Bone Health and Nutrition in Aging: Calcium and Vitamin D
Facebookdiggdel.icio.usReddit

See the Vitamin D category for more Vitamin D articles.

See the minerals category for more articles about minerals.

Bone Health Nutrition Issues in Aging: Calcium and Vitamin D

by Karen Plawecki and Karen Chapman-Novakofski

Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA;

Nutrients 2010

Bone health is an important issue in aging. Calcium and vitamin D currently have the most focus in published research on nutrition and bone health in aging, although evidence from published research is not conclusive. A systematic review was conducted to determine the impact of dietary and supplemental interventions focused on calcium and vitamin D over the past 10 years. Using key words to search, and search limits (aging population, English), 62 papers were found related to diet, nutrition, and bone; and 157 were found related to calcium and bone. Our review found a positive effect on bone health for supplements; food-based interventions; and educational strategies. Although there may be a publishing bias related to non-significant findings not being published, our results suggest the effectiveness of food based and educational interventions with less economic impact to the individual, as well as less risk of physiological side effects occurring.

RSS

feed-icon-14x14.png Get GUS by RSS
feed-icon-14x14.png New Forum Threads
feed-icon-14x14.png GUS RSS By Email
(What is RSS?)

More Calcium and Vitamin D Articles

Introduction

Osteoporosis is a systemic skeletal disease portrayed by low bone mass and structural weakening of the bone material that leads to reduced bone strength and increased susceptibility to fracture. Although all bones can be affected, the hip, vertebra and wrist bones are at high risk. Osteoporosis is commonly referred to as a .silent disease. as there are no symptoms until the fracture occurs [1].

Osteoporosis is a debilitating chronic disease that is a public health problem. It is estimated that 10 million individuals have osteoporosis while another 34 million suffer from low bone density. An estimated 61 million individuals will develop osteoporosis or low bone density by 2020 [1]. In 2002 annual direct care expenditures for osteoporotic fractures reached almost 18 billion dollars [2,3]. Beyond costs, there is the physical burden of living with osteoporosis and its impact on daily living, including restrictions in daily activities, loss of confidence (due to fear of falling and fracture) and loss of independence [4].

With people living longer, fracture risk is expected to increase. Each year an estimated 1.5 million individuals suffer a fracture due to bone disease. For those over 50 who suffer a hip fracture, approximately 4% will die in the hospital and 24% will die within the year. The risk of a fracture increases with age and is greatest in women. Approximately one in two women and one in four men aged 50 or older in the United States will experience an osteoporotic-related fracture sometime during the remainder of their lives. As people live longer, the lifetime risk of fractures will increase for all ethnic groups [2]. With the high costs of treating osteoporosis fractures [5], effective preventive interventions are needed.

Osteoporosis is primarily viewed as a woman’s disease. However, after age 50, 6% of all men will experience a hip fracture and 5% will have a vertebral fracture as a result of osteoporosis [1,2]. Bone loss occurs rapidly in women at menopause; for men the loss still occurs but later (in their late 60s and in their 70s). The topic of bone health and osteoporosis in men is not well studied, but it is believed to often occur due to secondary causes, such as corticosteroid therapy [6].

Risk factors for low bone density, osteoporosis and fractures, include both unchangeable and modifiable types of factors. Conditions increasing the chance for developing osteoporosis include: fracture history after age 50, family history, female gender, small bone frame, advanced age, estrogen deficiency, amenorrhea, low testosterone levels, some medications, certain chronic diseases, long-term low intake of calcium, vitamin D deficiency, inactivity, cigarette smoking and excessive alcohol [7]. Fortunately, there are many modifiable lifestyle factors (diet and activity) along with drug treatment which can prevent or slow the loss of bone.

The National Osteoporosis Foundation developed five steps to optimize bone health [1]. These include:

1. Get the daily recommended amounts of calcium and vitamin D;

2. Engage in regular weight-bearing and muscle-strengthening exercise;

3. Avoid smoking and excessive alcohol;

4. Talk to your healthcare provider about bone health;

5. Have a bone density test and take medication when appropriate.

Clinical studies have reported increases in calcium intake as a result of calcium supplementation and physical activity and intense supervision [2,8,9]. There is an inverse relationship between physical activity and future hip fracture risk for both women and men [10,11]. Resistance exercise combined with aerobic weight-bearing activity has been shown to improve bone mineral density (BMD) in postmenopausal women without a history of fractures. Calcium and vitamin D supplementation have been shown to increase BMD, but even within clinical trials adherence to taking supplements is not optimal. In fact, one large trial found no change in BMD in women enrolled in the supplement arm of the trial. However, when only those who actually took the supplements on most days were analyzed a significant improvement in hip BMD was found [12]. Clearly, exercise and diet can have a positive impact on bone health.

Review Section

Objectives

The objectives of this systematic review were to: Assess the impact of dietary intervention on dietary behavior measures, laboratory indices of bone health, bone mineral density, and other variables related to bone health; discuss the results of this review in terms of healthy aging; and identify gaps in the research related to bone health and aging.

