Dairy Products for Preventing Osteoporosis: History
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Breast milk is the best infant food, but milk should not be avoided later in life to prevent losing bone mass. On the other hand, more and more people limit their milk consumption and consume other dairy or non-dairy products. For example, they are usually replaced with plant beverages, which should be consumed carefully in several age groups. Additionally, an important element of milk and dairy products, as well as plant beverages, are probiotics and prebiotics, which may modulate bone turnover. Dietary recommendations focused on milk, and dairy products are an important element for the prevention of osteoporosis.

  • cow’s milk
  • plant milk
  • bone mineral density
  • lactose intolerance
  • cow’s milk allergy
  • nutrition
  • osteoporosis
  • bone health

1. Osteoporosis

Osteoporosis is a skeletal disorder with decreased bone mineral density (BMD) and bone strength, leading to increased risk of fractures. Osteoporosis may be divided into primary and secondary (70% and 30% of all cases, respectively). Secondary osteoporosis can be caused by several diseases, e.g., inflammatory bowel diseases, celiac disease, or endocrinology disorders [1]. Risk factors of osteoporosis are, among others, malabsorption, cigarette smoking, stress, air pollution, older age, low physical activity, and co-occurring diseases (Figure 1) [2][3]. Osteoporosis affects women twice as often as men. Additionally, it is estimated that 0.3 million and 1.7 million people have hip fractures in the USA and Europe, respectively [4]. Having a proper peak bone mass and maintaining it as long as possible is especially important for osteoporosis prevention.

Figure 1. Risk factors of osteoporosis.

It is vital to note that 1/3 adult people achieve their total bone mass between 2 and 4 Tanner stages, and 95% of peak bone mass is reached before the age of 16. For this reason, puberty is a key time for bone mass formation [5][6]. Data about the age of peak bone mass are inconsistent, and it is suggested that a peak bone mass is reached at around 18 years of age for women and 20 years of age for men [7]. However, other authors suggest peak bone mass is reached between 20 and 30 years of age [8].

Additionally, peak bone mass is influenced by genetic and environmental factors, including diet [9]. Therefore, proper intake of minerals and vitamins, especially vitamin D and calcium, is essential, especially in a period of rapid growth, such as childhood and adolescence. The next stage is bone remodeling, which leads to total rebuilding of the skeleton—once every ten years with no change in bone net weight. Proper intake of calcium and vitamin D helps maintain peak bone mass. The next stage is bone resorption, associated with higher activity of osteoclasts than osteoblasts, which results in a decreased bone mass and increased risk of fracture [5].

It is vital to notice that low vitamin D concentration causes hyperparathyroidism and decreases intestinal absorption of calcium, leading to bone resorption [10][11]. Vitamin D deficiency is associated with osteoporosis [12]. Moreover, women with fractures presented higher prevalence of vitamin D deficiency [13].

An important element of osteoporosis prevention is physical activity [14]. Physical activity increases BMD [15]. Additionally, regular exercise increases muscle strength, decreasing risk of fall and fracture [16].

Table 1 and Table 2 show calcium content in selected products and the Recommended Daily Intake of calcium for various age groups.

Table 2. Recommended Daily Intake of calcium for various age groups [18].

Age RDI (mg)
0–6 months 200
7–12 months 260
1–3 years 700
4–8 years 1000
9–13 years 1300
14–18 years 1300
19–50 years 1000
51–70 years  
Women 1200
Men 1000
71 years and older 1200
Pregnant and breastfeeding  
Teenagers 1300
Adults 1000

RDI-Recommended Daily Intake.

2. Breast Milk

Compounds of breast milk may come from three sources: the diet of the mother, stocks storage by mother, and lactocytes [19]. The amount of produced milk was negatively correlated with maternal age and weight gained during pregnancy, but these factors did not affect the content of fat in milk. Diet also did not influence the amount and compounds of milk, especially the content of protein, fat, carbohydrates, iron, and calcium. Additionally, fat-soluble vitamins content depended on a mother’s diet to a smaller extent and water-soluble vitamins to a significant one [20][21].

Lactose is the main carbohydrate of human milk. It is made up of glucose and especially important galactose, which supports the development of the central nervous system. Additionally, breast milk contains oligosaccharides (about 15–23 g/L in colostrum and 1–10 g/L in mature milk) [22].

