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Calcium intake and osteoporosis: the influence of calcium intake from dairy products on hip bone mineral density and fracture incidence – a population-based study in women over 55 years of age

Published online by Cambridge University Press:  10 December 2012

Dariusz Włodarek*
Affiliation:
Department of Dietetics, Faculty of Human Nutrition and Consumer Sciences, Warsaw University of Life Sciences–SGGW, 159c Nowoursynowska Street, 02-776 Warsaw, Poland
Dominika Głąbska
Affiliation:
Department of Dietetics, Faculty of Human Nutrition and Consumer Sciences, Warsaw University of Life Sciences–SGGW, 159c Nowoursynowska Street, 02-776 Warsaw, Poland
Aleksandra Kołota
Affiliation:
Chair of Nutritional Physiology, Department of Dietetics, Faculty of Human Nutrition and Consumer Sciences, Warsaw University of Life Sciences, Warsaw, Poland
Piotr Adamczyk
Affiliation:
Department and Clinic of Pediatrics, Medical University of Silesia, Katowice, Poland
Aleksandra Czekajło
Affiliation:
Department of Nephrology, Regional Hospital in Racibórz, Racibórz, Poland
Władysław Grzeszczak
Affiliation:
Department and Clinic of Internal Diseases, Diabetology and Nephrology, Medical University of Silesia, Katowice, Poland
Bogna Drozdzowska
Affiliation:
Department of Pathomorphology, Medical University of Silesia, Katowice, Poland
Wojciech Pluskiewicz
Affiliation:
Metabolic Bone Diseases Unit, Department and Clinic of Internal Diseases, Diabetology and Nephrology, Medical University of Silesia, Katowice, Poland
*
*Corresponding author: Email dariusz_wlodarek@sggw.pl
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Abstract

Objective

The incidence of osteoporosis increases with age and is most frequently observed in postmenopausal women. The objective of the present population-based cohort study was to assess the influence of Ca intake from dairy sources on hip bone mineral density and hip fracture incidence in a group of Polish women over 55 years of age.

Design

The main outcome measures included: bone mineral density, the number of previous fractures and the reported Ca intake from dairy sources, assessed by a diet questionnaire.

Setting

The RAC-OST-POL Study was conducted in the District of Raciborz in the south of Poland.

Subjects

The study was carried out in a group of 625 women, randomly recruited from the general population of women aged >55 years.

Results

Median Ca intake from dairy products was lower in the group of women with femoral neck T-score ≤–2·5 than in the group with T-score >–2·5 (275 v. 383 mg/d; P = 0·0019). For total hip score, the difference was close to borderline significance (P = 0·0698). Median Ca intake from dairy products was lower in the group of women with previous fractures than in those without fracture history (336 v. 395 mg/d; P = 0·0254). The main dairy source of Ca in the analysed group included milk drinks, rennet cheese and milk.

Conclusions

Higher dairy Ca intake is recommended, since a number of the women analysed were unable to satisfy their Ca requirement exclusively from their diet.

Type
Nutrition and health
Copyright
Copyright © The Authors 2012 

Osteoporosis is a skeletal disease associated with low bone mass, microarchitectural deterioration of bone tissue and, as a consequence, increased bone fragility and susceptibility to fracture( Reference Harvey, Dennison and Cooper 1 ). The incidence of osteoporosis increases with age and is most frequently observed in postmenopausal women, as bone tissue loss and remodelling are accelerated by decreased ovarian oestrogen levels associated with menopause( 2 ). Osteoporotic bone fractures may be particularly devastating in the case of elderly women. Fracture prevention is one of the key goals of osteoporosis therapy in postmenopausal women, with targets to inhibit bone loss processes, maintain proper bone strength, and minimise or eliminate the factors contributing to slips or falls( 3 ).

