Biomedical subjects
B E Ginsburg
Publications and source records attributed to B E Ginsburg.
Innateness of communicative behaviors.
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Molecular genetics of psychopathologies: a search for simple answers to complex problems.
Molecular genetics is helping define the contribution of genetic involvement in behavioral disorders. At this time, however, a severely limiting factor for DNA linkage studies of these disorders remains the definition of the phenotype. An example of this is found in the group of studies examining linkage of schizophrenia to the 5q location. Although various broad clinical interpretations of the schizophrenia phenotype were used to test for linkage, all but one study reported findings negative for linkage of schizophrenia to the 5q area. We offer a strategy based on family studies using segregation data of behavioral subtypes. We apply this strategy using molecular genetic technology to our study of psychopathology in patients. This approach offers the possibility of a clearer definition of the phenotype and is suggested for use in both linkage and association studies of neuropsychiatric disorders.
Alcohol and drug abusers subtyped by antisocial personality and primary or secondary depressive disorder.
Our data show that when substance abusers are subtyped simultaneously by antisocial personality disorder and the onset of depression relative to alcohol or drug abuse, groups of people with unique personality and affective profiles are identified. The profiles are represented by measures of affect-related personality variables such as trait anxiety, trait depression, histrionic traits, sensation seeking, and novelty seeking. These measures were chosen in an attempt to show that a "low arousal" personality type may be associated with antisocial personality and may thus indirectly be linked to a certain type (i.e., ASP/nondepressed) of substance abuser. By using a multi-symptomatic typological schema (i.e., a constellation of diagnostic categories rather than just one), we can show that different personality or affective profiles are indeed associated with certain subtypes of substance abusers and that depressed people who use drugs or alcohol are different affectively from antisocial types. We also show that the relationship between "low" and "high" arousal personality profile and subtypes based on co-morbid psychopathology is highlighted even more when we take into account the onset of dysthymia or depression that is primary versus secondary to substance abuse. Our findings are in accord with others' descriptions of the "affective arousal" dimensions of personality and are the first to link these dimensions with subtypes based on ASP and depression.
Effects of menstrual phase on intake of nicotine, caffeine, and alcohol and nonprescribed drugs in women with late luteal phase dysphoric disorder.
To investigate the possibility that cigarette smoking and other drug use are affected by menstrual phase in smokers with Late Luteal Phase Dysphoric Disorder (LLPDD), we examined daily diaries rating menstrual symptomatology, smoking, alcohol and nonprescription drug use, and caffeine intake in nine female smokers meeting criteria for LLPDD. Menstrual symptomatology peaked during the premenstrual phase. Smoking, alcohol, and nonprescription drug intake were increased during menses; caffeine intake was unaffected by phase. No systematic intrasubject correlation between symptomatology and smoking was detected. It was concluded that in women with LLPDD, smoking and alcohol and nonprescription drug intake appear to vary as a function of menstrual phase. The lack of intrasubject correlations between symptomatology and intake, and the failure of peak intake to coincide with peak symptomatology, however, indicate that these effects cannot be explained simply as "self-medication" of acute episodes of dysphoric mood.
The directional motor link in reading disabilities.
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[Health examinations of refugee children--whose needs control the content?].
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Urinary C-peptide excretion in obese and anorectic children.
To assess the total insulin secretion in children in different nutritional states we have analysed the 24 h urinary C-peptide excretion in 32 obese children (16 boys and 16 girls) 8-15 years of age as well as in 7 girls with anorexia nervosa 11-16 years of age. Obese children had a median urinary C-peptide excretion rate of 0.27 nmol/kg/24 h, which was not different from that of a group of normal-weight children. In the group of anorectic girls, on the other hand, the median value 0.47 nmol/kg/24 h was significantly (p less than 0.05) higher than for normal-weight girls of the same age (median = 0.26 nmol/kg/24 h). These results indicate that in obese children insulin secretion, measured as the 24 h urinary C-peptide excretion per kg body weight, is the same as in normal-weight children. Total insulin secretion is consequently increased. In anorexia nervosa, on the other hand, the higher C-peptide excretion per kg body weight compared with normal-weight children, indicates that insulin secretion is increased in relation to body weight.
The role of postnatal testosterone in the development of sexually dimorphic behaviors in DBA/1Bg mice.
The DBA/1 Y chromosome causes an increment in aggression and pubertal testosterone levels. The purpose of the following experiments was to determine whether pubertal testosterone is necessary for the normal development of both aggression and copulation in males. If it is, then the effect of the DBA/1 Y chromosome may be mediated by its influence on pubertal testosterone. Individuals were either castrated at 30 days of age (CAS30) or sham operated (Sham or CAS50). At 50 days of age, the CAS30 individuals were sham operated and replaced with testosterone, while the CAS50 group was castrated and replaced with the same quantity of testosterone. The shams were sham operated at 50 days of age. CAS30 individuals were less aggressive than the CAS50 group, while they were no less aggressive than the sham operated group. Additionally, no groups differed in male copulatory behaviors. The results are discussed in relation to Y chromosomal and developmental mechanisms of sexually dimorphic behaviors.
Plasma valine and urinary C-peptide in infants. The effect of substituting breast-feeding with formula or formula with human milk.
