Pablo Barttfeld’s research while affiliated with National University of Córdoba and other places

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Publications (47)


Study design, methodology and analyses
a, Image datasets. b, Groups. We collected 2,135 images from 958 HCs, 584 patients with FTLD and 593 patients with AD. c, Countries included: Latin America (n = 949; Argentina, Chile, Colombia, Mexico, Peru) and the United States (n = 1,186). d, States assessed. Latin America: Argentina (Buenos Aires -capital city and state, and San Juan); Chile (Atacama, Biobio, Metropolitana, O’Higgins, Valparaiso); Colombia (Antioquia, Bogota, Cundinamarca, Valle del Cauca); Mexico (Aguascalientes, Ciudad de Mexico, Estado de Mexico); Peru (Ancash, Arequipa, Callao, Huanuco, Ica, Junin, La Libertad, Lambayeque, Lima, Piura). United States (Alabama, Arizona, California, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Washington and Wisconsin). e, MRI image preparation. Voxel-based morphometry preprocessing was run with the Computational Anatomy Toolbox (CAT12). Outputs were normalized, smoothed and w-scored³¹. f, Resting-state fMRI (rs-fMRI) image preparation. Preprocessing was run using the fMRIPrep standard pipeline. We used weighted Symbolic Dependence Metric (wSDM) nonlinear correlation coefficients across the time series³² based on the Automated Anatomical Labeling (AAL) atlas⁴⁸ to build three FC matrices. Based on the GM results, these were shortened between all areas and the corresponding seed ROIs for all territories (Latin America, United States). Matrices were harmonized at the scanner level. g, Statistical Parametric Mapping (SPM12) associations between country-level and state-level Gini index and GM volume (black rectangle). Linear regressions assessed the link between country-level and state-level Gini indices and the significant GM volume clusters. Multiple regression models included age, sex, years of education and cognition as predictors.
Country-level Gini index and brain volume
Simple linear regressions were conducted with country-level Gini index (predictor) and the normalized significant-cluster GM volume maps per individual (dependent variable). The significant-cluster maps were calculated using binarized masks of the significant results from the SPM12 correlation on the normalized and smoothed images. We performed analyses in all groups together (HCs, FTLD and AD) and separately. Significant clusters from the SPM12 analyses are plotted next to each simple linear regression scatterplot. The shaded area around the regression lines indicates the 95% confidence interval, with the central tendency defined by the fitted mean values from the linear regression model. a, Significant-cluster GM volume from the regressions in all territories. No data are displayed in the AD groups in both the Latin America and United States plots because of nonsignificant GM volume results from the regression. b, Significant-cluster GM volume from the regressions in Latin America. c, Significant-cluster GM volume from the regressions in the United States. No significant results were obtained from the GM volume regressions in HCs, and individuals with FTLD and AD from the United States, separately. Source data are provided.
Source data
State-level Gini index and brain volume
Simple linear regressions were conducted with state-level Gini index (predictor) and the normalized significant-cluster GM volume maps per individual (dependent variable). Significant-cluster maps were calculated using binarized masks of the significant results from the SPM12 correlation on the normalized and smoothed images. We performed analyses in all groups together (HCs, and individuals with FTLD and AD) and separately. Significant clusters from the SPM12 analyses are plotted next to each simple linear regression scatterplot. The shaded area around the regression lines indicates the 95% confidence interval, with the central tendency defined by the fitted mean values from the linear regression model. a, Significant-cluster GM volume from the regressions in all territories. b, Significant-cluster GM volume from the regressions in Latin America. c, Significant-cluster GM volume from the regressions in the United States. No significant results were obtained in the GM volume regressions in HCs, and individuals with FTLD and AD, from the United States, separately.
Source data
Structural inequality and FC
Linear regression models were run to assess the predictive power of country-level and state-level Gini indices over the normalized connectivity of each matrix AAL pair. As regressors, we used country-level (a,b) and state-level (c–e) Gini indices. As dependent variables, we used the normalized FC between each seed and one AAL area of the matrix. We performed analyses in all groups together (HCs, individuals with FTLD and AD) and separately. Only significant results are plotted. The circularized plots represent the significant connectivity between each AAL area and the matrix seeds. In the brain plots, dots are AAL areas significantly connected (lines) with each seed (yellow dots). a, FC from country-level Gini index regressions in all territories. FC in all territories together was predicted according to country-level Gini index between AAL regions from matrix 1 (seed 1: left inferior temporal gyrus). b, FC from country-level Gini index regressions in Latin America. FC in Latin America was predicted according to country-level Gini index between AAL regions from matrix 2 (seed 1: left superior temporal gyrus; seed 2: left inferior temporal gyrus; seed 3: left fusiform). c, FC from state-level Gini regressions in all territories. FC in all territories together was predicted according to state-level Gini index between AAL regions from matrix 1 (seed 1: left inferior temporal gyrus). d, FC from state-level Gini regressions in Latin America. FC in Latin America was predicted according to state-level Gini index between AAL regions from matrix 2 (seed 1: left superior temporal gyrus; seed 2: left inferior temporal gyrus; seed 3: left fusiform). e, FC from state-level Gini index regressions in the United States. FC in the United States was predicted according to state-level Gini index between AAL regions from matrix 3 (seed 1: right inferior temporal gyrus; seed 2: right insula; seed 3: right middle cingulate).
Source data
Structural inequality linked to brain volume and network dynamics in aging and dementia across the Americas
  • Article
  • Publisher preview available

