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Dive into the research topics where Catherine Faget is active.

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Featured researches published by Catherine Faget.


Schizophrenia Bulletin | 2016

Chronic Peripheral Inflammation is Associated With Cognitive Impairment in Schizophrenia: Results From the Multicentric FACE-SZ Dataset

E. Bulzacka; Laurent Boyer; Franck Schürhoff; O. Godin; Fabrice Berna; Lore Brunel; M. Andrianarisoa; Bruno Aouizerate; Delphine Capdevielle; I. Chereau-Boudet; G. Chesnoy-Servanin; Jean-Marie Danion; Caroline Dubertret; J. Dubreucq; Catherine Faget; F. Gabayet; Tifenn Le Gloahec; Pierre-Michel Llorca; J. Mallet; D. Misdrahi; R. Rey; Raphaëlle Richieri; Christine Passerieux; Paul Roux; H. Yazbek; Marion Leboyer; Guillaume Fond; Face-Sz Fondamental Acad Ctr

OBJECTIVES Inflammation, measured by abnormal blood C-reactive protein (CRP) level, has been described in schizophrenia (SZ), being inconsistently related to impaired cognitive functions. The aim of the present study is to investigate cognitive impairment associated with abnormal CRP levels in a large multi-centric sample of community-dwelling SZ patients, using a comprehensive neuropsychological battery. METHOD Three hundred sixty-nine community-dwelling stable SZ subjects (76.2% men, mean age 32.7 y) were included and tested with a comprehensive battery of neuropsychological tests. Abnormal CRP level was defined as >3mg/L. RESULTS Multiple factor analysis revealed that abnormal CRP levels, found in 104 patients (28.2%), were associated with impaired General Intellectual Ability and Abstract Reasoning (aOR = 0.56, 95% CI 0.35-0.90, P = .014), independently of age, sex, education level, psychotic symptomatology, treatments, and addiction comorbidities. Abnormal CRP levels were also associated with the decline of all components of working memory (respectively effect size [ES] = 0.25, P = .033; ES = 0.27, P = .04; ES = 0.33, P = .006; and ES = 0.38, P = .004) and a wide range of other impaired cognitive functions, including memory (ES = 0.26, P = .026), learning abilities (ES = 0.28, P = .035), semantic memory (ES = 0.26, P = .026), mental flexibility (ES = 0.26, P = .044), visual attention (ES = 0.23, P = .004) and speed of processing (ES = 0.23, P = .043). CONCLUSION Our results suggest that abnormal CRP level is associated with cognitive impairment in SZ. Evaluating the effectiveness of neuroprotective anti-inflammatory strategies is needed in order to prevent cognitive impairment in SZ.


Schizophrenia Research | 2015

Metabolic syndrome, abdominal obesity and hyperuricemia in schizophrenia: Results from the FACE-SZ cohort

O. Godin; Marion Leboyer; Alexandru Gaman; Bruno Aouizerate; Fabrice Berna; Lore Brunel; Delphine Capdevielle; I. Chereau; J.M. Dorey; Caroline Dubertret; J. Dubreucq; Catherine Faget; F. Gabayet; Y. Le Strat; Pierre-Michel Llorca; D. Misdrahi; R. Rey; Raphaëlle Richieri; Christine Passerieux; A. Schandrin; Franck Schürhoff; M. Urbach; P. Vidalhet; Nicolas Girerd; Guillaume Fond; O. Blanc; E. Bulzacka; I. Chereau-Boudet; G. Chesnoy-Servanin; J.M. Danion

