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Guichet, C.

Publications and source records attributed to Guichet, C..

3 recordsLinked to original sources

Lifespan Oscillatory Dynamics in Lexical Production: A Population-based MEG Resting-State Analysis

Lexical production remains relatively preserved across the lifespan, but cognitive control demands increase with age to support efficient semantic access. It suggests a domain-general and a language-specific component. Current neurocognitive models suggest the Default Mode Network (DMN) may drive the interplay between these components, impacting the trajectory of production performance with a pivotal shift around midlife. However, the corresponding time-varying architecture still needs clarification. Here, we leveraged MEG resting-state data from healthy adults aged 18-88 from a CamCAN population-based sample. We found that DMN temporal dynamics shift from anterior-ventral to posterior-dorsal states until midlife to mitigate word-finding challenges. Similarly, sensorimotor integration along this posterior path enhances cross-talk with lower-level circuitry as the dynamic information flow with more anterior, higher-order cognitive states gets compromised. It suggests a bottom-up, exploitation-based form of cognitive control in the aging brain, highlighting the interplay between abstraction, control, and perceptive-motor systems in preserving lexical production. HighlightsO_LIMidlife is a pivotal period for time-varying functional connectivity C_LIO_LIDMN activation and deactivation drive the resting-state oscillatory architecture C_LIO_LIEnhanced posterior DMN temporal dynamics mitigates lexical production decline C_LI

neuroscience↗

Dynamics of White Matter Architecture in Lexical Production among Middle-Aged Adults

This study aimed to elucidate the white matter changes associated with lexical production (LP) difficulties that typically emerge in middle age, resulting in increased naming latencies. To delay the onset of LP decline, middle-aged adults may rely on domain-general (DG) and language-specific (LS) compensatory mechanisms as proposed by the LARA model (Lexical Access and Retrieval in Aging). However, our knowledge of the white matter changes supporting these mechanisms remains incomplete. Based on a sample of 155 middle-aged adults from the CAMCAN cohort, we combined dimensionality reduction techniques with multivariate statistical methods to jointly examine the relationships between diffusion-weighted imaging and LP-related neuropsychological data. Our findings (i) show that midlife constitutes a pivotal period marked by a discontinuity in brain structure within distributed networks within dorsal, ventral, and anterior cortico-subcortical pathways, and (ii) reveal that this discontinuity signals a neurocognitive transition around age 53-54, marking the onset of LP decline. Indeed, our results propose that middle-aged adults may initially adopt a "semantic strategy" to compensate for initial LP challenges. Still, this strategy may be compromised when late middle-aged adults (age 55-60) lose the ability to exert cognitive control over semantic representations (i.e., reduced semantic control). In summary, our study advances our comprehension of brain structure changes that underpin the neurocognitive profile of LP in middle age. Specifically, we underscore the importance of considering the interplay between DG and LS processes when studying the trajectory of LP performance in healthy aging. Furthermore, these findings offer valuable insights into identifying predictive biomarkers related to the compensatory dynamics observed in midlife, which can help understand language-related neurodegenerative pathologies. HighlightsO_LIMidlife constitutes a pivotal period characterized by a discontinuity in brain structure. C_LIO_LIEarly middle-aged adults (age 45-55) adopt a "semantic strategy" to facilitate semantic access and sustain lexical production (LP) performances. C_LIO_LILate middle-aged adults (age 55-60) gradually lose the ability to exert cognitive control over semantic representations, marking the onset of LP decline. C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=105 SRC="FIGDIR/small/579645v1_ufig1.gif" ALT="Figure 1"> View larger version (28K): org.highwire.dtl.DTLVardef@85346dorg.highwire.dtl.DTLVardef@13515b7org.highwire.dtl.DTLVardef@24a1fforg.highwire.dtl.DTLVardef@1078f4c_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

Modeling the Neurocognitive Dynamics of Language across the Lifespan

Healthy aging is associated with a heterogeneous decline across cognitive functions, typically observed between language comprehension and language production (LP). Examining resting-state fMRI and neuropsychological data from 628 healthy adults (age 18-88) from the CamCAN cohort, we performed state-of-the-art graph theoretical analysis to uncover the neural mechanisms underlying this variability. At the cognitive level, our findings suggest that LP is not an isolated function but is modulated throughout the lifespan by the extent of inter-cognitive synergy between semantic and domain-general processes. At the cerebral level, we show that DMN (Default Mode Network) suppression coupled with FPN (Fronto-Parietal Network) integration is the way for the brain to compensate for the effects of dedifferentiation at a minimal cost, efficiently mitigating the age-related decline in LP. Relatedly, reduced DMN suppression in midlife could compromise the ability to manage the cost of FPN integration. This may prompt older adults to adopt a more cost-efficient compensatory strategy that maintains global homeostasis at the expense of LP performances. Taken together, we propose that midlife represents a critical neurocognitive juncture that signifies the onset of LP decline, as older adults gradually lose control over semantic representations. We summarize our findings in a novel SENECA model (Synergistic, Economical, Nonlinear, Emergent, Cognitive Aging), integrating connectomic and cognitive dimensions within a complex system perspective. HighlightsO_LILexical production (LP) relies on the interplay between domain-general and semantic processes throughout life. C_LIO_LIDMN (Default Mode Network) suppression cooperates with FPN (Fronto-Parietal Network) integration to maintain LP performance at a minimal cost. C_LIO_LIMidlife marks a neurocognitive shift, with reduced DMN suppression prompting a more cost-efficient compensatory strategy that prioritizes homeostasis over LP performance. C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=135 SRC="FIGDIR/small/547510v2_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@85939aorg.highwire.dtl.DTLVardef@19d8bbcorg.highwire.dtl.DTLVardef@40f5e8org.highwire.dtl.DTLVardef@d0713f_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