Estimated Phytate Intake Is Associated with Bone Mineral Density in Mediterranean Postmenopausal Women
The main objective of this work was to explore the association of dietary phytate intake with bone mineral density (BMD) in a Mediterranean population of postmenopausal women. For this purpose, a cross-sectional analysis of 561 women aged 55-75 years with overweight/obesity and metabolic syndrome fr...
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Veröffentlicht in: | Nutrients 2023-04, Vol.15 (7), p.1791 |
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Zusammenfassung: | The main objective of this work was to explore the association of dietary phytate intake with bone mineral density (BMD) in a Mediterranean population of postmenopausal women. For this purpose, a cross-sectional analysis of 561 women aged 55-75 years with overweight/obesity and metabolic syndrome from a Mediterranean area and with data on dual-energy X-ray absorptiometry (DXA) scans in femur and lumbar spine was performed. Estimated phytate intake was calculated using a validated food frequency questionnaire. Our results indicated that phytate intake was associated with BMD [β(95%CI) per each 25 mg/100 kcal] in femoral neck [0.023(0.060-0.040) g/cm
], femoral Ward's triangle [0.033(0.013-0.054) g/cm
], total femur [0.018(0.001-0.035) g/cm
], and all the analyzed lumbar spine sites [L1-L4: 0.033(0.007-0.059) g/cm
] after adjusting for potential confounders. The sensitivity analysis showed that phytate intake was directly associated with lumbar spine BMD in women younger than 66 years, with a body mass index higher than 32.6 kg/cm
and without type 2 diabetes (all
-for interactions < 0.05). The overall results indicated that phytate, a substance present in food as cereals, legumes and nuts, was positively associated with BMD in Mediterranean postmenopausal women. Phytate may have a protective effect on bone resorption by adsorbing on the surfaces of HAP. Nevertheless, large, long-term, and randomized prospective clinical studies must be performed to assess the possible benefits of phytate consumption on BMD in postmenopausal women. |
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ISSN: | 2072-6643 2072-6643 |
DOI: | 10.3390/nu15071791 |