Supplementation of protein in the mother’s diet did not affect milk composition [23]. The main proteins in breast milk are casein, whey protein and mucin; however, protein content decreases with the child’s age [22].

Fats—mostly triacylglycerols (98%)—are a source of about 44% of total breast milk energy. Additionally, breast milk contains more than 200 various fatty acids (FA). The breast milk of European women contains 35–40% of saturated FA, 45–50% mono-unsaturated FA and 15% poly-unsaturated FA [22]. Moreover, the amount of long-chain FA and free FA is greater in human milk than cow’s milk [21]. Fat in human milk is absorbed at around 92%. It is vital to notice that the amount of cholesterol was lower in breast milk than in cow’s or sheep milk [24]. The composition of FA is dependent on the mother’s diet. Patin et al. have shown that, after consumption of 100g of fish (sardines) three times a week by breastfeeding women, the amount of omega-3 FA in breast milk was raised [25].

The optimum calcium:phosphorus (Ca:P) ratio is between 1:1 and 1:2 [26]. Furthermore, the Ca:P ratio is better in breast milk than cow’s milk (1.4–1.7:1 and 1.24:1, respectively) [27]. Additionally, the Ca:P ratio in cow’s milk is dependent on fat content and is higher in whole milk than skimmed [28].

Breast milk is also a source of immune factors, including Il2 (Interleukin 2), Il4, Il10, IgA (immunoglobulin A) total IgG, or macrophages. There were no significant differences in the amount of immune factors in breast milk from women after exposure to stress. However, two weeks after the stressful situation, the level of cortisol in milk was significantly higher. Moreover, breast milk also contains growth hormones [19][29].

3. Lactation and BMD

Breastfeeding may affect the BMD of both mother and child. Children who were initially (first six months of life) breastfed and later fed milk formula (up to 2 years old) had higher BMD than children only breastfed or only fed with milk formula (for the first two years of life) [30]. According to Blanco et al., exclusive breastfeeding for the first six months of life was associated with higher BMD in adolescents, when compared with mixed feeding [31]. Additionally, 6-year-old children who were breastfed presented higher BMD than children who were never breastfed. Among breastfed children, the group that was exclusively breastfed for minimum the first four months presented lower BMD and higher bone area (BA) than children who were not breastfed for the first four months [32].

On the other hand, among mothers, a breastfeeding period was negatively correlated with BMD of the lumbar spine. Additionally, the frequency of osteoporosis was higher among women who were breastfeeding for a minimum of 37 months than women who were breastfeeding for a shorter period. However, the age of the mother and number of deliveries did not correlate with BMD [33]. According to Tsvetov et al., a negative correlation between the number of deliveries and BMD was reported [34]. Moreover, breastfeeding for more than 18 months increased vertebral fracture risk more than twice in postmenopausal women [35]. In turn, Cooke-Hubley et al. reported that parity and lactation are not associated with higher risk of decreased BMD, clinical fragility or radiographic vertebral fractures over 10 years [36]. It is vital to notice that absorption of calcium during pregnancy increases, but this does not occur during lactation, and calcium is resorbed from the mother’s bones [37].

4. Cow’s Milk and Dairy Products and BMD

Milk and dairy products contain protein, minerals and vitamins (Figure 2), which may be beneficial for bone health [38]. Cultured dairy products (e.g., yoghurt and kefir) are formed by adding starter cultures, which convert the lactose in milk to lactic acid. For this reason, fermented dairy products may also contain bacteria, which are beneficial for human health [39].

Figure 2. The effect of cow’s milk on bone.

