Fujian Key Laboratory of Vascular Aging, Department of Geriatrics, Fujian Institute of Geriatrics, Fujian Clinical Research Center for Senile Vascular Aging and Brain Aging, Fujian Medical University Union Hospital, Fuzhou, Fujian, People's Republic of China.
Nursing Department, Fujian Medical University Union Hospital, Fuzhou, Fujian, People's Republic of China.
Clin Interv Aging. 2024 Nov 1;19:1773-1788. doi: 10.2147/CIA.S478461. eCollection 2024.
The prevalence of osteoporosis in elderly individuals is high, and osteoporosis is strongly associated with chronic inflammation. The monocyte-to-high-density lipoprotein ratio (MHR) is acknowledged as a marker for assessing systemic inflammation and oxidative stress, and changes in the MHR are associated with many chronic disease prevalent among the elderly population. This study investigated the relationships between the MHR and the incidence of osteoporosis in older adults, along with its predictive value.
Data from 563 participants aged ≥70 years were retrospectively analysed. The haematological parameters were evaluated via established methodologies, utilizing fasting blood samples collected from the participants. The absolute monocyte count was used to calculate the MHR (MHR=monocyte/HDL-C). BMD was measured by dual-energy X-ray absorptiometry. The results were evaluated via comparative statistical analyses, Spearman correlation, logistic regression analyses, and receiver operating characteristic (ROC) curve analysis.
The differences in the MHR were statistically significant among the osteoporosis groups ( < 0.001). Spearman correlation analysis revealed a positive correlation between the MHR and BMD. Furthermore, stratifying the sample into four groups on the basis of quartiles of MHR (M1, M2, M3, and M4) revealed a decreased risk of osteoporosis in the highest quartile compared with the lowest quartile ( <0.001). Multiple logistic regression analysis revealed that BMI and the MHR were independent risk factors for osteoporosis. The area under the ROC curve and the cut-off value of the MHR were 0.710 and 0.308(10/mmol), with specificity and sensitivity of 0.599 and 0.735, respectively (95% CI: 0.668~0.752, < 0.0001).
A low MHR was associated with a greater risk of senile osteoporosis. In clinical practice, the MHR has shown predictive value for senile osteoporosis, contributing to early intervention and treatment of this disease.
老年人骨质疏松症的患病率较高,骨质疏松症与慢性炎症密切相关。单核细胞与高密度脂蛋白比值(MHR)被认为是评估全身炎症和氧化应激的标志物,MHR 的变化与老年人中许多常见的慢性疾病有关。本研究探讨了 MHR 与老年人骨质疏松症的发生及其预测价值之间的关系。
回顾性分析了 563 名年龄≥70 岁的参与者的数据。通过使用参与者空腹采集的血液样本,采用既定方法评估血液学参数。用绝对单核细胞计数计算 MHR(MHR=单核细胞/HDL-C)。通过双能 X 线吸收法测量 BMD。通过比较统计学分析、Spearman 相关分析、逻辑回归分析和受试者工作特征(ROC)曲线分析来评估结果。
骨质疏松症组之间的 MHR 差异具有统计学意义(<0.001)。Spearman 相关分析显示 MHR 与 BMD 呈正相关。此外,根据 MHR 四分位数(M1、M2、M3 和 M4)将样本分为四组,结果显示最高四分位数组的骨质疏松症风险较最低四分位数组降低(<0.001)。多因素逻辑回归分析显示 BMI 和 MHR 是骨质疏松症的独立危险因素。ROC 曲线下面积和 MHR 的截断值分别为 0.710 和 0.308(10/mmol),特异性和敏感性分别为 0.599 和 0.735(95%CI:0.668~0.752,<0.0001)。
低 MHR 与老年骨质疏松症的风险增加相关。在临床实践中,MHR 对老年骨质疏松症具有预测价值,有助于对该疾病进行早期干预和治疗。