Schizophrenia comprises various symptom domains the two most important being positive and negative symptoms. Nevertheless, using (un)supervised machine learning techniques it was shown that a) negative symptoms are significantly interrelated with PHEM (psychosis, hostility, excitation, and mannerism) symptoms, formal thought disorders (FTD) and psychomotor retardation (PMR); and b) stable phase schizophrenia comprises two distinct classes, namely Major Neuro-Cognitive Psychosis (MNP, largely overlapping with deficit schizophrenia) and Simple NP (SNP). In this study, we recruited 120 MNP patients and 54 healthy subjects and measured the above-mentioned symptom domains. In MNP, there were significant associations between negative and PHEM symptoms, FTD and PMR. A single latent trait, which is essentially unidimensional, underlies these key domains of schizophrenia and additionally shows excellent internal consistency reliability, convergent validity, and predictive relevance. Confirmatory Tedrad Analysis indicates that this latent vector fits a reflective model. Soft Independent Modeling of Class Analogy (SIMCA) shows that MNP (diagnosis based on negative symptoms) is better modeled with PHEM symptoms, FTD and PMR than with negative symptoms. In conclusion, in MNP, a restricted sample of the schizophrenia population, negative and PHEM symptoms, FTD and PMR belong to one underlying latent vector reflecting general psychopathology and, therefore, may be used as an overall severity of schizophrenia (OSOS) index. The bi-dimensional concept of positive and negative symptoms and type I and II schizophrenia is revised.
To determine the mechanism(s) for the growth retardation associated with malnutrition early in life, the relationships among plasma somatomedin-C (SM-C), plasma GH, and hepatic bovine GH-binding sites were assessed in rat pups that were milk-deprived from birth until weaning (21 days). After this period of malnutrition, body weight, tail length, plasma SM-C, and liver GH-binding capacity of the malnourished animals were significantly (P < 0.001) reduced below those of control, well fed rats [SM-C at 21 days, 0.06 ± 0.01 vs. 0.30 ± 0.04 U/ml (mean ± SE); GH binding, 2.96 ± 0.39 vs. 7.19 ± 0.80 pmol/liver]. The number of GH-binding sites per mg DNA was also reduced (0.59 ± 0.06 vs. 1.08 ± 0.11 pmol/mg DNA; P < 0.001). After 1 week of ad libitum refeeding (days 21–28), body weight and tail length of malnourished pups increased significantly but showed no signs of catching up with that of control pups. Plasma SM-C and liver GH-binding capacity in the malnourished rats also rose significantly (P < 0.005) after refeeding, but remained as far below controls as at 21 days [SM-C on day 28, 0.19 ± 0.02 vs. 0.53 ± 0.02 U/ml (P < 0.001); GH binding, 6.59 ± 0.99 vs. 12.94 ± 1.60 pmol/liver (P < 0.005)]. After 7 weeks of refeeding (days 21–70), tail length but not body weight recovered, while plasma SM-C levels were normalized. The mean number of GH binding sites per mg DNA in the malnourished rats was not significantly different from that in controls and reached for the males and the females, respectively, 79% and 86% of control binding. When expressed per liver, GH binding followed a similar pattern; for the males, binding capacity returned to 73% of the control value (20.45 ± 1.82 vs. 27.93 ± 3.49 pmol/liver; P = NS), and for the females, it returned to 77% of the control value (36.42 ± 1.76 vs. 47.42 ± 4.13 pmol/liver; P < 0.01). In the young rats up to day 28, liver GH-binding capacities correlated with plasma SM-C concentrations (r = 0.81; P < 0.01), while in the adult rats no correlation was present. During malnutrition and refeeding, there were no changes in the affinity constants of the hepatic GH-binding sites or in plasma GH concentrations. The results suggest that in neonatal malnutrition, reduced liver GH-binding capacity could be one of the mechanisms whereby plasma SM-C concentrations are reduced. Prolonged, but not short term, refeeding leads to tail length catch-up growth, normalization of plasma SM-C concentrations, and restoration of near-normal liver GH-binding capacities. (Endocrinology115: 786–792, 1984)
Several neurochemical correlates of suicide were recently detected. Some authors found increased disorders in the hypothalamic-pituitary-adrenal (HPA) and -thyroid (HPT) axes and disturbances in serotonergic neurotransmission in suicidal patients. In order to investigate the biological correlates of suicidal ideation, we measured the following: basal thyrotropin-secreting hormone (TSH), free thyroxine (FT4), pre- and postdexamethasone cortisol, adrenocorticotropic hormone (ACTH) levels, the circulating concentrations of total L-tryptophan (L-TRP) and the ratio between L-TRP and competing amino acids (CAA). The subjects were 17 suicidal and 17 nonsuicidal major depressed females matched for age and severity of illness. We found no significant differences in any of the above-mentioned biological data between patients with suicidal ideation and those without.