Theory of Mind (ToM) is the ability to infer others’ mental states and thus to predict their behavior (Perner, 1991). Therefore, ToM is essential for the adequate adjustment of behavior in social situations. ToM can be divided into: 1) cognitive ToM encompassing inferences about intentions and beliefs and 2) affective ToM encompassing inferences about emotions (Shamay-Tsoory, Harari, Aharon-Peretz, & Levkovitz, 2010). Well-functioning skills of both ToM aspects are much-needed in the developmental period of adolescence because in this age phase peer relationships become more important and romantic relationships arise (Steinberg & Morris, 2001). Importantly, affective psychopathological disorders often have their onset in adolescence. ToM development in adolescence might be based on underlying cognitive mechanisms such as the ability to inhibit one’s own thoughts in order to understand another person’s thoughts (Carlson & Moses, 2001). Another possible mechanism relates to functional brain development across adolescence (Blakemore, 2008). Therefore, neurocognitive mechanisms may underlie ongoing ToM development in adolescence. First studies indicate an ongoing behavioral and functional brain development of ToM (e.g. Blakemore, 2008). However, ToM development in adolescence and how this might relate to underlying (neuro)cognitive functions remains largely underexamined. The major aims of the current thesis were first to answer the overall question whether there is an ongoing development of ToM in adolescence. This question relates to both behavioral and functional brain development. As a second major aim, the present work sought to elucidate possible (neuro)cognitive mechanisms of ongoing ToM development across adolescence. Specifically, these cognitive mechanisms might be basic cognitive functions as well as executive functions. Additionally, the present work aimed at exploring potential (neuro)cognitive mechanisms through an integration of both behavioral and functional brain studies. The current experimental work spans three cross-sectional studies investigating adolescents (aged around 12-15 years) and young adults (aged around 18-22 years) to examine for the first time both the behavioral (studies I and II) and functional brain development of ToM (study III) in adolescence and its underlying (neuro)cognitive mechanisms. In all three studies, more complex, advanced ToM tasks were employed to avoid ceiling effects. Study I was aimed at investigating if cognitive and affective ToM continues to develop in adolescence and at exploring if basic cognitive variables such as verbal ability, speed of processing, and working memory capacity underlie such development. Hence, two groups of adolescents and young adults completed tasks of ToM and basic cognitive abilities. Large age effects were revealed on both measures of ToM: adolescents performed lower than adults. These age differences remained significant after controlling for basic cognitive variables. However, verbal ability covaried with performance in affective ToM. Overall, results support the hypothesis of an ongoing development of ToM from adolescence to adulthood on both cognitive and affective aspects. Results may further indicate verbal ability being a basic cognitive mechanism of affective ToM. Study II was designed to further explore if affective ToM, as measured with a dynamic realistic task, continues to develop across adolescence. Importantly, this study sought to explore executive functions as higher cognitive mechanisms of developing affective ToM across adolescence. A large group spanning adolescents and young adults evaluated affective mental states depicted by actors in video clips. Additionally, participants were examined with three subcomponents of executive functions, inhibition, updating, and shifting following the classification of Miyake et al. (2000). Affective ToM performance was positively related to age and all three executive functions. Specifically, inhibition explained the largest amount of variance in age related differences of affective ToM performance. Overall, these results indicate the importance of inhibition as key underlying mechanism of developing an advanced affective ToM in adolescence. Study III set out to explore the functional brain development of affective ToM in adolescence by using functional magnetic resonance imaging (fMRI). The affective ToM measure was the behavioral developmentally sensitive task from study II. An additional control condition consisted of the same emotional stimuli with the instruction to focus on physical information. This study faced methodical challenges of developmental fMRI studies by matching performance of groups. The ventromedial prefrontal cortex (vMPFC) was significantly less deactivated in adolescents in comparison to adults, which might suggest that adolescents seem to rely more on self-referential processes for affective ToM. Furthermore, adolescents compared to adults showed greater activation in the dorsolateral prefrontal cortex (DLPFC) in the control condition, indicating that adolescents might be distracted by the emotional content and therefore needed to focus more on the physical content of the stimulus. These findings suggest affective ToM continues to develop on the functional brain level and reveals different underlying neurocognitive strategies for adolescents in contrast to adults. In summary, the current thesis investigated whether ToM continues to develop in adolescence until young adulthood and explored underlying (neuro)cognitive mechanisms. Findings suggest that there is indeed an ongoing development of both the cognitive and affective aspect of ToM, which importantly contributes to the conceptual debate. Moreover, the second benefit to the debate is to demonstrate how this change may occur. As a basic cognitive mechanism verbal ability and as an executive functioning mechanism inhibition was revealed. Furthermore, neurocognitive mechanisms in form of different underlying neurocognitive strategies of adolescents compared to adults were shown. Taken together, ToM development in adolescence seems to mirror a different adaptive cognitive style in adolescence (Crone & Dahl, 2012). This seems to be important for solving the wealth of socio-emotional developmental tasks that are relevant for this age span.

