATED WITH INCREASED BONE STRENGTH


IN MIDDLE-AGED AND ELDERLY CHINESE WOMEN
H. HUANG1, G.-Y. HAN1, L.-P. JING, Z.-Y. CHEN, Y.-M. CHEN, S.-M. XIAO
Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-Sen University, Guangzhou 510080, China. 1. These authors contributed equally to this work.
Corresponding author: Su-Mei Xiao and Yu-Ming Chen, Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-Sen University, 74 Zhongshan Er Road,
Guangzhou 510080, P. R. China, Tel: 86-20-87330151 and 86-20-87330605, Fax: 86-20-87330446, Email: xiaosm3@mail.sysu.edu.cn and chenyum@mail.sysu.edu.cn

Abstract: Objectives: Previous studies found that tea consumption was related to a reduction in the risks of some
chronic diseases, but limited data are available on bone health. This study aimed to examine the associations
of tea consumption with hip bone strength in Chinese women. Design: Cross-sectional study. Setting: The
participants were from the ongoing Guangzhou Nutrition and Health Study. This was a cohort study started
in 2008. The examination data conducted between June 2010 and December 2013 were used. Participants: A
total of 1,495 Chinese women aged more than 40 years were included. Measurements: Tea consumption, socio-
demographic information and lifestyle habits were collected by a face-to-face questionnaire. Hip bone mineral
density (BMD) and geometric parameters, i.e. cross-sectional area (CSA), section modulus (Z) and buckling
ratio (BR), were generated by dual-energy X-ray absorptiometry. The associations of tea consumption with bone
phenotypes were detected by analysis of covariance and multiple linear regression models after adjusting for
age, body mass index, years since menopause, physical activity, dietary-protein intake, dietary-calcium intake,
calcium tablet intake, drinking status and smoking status. Results: Tea drinkers (n = 732) had approximately
1.9% higher BMD (p < 0.05) and 3.6% lower BR (p < 0.05) than non-tea drinkers (n = 763). The dose-response
relationships of BMD, BR or CSA with total tea consumption were identified (p-trend < 0.05). Tea drinking was
found to be a significant and independent predictor of BMD (β = 0.068, p < 0.05) or BR (β = -0.079, p < 0.05).
Conclusion: Tea consumption was associated with increased bone strength in middle-aged and elderly Chinese
women.

Key words: Osteoporosis, tea consumption, bone mineral density, bone geometry.

Introduction production, and most of it is consumed in China and Japan.


Oolong tea, mainly cultivated in southern China, constitutes
Osteoporosis is a progressive systemic skeletal disorder ~2% of the total tea production (6). In addition, there is a
characterised by low bone mass and microarchitectural kind of post-fermented tea: dark tea, e.g. Pu-er tea, which is
deterioration of bone tissue that leads to a decrease in bone a well-known traditional tea in China (7). Previous studies
strength and an increased risk of fracture. With the aging of the found that tea drinking was related to a reduction in the risks
population, osteoporosis has become a serious public health of neurocognitive disorders, diabetes, cardiovascular diseases,
problem worldwide. Women are around four times more likely cancers and some other chronic disorders (8-11). Recently,
to develop osteoporosis than men because of their generally studies also indicated that tea may affect bone metabolism.
lighter and thinner bones in conjunction with a decrease in The polyphenols in tea may inhibit osteoclasts and stimulate
their estrogen levels after menopause (1). Approximately half osteoblasts by decreasing reactive oxygen species and pro-
of all women over 50 years old suffer an osteoporotic fracture inflammatory mediators (12, 13).
sometime in their life (2). Bone mineral density (BMD) and Some studies have detected the relationship between tea
bone geometry are two major determinants of bone strength and consumption and BMD, but the results are controversial.
two independent predictors in assessing the risk of osteoporotic Habitual tea consumption was found to have a positive effect
fracture (3, 4). Investigation of both is indispensable to improve (14, 15), no effect (16) or even a weak inverse effect (17, 18)
the accuracy of fracture risk prediction and the understanding of on BMD. In addition, studies about the effect of tea on bone
bone strength and osteoporosis. geometry were limited. Therefore, in this study, we aimed to
Tea, which is derived from Camellia sinensis, is one of the evaluate the associations of tea consumption with both BMD
most frequently consumed beverages throughout the world. and bone geometry in middle-aged and elderly Chinese women.
More than 30 countries cultivate tea, with an annual production
of 3.8 million tons (5). According to the degree of fermentation, Methods
tea is mainly classified into three categories: green tea (non-
fermented), oolong tea (semi-fermented) and black tea Subjects
(fermented). Black tea constitutes ~78% of the world’s tea The participants of this study were from the ongoing
production and is one of the most popular kinds consumed in Guangzhou Nutrition and Health Study, a cohort study started
Western countries. Green tea accounts for ~20% of the total in 2008 that was designed to assess the determinants of
Received October 25, 2016 Published online March 1, 2017, http://dx.doi.org/10.1007/s12603-017-0898-z
Accepted for publication January 4, 2017
216
J Nutr Health Aging
Volume 22, Number 2, 2018