Methods

The last 10 years in PubMed were searched using the keywords intervention, diet, and bone, as well as calcium, intervention, and bone (see Figure 1). Studies with vitamin D were included in both primary searches. The search limits included searching only for the classifications of middle-age and aged, humans, and publications in English. A secondary search was conducted on specific nutrients (protein, sodium, soy and vitamin K) which were in the results from the initial searches. The secondary searches were performed to identify additional studies that may not have been included in the initial search. Interventions that included drugs were not included in the review. For the purpose of this review, manuscripts of cross-sectional studies were eliminated.

Data extracted included type of intervention (randomized or quasi-experimental), number of subjects, length of study, description of the intervention, nutrient of interest, and outcome measures. Authors reviewed the manuscripts for consensus in data extraction and interpretation of results.

bone-health-search.JPG

Figure 1. Description of methods for systematic search.

Results

These research studies could be placed into one of four groups: calcium and vitamin D from food (Table 1 omitted), calcium and vitamin D from supplements (Table 2 omitted), other bone health-related nutrients (Table 3 omitted) and portfolio diets (Table 4 //omitted).

Calcium and Vitamin D Interventions Using Food

Interventions, including food rich in either calcium and/or vitamin D, have shown results with increased calcium intake and improving serum bone markers. Food sources used in the studies were dairy-based, either milk or yogurt [13-15]. Food was either provided to meet calcium and vitamin D needs [13,14] or as one source [15]. Moschonis et al. [13] studied the impact of fortified dairy (two servings of milk and one yogurt) over 30 months with biweekly counseling on bone health in post-menopausal women. During the first 12 months, the fortified dairy products provided a total of 1200 mg calcium and 7.5 µg vitamin D. For the final 18 months, vitamin D fortified levels were increased to 22.5 µg/day. The women consuming the fortified foods and receiving education showed an increase in arm, spinal and total BMD, in contrast to those staying on their usual diet and receiving no counseling.

In the study by Manios et al. [14], participants consumed calcium and vitamin D fortified dairy (provided via three servings of either milk or yogurt) to meet nutrient recommendations versus those consuming calcium supplements to reach 1200 mg calcium, or the control received neither .dairy. food nor supplements. Those in the dairy group also received instruction on osteoporosis and bone-healthy behaviors. In the study by Bonjour et al. [15], elderly women consumed two servings of vitamin D and calcium-enhanced soft cheese that provided a total of 2.5 µg vitamin D3, 302 mg calcium; 233 mg phosphorus, and 14.2 g protein. Participants tolerated the product and showed a modest increase in bone formation markers (insulin-like growth factor-1, osteocalcin and amino-terminal propeptide of type 1 procollagen) along with a decrease in parathyroid hormone (PTH) from baseline. Consumption of calcium and vitamin D rich foods generally resulted in reduced PTH levels.

In addition to providing food, providing instruction has seen a range of results in improving calcium intake [9,14,16-20]. Hein et al. [16] demonstrated the effectiveness of a training course. Participants in the intervention over a period of 18 months learned about osteoporosis, calcium-rich foods, local sources of calcium-rich foods, sample menus reviewed and various skills, including food preparation, were practiced. Those receiving the intervention increased their calcium intake versus the control group. The PTH levels were also decreased in the treatment group. Similar topics were addressed in the study by Manios et al. [14] where the intervention included fortified dairy servings. The bone density measures were improved in the intervention group versus the calcium supplement or control groups. Tailored and individualized education [19,20] yielded improved calcium intake over those receiving materials in the mail [17]. Tussing and Chapman-Novakofski [9] also reported increased calcium intake after an eight-week educational intervention.

Calcium and Vitamin D Interventions Using Supplements

Various calcium and vitamin D dosages have been used to improve bone health markers [21-27] or reduce falls [28-31]. A study by Kuwabara et al. [22] provided adults in residential facilities with either calcium, with or without vitamin D (800 IU). Even with additional vitamin D, participants did not reach recommended serum vitamin D (25(OH)D) levels but did show reduced PTH levels. In those who had experienced a fracture, supplemental calcium (1200 mg) and vitamin D (1400 IU) resulted in increased lumbar bone mineral density (BMD) and lower PTH; the effect of the supplement was more effective in participants under 70 years old [23]. Women who took a calcium supplement (600 mg twice per day) did not show a reduction of fracture risk for the entire intervention group but those that took the supplement over 80% of the time did have improved bone markers [24].