The relationship between Ca intake and bone mineral density (BMD) is a widely analysed issue; higher Ca intake is associated with increased bone density in children( Reference Wosje and Specker 4 ), as well as higher bone mass( Reference Nieves, Golden and Siris 5 ), reduced risk of osteoporosis( Reference Nieves, Barrett-Connor and Siris 6 ) and lower fracture risks( Reference Heaney 7 ) in adults and the elderly. The above-mentioned association is very complex and some authors emphasise the role of other factors, such as environmental factors for example, while doubting any strong correlation with Ca( Reference Badurski, Dobreńko and Nowak 8 , Reference Badurski, Jeziernicka and Dobreńko 9 ). Simultaneously, besides gender and age, body mass is the third important element which influences the risk of osteoporosis( Reference Varenna, Binelli and Casari 10 ), while being also associated with Ca intake( Reference Bueno, Cesar and Martini 11 , Reference Dicker, Belnic and Goldsmith 12 ).

The most important sources of Ca are dairy products, providing over 60 % of daily Ca intake in women's diets( Reference Gonnelli, Rossi and Montomoli 13 , Reference Poliquin, Joseph and Gray-Donald 14 ) and even 74 % in some Polish studies( Reference Wądołowska, Pabjan and Słowińska 15 ). Simultaneously, they are at least as efficacious as Ca supplements in osteoporosis prevention( Reference Heaney 16 ).

It was hypothesised that Ca intake from dairy sources will be associated with BMD in women over 55 years of age. The objective of the present population-based cohort study was to assess the influence of Ca intake from dairy sources on hip BMD and hip fracture incidence in a group of Polish women aged >55 years.

Methods

The RAC-OST-POL study was carried out in a group of Polish women aged >55 years, randomly recruited from the general population of women over 55 years of age in the District of Raciborz in the south of Poland. The total number of eligible women inhabiting the region at the time of enrolment was 17 500, from whom 1750 were randomly selected and invited by regular mail to participate in the study. A blind list of women, selected for the study, was provided by the local government and each woman was assigned a number without showing her name. A group of 625 women responded positively to the invitation and declared their intention to take part in the study, which was performed in May 2010. Among these women, six were still menstruating. All 625 participants were submitted to the study protocol, including BMD measurements and an FFQ to assess Ca intake. Body weight and height were measured with a standard medical balance and used to calculate BMI (kg/m2). The study complied with the guidelines of the Declaration of Helsinki and all procedures involving human subjects were approved by the Ethics Committee of the Medical University of Silesia, Katowice, Poland. A written informed consent was obtained from all participants. The study group was described in a previous paper( Reference Pluskiewicz, Adamczyk and Czekajło 17 ).

Osteoporosis has been operationally defined on the basis of BMD assessment. According to the WHO criteria, osteoporosis is defined as a BMD level that lies 2·5 sd or more below the average value for young healthy women (T-score of ≤–2·5)( 18 ). The skeletal status was assessed by a Lunar DPX bone densitometer (GE Healthcare, Waukesha, WI, USA), assessing femoral neck and total hip bone density. Densitometric variables are presented as BMD (g/cm2) and T-score. All measurements were performed by one operator. The CV for measurements (calculated on the basis of fifty measurements – two for each participant with reposition) was 1·6 % for femoral neck and 0·82 % for total hip. Participants were queried about previous fractures of non-traumatic origin, e.g. caused by a fall from standing height or less; since no radiograms were obtained, some spine fractures might have been missed.

Participants were asked questions from the applied FFQ to assess their Ca intake from dairy products; they were asked by a dietitian about the frequency of consumption of forty-nine dairy products most common in Poland (e.g. milk, yoghurt, other milk beverages, rennet cheese, cottage cheese) and of meals containing dairy products, as well as typical portion sizes. Ca intake from a particular product was estimated by the following formula: Ca intake (mg) = typical portion size (g) × Ca content (mg/g). The FFQ results were analysed using the Dietetyk 2 software package (the Polish dietetic software) and the Polish database of nutritional values of food products( Reference Kunachowicz, Nadolna and Przygoda 19 ). The use of an FFQ to assess Ca intake is a commonly accepted and widely applied method, taking into account specified sources of Ca in the diet, mainly dairy products( Reference Gonnelli, Rossi and Montomoli 13 , Reference Khan, Mai le and Hien 20 Reference Pereira, Genaro and Santos 23 ). The standard error of the Ca estimate for the FFQ administered (calculated on the basis of two measurements for fifty participants with repetition during the period of 6 weeks) was 180 mg, while the median difference for the two estimations of daily Ca intake was 12 %. A similar questionnaire, taking into account similar groups of products and applied to assess Ca intake in the Polish population, was also characterised by high sensitivity( Reference Szymelfejnik, Wądołowska and Cichon 24 ).

