Time trend analysis of osteoporosis prevalence among adults 50 years of age and older in the USA, 2005-2018.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Osteoporosis International Pub Date : 2025-03-01 Epub Date: 2025-01-28 DOI:10.1007/s00198-025-07395-3
Chris M Naso, Shuo-Yu Lin, Ge Song, Hong Xue
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引用次数: 0

Abstract

Using data from NHANES for years 2005-2018, we examined temporal trends in osteoporosis prevalence and the proportion of undiagnosed osteoporosis in the United States of America. Our results suggested statistically significant increases in osteoporosis prevalence across several demographic groups. These findings carry profound implications for public health, given increased life expectancy and burden of chronic diseases.

Introduction: This is the first study to assess osteoporosis prevalence trends over time and the proportion of undiagnosed osteoporosis across gender, ethnicity/race, and age groups.

Methods: Observational time trend analyses were conducted using the 2005-2006, 2007-2008, 2009-2010, 2013-2014, and 2017-2018 National Health and Nutrition Examination Survey (NHANES) datasets, along with a descriptive analysis using the 2017-2018 NHANES dataset to capture the proportion of undiagnosed osteoporosis.

Results: The findings showed a statistically significant increase in osteoporosis prevalence among women, non-Hispanic Whites, and all age groups (except for individuals 80 years of age and older) during the study period. A subsequent analysis examining individuals by both gender and ethnicity/race demonstrated a statistically significant increase among Other Hispanic men and non-Hispanic White women. Additional descriptive analyses found that 69.12% of individuals with osteoporosis went undiagnosed. Specifically, 86.88% of men and 84.77% of individuals 50-59 years of age with osteoporosis went undiagnosed, representing the two highest groups.

Discussion and conclusion: The substantial and increasing prevalence among certain groups and sub-groups, along with the lack of diagnostic capture of osteoporosis, highlights existing gaps in public health efforts and care delivery infrastructure. This paper highlights high-risk groups and sub-groups that may benefit most from accelerated initiatives to reduce the burden of illness associated with osteoporosis.

2005-2018年美国50岁及以上成年人骨质疏松症患病率时间趋势分析
使用NHANES 2005-2018年的数据,我们研究了美国骨质疏松症患病率的时间趋势和未确诊骨质疏松症的比例。我们的研究结果表明,骨质疏松症患病率在几个人口统计群体中有统计学意义的增加。鉴于预期寿命增加和慢性病负担加重,这些发现对公共卫生具有深远影响。这是第一个评估骨质疏松症随时间的流行趋势和未确诊骨质疏松症在性别、种族/种族和年龄组中的比例的研究。方法:使用2005-2006年、2007-2008年、2009-2010年、2013-2014年和2017-2018年国家健康与营养检查调查(NHANES)数据集进行观察性时间趋势分析,并使用2017-2018年NHANES数据集进行描述性分析,以捕获未确诊骨质疏松症的比例。结果:研究结果显示,在研究期间,骨质疏松症患病率在女性、非西班牙裔白人和所有年龄组(80岁及以上的个体除外)中均有统计学意义上的显著增加。随后的一项针对性别和种族的分析显示,其他西班牙裔男性和非西班牙裔白人女性的死亡率在统计上显著上升。另外的描述性分析发现,69.12%的骨质疏松症患者未被确诊。具体来说,86.88%的男性和84.77%的50-59岁的骨质疏松症患者未被诊断出来,代表了两个最高的群体。讨论和结论:在某些群体和亚群体中,骨质疏松症的发病率显著上升,同时缺乏对骨质疏松症的诊断,这突出了公共卫生工作和护理提供基础设施方面存在的差距。本文强调高危人群和亚群体可能受益于加速倡议,以减少与骨质疏松症相关的疾病负担。
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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
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