Another study evaluating calcium (1000 mg) and vitamin D (400 IU) in post-menopausal women demonstrated that the treatment group had a slightly higher hip BMD but no lower fracture risk [25]. Calcium and vitamin D supplementation (500 mg calcium and 200 IU vitamin D) indicated a protective effect of the supplement in peri- and postmenopausal women as those receiving the supplement showed no loss of total BMD, whereas the placebo group did lose BMD [26]. A study by Meier et al. [27] looked at the effect of calcium and vitamin D prescribed in winter months. During the first year of the study, calcitropic hormone changes were monitored and then measured the following winter with supplementation. Taking calcium (500 mg) and vitamin D (500 IU) during winter months helped to offset the effects of calcitropic hormones [27]. In another study, adults received vitamin D supplementation (0, 5, 10, 15 µg vitamin D) during wintertime. There was a dosage-related increase of serum vitamin D in the intervention groups and a decrease in PTH [21].

Interventions studying the effect of supplements on falls and fractures focused on vitamin D supplementation. A study by Sanders et al. [28] measured the effect of a single, annual dose of 500,000 IU of vitamin D given prior to the start of winter months. The intervention group had a higher number of falls and a relative risk for falls. Kärkkäinen et al. [29] conducted a large scale and smaller scale intervention. Both studies measured the effect of 1000 mg calcium and 800 IU vitamin D supplements given to community-dwelling women. In the large scale study, no difference between incidence of single or multiple falls was found but the smaller intervention resulted in a reduction in multiple falls, including those needing medical attention. Elderly, receiving calcium (1000 mg) with vitamin D (800 IU), had a decrease in first falls versus those who only received calcium [30]. Elderly, living in residential centers with minimum serum vitamin D level of 25 nmol/L, were given vitamin D (10,000 IU weekly dose and then 1000 IU/day), or placebo [31]. Those receiving the vitamin D supplement had a lower rate of falls and fractures.

Interventions Focusing on Additional Bone-Healthy Nutrients

Research in protein, sodium, soy and vitamin K interventions yielded additional details in
bone-health interventions. For protein, a cross-sectional intervention by Rapuri et al. [32] evaluated the effect of protein as a percentage of energy and its effect of calcium intake. Those in the higher protein quartile (mean 78 grams/day) had higher spine, radius and total BMD versus those with lower protein intakes. The effect was seen in those with at least 400 mg calcium.

A crossover study measured the effect of low and high sodium with low and high calcium intake on urinary calcium loss [33]. A diet high in sodium (11.2 g) increased calcium urinary loss leading to negative calcium balance with those on a high calcium diet (mean 1284 mg). Calcium balance was negative for low calcium intake (mean 518 mg), regardless of the sodium intake.

Soy-related interventions on bone-health have had varied results. A calcium and vitamin D supplement with isoflavones showed that the group receiving 120 mg of isoflavones was more protective at the femoral neck BMD [34] and total BMD [35]. Women with low BMD and taking genistein supplements (54 mg) had lower bone resorption markers (pyridinoline and deoxypyridinoline) and increased bone-specific alkaline phosphatase and insulin-like growth factor I. Post-menopausal women consuming 43 grams of soy protein with varying levels of isoflavones resulted in no changes in bone resorptive markers [36].

Varying levels of vitamin K supplementation has been studied. Booth et al. [37] measured the effect of an additional 500 µg phylloquinone in older men and women. There was no difference in BMD but the percent of undercarboxylated osteocalcin was reduced in those receiving additional vitamin K. In women with no osteoporosis, groups were supplemented with either a placebo, calcium and vitamin D, vitamin K or calcium (1000 mg), and vitamin D (400 IU) with vitamin K (200 µg) [38]. Those receiving the combination of calcium, vitamin D and vitamin K had an increase in bone mineral content (BMC) and BMD at the radius. Both vitamin K groups had lower percent of undercarboxylated osteocalcin. A study [39] of post-menopausal women measured the effect of a supplement with calcium/magnesium/zinc/vitamin D with or without vitamin K and a placebo. The group taking the combination with vitamin K show decreased bone loss at the femoral neck site [39].

Interventions Using Portfolio Diets

The Dietary Approaches to Stop Hypertension (DASH) and Mediterranean diets have been studied for impact on bone health markers. In an 18-month intervention, participants were randomized to control, standard diet for hypertension and the DASH diet. Those in the DASH diet had significant increases in nutrients positively impacting bone health, including calcium, potassium and magnesium [40]. The effect of the Mediterranean diet on bone markers was studied in elderly men and women [41]. Participants followed either a low fat diet (control), Mediterranean diet with olive oil as the monounsaturated fatty acid (MUFA) source, or Mediterranean diet with nuts as the MUFA source. The group consuming nuts had a higher acid load and slightly higher PTH levels but no other difference in biomarkers.

Discussion

More than a decade ago the Food and Drug Administration approved the label health claim that calcium-rich products can lower the risk for osteoporosis [42]. Since that time, the relative importance of calcium in bone health and fracture prevention has been an issue of many investigations. A primary function of vitamin D is to maintain serum calcium and phosphorus levels within a constant range, and to enhance calcium availability by intestinal uptake and osteoclast activation. In the last five years, scientific interest in vitamin D has blossomed, both in regards to bone and other medical conditions. Clearly both calcium and vitamin D contribute to healthy bone maintenance during aging, although the relative contribution may still be unclear. Nevertheless, all osteoporosis medication recommends adequate intake of calcium and vitamin D to ensure optimal effectiveness of the drug.