Die Ursache für das idiopathische Stottern ist bis zum jetzigen Zeitpunkt unbekannt. Typischerweise beginnt die Redeflussstörung im Vorschulalter. Es wird davon ausgegangen, dass 1% der Bevölkerung an Stottern leidet. Bei der Frage nach pathophysiologischen Hintergründen von Sprech- und Sprachstörungen ist der Zusammenhang zwischen einer pathologischen, funktionellen Lateralisierung und einer morphologischen Asymmetrie im Bereich von neuronalen Netzwerken der Sprachbildung bereits seit längerem Gegenstand der Forschung. Im Rahmen der vorliegenden Arbeit wurde die Lateralisierung von Sprache bei 17 stotternden Probanden und 20, im Alter entsprechenden, flüssig sprechenden Probanden untersucht. Hierbei wurde die Sprachlateralisierung mithilfe der fMRT sowohl mit einem Satz- als auch mit einem Wortgenerierungsparadigma ermittelt. Ausgehend von den in der fMRT ermittelten Sprachzentren wurde die angrenzende weiße Substanz unter Verwendung der DTI auf eine Asymmetrie hin untersucht. Im Vergleich zu der Gruppe der Normalprobanden zeigten die schwer stotternden Probanden eine Verschiebung der Indexwerte, deren endgültige Ursache offen bleibt. Gesteigerte funktionelle Aktivierung in Bereichen der rechtshemisphärischen Analoga der Sprachzentren scheint ein möglicher Erklärungsansatz. Vorausgegangene funktionelle Untersuchungen u. a. mittels PET und fMRT bei stotternden Probanden belegten eine Überaktivierung von Teilen des motorischen Kortex sowie eine atypische Lateralisierung bei der Produktion von Sprache mit rechtsseitiger Lateralisierung oder eine bilaterale Aktivität. Darüber hinaus zeigte sich eine morphologische Veränderung, im Sinne einer Abnahme einer linkshemisphärischen Asymmetrie bei den schwer stotternden Probanden, besonders in der an das Wernicke-Areal angrenzenden weißen Substanz. Mithilfe der VBM konnten in mehreren früheren Studien morphologische Unterschiede bei Stotternden gezeigt werden. Gegenüber dem rein morphologischen Untersuchungsansatz vorangegangener Untersuchungen berücksichtigte die Kombination der funktionellen und der diffusionsgewichteten Analyse stärker die intraindividuelle Variabilität der Sprachzentren.

No description available.

L'ectrostimulation dite conventionnelle (CONV) est délivrée par des impulsions électriques de basse fréquence (≤ 50 Hz), de courte durée (< 400 μs) et de haute intensité. Ce type d'ESNM permet ainsi d'évoquer une contraction musculaire grâce à l'activation directe des axones moteurs et est associé à une fatigue musculaire exagérée par rapport aux contractions volontaires (VOL). Au contraire, lors de l'utilisation d'impulsions de longues durées (1 ms), de hautes fréquences (≥ 80 Hz) et de faibles intensités (i.e. protocole « Wide-Pulse, High-Frequency » (WPHF)), une partie de la force musculaire évoquée aurait pour origine des mécanismes centraux. En effet, une augmentation de la force produite en réponse à WPHF a été rapportée alors que l'intensité de stimulation était constante. Cette « extra force » (EF) refléterait le recrutement par voie réflexe des motoneurones spinaux. L'objectif de ce travail de thèse était de mieux appréhender les mécanismes neurophysiologiques à l'origine de l'EF et d'évaluer les conséquences métaboliques et corticales du protocole WPHF (1 ms - 100 Hz) par rapport à des protocoles d'exercices VOL et de type CONV (50 μs - 25 Hz). Les réponses musculaires des fléchisseurs plantaires et les réponses cérébrales ont été évalué par résonance magnétique nucléaire (la spectroscopie par résonance magnétique du phosphore 31 du muscle et l'imagerie par résonance magnétique fonctionnelle du cerveau) et électrophysiologie (EMG). Ces résultats constituent une première étape importante vers une meilleure prise en charge des pathologies liées à des atteintes du neuromusculaire. / Conventional neuromuscular electrical stimulation (CONV) is delivered via surface electrodes at short pulse duration (< 400 μs), low frequencies (≤ 50 Hz) and high current intensities. The motor unit recruitment pattern of CONV, however, is different from the pattern of voluntary contractions (VOL) and leads to a hastened onset of muscle fatigue. The use of wide-pulses (1ms), high frequencies (100 Hz) (WPHF) and low current intensities might approach the natural activation pattern of VOL by enhancing the neural contribution to force production. Previous studies investigating WPHF reported progressive and unexpected force increments ("Extra Forces") despite a constant stimulation intensity which might reflect the more pronounced activation of sensory pathways within the central nervous system. The objective of this thesis was to investigate this "Extra Force" (EF) phenomenon and to evaluate the efficiency of WPHF (1 ms pulse duration at 100 Hz) in terms of metabolic demand and neural contribution to force production in comparison to CONV NMES (0.05 ms pulse duration at 25 Hz) and VOL. Our experiments comprised electrophysiological (EMG) and nuclear magnetic resonance techniques (31P spectroscopy of the muscle, functional imaging of the brain). The findings should be considered in future studies investigating the potential of NMES in a clinical context as a treatment for neuromuscular pathologies.