Data are presented as means and standard deviations, along with minimum, maximum and median values. The distribution of the analysed factors was verified using the Shapiro–Wilk test, while the Spearman correlation coefficient was used to characterise relationships among the analysed factors and the Mann–Whitney U test was used to analyse differences between groups.

An additional statistical analysis was performed in order to confirm that the analysed population might be treated as a representative sub-sample. It was verified whether the mean age in the analysed sub-population matched the mean age in the general population. The two-sided level of significance P ≤ 0·05 was accepted to define the significance of correlations. Statistical analysis was carried out using the Statistica software version 8·0.

Results

Table 1 presents the characteristic features of the participants: age, body weight, body height and BMI. According to the 2010 Statistical Yearbook, the general population of women over 55 years of age in Poland comprises the following age subgroups: 29·8 % aged 55–59 years, 14·3 % aged 60–64 years and 55·9 % aged 65 years and older( 25 ). These age subgroups accounted for respectively 27·0 %, 19·8 % and 53·2 % of the women in the present study. The χ 2 test performed for the subgroup aged 60–64 years revealed a significant difference between typical and observed numerical strength in the analysed group. A significant correlation was found between age and BMI values (P = 0·0017; r = 0·12).

Table 1 Characteristic features of the participants: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Variable was not normally distributed (verified by the Shapiro–Wilk test; P ≤ 0·05).

Dairy Ca intakes of the women, grouped according to femoral neck and total hip T-scores >–2·5 or ≤–2·5, are presented in Table 2. Ca intake from dairy products was lower in the group of women with femoral neck T-scores ≤–2·5 than in the group with T-scores >–2·5 (P = 0·0019). For the total hip scores, the difference was borderline significant (P = 0·0698).

Table 2 Dairy calcium intake (mg/d) according to femoral neck and total hip bone mineral density T-scores: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Differences assessed by the Mann–Whitney U test.

†Variable was not normally distributed (verified by the Shapiro–Wilk test; P ≤ 0·05).

Table 3 presents the associations between dairy Ca intake and fractures. Ca intake from dairy products was lower in the group of women with previous fractures than in those without fracture history (P = 0·0254).

Table 3 Dairy calcium intake (mg/d) according to fracture status: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Differences assessed by the Mann–Whitney U test.

†Variable was not normally distributed (verified by the Shapiro–Wilk test; P ≤ 0·05).

Ca intake from various dairy sources is presented in Table 4. The median Ca intake from total dairy products was 373·2 mg/d in the analysed group; however with a considerable variability among particular individuals, ranging from 3·6 mg/d to 1922·9 mg/d. Other milk drinks (i.e. drinks other than milk, such as yoghurt, kefir, buttermilk) were the main dairy source of Ca, providing a median of 99·1 mg Ca/d. Important sources of Ca included rennet cheese (median 72·6 mg/d) and milk (median 70·8 mg/d). The other analysed sources of Ca included cottage cheese, dairy dishes and other products.

Table 4 Calcium intake (mg/d) from dairy sources: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Variable was not normally distributed (verified by the Shapiro–Wilk test; P ≤ 0·05).

The correlations of age and BMI with Ca intake from various dairy sources are presented in Table 5. In the case of older individuals, a lower intake of Ca was observed, both from total dairy products and particular dairy products groups (including milk, other milk drinks, cottage and rennet cheese), while a higher intake of Ca from dairy dishes was confirmed. BMI values were inversely correlated with Ca intake levels from cottage cheese only.

Table 5 Correlations of age and BMI with calcium intake from dairy sources: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Significant correlations (assessed by the Spearman correlation coefficient; P ≤ 0·05).

Table 6 presents correlations between Ca intake from various dairy sources and measured BMD values. Positive correlations between femoral neck and total hip BMD were observed for total dairy Ca intake as well as Ca intake from milk and other milk drinks, while a negative correlation was found between total hip BMD values and Ca intake from dairy dishes.

Table 6 Correlations between calcium intake from dairy sources and femoral neck and total hip bone mineral density (BMD): Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

*Significant correlations (assessed by the Spearman correlation coefficient; P ≤ 0·05).