December 2024

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172 Reads

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4 Citations

Nature Aging

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Structural inequality, the uneven distribution of resources and opportunities, influences health outcomes. However, the biological embedding of structural inequality in aging and dementia, especially among underrepresented populations, is unclear. We examined the association between structural inequality (country-level and state-level Gini indices) and brain volume and connectivity in 2,135 healthy controls, and individuals with Alzheimer’s disease and frontotemporal lobe degeneration from Latin America and the United States. Greater structural inequality was linked to reduced brain volume and connectivity, with stronger effects in Latin America, especially in the temporo-cerebellar, fronto-thalamic and hippocampal regions. In the United States, milder effects were observed in the insular-cingular and temporal areas. Results were more pronounced in Alzheimer’s disease and were independent of age, sex, education, cognition and other confounding factors. The findings highlight the critical role of structural inequality in aging and dementia, emphasizing the biological embedding of macrosocial factors and the need for targeted interventions in underserved populations.

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Experimental task. In each trial, participants compared dot clouds in two circles, selecting the cloud with a larger amount of dots count using the keyboard arrow keys. They subsequently rated their confidence on a 4-point Likert scale. Each trial started with a fixation cross (500ms), followed by the dots displays (500ms), and unlimited response time
Regression models for explaining confidence levels based on specific facets. Multiple regression models were employed to examine the association between confidence level and dysfunctional personality traits. Separated beta regression models were run for each facet and domain (unitrait models). Additionally, a multitrait regression model encompassing all facets/domains was conducted, and an elastic-net regression approach was employed using personality facets as explanatory variables
Regression models for explaining metacognitive sensitivity based on specific facets. Multiple regression models were used to investigate the relation between metacognitive sensitivity and dysfunctional personality traits. Individual beta regression models were applied to each facet and domain (unitrait models). A comprehensive multitrait regression model was executed, encompassing all facets/domains. Furthermore, an elastic-net regression method was employed, employing personality facets as explanatory variables
Mean and Standard Deviation of Dysfunctional Personality Domains in the Collected Sample
Mean and Standard Deviation of Dysfunctional Personality Facets in the Collected Sample
Exploring the relationship between dysfunctional personality traits with metacognition and confidence

September 2024

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43 Reads

Current Psychology

The ability to assess one’s own cognitive processes across different domains is known as metacognition. Although it has been hypothesized that people with certain personality disorders have trouble understanding their own mental states, its relationship with metacognition remains unclear. In an online study, 224 adult participants (average age = 27.45; 63 males & 161 females) from the general population completed the Personality Inventory Disorders 5 (PID-5) for DSM-5 after completing a dot-density perceptual task. Participants reported their confidence levels on each trial. Using a bias-free metacognitive measure, we conducted several regression models to explore the relationship between metacognitive sensitivity and confidence with dysfunctional personality traits. We found evidence that Grandiosity, Perceptual Dysregulation, Restricted Affectivity, Separation Insecurity, Hostility, Impulsivity and Submissiveness dysfunctional personality facets are associated with confidence level. Moreover, Anxiousness and Emotional Lability showed connections with metacognitive sensitivity. These results support the idea of a potential link between metacognition and mental health in the context of a transdiagnostic framework for personality disorders.


