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1.
Psychol Med ; 53(13): 6288-6303, 2023 10.
Article de Anglais | MEDLINE | ID: mdl-36464660

RÉSUMÉ

BACKGROUND: The amygdala is a subcortical limbic structure consisting of histologically and functionally distinct subregions. New automated structural magnetic resonance imaging (MRI) segmentation tools facilitate the in vivo study of individual amygdala nuclei in clinical populations such as patients with anorexia nervosa (AN) who show symptoms indicative of limbic dysregulation. This study is the first to investigate amygdala nuclei volumes in AN, their relationships with leptin, a key indicator of AN-related neuroendocrine alterations, and further clinical measures. METHODS: T1-weighted MRI scans were subsegmented and multi-stage quality controlled using FreeSurfer. Left/right hemispheric amygdala nuclei volumes were cross-sectionally compared between females with AN (n = 168, 12-29 years) and age-matched healthy females (n = 168) applying general linear models. Associations with plasma leptin, body mass index (BMI), illness duration, and psychiatric symptoms were analyzed via robust linear regression. RESULTS: Globally, most amygdala nuclei volumes in both hemispheres were reduced in AN v. healthy control participants. Importantly, four specific nuclei (accessory basal, cortical, medial nuclei, corticoamygdaloid transition in the rostral-medial amygdala) showed greater volumetric reduction even relative to reductions of whole amygdala and total subcortical gray matter volumes, whereas basal, lateral, and paralaminar nuclei were less reduced. All rostral-medially clustered nuclei were positively associated with leptin in AN independent of BMI. Amygdala nuclei volumes were not associated with illness duration or psychiatric symptom severity in AN. CONCLUSIONS: In AN, amygdala nuclei are altered to different degrees. Severe volume loss in rostral-medially clustered nuclei, collectively involved in olfactory/food-related reward processing, may represent a structural correlate of AN-related symptoms. Hypoleptinemia might be linked to rostral-medial amygdala alterations.


Sujet(s)
Anorexie mentale , Femelle , Humains , Anorexie mentale/imagerie diagnostique , Anorexie mentale/anatomopathologie , Leptine , Amygdale (système limbique)/imagerie diagnostique , Amygdale (système limbique)/anatomopathologie , Substance grise/anatomopathologie , Imagerie par résonance magnétique/méthodes
2.
Int J Eat Disord ; 55(1): 135-140, 2022 01.
Article de Anglais | MEDLINE | ID: mdl-34799878

RÉSUMÉ

OBJECTIVE: Laboratory experiments using delay discounting tasks have delivered some evidence of an increased capacity to delay reward in anorexia nervosa (AN). Overall, however, findings have been inconclusive and no comprehensive studies of self-reported tendency to forgo immediate gratification in favor of long-term rewards exist in AN. METHOD: A total of 71 acutely underweight female inpatients with AN (acAN); 52 women long-term weight-recovered from AN (recAN); and 120 healthy control women completed the Delaying Gratification Inventory (DGI). Fifty-two acAN were reassessed after short-term weight rehabilitation. Separate cross-sectional and longitudinal group comparisons tested for differences in DGI subscales (food, physical pleasure, social interaction, money, and achievement) and total scores. RESULTS: DGI scores were elevated in acAN even after removing food-related items and accounting for comorbid symptoms. DGI scores remained relatively elevated following short-term weight rehabilitation, but no differences were evident between recAN and HC. DISCUSSION: This study delivers self-report evidence supporting the notion of an increased propensity to delay gratification in individuals acutely ill with AN which does not appear to change with partial weight restoration alone. A reduction in the tendency to delay reward may thus be an important cognitive correlate of long-term recovery in AN.


Sujet(s)
Anorexie mentale , Dévalorisation de la gratification différée , Anorexie mentale/diagnostic , Anorexie mentale/psychologie , Études transversales , Femelle , Humains , Plaisir , Récompense , Autorapport , Maigreur
3.
Neuroimage ; 238: 118223, 2021 09.
Article de Anglais | MEDLINE | ID: mdl-34098065

RÉSUMÉ

Studies on social cognition often use complex visual stimuli to asses neural processes attributed to abilities like "mentalizing" or "Theory of Mind" (ToM). During the processing of these stimuli, eye gaze, however, shapes neural signal patterns. Individual differences in neural operations on social cognition may therefore be obscured if individuals' gaze behavior differs systematically. These obstacles can be overcome by the combined analysis of neural signal and natural viewing behavior. Here, we combined functional magnetic resonance imaging (fMRI) with eye-tracking to examine effects of unconstrained gaze on neural ToM processes in healthy individuals with differing levels of emotional awareness, i.e. alexithymia. First, as previously described for emotional tasks, people with higher alexithymia levels look less at eyes in both ToM and task-free viewing contexts. Further, we find that neural ToM processes are not affected by individual differences in alexithymia per se. Instead, depending on alexithymia levels, gaze on critical stimulus aspects reversely shapes the signal in medial prefrontal cortex (MPFC) and anterior temporoparietal junction (TPJ) as distinct nodes of the ToM system. These results emphasize that natural selective attention affects fMRI patterns well beyond the visual system. Our study implies that, whenever using a task with multiple degrees of freedom in scan paths, ignoring the latter might obscure important conclusions.


Sujet(s)
Émotions , Fixation oculaire/physiologie , Mentalisation/physiologie , Cognition sociale , Théorie de l'esprit/physiologie , Adulte , Symptômes affectifs , Attention/physiologie , Cartographie cérébrale , Technologie d'oculométrie , Femelle , Humains , Individualité , Imagerie par résonance magnétique , Mâle , Lobe pariétal/imagerie diagnostique , Lobe pariétal/physiologie , Lobe pariétal/physiopathologie , Cortex préfrontal/imagerie diagnostique , Cortex préfrontal/physiologie , Cortex préfrontal/physiopathologie , Lobe temporal/imagerie diagnostique , Lobe temporal/physiologie , Lobe temporal/physiopathologie , Jeune adulte
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