THE JOURNAL OF NUTRITION, HEALTH & AGING©

osteoporosis and cardiometabolic outcomes (19). The data for BMD, CSA, Z and BR at the FN, respectively.
from the first follow-up examination conducted between June
2010 and December 2013 were used. Women over 40 years of Assessments of covariates
age were recruited by posting local advertisements, by sending Dietary intake was assessed using a quantitative and 81-item
invitation letters to residential buildings, by giving health talks food frequency questionnaire (22). For each food item, the
or from referrals in the local community. All of the participants subjects were asked how often (never, per year, per month,
were residents of urban Guangzhou, China for over 5 years. per week and per day) they had consumed over the past year.
Excluded were subjects with chronic diseases or conditions Dietary nutrients and total energy intake were calculated based
that might affect bone mass and metabolism, such as having a on the China Food Composition Table (23). Calcium tablet
history of metabolic bone disorder or left hip fracture, chronic intake was recorded if the subjects had taken the calcium
medical illness, endocrine diseases including hyperthyroidism, supplement over 30 times within the past year. The subjects
medications that might affect bone and calcium metabolism, who smoked more than 100 cigarettes in their lifetime were
bilateral oophorectomy, major gastrointestinal operations, defined as active smokers. Those who lived or worked in a
premature menopause at age < 40 years, or being prescribed room with an individual who smoked more than one cigarette or
medicines such as calcitonin, bisphosphonates, selective more than 5 minutes per day for at least one year were defined
estrogen receptor modulators and active vitamin D3 as passive smokers. Drinkers were individuals that had ever
metabolites. Ultimately, 1,495 women with bone measurement drunk alcoholic beverages at least once a week for more than
data and who responded to the questionnaires were included in 6 months. The daily physical activity including occupational
this study. The study was approved by the Ethics Committee activities, leisure-time activities and household-chores but
of the School of Public Health of Sun Yat-Sen University, and except for sitting and lying, was evaluated using metabolic
written informed consent was obtained from each participant. equivalent (MET) hours per day (24). Weight (kg) and height
(cm) were measured at the same time, and body mass index
Tea consumption (BMI, kg/m2) was calculated.
All of the participants completed a face-to-face interview
performed by trained staff using a structured questionnaire. Statistical analysis
Socio-demographic information, history of disease and Descriptive statistics were determined for all variables
medications, lifestyle habits and reproductive histories were according to their distribution. They are presented as the
collected. There were four questions on tea drinking. The first mean and standard deviation (SD), median and interquartile
question was: “Have you drunk tea twice or more times per range, or number (n) and percentage. Differences in bone
week in the past year?” Subjects who answered “yes” were phenotypes between tea drinkers and non-tea drinkers were
coded as tea drinkers and then completed questions on the assessed by using analysis of covariance. Further comparisons
number of times of tea drinking per week (times), the total were conducted among subgroups classified by total tea
consumed quantities (kg) of tea and the types of tea (i.e. green consumption or the times of tea drinking per week. Moreover,
tea, black tea, oolong tea and dark tea) over the past year. the assessments and inferences of the relationships between
tea consumption and bone phenotypes were conducted using
BMD and bone geometry multiple linear regression models. All analyses were adjusted
The BMD (g/cm2) at the femur neck (FN) of the left hip for confounding factors including age, BMI, years since
was measured by dual-energy X-ray absorptiometry (DXA, menopause (YSM), physical activity, dietary-protein intake,
Discovery W; Hologic Inc., Waltham, MA, USA). DXA images dietary-calcium intake, calcium tablet intake, drinking status
of the hip proximal femur were reprocessed with the Hip and smoking status. The dietary nutrient intakes were adjusted
Structure Analysis (HSA) program included in the APEX for total energy intake using a residual method. Statistical
software (v3.2, Hologic Inc.) (20). Three HSA-generated analyses were performed with SPSS 20.0 (SPSS, Inc., Chicago,
bone geometry parameters, i.e. cross-sectional area (CSA, IL, USA). A p < 0.05 in a two-tailed test was considered
cm 2), section modulus (Z, cm 3) and buckling ratio (BR), significant.
were analysed in this study. CSA is the amount of (cortical
equivalent) bone surface area in the cross-section after Results
excluding all of the trabecular and soft tissue spaces, and it
indicates the resistance to a loading force directed along the General characteristics of the participants
bone axis (21). Z indicates the bending strength for maximum The basic information of the participants is shown in Table
bending stress in the image plane. BR is the relative thickness 1. The median age of the 1,495 women was 58 years old, and
of the narrow neck cortex and represents an estimate of the the median YSM was 8 years. Among all subjects, 732 (49.0%)
cortical stability in buckling. An increase in BR indicates were tea drinkers and 763 (51.0%) were non-tea drinkers.
that the bone is becoming less stable and weaker. The in-vivo For the 732 tea drinkers, the median values of the times of
coefficients of variation were 1.92%, 1.55%, 2.99% and 4.62% tea drinking per week and total tea consumption over the past

