Xu Zi, Peng Yunsong, Zhang Mudan, Wang Rongpin, Yang Zhenlu
Department of Radiology, Guizhou Provincial Peoples Hospital, Guiyang, 550001, People's Republic of China.
Geroscience. 2025 Apr;47(2):2135-2148. doi: 10.1007/s11357-024-01394-8. Epub 2024 Oct 24.
Accurately estimating biological age is beneficial for measuring aging and predicting risk. It is widely accepted that the prevalence of spine compression increases significantly with age. However, biological age based on vertebral morphological data is rarely reported. In this study, a total of 2,364 participants from the National Health and Nutrition Examination Survey were enrolled, and morphological parameters of the spine were collected from lateral radiographs scanned by dual energy X-ray absorptiometry. The biological age of the spine, called SpineAge, was calculated with the parameters by machine learning models. The SHapley Additive exPlanation was used for better interpreting each parameter's contribution. Besides, an Accelerated Aging Index (AAI) was defined as SpineAge minus chronological age and was used to quantify the accelerating aging degree of the spine. The results indicated that the SpineAge performed better than chronological age did in predicting 2-year and 5-year all-cause mortality. After adjusting all covariates, there was a significant association between AAI and all-cause mortality risk. Specifically, each 1-year increase in AAI was associated with a 25.9% increase in all-cause mortality risk (Hazards ratio, 1.259; 95% CI, 1.087-1.457; P < 0.001). Considering the first quartile of AAI as a reference, the mortality risks for the second, third, and fourth quartiles were 2.389 (95% CI, 1.064-5.364; P = 0.035), 5.911 (95% CI, 2.241-15.590; P < 0.001) and 22.925 (95% CI, 4.744-110.769; P < 0.001) times higher, respectively. Our study developed a novel and highly applicable biological-age predictor for predicting individualized long-term prognosis and facilitating personalized care.
准确估计生物学年龄有助于衡量衰老程度和预测风险。人们普遍认为,脊柱压缩的患病率会随着年龄的增长而显著增加。然而,基于椎体形态学数据的生物学年龄却鲜有报道。在本研究中,共纳入了来自美国国家健康与营养检查调查的2364名参与者,并通过双能X线吸收法扫描的侧位X线片收集了脊柱的形态学参数。利用这些参数,通过机器学习模型计算出脊柱的生物学年龄,即脊柱年龄(SpineAge)。采用SHapley加性解释法来更好地解释每个参数的贡献。此外,加速衰老指数(AAI)被定义为脊柱年龄减去实际年龄,用于量化脊柱的加速衰老程度。结果表明,在预测2年和5年全因死亡率方面,脊柱年龄比实际年龄表现更好。在调整所有协变量后,加速衰老指数与全因死亡风险之间存在显著关联。具体而言,加速衰老指数每增加1岁,全因死亡风险就会增加25.9%(风险比,1.259;95%置信区间,1.087 - 1.457;P < 0.001)。以加速衰老指数的第一个四分位数为参照,第二个、第三个和第四个四分位数的死亡风险分别高出2.389倍(95%置信区间,1.064 - 5.364;P = 0.035)、5.911倍(95%置信区间,2.241 - 15.590;P < 0.001)和22.925倍(95%置信区间,4.744 - 110.769;P < 0.001)。我们的研究开发了一种新颖且高度适用的生物学年龄预测指标,用于预测个性化的长期预后并促进个性化医疗。