OBJECTIVE Abdominal obesity was suggested to be a better predictor than Metabolic Syndrome (MetS) for cardiovascular mortality, however this is has not been extensively studied in schizophrenia. Hyperuricemia (HU) was also suggested to be both an independent risk factor for greater somatic comorbidity and a global metabolic stress marker in patients with schizophrenia. The aim of this study was to estimate the prevalence of MetS, abdominal obesity and HU, to examine the association between metabolic parameters with HU in a cohort of French patients with schizophrenia or schizo-affective disorder (SZ), and to estimate the prevalence rates of treatment of cardio-vascular risk factors. METHOD 240 SZ patients (age=31.4years, male gender 74.3%) were systematically included. Metabolic syndrome was defined according to the International Diabetes Federation and HU if serum uric acid level was above 360μmol/L. RESULTS MetS, abdominal obesity and HU were found respectively in 24.2%, 21.3% and 19.6% of patients. In terms of risk factors, multiple logistic regression showed that after taking into account the potential confounders, the risk for HU was higher in males (OR=5.9, IC95 [1.7-21.4]) and in subjects with high waist circumference (OR=3.1, IC95 [1.1-8.3]) or hypertriglyceridemia (OR=4.9, IC95 [1.9-13]). No association with hypertension, low HDL cholesterol or high fasting glucose was observed. Only 10% of patients with hypertension received a specific treatment, 18% for high fasting glucose and 8% for dyslipidemia. CONCLUSIONS The prevalence of MetS, abdominal obesity and hyperuricemia is elevated in French patients with schizophrenia, all of which are considerably under-diagnosed and undertreated. HU is strongly associated with abdominal obesity but not with psychiatric symptomatology.


Schizophrenia Research | 2015

Elevated C-reactive protein is associated with sensory gating deficit in schizophrenia

Jean-Arthur Micoulaud-Franchi; Mélanie Faugere; Laurent Boyer; Guillaume Fond; Raphaëlle Richieri; Catherine Faget; M. Cermolacce; Pierre Philip; Jean Vion-Dury; Christophe Lançon

Sensory and cognitive impairments and inflammatory processes are contributing factors to the pathogenesis of schizophrenia. A previous study found that an elevated CRP level (≥5mg/L) was associated with higher cognitive impairments in schizophrenia. We aimed to investigate the association between an elevated CRP level and sensory impairments defined by a sensory gating deficit (abnormal P50 suppression) in 55 outpatients. Fifteen patients (27.3%) had an elevated CRP level that was associated with higher rate of sensory gating deficit (60% vs. 12.5%, p<0.001). This is the first study suggesting a relationship between sensory gating deficit and inflammatory processes in schizophrenia.


Schizophrenia Research | 2015

Akathisia: prevalence and risk factors in a community-dwelling sample of patients with schizophrenia. Results from the FACE-SZ dataset.

Fabrice Berna; D. Misdrahi; Laurent Boyer; Bruno Aouizerate; Lore Brunel; Delphine Capdevielle; I. Chereau; J.M. Danion; J.M. Dorey; Caroline Dubertret; J. Dubreucq; Catherine Faget; F. Gabayet; Christophe Lançon; J. Mallet; R. Rey; Christine Passerieux; A. Schandrin; Franck Schürhoff; A.M. Tronche; M. Urbach; Pierre Vidailhet; Pierre-Michel Llorca; Guillaume Fond; O. Blanc; E. Bulzacka; I. Chereau-Boudet; G. Chesnoy-Servanin; Thierry d'Amato; A. Deloge

The main objective of this study was to determine the prevalence of akathisia in a community-dwelling sample of patients with schizophrenia, and to determine the effects of treatments and the clinical variables associated with akathisia. 372 patients with schizophrenia or schizoaffective disorder were systematically included in the network of FondaMental Expert Center for Schizophrenia and assessed with validated scales. Akathisia was measured with the Barnes Akathisia Scale (BAS). Ongoing psychotropic treatment was recorded. The global prevalence of akathisia (as defined by a score of 2 or more on the global akathisia subscale of the BAS) in our sample was 18.5%. Patients who received antipsychotic polytherapy were at higher risk of akathisia and this result remained significant (adjusted odd ratio=2.04, p=.025) after controlling the influence of age, gender, level of education, level of psychotic symptoms, substance use comorbidities, current administration of antidepressant, anticholinergic drugs, benzodiazepines, and daily-administered antipsychotic dose. The combination of second-generation antipsychotics was associated with a 3-fold risk of akathisia compared to second-generation antipsychotics used in monotherapy. Our results indicate that antipsychotic polytherapy should be at best avoided and suggest that monotherapy should be recommended in cases of akathisia. Long-term administration of benzodiazepines or anticholinergic drugs does not seem to be advisable in cases of akathisia, given the potential side effects of these medications.


