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1.
J Neuropsychol ; 17(3): 564-583, 2023 09.
Artigo em Inglês | MEDLINE | ID: mdl-37159847

RESUMO

Patients with the 22q11.2 deletion syndrome (DS) show an increased risk of developing a psychotic illness lifetime. 22q11.2DS may represent a reliable model for studying the neurobiological underpinnings of schizophrenia. The study of social inference abilities in a genetic condition at high risk for psychosis, like 22q11.2DS, may shed light on the relationships between neurocognitive processes and patients' daily general functioning. The study sample consisted of 1736 participants, divided into four groups: 22q11.2DS patients with diagnosis of psychotic disorder (DEL SCZ, N = 20); 22q11.2DS subjects with no diagnosis of psychosis (DEL, N = 43); patients diagnosed with schizophrenia without 22q11.2DS (SCZ, N = 893); and healthy controls (HC, N = 780). Social cognition was assessed through The Awareness of Social Inference Test (TASIT) and general functioning through the Specific Levels of Functioning (SLoF) scale. We analysed data through regression analysis. The SCZ and DEL groups had similar levels of global functioning; they both had significantly lower SLoF Total scores than HC (p < .001); the DEL SCZ group showed significantly lower scores compared to the other groups (SCZ, p = .004; DEL, p = .003; HC, p < .001). A significant deficit in social cognition was observed in the three clinical groups. In the DEL SCZ and SCZ groups, TASIT scores significantly predicted global functioning (p < .05). Our findings of social cognition deficit in psychosis-prone patients point to the possible future adoption of rehabilitation programmes, like Social Skills Training and Cognitive Remediation, during premorbid stages of psychosis.


Assuntos
Síndrome de DiGeorge , Transtornos Psicóticos , Esquizofrenia , Humanos , Esquizofrenia/genética , Síndrome de DiGeorge/diagnóstico , Síndrome de DiGeorge/genética , Síndrome de DiGeorge/psicologia , Cognição Social , Transtornos Psicóticos/genética
2.
IEEE Trans Pattern Anal Mach Intell ; 45(3): 2816-2834, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35639680

RESUMO

We propose the first general and scalable framework to design certifiable algorithms for robust geometric perception in the presence of outliers. Our first contribution is to show that estimation using common robust costs, such as truncated least squares (TLS), maximum consensus, Geman-McClure, Tukey's biweight, among others, can be reformulated as polynomial optimization problems (POPs). By focusing on the TLS cost, our second contribution is to exploit sparsity in the POP and propose a sparse semidefinite programming (SDP) relaxation that is much smaller than the standard Lasserre's hierarchy while preserving empirical exactness, i.e., the SDP recovers the optimizer of the nonconvex POP with an optimality certificate. Our third contribution is to solve the SDP relaxations at an unprecedented scale and accuracy by presenting [Formula: see text], a solver that blends global descent on the convex SDP with fast local search on the nonconvex POP. Our fourth contribution is an evaluation of the proposed framework on six geometric perception problems including single and multiple rotation averaging, point cloud and mesh registration, absolute pose estimation, and category-level object pose and shape estimation. Our experiments demonstrate that (i) our sparse SDP relaxation is empirically exact with up to 60%- 90% outliers across applications; (ii) while still being far from real-time, [Formula: see text] is up to 100 times faster than existing SDP solvers on medium-scale problems, and is the only solver that can solve large-scale SDPs with hundreds of thousands of constraints to high accuracy; (iii) [Formula: see text] safeguards existing fast heuristics for robust estimation (e.g., [Formula: see text] or Graduated Non-Convexity), i.e., it certifies global optimality if the heuristic estimates are optimal, or detects and allows escaping local optima when the heuristic estimates are suboptimal.

