Browsing by Author "Mena, Carlos"
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- ItemDysconnectivity in Schizophrenia Revisited: Abnormal Temporal Organization of Dynamic Functional Connectivity in Patients With a First Episode of Psychosis(2023) Ramirez-Mahaluf, Juan P.; Tepper, Angeles; Maria Alliende, Luz; Mena, Carlos; Castaneda, Carmen Paz; Iruretagoyena, Barbara; Nachar, Ruben; Reyes-Madrigal, Francisco; Leon-Ortiz, Pablo; Mora-Duran, Ricardo; Ossandon, Tomas; Gonzalez-Valderrama, Alfonso; Undurraga, Juan; De la Fuente-Sandoval, Camilo; Crossley, Nicolas A.Background and Hypothesis Abnormal functional connectivity between brain regions is a consistent finding in schizophrenia, including functional magnetic resonance imaging (fMRI) studies. Recent studies have highlighted that connectivity changes in time in healthy subjects. We here examined the temporal changes in functional connectivity in patients with a first episode of psychosis (FEP). Specifically, we analyzed the temporal order in which whole-brain organization states were visited. Study Design Two case-control studies, including in each sample a subgroup scanned a second time after treatment. Chilean sample included 79 patients with a FEP and 83 healthy controls. Mexican sample included 21 antipsychotic-naive FEP patients and 15 healthy controls. Characteristics of the temporal trajectories between whole-brain functional connectivity meta-states were examined via resting-state functional MRI using elements of network science. We compared the cohorts of cases and controls and explored their differences as well as potential associations with symptoms, cognition, and antipsychotic medication doses. Study Results We found that the temporal sequence in which patients' brain dynamics visited the different states was more redundant and segregated. Patients were less flexible than controls in changing their network in time from different configurations, and explored the whole landscape of possible states in a less efficient way. These changes were related to the dose of antipsychotics the patients were receiving. We replicated the relationship with antipsychotic medication in the antipsychotic-naive FEP sample scanned before and after treatment. Conclusions We conclude that psychosis is related to a temporal disorganization of the brain's dynamic functional connectivity, and this is associated with antipsychotic medication use.
- ItemFunctional Dysconnectivity in Ventral Striatocortical Systems in 22q11.2 Deletion Syndrome(OXFORD UNIV PRESS, 2021) Tepper, Angeles; Cuiza Vasquez Analia; Alliende, Luz María; Mena, Carlos; Ramirez Mahaluf, Juan Pablo; Iruretagoyena, Barbara; Ornstein, Claudia; Fritsch, Rosemarie; Nachar, Ruben; Gonzalez Valderrama, Alfonso; Undurraga, Juan; Pablo Cruz, Juan; Tejos, Cristian; Fornito, Alex; Repetto, Gabriela; Crossley, Nicolas22q11.2 deletion syndrome (22q11.2DS) is a genetic neurodevelopmental disorder that represents one of the greatest known risk factors for psychosis. Previous studies in psychotic subjects without the deletion have identified a dopaminergic dysfunction in striatal regions, and dysconnectivity of striatocortical systems, as an important mechanism in the emergence of psychosis. Here, we used resting-state functional MRI to examine striatocortical functional connectivity in 22q11.2DS patients. We used a 2 x 2 factorial design including 125 subjects (55 healthy controls, 28 22q11.2DS patients without a history of psychosis, 10 22q11.2DS patients with a history of psychosis, and 32 subjects with a history of psychosis without the deletion), allowing us to identify network effects related to the deletion and to the presence of psychosis. In line with previous results from psychotic patients without 22q11.2DS, we found that there was a dorsal to ventral gradient of hypo- to hyperstriatocortical connectivity related to psychosis across both patient groups. The 22q11.2DS was additionally associated with abnormal functional connectivity in ventral striatocortical networks, with no significant differences identified in the dorsal system. Abnormalities in the ventral striatocortical system observed in these individuals with high genetic risk to psychosis may thus reflect a marker of illness risk.