As such, the results of this review are not initially surprising. One finding of this review is that most studies found that vitamin D supplementation would increase serum vitamin D levels [21,22] and an improvement in serum markers of bone health and/or PTH was reported [21-23,27]. In addition, BMD was improved with supplementation [23-26,29] and number of falls were reduced in some [29,30] but not all studies [28]. Our results concerning supplements are similar to other recently published reviews. A meta-analysis of vitamin D alone or vitamin D with calcium supplementation found that vitamin D with calcium was effective in reducing overall fracture risk and hip fracture risk [43]. Indeed this was also reported in a meta-analysis of calcium supplementation on hip fracture. Reid et al. reported that hip fracture risk was significantly increased with calcium supplementation alone, but decreased with both calcium and vitamin D supplementation [44]. This is in contrast to the meta-analysis reported by Tang et al. in [45] in which calcium supplementation decreased fracture risk, and little was added to the reduction when vitamin D was added. However a Cochran review concluded that vitamin D alone was ineffective in preventing hip fracture in older people, and although vitamin D with calcium did appear to reduce hip fracture incidence, hypercalcaemia was more common in older persons taking vitamin D with or without calcium, with some increases in gastrointestinal symptoms and renal disease [46].

One interesting result of this analysis was that few reviews and no meta-analyses have evaluated food as the source of calcium and/or vitamin D, which are far less likely to produce side effects. Our review found that studies providing calcium as food sources increased calcium and vitamin D intake [15]. When calcium and vitamin D intake was increased, an effect was seen on BMD, bone turnover markers, and PTH [13-15]. It is more difficult to quantify calcium or vitamin D intake when these nutrients are eaten as foods rather than as supplements. While there are several validated instruments published for assessing calcium intake in various groups [47-54], very few include calcium-fortified foods [55]. A significant gap in the research includes not only a vitamin D instrument for intake documentation, but a database containing the expanding list of vitamin D-fortified foods.

Of interest is those educational interventions without a food or supplement also increase calcium intake [9,15,19]. Decades of research on nutrition education have found that education would be more effective if focused on specific behaviors and if appropriate theory was used for designing the intervention [56]. A study of older adults (n = 162) found that attitudes and perceived control were important predictors of dairy product intake, whereas subjective norms were not (those significant people who influence our behavior) [57]. Not surprisingly in our review, when the education lacked depth and theory, e.g., mailings to participants, no improvement in calcium intake was found [17]. More importantly, studies examining mediators of bone-related dietary change in older adults are lacking. Similar to demonstrating a physiological mechanism for how nutrients affect health, investigations into educational strategies must investigate how behavioral theories mediate dietary change [58].

Concerning protein, both high and low protein intakes have been shown to have negative effects on bone, with negative effects more pronounced with inadequate calcium intake than with adequate intake [59-61]. The study supported a positive effect of protein on bone health. Other studies distinguish between animal and vegetable protein [62], or the acid load of protein and its effects on bone health. A review of all the studies related to bone and protein intake is beyond the scope of this paper. However, an educational interventional approach to adequate calcium, vitamin D, and protein intake with older persons is clearly lacking in the literature. One study did show that protein supplementation offered no additional increase in muscle mass in middle age and older men involved in a resistance exercise randomized control trial [63]. This is mentioned to highlight the other pertinent aspects of bone health, namely muscle mass and exercise.

Other nutritional issues highlighted in our review included vitamin K, soy, and portfolio diets. The latter presents the most holistic approach to investigating the optimal diet for bone health in aging, and may also include exercise and fall prevention training. The studies highlighted in this review demonstrate that key lifestyle habits can be utilized to strengthen bone health and reduce fracture risk. As previously mentioned, the National Osteoporosis Foundation [1] developed five steps to optimize bone health, the first of which is to improve calcium and vitamin D intake. As shown in the present review, this can be accomplished with either food or supplements in older adults. Medications certainly have a role for treating osteoporosis. However, with the number of medications that the older person is prescribed continuing to rise, there is a need to consider less aggressive measures when possible.

While most intervention studies and reviews concerning bone health have included medication as the primary intervention, relatively few have concentrated on diet or supplements alone. Pharmacological approaches will have a significantly higher effect on BMD, and possibly on falls and fractures, but at the same time pose a higher risk for medication-associated side effects, especially if continued for decades.