Studies have confirmed that dairy product consumption is essential for human health, especially in the pediatric group. Bone mineral content (BMC) was lower by about 5.6% in women aged 20–49 years who had consumed less than one portion of milk weekly during childhood, when compared with women who had consumed more than one portion. Additionally, low milk consumption during adolescence was associated with a 3% reduction in the BMD and BMC of the hip in adulthood. Among women over 50 years old, there was a non-linear association between milk consumption in childhood and adolescence and BMD and BMC of the hip. Moreover, low milk intake in childhood was linked with two times higher fracture risk [40]. For this reason, osteoporosis is called pediatric disease with geriatric consequences [41]. It is vital to note that children who had avoided milk and had not eaten food fortified with calcium reported fracture before puberty more frequently than children who had consumed cow’s milk [42]. Adults’ height correlated positively with the amount of milk consumed between the ages of 5–12 and 13–17 [43]. Higher consumption of dairy products was associated with higher total BMD among 6-year-old girls and boys. Additionally, positive association occurred between total BMD and intake of a minimum one portion of dairy products daily [44]. Sioen et al. have reported that consumption of dairy products by children (6–12 years old) positively affected total BMC and areal bone mineral density (aBMD) after adjusting for confounding factors [45]. Among young people (18–30 years old), total BMD was lower among people with lower dairy product consumption than subjects with proper intake. There was no significant difference in lumbar spine BMD among groups. It is vital to note that lower intake of dairy products was associated with higher BMI (Body Mass Index) and adipose tissue percentage [46]. On the other hand, as van Dongen et al. have shown, higher intake of milk, milk + yoghurt, and milk + yogurt + cheese was associated with higher trabecular and integral vBMD and VCS among men but not women [47]. Additionally, the positive impact of dairy products on BMD may depend on serum vitamin D levels. Intake of dairy products, fluid dairy and milk was associated with higher BMD of the femoral neck and lumbar spine among subjects with normal 25(OH)D concentration but not in a group with vitamin D deficiency [48]. Among 70-year-old women and men, total dairy product intake was positively associated with trabecular and cortical cross-sectional areas in the tibia and the areal bone mineral density of the radius [49].

On the other hand, as Michaëlsson et al. have reported, dairy product intake was linked with higher mortality in women and men and a higher risk of fracture among women in Sweden [50]. However, it should be mentioned that in Sweden, milk was fortified with vitamin A in the years 1987–1990 and 1997, which may influence the abovementioned results [51]. About 60% of dietary calcium should come from dairy products. Meeting dairy calcium requirements correlated positively with children’s BMD [52]. Meta-analysis has not shown a clear association between the group with an enormous amount of milk intake and risk of osteoporotic fracture and hip fracture. Additionally, results were heterogeneous and did not allow for clear conclusions [53].

5. Plant Milk (Plant Beverages) and BMD

In the last years, the market availability of plant products, substitutes for cow’s milk, has increased. These products are made from, among others, soybeans, rice, oats, almonds, coconut and are called plant milk or plant beverages. The most similar protein content to cow’s milk occurs in soya beverages. In turn, the content of protein in rice, oats and almond milk is very low. Plant beverages contain a lower amount of saturated fatty acids and do not contain cholesterol. However, producers frequently add fat and sugar to these products, which may increase the risk of metabolic disorders. Moreover, plant beverages contain a lower amount of iodine, potassium, phosphorus and selenium compared with semi-skimmed milk [41].

Data about the differences between the absorption of calcium from dairy and soy products are unclear [54][55]. It is vital to note that the Ca:P ratio in unfortified soya milk is lower than in cow’s milk (2:1 and 1.3:1, respectively). However, calcium fortification changes this ratio for the better (1.8:1) [56]. Nevertheless, calcium and vitamin D fortification of plant beverages is not obligatory in every country [57].

Soy products contain isoflavones, which show an affinity with the estrogen receptor and protects from loss of bone mass. 18-months of intake of cow’s milk fortified with calcium by postmenopausal women increased the BMD of the femoral neck significantly. However, consumption of soy-fortified milk decreased (not significantly) femoral neck BMD [58]. Additionally, intake of cow’s milk with soy isoflavones led to an increase in the level of 25OHD and a decrease in the concentration of bone turnover markers (osteoprotegerin and tartrate-resistant acid phosphatase) [59]. As Lydeking-Olsen et al. have reported among women divided into four groups—consuming soy products, treated with transdermal progesterone (TDP), combined group (consuming soy products and treated with TDP) and control group—BMD and BMC decreased significantly in combined and control groups. BMD and BMC increased in the soy group only, but differences were not significant [60]. An animal study has shown that isoflavones inhibited bone loss in mature female rats with a decreased level of estradiol [61].

An in vitro study has shown that germinated soy germ extracts increased expression of osteocalcin and alkaline phosphatase [62].

