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使用狭窄年龄队列在认知、速度和生物学变量中寻找共同的原因因素。

Search for a common cause factor amongst cognitive, speed and biological variables using narrow age cohorts.

作者信息

Mackinnon Andrew, Christensen Helen, Jorm Anthony F

机构信息

Centre for Mental Health Research, Australian National University, Canberra, Australia.

出版信息

Gerontology. 2006;52(4):243-57. doi: 10.1159/000093657.

Abstract

BACKGROUND

Cross-sectional studies have demonstrated that age-related effects on many cognitive and biological functioning variables are shared. A number of theories postulate that these associations arise from a common causal mechanism responsible for change across a wide range of functions. However, it has been claimed that the finding of shared variance among variables in these studies may be spurious because most studies have been cross-sectional and based on age-heterogeneous samples.

OBJECTIVE

To examine evidence for changes with age in variance shared by cognitive variables using a narrow-age cohort design.

METHODS

Three samples of adults with age ranges 20-24 years (n = 2,404), 40-44 years (n = 2,530) and 60-64 years (n = 2,510) were drawn from a population-based study. These groups were supplemented by data from an older sample of individuals (77 years and over) from a second population-based study (n = 374). Four models of the structure of a range of cognitive, speed and biological variables derived from previous cross-sectional research were fitted to data. These models were complete independence of variables within a cohort, a single common factor, multiple independent factors, and a second order factor model.

RESULTS

Model fit and the magnitude of loadings from multiple-group confirmatory factor analyses was compared between age groups. The fit for all four models was worse in the 60-64 year age group. Factor loadings on the common factor specified in these models varied between the groups, but the speed factor rather than the biological factor showed increased loadings as a function of age.

CONCLUSIONS

This narrow age-cohort study did not support the existence of developmental changes in the structure of cognitive and biological variables across the lifespan. Shared variation between measures of cognition and biological function may be an artifact of the research designs that have generated these findings. This casts doubt of the existence of a common causal mechanism. However, it may be that such changes manifest only in later old age.

摘要

背景

横断面研究表明,年龄对许多认知和生物功能变量的影响具有共性。一些理论假定,这些关联源于一个共同的因果机制,该机制负责多种功能的变化。然而,有人认为,这些研究中变量间共享方差的发现可能是虚假的,因为大多数研究都是横断面研究且基于年龄异质性样本。

目的

使用年龄范围狭窄的队列设计,研究认知变量共享方差随年龄变化的证据。

方法

从一项基于人群的研究中抽取了三个年龄组的成年人样本,年龄范围分别为20 - 24岁(n = 2404)、40 - 44岁(n = 2530)和60 - 64岁(n = 2510)。这些组还补充了来自另一项基于人群研究的老年个体样本(77岁及以上)的数据(n = 374)。将先前横断面研究得出的一系列认知、速度和生物变量结构的四种模型应用于数据。这些模型分别是队列内变量完全独立、单一共同因素、多个独立因素以及二阶因素模型。

结果

比较了年龄组之间多组验证性因素分析的模型拟合度和负荷大小。在60 - 64岁年龄组中,所有四种模型的拟合度都更差。这些模型中指定的共同因素的因素负荷在各组之间有所不同,但速度因素而非生物因素显示出随年龄增长负荷增加。

结论

这项年龄范围狭窄的队列研究不支持认知和生物变量结构在整个生命周期中存在发育变化。认知和生物功能测量之间的共享变异可能是产生这些发现的研究设计的人为产物。这使人对共同因果机制的存在产生怀疑。然而,可能这种变化仅在老年后期才会显现。

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