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Duarte, A.

Publications and source records attributed to Duarte, A..

At least 19 recordsLinked to original sources

Effects of predictability and error on corticospinal excitability during an electronic prediction game

Background: Detecting environmental regularities is a sophisticated cognitive skill, but its neural basis remains unclear. We tested whether corticospinal excitability tracks stimulus predictability, prediction errors, and task progression while the participants played the Goalkeeper Game. Methods: Sixteen right-handed males (24.4 +/- 6.8 years) saved penalty kicks using index, middle, or ring fingers (left, center, right). Kick sequences were generated by a context tree model, in which contexts represent the minimum recent history required to predict the next event. Participants completed 1,200 trials (6 blocks x 200 trials each). Transcranial magnetic stimulation (TMS) delivered 400 ms before the go signal elicited motor evoked potentials (MEPs) in the first dorsal interosseous (FDI) and flexor digitorum superficialis (FDS) muscles during blocks 2, 4, and 6. Contexts were classified as unpredictable (1, 10) or predictable (2, 20, 00); prediction errors were defined for non-deterministic transitions after context 1. Log-MEPs were analyzed using mixed-effects models. Results: In FDI, a Predictability x Previous-Error x Block interaction emerged (F(2,8997)=6.89, p=.001), confined to the final block. Predictability increased MEP amplitudes after successful transitions (+6.3%; p=0.006) but decreased MEP amplitudes after failed transitions (-7.0%; p=0.007). For FDS, unpredictable trials elicited larger MEPs (+7.2%; p=0.002), and MEPs increased from block 2 to 6 (+16.8%; p=0.003). Conclusions: FDS MEP responses were broadly associated with uncertainty and task progression, whereas FDI MEP responses showed context-specific, error-dependent modulation after extended exposure, suggesting fine-grained predictive coding in goal-executing effectors.

neuroscience↗

Individual differences in post-encoding sleep continuity predict context memory accuracy and supporting ERPs in younger and older adults

Post-encoding sleep plays an essential role in episodic memory consolidation. Much of the existing literature on sleep and memory relies on deprivation paradigms or laboratory-controlled sleep. Relatively few studies have examined how naturalistic post-encoding sleep relates to memory retrieval and its supporting neural activity, or whether age-related impairments in this sleep are linked to those in episodic memory. In the present study, we used actigraphy and electroencephalography to examine how post-encoding sleep quality relates to context memory performance and retrieval-related ERPs supporting performance in younger and older adults. Participants encoded object-scene pairs and were tested on matching and mismatching pairs after a 96-hour sleep-filled delay. We found that greater post-encoding sleep continuity predicted better delayed context memory performance for mismatching pairs across age groups. Post-encoding sleep continuity was also associated with larger ERP differences between context hits and misses for context-matching pairs, for ERP effects associated with post-retrieval monitoring operations across age groups. Together, these findings suggest that more continuous, naturalistic post-encoding sleep facilitates episodic memory performance and neural mechanisms supporting episodic memory retrieval across adult age.

neuroscience↗

Age Alters the Relationship between Post-Encoding Sleep Quality and Context Memory Neural Reinstatement

Sleep supports episodic memory consolidation, yet it remains unclear how naturalistic post-encoding sleep quality relates to the neural reinstatement of episodic representations across adulthood. The present study examined whether sleep discontinuity during the retention interval predicted delayed context memory and encoding-retrieval similarity (ERS) of EEG in younger and older adults. Participants completed an object-scene context memory task with immediate and delayed retrieval, while EEG was recorded during encoding and retrieval. Actigraphy was used to measure sleep across the post-encoding retention period, and principal component analysis identified sleep discontinuity and sleep time components. Behavioral results showed that greater post-encoding sleep discontinuity, but not sleep time, was associated with poorer delayed memory accuracy for mismatching object-context pairs across age. ERS analyses further showed that greater sleep discontinuity was associated with reduced ERS for correctly rejected mismatching pairs across frontal and posterior spatiotemporal clusters. Age moderated sleep-ERS associations: greater sleep discontinuity was generally related to lower ERS in younger adults, whereas some spatiotemporal clusters showed positive associations in older adults, potentially reflecting compensatory or effortful retrieval-related processing in poorer sleepers. Together, these findings suggest that sleep continuity during the post-encoding retention interval is important for preserving high-fidelity episodic representations needed for later context discrimination. More broadly, the results demonstrate that naturalistic sleep fragmentation is linked to both behavioral memory outcomes and neural reinstatement across adults.