No description available.

Ce travail de thèse vise à améliorer notre compréhension des mécanismes sous-tendant la perception et la mémorisation des structures sonores complexes. Nous avons étudié les corrélats comportementaux et cérébraux de la perception et de la mémoire auditive pour des notes isolées, des séquences musicales et des séquences de mots, chez des auditeurs typiques et dans l'amusie congénitale, un trouble permanent de la perception de la musique. En utilisant des approches comportementales, nous avons démontré que les déficits des individus amusiques dans la dimension de la hauteur sont liés à des déficits à la fois durant l’encodage des sons courts et dans la rétention à court terme de l'information musicale. En utilisant des mesures neurophysiologiques (IRM, MEG, IRMf) nous avons démontré l’existence d’anomalies anatomiques et fonctionnelles dans le cerveau amusique, principalement dans les cortex frontal et auditif droits. De plus des anomalies fonctionnelles ont été observées à la fois durant l'encodage, la rétention et la reconnaissance de l'information mélodique lors d’une tâche de mémoire à court terme. En revanche, pour le matériel verbal, les participants amusiques recrutaient des régions cérébrales similaires à celles des contrôles, ceci suggérant que des ressources neuronales distinctes sous-tendent la mémoire tonale et verbale. A partir des conclusions de ces trois premières études, nous avons exploré deux approches visant à renforcer les capacités de traitement de la hauteur dans l'amusie: 1) en étudiant si des connaissances implicites du système musical occidental tonal pouvaient améliorer leurs capacités de mémoire à court terme pour les notes, et 2) en explorant si les capacités d’encodage altérées des participants amusiques pouvaient être améliorées par des interactions audio-visuelles. Ces études ont été encourageantes et pourraient guider la conception d'outils de réhabilitation dans ce déficit. Enfin, il convient de souligner que nos recherches contribuent également à améliorer la compréhension des mécanismes sous-tendant le traitement de la musique en général, un domaine de recherche émergeant qui fait le parallèle avec le traitement du langage / The aim of this PhD thesis is to further our understanding about how humans perceive and nmemorize complex sound structures. We investigated the behavioral and cerebral correlates of auditory perception and memory for isolated tones, musical sequences, and verbal material both in typical listeners and in individuals presenting a lifelong disorder of music perception that has been referred to as congenital amusia. Using behavioral approaches, we demonstrated that amusic individuals’ deficits in the pitch dimension are related to impairments both in the encoding of short tones and in the short term retention of pitch information. Using multimodal neuroimaging methods (MRI, MEG, fMRI) we observed anatomical and functional abnormalities in the amusic brain, mostly in the right frontal cortex and in the right auditory cortex. Functional abnormalities were observed at each level of processing in short-term memory tasks, that is for encoding, retention, and retrieval of the melodic information. In contrast, for verbal material, amusic participants recruited similar brain regions as those observed for controls, thus suggesting that separate neural resources support tonal and verbal memory. Based on the conclusions made on these first three studies, we explored two approaches aiming to boost pitch processing abilities in amusia; 1) by investigating whether implicit knowledge of the western tonal musical system could influence their short-term memory abilities, and 2) by exploring whether amusic individuals’ altered encoding of short tones could be improved by audio-visual interactions These investigations were encouraging and provide the first steps toward designing tools of rehabilitation in this musical disorder. To conclude, it is worth underlining that these studies also improve our understanding of music processing in general, which is the subject of an increasing research domain that is often making the parallel to language processing

A number of studies have concluded that cognitive control is not fully established until late adolescence. The precise differences in brain function between adults and adolescents with respect to cognitive control, however, remain unclear. To address this issue, we conducted a study in which 185 adolescents (mean age (SD) 14.6 (0.3) years) and 28 adults (mean age (SD) 25.2 (6.3) years) performed a single task that included both a stimulus-response (S-R) interference component and a task-switching component. Behavioural responses (i.e. reaction time, RT; error rate, ER) and brain activity during correct, error and post-error trials, detected by functional magnetic resonance imaging (fMRI), were measured. Behaviourally, RT and ER were significantly higher in incongruent than in congruent trials and in switch than in repeat trials. The two groups did not differ in RT during correct trials, but adolescents had a significantly higher ER than adults. In line with similar RTs, brain responses during correct trials did not differ between groups, indicating that adolescents and adults engage the same cognitive control network to successfully overcome S-R interference or task switches. Interestingly, adolescents with stronger brain activation in the bilateral insulae during error trials and in fronto-parietal regions of the cognitive control network during post-error trials did have lower ERs. This indicates that those mid-adolescents who commit fewer errors are better at monitoring their performance, and after detecting errors are more capable of flexibly allocating further cognitive control resources. Although we did not detect a convincing neural correlate of the observed behavioural differences between adolescents and adults, the revealed interindividual differences in adolescents might at least in part be due to brain development.