Schizophrenia Research | 2017

Childhood trauma, depression and negative symptoms are independently associated with impaired quality of life in schizophrenia. Results from the national FACE-SZ cohort

M. Andrianarisoa; L. Boyer; O. Godin; Lore Brunel; E. Bulzacka; Bruno Aouizerate; Fabrice Berna; Delphine Capdevielle; J.M. Dorey; Caroline Dubertret; J. Dubreucq; Catherine Faget; F. Gabayet; Pierre-Michel Llorca; J. Mallet; D. Misdrahi; R. Rey; Raphaëlle Richieri; Christine Passerieux; A. Schandrin; A.M. Tronche; M. Urbach; Pierre Vidailhet; Franck Schürhoff; Guillaume Fond; O. Blanc; I. Chereau-Boudet; G. Chesnoy-Servanin; J.M. Danion; Thierry d'Amato

OBJECTIVES Depression and negative symptoms have been associated with impaired Quality of life (QoL) in schizophrenia (SZ). However, childhood trauma may influence both QoL and depression in SZ patients, with consequences for the management of impaired QoL in SZ patients. The aim of the present study was to determine if childhood trauma was associated with impaired QoL in schizophrenia. METHOD A sample of 544 community-dwelling stabilized SZ patients enrolled in FACE-SZ cohort were utilized in this study (74.1% males, mean aged 32.3years, mean illness duration 10.6years). QoL was self-reported with the S-QoL18 questionnaire. Childhood trauma was self-reported with the Childhood Trauma Questionnaire. Depression was measured by the Calgary Depression Rating Scale for Schizophrenia. Psychotic severity was measured by the Positive and Negative Syndrome Scale for Schizophrenia (PANSS). Other clinical factors, treatments, comorbidities, functioning and sociodemographical variables were also recorded, with validated scales. RESULTS Overall, 151 participants (27.8%) had a current major depressive episode and 406 (82.5%) reported at least one episode of historical childhood trauma. In multivariate analyses, lower QoL total score was associated with a history of childhood trauma (β=-0.21, p<0.0001), psychotic negative symptoms (β=-0.11, p=0.04), current depression (β=-0.0.38, p<0.0001) and male gender (β=-0.16, p<0.0001). CONCLUSION Impaired QoL is independently associated with negative symptoms, depression and childhood trauma in schizophrenia.


Schizophrenia Bulletin | 2016

Working Memory Deficit as a Risk Factor for Severe Apathy in Schizophrenia: A 1-Year Longitudinal Study

Stéphane Raffard; Laure-Anne Gutierrez; H. Yazbek; Aurore Larue; Jean-Philippe Boulenger; Christophe Lançon; Michel Benoit; Catherine Faget; Joanna Norton; Delphine Capdevielle

Apathy, described as impaired motivation and goal-directed behavior, is a common yet often overlooked multidimensional psychopathological state in schizophrenia. Its underlying cognitive processes remain largely unexplored. Data was drawn from a longitudinal hospital study of patients with a DSM-IV diagnosis of schizophrenia; 137 (82.5%) participated at the 1-month follow-up and 81 (59.1%) at the 1-year follow-up. Apathy was assessed with the Lille Apathy Rating Scale, validated in French and in schizophrenia. Severe apathy, overall (total score > -13) and on 4 previously identified distinct dimensions, was considered. Episodic verbal learning was assessed with the California Verbal Learning Test, executive functioning with the Trail Making Test, the Six Element Test and the Stop Signal Paradigm and working memory with the Letter-Number Sequencing Test. After controlling for confounding variables, only episodic verbal learning was associated with severe overall apathy in the cross-sectional study. At 1 year, working memory was associated with an increased risk of severe overall apathy, adjusting for baseline apathy. Using a dimensional approach to apathy, specific types of cognition were found to be associated with specific dimensions of apathy. Our findings confirm the need for a multidimensional approach of negative symptoms in schizophrenia. Moreover, cognitive functioning could be a risk factor for developing severe apathy. Cognitive remediation may thus be a useful non-pharmacological intervention for treating apathy in schizophrenia patients.


