89 research outputs found

    P300 component in euthymic patients with bipolar disorder type I, bipolar disorder type II and healthy controls: a preliminary event-related potential study

    Get PDF
    The aim of the present study was to investigate P300 event-related potential components in euthymic bipolar disorder type I (BDI) and bipolar disorder type II (BDII) patients and matched controls. A total of 10 BDI patients, 10 BDII patients and 10 healthy individuals were enrolled in the study. Event-related potential data were collected according to a standard auditory 'oddball' paradigm. A significant groups effect in both the peak amplitude (P<0.001) and the mean amplitude (P<0.001) was observed; post-hoc comparisons showed that the peak and mean amplitudes of BDI and BDII patients were significantly lower than the peak and mean amplitudes of the healthy controls. The neurophysiological patterns found in the present study might at least partially reflect the presence of a mild selective cognitive impairment in euthymic BDI and BDII patients. From a clinical point of view, these evidences support the potential role of cognitive interventions in the treatment of BD

    Negative symptoms as key features of depression among cannabis users: a preliminary report.

    Get PDF
    OBJECTIVE: Cannabis use is frequent among depressed patients and may lead to the so-called "amotivational syndrome", which combines symptoms of affective flattening and loss of emotional reactivity (i.e. the so-called "negative" symptomatology). The aim of this study was to investigate the negative symptomatology in depressed patients with concomitant cannabis use disorders (CUDs) in comparison with depressed patients without CUDs. PATIENTS AND METHODS: Fifty-one patients with a diagnosis of Major Depressive Disorder (MDD) and concomitant CUD and fifty-one MDD patients were enrolled in the study. The 21-Item Hamilton Depression Rating Scale (HDRS) and the negative symptoms subscales of the Positive and Negative Syndrome Scale (PANSS) were used to assess depressive and negative symptomatology. RESULTS: Patients with cannabis use disorders presented significantly more severe negative symptoms in comparison with patients without cannabis use (15.18 ± 2.25 vs 13.75 ± 2.44; t100 = 3.25 p = 0.002). DISCUSSION: A deeper knowledge of the "negative" psychopathological profile of MDD patients who use cannabis may lead to novel etiopathogenetic models of MDD and to more appropriate treatment approaches

    Metabolic abnormalities and low dietary Omega 3 are associated with symptom severity and worse functioning prior to the onset of psychosis: Findings from the North American Prodrome Longitudinal Studies Consortium

    Get PDF
    Objective: Patients with schizophrenia have a high prevalence of metabolic disorders and cardiovascular mortality. It is possible that a vulnerability to metabolic abnormalities is associated with risk for psychosis, symptoms and functionality. In this study, we evaluate demographic information, cardiometabolic indices, symptoms and functioning in an antipsychotic free cohort at Clinical High Risk (CHR) for psychosis from the NAPLS Omega 3 fatty acid clinical trial. Method: Subjects received physical exams and metabolic monitoring prior to randomization into the Omega 3 versus Placebo trial. Anthropometrical measures, vital signs, glucose, and lipids were assessed along with symptoms, functioning, dietary Omega 3 fatty acids, erythrocyte polyunsaturated fatty acid content and a measure of lipid peroxidation (TBARS, Thiobarbituric acid-reactive substances). Results: The sample included 113 CHR subjects (42.1% female; 17.5% Latino) ages 12–29. The mean BMI was 24.3 with a trend toward higher BMI and a higher incidence of metabolic syndrome in Latino subjects; 36% of the sample was obese/overweight; 37.6% met criteria for prehypertension/hypertension; 4.2% met criteria for prediabetes/diabetes; 9.6% showed evidence of insulin resistance and 44.7% had dyslipidemia. The TBARS was elevated at 9.8 ÎŒM ± 6.1 (normal 1.86–3.94 ÎŒM). Metabolic parameters and a diet low in Omega 3 rich foods were significantly associated with prodromal symptoms and poor functioning. Conclusions: CHR subjects show a high percentage of metabolic abnormalities prior to exposure to antipsychotic medication. These findings reinforce that early detection of metabolic disturbances and food insecurity is crucial since these factors are modifiable with the potential for significant gains in terms of quality of life, physical and mental health

    Acute and repetitive fronto-cerebellar tDCS stimulation improves mood in non-depressed participants

    Get PDF

    Abstracts: NRC Waste Management Program reports

    No full text
    This document consists of abstracts of all reports published by the Nuclear Regulatory Commission (NRC) Waste Management Program at Lawrence Livermore Laboratory (LLL). It will be updated at regular intervals. Reports are arranged in numerical order, within each category. Unless otherwise specified, authors are LLL scientists and engineers