De nombreux changements cérébraux s’opèrent au cours du vieillissement normal, et ce, tant au niveau structurel que fonctionnel. Ces changements résultent le plus souvent en une certaine détérioration du fonctionnement cognitif et se répercutent ainsi sur la qualité de vie des personnes âgées. Il appert toutefois que certaines personnes se voient relativement épargnées et parviennent à maintenir un niveau de fonctionnement cognitif comparativement élevé en dépit de l’avancement en âge. En présence d’une accélération du vieillissement populationnel, il devient donc criant de comprendre les facteurs et les mécanismes neurobiologiques qui contribueraient à cette meilleure résilience face aux effets du vieillissement sur le cerveau et la cognition. Bien que plusieurs modèles aient tenté de rendre compte de ce phénomène, la compréhension des mécanismes qui le sous-tendent demeure à ce jour relativement lacunaire. L’objectif principal de cette thèse était ainsi d’exposer les corrélats neurobiologiques associés à une meilleure résilience face aux effets du vieillissement normal sur le cerveau et la cognition, et ce, par l’entremise de mesures d’imagerie par résonance magnétique structurelle (IRM) et fonctionnelle (IRMf). Cette thèse contient quatre articles. L’intention du premier article (Chapitre II) était de faire une synthèse des connaissances quant aux mécanismes impliqués dans la résilience contre les effets délétères du vieillissement normal sur la cognition. Dans cette revue de la littérature, nous nous sommes intéressés à deux des principaux modèles visant à rendre compte de ce phénomène de protection : la réserve cérébrale et la réserve cognitive. L’examen de la littérature empirique amène à la conclusion qu’une meilleure résilience pourrait reposer sur des différences cérébrales à la fois structurelles et fonctionnelles, et donc que les deux modèles proposés pourraient amener une contribution indépendante au phénomène de résilience. Par ailleurs, nous soulevons l’hypothèse que les corrélats de la résilience s’apparentent grandement aux différences cérébrales associées aux entraînements cognitifs. Les trois articles suivants sont des articles empiriques qui s’intéressent à la mémoire de travail, une fonction qui décline avec l’âge, mais qui montre d’importantes différences interindividuelles. L’objectif du second article (Chapitre III) était d’investiguer la relation entre la scolarité, un indicateur de réserve (reserve proxy) bien établi, et le volume régional de la substance grise, ainsi qu’entre la scolarité et les activations cérébrales lors d’une tâche de mémoire de travail chez des participants âgés et cognitivement sains. Les résultats indiquent qu’un nombre d’années de scolarité plus élevé est à la fois associé à une moindre perte de volume liée à l’âge dans les régions frontales et pariétales, ainsi qu’à une plus grande activation liée à l’âge dans certaines régions préfrontales faisant partie du réseau de la mémoire de travail. La troisième étude (Chapitre IV) visait à examiner si les différences cérébrales fonctionnelles associées à la scolarité sont compatibles avec des mécanismes d’efficacité ou de flexibilité neuronale. Elle avait ensuite pour objectif d’examiner l’effet « protecteur » de ces différences fonctionnelles sur le plan de la performance en mémoire de travail. Les résultats suggèrent que les deux mécanismes posés seraient associés à une meilleure préservation de la mémoire de travail face aux effets de l’âge, mais que leur implication respective dépendrait du niveau d’exigence de la tâche. Enfin, l’objectif de la quatrième étude (Chapitre V) était de tester, dans un premier temps, la relation entre l’engagement dans un style de vie stimulant et le maintien de l’intégrité de la substance blanche. Puis, l’étude visait dans un second temps à examiner si une plus grande intégrité de la substance blanche diminuait l’impact de l’âge sur la mémoire de travail. Les résultats de l’étude suggèrent qu’un style de vie plus stimulant serait associé à un moindre volume de lésions de la substance blanche liées à l’âge et que ce moindre volume de lésions de la substance blanche serait en retour associé à de meilleures performances en mémoire de travail. / Many changes to the brain occur in normal aging, both structurally and functionally. These changes most often result in a certain deterioration of cognitive functioning, and thus affect the quality of life of the elderly. It appears, however, that some people are relatively spared and manage to maintain a comparatively high level of cognitive functioning despite advancing in age. In the presence of an acceleration of population aging, there is a striking need to understand the factors and neurobiological mechanisms that may contribute to this better resilience to the effects of aging on the brain and on cognition. Although several models have attempted to account for this phenomenon, the understanding of the mechanisms