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Biomedical subjects

S Ledoux

Publications and source records attributed to S Ledoux.

47 records · Page 3Linked to original sources

Associated factors for self-reported binge eating among male and female adolescents.

As part of an epidemiological study, adolescents aged 12-19 (n = 3287) filled out a self-administered questionnaire concerning their eating behaviours. The analysis showed that binge eaters (BE) had disorderly eating habits (skipping meals, snacking, eating sweets, unbalanced diets), concern with body shape (feeling too fat) and depressive symptoms more often than non binge-eaters (NBE) did. This relationship between binging episodes on the one hand, and eating habits, concern with body shape, and depressiveness on the other, has been observed for both sexes, in separate logistic regression analyses.

Body Image↗

[Functional and humor disorders as health indicators in adolescence].

In 1988, an epidemiological study concerning self-perceived health problems was carried out on a sample of 3,288 adolescents aged 11 to 19. Eight functional and depressive symptoms (FDS) were investigated. Among girls, FDS (especially sleep disorders, headaches, feelings of nervousness or depression) appeared to be common and increased between ages 11 and 19. Among boys, FDS were less common and did not increase during adolescence. Thus, at age 18, sex differences were clearly established. Results suggest a link between FDS and intrafamilial relationships, especially the aggressive attitude or the rejection of the parents and their lack of interest. For the 11-15 age group, FDS are related to school behavior, but not to school performance.

Adolescent↗

Self-reported alcohol consumption among adolescents and the signification of early onset. A longitudinal approach.

A cohort study of 327 French adolescents was carried out from 1983 to 1985 to investigate 1) the prevalence, incidence and remission rates of alcohol consumption 2) the significance of alcohol consumption before age 16 and its evolution. Among the young people with high alcohol consumption at age 16 (20%), 40% (30% among boys, 68% among girls) decrease their consumption at age 17 or 18. There are great differences between problem drinkers at age 16, and the others. They reveal more risky behaviour, more psychosomatic symptoms and have a more active life style. Even if they decrease their alcohol consumption between age 16 and their 18, their behaviour and psychosomatic problems persist.

Adolescent↗

Progressive multifocal leukoencephalopathy with gray matter involvement.

An unusual case of Progressive Multifocal Leukoencephalopathy (PML) in a Haitian man with AIDS is reported. The lesions involving both white and gray matter are described radiologically and at post-mortem. The implications regarding neuroradiological differential diagnosis in AIDS as well as PML virulence in this type of patient are discussed.

Acquired Immunodeficiency Syndrome↗

Self-reported alcohol consumption among high school students in France. Epidemiological approach of the alcoholisation process and its evolution.

Very few data are available concerning alcohol consumption among adolescents in France. Three epidemiological surveys carried out by INSERM (Unit 185), focused on the evolution of drinking behaviour patterns among high school students. Consumption trends from 1971 to 1984 were studied: daily wine consumption fell by one-third between these periods; daily beer consumption remained steady; regular hard liquor use fell by about 50% between 1971 and 1978 but showed a marked increase thereafter. The experience of drunkeness increased very significantly among young people, especially among girls. It seems that alcohol consumption became of a more addictive type recently.

Adolescent↗

Immunocytochemical localization of atrial natriuretic factor in the heart and salivary glands.

Antibodies produced in the mouse by repeated intraperitoneal injections of partly purified atrial natriuretic factor (low molecular weight peptide (LMWP) and high molecular weight peptide (HMWP)) have been used to localize these factors by immunohistochemistry (immunofluorescence and immunoperoxidase method) and by immunocytochemistry (protein A-gold technique) in the heart of rats and of a variety of animal species including man and in the rat salivary glands. Immunofluorescence and the immunoperoxidase method gave identical results; in the rat, atrial cardiocytes gave a positive reaction at both nuclear poles while ventricular cardiocytes were consistently negative. The cardiocytes of the right atrial appendage were more intensely reactive than those localized in the left appendage. A decreasing gradient of intensity was observed from the subpericardial to the subendocardial cardiocytes. The cardiocytes of the interatrial septum were only lightly granulated. Sodium deficiency and thirst (deprivation of drinking water for 5 days) produced, as already shown at the ultrastructural level, a marked increase in the reactivity of all cardiocytes from both atria with the same gradient of intensity as in control animals. Cross-reactivity of intragranular peptides with the rat antibodies allowed visualization of specific granules in a variety of animal species (mouse, guinea pig, rabbit, rat, dog) and in human atrial appendages. No reaction could be elicited in the frog atrium and ventricle although, in this species, specific granules have been shown to be present by electron microscopy in all cardiac chambers. With the protein A-gold technique, at the ultrastructural level, single labeling (use of one antibody on one face of a fine section) or double labeling (use of two antibodies on the two faces of a fine section) showed that the two peptides are localized simultaneously in all three types (A, B and D) of specific granules. In the rat salivary glands, immunofluorescence and the immunoperoxidase method showed reactivity exclusively in the acinar cells. The reaction was most intense in the acinar cells of the parotid gland. In the sublingual gland, only the serous cells, sometimes forming abortive "demi-lunes", were reactive. In the submaxillary gland, the reaction was weaker and distributed seemingly haphazardly in the gland. The most constantly reactive cells were localized near the capsule while many cells did not contain visible reaction product.

