Division of Endocrinology and Metabolism, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Poongnap2-Dong, 138-736, Songpa-Gu, Seoul, Korea.
Osteoporos Int. 2013 Oct;24(10):2627-37. doi: 10.1007/s00198-013-2363-0. Epub 2013 Apr 17.
Data gathered from a nationally representative cohort demonstrate that higher serum ferritin levels are significantly associated with lower bone mass at various skeletal sites and the increased prevalence of osteoporosis and fractures, especially in women ≥45 years of age.
Despite extensive in vitro and in vivo studies showing the detrimental effects of iron on bone metabolism, the clinical studies relating to osteoporosis-related phenotypes have not been evaluated extensively. In the present study, we investigated and compared the association between serum ferritin and bone mineral density (BMD), depending on the stratified age groups in both genders.
This is a population-based, cross-sectional study from the Korea National Health and Nutrition Examination Surveys, including 14,017 Koreans (6,817 men and 7,200 women) aged 10-80 years. BMD was measured using dual X-ray absorptiometry, and osteoporosis was diagnosed by the World Health Organization definition.
Initially, we divided the subjects into three age groups, based on the patterns of age-related BMD changes in this national cohort (i.e., ≤24, 25-44, and ≥45 years old). Serum ferritin concentrations were inversely associated with BMD values at all measured sites after adjustment for confounders, only in women ≥45 years of age (P = 0.041 to <0.001). Furthermore, when we divided these women into serum ferritin quartiles, the odds for prevalent osteoporosis and fractures were 1.55-fold (95 % CI = 1.09-2.23) and 1.52-fold (95 % CI = 1.02-2.27) higher, respectively, in subjects in the highest quartile compared with those in the lowest quartile.
These results provide the first clinical evidence that the associations between serum ferritin level and bone parameters could be the most prominent in women ≥45 years of age.
一项全国代表性队列研究的数据表明,血清铁蛋白水平较高与各种骨骼部位的骨量较低以及骨质疏松症和骨折的发生率增加显著相关,尤其是在 45 岁以上的女性中。
尽管大量的体外和体内研究表明铁对骨代谢有不良影响,但与骨质疏松症相关表型相关的临床研究尚未得到广泛评估。在本研究中,我们根据两性的分层年龄组,调查并比较了血清铁蛋白与骨矿物质密度(BMD)之间的关系。
这是一项来自韩国国家健康和营养检查调查的基于人群的横断面研究,共纳入 14017 名韩国人(6817 名男性和 7200 名女性),年龄在 10-80 岁之间。使用双能 X 线吸收法测量 BMD,采用世界卫生组织的定义诊断骨质疏松症。
最初,我们根据该国家队列中与年龄相关的 BMD 变化模式(即≤24、25-44 和≥45 岁)将受试者分为三组。在调整了混杂因素后,仅在 45 岁以上的女性中,血清铁蛋白浓度与所有测量部位的 BMD 值呈负相关(P = 0.041 至 <0.001)。此外,当我们将这些女性分为血清铁蛋白四分位数时,与最低四分位数相比,最高四分位数的女性发生骨质疏松症和骨折的几率分别高出 1.55 倍(95 % CI = 1.09-2.23)和 1.52 倍(95 % CI = 1.02-2.27)。
这些结果首次提供了临床证据,表明血清铁蛋白水平与骨参数之间的关联在 45 岁以上的女性中最为显著。