that underpin it is still relatively incomplete. The main objective of this thesis was to expose the neurobiological correlates associated with a better resilience to the effects of normal aging on the brain and cognition, through structural (MRI) and functional magnetic resonance imaging (fMRI). This thesis contains four articles. The intention of the first article (Chapter II) was to synthesize knowledge about the mechanisms involved in the resilience against the degenerative effects of normal aging on cognition. In this literature review, we were interested in the two main models attempting to account for this protective phenomenon: the brain reserve and cognitive reserve. Examining the empirical literature leads to the conclusion that better resilience might be based on both structural and functional brain differences, and therefore that the two proposed models could make an independent contribution to the resilience phenomenon. In addition, we hypothesize that the correlates of resilience are very similar to the brain differences associated with cognitive training. The following three articles are empirical articles which focus on working memory, a function that declines with age but shows significant inter-individual differences. The purpose of the second article (Chapter III) was to investigate the relationship between education, a well-established reserve proxy, and the regional volume of gray matter, as well as between education and brain activation during a working memory task in cognitively healthy elderly participants. Results indicate that higher years of education are associated with lower age-related loss of volume in the frontal and parietal areas, as well as greater age-related activation in some prefrontal regions that are part of the working memory network. The third study (Chapter IV) sought to examine whether functional education-related brain differences are compatible with neuronal efficiency and/or flexibility mechanisms. It further aimed to examine the "protective" effect of these functional differences on working memory performance. The results suggest that the two proposed mechanisms would be associated with a better preservation of working memory in the face of the effects of age, but that their respective involvement would depend on the level of the task requirement. Finally, the objective of the fourth study (Chapter V) was to first test the relationship between engagement in a stimulating lifestyle and white matter integrity maintaining. Then, the study aimed to examine whether greater white matter integrity decreased the impact of age on working memory. The results of the study suggest that a more stimulating lifestyle would be associated with a lesser age-related white matter lesions volume, and that this smaller white matter lesions volume would in turn be associated with better working memory performance.

Theory of Mind (ToM) is the ability to infer others’ mental states and thus to predict their behavior (Perner, 1991). Therefore, ToM is essential for the adequate adjustment of behavior in social situations. ToM can be divided into: 1) cognitive ToM encompassing inferences about intentions and beliefs and 2) affective ToM encompassing inferences about emotions (Shamay-Tsoory, Harari, Aharon-Peretz, & Levkovitz, 2010). Well-functioning skills of both ToM aspects are much-needed in the developmental period of adolescence because in this age phase peer relationships become more important and romantic relationships arise (Steinberg & Morris, 2001). Importantly, affective psychopathological disorders often have their onset in adolescence. ToM development in adolescence might be based on underlying cognitive mechanisms such as the ability to inhibit one’s own thoughts in order to understand another person’s thoughts (Carlson & Moses, 2001). Another possible mechanism relates to functional brain development across adolescence (Blakemore, 2008). Therefore, neurocognitive mechanisms may underlie ongoing ToM development in adolescence. First studies indicate an ongoing behavioral and functional brain development of ToM (e.g. Blakemore, 2008). However, ToM development in adolescence and how this might relate to underlying (neuro)cognitive functions remains largely underexamined. The major aims of the current thesis were first to answer the overall question whether there is an ongoing development of ToM in adolescence. This question relates to both behavioral and functional brain development. As a second major aim, the present work sought to elucidate possible (neuro)cognitive mechanisms of ongoing ToM development across adolescence. Specifically, these cognitive mechanisms might be basic cognitive functions as well as executive functions. Additionally, the present work aimed at exploring potential (neuro)cognitive mechanisms through an integration of both behavioral and functional brain studies. The current experimental work spans three cross-sectional