Dataset characterization and analysis pipeline
Datasets included LAC and non-LAC healthy controls (HC, total n = 3,509) and participants with Alzheimer disease (AD, total n = 828), bvFTD (total n = 463) and MCI (total n = 517). The fMRI dataset included 2,953 participants from LAC (Argentina, Chile, Colombia, Mexico and Peru) as well as non-LAC (the USA, China and Japan). The EEG dataset involved 2,353 participants from Argentina, Brazil, Chile, Colombia and Cuba (LAC) as well as Greece, Ireland, Italy, Turkey and the UK (non-LAC). The raw fMRI and EEG signals were preprocessed by filtering and artifact removal and the EEG signals were normalized to project them into source space. A parcellation using the automated anatomical labeling (AAL) atlas for both the fMRI and EEG signals was performed to build the nodes from which we calculated the high-order interactions using the Ω-information metric. A connectivity matrix was obtained for both modalities, which was later represented by graphs. Data augmentation was performed only in the testing dataset. The graphs were used as input for a graph convolutional deep learning network (architecture shown in the last row), with separate models for EEG and fMRI. Finally, age prediction was obtained, and the performance was measured by comparing the predicted versus the chronological ages. This figure was partially created with BioRender.com (fMRI and EEG devices).
FMRI training and testing the deep learning model in different datasets
a, Ordinary least squares (OLS) regression comparing chronological age versus predicted age with the feature importance list for training (n = 1,155) and testing (n = 289) in the whole sample (P < 1 × 10⁻¹⁵). b, Regression comparing chronological age versus predicted age with the feature importance list for training (n = 773) and testing (n = 194) in the non-LAC dataset (P < 1 × 10⁻¹⁵). c, Regression comparing chronological age versus predicted age with the feature importance list for training (n = 381) and testing (n = 91) in the LAC dataset (P = 4.91 × 10⁻⁷). For a, b and c, the bars show the brain region feature importance list in descending order, with ring plots and glass brain representations of the most important network-edge connections. Feature importance (top 10) data are presented as mean values and 99% CI. The values for the features (mean, left limit, right limit) are: feature 1 = (0.975, 0.952, 0.999), feature 2 = (0.735, 0.715, 0.756), feature 3 = (0.627, 0.597, 0.656), feature 4 = (0.470, 0.449, 0.490), feature 5 = (0.375, 0.353, 0.397), feature 6 = (0.314, 0.285, 0.342), feature 7 = (0.239, 0.217, 0.262), feature 8 = (0.198, 0.169, 0.228), feature 9 = (0.161, 0.128, 0.193), feature 10 = (0.119, 0.093, 0.145) (a); feature 1 = (0.968, 0.937, 0.999), feature 2 = (0.736, 0.707, 0.764), feature 3 = (0.541, 0.518, 0.565), feature 4 = (0.434, 0.403, 0.464), feature 5 = (0.315, 0.290, 0.339), feature 6 = (0.253, 0.220, 0.286), feature 7 = (0.177, 0.156, 0.197), feature 8 = (0.140, 0.114, 0.166), feature 9 = (0.111, 0.078, 0.144), feature 10 = (0.079, 0.053, 0.106) (b); and feature 1 = (0.971, 0.944, 0.999), feature 2 = (0.847, 0.816, 0.878), feature 3 = (0.698, 0.667, 0.730), feature 4 = (0.533, 0.512, 0.555), feature 5 = (0.458, 0.430, 0.487), feature 6 = (0.371, 0.344, 0.399), feature 7 = (0.298, 0.272, 0.325), feature 8 = (0.242, 0.216, 0.269), feature 9 = (0.198, 0.169, 0.227), feature 10 = (0.163, 0.130, 0.196) (c). d, Histogram of the prediction error when training in non-LAC dataset (n = 967) and testing in LAC dataset (n = 477). e, Violin plot of the distribution and statistical comparison of training and testing with different regions using a two-sided permutation test without multiple comparisons (5,000 algorithm iterations) with a result of P < 1 × 10⁻¹⁵. Mean, first quartile (q1), third quartile (q3), whisker low, whisker high, minima and maxima values for violin plots are: LAC/non-LAC (−2.52, −7.74, 3.31, −22.52, 17.33, −22.52, 17.33); non-LAC/LAC (5.60, 0.85, 12.14, −12.82, 27.75, −12.82, 27.75). f, Violin plot of the distribution and statistical comparison of testing the models on females (n = 261) and males (n = 216) in LAC using a permutation test (5,000 iterations) with a result of P = 0.042. Mean, q1, q3, whisker low, whisker high, minima and maxima values for violin plots are: male (3.66, −1.83, 9.45, −12.49, 16.32, −12.49, 16.32); and female (6.93, 2.21, 12.78, −12.82, 27.75, −12.82, 27.75). ROI, region of interest. This figure was partially created with BioRender.com (fMRI device).
EEG training and testing the deep learning model in different samples