    BOND ENERGIES AND BOND DISSOCIATION ENERGIES

    No full text
    La dissociation d'un lien, R1R2 → R1 ‱ + R2 ‱, est dĂ©crite en tenant compte que dans la molĂ©cule les fragments R1 et R2 ne sont pas habituellement Ă©lectriquement neutres Ă  titre individuel, tandis que les radicaux correspondants le sont certainement. On dĂ©duit une Ă©quation pour l'Ă©nergie de neutralisation de charge, ENC, dĂ©crivant la neutralisation de R1 par R2. Il en dĂ©coule une formule pour 1'Ă©nergie de dissociation, D* = Δ + ENC + ΔEnl + RE(R1) + RE(R2), oĂč Δ est l'Ă©nergie de lien (qui dĂ©pend des charges) et ΔEnl est un terme d'interaction entre atomes non liĂ©s, les derniers deux termes Ă©tant chacun l'Ă©nergie de rĂ©organisation d'un fragment neutre devenant un radical. Cette formule est gĂ©nĂ©rale. Elle se rĂ©duit Ă  D* = Δ pour les molĂ©cules diatomiques. Pour un lien Ă  l'"intĂ©rieur" d'une molĂ©cule (i.e., un lien entre groupes polyatomiques) on obtient D* ≈ Δ. Les liens pĂ©riphĂ©riques (e.g., C-X avec X = H, Cl, Br, I) sont dĂ©crits par D* ≈ constante + RE. Finalement, les liens impliquant l'"extĂ©rieur" d'une molĂ©cule (p. ex. les liaisons hydrogĂšne) sont dĂ©crits par D* = ENC + ΔEnl. Bien que les "liens" de ce dernier type puissent ĂȘtre relativement faibles, tout transfert de charge accompagnant leur formation peut dĂ©clencher d'importantes modifications dans l'"intĂ©rieur" des partenaires liĂ©s, se reflĂ©tant dans leur rĂ©activitĂ©. C'est dans ce contexte que des analyses de populations Ă©lectroniques et le calcul des Ă©nergies de lien qui en dĂ©pendent peuvent s'avĂ©rer utiles.The problem of bond dissociation, R1R2 → R1 ‱ +R2 ‱, is addressed from the view point that the fragments, R1 and R2, may not be individually electroneutral in the host molecule, whereas the corresponding radicals certainly are. An expression is derived for the charge neutralization energy, CNE, accounting for the neutralization of R1 by R2. This leads to a new formula for the dissociation energy, D* = Δ + CNE + ΔEnb + RE(R1) + RE(R2), where Δ is the charge-dependent bond energy, ΔEnb is a small nonbonded contribution and the last two terms are reorganizational energies which measure the relaxation of an electroneutral fragment to yield the final product. This new formula is general. For diatomics it reduces to D* = Δ. For a bond in the "interior" of a molecule (i.e. a bond linking sufficiently large groups), the appropriate expression is D* ≈ Δ + RE(R1) + RE(R2). Peripheral bonds (e.g., C-X with X = H, Cl, Br, I) are described by D* ≈ constant + RE. Finally, bonds involving the "exterior" of a molecule (e-g., hydrogen bonds) are described by D* = CNE + ΔEnb. Even though the latter "bonds" may be relatively weak, any charge imbalance resulting from their formation is capable of inducing significant modifications in the "interior" of the bonded partners and thus can affect their reactivities. This is where detailed charge analyses and the calculation of charge-dependent bond energies can prove valuable

    From Concepts to Algorithms for the Characterization of Reaction Mechanisms- H2CS as a Case Study

    No full text
    All the stationary points on the S0 surface of H2CS and their quadratic force fields have been determined by correlated methods using large multiply polarized basis sets. Complete quartic force fields of all stationary points and reaction paths connecting each pair of minima through a first?order saddle point have been obtained at the MP2 level using smaller polarized basis sets. These data allow the computation of reliable isomerization and fragmentation rates by semiclassical expressions which take into account tunneling as well as curvature and mode–mode couplings. Further insight into the characteristics of the different reaction channels has been gained from the parameters of the so?called reaction path Hamiltonian (RPH) both in adiabatic and diabatic representations. The bookkeeping and processing of the large body of data involved in this study has been possible through the development of a package which is able to perform anharmonic and reaction path computations. The results are discussed with special reference to the H2CO system and to the interplay of potential, kinetic, and statistic effects in determining reaction mechanisms and rates
    • 

    corecore