Adult↗

Ultrastructural immunocytochemical localization of renin and angiotensin II in the juxtaglomerular cells of the ischemic kidney in experimental renal hypertension.

Partial ligation of the rat aorta between the renal arteries induces acute hypertension with atrophy of the left (ischemic) kidney, intense stimulation of juxtaglomerular cell (JGC) secretory activity, and significant increases in renal cortical renin activity, in plasma renin activity, and in the plasma levels of angiotensin I (AI) and angiotensin II (AII). With the unlabeled antibody technique at the light-microscopic level and various dilutions of renin antiserum, immunoreactive renin can be visualized in the JGC of sham-operated controls with high dilutions of antiserum that do not reveal renin in the JGC of ischemic kidney. The reverse is true with AII antisera; ie, high dilutions of AII antisera immunostain the JGCs of ischemic kidney but not those of control kidney. With the protein A-gold technique at the electron-microscopic level, using gold particles of small and large size and immunoreacting the two faces of a fine section, renin and AII can be localized in the same JGC secretory granules. With the same technique (immunoreacting only one face of a fine section with small gold particles), quantitative analysis reveals a lower concentration of renin and a higher concentration of AII in the secretory granules of the ischemic kidney JGCs; these granules are also of smaller size than those of control kidney JGCs. AI cannot be visualized in these cells at either the light- or electron-microscopic level. These results indicate that AII co-localized with renin in JGC secretory granules and probably co-secreted, is not synthetized by these cells but is internalized following receptor binding.

Angiotensin II↗

Immunohistochemical localization of tonin in rat salivary glands and kidney.

Tonin has been localized in salivary glands and kidney by the indirect immunofluorescence technique of Coons and by the unlabeled antibody technique of Sternberger. Both techniques gave identical results. Immunoreactive tonin was localized in the cytoplasm of granular convoluted tubular cells and on the apical surface of striated duct cells and collecting duct cells of the submandibular gland. In the parotid and sublingual glands, which lack granular cells, tonin was only found on the apical surface of striated duct and collecting duct cells. In the kidney, immunoreactive tonin was found only associated with cells of the distal convoluted tubules. After fixation with Bouin fluid or with ethanol, tonin was found not only on the apical surface of the cells but also in the apical and perinuclear cytoplasm. This cytoplasmic staining has been attributed to artefactual diffusion since, after fixation with formol-picric acid, the enzyme could only be localized on the apical surface of the tubular cells.

Aging↗

[Prognostic value of early risk indicators. Longitudinal 3-year study of children at risk].

Four hundred and fifteen Parisian pre-school children were followed for 3 years (1974-1977). Four epidemiological questionnaires carried out at the ages of 3, 9, 18 and 36 months provided information on the familial and social situation as well as the physical and psychological development of the children. A cluster analysis was carried out on the behaviour variables of the 3 year-old children and 3 different groups were identified. Most children (69%) belonged to the first group, characterized by the absence of difficulties or the presence of few minor symptoms and 10% of the children belonged to the third group, a "high risk group" because of the frequency of the symptoms. Children of the "high risk group" and matched controls were followed up till their school entrance (7 years of age) and compared on different variables: health problems, sleep disorders, school problems, psychosomatic symptoms, difficulties in communicating with others. Comparison between the high risk group and controls permits discussion of the predictive value of early functional disorder risk indicators.

Child, Preschool↗