Among individuals who weekly drink 1.3 cups of soy milk fortified with calcium, decreased low T-score risk was decreased by 57% when compared with individuals who did not drink soy milk, even if they consumed dairy products [63]. Children are the group who are particularly vulnerable to nutrients deficiencies. Children that consumed plant beverages presented lower serum concentration of vitamin D than children who drank cow’s milk [57].

Cow’s milk is often replaced with plant milk by vegans. According to Ambroszkiewicz et al., people on a vegan diet consume an insufficient amount of calcium and vitamin D, which may lead to osteoporosis [64].

Consumption of unfortified beverages instead of breast milk, cow’s or modified milk may be especially harmful to children in the first year of life because it could lead to the development of rickets, failure in thrive, kwashiorkor, anaemia, metabolic alkalosis, scurvy and hyperoxaluria [65].

Table 3 and Table 4 present the content of nutrients in dairy products and various milks.

This entry is adapted from the peer-reviewed paper 10.3390/nu13041329

References

  1. Janiszewska, M.; Kulik, T.; Dziedzic, M.; Żołnierczuk-Kieliszek, D.; Barańska, A. Osteoporosis as a Social Problem- Pathogenesis, Symptoms and Risk Factors of Postmenopausal Osteoporosis. Probl. Hig. Epidemiol. 2015, 96, 106–114.
  2. Pouresmaeili, F.; Kamalidehghan, B.; Kamarehei, M.; Goh, Y.M. A Comprehensive Overview on Osteoporosis and Its Risk Factors. Ther. Clin. Risk Manag. 2018, 14, 2029–2049.
  3. Ratajczak, A.E.; Rychter, A.M.; Zawada, A.; Dobrowolska, A.; Krela-Kaźmierczak, I. Nutrients in the Prevention of Osteoporosis in Patients with Inflammatory Bowel Diseases. Nutrients 2020, 12, 1702.
  4. Rosen, C.J. The Epidemiology and Pathogenesis of Osteoporosis; MDText.com, Inc.: South Dartmouth, MA, USA, 2020.
  5. Hodges, J.K.; Cao, S.; Cladis, D.P.; Weaver, C.M. Lactose Intolerance and Bone Health: The Challenge of Ensuring Adequate Calcium Intake. Nutrients 2019, 11, 718.
  6. Gordon, C.M.; Zemel, B.S.; Wren, T.A.L.; Leonard, M.B.; Bachrach, L.K.; Rauch, F.; Gilsanz, V.; Rosen, C.J.; Winer, K.K. The Determinants of Peak Bone Mass. J. Pediatrics 2017, 180, 261–269.
  7. Osteoporosis: Peak Bone Mass in Women|NIH Osteoporosis and Related Bone Diseases National Resource Center. Available online: (accessed on 19 December 2020).
  8. Weaver, C.M.; Gordon, C.M.; Janz, K.F.; Kalkwarf, H.J.; Lappe, J.M.; Lewis, R.; O’Karma, M.; Wallace, T.C.; Zemel, B.S. The National Osteoporosis Foundation’s Position Statement on Peak Bone Mass Development and Lifestyle Factors: A Systematic Review and Implementation Recommendations. Osteoporos. Int. 2016, 27, 1281–1386.
  9. McGuigan, F.E.A.; Murray, L.; Gallagher, A.; Davey-Smith, G.; Neville, C.E.; Van’t Hof, R.; Boreham, C.; Ralston, S.H. Genetic and Environmental Determinants of Peak Bone Mass in Young Men and Women. J. Bone Miner. Res. 2002, 17, 1273–1279.
  10. Muscogiuri, G.; Barrea, L.; Altieri, B.; Di Somma, C.; Bhattoa, H.P.; Laudisio, D.; Duval, G.T.; Pugliese, G.; Annweiler, C.; Orio, F.; et al. Calcium and Vitamin D Supplementation. Myths and Realities with Regard to Cardiovascular Risk. Curr. Vasc. Pharmacol. 2019, 17, 610–617.
