Early lifestyle determinants of adiposity trajectories from childhood into late adolescence

Contexte: L'obésité infantile est un facteur de risque majeur de mortalité et de morbidité, car les enfants avec obésité ont tendance à maintenir leur obésité à l’âge adulte. Parmi les enfants canadiens, 27% ont un surpoids ou une obésité, ce qui pose un grave problème de santé publique, vu les conséquences en termes de morbidité et mortalité de l’obésité à l’âge adulte. Objectifs: Les principaux objectifs de ma recherche sont les suivants: (1) examiner le lien entre l'activité physique durant la pré-puberté et les trajectoires d'adiposité de l’enfance à l'adolescence; (2) examiner le lien entre les comportements sédentaires dans la pré-puberté et les trajectoires d'adiposité de l’enfance à l'adolescence; et (3) examiner les associations entre les apports alimentaires dans la pré-puberté et les trajectoires d'adiposité de l’enfance à l'adolescence. Mon hypothèse est que moins d'activité physique, plus de temps sédentaire et une alimentation moins saine (ex. moins de fruits et légumes, plus de boissons sucrées) pendant l'enfance seront associés à des trajectoires défavorables d’obésité de l’enfance à l'adolescence. Méthodes: Cette recherche porte sur les données de l’étude QUALITY (QUebec Adipose and Lifestyle Investigation in Youth). Cette cohorte comprend 630 enfants caucasiens âgés de 8 à 10 ans, recrutés au départ sur la base d’antécédent d'obésité chez leurs parents. De ce nombre, 377 ont été suivis à 10-12 ans et à 15-17 ans. Les comportements sédentaires et l'activité physique ont été mesurés par accélérométrie sur une période de 7 jours, le temps d'écran a été mesuré par questionnaire et l'apport alimentaire avec trois rappels alimentaires de 24 heures. Le poids et la taille ont été mesurés à chaque période et transformés en scores z de l'indice de masse corporelle (IMC-z) selon les normes de l'OMS (Organisation Mondiale de la Santé). La modélisation des trajectoires basée sur les groupes a été utilisée pour identifier les trajectoires longitudinales de l'IMC-z. Des régressions logistiques multinomiales ont ensuite été utilisées pour examiner les associations entre les habitudes de vie durant l’enfance et les trajectoires d’adiposité, en ajustant l’âge, le sexe, les stades du développement pubertaire de Tanner et l’éducation parentale. Résultats principaux: Six trajectoires distinctes d’IMC-z ont été identifiées: Poids-Faible-à-Normal-Stable (5,7%), deux groupes de Poids-Normal-Stable qui ont ensuite été combinés (33,0% et 24,8%), Surpoids-Stable (19,8%), Obèse-Stable (8,8%) et Surpoids-Décroissants (7,9%). Pour chaque portion supplémentaire de fruits et légumes à 8-10 ans, la probabilité de faire partie du groupe en Surpoids-Décroissants est augmentée de 26% (OR 1,26, IC 95% 1,06-1,49) par rapport à ceux du groupe Poids-Normal-Stable. Pour chaque heure supplémentaire de comportement sédentaire mesurée par l'accéléromètre à 8-10 ans, la probabilité d'appartenir au groupe Surpoids-Décroissants est augmentée de 51% (OR 1,51, IC à 95% 1,03- 2,22) par rapport au groupe Poids-Normal-Stable. En termes d'activité physique, toutes les 10 minutes supplémentaires d'activité physique modérée à vigoureuse (APMV) au départ étaient associées à une probabilité plus faible d'appartenir au groupe Obèse-Stable (OR 0,75, IC à 95% 0,61-0,91) et Groupe Surpoids-Décroissants (OR 0,78, IC 95% 0,62-0,98) par rapport au groupe Poids-Normal-Stable. Importance: Cette étude a permis d’identifier différents groupes de trajectoires de développement du score IMC-z qui restent stables de l’enfance à la fin de l'adolescence ainsi qu’un groupe d’enfants qui sont passés d'un surpoids à un poids normal. Ces derniers avaient un apport alimentaire plus favorable en fruits et légumes à 8-10 ans. Cependant, ils avaient également une APMV inférieure et un comportement plus sédentaire comparativement au groupe de Poids-Normal-Stable.Background: Childhood obesity is a major risk factor for mortality and morbidity as children with obesity tend to remain obese into adulthood. Among Canadian children, 27 % have overweight or obesity, which is a serious public health concern. Objectives: The main objectives of my research are to (1) examine the associations between physical activity in pre-puberty or early puberty and obesity trajectories across childhood and adolescence; (2) examine the associations between sedentary behaviors in pre-puberty or early puberty and obesity trajectories across childhood and adolescence; and (3) to examine associations between dietary intake in pre-puberty or early puberty and obesity trajectories across childhood and adolescence. My hypothesis is that lower physical activity, more time spent in sedentary behaviours and unhealthy diets (e.g., higher sugar-sweetened beverage consumption, lower fruit and vegetable intake) in childhood (pre to early puberty) will be associated with adverse patterns of obesity into adolescence. Methods: This study uses data from the Quebec Adipose and Lifestyle Investigation in Youth (QUALITY) study. This cohort includes 630 Caucasian children aged 8-10 years, recruited at baseline based on a parental history of obesity. Of these, 377 were re-assessed at 10-12 years and at 15-17 years. Sedentary behavior and physical activity using 7-day accelerometry, self-reported screen time and dietary intake with three 24-hr diet recalls were measured. Weight and height were measured at each time period and transformed to body mass index (BMI) z-scores using WHO (World Health Organization) Standards. Group based trajectory modeling was used to identify longitudinal trajectories of z-BMI. Multinomial logistic regressions were used to examine associations between lifestyle behaviors at 8-10 years and distinct obesity trajectory groups, while adjusting for age, sex, tanner stage and parental education. Results: Six distinct z-BMI trajectory groups were identified: Stable-Low-Normal-Weight (5.7%), two Stable-Normal-Weight groups that were subsequently combined (33.0% and 24.8%), Stable-Overweight (19.8%), Stable-Obese (8.8%) and Overweight-Decreasers (7.9%). For every additional vegetable and fruit serving at baseline, the likelihood of being in the Overweight–Decreasers group increased by 26% (OR 1.26, 95% CI: 1.06, 1.49) compared to those in the Stable-Normal-Weight group. For every additional hour of sedentary behavior at baseline, the likelihood of belonging to the Overweight-Decreasers group increased by 51% (OR 1.51, 95% CI: 1.03, 2.22) as compared to Stable-Normal-Weight group. In terms of physical activity, every additional 10 mins of Moderate to Vigorous Physical Activity (MVPA) at baseline was associated with a lower likelihood of belonging to the Stable-Obese group (OR 0.75, 95% CI: 0.61, 0.91) and to the Overweight-Decreasers group (OR=0.78, 95% CI: 0.62, 0.98) compared to the Stable-Normal-Weight group. Conclusion: Stable trajectories of z-BMI from childhood to late adolescence were found, with the exception of one decreasing trajectory from overweight in childhood to normal weight in adolescence. The latter had more favourable dietary intake of fruits and vegetables at baseline, however, they also had lower MVPA and more sedentary behavior