studies investigating adolescents (aged around 12-15 years) and young adults (aged around 18-22 years) to examine for the first time both the behavioral (studies I and II) and functional brain development of ToM (study III) in adolescence and its underlying (neuro)cognitive mechanisms. In all three studies, more complex, advanced ToM tasks were employed to avoid ceiling effects. Study I was aimed at investigating if cognitive and affective ToM continues to develop in adolescence and at exploring if basic cognitive variables such as verbal ability, speed of processing, and working memory capacity underlie such development. Hence, two groups of adolescents and young adults completed tasks of ToM and basic cognitive abilities. Large age effects were revealed on both measures of ToM: adolescents performed lower than adults. These age differences remained significant after controlling for basic cognitive variables. However, verbal ability covaried with performance in affective ToM. Overall, results support the hypothesis of an ongoing development of ToM from adolescence to adulthood on both cognitive and affective aspects. Results may further indicate verbal ability being a basic cognitive mechanism of affective ToM. Study II was designed to further explore if affective ToM, as measured with a dynamic realistic task, continues to develop across adolescence. Importantly, this study sought to explore executive functions as higher cognitive mechanisms of developing affective ToM across adolescence. A large group spanning adolescents and young adults evaluated affective mental states depicted by actors in video clips. Additionally, participants were examined with three subcomponents of executive functions, inhibition, updating, and shifting following the classification of Miyake et al. (2000). Affective ToM performance was positively related to age and all three executive functions. Specifically, inhibition explained the largest amount of variance in age related differences of affective ToM performance. Overall, these results indicate the importance of inhibition as key underlying mechanism of developing an advanced affective ToM in adolescence. Study III set out to explore the functional brain development of affective ToM in adolescence by using functional magnetic resonance imaging (fMRI). The affective ToM measure was the behavioral developmentally sensitive task from study II. An additional control condition consisted of the same emotional stimuli with the instruction to focus on physical information. This study faced methodical challenges of developmental fMRI studies by matching performance of groups. The ventromedial prefrontal cortex (vMPFC) was significantly less deactivated in adolescents in comparison to adults, which might suggest that adolescents seem to rely more on self-referential processes for affective ToM. Furthermore, adolescents compared to adults showed greater activation in the dorsolateral prefrontal cortex (DLPFC) in the control condition, indicating that adolescents might be distracted by the emotional content and therefore needed to focus more on the physical content of the stimulus. These findings suggest affective ToM continues to develop on the functional brain level and reveals different underlying neurocognitive strategies for adolescents in contrast to adults. In summary, the current thesis investigated whether ToM continues to develop in adolescence until young adulthood and explored underlying (neuro)cognitive mechanisms. Findings suggest that there is indeed an ongoing development of both the cognitive and affective aspect of ToM, which importantly contributes to the conceptual debate. Moreover, the second benefit to the debate is to demonstrate how this change may occur. As a basic cognitive mechanism verbal ability and as an executive functioning mechanism inhibition was revealed. Furthermore, neurocognitive mechanisms in form of different underlying neurocognitive strategies of adolescents compared to adults were shown. Taken together, ToM development in adolescence seems to mirror a different adaptive cognitive style in adolescence (Crone & Dahl, 2012). This seems to be important for solving the wealth of socio-emotional developmental tasks that are relevant for this age span.:Abstract 1 1 General Introduction 4 1.1 Concept of ToM: cognitive and affective aspects 7 1.2 ToM Development 8 1.2.1 ToM Development until Adolescence 9 1.2.2 ToM Development in Adolescence 12 1.3 Cognitive Mechanisms 14 1.3.1 Basic Cognitive Functions 15 1.3.2 Executive Functions 17 1.4 Neurocognitive Mechanisms 19 1.4.1 Functional brain development of ToM 20 1.4.2 Integrating behavioral and functional brain studies 21 2 Outline and Central Questions 24 2.1 Does ToM continue to develop in adolescence? 24 2.1.1 Does ToM continue to develop on the behavioral level? 24 2.1.2 Does ToM continue to develop on the level of brain function? 25 2.2 What are (neuro)cognitive mechanisms of ToM development in adolescence? 