217
J Nutr Health Aging
Volume 22, Number 2, 2018

TEA CONSUMPTION IS ASSOCIATED WITH INCREASED BONE STRENGTH IN MIDDLE-AGED

year were 7 times and 4.2 kg, respectively. The numbers of Differences in bone phenotypes between tea drinkers and
individuals who drank green tea, black tea, oolong tea and non-tea drinkers
dark tea were 109 (14.9%), 110 (15.0%), 229 (31.3%) and 284 Table 2 shows the differences in the mean values of BMD,
(38.8%), respectively. The medium values of dietary nutrient BR, CSA and Z between tea drinkers and non-tea drinkers. Tea
intakes were around 65.90 g/d and 575.03 mg/d for protein and drinkers had a higher BMD (p = 0.032) and a lower BR (p =
calcium, respectively. Approximately 29.6% of the participants 0.005) than non-tea drinkers after adjusting for confounding
had taken calcium tablets more than 30 times in the past year, factors, including age, BMI, YSM, physical activities, dietary-
28.5% were active or passive smokers and 3.3% were alcohol protein intake, dietary-calcium intake, calcium tablet intake,
drinkers. The mean (SD) values of BMD, BR, CSA and Z of drinking status and smoking status. For CSA and Z, the mean
all subjects were 0.844 (0.144) g/cm2, 10.929 (2.784), 2.434 values were all consistently higher in tea drinkers than non-
(0.394) cm2 and 1.105 (0.224) cm3, respectively. tea drinkers, although the differences were not statistically
significant in this sample (p > 0.05). The mean differences
Table 1 in BMD, BR, CSA and Z between tea drinkers and non-tea
Basic characteristics of studied women (n = 1,495) drinkers were 0.016 g/cm2 (1.9%), -0.400 (3.6%), 0.028 cm2
(1.2%) and 0.011cm3 (1.0%), respectively.
Variable Mean ± SD / median (25th~75th)
/ n (%) Table 2
Age (year) 58.0 (55.0~62.0) Differences of BMD and bone geometric parameters between
Height (cm) 155.07 ± 5.37 the groups of non-tea drinker and tea drinker (n = 1,495)
Weight (kg) 56.16 ± 8.33
Variable Non-tea drinkers Tea drinkers p-value
BMI (kg/m2) 23.34 ± 3.20
(n = 763) (n = 732)
YSM (year) 8.0 (5.0~12.0)
BMD (g/cm2) 0.836 (0.005) 0.852 (0.005) 0.032
Physical activities (MET · h/d) a 33.18 (30.31~37.24) BR 11.125 (0.100) 10.725 (0.102) 0.005
Energy intake (kcal/d) 1505.59 (1264.86~1777.62) CSA (cm2) 2.420 (0.014) 2.448 (0.014) >0.050
Dietary-protein intake (g/d) 65.90 (52.95~80.52) Z (cm3) 1.100 (0.008) 1.111 (0.008) >0.050
Dietary-calcium intake (mg/d) 575.03 (437.40~715.85) Values were expressed as mean and standard error. Bone phenotypes were adjusted for
Calcium tablets intake (n, %) 443 (29.6) age, body mass index, years since menopause, physical activities, dietary-protein intake,
dietary-calcium intake, calcium tablet intake, drinking status and smoking status. BMD,
Smoker (n, %) 426 (28.5) bone mineral density; BR, buckling ratio; CSA, cross sectional area; Z, section modulus.
Alcohol drinker (n, %) 49 (3.3)
Tea drinker (n, %) 732 (49.0) Dose-response relationships of tea consumption with bone
phenotypes
Times of tea drinking (times/week) 7.0 (3.0~7.0)