  11. Fischer, V.; Haffner-Luntzer, M.; Amling, M.; Ignatius, A. Calcium and Vitamin D in Bone Fracture Healing and Post-Traumatic Bone Turnover. Eur. Cell Mater. 2018, 35, 365–385.
  12. Dadra, A.; Aggarwal, S.; Kumar, P.; Kumar, V.; Dibar, D.P.; Bhadada, S.K. High Prevalence of Vitamin D Deficiency and Osteoporosis in Patients with Fragility Fractures of Hip: A Pilot Study. J. Clin. Orthop. Trauma 2019, 10, 1097–1100.
  13. Lee, J.S.; Kim, J.W. Prevalence of Vitamin D Deficiency in Postmenopausal High- and Low-Energy Fracture Patient. Arch. Osteoporos. 2018, 13, 109.
  14. Warburton, D.E.R.; Nicol, C.W.; Bredin, S.S.D. Health Benefits of Physical Activity: The Evidence. CMAJ 2006, 174, 801–809.
  15. Maggio, A.B.R.; Rizzoli, R.R.; Marchand, L.M.; Ferrari, S.; Beghetti, M.; Farpour-Lambert, N.J. Physical Activity Increases Bone Mineral Density in Children with Type 1 Diabetes. Med. Sci. Sports Exerc. 2012, 44, 1206–1211.
  16. Chan, D.-C.; Chang, C.-B.; Han, D.-S.; Hong, C.-H.; Hwang, J.-S.; Tsai, K.-S.; Yang, R.-S. Effects of Exercise Improves Muscle Strength and Fat Mass in Patients with High Fracture Risk: A Randomized Control Trial. J. Formos. Med. Assoc. 2018, 117, 572–582.
  17. Calcium Content of Common Foods | International Osteoporosis Foundation. Available online: (accessed on 14 December 2020).
  18. Office of Dietary Supplements-Calcium. Available online: (accessed on 8 December 2020).
  19. Ballard, O.; Morrow, A.L. Human Milk Composition: Nutrients and Bioactive Factors. Pediatr. Clin. North. Am. 2013, 60, 49–74.
  20. Hytten, F.E. Clinical and Chemical Studies in Human Lactation. VIII. Relationship of the Age, Physique, and Nutritional Status of the Mother to the Yield and Composition of Her Milk. Br. Med. J. 1954, 2, 844–845.
  21. Thomson, A.M.; Black, A.E. Nutritional Aspects of Human Lactation. Bull. World Health Organ. 1975, 52, 163–177.
  22. Mosca, F.; Giannì, M.L. Human Milk: Composition and Health Benefits. Pediatr. Med. Chir. 2017, 39, 155.
  23. Gopalan, C. Effect of Nutrition on Pregnancy and Lactation. Bull. World Health Organ. 1962, 26, 203–211.
  24. Pietrzak-Fiećko, R.; Kamelska-Sadowska, A.M. The Comparison of Nutritional Value of Human Milk with Other Mammals’ Milk. Nutrients 2020, 12, 1404.
  25. Patin, R.V.; Vítolo, M.R.; Valverde, M.A.; Carvalho, P.O.; Pastore, G.M.; Lopez, F.A. The Influence of Sardine Consumption on the Omega-3 Fatty Acid Content of Mature Human Milk. J. Pediatr. 2006, 82, 63–69.
  26. Loughrill, E.; Wray, D.; Christides, T.; Zand, N. Calcium to Phosphorus Ratio, Essential Elements and Vitamin D Content of Infant Foods in the UK: Possible Implications for Bone Health. Matern. Child. Nutr. 2017, 13, e12368.
  27. Mahdi, A.A.; Brown, R.B.; Razzaque, M.S. Osteoporosis in Populations with High Calcium Intake: Does Phosphate Toxicity Explain the Paradox? Ind. J. Clin. Biochem. 2015, 30, 365–367.
  28. Burgess, K. Milk and Dairy Products in Human Nutrition; Muehlhoff, E., Bennett, A., McMahon, D., Eds.; Food and Agriculture Organisation of the United Nations (FAO): Rome, Italy, 2013; ISBN 978-92-5-107864-8.
