RESUMO
BACKGROUND: Social cognition (SC) and Theory of Mind (ToM) are compromised in patients with Schizophrenia (SKZ) and Bipolar Disorder (BD) and an increased frequency of metabolic abnormalities is reported in both disorders. Obesity seems associated with cognitive impairments The aim of our study is thus to assess the relationship between obesity and ToM in SKZ and BD. METHODS: 36 stabilized outpatients (18 SKZ and 18 BD) were recruited and completed Reading the Mind in the Eyes Test, Italian version and Faux Pas Recognition Test, adult version. BMI was calculated from self-reported height and weight. Two different Generalized Linear Models were created including performance in Eyes test and in Faux Pas test as outcomes and BMI as covariate. RESULTS: After stratifying for sex, we found a significant relationship between BMI and Faux Pas performance for male patients (pâ¯=â¯0.017), without significant interactions between sex and diagnosis. These results suggest a BMI effect on both affective and cognitive ToM in male patients. LIMITATIONS: Major confounders need to be considered: the greater number of subjects with SKZ in male subsample, a possible influence of neurocognitive performance, small sample size and self-reported BMI. CONCLUSIONS: There could be a relationship between ToM and metabolic dysfunctions, at least in male patients. The exact nature of this relationship has yet to be determined; an interesting theoretical framework is based on a combination of increased brain energy request and inefficient peripheral compensatory mechanisms, resulting in inefficient energy allocation to the brain.
Assuntos
Transtorno Bipolar/psicologia , Cognição , Obesidade/psicologia , Psicologia do Esquizofrênico , Comportamento Social , Teoria da Mente , Adulto , Transtorno Bipolar/complicações , Transtorno Bipolar/metabolismo , Feminino , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Testes Neuropsicológicos , Obesidade/complicações , Esquizofrenia/complicações , Esquizofrenia/metabolismoRESUMO
BACKGROUND: Bipolar disorder (BD) may be characterized by the presence of psychotic symptoms and comorbid substance abuse. In this context, structural and metabolic dysfunctions have been reported in both BD with psychosis and addiction, separately. In this study, we aimed at identifying neural substrates differentiating psychotic BD, with or without substance abuse, versus substance-induced psychosis (SIP) by coupling, for the first time, magnetic resonance imaging (MRI) and positron emission tomography (PET). METHODS: Twenty-seven BD type I psychotic patients with (n=10) or without (n=17) substance abuse, 16 SIP patients and 54 healthy controls were enrolled in this study. 3T MRI and 18-FDG-PET scanning were acquired. RESULTS: Gray matter (GM) volume and cerebral metabolism reductions in temporal cortices were observed in all patients compared to healthy controls. Moreover, a distinct pattern of fronto-limbic alterations were found in patients with substance abuse. Specifically, BD patients with substance abuse showed volume reductions in ventrolateral prefrontal cortex, anterior cingulate, insula and thalamus, whereas SIP patients in dorsolateral prefrontal cortex and posterior cingulate. Common alterations in cerebellum, parahippocampus and posterior cingulate were found in both BD with substance abuse and SIP. Finally, a unique pattern of GM volumes reduction, with concomitant increased of striatal metabolism, were observed in SIP patients. CONCLUSIONS: These findings contribute to shed light on the identification of common and distinct neural markers associated with bipolar psychosis and substance abuse. Future longitudinal studies should explore the effect of single substances of abuse in patients at the first-episode of BD and substance-induced psychosis.
Assuntos
Transtorno Bipolar/diagnóstico por imagem , Transtorno Bipolar/patologia , Transtornos Psicóticos/diagnóstico por imagem , Transtornos Psicóticos/patologia , Lobo Temporal/patologia , Adulto , Transtorno Bipolar/complicações , Estudos de Casos e Controles , Córtex Cerebral/patologia , Feminino , Substância Cinzenta/patologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Tomografia por Emissão de Pósitrons , Transtornos Psicóticos/complicações , Tálamo/patologia , Adulto JovemRESUMO
We tested sera from 22 women and their singleton full-term infants for inhibition in one-way mother/father mixed lymphocyte culture (MLC). Ten of these infants were small for gestational age (SGA) and 12 of them adequate for gestational age (AGA). Twenty placentas from these cases (ten from SGA infants and ten from AGA infants) were histologically studied. The results show evidence that blocking factors capable of inhibiting responses of wife's lymphocytes to husband's cells in MLC are present in sera from women with normal pregnancies but not in women with SGA infants. Sera from AGA infants showed a blocking activity on responses of husband's lymphocytes to wife's cells and this was not observed in sera from SGA infants. Lesions of chronic villitis were found in six placentas from SGA infants and in none from AGA infants. A deficit of blocking protective factors and its relationship with placental lesions is in favor of an immunological mechanism for intrauterine growth retardation.
Assuntos
Retardo do Crescimento Fetal/imunologia , Isoanticorpos/imunologia , Doenças Placentárias/imunologia , Arteriosclerose/imunologia , Arteriosclerose/patologia , Ligação Competitiva , Vilosidades Coriônicas/patologia , Feminino , Sangue Fetal/imunologia , Humanos , Técnicas In Vitro , Recém-Nascido , Recém-Nascido Pequeno para a Idade Gestacional , Inflamação/imunologia , Inflamação/patologia , Ativação Linfocitária , Teste de Cultura Mista de Linfócitos , Doenças Placentárias/patologia , GravidezRESUMO
The cases of twenty-six patients who received a massive allotransplant of frozen bone, with a known degree of histocompatibility between the donor and the recipient, were studied. Twenty-two patients were followed for more than two years (range, twenty-four to ninety-two months). Twenty-three biopsies were performed in sixteen patients from nine to seventy-eight months after transplantation. No clear relationship could be established between the degree of histocompatibility of the donor and the recipient and the incorporation of the graft, probably in part due to the number of variables involved and the polymorphism of the HLA system. However, no early massive resorption of the transplant was seen in this series, in which, by the design of the protocol, no recipients had pre-existing circulating antibodies to the antigens of the donor. Two allografts showed infiltration by round cells and vascular lesions in the absence of infection, which is suggestive of an immune response against antigens from the donor. Both matched poorly with the donor for HLA antigens. The individual who had the strongest reaction was the only recipient in the series who had a massive failure of the transplant.
Assuntos
Transplante Ósseo , Teste de Histocompatibilidade , Osso e Ossos/imunologia , Osso e Ossos/patologia , Seguimentos , Congelamento , Rejeição de Enxerto , Sobrevivência de Enxerto , Antígenos HLA/análise , Humanos , Teste de Cultura Mista de Linfócitos , Preservação de Tecido , Transplante HomólogoRESUMO
A survey of sheep with chronic respiratory tract disease was conducted in the central sierra of Peru. Histopathologic examinations coupled with an agar-gel immunodiffusion test for ovine progressive pneumonia (OPP) revealed that sheep pulmonary adenomatosis and OPP were present in these flocks. Of 80 sheep examined, 22 had lesions of sheep pulmonary adenomatosis, and 4 had metastases to regional lymph nodes. Four sheep had lesions consistent with OPP and 9 had lesions indicating the coexistence of both diseases. The agar-gel immunodiffusion test revealed that at least 26% of the sheep had been exposed to the OPP (or an antigenically similar) virus. A variety of other respiratory tract diseases complicated the evaluations of these sheep, including verminous pneumonia, hydatid disease, lung abscesses, and other nonspecific acute and chronic pneumonias.