- ItemGender, age and geographical representation over the past 50 years of schizophrenia research(2022) Alliende, Luz MarÍa; Czepielewski, Leticia S.; Aceituno Farías, David; Paz Castaneda, Carmen; Díaz, Camila; Iruretagoyena Bruce, Bárbara Arantzazu; Mena, Carlos; Mena, Cristian; Ramírez Mahaluf, Juan Pablo; Tepper, Ángeles; Vásquez, Javiera; Fonseca, Lais; Machado, Viviane; Hernández, Camilo E.; Vargas Upegui, Cristian; Gómez Cruz, Gladys; Kobayashi Romero, Luis F.; Moncada Habib, Tomas; Evans Lacko, Sara; Bressan, Rodrigo; Gama, Clarissa S.; López Jaramillo, Carlos; de la Fuente Sandoval, Camilo; González Valderrama, Alfonso; Undurraga, Juan; Gadelha, Ary; Crossley Karmelic, Nicolás Andrés; ANDES NetworkPrevious studies have suggested that subjects participating in schizophrenia research are not representative of the demographics of the global population of people with schizophrenia, particularly in terms of gender and geographical location. We here explored if this has evolved throughout the decades, examining changes in geographical location, gender and age of participants in studies of schizophrenia published in the last 50 years. We examined this using a meta-analytical approach on an existing database including over 3,000 studies collated for another project. We found that the proportion of studies and participants from low-and-middle income countries has significantly increased over time, with considerable input from studies from China. However, it is still low when compared to the global population they represent. Women have been historically underrepresented in studies, and still are in high-income countries. However, a significantly higher proportion of female participants have been included in studies over time. The age of participants included has not changed significantly over time. Overall, there have been improvements in the geographical and gender representation of people with schizophrenia. However, there is still a long way to go so research can be representative of the global population of people with schizophrenia, particularly in geographical terms.
- ItemQuantitative Susceptibility Mapping MRI in Deep-Brain Nuclei in First-Episode Psychosis(2023) García Saborit, Marisleydis; Jara Vallejos, Alejandro Antonio; Muñoz Camelo, Néstor Andrés; Milovic, Carlos; Tepper, Angeles; Alliende Correa, Luz María; Mena, Carlos; Iruretagoyena Bruce, Bárbara Arantzazu; Ramírez Mahaluf, Juan Pablo; Diaz, Camila; Nachar, Rubén; Castaneda, Carmen Paz; Gonzalez, Alfonso; Undurraga, Juan; Crossley, Nicolás; Tejos Núñez, Cristián AndrésBackground Psychosis is related to neurochemical changes in deep-brain nuclei, particularly suggesting dopamine dysfunctions. We used an magnetic resonance imaging-based technique called quantitative susceptibility mapping (QSM) to study these regions in psychosis. QSM quantifies magnetic susceptibility in the brain, which is associated with iron concentrations. Since iron is a cofactor in dopamine pathways and co-localizes with inhibitory neurons, differences in QSM could reflect changes in these processes. Methods We scanned 83 patients with first-episode psychosis and 64 healthy subjects. We reassessed 22 patients and 21 control subjects after 3 months. Mean susceptibility was measured in 6 deep-brain nuclei. Using linear mixed models, we analyzed the effect of case-control differences, region, age, gender, volume, framewise displacement (FD), treatment duration, dose, laterality, session, and psychotic symptoms on QSM. Results Patients showed a significant susceptibility reduction in the putamen and globus pallidus externa (GPe). Patients also showed a significant R2* reduction in GPe. Age, gender, FD, session, group, and region are significant predictor variables for QSM. Dose, treatment duration, and volume were not predictor variables of QSM. Conclusions Reduction in QSM and R2* suggests a decreased iron concentration in the GPe of patients. Susceptibility reduction in putamen cannot be associated with iron changes. Since changes observed in putamen and GPe were not associated with symptoms, dose, and treatment duration, we hypothesize that susceptibility may be a trait marker rather than a state marker, but this must be verified with long-term studies.