To assess the dose-response relationships of tea consumption
Total tea consumption (kg) 4.2 (2.0~8.3)
with bone phenotypes, the subjects were further categorised into
Types of tea several subgroups by their tea drinking habits. As displayed
Green tea (n, %) 109 (14.9) in Table 3 and Figure 1, there were significant trends of
Black tea (n, %) 110 (15.0) increased BMD, CSA (p = 0.006 and 0.042) and decreased BR
Oolong tea (n, %) 229 (31.3) (p = 0.003) with the larger quantity of total tea consumption.
Compared with those who consumed less than 1.0 kg over the
Dark tea (n, %) 284 (38.8)
past year, the individuals who consumed more than 4.2 kg of
BMD (g/cm ) 2
0.844 ± 0.144
tea had approximately 3.0% higher BMD, 4.7% lower BR and
BR 10.929 ± 2.784 2.0% higher CSA, respectively. In the 732 tea drinkers, the
CSA (cm2) 2.434 ± 0.394 differences in bone phenotypes among the subgroups classified
Z (cm3) 1.105 ± 0.224 by the types of tea (green, black, oolong and dark tea) were not
Values were presented as mean ± standard deviation (SD), median and interquartile significant (p > 0.05).
range (25th~75th), or number (n) and percentage (%). a. Physical activities including
daily occupational activities, leisure time and household chores, were evaluated using
metabolic equivalent hours per day (MET · h/d). BMI, body mass index; YSM, years
Contributions of tea consumption to bone phenotypes
since menopause; BMD, bone mineral density; BR, buckling ratio; CSA, cross sectional Multiple linear regression models were then performed
area; Z, section modulus. to evaluate the contributions of tea consumption to bone
phenotypes (Table 4). The results showed that tea consumption
was a significant predictor of BMD and BR independent of
age, BMI, YSM, physical activities, dietary-protein intake,
dietary-calcium intake, calcium tablet intake, drinking status

218
J Nutr Health Aging
Volume 22, Number 2, 2018

THE JOURNAL OF NUTRITION, HEALTH & AGING©

Table 3
Results of dose-response relationships of bone phenotypes with the studied variables of tea consumption (n = 1,495)

BMD (g/cm2) BR CSA (cm2) Z (cm3)


Total tea consumption (kg)
<1.0 (n = 763) 0.836 (0.005) 11.125 (0.100) 2.420 (0.014) 1.099 (0.008)
1.0~4.2 (n = 373) 0.843 (0.007) 10.847 (0.141) 2.428 (0.019) 1.100 (0.011)
>4.2 (n = 359) 0.861 (0.007) 10.597 (0.145) 2.470 (0.020) 1.122 (0.012)
p-trend 0.006 0.003 0.042 >0.050
Times of tea drinking per week
≤1 (n = 763) 0.836 (0.005) 11.125 (0.100) 2.420 (0.014) 1.099 (0.008)
2~6 (n = 309) 0.851 (0.008) 10.642 (0.155) 2.435 (0.021) 1.096 (0.012)
≥7 (n = 423) 0.853 (0.007) 10.788 (0.135) 2.458 (0.018) 1.121 (0.011)
p-trend >0.050 >0.050 >0.050 >0.050
Values were expressed as mean and standard error. Bone phenotypes were adjusted for age, body mass index, years since menopause, physical activities, dietary-protein intake, dietary-
calcium intake, calcium tablet intake, drinking status and smoking status. BMD, bone mineral density; BR, buckling ratio; CSA, cross sectional area; Z, section modulus

