ARTICLE INFO | ABSTRACT | |
SYSTEMATIC REVIEW | Background: There is a direct relationship between taking soy isoflavones and higher bone density, but there is a paucity of studies examining the relationship between flavonoid consumption and fracture risk. This study aimed to assess the bone fracture and its relationship to soy product intake by performing a systematic review. Methods: Scopus, PubMed, and Web of science were searched to find studies on the effect of soy isoflavones on bone fracture, without any time and language of publication restrictions. Key words of SoyMilk, soymilk, soybeans, soybean, soy, soya, Isoflavones, Isoflavone, ipriflavone, equol, genistein, daidzein, glycitin, fractures, and broken bone were used. Results: From a total of 1675 articles, 27 studies (cross-sectional studies (n=1), case-control studies (n=1), cohort (n=11), and randomized control trials (n=14)) were identified, and their quality was assessed. Eighteen studies highlighted mainly positive results in preventive influence of soy bone fractures. Two papers reported a positive effect was observed in men with cancer. No significant association was found between soy intake and bone prevention fracture in eight distinct papers. Conclusion: Intake of soy isoflavones can make a significant preventive effect on bone fracture; however, the results of some studies are controversial. Therefore, it is necessary to survey more studies to identify the relationship between isoflavones and bone fracture. Keywords: Isoflavones; Bone; Fracture |
|
Article history: Received: 3 Apr 2022 Revised: 28 Jul 2022 Accepted: 28 Aug 2022 |
||
*Corresponding author: najmehhejazi@gmail.com Nutrition Research Center, Department of Clinical Nutrition, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran. Postal code: 7153675500 Tel: +98 71 37251004 |
Bone with frequent renovation during the lifespan is an active tissue (Shetty et al., 2016). Bone renovation contains two stages including formation of new bone tissue and reabsorption of the old bone tissue (Eastell and Szulc, 2017). During growth, the amount of new bone tissue formation surpasses that of reabsorption of old bone tissue, but with age, this trend is reversed. Augmented and non-stop bone reabsorption in aging causes osteoporosis. Osteoporosis is categorized by decreased bone mass related to augmented bone fragility and vulnerability to fracture (Shetty et al., 2016).
Pelvic fractures increase the financial burden by 20 percent due to long-term care of the elderly and in some cases even death (Bunout et al., 2006). Isoflavone soy is classified as phytoestrogens, because of its similarity with estrogen herbal mixtures that can attach to estrogen receptors, and performs the same function as estrogen (Taku et al., 2011). Isoflavones are found in abundance in soy, so in the case of estrogen deficiency (menopause), they can prevent bone loss and bone fracture (Taku et al., 2011, Zhang et al., 2005, Zheng et al., 2016).
Soybean production and dietary consumption have increased within Western nations with postulated health benefits by increasing bone health, especially in women (Xiao, 2008). There has also been an association between the use of phytoestrogens and increased bone density (Greendale et al., 2002, Zhang et al., 2005); however, studies in Caucasian people are incomplete due to lower habitual consumption of phytoestrogens.
In a study in Shanghai, the average soy isoflavone intake in postmenopausal women was 38 mg / day, which was associated with a reduction in bone fractures (Zhang et al., 2005). Even though genetic factors affect the peak bone mass, regimen is one of the risk factors for osteoporosis (Chan et al., 2011). Natto is a kind of fermented soybean that is taken. This food is rich in menaquinone-7and comprises 100 times more menaquinone-7 than numerous types of cheese (Katsuyama et al., 2002). Based on the present evidence, the consequences of epidemiological studies are still controversial about the effect of soy isoflavone on bone fraction. To the best of the authors’ knowledge, this systematic review is the first to survey the effect of soy isoflavone on preventing bone fraction in patients. Bone fracture, especially in menopause women is an important problem worldwide, so in this systematic review, literature was searched to investigate the probable effect of soy isoflavones on bone fracture to reveal the positive effect of soy products on ameliorating fracture of bone in human to help them enjoy their life better. Thus, the main aim of this study was to survey the efficiency of soy isoflavone on fraction in patients by searching randomized controlled trials (RCTs), cohort studies, and case report studies. The study also aimed to examine which type, quantity, and duration of soy isoflavone is more effective for preventing bone fraction.
Phytoestrogens are derivatives of plant compounds that have both antiestrogenic and estrogenic properties. Soy contains large amounts of isoflavones with a structure of 17 b-estradiol. Isoflavones bind to estrogen-binding receptors and function similarly to estrogen (Kuiper et al., 1997). Genistein and daidzine are key isoflavones found in soy (Anderson et al., 1999).