neuroscience↗

Thalassoporum longitrichum sp. nov., a marine epizoic cyanobacterium with anti-inflammatory potential, and the taxonomic reassessment of Limnothrix Meffert

The strain LEGE 10371, isolated from the surface of a marine sponge at Praia da Memoria, Portugal, was characterized as a new Thalassoporum species (Pseudanabaenales) using a polyphasic approach that included 16S rRNA gene phylogenetic analysis (Maximum Likelihood and Bayesian Inference), 16S-23S ITS secondary structures, p-distance calculations, MALDI-TOF MS profiling, and morphological analysis by optical and scanning electron microscopy, as well as ecological and biochemical characterization. Phylogenetically, LEGE 10371 clustered within the Thalassoporum clade, however distant from the other existent species of the genus. The p-distance analysis revealed low sequence identity with other Thalassoporum species, with a maximum value of 97.2% to Th. komareki. The MALDI-TOF profile displayed high-intensity peaks at approximately 3,000, 4,000, 6,000 and 8,000 m/z, representing strong candidates for diagnostic markers of the new species. Morphologically, the new species differ from the other species of the genus by presenting trichomes with more than 10 cells and lack of aerotopes. Biocompatibility of the fractions was evaluated in HaCaT keratinocytes, showing no cytotoxic effects at most tested concentrations. PCR screening targeting mcyE, sxtG, anaC, and cyrA confirmed the absence of the genetic potential for the production of major cyanotoxins. Chemical characterization revealed a pigment-rich profile dominated by chlorophyll-a and carotenoids, including {beta}-carotene, zeaxanthin, lutein, and mixoxanthophyll. Bioactivity assays showed superoxide anion radical scavenging by the aqueous fraction (IC2 {approx} 0.042-0.045 mg mL-{superscript 1}), strong nitric oxide radical scavenging by the acetonic fraction (IC = 0.045 mg mL-{superscript 1}), and lipoxygenase inhibition ([~]41%, for a fraction concentration of 0.25 mg mL-), suggesting a potential contribution of these fractions to modulate inflammation-related pathways. Additionally to this results, the polyphasic analysis permitted to confirm previous data that Pseudanabaena and Limnothrix represent the same generic entity. Both genera clustered together, presented high 16S rRNA gene identity (up to 99.9%) and share the same morphological and ecological features. Consequently, we formally proposed the synonimization of Limnothrix into Pseudanabaena.

microbiology↗

CyTOF-based profiling of circulating tumor cells predicts aggressiveness and therapy response in SCLC liquid biopsies at a personalized level

Small-cell lung cancer (SCLC) is an aggressive neuroendocrine carcinoma characterized by high numbers of circulating tumor cells (CTCs). We applied CyTOF and a 20-marker antibody panel to detect and phenotype CTCs directly in liquid biopsies of 51 SCLC patients (treatment-naive, chemotherapy and immunotherapy-treated, and tarlatamab-treated), of which a subset were longitudinally tracked. Unsupervised clustering revealed distinct cell populations enriched in patient liquid biopsies compared to those from healthy donors. Further analysis identified CTC populations of the three established SCLC subtypes driven by the high expression of ASCL1, NeuroD1, and POU2F3 transcription factors respectively. Significant differences in CTC EMT markers, established therapeutic targets (e.g. DLL3), and subtype heterogeneity were observed between naive versus treated samples. Changes in subtype proportions were observed in longitudinally tracked samples in both treatment modalities. Our study demonstrates the utility of CyTOF for high-resolution CTC profiling, offering dynamic insights into CTC heterogeneity, treatment response, and resistance mechanisms. HighlightsO_LICTCs can be detected, subtyped and phenotyped in SCLC liquid biopsies using CyTOF C_LIO_LICTC subtypes and EMT states are differentially associated with treatment modality C_LIO_LICTC DLL3 levels and epithelial features increase following anti-DLL3 BiTE therapy C_LIO_LICyTOF CTC subtyping can predict disease aggressiveness C_LIO_LILongitudinal tracking reveals CTC plasticity and therapy response correlations C_LI Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=132 SRC="FIGDIR/small/694669v1_ufig1.gif" ALT="Figure 1"> View larger version (46K): org.highwire.dtl.DTLVardef@384cbcorg.highwire.dtl.DTLVardef@35dd37org.highwire.dtl.DTLVardef@4e7d61org.highwire.dtl.DTLVardef@1098e4f_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗

The Role of Sleep Duration and Age in Neural Reactivation and Episodic Memory Performance Across the Adult Lifespan

Sleep is essential for episodic memory consolidation, involving the reactivation of neural patterns during encoding and retrieval. This study examined how sleep duration influences encoding-retrieval similarity (ERS) and memory performance across the adult lifespan. Fifty-five adults (18-79 years) participated in a seven-day protocol, combining actigraphy-based sleep monitoring with EEG and memory assessments during a paired associate learning task. Significant correlations between sleep duration and ERS were observed, with clusters showing positive and negative associations across brain regions. In match context trials, ERS in the left frontal region correlated with sleep duration, and age moderated these effects. In mismatch context trials, positive correlations were identified in the left posterior, left frontal, and right posterior regions. These results highlight the role of sleep in modulating neural reactivation patterns during memory retrieval and emphasize the influence of age. The study advances our understanding of how sleep variability impacts memory consolidation and provides a basis for exploring targeted sleep interventions. Clinical RelevanceThis study highlights the impact of habitual sleep variability on neural reactivation patterns and memory retrieval across the adult lifespan. The findings emphasize the moderating role of age and suggest that improving sleep duration may enhance episodic memory performance. These insights could guide clinicians in developing personalized sleep interventions to support cognitive health and mitigate age-related memory decline.

neuroscience↗

Investigating the Impact of Habitual Sleep Quality on Episodic Memory Performance: An EEG-Based Representational Similarity Analysis

Sleep is crucial for episodic memory consolidation, yet the impact of habitual sleep quality on memory performance remains underexplored. This study investigates the relationship between sleep quality and episodic memory retrieval using EEG-based representational similarity analysis (RSA). Thirty-six participants wore wrist accelerometers for one week to capture habitual sleep patterns, including total sleep time and restlessness. Memory performance was assessed through a paired associate learning task, with EEG data recorded during encoding and retrieval phases. RSA was applied to EEG oscillatory power across time-frequency windows to examine the neural similarity between encoding and retrieval. The results showed both positive and negative correlations between sleep metric and memory performance, with sleep restlessness being linked to both increases and decreases in neural similarity across specific clusters. These findings emphasize the important role of sleep quality in shaping the neural processes underlying episodic memory retrieval, indicating a strong connection between sleep patterns and memory function.

neuroscience↗

Enhancing cryopreservation of human iPSCs: Bottom-up vs Conventional freezing geometry

Induced pluripotent stem cells (iPSCs) hold large potential on regenerative medicine due to their pluripotency and unlimited self-renewal capacity without the ethical issues of embryonic stem cells. To provide quality-controlled iPSCs for clinical therapies, it is essential to develop safe cryopreservation protocols for long-term storage, preferable amenable for scale-up and automation. We have compared the impact of two different freezing geometries (bottom-up and conventional radial freezing) on the viability and differentiation capability of human iPSCs. Our results demonstrate that the bottom-up freezing under optimized conditions significantly increases iPSCs viability, up to 9% for the cell membrane integrity and up to 21% for the cell metabolic state, compared to conventional freezing. The improvement achieved for bottom-up versus conventional freezing was maintained after scale-up from cryogenic vials to 30 mL bags, highlighting the methods potential for clinical applications. These findings show that bottom-up freezing can offer a more controlled and scalable cryopreservation strategy for iPSCs, promoting their future use in regenerative medicine.

cell biology↗

SimMS: A GPU-Accelerated Cosine Similarity implementation for Tandem Mass Spectrometry

Untargeted metabolomics involves a large-scale comparison of the fragmentation pattern of a mass spectrum against a database containing known spectra. Given the number of comparisons involved, this step can be time-consuming. In this work, we present a GPU-accelerated cosine similarity implementation for Tandem Mass Spectrometry (MS) with approximately 1000-fold speedup compared to the MatchMS reference at a rate of 0.005% incorrect matches and a rate of 0.002% incorrect scores. We describe the underlying reasons for these errors and provide means to avoid them.

bioinformatics↗

Developing epidemiological preparedness for a plant disease invasion: modelling citrus huanglongbingin the European Union