Discussion

The present data were obtained from research carried out in a group of Polish women aged >55 years, analysing their dietary Ca intake from dairy products and its association with osteoporosis. The correlation between dietary Ca intake and osteoporosis development arouses a great deal of controversy, as Ca intake is not the only factor affecting BMD( Reference Badurski, Jeziernicka and Dobreńko 9 ), but remains a vital issue that is evaluated intensively in various countries( Reference Fardellone, Cotté and Roux 26 Reference Park, Heo and Park 30 ).

The group of women analysed in the present study was characterised by excessive body mass, with a median BMI of 30·84 kg/m2. The high BMI values in these women are congruent with BMI levels observed in osteoporosis studies conducted in Europe( Reference Fardellone, Cotté and Roux 26 , Reference Manios, Moschonis and Panagiotakos 27 ). Increased BMI may be associated with bone mineral loss( Reference Tseng, Huang and Liu 31 ) and during weight reduction overweight postmenopausal women are also more susceptible to bone loss, even if they are characterised by daily Ca intake of 1000 mg( Reference Riedt, Cifuentes and Stahl 32 ).

Femoral neck T-score is the main indicator of osteoporosis in BMD assessment( 18 ), with fractures being the most adverse effect of the disease( Reference Burge, Dawson-Hughes and Solomon 33 ). In the present study, women with either lower femoral neck T-scores or previous fractures were characterised by lower dairy Ca intake. Other reports indicate that postmenopausal women with higher intakes of dairy products are also characterised by higher lumbar BMD values( Reference Varenna, Binelli and Casari 10 ). Some researchers have emphasised a strong negative correlation between Ca intake and hip fracture incidence among women( Reference Yaegashi, Onoda and Tanno 34 ), as well as a correlation between Ca intake and broadband ultrasound attenuation Z-score in elderly women( Reference Lin, Chiu and Lin 35 ). However, other studies of Ca intake and osteoporosis indicated associations between Ca intake and BMD to be rather contradictory. Some researchers claim that, even if a certain influence of Ca intake on bone mass improvement is observed, neither Ca nor vitamin D supplementation demonstrates any short-term effect on fracture risk( Reference Nieves, Barrett-Connor and Siris 6 ); thus coming to the conclusion that no correlation exists between Ca intake and fracture incidence( Reference Zhong, Okoro and Balluz 28 ).

Dairy Ca intake may be perceived as a strong predictor of total Ca intake, as Ca intake from products other than dairy products is fairly constant. The results of other authors indicate that dairy products provide over 60 % of daily Ca intake in women's diets; in a group characterised by Ca intake of about 800 mg/d the contribution from dairy products was about 62 %, while in group characterised by Ca intake of about 900 mg/d the contribution amounted to about 84 %( Reference Gonnelli, Rossi and Montomoli 13 ). As the daily Ca intake from non-dairy products remains at a fairly stable level, a higher total daily Ca intake suggests a higher contribution of Ca from dairy products in the diet. The total Ca intake of the women in the present study may be estimated as the sum of Ca intakes from all products in the FFQ and about 250 mg Ca from products other than dairy products. Thus, in the present group of Polish women, Ca intake can be estimated at the level of about 675 mg/d. In other research conducted in postmenopausal women in Poland, the total Ca intake was similar – over 600 mg daily( Reference Bruyere, De Cock and Mottet 36 ). The latter study, performed in nine European countries, indicated that Polish women are characterised by low Ca intake compared with women in the other countries evaluated( Reference Bruyere, De Cock and Mottet 36 ). Ca intake in non-European populations was lower than in Poland – below 600 mg/d( Reference Pongchaiyakul, Kosulwat and Charoenkiatkul 37 Reference Kumar, Mittal and Orito 39 ). The recommended daily Ca intake for postmenopausal women is 1000–1500 mg, depending on age and recommending institution( 40 ). As a result, a number of women in the present study were unable to satisfy their Ca requirement exclusively from their diet.

