» Articles » PMID: 37036532

Association Between Dietary Intake of α-tocopherol and Cadmium Related Osteoporosis in Population ≥ 50 years

Overview
Specialty Endocrinology
Date 2023 Apr 10
PMID 37036532
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: To analyze the association between α-tocopherol intake and cadmium (Cd) exposure and osteoporosis in population ≥ 50 years.

Materials And Methods: Sociodemographic data, physical examination, and laboratory indicators including serum Cd level and dietary α-tocopherol intake of 8459 participants were extracted from the National Health and Nutrition Examination Survey (NHANES) database in this cross-sectional study. The associations between α-tocopherol intake, serum Cd levels and osteoporosis were evaluated using univariate and multivariate logistic regression analyses, with the estimated value (β), odds ratios (ORs) and 95% confidence intervals (CIs). We further explored the impact of α-tocopherol intake on Cd exposure and the bone mineral density (BMD) in total femur and femur neck.

Results: A total of 543 old adults suffered from osteoporosis. The serum Cd level (0.52 μg/L vs. 0.37 μg/L) and α-tocopherol intake (5.28 mg vs. 6.50 mg) were statistical different in osteoporosis group and non-osteoporosis group, respectively. High level of Cd exposure was related to the increased risk of osteoporosis [OR = 1.60, 95% CI (1.15-2.21)]. In the total femur, α-tocopherol intake may improve the loss of BMD that associated with Cd exposure [β = - 0.047, P = 0.037]. Moreover, high α-tocopherol intake combined with low Cd exposure [OR = 0.54, 95% CI (0.36-0.81)] was linked to the decreased risk of osteoporosis comparing with low α-tocopherol intake combined with high Cd exposure.

Conclusion: High α-tocopherol intake may improve the Cd-related osteoporosis and loss of BMD that could provide some dietary reference for prevention of osteoporosis in population ≥ 50 years old.

Citing Articles

Treatment of Osteoporosis and Osteoarthritis in the Oldest Old.

Fuggle N, Laslop A, Rizzoli R, Al-Daghri N, Alokail M, Balkowiec-Iskra E Drugs. 2025; 85(3):343-360.

PMID: 39969778 PMC: 11891106. DOI: 10.1007/s40265-024-02138-w.


Association between dietary vitamin E and osteoporosis in older adults in the United States.

Zhuang R, Hou W, Zhang T, Wang T Front Endocrinol (Lausanne). 2024; 15:1410581.

PMID: 39497806 PMC: 11532079. DOI: 10.3389/fendo.2024.1410581.

References
1.
Duan W, Meng X, Sun Y, Jia C . Association between polycyclic aromatic hydrocarbons and osteoporosis: data from NHANES, 2005-2014. Arch Osteoporos. 2018; 13(1):112. DOI: 10.1007/s11657-018-0527-4. View

2.
Wang N, Wang Y, Zhang H, Guo Y, Chen C, Zhang W . Association of bone mineral density with nine urinary personal care and consumer product chemicals and metabolites: A national-representative, population-based study. Environ Int. 2020; 142:105865. DOI: 10.1016/j.envint.2020.105865. View

3.
Kim Y, Kim J, Cho D . [Gender difference in osteoporosis prevalence, awareness and treatment: based on the Korea national health and nutrition examination survey 2008~2011]. J Korean Acad Nurs. 2015; 45(2):293-305. DOI: 10.4040/jkan.2015.45.2.293. View

4.
Hsueh Y, Huang Y, Chen H, Shiue H, Lin Y, Hsieh R . Alcohol Consumption Moderated the Association Between Levels of High Blood Lead or Total Urinary Arsenic and Bone Loss. Front Endocrinol (Lausanne). 2021; 12:782174. PMC: 8678633. DOI: 10.3389/fendo.2021.782174. View

5.
Lim H, Lee H, Kim T, Lee B . Relationship between Heavy Metal Exposure and Bone Mineral Density in Korean Adult. J Bone Metab. 2016; 23(4):223-231. PMC: 5153379. DOI: 10.11005/jbm.2016.23.4.223. View