  29. Aparicio, M.; Browne, P.D.; Hechler, C.; Beijers, R.; Rodríguez, J.M.; de Weerth, C.; Fernández, L. Human Milk Cortisol and Immune Factors over the First Three Postnatal Months: Relations to Maternal Psychosocial Distress. PLoS ONE 2020, 15, e0233554.
  30. Al-Agha, A.E.; Kabli, Y.O.; AlBeiruty, M.G.; Milyani, A.A. Determinants of Bone Mineral Density through Quantitative Ultrasound Screening of Healthy Children Visiting Ambulatory Paediatric Clinics. Saudi Med. J. 2019, 40, 560–567.
  31. Blanco, E.; Burrows, R.; Reyes, M.; Lozoff, B.; Gahagan, S.; Albala, C. Breastfeeding as the Sole Source of Milk for 6 Months and Adolescent Bone Mineral Density. Osteoporos. Int. 2017, 28, 2823–2830.
  32. van den Hooven, E.H.; Gharsalli, M.; Heppe, D.H.M.; Raat, H.; Hofman, A.; Franco, O.H.; Rivadeneira, F.; Jaddoe, V.W.V. Associations of Breast-Feeding Patterns and Introduction of Solid Foods with Childhood Bone Mass: The Generation R Study. Br. J. Nutr. 2016, 115, 1024–1032.
  33. Hwang, I.R.; Choi, Y.K.; Lee, W.K.; Kim, J.G.; Lee, I.K.; Kim, S.W.; Park, K.G. Association between Prolonged Breastfeeding and Bone Mineral Density and Osteoporosis in Postmenopausal Women: KNHANES 2010–2011. Osteoporos. Int. 2016, 27, 257–265.
  34. Tsvetov, G.; Levy, S.; Benbassat, C.; Shraga-Slutzky, I.; Hirsch, D. Influence of Number of Deliveries and Total Breast-Feeding Time on Bone Mineral Density in Premenopausal and Young Postmenopausal Women. Maturitas 2014, 77, 249–254.
  35. Bolzetta, F.; Veronese, N.; De Rui, M.; Berton, L.; Carraro, S.; Pizzato, S.; Girotti, G.; De Ronch, I.; Manzato, E.; Coin, A.; et al. Duration of Breastfeeding as a Risk Factor for Vertebral Fractures. Bone 2014, 68, 41–45.
  36. Cooke-Hubley, S.; Gao, Z.; Mugford, G.; Kaiser, S.M.; Goltzman, D.; Leslie, W.D.; Davison, K.S.; Brown, J.P.; Probyn, L.; Lentle, B.; et al. Parity and Lactation Are Not Associated with Incident Fragility Fractures or Radiographic Vertebral Fractures over 16 Years of Follow-up: Canadian Multicentre Osteoporosis Study (CaMos). Arch. Osteoporos. 2019, 14, 49.
  37. Kovacs, C.S. Calcium and Phosphate Metabolism and Related Disorders during Pregnancy and Lactation. In Endotext; Feingold, K.R., Anawalt, B., Boyce, A., Chrousos, G., de Herder, W.W., Dungan, K., Grossman, A., Hershman, J.M., Hofland, J., Kaltsas, G., et al., Eds.; MDText.com, Inc.: South Dartmouth, MA, USA, 2000.
  38. Tunick, M.H.; Van Hekken, D.L. Dairy Products and Health: Recent Insights. J. Agric. Food Chem. 2015, 63, 9381–9388.
  39. Aryana, K.J.; Olson, D.W. A 100-Year Review: Yogurt and Other Cultured Dairy Products. J. Dairy Sci. 2017, 100, 9987–10013.
  40. Kalkwarf, H.J.; Khoury, J.C.; Lanphear, B.P. Milk Intake during Childhood and Adolescence, Adult Bone Density, and Osteoporotic Fractures in US Women. Am. J. Clin. Nutr. 2003, 77, 257–265.
  41. Thorning, T.K.; Raben, A.; Tholstrup, T.; Soedamah-Muthu, S.S.; Givens, I.; Astrup, A. Milk and Dairy Products: Good or Bad for Human Health? An Assessment of the Totality of Scientific Evidence. Food Nutr. Res. 2016, 60, 32527.
  42. Goulding, A.; Rockell, J.E.P.; Black, R.E.; Grant, A.M.; Jones, I.E.; Williams, S.M. Children Who Avoid Drinking Cow’s Milk Are at Increased Risk for Prepubertal Bone Fractures. J. Am. Diet. Assoc. 2004, 104, 250–253.