Conclusions

Many nutrients play a role in optimizing skeletal mass. In addition to vitamin D and calcium, deficiency, and in some cases excesses, of other nutrients can impact bone mineral density. These nutrients are commonly obtained by following the U.S. Dietary Guidelines [54]. Interventions, including foods or supplements, or targeting behaviors, have shown positive results. Additional research is needed to examine the impact of educational strategies that combine all nutritional factors into one randomized controlled intervention; then further to examine the impact of education plus supplemental foods. The results of these trials will perhaps provide an effective strategy for bone health in aging adults who prefer not to take supplements or medication. Future research may also combine these proposed projects with balance, flexibility, and impact exercise, to determine their additional effects on bone density, fracture rates, and markers of bone health. With the economic factors of supplements and medication, as well as quality of life issues, additional research is needed to examine the potential role of education strategies concerning bone health in aging.

Limitations

An inherent limitation in evaluating impact of interventions is publication bias. Significant changes are commonly needed in order to be published. If an intervention produced no change, this may not be published and consequently data were not available for review.

With the focus of the review being nutritional interventions, the review excluded studies that focused on drug treatment. These studies may have provided additional nutritional information but the diet variable is often held constant in these studies.

References

1. National Osteoporosis Foundation. Osteoporosis: A debilitating disease that can be prevented and treated. Available online: http://www.nof.org/osteoporosis/index.htm (accessed on 15 June 2009).

2. Carmona, R.H. Surgeon General. Bone Health and Osteoporosis: A Report from the Surgeon
General, 2004. Available online: http://www.surgeongeneral.gov/library/bonehealth/ (accessed on 8 March 2007).

3. Compston, J. Osteoporosis: Social and economic impact. Radiol. Clin. North Am. 2010, 48, 477-482.

4. Pasco, J.A.; Sanders, K.M.; Hoekstra, F.M.; Henry, M.J.; Nicholson, G.C.; Kotowicz, M.A. The human cost of fracture. Osteoporos. Int. 2005, 16, 2046-2052.

5. Burge, R.; Dawson-Hughes, B.; Solomon, D.H.; Wong, J.B.; King, A.; Tosteson, A. Incidence and Economic Burden of Osteoporosis-Related Fractures in the United States 2005–2025. J. Bone Miner. Res. 2007, 22, 465-475.

6. Al Attia, H.; Adams, B. Osteoporosis in men: Are we referring enough for DXA and how? Clin. Rheumatol. 2007, 26, 1123-1126.

7. Poole, K.; Compston, J. Osteoporosis and its management. BMJ 2006, 333, 1251-1256.

8. Gass, M.; Dawson-Hughes, B. Preventing Osteoporosis-related fractures: An overview. Am. J. Med. 2006, 119, 3S-11S.

9. Tussing, L.; Chapman-Novakofski, K. Osteoporosis prevention education: Behavior theories and calcium intake. J. Am. Diet. Assoc. 2005, 105, 92-97.

10. Schmitt, N.M.; Schmitt, J.; Dören, M. The role of physical activity in the prevention of osteoporosis in postmenopausal women—An update. Maturitas 2009, 63, 34-38.

11. Thomas-John, M.; Codd, M.B.; Manne, S.; Watts, N.B.; Mongey, A.B. Risk Factors for the Development of Osteoporosis and Osteoporotic Fractures Among Older Men. J. Rheumatol. 2009, 36, 1947-1952.

12. Shea, B.; Wells, G.; Cranney, A.; Zytaruk, N.; Robinson, V.; Griffith, L.; Hamel, C.; Ortiz, Z.; Peterson, J.; Adachi, J.; et al. Calcium supplementation on bone loss in postmenopausal women. Cochrane Database Syst. Rev. 2004, CD004526; doi:10.1002/14651858.CD004526.pub2.

13. Moschonis, G.; Katsaroli, I.; Lyritis, G.P.; Manios, Y. The effects of a 30-month dietary intervention on bone mineral density: The Postmenopausal Health Study. Br. J. Nutr. 2010, 104, 100-107.

14. Manios, Y.; Moschonis, G.; Katsaroli, I.; Grammatikaki, E.; Tanagra, S. Changes in diet quality score, macro- and micronutrients intake following a nutrition education intervention in postmenopausal women. J. Hum. Nutr. Diet. 2007, 20, 126-131.

15. Bonjour, J.P.; Benoit, V.; Pourchaire, O.; Ferry, M.; Rousseau, B.; Souberbielle, J.C. Inhibition of markers of bone resorption by consumption of vitamin D and calcium-fortified soft plain cheese by institutionalised elderly women. Br. J. Nutr. 2009, 102, 962-966.

16. Hien, V.T.; Khan, N.C.; Mai le, B.; Lam, N.T.; Phuong, T.M.; Nhung, B.T.; Nhien, N.V.; Nakamori, M.; Yamamoto, S. Effect of community-based nutrition education intervention on calcium intake and bone mass in postmenopausal Vietnamese women. Public Health Nutr. 2009, 12, 674-679.

17. Solomon, D.H.; Finkelstein, J.S.; Polinski, J.M.; Arnold, M.; Licari, A.; Cabral, D.; Canning, C.; Avorn, J.; Katz, J.N. A randomized controlled trial of mailed osteoporosis education to older adults. Osteoporos. Int. 2006, 17, 760-767.

