Critical ages in the life course of the adult brain: Nonlinear subcortical aging
Research Group for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo, Norway Neurobiology of aging
(Impact Factor: 5.01).
05/2013; 34(10). DOI: 10.1016/j.neurobiolaging.2013.04.006
Age-related changes in brain structure result from a complex interplay among various neurobiological processes, which may contribute to more complex trajectories than what can be described by simple linear or quadratic models. We used a nonparametric smoothing spline approach to delineate cross-sectionally estimated age trajectories of the volume of 17 neuroanatomic structures in 1100 healthy adults (18-94 years). Accelerated estimated decline in advanced age characterized some structures, for example hippocampus, but was not the norm. For most areas, 1 or 2 critical ages were identified, characterized by changes in the estimated rate of change. One-year follow-up data from 142 healthy older adults (60-91 years) confirmed the existence of estimated change from the cross-sectional analyses for all areas except 1 (caudate). The cross-sectional and the longitudinal analyses agreed well on the rank order of age effects on specific brain structures (Spearman ρ = 0.91). The main conclusions are that most brain structures do not follow a simple path throughout adult life and that accelerated decline in high age is not the norm of healthy brain aging.
Available from: Rosanna Kathleen Olsen
- "In grey matter, the trajectory of these age-related changes is variable across the brain such that more rapid decline is observed in regions of the frontal and parietal lobes than in the temporal and occipital lobes (Fjell et al., 2013; Kennedy and Raz, 2009; Raz et al., 2004, 2005; Resnick et al., 2000, 2003; Walhovd et al., 2005, 2011). In white matter, some studies have reported a more diffuse pattern of volumetric reductions across the brain with age (Fjell et al., 2013; Resnick et al., 2000, 2003; Salat et al., 2009; Walhovd et al., 2005, 2011), whereas others have reported greater reduction in frontal lobe white matter compared to other regions (Brickman et al., 2006; Ferreira et al., 2014; Head et al., 2004). In addition to neocortical changes, it is well documented that the hippocampus decreases in volume with increasing age (Jack et al., 1998; Mueller et al., 1998; Resnick et al., 2003; Walhovd et al., 2005). "
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ABSTRACT: Lifelong bilingualism is associated with the delayed diagnosis of dementia, suggesting bilingual experience is relevant to brain health in aging. While the effects of bilingualism on cognitive functions across the lifespan are well documented, less is known about the neural substrates underlying differential behavior. It is clear that bilingualism affects brain regions that mediate language abilities and that these regions are at least partially overlapping with those that exhibit age-related decline. Moreover, the behavioral advantages observed in bilingualism are generally found in executive function performance, suggesting that the frontal lobes may also be sensitive to bilingualism, which exhibit volume reductions with age. The current study investigated structural differences in the brain of lifelong bilingual older adults (n=14, mean age=70.4) compared with older monolinguals (n=14, mean age= 70.6). We employed two analytic approaches: 1) we examined global differences in grey and white matter volumes; and, 2) we examined local differences in volume and cortical thickness of specific regions of interest previously implicated in bilingual/monolingual comparisons (temporal pole) or in aging (entorhinal cortex and hippocampus). We expected bilinguals would exhibit greater volume of the frontal lobe and temporal lobe (grey and white matter), given the importance of these regions in executive and language functions, respectively. We further hypothesized that regions in the medial temporal lobe, which demonstrate early changes in aging and exhibit neural pathology in dementia, would be more preserved in the bilingual group. As predicted, bilinguals exhibit greater frontal lobe white matter compared with monolinguals. Moreover, increasing age was related to decreasing temporal pole cortical thickness in the monolingual group, but no such relationship was observed for bilinguals. Finally, Stroop task performance was positively correlated with frontal lobe white matter, emphasizing the importance of preserved white matter in maintaining executive function in aging. These results underscore previous findings implicating an association between bilingualism and preserved frontal and temporal lobe function in aging.
Copyright © 2015. Published by Elsevier B.V.
Brain Research 02/2015; 1612. DOI:10.1016/j.brainres.2015.02.034 · 2.84 Impact Factor
Available from: José Miguel Soares
- "volumetric decreases with age. Similar findings have been consistently reported in the literature, both in cross-sectional and longitudinal studies (Raz et al., 2005; Smith et al., 2007; Abe et al., 2008; Fjell et al., 2009; Walhovd et al., 2011; Tamnes et al., 2013). Specifically, however, herein we found a higher decrease in global WM than GM, confirming a striker WM deterioration after the fifth decade (Gunning-Dixon et al., 2009; Lemaitre et al., 2012). "
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ABSTRACT: Normal brain aging is an inevitable and heterogeneous process characterized by a selective pattern of structural changes. Such heterogeneity arises as a consequence of cumulative effects over the lifespan, including stress and mood effects, which drive different micro- and macro-structural alterations in the brain. Investigating these differences in healthy age-related changes is a major challenge for the comprehension of the cognitive status. Herein we addressed the impact of normal aging, stress, mood, and their interplay in the brain gray and white matter (WM) structure. We showed the critical impact of age in the WM volume and how stress and mood influence brain volumetry across the lifespan. Moreover, we found a more profound effect of the interaction of aging/stress/mood on structures located in the left hemisphere. These findings help to clarify some divergent results associated with the aging decline and to enlighten the association between abnormal volumetric alterations and several states tha
Frontiers in Aging Neuroscience 11/2014; 6:330. DOI:10.3389/fnagi.2014.00330 · 4.00 Impact Factor
Available from: Didac Vidal-Piñeiro
- "such as the hippocampus may exhibit an increased rate of atrophy with ageing ( Fjell et al . , 2013 ) . Both macrostructural and microstructural WM alterations that includes damage in the myelin sheath and reduction in the total number of nerve fibers have been widely reported in aged humans ( Tang et al . , 1997 ; Bartzokis et al . , 2004 ; Davis et al . , 2009 ; Westlye et al . , 2010 ; Sala et al . , 2012 ) . These changes are beli"
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ABSTRACT: Ageing entails cognitive and motor decline as well as brain changes such as loss of gray (GM) and white matter (WM) integrity, neurovascular and functional connectivity alterations. Regarding connectivity, reduced resting-state fMRI connectivity between anterior and posterior nodes of the Default Mode Network (DMN) relates to cognitive function and has been postulated to be a hallmark of ageing. However, the relationship between age-related connectivity changes and other neuroimaging-based measures in ageing is fragmentarily investigated. In a sample of 116 healthy elders we aimed to study the relationship between antero-posterior DMN connectivity and measures of WM integrity, GM integrity and cerebral blood flow (CBF), assessed with an arterial spin labeling sequence. First, we replicated previous findings demonstrating DMN connectivity decreases in ageing and an association between antero-posterior DMN connectivity and memory scores. The results showed that the functional connectivity between posterior midline structures and the medial prefrontal cortex was related to measures of WM and GM integrity but not to CBF. Gray and WM correlates of anterio-posterior DMN connectivity included, but were not limited to, DMN areas and cingulum bundle. These results resembled patterns of age-related vulnerability which was studied by comparing the correlates of antero-posterior DMN with age-effect maps. These age-effect maps were obtained after performing an independent analysis with a second sample including both young and old subjects. We argue that antero-posterior connectivity might be a sensitive measure of brain ageing over the brain. By using a comprehensive approach, the results provide valuable knowledge that may shed further light on DMN connectivity dysfunctions in ageing.
Frontiers in Aging Neuroscience 09/2014; 6:256. DOI:10.3389/fnagi.2014.00256 · 4.00 Impact Factor
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