The present women had lower intakes of Ca from milk and milk drinks, as well as from cheeses and other products, as compared with the results of other studies( Reference Gonnelli, Rossi and Montomoli 13 ). The proportion of dairy products as sources of Ca was also different. In the study by Poliquin et al.( Reference Poliquin, Joseph and Gray-Donald 14 ) the proportion of Ca from milk to Ca from other dairy products was about 3·2:4 and in the study by Fardellone et al.( Reference Fardellone, Cotté and Roux 26 ) it was about 1·8:4, whereas the proportion was 0·7:4 in the present study. Simultaneously, Gonelli et al.( Reference Gonnelli, Rossi and Montomoli 13 ) found the proportion of Ca from milk and milk drinks to Ca from cheeses and other dairy products to be about 3:4, while this proportion was 5·5:4 in our study. Therefore it may be concluded that while milk consumption was low in the present study group, the consumption of other milk drinks was fairly high in comparison with the results from other research.

The strong effect of age on Ca intake we observed is also reported by other researchers( Reference Fardellone, Cotté and Roux 26 , Reference Pongchaiyakul, Kosulwat and Charoenkiatkul 37 , Reference Kumar, Mittal and Orito 39 ). According to other authors, the daily Ca intake of postmenopausal women is significantly lower than that of premenopausal women( Reference Kumar, Mittal and Orito 39 ) and the proportion of women with low Ca intake rises with age( Reference Fardellone, Cotté and Roux 26 , Reference Pongchaiyakul, Kosulwat and Charoenkiatkul 37 ). However, the character of the relationship is not obvious, as other authors report lower Ca inadequacy in women above 75 years of age( Reference Bruyere, De Cock and Mottet 36 ), probably associated with higher intake of Ca supplements( Reference Poliquin, Joseph and Gray-Donald 14 ).

In the present study it can be concluded that the lower Ca intake observed in the case of older women can be attributed to lower consumption of dairy products, probably as a result of changing nutritional habits. Simultaneously, milk consumption remains stable, independently of age, while the consumption of dairy dishes is higher, without any major impact on the total dairy Ca intake. With age, everyday activities such as preparing meals become more difficult( Reference Seidel, Brayne and Jagger 41 ) and chewing ability also decreases( Reference Locker 42 ). So, the above-mentioned higher consumption of dairy dishes may probably result from the fact that dairy dishes are easy to prepare and eat.

In the research of Zhong et al.( Reference Zhong, Okoro and Balluz 28 ), a close to significant association was observed between Ca intake and BMI: postmenopausal women with higher BMI values reported lower Ca intake. No such correlation was observed in our study group. The only correlation we observed, that between cottage cheese consumption and BMI, could have been attributed to the general observation that individuals with lower BMI consume more cottage cheese, also confirmed by other researchers( Reference Mullie, Godderis and Clarys 43 ).

In the present group of females, correlations were observed between Ca intake from various dairy sources and BMD that corresponded to the results of other authors, claiming similar correlations between Ca intake and BMD( Reference Kumar, Mittal and Orito 39 , Reference Napoli, Thompson and Civitelli 44 , Reference Farrell, Harris and Lohman 45 ).

In contrast, the observed negative correlation between Ca intake from dairy dishes and total hip BMD score is rather difficult to explain. Only the fact indicated previously, that dairy dishes are generally easier to prepare and to eat and may be more often chosen by elderly people, may provide an explanation. The positive correlation between dairy Ca intake and BMD in the case of Ca from milk and other milk drinks, but not for Ca from rennet cheese and cottage cheese, may be associated with lactose. Lactose is contained in milk and other milk drinks, being a factor promoting Ca absorption( Reference Uenishi and Yamaura 46 ). The content of lactose in milk and other milk drinks is significantly higher than in either rennet cheese or cottage cheese; according to the Polish food composition database, the lactose content is 4·6–4·9 g/100 g and 4·1–5·0 g/100 g for cow's milk and other milk drinks, as opposed to 0·1–1·0 g/100 g and 1·0–3·3 g/100 g for rennet cheese and cottage cheese, respectively( Reference Kunachowicz, Nadolna and Przygoda 19 ). So, it may be concluded that BMD is correlated not only with Ca from dairy products but with Ca intake from lactose-containing dairy products, where lactose improves Ca absorption.