Psychiatry Research-neuroimaging | 2014

Validation of the French sensory gating inventory: A confirmatory factor analysis

Jean-Arthur Micoulaud-Franchi; William P. Hetrick; Laurent Boyer; Amanda R. Bolbecker; Mitsuko Aramaki; Sølvi Ystad; Raphaëlle Richieri; Alexandre El-Kaim; Catherine Faget; Mélanie Faugere; M. Cermolacce; Richard Kronland-Martinet; Christophe Lançon; Jean Vion-Dury

The Sensory Gating Inventory (SGI) is an instrument investigating daily experiences of sensory gating deficit developed for English speaking schizophrenia patients. The purpose of this study is to design and validate a French version of the SGI. A forward-backward translation of the SGI was performed. The psychometric properties of the French SGI version were analyzed. A confirmatory factor analysis (CFA) was carried out to determine whether factor structure of the French version is similar to the original English version. In a sample of 363 healthy subjects (mean age=31.8 years, S.D.=12.2 years) the validation process revealed satisfactory psychometric properties: the internal consistency reliability was confirmed for each dimension; each item achieved the 0.40 standard threshold for item-internal consistency; each item was more highly correlated with its contributive dimension than with the other dimensions; and based on a CFA, we found a 4-factor structure for the French version of the SGI similar to the original instrument. Test-retest reliability was not determined. The French version of the SGI is a psychometrically sound self-report for measuring phenomenological sensory gating experiences.


Journal of Clinical Psychopharmacology | 2015

Effects of Clozapine on Perceptual Abnormalities and Sensory Gating A Preliminary Cross-Sectional Study in Schizophrenia

Jean-Arthur Micoulaud-Franchi; Mitsuko Aramaki; Pierre Alexis Geoffroy; Raphaëlle Richieri; M. Cermolacce; Catherine Faget; Sølvi Ystad; Richard Kronland-Martinet; Christophe Lançon; Jean Vion-Dury

Abstract The aim of the present study was to investigate the effect of second-generation antipsychotics (clozapine or another second-generation antipsychotic) on perceptual abnormalities related to sensory gating deficit. Although clozapine is known to improve sensory gating assessed neurophysiologically, we hypothesized that patients with schizophrenia treated with clozapine would report less perceptual abnormalities related to sensory gating deficit than patients treated with other second-generation antipsychotics do. Forty patients with a diagnosis of schizophrenia were investigated (10 patients treated with clozapine and 30 patients treated with another second-generation antipsychotic drug). Perceptual abnormalities were assessed with the Sensory Gating Inventory. Sensory gating was assessed through electroencephalogram with the auditory event-related potential method by measuring P50 amplitude changes in a dual click conditioning-testing procedure. Patients treated with clozapine present normal sensory gating and report less perceptual abnormalities related to sensory gating than patients treated with other second-generation antipsychotics do. Although the cross-sectional design of this study is limited because causal inferences cannot be clearly concluded, the present study suggests clinical and neurophysiological advantages of clozapine compared with other second-generation antipsychotics and provides a basis for future investigations on the effect of this treatment on perceptual abnormalities related to sensory gating deficit in patients with schizophrenia.


