Distribution and diagnostic modeling of osteoporosis and comorbidities across demographic factors: A cross-sectional study of 2224 female patients

Li Dingpeng , Bai Bihui , Xie Ruixuan , Yao Fei , Xie Xingwen , Lin Demin
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Abstract

Objective

This study investigates the distribution of osteoporosis (OP) and its associated comorbidities across different demographic factors. Furthermore, this study seeks to develop a statistically-based diagnostic model leveraging demographic and health indicators to provide personalized risk assessments for OP.

Methods

A retrospective analysis was conducted on the demographic data, health profiles, and bone density measurements of 2224 female patients. Key variables associated with OP were identified using chi-square tests. Feature selection was refined through Lasso regression and recursive feature elimination (RFE), which guided the development of a logistic regression-based dynamic nomogram. This model was subsequently implemented on the Shiny platform for personalized online OP risk assessments.

Results

Among 2224 female patients, 801 (36.0 %) were diagnosed with OP. Women aged 70 and older exhibited a significantly higher prevalence of OP compared to younger age groups (OR = 5.83, 95 % CI: 1.74–19.61, P = 0.004), and this remained significant in the multivariable analysis (OR = 5.18, 95 % CI: 1.19–22.52, P = 0.028). Later age at menarche was associated with increased OP risk (OR = 1.31, 95 % CI: 1.09–1.57, P = 0.004), persisting in multivariable analysis (OR = 1.25, 95 % CI: 1.03–1.52, P = 0.023). In rheumatoid arthritis (RA) patients, higher education reduced OP risk, with secondary education (OR = 0.09, P = 0.024) and college education (OR = 0.04, P = 0.009) showing protective effects. Diabetic patients who were unmarried or had non-traditional marital statuses showed increased OP risk (univariate OR = 2.73, P = 0.006; multivariate OR = 2.34, P = 0.029). Among nonalcoholic fatty liver disease (NAFLD) patients, age at menopause was significantly linked to OP risk (univariate OR = 1.04, P = 0.012). The prediction model showed strong performance (AUC = 0.720), and the dynamic nomogram on the Shiny platform provided effective personalized OP risk assessments.

Conclusion

Age and age at menarche are significant risk factors for OP, with later menarche increasing the risk. In RA patients, higher education levels were associated with a lower risk of OP. In contrast, unmarried or non-traditional marital statuses increased OP risk among diabetic patients. Additionally, age at menopause was found to be a significant factor for OP risk in NAFLD patients. The prediction model developed in this study, with an AUC of 0.720, provides a reliable method for personalized OP risk assessment through a dynamic nomogram. These findings highlight the crucial role of demographic factors in predicting OP risk and underscore the importance of personalized treatment strategies for effective OP prevention and management.
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骨质疏松症和合并症在不同人口统计学因素中的分布和诊断模型:一项针对 2224 名女性患者的横断面研究。
研究目的本研究调查了骨质疏松症(OP)及其相关合并症在不同人口因素中的分布情况。此外,本研究还试图开发一种基于统计学的诊断模型,利用人口统计学和健康指标提供个性化的骨质疏松症风险评估:方法:对 2224 名女性患者的人口统计学数据、健康状况和骨密度测量结果进行了回顾性分析。通过卡方检验确定了与 OP 相关的关键变量。通过拉索回归和递归特征剔除(RFE)对特征选择进行了改进,从而指导开发了基于逻辑回归的动态提名图。该模型随后在 Shiny 平台上实施,用于个性化在线 OP 风险评估:在 2224 名女性患者中,有 801 人(36.0%)被确诊为 OP。与年轻群体相比,70 岁及以上女性的 OP 患病率明显更高(OR = 5.83,95 % CI:1.74-19.61,P = 0.004),而且在多变量分析中仍有显著意义(OR = 5.18,95 % CI:1.19-22.52,P = 0.028)。月经初潮年龄较晚与 OP 风险增加有关(OR = 1.31,95 % CI:1.09-1.57,P = 0.004),在多变量分析中依然如此(OR = 1.25,95 % CI:1.03-1.52,P = 0.023)。在类风湿性关节炎(RA)患者中,较高的教育程度可降低 OP 风险,中等教育程度(OR = 0.09,P = 0.024)和大学教育程度(OR = 0.04,P = 0.009)具有保护作用。未婚或非传统婚姻状况的糖尿病患者 OP 风险增加(单变量 OR = 2.73,P = 0.006;多变量 OR = 2.34,P = 0.029)。在非酒精性脂肪肝(NAFLD)患者中,绝经年龄与 OP 风险显著相关(单变量 OR = 1.04,P = 0.012)。预测模型显示出很强的性能(AUC = 0.720),Shiny 平台上的动态提名图提供了有效的个性化 OP 风险评估:结论:年龄和初潮年龄是 OP 的重要风险因素,初潮年龄越晚,风险越高。在 RA 患者中,受教育程度越高,罹患 OP 的风险越低。相反,未婚或非传统婚姻状况会增加糖尿病患者的 OP 风险。此外,在非酒精性脂肪肝患者中,绝经年龄也是影响 OP 风险的一个重要因素。本研究建立的预测模型的AUC为0.720,为通过动态提名图进行个性化OP风险评估提供了一种可靠的方法。这些发现凸显了人口统计学因素在预测 OP 风险中的关键作用,并强调了个性化治疗策略对有效预防和管理 OP 的重要性。
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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
CiteScore
6.70
自引率
0.00%
发文量
0
审稿时长
66 days
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