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Plasma valine and urinary C-peptide in breast-fed and artificially fed infants up to 6 months of age.
Plasma branched-chain amino acids and urinary C-peptide-creatinine excretion was determined at 3, 4 1/2 and 6 months of age in a group of 50 infants who were either breast-fed or artificially fed and selected at random. The average concentrations of valine in plasma and C-peptide in urine as well as the ratio between C-peptide and creatinine in urine were 2-3 times higher (p less than 0.01) in artificially fed as compared to breast-fed infants at all the ages studied. Plasma valine values correlated significantly with the urinary C-peptide/creatinine ratio (r = 0.76, p less than 0.01), which suggests that the enhanced insulin response induced by the artificial formula is related to its protein content.
A mutant for spontaneous seizures in C57BL/10Bg mice.
The symptomatology, electroencephalographic and other correlates, development, and genetics of a new mutant in mice for spontaneous seizures are described. This recessive mutant is designated "spontaneous seizures" and is assigned the gene symbol sps. Just at or after puberty, 25% of the sps/sps homozygotes show behavioral arrest and spontaneous generalized convulsions. The behavioral arrest is associated with 1-2/s high-voltage spikes in the neocortex and the generalized convulsions are associated with paroxysmal activity in the neocortex. The effects of this mutant are compared with those of others for reflex or spontaneous seizures in mice.
Workshop on Human Behavior Genetics.
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Y-chromosome length in sublines of two mouse strains.
Differences in intermale aggression have been repeatedly reported for DBA/1 and C57BL/10 mice. The results of rreciprocal crosses combined with cross-fostering procedures suggest an involvement of the Y chromosome. In the present study, the length of the Y chromosome relative to that of chromosome 19 was ascertained in five sublines of DBA/1Bg, three sublines of C57BL/10Bg, and C57BL/10.DBA/1-Y congenic stock of mice, which carries the DBA/1Bg Y chromosome. With respect to the length of the Y chromosome relative to that of chromosome of 19, two of the DBA/1 sublines are shorter than the other three DBA/1 sublines, and all DBA/1 sublines are shorter than the three C57BL/10 sublines. This is attributable primarily to the length of the Y chromosome. The C57BL/10 sublines and the BL10.D1-Y congenic stock tested exhibit the same relative lengths of the Y chromosome, suggesting that its length has changed on the C57BL/10 genetic background. There is a parallel dependence on autosomal background of the effect of the Y chromosome on intermale aggression.
Development of susceptibility to audiogenic seizures in DBA/2J and Rb mice: toward a systematic nomenclature of audiogenic seizure levels.
A systematic nomenclature of levels of audiogenic seizures has been proposed and applied to describe the developmental changes in susceptibility in Rb-1, Rb-2 and DBA/2J mice.
Serum cholesterol concentrations in early infancy.
Sixteen healthy term infants were followed from birth to the age of 3-6 months. Total cholesterol, VLDL-LDL-cholesterol and HDL-cholesterol were determined in cord serum, in serum obtained 3-10 days after birth (mean age 4.6 days) and at the age of 3-6 months (mean 4.1 months). Mean total cholesterol increased by 1.5 mmol/l during the first 3-10 days and by an additional 1.1 mmol/l during the following 3-6 months. Mean VLDL-LdL-cholesterol increased by 1.0 mmol/l and 0.9 mmol/l, respectively, and mean HDL-cholesterol by 0.4 mmol/l and 0.3 mmol/l, respectively, during the same periods. The HDL-cholesterol: VLDL-LDL-cholesterol ratio thus fell from 1.5 at birth to 0.8 at the age of 3-10 days and to 0.6 at 3-6 months. In eight breast-fed infants, the mean total cholesterol level increased by 2.9 mmol/l from birth to the age of 3-6 months. This increase was significantly higher than the increase found in eight infants who received a cow's milk formula--i.e. 2.3 mmol/l. Free and esterified cholesterol were determined in 10 infants. Free cholesterol accounted for about one-third of the total cholesterol from birth to the age of 3-6 months.
Serum cholesterol concentrations in newborn infants with gestational ages of 28-42 weeks.
Serum total cholesterol, HDL-cholesterol and VLDL-LDL-cholesterol were determined in 53 newborn infants with gestational ages of 28-42 weeks. In pre-term infants (gestational age less than 37 weeks) the total cholesterol concentration in cord blood was higher than in term infants. Mean values were 2.4 and 1.7 mmol/l, respectively. The HDL-cholesterol/VLDL-LDL-cholesterol ratio was 1.8 in pre-term and term infants. In 11 pre-term and 17 term infants a second determination was made 3-4 days after birth. Total cholesterol had increased more in term than in pre-term infants and the difference found at birth and already levelled out. Mean value was 3.0 mmol/l in pre-term and term infants. The HDL-cholesterol/VLDL-LDL-cholesterol ratio had changed to 0.6 in pre-term and term infants. Six-pre-term infants who received intravenous fluids only were also studied. Their values did not differ from those in pre-term infants fed orally. Free and esterified cholesterol were determined in 26 infants of varying gestational ages. About one-third of the total cholesterol was in the free form in pre-term and term infants at birth and during the first days of life.
Neurochemical investigation of an endogenous model of the "hyperkinetic syndrome" in a hybrid dog.
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