Table 4
Results of multiple linear regression analysis of tea consumption variables with BMD and bone geometric parameters (n = 1,495)

Variable Tea drinking (yes/no) Total tea consumption (kg)


Standardized β p-value Standardized β p-value
BMD (g/cm2) 0.054 0.032 0.068 0.007
BR -0.072 0.005 -0.079 0.002
CSA (cm2) 0.035 >0.050 0.048 >0.050
Z (cm3) 0.025 >0.050 0.037 >0.050
Bone phenotypes were adjusted for age, body mass index, years since menopause, physical activities, dietary-protein intake, dietary-calcium intake, calcium tablet intake, drinking status
and smoking status. BMD, bone mineral density; BR, buckling ratio; CSA, cross sectional area; Z, section modulus.

and smoking status. The standardized regression coefficients of also observed to have a significant and negative dose-response
tea drinking and total tea consumption were 0.054 (p = 0.032) relationship with total tea consumption. Previous association
and 0.068 (p = 0.007) for BMD, -0.072 (p = 0.005) and -0.079 studies of tea consumption and bone geometric structure are
(p = 0.002) for BR, respectively. limited. Nonetheless, the findings from the animal model study
into the influence of tea on bone may be instructive. Chen et
Discussion al (26) observed that with the 12 weeks supplementation of
(-)-epigallocatechin-3-gallate (EGCG), a bioactive substance in
The associations of tea consumption-related variables with tea, the ovariectomy-induced osteopenic rats showed increased
hip BMD and bone geometry in middle-aged and elderly bone volume, trabecular number, and trabecular thickness and
Chinese women were evaluated in this study. The results decreased trabecular separation, which suggested the protective
showed that tea drinking was a protective factor for BMD and effects of EGCG on bone microarchitecture. Recently, Ng et
BR, and the habit of drinking tea could also be beneficial for the al (27) in 2,398 individuals aged more than 55 years found
other parameter of bone strength, i.e. CSA. that tea consumption was related to the better performance in
Our data suggested that tea drinking could maintain the physical function. In addition, a 6-month randomised placebo-
cortical stability and strength of bone. BR is the relative controlled trial conducted in postmenopausal osteoporotic
thickness of the narrow neck cortex and is an estimate of the women suggested that the polyphenols in tea could improve leg
cortical stability in buckling. Gnudi et al. evaluated the ability strength (28). These studies indirectly support the role of tea in
of bone structural parameters measured at the FN, i.e. CSA, Z promoting the stability and strength of bone.
and BR, to predict the risk of hip fracture. They found that BR The positive association between tea drinking and BMD at
was the best predictor, and its ability to predict fracture risk the hip was also observed in this study. This was consistent
was equal to that of FN BMD (25). In the present study, the with the findings in previous studies conducted in both Chinese
tea drinkers had lower BR than the non-tea drinkers. BR was and other populations (15). Hegarty et al (29) carried out
219
J Nutr Health Aging
Volume 22, Number 2, 2018

