Li Hong, Li Johnny Siu-Hang
School of Finance, Nankai University, Tongyan Road 38, 300350, Tianjin, People's Republic of China.
Department of Statistics and Actuarial Science, University of Waterloo, 200 University Avenue West, Waterloo, ON, Canada.
Demography. 2017 Jun;54(3):1073-1095. doi: 10.1007/s13524-017-0579-x.
Researchers using the Lee-Carter approach have often assumed that the time-varying index evolves linearly and that the parameters describing the age pattern of mortality decline are time-invariant. However, as several empirical studies suggest, the two assumptions do not seem to hold when the calibration window begins too early. This problem gives rise to the question of identifying the longest calibration window for which the two assumptions hold true. To address this question, we contribute a likelihood ratio-based sequential test to jointly test whether the two assumptions are satisfied. Consistent with the mortality structural changes observed in previous studies, our testing procedure indicates that the starting points of the optimal calibration windows for most populations fall between 1960 and 1990. Using an out-of-sample analysis, we demonstrate that in most cases, models that are estimated to the optimized calibration windows result in more accurate forecasts than models that are fitted to all available data or data beyond 1950. We further apply the proposed testing procedure to data over different age ranges. We find that the optimal calibration windows for age group 0-49 are generally shorter than those for age group 50-89, indicating that mortality at younger ages might have undergone (another) structural change in recent years.
使用李-卡特方法的研究人员通常假定时变指数呈线性演变,且描述死亡率下降年龄模式的参数不随时间变化。然而,正如一些实证研究所表明的,当校准窗口开始得太早时,这两个假设似乎并不成立。这个问题引发了一个问题,即确定这两个假设成立的最长校准窗口。为了解决这个问题,我们提出了一种基于似然比的序贯检验,以联合检验这两个假设是否得到满足。与先前研究中观察到的死亡率结构变化一致,我们的检验程序表明,大多数人群的最优校准窗口的起始点在1960年至1990年之间。通过样本外分析,我们证明,在大多数情况下,针对优化校准窗口进行估计的模型比拟合所有可用数据或1950年以后数据的模型能产生更准确的预测。我们进一步将所提出的检验程序应用于不同年龄范围的数据。我们发现,0 - 49岁年龄组的最优校准窗口通常比50 - 89岁年龄组的短,这表明近年来较年轻年龄段的死亡率可能经历了(另一次)结构变化。