a, OLS regression comparing chronological age versus predicted age with the feature importance list for training (n = 1,644) and testing (n = 411) in the whole sample (P < 1 × 10⁻¹⁵). b, Regression comparing chronological age versus predicted age with the feature importance list for training (n = 471) and testing (n = 118) in the non-LAC dataset (P < 1 × 10⁻¹⁵). c, Regression comparing chronological age versus predicted age with the feature importance list for training (n = 1,188) and testing (n = 298) in the LAC dataset (P = 3.51 × 10⁻⁷). For a, b and c, the bars show the brain region feature importance list in descending order, with ring plots and glass brain representations of the most important network-edge connections. Feature importance (top 10) data are presented as mean values and 99% CI. The values for the features (mean, left limit, right limit) are: feature 1 = (0.968, 0.946, 0.991), feature 2 = (0.759, 0.739, 0.779), feature 3 = (0.644, 0.617, 0.670), feature 4 = (0.531, 0.500, 0.561), feature 5 = (0.410, 0.384, 0.436), feature 6 = (0.336, 0.309, 0.363), feature 7 = (0.259, 0.239, 0.279), feature 8 = (0.218, 0.191, 0.245), feature 9 = (0.184, 0.150, 0.217), feature 10 = (0.146, 0.114, 0.177) (a); feature 1 = (0.967, 0.935, 0.999), feature 2 = (0.764, 0.741, 0.786), feature 3 = (0.569, 0.549, 0.590), feature 4 = (0.460, 0.435, 0.485), feature 5 = (0.354, 0.330, 0.377), feature 6 = (0.283, 0.256, 0.311), feature 7 = (0.216, 0.192, 0.241), feature 8 = (0.169, 0.145, 0.193), feature 9 = (0.129, 0.107, 0.150), feature 10 = (0.101, 0.077, 0.124) (b); feature 1 = (0.972, 0.949, 0.995), feature 2 = (0.833, 0.805, 0.860), feature 3 = (0.705, 0.677, 0.733), feature 4 = (0.564, 0.543, 0.584), feature 5 = (0.488, 0.463, 0.514), feature 6 = (0.408, 0.385, 0.431), feature 7 = (0.363, 0.334, 0.393), feature 8 = (0.292, 0.269, 0.314), feature 9 = (0.243, 0.222, 0.264), feature 10 = (0.221, 0.188, 0.254) (c). d, Histogram of the prediction error when training in non-LAC dataset (n = 569) and testing in LAC dataset (n = 1,486). e, Violin plot of the distribution and statistical comparison of training and testing with different regions using a two-sided permutation test without multiple comparisons (5,000 algorithm iterations) with a result of P < 1 × 10⁻¹⁵. Mean, q1, q3, whisker low, whisker high, minima and maxima values for violin plots are: LAC/non-LAC (−2.34, −6.07, 1.26, −13.25, 11.52, −20.08, 17.52); non-LAC/LAC (5.24, 1.95, 8.61, −5.24, 16.18, −12.73, 16.18). f, Violin plot of the distribution and statistical comparison of testing the models on females and males using a permutation test (5,000 iterations) with a result of P = 0.012. Mean, q1, q3, whisker low and whisker high values for violin plots are: male (3.66, 1.87, 7.83, −5.24, 16.18, −12.73, 16.18); female (6.19, 2.67, 9.39, −3.08, 15.52, −3.08, 15.52). This figure was partially created with BioRender.com (EEG device).
Groups, sex and macrosocial influences in brain-age gaps
a,b, Violin plots for the distribution of prediction gaps for different groups and sex effects using (a) fMRI and (b) EEG datasets. Statistical comparisons were calculated using two-sided subsample permutation testing without multiple comparisons and with 5,000 algorithm iterations. c, Associations between macrosocial and disease disparity factors with brain-age gaps were assessed with a multi-method approach comprising SHAP values, feature importance (MDI) and permutation importance. Plots show the mean importance values for each method, along with their 99% CI, as well as the average R² and Cohen’s f². *Features whose lower CI boundary does not cross zero. Shaded bars indicate significance across the three methods. We conducted a two-sided F-test to evaluate the overall significance of the regression models. The three models were significant: healthy controls LAC (R² = 0.37 (99% CI ±0.17), F² = 0.59 (99% CI ±0.21), r.m.s.e. = 6.9 (99% CI ±0.92), F = 138.78 (P < 1 × 10⁻¹⁵)); healthy controls non-LAC (R² = 0.41 (99% CI ±0.17), F² = 0.71 (99% CI ±0.21), r.m.s.e. = 6.57 (99% CI ±1.31), F = 135.91 (P < 1 × 10⁻¹⁵)) and total dataset (R² = 0.41 (99% CI ±0.12), F² = 0.71 (99% CI ±0.14), r.m.s.e. = 6.76 (99% CI ±0.89), F = 253.39 (P < 1 × 10⁻¹⁵)). The relevance of the features and their respective CI values are available in Supplementary Table 2. F, females; HC LAC, healthy controls from LAC; HC non-LAC, healthy controls from non-LAC; M, males. This figure was partially created with BioRender.com (fMRI and EEG devices).
Sensitivity analysis
a, Violin plots for the distribution of data quality metrics of fMRI (healthy controls non-LAC, n = 967, MCI non-LAC n = 215, Alzheimer disease non-LAC n = 214, bvFTD non-LAC n = 190, HC LAC n = 477, MCI LAC n = 169, AD LAC n = 505, bvFTD LAC n = 216). b, Violin plots for the distribution of data quality metrics of EEG datasets (HC non-LAC n = 569, HC LAC n = 1486, MCI LAC n = 133, Alzheimer disease LAC n = 108, bvFTD LAC n = 57). Both a and b indicate null results between groups in terms of data quality. c, Linear regression effects of scanner type, evidencing that the fMRI data quality was not significantly associated with fMRI brain-age gaps differences (P = 0.184). d, fMRI brain-age gap differences across groups controlling for scanner differences. The statistical comparisons were calculated using two-sided subsample permutation testing with 5,000 iterations. NS, not significant; ODQ, overall data quality.
Brain clocks capture diversity and disparities in aging and dementia across geographically diverse populations

