Sanders Jason L, Singh Jatinder, Minster Ryan L, Walston Jeremy D, Matteini Amy M, Christensen Kaare, Mayeux Richard, Borecki Ingrid B, Perls Thomas, Newman Anne B
Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Human Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania.
J Am Geriatr Soc. 2016 Aug;64(8):1679-83. doi: 10.1111/jgs.14190. Epub 2016 Jun 13.
To investigate the association between mortality and heritability of a rescaled Fried frailty index, the Scale of Aging Vigor in Epidemiology (SAVE), to determine its value for genetic analyses.
Longitudinal, community-based cohort study.
The Long Life Family Study (LLFS) in the United States and Denmark.
Long-lived individuals (N = 4,875, including 4,075 genetically related individuals) and their families (N = 551).
The SAVE was administered to 3,599 participants and included weight change, weakness (grip strength), fatigue (questionnaire), physical activity (days walked in prior 2 weeks), and slowness (gait speed); each component was scored 0, 1, or 2 using approximate tertiles, and summed (range 0 (vigorous) to 10 (frail)). Heritability was determined using a variance component-based family analysis using a polygenic model. Association with mortality in the proband generation (N = 1,421) was calculated using Cox proportional hazards mixed-effect models.
Heritability of the SAVE was 0.23 (P < .001) overall (n = 3,599), 0.31 (P < .001) in probands (n = 1,479), and 0.26 (P < .001) in offspring (n = 2,120). In adjusted models, higher SAVE scores were associated with higher mortality (score 5-6: hazard ratio (HR) = 2.83, 95% confidence interval (CI) = 1.46-5.51; score 7-10: HR = 3.40, 95% CI = 1.72-6.71) than lower scores (0-2).
The SAVE was associated with mortality and was moderately heritable in the LLFS, suggesting a genetic component to age-related vigor and frailty and supporting its use for further genetic analyses.
研究重新调整后的弗里德衰弱指数(即流行病学衰老活力量表,SAVE)与死亡率及遗传力之间的关联,以确定其在基因分析中的价值。
基于社区的纵向队列研究。
美国和丹麦的长寿家庭研究(LLFS)。
长寿个体(N = 4875,包括4075名有基因关联的个体)及其家庭(N = 551)。
对3599名参与者进行SAVE评估,包括体重变化、虚弱程度(握力)、疲劳感(问卷调查)、身体活动量(前两周行走天数)和行动迟缓程度(步速);每个组成部分使用近似三分位数分别评分为0、1或2,并求和(范围从0(活力充沛)到10(衰弱))。使用基于多基因模型的方差成分家庭分析来确定遗传力。使用Cox比例风险混合效应模型计算先证者一代(N = 1421)中与死亡率的关联。
总体而言(n = 3599),SAVE的遗传力为0.23(P <.001),先证者中(n = 1479)为0.31(P <.001),后代中(n = 2120)为0.26(P <.001)。在调整模型中,与较低分数(0 - 2)相比,较高的SAVE分数与较高的死亡率相关(分数5 - 6:风险比(HR)= 2.83,95%置信区间(CI)= 1.46 - 5.51;分数7 - 10:HR = 3.40,95% CI = 1.72 - 6.71)。
SAVE与死亡率相关,且在LLFS中具有中度遗传性,这表明与年龄相关的活力和衰弱存在遗传成分,并支持其用于进一步的基因分析。