One of the factors that influences Ca metabolism in the human body, and as a consequence reduces the risk of osteoporosis, is vitamin D3. In the present study, neither vitamin D intake nor its serum level was assessed. This may be a limitation of the study, but nevertheless the proper intake of Ca is the main dietary factor influencing bone density, and in the research of other authors a similar attitude is chosen( Reference Varenna, Binelli and Casari 10 , Reference Nguyen, Center and Eisman 47 ). Other potential limitations of our study may be associated with the fact that only 36 % of invited women participated and that BMD was measured at the hip only and spine radiograms were not available, thus some spine fractures might not have been taken into account.

Conclusions

In the present group of Polish women above 55 years of age, it may be concluded that lower BMD (femoral neck T-score ≤–2·5) and previous fractures were associated with lower reported dairy Ca intake. Due to the insufficient consumption of dairy products, a number of women were unable to satisfy their Ca requirement exclusively from their diet. The main dairy sources of Ca in the analysed group included milk, other milk drinks and rennet cheese. It is therefore important to recommend the consumption of dairy products with lactose, a Ca-absorption improving factor, such as milk and milk drinks, to improve BMD and reduce fracture risks in the population of postmenopausal women with osteoporosis.

Acknowledgements

Sources of funding: This research received no specific grant from any funding agency in the public, commercial or non-for-profit sectors. Conflicts of interest: The authors have no conflicts of interest to declare. Authors’ contributions: D.W. and W.P. designed study; D.W., D.G., A.K., P.A., A.C., W.G., B.D. and W.P. conducted the research; D.W., D.G. and A.K. analysed the data and performed the statistical analysis; D.W. and D.G. wrote the paper; D.W. had primary responsibility for final content.