August 2024

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494 Reads

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17 Citations

Nature Medicine

Brain clocks, which quantify discrepancies between brain age and chronological age, hold promise for understanding brain health and disease. However, the impact of diversity (including geographical, socioeconomic, sociodemographic, sex and neurodegeneration) on the brain-age gap is unknown. We analyzed datasets from 5,306 participants across 15 countries (7 Latin American and Caribbean countries (LAC) and 8 non-LAC countries). Based on higher-order interactions, we developed a brain-age gap deep learning architecture for functional magnetic resonance imaging (2,953) and electroencephalography (2,353). The datasets comprised healthy controls and individuals with mild cognitive impairment, Alzheimer disease and behavioral variant frontotemporal dementia. LAC models evidenced older brain ages (functional magnetic resonance imaging: mean directional error = 5.60, root mean square error (r.m.s.e.) = 11.91; electroencephalography: mean directional error = 5.34, r.m.s.e. = 9.82) associated with frontoposterior networks compared with non-LAC models. Structural socioeconomic inequality, pollution and health disparities were influential predictors of increased brain-age gaps, especially in LAC (R² = 0.37, F² = 0.59, r.m.s.e. = 6.9). An ascending brain-age gap from healthy controls to mild cognitive impairment to Alzheimer disease was found. In LAC, we observed larger brain-age gaps in females in control and Alzheimer disease groups compared with the respective males. The results were not explained by variations in signal quality, demographics or acquisition methods. These findings provide a quantitative framework capturing the diversity of accelerated brain aging.


Figure 1. Detailed pipeline for identification, screening and selection of reports, based on PRISMA guidelines (Page et al., 2021). The asterisk (*) denotes citations in identified papers and additional web searches. L2p: foreign-language proficiency.
Figure 2. L2p normalization formula. x is the reported L2p mean and a and b represent the minimum and maximum values of the scale, respectively. The normalization formula offers percent values for each average L2p. Finally, the percent scale values are classified between ten different qualitative levels to ease their descriptive analysis. Intermediate and high L2p levels are distinguished in color.
Figure 3. MFLE on impersonal (A) and personal (B) dilemmas. Studies are sorted from left to right on the X axis based on their samples' normalized L2p level. Black circles (•) denote significant MFLEs. Crossed circles (⊗) denote non-significant MFLEs. Stars (★) indicate that the experiment used solely the footbridge dilemma. Only studies that exclusively distinguish personal and impersonal dilemmas are included; a figure with all studies included in the review can be found in the Supplementary material (Figure S1).
Figure 4. Outstanding results showing the role of L2p on impersonal and personal moral dilemmas. (A) Utilitarian choices resulting from a moral decision task with an impersonal (trolley) and a personal (footbridge) dilemma, showcasing an MFLE only on the personal one. Divided in above average and below average groups of self-rated L2p, the MFLE seems stronger on the lower L2p subjects. (B) Results from a footbridge dilemma task on two groups with different L2 and different L2p levels. The Swedish-English group had a high normalized L2p = 77.77% and failed to show an MFLE. The Swedish-French group had an intermediate normalized L2p = 48.88% and showed a significant increase on utilitarian choices for L2 responses. Panel A: reprinted from PLoS ONE 9(4): e94842, by Albert Costa, Alice Foucart, Sayuri Hayakawa, Melina Aparici, Jose Apesteguia, Joy Heafner and Boaz Keysar, "Your Morals Depend on Language" (open access), Copyright 2014, https://doi.org/10.1371/journal.pone.0094842. Authorized reproduction under the terms of the Creative Commons Attribution License. Panel B: reprinted from Cognition, Volume 196, by Alexandra S. Dylman and Marie-France Champoux-Larsson, "It's (not) all Greek to me: Boundaries of the foreign language effect," 104148, Copyright (2020), with permission from Elsevier.
Figure 5. Factors mediating the impact of L2p on L2 personal moral decision tasks, leading to the MFLE. Across columns, from left to right, the figure shows (i) mediating factors, (ii) relevant affective and cognitive processes, (iii) impact of lower L2p on each process and (iv) proposed effects on action aversion. L2: second language; L2p: second language proficiency; MFLE: moral foreign-language effect.
Bilinguals on the footbridge: the role of foreign-language proficiency in moral decision making