Huanglongbing (HLB; citrus greening) is the most damaging disease of citrus worldwide. While citrus production in the USA and Brazil have been affected for decades, HLB has not been detected in the European Union (EU). However, psyllid vectors have already invaded and spread in Portugal and Spain, and in 2023 the psyllid species known to vector HLB in the Americas was first reported within the EU. We develop a landscape-scale, epidemiological model, accounting for heterogeneous citrus cultivation and vector dispersal, as well as climate and disease management. We use our model to predict HLB dynamics following introduction into high-density citrus areas in Spain, assessing detection and control strategies. Even with significant visual surveillance, we predict any epidemic will be widespread on first detection, with eradication unlikely. Introducing increased inspection and roguing following first detection, particularly if coupled with intensive insecticide use, could potentially sustain citrus production for some time. However, this may require chemical application rates that are not permissible in the EU. Disease management strategies targeting asymptomatic infection will likely lead to more successful outcomes. Our work highlights modelling as a key component of developing epidemiological preparedness for a pathogen invasion that is, at least somewhat, predictable in advance.

ecology↗

More than the sum of its parts: investigating episodic memory as a multidimensional cognitive process

Why do we remember some events but forget others? Previous studies attempting to decode successful vs. unsuccessful brain states to investigate this question have met with limited success, potentially due, in part, to assessing episodic memory as a unidimensional process, despite evidence that multiple domains contribute to episodic encoding. Using a novel machine learning algorithm known as "transfer learning", we leveraged visual perception, sustained attention, and selective attention brain states to better predict episodic memory performance from trial-to-trial encoding electroencephalography (EEG) activity. We found that this multidimensional treatment of memory decoding improved prediction performance compared to traditional, unidimensional, methods, with each cognitive domain explaining unique variance in decoding of successful encoding-related neural activity. Importantly, this approach could be applied to cognitive domains outside of memory. Overall, this study provides critical insight into the underlying reasons why some events are remembered while others are not.

neuroscience↗

Worldwide soundscape ecology patterns across realms

Abstract and keywordsO_ST_ABSAimC_ST_ABSThe urgency for remote, reliable, and scalable biodiversity monitoring amidst mounting human pressures on ecosystems has sparked worldwide interest in Passive Acoustic Monitoring (PAM), which can track life underwater and on land. However, we lack a unified methodology to report this sampling effort and a comprehensive overview of PAM coverage to gauge its potential as a global research and monitoring tool. To remediate this, we created the Worldwide Soundscapes project, a collaborative network and growing database comprising metadata from 409 datasets across all realms (terrestrial, marine, freshwater, and subterranean). LocationWorldwide, 12 200 sites, all ecosystems. Time period1991 to present. Major taxa studiedAll soniferous taxa. MethodsWe synthesise sampling coverage across spatial, temporal, and ecological scales using metadata describing sampling locations, deployment schedules, focal taxa, and recording parameters. We explore global trends in biological, anthropogenic, and geophysical sounds based on 168 recordings from twelve ecosystems across all realms. ResultsTerrestrial sampling is spatially denser (45 sites/Mkm2) than aquatic sampling (0.3 and 1.8 sites/Mkm2 in oceans and fresh water) with only two subterranean datasets. Although diel and lunar cycles are well-covered in all realms, only marine datasets (56%) comprehensively sample all seasons. Across twelve ecosystems, biological sounds show contrasting diel patterns, decline with distance from the equator and negatively correlate with anthropogenic sounds. Main conclusionsPAM can inform macroecology studies as well as global conservation and phenology syntheses, but representation can be improved by expanding terrestrial taxonomic scope, sampling coverage in the high seas and subterranean ecosystems, and spatio-temporal replication in freshwater habitats. Overall, this global PAM network holds promise to support global biodiversity research and monitoring efforts.

ecology↗

Dissecting an ancient stress resistance trait syndrome in the compost yeast Kluyveromyces marxianus