European Archives of Psychiatry and Clinical Neuroscience | 2017

Nicotine dependence is associated with depression and childhood trauma in smokers with schizophrenia: results from the FACE-SZ dataset

R. Rey; Thierry d’Amato; Laurent Boyer; Lore Brunel; Bruno Aouizerate; Fabrice Berna; Delphine Capdevielle; I. Chereau; G. Chesnoy-Servanin; H. Denizot; J.M. Dorey; Caroline Dubertret; J. Dubreucq; Catherine Faget; F. Gabayet; Christophe Lançon; J. Mallet; D. Misdrahi; Christine Passerieux; A. Schandrin; Franck Schürhoff; M. Urbach; Pierre Vidailhet; Pierre-Michel Llorca; Guillaume Fond

In a perspective of personalized care for smoking cessation, a better clinical characterization of smokers with schizophrenia (SZ) is needed. The objective of this study was to determine the clinical characteristics of SZ smokers with severe nicotine (NIC) dependence. 240 stabilized community-dwelling SZ smokers (mean age = 31.9 years, 80.4% male gender) were consecutively included in the network of the FondaMental Expert Centers for Schizophrenia and assessed with validated scales. Severe NIC dependence was defined by a Fagerstrom questionnaire score ≥ 7. Depression was defined by a Calgary score ≥ 6. Childhood trauma was self-reported by the Childhood Trauma Questionnaire score (CTQ). Ongoing psychotropic treatment was recorded. Severe NIC dependence was identified in 83 subjects (34.6%), depression in 60 (26.3%). 44 (22.3%) subjects were treated by antidepressants. In a multivariate model, severe NIC dependence remained associated with depression (OR = 3.2, p = 0.006), male gender (OR = 4.5, p = 0.009) and more slightly with childhood trauma (OR = 1.03, p = 0.044), independently of socio-demographic characteristics, psychotic symptoms severity, psychotropic treatments and alcohol disorder. NIC dependence was independently and strongly associated with, respectively, depression and male gender in schizophrenia, and only slightly with history of childhood trauma. Based on these results, the care of both nicotine dependence and depression should be evaluated for an effective smoking cessation intervention in schizophrenia.


Schizophrenia Research | 2016

Differential effects of childhood trauma and cannabis use disorders in patients suffering from schizophrenia

G. Baudin; O. Godin; M. Lajnef; Bruno Aouizerate; Fabrice Berna; Lore Brunel; Delphine Capdevielle; I. Chereau; J.M. Dorey; Caroline Dubertret; J. Dubreucq; Catherine Faget; Guillaume Fond; F. Gabayet; H. Laouamri; Christophe Lançon; Y. Le Strat; A.M. Tronche; D. Misdrahi; R. Rey; Christine Passerieux; A. Schandrin; M. Urbach; P. Vidalhet; Pierre-Michel Llorca; Franck Schürhoff

BACKGROUND Childhood trauma (CT) and cannabis use are both environmental and modifier risk factors for schizophrenia. However, little is known about how they interact in schizophrenia. We examined the main effect of each of these two environmental factors on the clinical expression of the disease using a large set of variables, and we tested whether and how cannabis and CT interact to influence the course and the presentation of the illness. METHODS A sample of 366 patients who met the DSM-IV-TR criteria for schizophrenia was recruited through the FACE-SCZ (Fondamental Advanced Centre of Expertise - Schizophrenia) network. Patients completed a large standardized clinical evaluation including Structured Clinical Interview for DSM Disorders-I (SCID-I), Positive and Negative Symptoms Scale (PANSS), Columbia-Suicide Severity Rating Scale (C-SSRS), Global Assessment of Functioning (GAF), Short-Quality of Life-18 (S-QoL-18), and Medication Adherence Rating Scale (MARS). We assessed CT with the Childhood Trauma Questionnaire and cannabis status with SCID-I. RESULTS CT significantly predicted the number of hospitalizations, GAF, and S-QoL-18 scores, as well as the PANSS total, positive, excitement, and emotional distress scores. Cannabis use disorders significantly predicted age of onset, and MARS. There was no significant interaction between CT and cannabis use disorders. However, we found evidence of a correlation between these two risk factors. CONCLUSIONS CT and cannabis both have differential deleterious effects on clinical and functional outcomes in patients with schizophrenia. Our results highlight the need to systematically assess the presence of these risk factors and adopt suitable therapeutic interventions.

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Guillaume Fond

Aix-Marseille University

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J. Dubreucq

Centre national de la recherche scientifique

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Fabrice Berna

University of Strasbourg

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D. Misdrahi

University of Bordeaux

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