  43. Wiley, A.S. Does Milk Make Children Grow? Relationships between Milk Consumption and Height in NHANES 1999–2002. Am. J. Hum. Biol. 2005, 17, 425–441.
  44. Bielemann, R.M.; dos S Vaz, J.; Domingues, M.R.; Matijasevich, A.; Santos, I.S.; Ekelund, U.; Horta, B.L. Are Consumption of Dairy Products and Physical Activity Independently Related to Bone Mineral Density of 6-Year-Old Children? Longitudinal and Cross-Sectional Analyses in a Birth Cohort from Brazil. Public Health Nutr. 2018, 21, 2654–2664.
  45. Sioen, I.; Michels, N.; Polfliet, C.; De Smet, S.; D’Haese, S.; Roggen, I.; Deschepper, J.; Goemaere, S.; Valtueña, J.; De Henauw, S. The Influence of Dairy Consumption, Sedentary Behaviour and Physical Activity on Bone Mass in Flemish Children: A Cross-Sectional Study. BMC Public Health 2015, 15, 717.
  46. Torres-Costoso, A.; López-Muñoz, P.; Ferri-Morales, A.; Bravo-Morales, E.; Martínez-Vizcaíno, V.; Garrido-Miguel, M. Body Mass Index, Lean Mass, and Body Fat Percentage as Mediators of the Relationship between Milk Consumption and Bone Health in Young Adults. Nutrients 2019, 11, 2500.
  47. van Dongen, L.H.; Kiel, D.P.; Soedamah-Muthu, S.S.; Bouxsein, M.L.; Hannan, M.T.; Sahni, S. Higher Dairy Food Intake Is Associated With Higher Spine Quantitative Computed Tomography (QCT) Bone Measures in the Framingham Study for Men But Not Women. J. Bone Miner. Res. 2018, 33, 1283–1290.
  48. Mangano, K.M.; Noel, S.E.; Sahni, S.; Tucker, K.L. Higher Dairy Intakes Are Associated with Higher Bone Mineral Density among Adults with Sufficient Vitamin D Status: Results from the Boston Puerto Rican Osteoporosis Study. J. Nutr. 2019, 149, 139–148.
  49. Hallkvist, O.M.; Johansson, J.; Nordström, A.; Nordström, P.; Hult, A. Dairy Product Intake and Bone Properties in 70-Year-Old Men and Women. Arch. Osteoporos. 2018, 13, 9.
  50. Michaëlsson, K.; Wolk, A.; Langenskiöld, S.; Basu, S.; Warensjö Lemming, E.; Melhus, H.; Byberg, L. Milk Intake and Risk of Mortality and Fractures in Women and Men: Cohort Studies. BMJ 2014, 349, g6015.
  51. Rozenberg, S.; Body, J.-J.; Bruyère, O.; Bergmann, P.; Brandi, M.L.; Cooper, C.; Devogelaer, J.-P.; Gielen, E.; Goemaere, S.; Kaufman, J.-M.; et al. Effects of Dairy Products Consumption on Health: Benefits and Beliefs—Commentary from the Belgian Bone Club and the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases. Calcif. Tissue Int. 2016, 98, 1–17.
  52. Infante, D.; Tormo, R. Risk of Inadequate Bone Mineralization in Diseases Involving Long-Term Suppression of Dairy Products. J. Pediatric Gastroenterol. Nutr. 2000, 30, 310–313.
  53. Matía-Martín, P.; Torrego-Ellacuría, M.; Larrad-Sainz, A.; Fernández-Pérez, C.; Cuesta-Triana, F.; Rubio-Herrera, M.Á. Effects of Milk and Dairy Products on the Prevention of Osteoporosis and Osteoporotic Fractures in Europeans and Non-Hispanic Whites from North America: A Systematic Review and Updated Meta-Analysis. Adv. Nutr. 2019, 10, S120–S143.
  54. Tang, A.L.; Walker, K.Z.; Wilcox, G.; Strauss, B.J.; Ashton, J.F.; Stojanovska, L. Calcium Absorption in Australian Osteopenic Post-Menopausal Women: An Acute Comparative Study of Fortified Soymilk to Cows’ Milk. Asia Pac. J. Clin. Nutr. 2010, 19, 243–249.