April 2024

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148 Reads

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2 Citations

Bilingualism: Language and Cognition

Socio-cognitive research on bilinguals points to a moral foreign-language effect (MFLE), with more utilitarian choices (e.g., sacrificing someone to save more people) for moral dilemmas presented in the second language (L2) relative to the first language. Yet, inconsistent results highlight the influence of subject-level variables, including a critical underexplored factor: L2 proficiency (L2p). Here we provide a systematic review of 57 bilingualism studies on moral dilemmas, showing that L2p rarely modulates responses to impersonal dilemmas, but it does impact personal dilemmas (with MFLEs proving consistent at intermediate L2p levels but unsystematic at high L2p levels). We propose an empirico-theoretical framework to conceptualize such patterns, highlighting the impact of L2p on four affective mediating factors: mental imagery, inhibitory control, prosocial behavior and numerical processing. Finally, we outline core challenges for the field. These insights open new avenues at the crossing of bilingualism and social cognition research.


Figure 5
Brain clocks capture diversity and disparity in aging and dementia

March 2024

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225 Reads

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1 Citation

Brain clocks, which quantify discrepancies between brain age and chronological age, hold promise for understanding brain health and disease. However, the impact of multimodal diversity (geographical, socioeconomic, sociodemographic, sex, neurodegeneration) on the brain age gap (BAG) is unknown. Here, we analyzed datasets from 5,306 participants across 15 countries (7 Latin American countries -LAC, 8 non-LAC). Based on higher-order interactions in brain signals, we developed a BAG deep learning architecture for functional magnetic resonance imaging (fMRI=2,953) and electroencephalography (EEG=2,353). The datasets comprised healthy controls, and individuals with mild cognitive impairment, Alzheimer’s disease, and behavioral variant frontotemporal dementia. LAC models evidenced older brain ages (fMRI: MDE=5.60, RMSE=11.91; EEG: MDE=5.34, RMSE=9.82) compared to non-LAC, associated with frontoposterior networks. Structural socioeconomic inequality and other disparity-related factors (pollution, health disparities) were influential predictors of increased brain age gaps, especially in LAC (R²=0.37, F²=0.59, RMSE=6.9). A gradient of increasing BAG from controls to mild cognitive impairment to Alzheimer’s disease was found. In LAC, we observed larger BAGs in females in control and Alzheimer’s disease groups compared to respective males. Results were not explained by variations in signal quality, demographics, or acquisition methods. Findings provide a quantitative framework capturing the multimodal diversity of accelerated brain aging.


Decision and metacognitive computations carry evidence of unchosen options in multialternative decisions

January 2024

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7 Reads

Humans often face decisions between multiple alternatives. However, our grasp of the computations underlying this process is still limited. While some evidence suggests that only the chosen alternative is represented at the decision stage, other findings indicate that information from unchosen alternatives remains accessible for decision computations. Furthermore, the amount and kind of information that reaches metacognitive levels remains unexplored. We ran two pre-registered experiments using a second-guess paradigm to understand to what extent humans retain information from choices that were discarded in a first guess. We found consistent above chance performance and metacognition in a second-guess with a 4 alternative (Exp. 1) and 12 alternative task (Exp. 2). Computational modeling suggests both the decision and metacognitive systems maintain a noisy version of the information from all alternatives. Overall, our results suggest that, although suboptimally, humans take into account evidence from unchosen options in multialternative perceptual decision making and metacognition.


Exploring the Relationship between Dysfunctional Personality Traits with Metacognition and Confidence

December 2023

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60 Reads

The ability to assess one's own cognitive processes is known as metacognition. Although it has been hypothesized that people with certain personality disorders have trouble understanding their own mental states, the relationship between dysfunctional personality traits (DPT) and metacognition remains unclear. In an online study, neurotypical participants completed the Personality Inventory Disorders 5 (PID-5) for DSM-5 after completing a dot-density perceptual task. We found evidence that Grandiosity, Perceptual Dysregulation, Restricted Affectivity, Separation Insecurity, Hostility, Impulsivity and Submissiveness DPT facets are associated with confidence level. Moreover, Anxiousness and Emotional Lability showed connections with metacognitive sensitivity. These results support the idea of a potential link between metacognition and mental health in the context of a transdiagnostic framework for personality disorders.


