First growth reference curves for Tunisian children and adolescents

International audienceA growth chart is a powerful graphical tool displaying children’s growth patterns. The aim of this study was to develop growth reference curves appropriate for Tunisian children. The collection of data from this cross-sectional study was conducted on 4358 healthy subjects (2182 girls and 2176 boys) in three pediatric centers and 15 schools. Smoothed growth curves were estimated using the LMS method. The smoothed percentile curves for height, weight, sitting height (SH), and leg length (LL) increase rapidly during the 1st years of life and then progress slowly until 18 years. However, the sitting height-to-height ratio (SHTHR) curves decrease sharply before the age of 4 and then stabilize in both sexes. In addition, the comparison between boys and girls indicated that the values are very similar at most ages. Except during puberty, the values in boys increase (P<0.0001) for the weight, height, SH, and LL parameters and decline (P<0.0001) in the SHTHR compared to the values in girls. The growth rate curves presented two remarkable velocity peaks: the first appears during the 1st years of life and the second at puberty. Height gains at the last stage of growth (puberty) are around 15.45% of final height for boys and 15.52% for girls. This study showed a number of discrepancies for certain age groups when comparing the median weight and height values with those of the World Health Organization, the National Center for Health Statistics, and Algerian references in both sexes. Conclusion: The smoothed percentile curves for weight and height will be useful to access the general growth of Tunisian children. Furthermore, the SH, LL, and SHTHR curves can be used to monitor body proportions during childhood

Molecular Analysis of the Mechanical Behavior of Plasticized Amorphous Polymer

Plasticization effects on the mechanical behavior were investigated on two families of materials based on poly(methyl methacrylate) (PMMA) and poly(vinyl chloride) (PVC), respectively. For this purpose, PMMA was blended with poly(vinylidene fluoride) (PVDF) by co-precipitation from solution, all over the PVDF range 0-40 wt% where the samples remain amorphous. Di-octylphtalate (DOP) was mechanically dispersed in PVC over the DOP range 0-20 wt%. The relaxation behavior of the samples was studied by differential scanning calorimetry at heating rate of 10 °C$\cdot$min-1 and by dynamic mechanical analysis at the frequency 1 Hz over the temperature range $-100~^{\circ}$C/150 °C. Stress strain curves were recorded during compression testing at a deformation rate of 2.10-3 s-1. Data analysis was carried out on the molecular scale; it permitted to highlight the influence of the β elaxation motions on the plastic behavior. Consideration of the non elastic part of the energy to yield was clearly related to the contribution of $\alpha$ and $\beta$ motions

Exposure to Mimivirus Collagen Promotes Arthritis

Collagens, the most abundant proteins in animals, also occur in some recently described nucleocytoplasmic large DNA viruses such as Mimiviridae, which replicate in amoebae. To clarify the impact of viral collagens on the immune response of animals exposed to Mimiviridae, we have investigated the localization of collagens in Acanthamoeba polyphaga mimivirus particles and the response of mice to immunization with mimivirus particles. Using protein biotinylation, we have first shown that viral collagen encoded by the ORF L71 is present at the surface of mimivirus particles. Exposure to mimivirus collagens elicited the production of anti-collagen antibodies in DBA/1 mice immunized intra-dermally with mimivirus protein extracts. This antibody response also targeted mouse collagen type II and was accompanied by T-cell reactivity to collagen and joint inflammation as observed in collagen-induced arthritis following immunization of mice with bovine collagen type II. The broad distribution of nucleocytoplasmic large DNA viruses in the environment suggests that humans are constantly exposed to such large virus particles. A survey of blood sera from human healthy subjects and from rheumatoid arthritis patients indeed demonstrated that 30% of healthy subject and 36% of rheumatoid arthritis sera recognized the major mimivirus capsid protein L425. Moreover, whereas 6% of healthy subject sera recognized the mimivirus collagen protein L71, 22% of rheumatoid arthritis sera were positive for mimivirus L71. Accordingly, our study shows that environmental exposure to mimivirus represents a risk factor in triggering autoimmunity to collagens