Organisms specialized to extreme environments can be the product of millions of years of evolutionary engineering and refinement. The underlying genetics can be quite distinct from the ones operating at earlier stages of trait innovation. In this work, we have developed the multi-stress resistant yeast Kluyveromyces marxianus, which diverged from its closest relative >20 million years ago, as a model for interspecies comparative biology and genomics. In growth assays of the Kluyveromyces genus, we found that K. marxianus exhibited unique tolerance of high heat and a subset of chemical stress conditions. We then generated and analyzed omic profiles from across the genus to find molecular features associated with- and potentially causal for - K. marxianus traits. Expression profiling revealed divergent lipid processing and membrane transport programs in K. marxianus, borne out in changes in lipid utilization in experimental assays. Sequence analyses found robust evidence for expansions in gene families in the K. marxianus genome, most notably among transmembrane transporters and in metabolic enzymes. In molecular-evolution tests, we identified adaptive protein variants throughout the K. marxianus genome among which plasma membrane transporters were over-represented. These data enable a model of the molecular mechanisms and evolutionary pressures underlying K. marxianus traits, including adaptive changes to transporters, lipid processing, and membrane functions mediating stress resistance. Significance statementMany traits of basic and applied interest arose long ago and manifest in the modern day as fixed in a given species; understanding how evolution built them, potentially over millions of years, remains a key challenge in the field. In this study, we report stress-resistance phenotypes that distinguish the yeast Kluyveromyces marxianus from its relatives, and we discover unique patterns of genetic and regulatory variation in membrane-protein genes, as well as unique properties of lipid metabolism, in this species. We propose a broadly applicable model in which evolution can tune membrane lipid composition and membrane-protein function to boost cellular fitness in challenging environments.

evolutionary biology↗

YAP1 status defines two intrinsic subtypes of LCNEC with distinct molecular features and therapeutic vulnerabilities

Large cell neuroendocrine carcinoma (LCNEC) is a high-grade neuroendocrine malignancy that, like the more common small cell lung cancer (SCLC), is associated with an absence of druggable oncogenic driver mutations, a clinically aggressive disease course, and dismal prognosis. In contrast to SCLC, however, there is little evidence to guide optimal treatment strategies which are, instead, often adapted from SCLC and non-small cell lung cancer (NSCLC) approaches. While there have been some efforts to describe the molecular landscape of LCNEC, to date there are few links between distinct biologic phenotypes of LCNEC and therapeutic vulnerabilities. Here, we demonstrate that the presence or absence of the transcription factor YAP1 distinguishes two roughly equal subsets of LCNEC. The YAP1-high subset is mesenchymal and inflamed and characterized, alongside TP53 mutations, by co-occurring alterations in CDKN2A/B and SMARCA4. Therapeutically, the YAP1-high subset demonstrates vulnerability to MEK and AXL targeting strategies, including a novel preclinical AXL CAR-T cell, as well as predicted vulnerability to SMARCA2 degraders and CDK4/6 inhibitors. Meanwhile, the YAP1-low subset is epithelial and immune-cold and more commonly features TP53 and RB1 co-mutations, similar to those observed in pure SCLC. Notably, the YAP1-low subset is also characterized by expression of SCLC subtype-defining transcription factors -especially ASCL1 and NEUROD1 - and, as expected given its transcriptional similarities to SCLC, exhibits putative vulnerabilities reminiscent of SCLC, including Delta-like ligand 3 (DLL3) and CD56 targeting, as with novel preclinical DLL3 and CD56 CAR T-cells, and DNA damage repair (DDR) inhibition. These findings highlight the potential for YAP1 to guide the first personalized treatment strategies for LCNEC.

cancer biology↗

H2AX promotes replication fork degradation and chemosensitivity in BRCA-deficient tumours

Histone H2AX plays a key role in DNA damage signalling in the surrounding regions of DNA double-strand breaks (DSBs)1,2. In response to DNA damage, H2AX becomes phosphorylated on serine residue 139 (known as {gamma}H2AX), resulting in the recruitment of the DNA repair effectors 53BP1 and BRCA13-6. Here, by studying resistance to poly(ADP-ribose) polymerase (PARP) inhibitors in BRCA1/2-deficient mammary tumours7,8, we identify a novel function for {gamma}H2AX in orchestrating drug-induced replication fork degradation. Mechanistically, {gamma}H2AX-dependent replication fork degradation is elicited by the inhibition of CtIP-mediated fork protection. As a result, H2AX loss restores replication fork stability and increases chemoresistance in BRCA1/2-deficient tumour cells without restoring homology-directed DNA repair, as highlighted by the lack of DNA damage-induced RAD51 foci. Furthermore, in the attempt to discover acquired genetic vulnerabilities, we find that ATM inhibition overcomes PARP inhibitor (PARPi) resistance in H2AX-deficient tumours by interfering with CtIP-mediated fork protection of stalled forks. In summary, our results demonstrate a novel role for H2AX in replication fork biology in BRCA-deficient tumours and establish a function of H2AX separable from its classical role in DNA damage signalling and DSB repair.