  55. Heaney, R.P.; Dowell, M.S.; Rafferty, K.; Bierman, J. Bioavailability of the Calcium in Fortified Soy Imitation Milk, with Some Observations on Method. Am. J. Clin. Nutr. 2000, 71, 1166–1169.
  56. Geiker, N.R.W.; Mølgaard, C.; Iuliano, S.; Rizzoli, R.; Manios, Y.; van Loon, L.J.C.; Lecerf, J.-M.; Moschonis, G.; Reginster, J.-Y.; Givens, I.; et al. Impact of Whole Dairy Matrix on Musculoskeletal Health and Aging–Current Knowledge and Research Gaps. Osteoporos. Int. 2020, 31, 601–615.
  57. Lee, G.J.; Birken, C.S.; Parkin, P.C.; Lebovic, G.; Chen, Y.; L’Abbé, M.R.; Maguire, J.L. TARGet Kids! Collaboration Consumption of Non-Cow’s Milk Beverages and Serum Vitamin D Levels in Early Childhood. CMAJ 2014, 186, 1287–1293.
  58. Gui, J.-C.; Brašić, J.R.; Liu, X.-D.; Gong, G.-Y.; Zhang, G.-M.; Liu, C.-J.; Gao, G.-Q. Bone Mineral Density in Postmenopausal Chinese Women Treated with Calcium Fortification in Soymilk and Cow’s Milk. Osteoporos. Int. 2012, 23, 1563–1570.
  59. García-Martín, A.; Quesada Charneco, M.; Alvárez Guisado, A.; Jiménez Moleón, J.J.; Fonollá Joya, J.; Muñoz-Torres, M. Effect of milk product with soy isoflavones on quality of life and bone metabolism in postmenopausal Spanish women: Randomized trial. Med. Clin. 2012, 138, 47–51.
  60. Lydeking-Olsen, E.; Beck-Jensen, J.-E.; Setchell, K.D.R.; Holm-Jensen, T. Soymilk or Progesterone for Prevention of Bone Loss—A 2 Year Randomized, Placebo-Controlled Trial. Eur. J. Nutr. 2004, 43, 246–257.
  61. Yanaka, K.; Higuchi, M.; Ishimi, Y. Anti-Osteoporotic Effect of Soy Isoflavones Intake on Low Bone Mineral Density Caused by Voluntary Exercise and Food Restriction in Mature Female Rats. J. Nutr. Sci. Vitam. 2019, 65, 335–342.
  62. Choi, C.-W.; Choi, S.-W.; Kim, H.-J.; Lee, K.-S.; Kim, S.-H.; Kim, S.-L.; Do, S.H.; Seo, W.-D. Germinated Soy Germ with Increased Soyasaponin Ab Improves BMP-2-Induced Bone Formation and Protects against in Vivo Bone Loss in Osteoporosis. Sci. Rep. 2018, 8, 12970.
  63. Matthews, V.L.; Knutsen, S.F.; Beeson, W.L.; Fraser, G.E. Soy Milk and Dairy Consumption Are Independently Associated with Ultrasound Attenuation of the Heel Bone among Postmenopausal Women: The Adventist Health Study-2 (AHS-2). Nutr. Res. 2011, 31, 766–775.
  64. Ambroszkiewicz, J.; Klemarczyk, W.; Gajewska, J.; Chełchowska, M.; Franek, E.; Laskowska-Klita, T. The Influence of Vegan Diet on Bone Mineral Density and Biochemical Bone Turnover Markers. Pediatr. Endocrinol. Diabetes Metab. 2010, 16, 201–204.
  65. Vitoria, I. The Nutritional Limitations of Plant-Based Beverages in Infancy and Childhood. Nutr. Hosp. 2017, 34, 1205–1214.
  66. Kowalska, D.; Gruczyńska, E.; Bryś, J. Mother’s Milk—First Food in Human Life. Probl. Hig. Epidemiol. 2015, 96, 387–398.
  67. Guetouache, M.; Guessas, B.; Medjekal, S. Composition and Nutritional Value of Raw Milk. Issues Biol. Sci. Pharm. Res. 2014, 2, 115–122.
  68. Paul, A.A.; Kumar, S.; Kumar, V.; Sharma, R. Milk Analog: Plant Based Alternatives to Conventional Milk, Production, Potential and Health Concerns. Crit. Rev. Food Sci. Nutr. 2020, 60, 3005–3023.
  69. Kunachowicz, H.; Przygoda, B.; Nadolna, I.; Iwanow, K. Tabele Skłądu I Wartości Odżywczej Żywności, 2nd ed.; PZWL Wydawnictwo Lekarskie: Warszawa, Poland, 2017.
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