References

1. Harvey, N, Dennison, E & Cooper, C (2008) Epidemiology of osteoporotic fracture. In Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism, 7th ed., pp. 198203 [MJ Favus, editor]. Washington, DC: American Society for Bone and Mineral Research.Google Scholar
2. North American Menopause Society (2006) The role of calcium in peri- and postmenopausal women: 2006 position statement of the North American Menopause Society. Menopause 13, 862877.CrossRefGoogle Scholar
3. North American Menopause Society (2002) Management of postmenopausal osteoporosis: position statement of the North American Menopause Society. Menopause 9, 84101.Google Scholar
4. Wosje, KS & Specker, BL (2000) Role of calcium in bone health during childhood. Nutr Rev 58, 253268.Google Scholar
5. Nieves, JW, Golden, AL, Siris, E et al. (1995) Teenage and current calcium intake are related to bone mineral density of the hip and forearm in women aged 30–39 years. Am J Epidemiol 141, 342351.Google Scholar
6. Nieves, JW, Barrett-Connor, E, Siris, ES et al. (2008) Calcium and vitamin D intake influence bone mass, but not short-term fracture risk, in Caucasian postmenopausal women from the National Osteoporosis Risk Assessment (NORA) study. Osteoporos Int 19, 673679.Google Scholar
7. Heaney, RP (1992) Calcium in the prevention and treatment of osteoporosis. J Intern Med 231, 169180.Google Scholar
8. Badurski, J, Dobreńko, A, Nowak, N et al. (2008) Bialystok osteoporosis study-2: epidemiology of osteoporotic fractures and 10 year fracture risk assessment in population of women in Bialystok region by FRAX™ – WHO algorithm. Reumatol 46, 7279.Google Scholar
9. Badurski, J, Jeziernicka, E, Dobreńko, A et al. (2011) The characteristics of osteoporotic fractures in the region of Bialystok (BOS-2). The application of the WHO algorithm, FRAX®BMI and FRAX®BMD assessment tools to determine patients for intervention. Pol J Endocrinol 62, 290298.Google ScholarPubMed
10. Varenna, M, Binelli, L, Casari, S et al. (2007) Effects of dietary calcium intake on body weight and prevalence of osteoporosis in early postmenopausal women. Am J Clin Nutr 86, 639644.Google Scholar
11. Bueno, MB, Cesar, CLG, Martini, LA et al. (2008) Dietary calcium intake and overweight: an epidemiologic view. Nutrition 24, 11101115.CrossRefGoogle ScholarPubMed
12. Dicker, D, Belnic, Y, Goldsmith, R et al. (2008) Relationship between dietary calcium intake, body mass index, and waist circumference in MABAT – the Israeli National Health and Nutrition Study. Isr Med Assoc J 10, 512515.Google Scholar
13. Gonnelli, S, Rossi, S, Montomoli, M et al. (2009) Accuracy of different reduced versions of a validated food-frequency questionnaire in Italian men and women. Calcif Tissue Int 85, 221227.Google Scholar
14. Poliquin, S, Joseph, L & Gray-Donald, K (2009) Calcium and vitamin D intakes in an adult Canadian population. Can J Diet Pract Res 70, 2127.Google Scholar
15. Wądołowska, L, Pabjan, K, Słowińska, MA et al. (2010) Bone mineral density and consumption of calcium, calcium-fortified food and calcium supplements by women – a short report. Pol J Food Nutr Sci 60, 183187.Google Scholar
16. Heaney, RP (2000) Calcium, dairy products and osteoporosis. J Am Coll Nutr 19, 2 Suppl., S83S99.Google Scholar
17. Pluskiewicz, W, Adamczyk, P, Czekajło, A et al. (2012) Epidemiological data on osteoporosis in women from the RAC-OST-POL Study. J Clin Densitom 15, 308314.Google Scholar
18. World Health Organization (2004) Scientific Group on the Assessment of Osteoporosis at Primary Health Care Level. Summary meeting report – Brussels, Belgium, 5–7 May 2004. Geneva: WHO.Google Scholar
19. Kunachowicz, H, Nadolna, J, Przygoda, B et al. (2005) Food Composition Tables. Warsaw: PZWL (in Polish).Google Scholar
20. Khan, NC, Mai le, B, Hien, VT et al. (2008) Development and validation of food frequency questionnaire to assess calcium intake in postmenopausal Vietnamese women. J Nutr Sci Vitaminol 54, 124129.Google Scholar
21. Uenishi, K, Ishida, H & Nakamura, K (2008) Development of a simple food frequency questionnaire to estimate intakes of calcium and other nutrients for the prevention and management of osteoporosis. J Nutr Sci Vitaminol 54, 2529.Google Scholar
22. Hacker-Thompson, A, Robertson, TP & Sellmeyer, DE (2009) Validation of two food frequency questionnaires for dietary calcium assessment. J Am Diet Assoc 109, 12371240.Google Scholar
23. Pereira, GA, Genaro, PS, Santos, LC et al. (2009) Validation of a food frequency questionnaire for women with osteoporosis. J Nutr Health Aging 13, 403407.Google Scholar
24. Szymelfejnik, EJ, Wądołowska, L, Cichon, R et al. (2006) Dairy products frequency questionnaire (ADOS-Ca) calibration for calcium intake evaluation. Pol J Food Nutr Sci 15, 229236.Google Scholar
25. Central Statistical Office (2010) 2010 Statistical Yearbook. Warsaw: Central Statistical Office (in Polish).Google Scholar
26. Fardellone, P, Cotté, FE, Roux, C et al. (2010) Calcium intake and the risk of osteoporosis and fractures in French women. Joint Bone Spine 77, 154158.Google Scholar