Isoflavones are involved in the formation of the bone tissue by binding to osteoblast receptors through a genomic mechanism involved in inhibiting the function of nuclear estrogen receptors (Blair et al., 1996). Its receptor osteoprotein (OPG) and receptor activator of nuclear factor kappa beta (RANKL) are involved in tissue analysis and hemostatic bone resorption. Postmenopausal women receiving genistein have lower sRANKL levels, indicating a possible mechanism of the phytoestrogens in the bone (Marini et al., 2008). Excessive consumption of animal protein increases the urinary excretion of calcium which is effective in the process of osteoporosis, while this trend has not been observed in the consumption of soy protein (Breslau et al., 1988).
Results
Table 1. Features of the studies on the effect of isoflavones. | ||||||||
Study | Location | Number | Characteristics | Sex | Age(y) | Interventions and groups | Study design | Outcomes |
(Kojima et al., 2020) | Japanese |
1417 |
Postmenopausal |
Female |
15–79 |
FFQ of natto, tofu, and another soybean |
Prospective cohort | Decrease the risk of hip fracture |
(Zheng et al., 2019) |
China |
N1=4139 N2= 1987 N3=2152 |
N1= stage 0–III breast cancer patients N2= pre-/perimenopausal N3= postmenopausal patients |
Female |
20-75 |
Consume soy using Frequency questionnaire
|
Prospective |
Decrease the risk of hip fracture |
(Nayeem et al., 2019) |
America |
99 |
Healthy premenopausal women | Female |
30-42 |
Isoflavones (136.6 mg) and placebo |
Clinical trial |
Decrease the risk of hip fracture |
(Yoshikata et al., 2018) |
China |
74 |
Menopause |
Female |
44–74 |
Per oral equol-containing supplement, 10 mg/day |
A Prospective Observational Study | Decrease the risk of hip fracture |
(Zhang et al., 2017) | China |
1050 |
Elderly |
Male/ female |
52-83 |
Validated 79-item food frequency questionnaire | Case-control study of | Decrease the risk of hip fracture |
(Arcoraci et al., 2017) |
Italy |
121 |
Postmenopausal |
Female |
Mean 54.5 |
With either 1000 mg of calcium and 800 IU vitamin D3 in placebo group and vitamin D3,calcium, and Genistein aglycone (54 mg/day in intervention group | Clinical trial |
Decrease the risk of hip fracture |
(Myers et al., 2015) |
Australia |
1188 |
Postmenopausal |
Female |
Mean 80.0 |
A validated food-frequency questionnaire |
Prospective cohort |
Decrease the risk of hip fracture |
(Baglia et al., 2015) |
China |
1,587 |
Breast cancer diagnosis |
Male and female | 20 - 75 |
Food frequency questionnaire |
Cohort |
Decrease the risk of hip fracture |
(Dai et al., 2014) |
Singapore Chinese |
63,257 |
Both pre- and postmenopausal |
Male and female | 45–74 |
A validated food-frequency questionnaire |
Prospective population-based cohort | Decrease the risk of hip fracture |
(Lappe et al., 2013) |
USA |
70 |
Postmenopausal |
Female |
Mean age 54.8 | Case: genistein (30 mg/days), vitamin K1 (150 μg/days) vitamin D3 (800 IU/days), vitamin K1 (150 μg/days) and polyunsaturated fatty acids (1 g Controle: calcium |
Clinical trial |
Decrease the risk of hip fracture |
(Tai et al., 2012) |
Taiwan |
431 |
Postmenopausal |
Female |
45-65 |
00-mg/day isoflavones (aglycone equivalents) (172.5 mg genistein + 127.5 mg daidzein) and600 mg of calcium and 125 IU of vitamin D3 per day | Clinical trial |
The relative risk of bone fracture and its 95% CI for the isoflavone group were 1.64 (0.74, 3.67) |
(Hasnah et al., 2012) |
Malaysia |
125 |
Postmenopausal |
Female |
Mean age 60 |
A dietary history Questionnaire |
A cross-sectional study |
A diet without dairy increased the risk of bone fractures |
(Lousuebsakul Matthews et al., 2011) | Canada |
337 |
Postmenopausal |
Female |
54-75 |
Completed a lifestyle and dietary questionnaire and FFQ |
Cohort study |
BUA measurement related to soy foods intake and history of minor accident fracturesp= 0.25 |
