Department of Rehabilitation and Geriatrics, Geneva University Hospitals and University of Geneva, Thônex, Switzerland.
J Nutr Health Aging. 2012 Mar;16(3):225-30. doi: 10.1007/s12603-011-0138-x.
Telomere length has been considered in many cross-sectional studies as a biomarker of aging. However the association between shorter telomeres with lower survival at advanced ages remains a controversial issue. This association could reflect the impact of other health conditions than a direct biological effect.
To test whether leukocyte telomere length is associated with 5-year survival beyond the impact of other risk factors of mortality like comorbidity, functional, nutritional and cognitive status.
Prospective study.
A population representative sample of 444 patients (mean age 85 years; 74% female) discharged from the acute geriatric hospital of Geneva University Hospitals (January-December 2004), since then 263 (59.2%) had died (December 2009).
Telomere length in leukocytes by flow cytometry.
In univariate model, telomere length at baseline and cognitive status were not significantly associated with mortality even when adjusting for age (R²=9.5%) and gender (R²=1.9%). The best prognostic predictor was the geriatric index of comorbidity (GIC) (R²=8.8%; HR=3.85) followed by more dependence in instrumental (R²=5.9%; HR=3.85) and based (R²=2.3%; HR=0.84) activities of daily living and lower albumin levels (R²=1.5%; HR=0.97). Obesity (BMI>30: R²=1.6%; HR=0.55) was significantly associated with a two-fold decrease in the risk of mortality compared to BMI between 20-25. When all independent variables were entered in a full multiple Cox regression model (R²=21.4%), the GIC was the strongest risk predictor followed by the nutritional and functional variables.
Neither telomeres length nor the presence of dementia are predictors of survival whereas the weight of multiple comorbidity conditions, nutritional and functional impairment are significantly associated with 5-year mortality in the oldest old.
端粒长度在许多横断面研究中被认为是衰老的生物标志物。然而,端粒较短与高龄时存活率较低之间的关联仍然是一个有争议的问题。这种关联可能反映了其他健康状况的影响,而不是直接的生物学效应。
测试白细胞端粒长度是否与 5 年生存率相关,而其他死亡率的危险因素(如合并症、功能、营养和认知状态)的影响除外。
前瞻性研究。
来自日内瓦大学医院急性老年医院的 444 名患者(平均年龄 85 岁,74%为女性)的代表性样本(2004 年 1 月至 12 月),其中 263 人(59.2%)死亡(2009 年 12 月)。
通过流式细胞术测量白细胞中端粒长度。
在单变量模型中,基线时的端粒长度和认知状态与死亡率没有显著关联,即使在调整年龄(R²=9.5%)和性别(R²=1.9%)后也是如此。最佳预后预测因子是老年合并症指数(GIC)(R²=8.8%;HR=3.85),其次是工具性(R²=5.9%;HR=3.85)和基于(R²=2.3%;HR=0.84)日常生活活动的依赖性和较低的白蛋白水平(R²=1.5%;HR=0.97)。与 BMI 为 20-25 之间的人相比,肥胖(BMI>30:R²=1.6%;HR=0.55)与死亡率降低两倍显著相关。当所有独立变量都被纳入全 Cox 回归模型(R²=21.4%)时,GIC 是最强的风险预测因子,其次是营养和功能变量。
端粒长度或痴呆的存在都不是生存的预测因子,而多种合并症状况、营养和功能障碍的严重程度与最年长人群的 5 年死亡率显著相关。