27. Manios, Y, Moschonis, G, Panagiotakos, DB et al. (2009) Changes in biochemical indices of bone metabolism in post-menopausal women following a dietary intervention with fortified dairy products. J Hum Nutr Diet 22, 156165.CrossRefGoogle ScholarPubMed
28. Zhong, Y, Okoro, CA & Balluz, LS (2009) Association of total calcium and dietary protein intakes with fracture risk in postmenopausal women: the 1999–2002 National Health and Nutrition Examination Survey (NHANES). Nutrition 25, 647654.Google Scholar
29. Daly, RM, Brown, M, Bass, S et al. (2006) Calcium- and vitamin D3-fortified milk reduces bone loss at clinically relevant skeletal sites in older men: a 2-year randomized controlled trial. J Bone Miner Res 21, 397405.CrossRefGoogle Scholar
30. Park, H-M, Heo, J & Park, Y (2011) Calcium from plant sources is beneficial to lowering the risk of osteoporosis in postmenopausal Korean women. Nutr Res 31, 2731.Google Scholar
31. Tseng, YH, Huang, KC, Liu, ML et al. (2009) Association between metabolic syndrome (MS) and bone mineral loss: a cross-sectional study in Puli Township in Taiwan. Arch Gerontol Geriatr 49, Suppl. 2, S37S40.CrossRefGoogle Scholar
32. Riedt, CS, Cifuentes, M, Stahl, T et al. (2005) Overweight postmenopausal women lose bone with moderate weight reduction and 1 g/day calcium intake. J Bone Miner Res 20, 455463.Google Scholar
33. Burge, R, Dawson-Hughes, B, Solomon, DH et al. (2007) Incidence and economic burden of osteoporosis-related fractures in the United States, 2005–2025. J Bone Miner Res 22, 465475.Google Scholar
34. Yaegashi, Y, Onoda, T, Tanno, K et al. (2008) Association of hip fracture incidence and intake of calcium, magnesium, vitamin D, and vitamin K. Eur J Epidemiol 23, 219225.CrossRefGoogle ScholarPubMed
35. Lin, YC, Chiu, JF, Lin, MC et al. (2005) Bone health status of the elderly in Taiwan by quantitative ultrasound. Asia Pac J Clin Nutr 14, 270277.Google ScholarPubMed
36. Bruyere, O, De Cock, C, Mottet, C et al. (2009) Low dietary calcium in European postmenopausal osteoporotic women. Public Health Nutr 12, 111114.Google Scholar
37. Pongchaiyakul, C, Kosulwat, V, Charoenkiatkul, S et al. (2008) The association of dietary calcium, bone mineral density and biochemical bone turnover markers in rural Thai women. J Med Assoc Thai 91, 295302.Google Scholar
38. Miura, S, Nakamori, M, Yagi, M et al. (2009) Daily calcium intake and physical activity status in urban women living on low incomes in Davao, Philippines: a primary study for osteoporosis prevention. J Med Invest 56, 130135.Google Scholar
39. Kumar, A, Mittal, S, Orito, S et al. (2010) Impact of dietary intake, education, and physical activity on bone mineral density among North Indian women. J Bone Miner Metab 28, 192201.Google Scholar
40. North American Menopause Society (2001) The role of calcium in peri- and postmenopausal women: consensus opinion of the North American Menopause Society Menopause. Menopause 8, 8495.Google Scholar
41. Seidel, D, Brayne, C & Jagger, C (2011) Limitations in physical functioning among older people as a predictor of subsequent disability in instrumental activities of daily living. Age Ageing 40, 463469.Google Scholar
42. Locker, D (2002) Changes in chewing ability with ageing: a 7-year study of older adults. J Oral Rehabil 29, 10211029.Google Scholar
43. Mullie, P, Godderis, L & Clarys, P (2011) Determinants and nutritional implications associated with low-fat food consumption. Appetite 58, 3438.Google Scholar
44. Napoli, N, Thompson, J, Civitelli, R et al. (2007) Effects of dietary calcium compared with calcium supplements on estrogen metabolism and bone mineral density. Am J Clin Nutr 85, 14281433.Google Scholar
45. Farrell, VA, Harris, M, Lohman, TG et al. (2009) Comparison between dietary assessment methods for determining associations between nutrient intakes and bone mineral density in postmenopausal women. J Am Diet Assoc 109, 899904.Google Scholar
46. Uenishi, K & Yamaura, T (2010) Nutrition and bone health – lactose and bone. Clin Calcium 20, 424429.Google Scholar
47. Nguyen, TV, Center, JR & Eisman, JA (2000) Osteoporosis in elderly men and women: effects of dietary calcium, physical activity, and body mass index. J Bone Miner Res 15, 322331.Google Scholar
Figure 0

Table 1 Characteristic features of the participants: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

Figure 1

Table 2 Dairy calcium intake (mg/d) according to femoral neck and total hip bone mineral density T-scores: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

Figure 2

Table 3 Dairy calcium intake (mg/d) according to fracture status: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

Figure 3

Table 4 Calcium intake (mg/d) from dairy sources: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

Figure 4

Table 5 Correlations of age and BMI with calcium intake from dairy sources: Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010

Figure 5

Table 6 Correlations between calcium intake from dairy sources and femoral neck and total hip bone mineral density (BMD): Polish women (n 625) aged >55 years, RAC-OST-POL Study, May 2010