TEA CONSUMPTION IS ASSOCIATED WITH INCREASED BONE STRENGTH IN MIDDLE-AGED

a cross-section study in 1,256 Britain women aged 65-76 EGCG was shown to reduce the levels of excessive reactive
years. They observed that BMD in tea drinkers was around oxygen species, increase the activity of alkaline phosphatase,
3.0% greater than those who did not drink tea. A study in and up-regulate the expression of runt-related transcription
Taiwanese found that tea drinkers had an increased BMD factor 2 through the bone morphogenetic protein 2 signalling
than non-tea drinkers at the total body, hip regions and pathway, thus promoting the proliferation of osteoblasts and
lumbar spine, especially in tea drinkers with a larger quantity formation of bone (32). The chemical constituents differ for
of tea consumption (30). In this study, we also identified different types of tea with varied levels of fermentation (33).
the significant and positive trend of BMD with total tea The amount of EGCG was found to be much lower in other
consumption over the past year. In addition, a prospective types of tea than in green tea (34). Theaflavins and thearubigins
analysis in 1,027 Australian women found that after a 4-year are the representative substances in black tea. Recently, Das
follow-up, tea drinkers lost about 1.6% hip BMD, but non- et al (35) observed that the extract of black tea could protect
tea drinkers lost approximately 4.0% (31). All these results against ovariectomy-induced oxidative stress of mononuclear
supported that tea consumption was favorable for bone mass. cells and its associated progression of bone loss by reducing
the activated osteoclasts. In addition, studies also found that the
Figure 1 bioactive substances in oolong tea or Pu-er tea had the strong
The relative values of bone phenotypes of each subgroup of (a) antioxidative effects and the scavenging capacity of free radical
total tea consumption or (b) times of tea drinking per week to (36, 37).
the reference group The findings in this study might be generalisable to ordinary
urban middle-aged and elderly women in southern China. The
results were obtained from a considerable sample size of 1,495
women recruited from communities in Guangzhou city, with
consideration given to a relatively large range of confounding
factors and with good assessments of bone phenotypes.
Nonetheless, there were also several limitations. This study
only investigated the tea drinking habits of subjects over the
past year, which might not accurately reflect their long-term
habits of tea drinking. However, tea drinking is generally a
relatively stable habit, and Guangzhou is a city with a very
long history of tea culture and with a large proportion of tea
drinkers. Approximately half of the studied subjects were tea
drinkers, and the times of tea drinking per week and the total tea
consumption over the past year were highly correlated (r = 0.94,
p < 0.001). Thus, the present data might reflect the long-term
habits of tea drinking to some extent. Finally, this was a cross-
sectional study, and thus the findings cannot establish temporal
relationships or causality. A future longitudinal analysis of the
effects of tea consumption on bone strength will be of interest
when the ongoing cohort study is completed.
In summary, this study suggested a protective effect of tea
drinking on both bone mass and geometric structure in middle-
aged and elderly Chinese women. As tea is a traditional and
Vertical bars were the percentage differences of each sub-group relative to the group of popular beverage in China, its role in bone health merits further
total tea consumption < 1.0 kg (a) or times of tea drinking per week ≤ 1 time (b). Error
bars were the standard errors of the mean values. Values were adjusted for age, body mass investigations.
index, years since menopause, physical activities, dietary-protein intake, dietary-calcium
intake, calcium tablet intake, drinking status and smoking status. *p-trend < 0.05. BMD, Acknowledgments: This study was supported by the National Natural Science
bone mineral density; BR, buckling ratio; CSA, cross sectional area; Z, section modulus. Foundation of China (No. 81273049, 81400857), the Natural Science Foundation
of Guangdong Province (No.2014A030313132), and the 5010 Program for Clinical
Researches by Sun Yat-Sen University, Guangzhou, China (No. 2007032). We thank other
The bone-protective effects of tea may be attributed to team members for their contribution in the data collection.
the chemical compounds in it. Animal studies found that a
Conflicts of Interest: The authors declare no conflict of interest.
moderate intake of tea polyphenols could enhance bone strength
and quality (12). Tea catechins, including EGCG, epicatechin- Ethical standards: The experiments comply with the current laws of China in which
3-gallate, epigallocatechin and epicatechin, are the main they were performed. The protocol was approved by the Ethics Committee of the School of
Public Health of Sun Yat-Sen University.
components in tea polyphenols. These substances can benefit
bone via their antioxidant activities and their capability to
scavenge reactive oxygen species (12). As a potent antioxidant,