26 2.2.1 What are basic cognitive and executive functioning mechanisms? 26 2.2.2 Can mechanisms be concluded from the integration of behavioral data and functional brain processes? 26 3 Study I – ToM Development in Adolescence and its Basic Cognitive Mechanisms 28 3.1 Introduction 28 3.2 Method 32 3.2.1 Participants 32 3.2.2 Materials 33 3.3 Results 36 3.3.1 Age Effects 36 3.3.2 Influence of puberty on social cognition 37 3.3.3 Controlling for Basic Cognitive Abilities 39 3.4 Discussion 40 3.4.1 Overview 40 3.4.2 Age differences in social cognition 40 3.4.3 Influence of puberty on social cognition 42 3.4.4 Covariates of age differences in social cognition 42 3.4.5 Conclusions 43 4 Study II – ToM Development in Adolescence and its Executive Functioning Mechanisms 45 4.1 Introduction 45 4.2 Method 49 4.2.1 Participants 49 4.2.2 Materials 49 4.3 Results 52 4.3.1 Decomposing the Age Effect in Affective Theory of Mind 54 4.4 Discussion 55 4.4.1 Overview 55 4.4.2 Conclusions 57 5 Study III – ToM Development in Adolescence and its Neurocognitive Mechanisms 59 5.1 Introduction 59 5.2 Method 61 5.2.1 Participants 61 5.2.2 Stimuli, design and procedure 62 5.2.3 Statistical analysis of behavioral data 65 5.2.4 Functional imaging 65 5.2.5 Statistical analysis of fMRI data 66 5.3 Results 67 5.3.1 Behavioral results 67 5.3.2 fMRI results 68 5.4 Discussion 71 5.4.1 Developmental differences in brain activations 71 5.4.2 Conclusions 74 6 General Discussion 75 6.1 Summary of empirical findings 75 6.2 Discussion and integration of the main empirical findings 76 6.2.1 Continued ToM development in adolescence 76 6.2.2 (Neuro)cognitive mechanisms of ToM development in adolescence 80 6.3 Implications and outlook 89 6.3.1 Current findings and their conceptual fit to present models of ToM 90 6.3.2 Underpinning the concept of cognitive and affective ToM 91 6.3.3 Conceptual and methodical implications of performance matching 92 6.3.4 The role of puberty on ToM 94 6.3.5 Predicting other’s economic behavior 95 6.3.6 Structural brain development 96 6.3.7 Applied perspective 97 6.4 Summary 98 References 99

La maladie d’Alzheimer (MA) est à l’origine de la majorité des cas de démence chez les personnes âgées. Son diagnostic précoce est essentiel pour mieux comprendre les mécanismes cérébraux sous-tendant la manifestation phénotypique de la maladie et développer des interventions conséquentes. Le fait d’étudier des individus à risque de développer la MA, par exemple ceux présentant un déclin cognitif subjectif (DCS) ou un trouble cognitif léger (TCL), offre l’opportunité d’examiner les processus neuropathophysiologiques qui précèdent le stade démentiel. Cela permettrait, entre autres, d’identifier des biomarqueurs avant-coureurs de la maladie. Cette thèse avait pour but d’investiguer la présence d’hyperactivation cérébrale chez des individus à risque de développer la MA, et d’examiner les réseaux cérébraux fonctionnels associés à l’hyperactivation. L’hyperactivation se définit par la présence de niveaux supérieurs d’activation cérébrale chez des personnes faisant partie de groupes à risque pour la MA (p.ex. DCS ou TCL), comparativement à des participants contrôles cognitivement sains. L’hyperactivation est le plus souvent mesurée par l’imagerie par résonance magnétique fonctionnelle (IRMf) en condition de réalisation de tâche. Dans cette thèse, le lecteur ou la lectrice sera d’abord exposée aux études ayant utilisé l’IRMf pour examiner les patrons d’activation cérébrale et de connectivité fonctionnelle chez les individus ayant reçu un diagnostic clinique de MA, de TCL ou présentant un DCS. Les modèles théoriques découlant de ces études seront ensuite présentés. Afin de mieux comprendre le phénomène d’hyperactivation et sa relation avec les patrons de connectivité fonctionnelle, les divers enjeux scientifiques qui demeurent à être abordés seront ensuite décrits (Chapitre 1). Trois articles exposant les études empiriques formant le corps de la thèse seront ensuite présentés. La première étude avait pour but de documenter la présence, la localisation et l’évolution longitudinale de l’hyperactivation iv associée à une tâche de mémoire épisodique chez des individus qui rencontrent les critères de TCL et qui ont ultérieurement progressé vers une démence (Chapitre 2). La deuxième étude visait à déterminer la trajectoire de l’activation cérébrale associée à une tâche de mémoire associative en fonction du degré de sévérité de la maladie chez un groupe d’individus à risque de développer la MA. Elle avait également pour but de déterminer la présence d’hyperactivation chez des personnes rencontrant les critères de DCS plus (ou DCS+), qui sont des individus présentant une plainte de mémoire ainsi que des marqueurs génétiques et/ou de neurodégénérescence pour la MA (Chapitre 3). La troisième étude avait pour but d’examiner les réseaux cérébraux fonctionnels associés aux régions montrant de