Graduate School of Public Health, University of Pittsburgh, A527 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261.
J Gerontol A Biol Sci Med Sci. 2014 Apr;69(4):479-85. doi: 10.1093/gerona/glt117. Epub 2013 Aug 2.
Longevity-associated genes may modulate risk for age-related diseases and survival. The Healthy Aging Index (HAI) may be a subphenotype of longevity, which can be constructed in many studies for genetic analysis. We investigated the HAI's association with survival in the Cardiovascular Health Study and heritability in the Long Life Family Study.
The HAI includes systolic blood pressure, pulmonary vital capacity, creatinine, fasting glucose, and Modified Mini-Mental Status Examination score, each scored 0, 1, or 2 using approximate tertiles and summed from 0 (healthy) to 10 (unhealthy). In Cardiovascular Health Study, the association with mortality and accuracy predicting death were determined with Cox proportional hazards analysis and c-statistics, respectively. In Long Life Family Study, heritability was determined with a variance component-based family analysis using a polygenic model.
Cardiovascular Health Study participants with unhealthier index scores (7-10) had 2.62-fold (95% confidence interval: 2.22, 3.10) greater mortality than participants with healthier scores (0-2). The HAI alone predicted death moderately well (c-statistic = 0.643, 95% confidence interval: 0.626, 0.661, p < .0001) and slightly worse than age alone (c-statistic = 0.700, 95% confidence interval: 0.684, 0.717, p < .0001; p < .0001 for comparison of c-statistics). Prediction increased significantly with adjustment for demographics, health behaviors, and clinical comorbidities (c-statistic = 0.780, 95% confidence interval: 0.765, 0.794, p < .0001). In Long Life Family Study, the heritability of the HAI was 0.295 (p < .0001) overall, 0.387 (p < .0001) in probands, and 0.238 (p = .0004) in offspring.
The HAI should be investigated further as a candidate phenotype for uncovering longevity-associated genes in humans.
与长寿相关的基因可能调节与年龄相关的疾病和生存风险。健康老龄化指数 (HAI) 可能是长寿的一个亚表型,可以在许多研究中构建用于遗传分析。我们调查了 HAI 与心血管健康研究中的生存的关系,并在长寿家族研究中调查了其遗传性。
HAI 包括收缩压、肺活量、肌酐、空腹血糖和改良的 Mini-Mental 状态检查评分,每个评分使用近似三分位数评为 0、1 或 2,并从 0(健康)到 10(不健康)进行求和。在心血管健康研究中,使用 Cox 比例风险分析和 c 统计量分别确定与死亡率的关联和准确预测死亡的能力。在长寿家族研究中,使用基于方差分量的家族分析,使用多基因模型确定遗传性。
心血管健康研究中,指数得分(7-10)不健康的参与者的死亡率是指数得分(0-2)健康的参与者的 2.62 倍(95%置信区间:2.22,3.10)。HAI 本身对死亡的预测效果较好(c 统计量=0.643,95%置信区间:0.626,0.661,p<.0001),略逊于年龄本身(c 统计量=0.700,95%置信区间:0.684,0.717,p<.0001;c 统计量比较差异有统计学意义,p<.0001)。调整人口统计学、健康行为和临床合并症后,预测能力显著增加(c 统计量=0.780,95%置信区间:0.765,0.794,p<.0001)。在长寿家族研究中,HAI 的遗传度为 0.295(p<.0001),总体而言,先证者为 0.387(p<.0001),后代为 0.238(p=0.0004)。
HAI 应作为人类长寿相关基因的候选表型进一步研究。