220
J Nutr Health Aging
Volume 22, Number 2, 2018

THE JOURNAL OF NUTRITION, HEALTH & AGING©

References 19. Cao Y, Wang C, Guan K, Xu Y, Su Y, Chen Y. Association of magnesium in serum


and urine with carotid intima-media thickness and serum lipids in middle-aged and
1. Looker AC, Johnston CJ, Wahner HW, et al. Prevalence of low femoral bone density elderly Chinese: a community-based cross-sectional study. Eur J Nutr. 2016; 55(1):
in older U.S. women from NHANES III. J Bone Miner Res. 1995; 10(5): 796-802. 219-226.
2. Li GW, Chang SX, Xu Z, Chen Y, Bao H, Shi X. Prediction of hip osteoporotic 20. Beck TJ. Extending DXA beyond bone mineral density: understanding hip structure
fractures from composite indices of femoral neck strength. Skeletal Radiol. 2013; analysis. Curr Osteoporos Rep. 2007; 5(2): 49-55.
42(2): 195-201. 21. Esenyel M, Ozen A, Esenyel CZ, Rezvani A, Sariyildiz MA, Ergin O. Hip Structural
3. LaCroix AZ, Beck TJ, Cauley JA, et al. Hip structural geometry and incidence of hip Changes and Fracture Risk in Osteopenia and Osteoporosis. The Eurasian Journal of
fracture in postmenopausal women: what does it add to conventional bone mineral Medicine. 2011; 43(2): 73-78.
density? Osteoporosis Int. 2010; 21(6): 919-929. 22. Zhang CX, Ho SC. Validity and reproducibility of a food frequency Questionnaire
4. Kaptoge S, Beck TJ, Reeve J, et al. Prediction of Incident Hip Fracture Risk by among Chinese women in Guangdong province. Asia Pac J Clin Nutr. 2009; 18(2):
Femur Geometry Variables Measured by Hip Structural Analysis in the Study of 240-250.
Osteoporotic Fractures. J Bone Miner Res. 2008; 23(12): 1892-1904. 23. Yang YX, Wang GY, Pan XC. China food composition tables. 1st ed. Beijing: Peking
5. Yang CS, Hong J. Prevention of Chronic Diseases by Tea: Possible Mechanisms and University Medical Press; 2002.
Human Relevance. Annu Rev Nutr. 2013; 33: 161-181. 24. Wang P, Chen Y, He L, et al. Association of Natural Intake of Dietary Plant Sterols
6. Sanga S, Lambertb JD, Hoc C, Yang CS. The chemistry and biotransformation of tea with Carotid Intima – Media Thickness and Blood Lipids in Chinese Adults: A Cross-
constituents. Pharmacol Res. 2011; 64(2): 87-99. Section Study. PLoS ONE. 2012; 7(3): e32736.
7. Zhao M, Zhang D, Su X, et al. An Integrated Metagenomics/ Metaproteomics 25. Gnudi S, Sitta E, Fiumi N. Bone density and geometry in assessing hip fracture risk in
Investigation of the Microbial Communities and Enzymes in Solid-state Fermentation post-menopausal women. Br J Radiol. 2007; 80(959): 893-897.
of Pu-erh tea. Sci Rep. 2015; 5: 10117. 26. Chen C, Kang L, Lin R, et al. (−)-Epigallocatechin-3-gallate improves bone
8. Feng L, Chong MS, Lim WS, et al. Tea Consumption Reduces the Incidence of microarchitecture in ovariectomized rats. Menopause. 2013; 20(6): 687-694.
Neurocognitive Disorders: Findings from the Singapore Longitudinal Aging Study. J 27. Ng TP, Aung KC, Feng L, Feng L, Nyunt MS, Yap KB. Tea consumption and
Nutr Health Aging. 2016; 20(10): 1002-1009. physical function in older adults: a cross-sectional study. J Nutr Health Aging. 2014;
9. Yang J, Mao QX, Xu HX, Ma X, Zeng CY. Tea consumption and risk of type 2 18(2): 161-166.
diabetes mellitus: a systematic review and meta-analysis update. BMJ Open. 2014; 28. Shen CL, Chyu MC, Yeh JK, et al. Effect of green tea and Tai Chi on bone health in