Social and non-social working memory in neurodegeneration

May 2023

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84 Reads

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7 Citations

Neurobiology of Disease

Although social functioning relies on working memory, whether a social-specific mechanism exists remains unclear. This undermines the characterization of neurodegenerative conditions with both working memory and social deficits. We assessed working memory domain-specificity across behavioral, electrophysiological, and neuroimaging dimensions in 245 participants. A novel working memory task involving social and non-social stimuli with three load levels was assessed across controls and different neurodegenerative conditions with recognized impairments in: working memory and social cognition (behavioral-variant frontotemporal dementia); general cognition (Alzheimer's disease); and unspecific patterns (Parkinson's disease). We also examined resting-state theta oscillations and functional connectivity correlates of working memory domain-specificity. Results in controls and all groups together evidenced increased working memory demands for social stimuli associated with frontocinguloparietal theta oscillations and salience network connectivity. Canonical frontal theta oscillations and executive-default mode network anticorrelation indexed non-social stimuli. Behavioral-variant frontotemporal dementia presented generalized working memory deficits related to posterior theta oscillations, with social stimuli linked to salience network connectivity. In Alzheimer's disease, generalized working memory impairments were related to temporoparietal theta oscillations, with non-social stimuli linked to the executive network. Parkinson's disease showed spared working memory performance and canonical brain correlates. Findings support a social-specific working memory and related disease-selective pathophysiological mechanisms.


Is visual metacognition associated with autistic traits? A regression analysis shows no link between visual metacognition and Autism-Spectrum Quotient scores

March 2023

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4 Citations

Consciousness and Cognition

Metacognition -the human ability to recognize correct decisions- is a key cognitive process linked to learning and development. Several recent studies investigated the relationship between metacognition and autism. However, the evidence is still inconsistent. While some studies reported autistic people having lower levels of metacognitive sensitivity, others did not. Leveraging the fact that autistic traits are present in the general population, our study investigated the relationship between visual metacognition and autistic traits in a sample of 360 neurotypical participants. We measured metacognition as the correspondence between confidence and accuracy in a visual two alternative forced choice task. Autistic-traits were assessed through the Autism-spectrum Quotient (AQ) score. A regression analysis revealed no statistically significant association between autistic traits and metacognition or confidence. Furthermore, we found no link between AQ sub-scales and metacognition. We do not find support for the hypothesis that autistic traits are associated with metacognition in the general population.


Citations (29)


... [1][2][3][4][5][6] In underrepresented populations, social and health disparities have larger effects than standard risk factors such as age or gender for healthy aging. 2 Even universal models fail to be applied to underrepresented populations in terms of risk factors or brain-phenotype associations. 7,8 Engaging local researchers beyond the US and Europe fosters innovation and scientific discovery. 1 This diversity in research enhances our global understanding of dementia and ensures that Amid these difficulties, I found joy and resilience through my two daughters, Anahí and Bianca, who have deeply shaped me into a better person. ...

Reference:

Inspired by struggle: A personal journey to global precision brain health
Structural inequality linked to brain volume and network dynamics in aging and dementia across the Americas

Nature Aging

... For instance, factors like socioeconomic status, education levels, cultural practices, and environmental exposures can significantly impact the onset, progression, and multimodal phenotypes of aging and dementia. [1][2][3][4][5][6] In underrepresented populations, social and health disparities have larger effects than standard risk factors such as age or gender for healthy aging. 2 Even universal models fail to be applied to underrepresented populations in terms of risk factors or brain-phenotype associations. 7,8 Engaging local researchers beyond the US and Europe fosters innovation and scientific discovery. ...

Brain clocks capture diversity and disparities in aging and dementia across geographically diverse populations

Nature Medicine

... Consequently, bilinguals are more likely to make less emotional and thus more rational decisions in response to emotionally charged moral dilemmas in their LX, particularly if their proficiency level in that language is low to intermediate. This assumption aligns with a recent metanalysis of 57 studies addressing bilinguals' decision-making, which revealed that the MFLe has been systematically found in personal moral dilemmas at intermediate LX proficiency levels but tends to diminish as LX proficiency increases (Teitelbaum Dorfman et al., 2024;but see Del Maschio et al., 2022). Nevertheless, evidence of the interplay between LX proficiency level and moral decision-making across different types of moral dilemmas (e.g., unrealistic/classic versus realistic) is still limited and the existing findings do not always converge. ...

Bilinguals on the footbridge: the role of foreign-language proficiency in moral decision making

Bilingualism: Language and Cognition

... In addition to agitation/aggression, depression, anxiety, sleep dysregulation, psychosis, and apathy, AD significantly impacts social behavior in affected individuals [58,[152][153][154][155][156]. Social deficits and dysregulation of social interactions are common NPS associated with AD ( Table 2). ...