(Kuhnle et al., 2011) |
UK |
F=2580M=4973 |
Cancer |
Male and female | 45–75 |
Survey of soy intake using a newly developed food composition database
|
Prospective study cohort |
Decrease the risk of hip fracture |
(Haron et al., 2010) |
Malaysia |
21 |
Postmenopausal |
Female |
55-65 |
A glass of milk (114 g) or from a meal of tempeh (206 g); each containing 130 mg calcium. At each study of Phase and Phase 2 (mid-August), intravenous 42Ca and oral 44Ca |
Clinical trial |
No effect |
(Koh et al., 2009) |
Chinese |
63,257 |
Healthy |
Male and female | 45–74 |
Using food frequency questionnaire , lifestyle factors and questions on medical history |
Prospective cohort |
Decrease the risk of hip fracture |
(Newton et al., 2006) |
USA |
F=13 M=98 |
Healthy |
Male and female |
50–80 |
Soy protein comprising 83 mg isoflavones (45.6 mg genistein, 31.7 mg daidzein), aglycone units; the control group comprising 3mg isoflavones | Clinical trial |
No effect |
(Ikeda et al., 2006) |
Japan |
944 |
Postmenopausal |
Female |
20-79 |
Dietary natto intake was assessed by a FFQ on both occasions |
Cohort |
Reduced risk |
(Bunout et al., 2006) |
Chile |
100 |
Elderly with femoral osteoporosis. |
Male and female | Mean age 70 |
31 g proteins per and 90 mg isoflavones, 400 IU vitamin D, 800 mg calcium, 60 ug vitamin K day |
Clinical trial |
No effect |
(Zhang et al., 2005) |
USA |
75,000 |
Postmenopausal |
Female |
40-70 |
FFQ |
Cohort |
May reduce the risk of fracture |
(Welch et al., 2005) |
UK |
F=5,379 M=6,369 |
Cancer |
Male and female |
42 -82 |
Individuals were divided into four groups based on soy consumption and vegetarian status and a food frequency questionnaire was used. | Prospective study |
Calcaneum BUA in vegetarian men was significantly lower than but in female had no effect |
(Harada et al., 2004) |
Japan |
2035 |
Elderly |
Male and female | Mean age 65 |
An anonymous survey consisting of 12 questions |
Clinical trial |
Reduced risk |
(Kaneki et al., 2001) | Japan |
105 |
Postmenopausal |
Female |
50–84 |
Examined the influence of Japanese fermented soybean, on serum vitamin K | Clinical trial |
Reduced risk |
(Alexandersen et al., 2001) |
Denmark |
474 |
Postmenopausal |
Female |
45-75 |
200 mg 3 r placebo all received 500 mg/d of calcium |
Clinical trials |
No effect |
(Sato et al., 2000) | Japan |
9 |
Long-Distance Runners | Female |
20-24 |
1350 g of vitamin K2 and 72 mg of soybean isoflavones | Clinical trial |
Reduced risk |
(Reginster et al., 1997) |
Denmark |
460 |
Menopause |
Female |
45-75 |
IP (200 mg, and 500 g oral calcium everyday |
Clinical trial |
Reduced risk |
(Agnusdei and Bufalino, 1997) |
Italy |
149 |
Elderly, osteoporotic women |
Female |
65–79 |
IP (200 mg, and 1 g oral calcium everyday |
Clinical trial |
Reduced risk |
Table 2. Jadad scale quality assessment for RCTs. | |||||
Quality | Total | An account of all patients | Blinding | Randomization | Study |
High | 5 | 1 | 2 | 2 | (Nayeem et al., 2019) |
High | 4 | 0 | 2 | 2 | (Arcoraci et al., 2017) |
High | 5 | 1 | 2 | 2 | (Lappe et al., 2013) |
High | 5 | 1 | 2 | 2 | (Tai et al., 2012) |
Low | 3 | 1 | 1 | 1 | (Haron et al., 2010) |
High | 5 | 1 | 2 | 2 | (Newton et al., 2006) |
Low | 3 | 1 | 1 | 1 | (Bunout et al., 2006) |
Low | 3 | 1 | 1 | 1 | (Kaneki et al., 2001) |
High | 5 | 1 | 2 | 2 | (Alexandersen et al., 2001) |
Low | 3 | 1 | 1 | 1 | (Sato et al., 2000) |
High | 4 | 0 | 2 | 2 | (Reginster et al., 1997) |
High | 4 | 0 | 2 | 2 | (Agnusdei and Bufalino, 1997) |
Table 3. Newcastle-Ottawa quality assessment for cohort, case control, and cross sectional studies. | |||||
Quality | Total | Outcome | Comparability | Selection | Study |
Good | 7 | 3 | 1 | 3 | (Kojima et al., 2020) |
Fair | 6 | 2 | 1 | 3 | (Zheng et al., 2019) |
Fair | 5 | 2 | 1 | 2 | (Yoshikata et al., 2018) |