18. Sedlak, C.A.; Doheny, M.O.; Estok, P.J.; Zeller, R.A. Tailored interventions to enhance osteoporosis prevention in women. Orthop. Nurs. 2005, 24, 270-276.

19. Wong, S.Y.; Lau, E.M.; Lau, W.W.; Lynn, H.S. Is dietary counseling effective in increasing dietary calcium, protein and energy intake in patients with osteoporotic fractures? A randomized controlled clinical trial. J. Hum. Nutr. Diet. 2004, 17, 359-364.

20. Heaney, R.P.; McCarron, D.A.; Dawson-Hughes, B.; Oparil, S.; Berga, S.L.; Stern, J.S.; Barr, S.I.; Rosen, C.J. Dietary changes favorably affect bone remodeling in older adults. J. Am. Diet. Assoc. 1999, 99, 1228-1233.

21. Seamans, K.M.; Hill, T.R.; Wallace, J.M.; Horigan, G.; Lucey, A.J.; Barnes, M.S.; Taylor, N.; Bonham, M.P.; Muldowney, S.; Duffy, E.M.; Strain, J.J.; Kiely, M.; Cashman, K.D. Cholecalciferol supplementation throughout winter does not affect markers of bone turnover in healthy young and elderly adults. J. Nutr. 2010, 140, 454-460.

22. Kuwabara, A.; Tsugawa, N.; Tanaka, K.; Fujii, M.; Kawai, N.; Mukae, S.; Kato, Y.; Kojima, Y.; Takahashi, K.; Omura, K.; et al. Improvement of vitamin D status in Japanese institutionalized elderly by supplementation with 800 IU of vitamin D(3). J. Nutr. Sci. Vitaminol. 2009, 55, 453-458.

23. Hits, M.F.; Jensen, J.E.; Eskildsen, P.C. Bone mineral density and bone markers in patients with a recent low-energy fracture: Effect of 1 y of treatment with calcium and vitamin D. Am. J. Clin. Nutr. 2007, 86, 251-259.

24. Prince, R.L.; Devine, A.; Dhaliwal, S.S.; Dick, I.M. Effects of calcium supplementation on clinical fracture and bone structure: Results of a 5-year, double-blind, placebo-controlled trial in elderly women. Arch. Intern. Med. 2006, 24, 869-875.

25. Jackson, R.D.; LaCroix, A.Z.; Gass, M.; Wallace, R.B.; Robbins J.; Lewis, C.E.; Bassford, T.; Beresford, S.A.; Black, H.R.; Blanchette, P.; et al. Calcium plus vitamin D supplementation and the risk of fractures. N. Engl. J. Med. 2006, 354, 669-683.

26. Di Daniele, N.; Carbonelli, M.G.; Candeloro, N.; Iacopino, L.; De Lorenzo, A.; Andreoli, A. Effect of supplementation of calcium and vitamin D on bone mineral density and bone mineral content in peri- and post-menopause women; a double-blind, randomized, controlled trial. Pharmacol. Res. 2004, 50, 637-641.

27. Meier, C.; Woitge, H.W.; Witte, K.; Lemmer, B.; Seibel, M.J. Supplementation with oral vitamin D3 and calcium during winter prevents seasonal bone loss: A randomized controlled open-label prospective trial. J. Bone Miner. Res. 2004, 19, 1221-1230.

28. Sanders, K.M.; Stuart, A.L.; Williamson, E.J.; Simpson, J.A.; Kotowicz, M.A.; Young, D.; Nicholson, G.C. Annual high-dose oral vitamin D and falls and fractures in older women: A randomized controlled trial. JAMA 2010, 303, 1815-1822.

29. Kärkkäinen, M.K.; Tuppurainen, M.; Salovaara, K.; Sandini, L.; Rikkonen, T.; Sirola, J.;
Honkanen, R.; Arokoski, J.; Alhava, E.; Kröger, H. Does daily vitamin D 800 IU and calcium 1000 mg supplementation decrease the risk of falling in ambulatory women aged 65–71 years? A 3-year randomized population-based trial (OSTPRE-FPS). Maturitas 2010, 65, 359-365.

30. Pfeifer, M.; Begerow, B.; Minne, H.W.; Suppan, K.; Fahrleitner-Pammer, A.; Dobnig, H. Effects of a long-term vitamin D and calcium supplementation on falls and parameters of muscle function in community-dwelling older individuals. Osteoporos. Int. 2009, 20, 315-322.

31. Flicker, L.; MacInnis, R.J.; Stein, M.S.; Scherer, S.C.; Mead, K.E.; Nowson, C.A, Thomas, J.; Lowndes, C.; Hopper, J.L.; Wark, J.D. Should older people in residential care receive vitamin D to prevent falls? Results of a randomized trial. J. Am. Geriatr. Soc. 2005, 53, 1881-1888.

32. Rapuri, P.B.; Gallagher, J.C.; Haynatzka, V. Protein intake: Effects on bone mineral density and the rate of bone loss in elderly women. Am. J. Clin. Nutr. 2003, 77, 1517-1525.

33. Teucher, B.; Dainty, J.R.; Spinks, C.A.; Majsak-Newman, G.; Berry, D.J.; Hoogewerff, J.A.; Foxall, R.J.; Jakobsen, J.; Cashman, K.D.; Flynn, A.; Fairweather-Tait, S.J.. Sodium and bone health: Impact of moderately high and low salt intakes on calcium metabolism in postmenopausal women. J. Bone Miner. Res. 2008, 23, 1477-1485.

34. Alekel, D.L.; Van Loan, M.D.; Koehler, K.J.; Hanson, L.N.; Stewart, J.W.; Hanson, K.B.; Kurzer, M.S.; Peterson, C.T. The soy isoflavones for reducing bone loss (SIRBL) study: A 3-y randomized controlled trial in postmenopausal women. Am. J. Clin. Nutr. 2010, 91, 218-230.

35. Wong, W.W.; Lewis, R.D.; Steinberg, F.M.; Murray, M.J.; Cramer, M.A.; Amato, P.; Young, R.L.; Barnes, S.; Ellis, K.J.; Shypailo, R.J.; Fraley, J.K.; Konzelmann, K.L.; Fischer, J.G.; Smith, E.O. Soy isoflavone supplementation and bone mineral density in menopausal women: A 2-y multicenter clinical trial. Am. J. Clin. Nutr. 2009, 90, 1433-1439.

36. Cheong, J.M.; Martin, B.R.; Jackson, G.S.; Elmore, D.; McCabe, G.P.; Nolan, J.R.; Barnes, S.; Peacock, M.; Weaver, C.M. Soy isoflavones do not affect bone resorption in postmenopausal women: A dose-response study using a novel approach with 41Ca. J. Clin. Endocrinol. Metab. 2007, 92, 577-582.

37. Booth, S.L.; Dallal, G.; Shea, M.K.; Gundberg, C.; Peterson, J.W.; Dawson-Hughes, B. Effect of vitamin K supplementation on bone loss in elderly men and women. J. Clin. Endocrinol. Metab. 2008, 93, 1217-1223.

38. Bolton-Smith, C.; McMurdo, M.E.; Paterson, C.R.; Mole, P.A.; Harvey, J.M.; Fenton, S.T.; Prynne, C.J.; Mishra, G.D.; Shearer, M.J. Two-year randomized controlled trial of vitamin K1 (phylloquinone) and vitamin D3 plus calcium on the bone health of older women. J. Bone Miner. Res. 2007, 22, 509-519.

39. Braam, L.A.; Knapen, M.H.; Geusens, P.; Brouns, F.; Hamulyák, K.; Gerichhausen, M.J.;
Vermee, C. Vitamin K1 supplementation retards bone loss in postmenopausal women between
50 and 60 years of age. Calcif. Tissue Int. 2003, 73, 21-26.

40. Lin, P.H.; Appel, L.J.; Funk, K.; Craddick, S.; Chen, C.; Elmer, P.; McBurnie, M.A.;
Champagne, C. The PREMIER intervention helps participants follow the Dietary Approaches to
Stop Hypertension dietary pattern and the current Dietary Reference Intakes recommendations. J. Am. Diet. Assoc. 2007, 107, 1541-1551.

41. Bulló, M.; Amigó-Correig, P.; Márquez-Sandoval, F.; Babio, N.; Martínez-González, M.A.; Estruch, R.; Basora, J.; Solà, R.; Salas-Salvadó, J. Mediterranean diet and high dietary acid load associated with mixed nuts: Effect on bone metabolism in elderly subjects. J. Am. Geriatr. Soc. 2009, 57, 1789-1798.

42. FDA (Food and Drug Administration). Title 21: Food and Drugs, Part 101 Food labeling. Subpart E. Specific requirements for health claims. Health claims: Calcium and osteoporosis. Available online: http://www.cfsan.fda.gov/~dms/lab-ssa.html (accessed on 15 August 2008).

43. DIPART (Vitamin D Individual Patient Analysis of Randomized Trials) Group. Patient level pooled analysis of 68 500 patients from seven major vitamin D fracture trials in US and Europe. BMJ 2010, 340, b5463.

44. Reid, I.R.; Bolland, M.J.; Grey, A. Effect of calcium supplementation on hip fractures. Osteoporos. Int. 2008, 19, 1119-1123.

45. Tang, B.M.; Eslick, G.D.; Nowson, C.; Smith, C.; Bensoussan, A. Use of calcium or calcium in combination with vitamin D supplementation to prevent fractures and bone loss in people aged 50 years and older: A meta-analysis. Lancet 2007, 370, 657-666.

46. Avenell, A.; Gillespie, W.J.; Gillespie, L.D.; O’Connell, D. Vitamin D and vitamin D analogues for preventing fractures associated with involutional and post-menopausal osteoporosis. Cochrane Database Syst. Rev. 2009, CD000227; doi:10.1002/14651858.CD000227.pub3.

47. Blalock, S.J.; Currey, S.S.; DeVellis, R.F.; Anderson, J.J.; Gold, D.T.; Dooley, M.A. Using a short food frequency questionnaire to estimate dietary calcium consumption: A tool for patient education. Arthritis Care Res. 1998, 11, 479-484.

48. Blalock, S.J.; Norton, L.L.; Patel, R.A.; Cabral, K.; Thomas, C.L. Development and assessment of a short instrument for assessing dietary intakes of calcium and vitamin D. J. Am. Pharm. Assoc. 2003, 43, 685-693.

49. Cook, A.J.; Friday, J.E. Food mixture or ingredient sources for dietary calcium: Shifts in food group contributions using four grouping protocols. J. Am. Diet. Assoc. 2003, 103, 1513-1519.

50. Harnack, L.J.; Lytle, L.A.; Story, M.; Galuska, D.A.; Schmitz, K.; Jacobs, D.R., Jr.; Gao, S. Reliability and validity of a brief questionnaire to assess calcium intake of middle-school-aged children. J. Am. Diet. Assoc. 2006, 106, 1790-1795.

51. Jensen, J.K.; Gustafson, D.; Boushey, C.J.; Auld, G.; Bock, M.A.; Bruhn, C.M.; Gabel, K.; Misner, S.; Novotny, R.; Peck, L.; Read, M. Development of a food frequency questionnaire to estimate calcium intake of Asian, Hispanic, and white youth. J. Am. Diet. Assoc. 2004, 104, 762-769.

52. Montomoli, M.; Gonnelli, S.; Giacchi, M.; Mattei, R.; Cuda, C.; Rossi, S.; Gennari, C. Validation of a food frequency questionnaire for nutritional calcium intake assessment in Italian women. Eur. J. Clin. Nutr. 2002, 56, 21-30.

53. Ward, K.D.; Hunt, K.M.; Berg, M.B.; Slawson, D.A.; Vukadinovich, C.M.; McClanahan, B.S.; Clemens, L.H. Reliability and validity of a brief questionnaire to assess calcium intake in female collegiate athletes. Int. J. Sport Nutr. Exerc. Metab. 2004, 14, 209-221.

54. Yanek, L.R.; Moy, T.F.; Becker, D.M. Comparison of food frequency and dietary recall methods in African-American women. J. Am. Diet. Assoc. 2001, 101, 1361-1364.

55. Plawecki, K.; Evans, E.; Mojtahedi, M.; McAuley, E.; Chapman-Novakofski, K. Assessing
calcium intake in postmenopausal women. Prev. Chronic Dis. 2009, 6, A124. Available online: http://www.cdc.gov/pcd/issues/2009/oct/08_0197.htm (accessed on 8 October 2009).

56. Contento, I. Review of Nutrition Education Research in the Journal of Nutrition Education and Behavior, 1998 to 2007. J. Nutr. Educ. Behav. 2008, 40, 331-340.

57. Kim, K.; Reicks, M.; Sjoberg, S. Applying the Theory of Planned Behavior to Predict Dairy Product Consumption by Older Adults. J. Nutr. Educ. Behav. 2003, 35, 294-301.

58. Cerin, E.; Barnett, A.; Baranowski, T. Testing Theories of Dietary Behavior Change in Youth Using the Mediating Variable Model with Intervention Programs. J. Nutr. Educ. Behav. 2009, 41, 309-318.

59. Dawson-Hughes, B. Interaction of dietary calcium and protein in bone health in humans. J. Nutr. 2003, 133, 852S-854S.

60. Kerstetter, J.E.; O’Brien, K.O.; Insogna, K.L. Low protein intake: The impact on calcium and bone homeostasis. J. Nutr. 2003, 133, 855S-861S.

61. Spence, L.A.; Weaver, C.M. New perspectives on dietary protein and bone health: Preface. J. Nutr. 2003, 133, 850S-851S.

62. Weikert, C.; Walter, D.; Hoffmann, K.; Kroke, A.; Bergmann, M.M.; Boeing, H. The relation between dietary protein, calcium and bone health in women: Results from the EPIC-Potsdam cohort. Ann. Nutr. Metab. 2005, 49, 312-318.

63. Bemben, M.G.; Witten, M.S.; Carter, J.M.; Eliot, K.A.; Knehans, A.W.; Bemben, D.A. The effects of supplementation with creatine and protein on muscle strength following a traditional resistance training program in middle-aged and older men. J. Nutr. Health Aging 2010, 14, 155-159.

© 2010 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license http://creativecommons.org/licenses/by/3.0






This page created 21 Nov 2010 16:31
Last updated 11 Dec 2013 22:18

© 2014 by Eric Troy and Ground Up Strength. All Rights Reserved. Please contact for permissions.