l’hyperactivation chez des individus à risque de développer la MA. Elle avait également pour objectif d’évaluer comment l’hyperactivation et ces réseaux cérébraux fonctionnels sont reliés aux performances en mémoire (Chapitre 4). Les résultats découlant de l’étude 1 ont permis de mettre en évidence la présence d’hyperactivation chez des individus présentant un TCL et ayant ultérieurement progressé vers le stade de démence. Les trouvailles de l’étude 2 indiquent qu’une fonction quadratique décrit la relation entre des indices de sévérité de la maladie et l’activation pariétale supérieure gauche chez un groupe d’individus à risque de développer la MA (DCS+ et TCL). Par ailleurs, des niveaux supérieurs d’activation, c’est-à-dire de l’hyperactivation, étaient retrouvés dans les hippocampes + et plusieurs régions temporo-pariétales dans le groupe d’individus DCS . Une hypoactivation pariétale supérieure gauche était plutôt retrouvée chez les individus TCL. Enfin, les résultats de l’étude 3 indiquent que l’hyperactivation de régions prédéterminées est associée à la dysfonction de réseaux cérébraux fonctionnels impliqués dans les processus de mémoire associative dans le DCS+ et le TCL. De plus, ces interactions hyperactivation-réseaux étaient associées à une symptomatologie cognitive croissante. Les implications de cette thèse et ses limites sont abordées dans la discussion (Chapitre 5). / Alzheimer's disease (AD) is the most common cause of dementia in older adults. Its early diagnosis is essential to better understand the brain mechanisms underlying the phenotypical manifestation of the disease and develop consequent interventions. The study of individuals at risk of AD, for example those presenting with subjective cognitive decline (SCD) or mild cognitive impairment (MCI), offers the opportunity to examine the neuropathophysiological processes preceding the dementia stage. This would allow, among other things, to identify early biomarkers of the disease. The general aim of this thesis was to determine the presence of cerebral hyperactivation and to assess functional brain networks associated with hyperactivation. Hyperactivation is defined by the presence of higher levels of brain activation in individuals at risk of AD (i.e. SCD, MCI) in comparison to cognitively healthy controls. Hyperactivation is most often measured with functional magnetic resonance imaging (fMRI) while participants perform a cognitive task. In this thesis, the reader will first be exposed to the studies which used fMRI to examine patterns of brain activation and connectivity in individuals with a clinical diagnosis of AD, MCI or presenting with SCD. Theoretical models resulting from these studies will then be presented. The scientific issues remaining to be addressed to better understand the phenomenon of hyperactivation and its relation to functional brain networks will then be described (Chapter 1). Three empirical studies forming the core of this thesis will be presented. The first study aimed to assess the presence, localization and longitudinal evolution of hyperactivation associated with an episodic memory task in individuals meeting criteria for MCI and having subsequently progressed towards dementia (Chapter 2). The second study aimed to determine the trajectory of brain activation associated with an associative memory task as a function of disease severity in a group of individuals at risk of AD. It also aimed to determine if hyperactivation is present in viii participants meeting criteria for SCD plus (or SCD+), who are individuals presenting with memory complaint in addition to genetic and/or neurodegeneresence markers of AD (Chapter 3). The third and last study aimed to examine patterns of functional connectivity related to regions of hyperactivation, and to assess how hyperactivation and its associated functional networks relate to memory performance in individuals at risk of AD (Chapter 4). Results from the first study highlighted the presence of hyperactivation in individuals with MCI who subsequently progressed to the dementia stage. Findings from the second study revealed a quadratic function describing the relationship between proxies of disease severity (neurodegeneration, memory performance) and left superior parietal activation in a group of individuals at risk of AD (SCD+ and MCI). Moreover, higher levels of activation, i.e. hyperactivation, were found in hippocampal and temporo-parietal regions in the SCD+ group. Hypoactivation was rather found in the left superior parietal area in the MCI group. Finally, results from the third study revealed that hyperactivation of predetermined regions was associated with dysfunction of functional brain networks underlying associative memory in SCD+ and MCI. Moreover, these hyperactivation-network interactions were associated with increasing symptomatology. The implications of this thesis and its limits are addressed in the discussion section (Chapter 5).