Good | 6 | 2 | 1 | 3 | (Zhang et al., 2017) |
Good | 6 | 2 | 1 | 3 | (Myers et al., 2015) |
Good | 6 | 3 | 1 | 2 | (Baglia et al., 2015) |
Good | 6 | 2 | 1 | 3 | (Dai et al., 2014) |
Fair | 5 | 2 | 0 | 3 | (Hasnah et al., 2012) |
Good | 6 | 2 | 1 | 3 | (Lousuebsakul Matthews et al., 2011) |
Good | 6 | 2 | 1 | 3 | (Kuhnle et al., 2011) |
Good | 6 | 2 | 1 | 3 | (Koh et al., 2009) |
Good | 6 | 2 | 1 | 3 | (Ikeda et al., 2006) |
Good | 6 | 2 | 1 | 3 | (Zhang et al., 2005) |
Good | 7 | 3 | 1 | 3 | (Welch et al., 2005) |
Fair | 5 | 2 | 1 | 2 | (Harada et al., 2004) |
Discussion
Soy also increases the production of insulin-like growth factor 1, an indicator recognized to increase osteoblastic activity related to bone formation (Arjmandi and Smith, 2002).The amount of IGF-I in both sexes decreases with age, which intensifies in menopause (George et al., 2020). IGF-I, like growth hormone, stimulates bone formation (George et al., 2020). It may also increase the production of 1,25 (OH)2 vitamin D by regulating 1α-hydroxylase activity (George et al., 2020). Soy consumption in postmenopausal women has caused a reduction in urinary excretion of bone indicators (Nikander et al., 2004). Menaquinone-7 (MK-7) enables osteocalcin γ -carboxylation (Shetty et al., 2016), and mineralization (Bruge et al., 2011). In a study in the Caucasus, MK-7 consumption was effective in preventing bone fractures in postmenopausal women (Knapen et al., 2013). Thus, soy products prevent bone fractures by preserving bone mass and bone microarchitecture (Rønn et al., 2016). Soy products can decrease bone loss (Wong et al., 2009) and provoke bone formation (Ma et al., 2008b, Marini et al., 2007); this association was not found in 8 studies. This can be attributed to different types of isoflavones in different soy products (Kojima et al., 2020). Isoflavone aglycones in unfermented soy products, such as tofu, are absorbed faster and have more bioavailability than other soy products (Izumi et al., 2000). The phytoestrogens in soy reduce the process of bone loss (Ma et al., 2008a). The effect of soy in avoiding osteoporosis in men has not been determined (Newton et al., 2006). The exact mechanism of genistein in men is unknown (Piekarz and Ward, 2007). Genistein prevents bone loss by increasing the activity of osteoblasts in male rodents (Khalil et al., 2005). Decreased testosterone is observed in men with age (Orwoll et al., 2006), since testosterone helps maintain bone health in men (Amin et al., 2006). Therefore, isoflavones can be effective in preventing bone fractures in older men and soy products, due to the mentioned properties, can be effective in preventing bone fractures.
Limitation
This review study had some limitations. Each study had different interventions, evaluating different results, which made impossible to compare the results. Also, confounding factors such as age, BMI, and dietary calcium intake were not investigated.
Conclusion
Various diseases and factors that affect bone fractures mainly affect the quality of life of people. Therefore, the results of this review revealed that soy consumption may have a beneficial effect on preventing bone fraction. More studies with a longer time of intervention on a larger sample size are recommended to approve these results.
Acknowledgement
Funding
Author contributions
Hamidian Shirazi M, Mollaei M, Hamidian Shirazi A and Hejazi N. contributed to the research concept; Hamidian Shirazi M, Hejazi N and Ramezani A searched databases, screened articles, and extracted data. All authors contributed to the writing and revision of the manuscript. All authors have read and agreed to the published version of the manuscript.
Conflict of interest
Reference
Rights and permissions | |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |