Department of Senior Official Ward, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Beijing, 100029, China.
Arch Osteoporos. 2021 Jan 6;16(1):9. doi: 10.1007/s11657-020-00850-0.
Using national representative data, we found the prevalence of and risk factors associated with low BMD differed by race and ethnicity.
Race/ethnicity is an important determinant of osteoporosis risk. The study aims were to (1) estimate the racial and ethnic differences in the prevalence of low BMD, (2) identify factors associated with low BMD by race and ethnic group, and (3) evaluate if the association between sleep duration and low BMD is modified by age, sex, gender, and/or race/ethnicity.
Using data from the National Health and Nutrition Examination Survey (NHANES) database from 2005 to 2014, totally, 7992 participants aged ≥ 50 years were included as the primary cohort. Three race/ethnic groups were included: non-Hispanic Whites, Hispanics, and non-Hispanic Blacks. Low BMD was defined by femoral neck BMD T-scores less than - 1, as measured by DXA scan. Univariate and multivariate analyses were performed to determine associations between participants' demographics, comorbidities, lifestyle characteristics, and prevalent low BMD.
Prevalence of low BMD was 50.8% among non-Hispanic Whites, 23.7% among non-Hispanic Blacks, and 44.0% among Hispanics. After adjusting for confounders, advanced age, female gender, and fracture history were significantly associated with increased odds of low BMD in all three race/ethnic groups. Family history of osteoporosis, ever used glucocorticoids daily, and vitamin D deficiency or insufficiency were associated with increased odds of low BMD only among non-Hispanic Whites. Cardiovascular disease (CVD) history and diabetes were associated with low BMD only among non-Hispanic Blacks. Short sleep duration was not associated with low BMD in all ethnic groups, but was significantly associated with low BMD in older adults (> 65 years) and females.
Prevalence of low BMD among three race/ethnic groups in the USA is determined, with race/ethnic disparities in several risk factors associated with low BMD identified. By contrast, advanced age, female gender, and fracture history are associated with increased odds of low BMD across all race/ethnic groups. The association between sleep duration and low BMD is modified by age and sex. Together, these findings may help clinicians and healthcare providers formulate better care for individual's bone health.
利用全国代表性数据,我们发现,骨密度低的患病率和相关风险因素因种族和族裔而异。
种族/族裔是骨质疏松风险的一个重要决定因素。本研究的目的是:(1) 估计不同种族和族裔之间低骨密度的患病率差异;(2) 按种族和族裔群体确定与低骨密度相关的因素;(3) 评估睡眠持续时间与低骨密度之间的关联是否受年龄、性别、性别认同和/或种族/族裔的影响。
使用 2005 年至 2014 年全国健康与营养调查(NHANES)数据库中的数据,共纳入 7992 名年龄≥50 岁的参与者作为主要队列。包括三个种族/族裔群体:非西班牙裔白人、西班牙裔和非西班牙裔黑人。通过 DXA 扫描测量股骨颈骨密度 T 评分小于-1,定义为低骨密度。进行单变量和多变量分析,以确定参与者的人口统计学、合并症、生活方式特征与普遍存在的低骨密度之间的关联。
非西班牙裔白种人低骨密度的患病率为 50.8%,非西班牙裔黑种人低骨密度的患病率为 23.7%,西班牙裔低骨密度的患病率为 44.0%。在调整混杂因素后,所有三个种族/族裔群体中,年龄较大、女性和骨折史与低骨密度的患病几率增加显著相关。骨质疏松家族史、每日使用糖皮质激素以及维生素 D 缺乏或不足与非西班牙裔白种人低骨密度的患病几率增加相关。心血管疾病(CVD)史和糖尿病仅与非西班牙裔黑种人低骨密度相关。所有族裔群体中,睡眠持续时间较短与低骨密度无关,但在年龄较大(>65 岁)和女性中与低骨密度显著相关。
确定了美国三个种族/族裔群体中低骨密度的患病率,并确定了与低骨密度相关的几个风险因素存在种族/族裔差异。相比之下,所有种族/族裔群体中,年龄较大、女性和骨折史与低骨密度的患病几率增加相关。睡眠持续时间与低骨密度之间的关联受年龄和性别影响。这些发现可能有助于临床医生和医疗保健提供者制定针对个人骨骼健康的更好的护理方案。