4(7): e5632. postmenopausal osteopenic women: a 6-month randomized placebo-controlled trial.
10. Liu J, Liu S, Zhou H, et al. Association of green tea consumption with mortality from Osteoporosis Int. 2012; 23(5): 1541-1552.
all-cause, cardiovascular disease and cancer in a Chinese cohort of 165,000 adult 29. Hegarty VM, May HM, Khaw KT. Tea drinking and bone mineral density in older
men. Eur J Epidemiol. 2016; 31(9): 853-865. women. Am J Clin Nutr. 2000; 71(4): 1003-1007.
11. Butt MS, Ahmad RS, Sultan MT, Qayyum MM, Naz A. Green tea and anticancer 30. Wu C, Yang Y, Yao W, Lu F, Wu J, Chang. C. Epidemiological Evidence of
perspectives: updates from last decade. Crit Rev Food Sci Nutr. 2015; 55(6): 792- Increased Bone Mineral Density in Habitual Tea Drinkers. Arch Intern Med. 2002;
805. 162(9): 1001-1006.
12. Shen CL, Chyu MC, Wang JS. Tea and bone health: steps forward in translational 31. Devine A, Hodgson JM, Dick IM, Prince RL. Tea drinking is associated with benefits
nutrition. Am J Clin Nutr. 2013; 98(6): 1694S-1699S. on bone density in older women. Am J Clin Nutr. 2007; 86(4): 1243-1247.
13. Nash LA, Ward WE. Tea and Bone Health: Findings from Human Studies, Potential 32. Jin P, Wu H, Xu G, Zheng L, Zhao J. Epigallocatechin-3-gallate (EGCG) as a pro-
Mechanisms, and Identification of Knowledge Gaps. Crit Rev Food Sci. 2015: 00-00. osteogenic agent to enhance osteogenic differentiation of mesenchymal stem cells
14. Wang G, Liu LH, Zhang Z, et al. Oolong Tea Drinking Could Help Prevent Bone from human bone marrow: an in vitro study. Cell Tissue Res. 2014; 356(2): 381-390.
Loss in Postmenopausal Han Chinese Women. Cell Biochem Biophys. 2014; 70(2): 33. Wu CH, Yang YC, Yao WJ, Lu FH, Wu JS, Chang CJ. Epidemiological evidence
1289-1293. of increased bone mineral density in habitual tea drinkers. Arch Intern Med. 2002;
15. Chen Z. Habitual Tea Consumption and Risk of Osteoporosis: A Prospective Study in 162(9): 1001-1006.
the Women’s Health Initiative Observational Cohort. Am J Epidemiol. 2003; 158(8): 34. Cabrera C, Giménez R, López MC. Determination of Tea Components with
772-781. Antioxidant Activity. J Agr Food Chem. 2003; 51(15): 4427-4435.
16. Hamdi KI, Aydin S, Gemalmaz A, et al. Habitual tea drinking and bone mineral 35. Das AS, Mukherjee M, Das D, Mitra C. Protective Action of Aqueous Black Tea
density in postmenopausal Turkish women: investigation of prevalence of (Camellia sinensis) Extract (BTE) against Ovariectomy-induced Oxidative Stress
postmenopausal osteoporosis in Turkey (IPPOT Study). Int J Vitam Nutr Res. 2007; of Mononuclear Cells and its Associated Progression of Bone Loss. Phytother. Res.
77(6): 389-397. 2009; 23(9): 1287-1294.
17. Saitoglu M, Ardicoglu O, Ozgocmen S, Kamanli A, Kaya A. Osteoporosis Risk 36. Zhang X, Wu Z, Weng P. Antioxidant and Hepatoprotective Effect of
Factors and Association with Somatotypes in Males. Arch Med Res. 2007; 38(7): (−)-Epigallocatechin 3-O-(3-O-Methyl) gallate (EGCG3-Me) from Chinese Oolong
746-751. Tea. J Agr Food Chem. 2014; 62(41): 10046-10054.
18. Hernandez-Avila M, Stampfer MJ, Ravnikar VA, et al. Caffeine and other predictors 37. Zhang L, Zhang Z, Zhou Y, Ling T, Wan X. Chinese dark teas: Postfermentation,
of bone density among pre- and perimenopausal women. Epidemiology (Cambridge, chemistry and biological activities. Food Res Int. 2013; 53(2): 600-607.
Mass.). 1993; 4(2): 128-134.

221

You might also like