Social and non-social working memory in neurodegeneration
  • Citing Article
  • May 2023

Neurobiology of Disease

... Metacognition studies on PwASD demonstrate an overall metacognitive di culty in various cognitive domains, such as memory (Teunisse & de Gelder, 2003;Zhao et al., 2016). However, as ASD represents a heterogeneous condition for the etiology, phenotype, and outcome (Masi et al., 2017), not all PwASD may experience the same type of metacognitive di culties (Embon et al., 2023). Speci cally, visual metacognition is the ability to evaluate one's performance on visual perceptual tasks, such as recognizing our ability to distinguish between colors or shapes accurately. ...

Is visual metacognition associated with autistic traits? A regression analysis shows no link between visual metacognition and Autism-Spectrum Quotient scores
  • Citing Article
  • March 2023

Consciousness and Cognition

... In previous research conducted in our lab, we observed that anodal transcranial direct current stimulation on the right fronto-parietal network specifically mitigates executive vigilance loss across time-on-task but not arousal vigilance nor modulates phasic alertness, attentional orienting, or cognitive control effects 8,36 . Moreover, we have also observed that changes in alpha but not delta, theta, beta, or gamma power anticipate failures in executive but not arousal vigilance 10 . Therefore, analyzing multiple effects measured at the same time in a task like the ANTI -Vea provides the possibility of examining beneficial or detrimental modulations by other factors on attentional networks' functioning under the same participant' state. ...

Different oscillatory rhythms anticipate failures in executive and arousal vigilance

Frontiers in Cognition

... (2) orienting, induced by location cue facilitating target detection or causing reorientation; (3) executive control, resolving the conflicts between the targets and the distractors; (4) executive vigilance, maintaining the ability to detect critical signals that occur rarely by executing a specific response; and (5) arousal vigilance, maintaining a fast and stable reaction to stimuli occurring rarely without specific response [5,15,16]. Furthermore, the contributions of the possible deficits in these networks to the clinical characteristics of migraine were evaluated by developing a classification model to distinguish patients from healthy controls, as well as a regression model to predict clinical characteristics. This study seeks to provide a better understanding of the attentional dysfunctions in migraine. ...

Event-related potentials associated with attentional networks evidence changes in executive and arousal vigilance
  • Citing Article
  • February 2023

Psychophysiology

... The prospect of employing different data sources, such as electroencephalography (EEG) or magnetoencephalography (MEG), to substantiate the identified consciousness states introduces an avenue for expanding the horizon of the current methodology, and enhances the robustness of the method and the findings (Vidaurre et al. 2018(Vidaurre et al. , 2016Baker et al. 2014;Sitt et al. 2014). Generalisations of the present method to EEG are under development (Della Bella et al. 2022), and may be of particular relevance , for example, for the study of unconsciousness induced by epileptic seizures. Alternatively, other species under general anaesthesia can be studied as has been done in the past with the sliding window technique (Barttfeld, Uhrig, et al. 2015;Uhrig et al. 2018) Envisioning a broader context, the study prompts consideration of consciousness-altering scenarios beyond those encountered within wakefulness or unconscious states. ...

EEG brain states for real-time detection of covert cognition in disorders of consciousness
  • Citing Preprint
  • October 2022

... Recent studies have also found that subjects with Autism Spectrum Disorder (ASD) show impairments both in measures of mentalising about others, and of explicit self-directed metacognitive efficiency (Johnstone et al., 2022;Nicholson et al., 2021;Plas et al., 2021); although see Embon et al., (2022)). For example, in a dual-task scenario, a mentalising task (but not a similarly demanding non-mentalising task) impairs the fidelity of (self-directed) confidence ratings on a metacognition task, indicating a sharing of cognitive resources between self-directed metacognition and mentalising about others (Nicholson et al., 2021). ...

Is visual metacognition associated with ASD traits? A regression analysis shows no link between visual metacognition and AQ scores.
  • Citing Preprint
  • September 2022

... Dissociable patterns at the behavioral (Luna, Barttfeld, et al., 2022;Luna, Tortajada, et al., 2022;Román-Caballero et al., 2021), physiological (Feltmate et al., 2020;Sanchis et al., 2020;Sanchis-Navarro et al., 2024), and neural (Hemmerich et al., 2023(Hemmerich et al., , 2024Luna et al., 2020Luna et al., , 2023aLuna et al., , 2023b) levels were observed for EV and AV when measuring vigilance components via the ANTI-Vea task. Most importantly, the EV and AV decrements were independently mitigated by modulating different mechanisms of sustained attention. ...

Cognitive load mitigates the executive but not the arousal vigilance decrement

Consciousness and Cognition