cancer biology↗

Antimicrobial Susceptibility Profiles of Bacteria Isolated from The Ozama River in Santo Domingo, Dominican Republic

The dissemination of antimicrobial-resistant bacteria in environmental waters is an emerging concern in medical and industrial settings. In the present study, our research team analyzed superficial water samples from 3 different collection sites along the Ozama River, the most important river in the Dominican metropolitan area. Seventy-six isolates were obtained from culture media previously enriched with cefotaxime and imipenem and subsequently identified by MALDI-ToF. Our isolates spanned 12 genera of bacteria; over 30% were of clinical relevance, and 43% exhibited a phenotype classified as multi-drug resistance. The most frequent species identified as Stenotrophomonas maltophilia (n = 33), an emerging nosocomial pathogen. This study constitutes part of the initiative to understand the profiles of the perils of multi-drug resistance in metropolitan areas of the Dominican Republic: a nation with poor antibiotic use regulation. IMPORTANCENearly two billion people are sourcing their water from low-quality reservoirs world-wide. These reservoirs consist of contaminated waters with anthropogenic pollutants such as antibiotics, disinfectants, and other substances used to treat water in societies with scarce resources and unregulated industries. Furthermore, the exposure of these antibiotics to potable water reservoirs promotes the increase of clinically relevant bacteria with antibiotic-resistance capabilities, becoming a public health crisis. Therefore, treating patients with infectious diseases and providing prophylactic measures against infection-associated conditions (such as post-surgical recovery) has become progressively more difficult. Based on this evidence frame, it is of considerable importance to analyze the bacterial profiles of rivers that fall prey to anthropogenic contamination, as these investigations on antibiotic resistance will, of course, benefit the life of humans.

microbiology↗

Multi-omics analysis reveals distinct non-reversion mechanisms of PARPi resistance in BRCA1- versus BRCA2-deficient mammary tumors

BRCA1 and BRCA2 both function in DNA double-strand break repair by homologous recombination (HR). Due to their HR-defect, BRCA1/2-deficient cancers are sensitive to poly(ADP-ribose) polymerase inhibitors (PARPi) but they eventually acquire resistance. Preclinical studies yielded several PARPi resistance mechanisms that do not involve BRCA1/2 reactivation, but their relevance in the clinic remains elusive. To investigate which BRCA1/2-independent mechanisms drive spontaneous resistance in vivo, we combined molecular profiling with functional analysis of the HR status of matched PARPi-naive and PARPi-resistant mouse mammary tumors harboring large intragenic deletions that prevent functional restoration of BRCA1/2. We observed restoration of HR in 64% of PARPi-resistant BRCA1-deficient tumors but none in the PARPi-resistant BRCA2-deficient tumors. Moreover, we found that 53BP1 loss is the prevalent resistance mechanism in HR-proficient BRCA1-deficient tumors, whereas resistance in BRCA2-deficient tumors is mainly induced by the loss of PARG. Our combined multi-omics analysis catalogued additional genes and pathways potentially involved in modulating PARPi response.

cancer biology↗

Preparing for the worst: Evidence that older adults proactively downregulate negative affect

Age-related differences in processing emotional stimuli are well established. However, previous studies have only assessed the impact of age on emotional processing and encoding in response to, not in anticipation of, emotional stimuli. In the current study, we investigated age-related differences in the impact of emotional anticipation on affective responses and episodic memory for emotional images. Young and older were scanned while encoding negative and neutral images preceded by cues that were either valid or invalid predictors of image valence. Participants were asked to rate the emotional intensity of the images and to complete an episodic recognition task immediately after scanning. Using multivariate behavioral partial least squares (PLS) analysis, we found that young and older adults recruit the same set of brain regions to differentially support emotional processing during the anticipation of emotional images. Specifically, anticipatory recruitment of the amygdala, ventromedial PFC, and hippocampus in older adults predicts reduced memory for negative than neutral images for older adults and the opposite for young adults. Seed PLS analyses further show inverse coupling between the amygdala and ventromedial PFC activation following negative cues, consistent with the top-down spontaneous suppression of negative affect. To the best of our knowledge, this is the first study to provide evidence that the \"positivity effect\" seen in older adults memory performance is related to the spontaneous suppression of negative affect in anticipation of, not just in response to, negative stimuli.

neuroscience↗