Beekman Marian, Uh Hae-Won, van Heemst Diana, Wuhrer Manfred, Ruhaak L Renee, Gonzalez-Covarrubias Vanessa, Hankemeier Thomas, Houwing-Duistermaat Jeanine J, Slagboom P Eline
Molecular Epidemiology, Leiden University Medical Center , Leiden , Netherlands.
Medical Statistics and Bioinformatics, Leiden University Medical Center , Leiden , Netherlands.
Front Public Health. 2016 Oct 28;4:233. doi: 10.3389/fpubh.2016.00233. eCollection 2016.
In older people, chronological age may not be the best predictor of residual lifespan and mortality, because with age the heterogeneity in health is increasing. Biomarkers for biological age and residual lifespan are being developed to predict disease and mortality better at an individual level than chronological age. In the current paper, we aim to classify a group of older people into those with longevity potential or controls.
In the Leiden Longevity Study participated 1671 offspring of nonagenarian siblings, as the group with longevity potential, and 744 similarly aged controls. Using known risk factors for cardiovascular disease, previously reported markers for human longevity and other physiological measures as predictors, classification models for longevity potential were constructed with multiple logistic regression of the offspring-control status.
The Framingham Risk Score (FRS) is predictive for longevity potential [area under the receiver operating characteristic curve (AUC) = 64.7]. Physiological parameters involved in immune responses and glucose, lipid and energy metabolism further improve the prediction performance for longevity potential (AUCmale = 71.4, AUCfemale = 68.7).
Using the FRS, the classification of older people in groups with longevity potential and controls is moderate, but can be improved to a reasonably good classification in combination with markers of immune response, glucose, lipid, and energy metabolism. We show that individual classification of older people for longevity potential may be feasible using biomarkers from a wide variety of different biological processes.
在老年人中,实际年龄可能并非剩余寿命和死亡率的最佳预测指标,因为随着年龄增长,健康状况的异质性在增加。目前正在开发生物学年龄和剩余寿命的生物标志物,以便在个体层面上比实际年龄更好地预测疾病和死亡率。在本文中,我们旨在将一组老年人分为具有长寿潜力者或对照组。
莱顿长寿研究纳入了1671名百岁老人兄弟姐妹的后代作为具有长寿潜力的群体,以及744名年龄相仿的对照组。以已知的心血管疾病风险因素、先前报道的人类长寿标志物和其他生理指标作为预测因子,通过后代与对照组状态的多重逻辑回归构建长寿潜力的分类模型。
弗雷明汉风险评分(FRS)可预测长寿潜力[受试者工作特征曲线下面积(AUC)=64.7]。涉及免疫反应以及葡萄糖、脂质和能量代谢的生理参数进一步提高了长寿潜力的预测性能(男性AUC=71.4,女性AUC=68.7)。
使用FRS对老年人进行具有长寿潜力组和对照组的分类效果中等,但结合免疫反应、葡萄糖、脂质和能量代谢的标志物可将分类改善至相当好的水平。我们表明,利用来自各种不同生物学过程的生物标志物对老年人的长寿潜力进行个体分类可能是可行的。