3.
J Clin Med ; 11(3)2022 Jan 19.
Artigo em Inglês | MEDLINE | ID: mdl-35159957

RESUMO

BACKGROUND: There is a growing body of literature on the association between psychosis and sexual dysfunction. However, most studies have focused on sexual dysfunction and have not investigated the sexual lives of patients with psychosis across a broader range. MATERIAL AND METHODS: Consecutive patients with a diagnosis of acute psychosis or schizophrenia were recruited to the study after obtaining informed consent (n = 46). In addition, healthy control subjects were recruited (n = 52). Sociodemographic and clinical data, psychopathology, and sexual functioning were assessed. Independent sample t-test to determine group differences was obtained. RESULTS: In both the male and female groups, there are significant differences between psychotic individuals and healthy controls in several areas of their sexual functioning: the control group seemed to better perceive Couple sexuality, Self-eroticism, and overall appeared to have a higher Quality of sexual life; on the other hand, the group of patients with psychosis displayed higher scores in Sexual dysfunction. CONCLUSIONS: A poor sexual quality of life may be found in patients with psychotic disorders. Assessment of sexual function in these patients is necessary to identify and manage issues and provide support and help to patients in this important area of life.

4.
Clin Case Rep ; 9(5): e04134, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-34084508

RESUMO

Despite entailing more severe and uncommon side effects in 22q11.2DS compared to idiopathic schizophrenia, we strongly believe that clozapine should continue to be considered the gold standard for all treatment-resistant schizophrenia, even in 22qDS.

5.
Ann Ist Super Sanita ; 56(1): 107-113, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32242542

RESUMO

INTRODUCTION: 22q11.2 microdeletion syndrome (22q11DS) is associated with a 25% risk of psychotic onset. MATERIALS AND METHODS: The sample consist of 120 subjects: 39 schizophrenics (SCZ); 20 siblings of schizophrenic patients (SIB); 34 22q11DS non-psychotic patients (DEL); 17 22q11DS psychotic patients (DEL_scz); 30 control subjects (CS). Social cognition was evaluated with the awareness of social interference test. Intelligence Quotient (IQ) was calculated with Wechsler Adult Intelligence Scale. TASIT (Awareness of Social Inference Test) performance was analyzed via MANOVA, including IQ as covariate. RESULTS: Group and IQ showed significant effect (p < 0.001; p = 0.037). The only TASIT variables where IQ showed no effect were paradoxical sarcasm; sincerity; lie. In sincerity, CS group shows a better performance than both 22q11DS groups (p < 0.05). In paradoxical sarcasm and lie, CS group performed better than each clinical group (p < 0.05). Regarding lie, DEL group was worst also respect to SCZ group (p = 0.029). CONCLUSIONS: Our results show a specific social cognition deficit in 22q11DS and schizophrenia.


Assuntos
Transtornos Cognitivos/psicologia , Síndrome de DiGeorge/psicologia , Esquizofrenia/genética , Psicologia do Esquizofrênico , Cognição Social , Adulto , Transtornos Cognitivos/etiologia , Síndrome de DiGeorge/genética , Saúde da Família , Feminino , Predisposição Genética para Doença , Humanos , Masculino , Testes Psicológicos , Transtornos Psicóticos/genética , Transtornos Psicóticos/psicologia , Irmãos , Escalas de Wechsler , Adulto Jovem
6.
J Neural Transm (Vienna) ; 125(7): 1043-1052, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29520614

RESUMO

The 22q11 deletion syndrome (22q11DS), or DiGeorge syndrome (DG), is one of the most common genetic deletion syndromes. DG also carries a high risk for psychiatric disorders, with learning disabilities frequently being reported. Impairments in specific cognitive domains, such as executive functioning and attention, have also been described. The aim of this study was to investigate attentional functioning in a group of subjects with DG using ERPs, and in particular the P300 and CNV components. We studied ten patients with DG and ten healthy subjects that performed a P300 Novelty task and a CNV motor task. P3b amplitude was significantly lower in patients than in controls, while P3b latency was comparable in patients and controls. The P3a parameters were similar in both groups. All CNV amplitudes were significantly lower in DG patients than in controls. DG patients displayed slower reaction times in the CNV motor task than healthy subjects. These results point to a cognitive dysfunction related above all to executive attentional processing in DG patients. In particular, a specific difficulty emerged in selective attention and in the ability to orient and to sustain the anticipatory attention required for an executive motor response.


Assuntos
Atenção/fisiologia , Disfunção Cognitiva/diagnóstico , Síndrome de DiGeorge/complicações , Potenciais Evocados/fisiologia , Adulto , Disfunção Cognitiva/etiologia , Síndrome de DiGeorge/psicologia , Feminino , Humanos , Masculino
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