Lipids, lipoprotein distribution and nutritional parameters over the ramadan period in hemodialysis patients

The period of Ramadan (R) is associated with dramatic changes in eating habits involving extended periods of fasting on a daily basis. The current study assessed whether lipids and lipoproteins were impacted during R in chronic hemodialysis (HD) patients. Forty-five subjects in an outpatient dialysis clinic in Saudi Arabia were evaluated for anthropometric and lipid changes on a monthly basis before, during as well as one and two months after R. In addition to routine biochemical measures, anthropometric assessments including hand-grip strength (HGS), mid-arm muscle circumference (MAMC), plasma lipids and lipoproteins were evaluated. Dietary assessment was carried out using 24 h recalls. Over the course of the study, changes in renal-related parameters (creatinine, albumin, Kt/V) were minor, as were changes in plasma lipids. Large high-density lipoproteins (HDLs) and low-density lipoproteins (LDLs) accounted for the majority of their respective lipoproteins and their proportions did not change over the study period. Mean LDL particle diameters were higher during the R period, but the changes over the study period were small. Calorie intake during R (2139 ± 709 kcal/d) was significantly higher than the value noted two month post-R (1755 ± 424 kcal/d) and this was associated with significant increases in protein (69 ± 24 vs. 60 ± 24 g/d) and fat (97 ± 38, vs. 73 ± 35 g/d), respectively. No changes were noted with respect to HGS and MAMC. These data show that for HD patients, the period of R results in temporal or non-significant effects on plasma lipids, despite changes in nutrient intake

MAO-B Elevation in Mouse Brain Astrocytes Results in Parkinson's Pathology

Age-related increases in monoamine oxidase B (MAO-B) may contribute to neurodegeneration associated with Parkinson's disease (PD). The MAO-B inhibitor deprenyl, a long-standing antiparkinsonian therapy, is currently used clinically in concert with the dopamine precursor L-DOPA. Clinical studies suggesting that deprenyl treatment alone is not protective against PD associated mortality were targeted to symptomatic patients. However, dopamine loss is at least 60% by the time PD is symptomatically detectable, therefore lack of effect of MAO-B inhibition in these patients does not negate a role for MAO-B in pre-symptomatic dopaminergic loss. In order to directly evaluate the role of age-related elevations in astroglial MAO-B in the early initiation or progression of PD, we created genetically engineered transgenic mice in which MAO-B levels could be specifically induced within astroglia in adult animals. Elevated astrocytic MAO-B mimicking age related increase resulted in specific, selective and progressive loss of dopaminergic neurons in the substantia nigra (SN), the same subset of neurons primarily impacted in the human condition. This was accompanied by other PD-related alterations including selective decreases in mitochondrial complex I activity and increased mitochondrial oxidative stress. Along with a global astrogliosis, we observed local microglial activation within the SN. These pathologies correlated with decreased locomotor activity. Importantly, these events occurred even in the absence of the PD-inducing neurotoxin MPTP. Our data demonstrates that elevation of murine astrocytic MAO-B by itself can induce several phenotypes of PD, signifying that MAO-B could be directly involved in multiple aspects of disease neuropathology. Mechanistically this may involve increases in membrane permeant H2O2 which can oxidize dopamine within dopaminergic neurons to dopaminochrome which, via interaction with mitochondrial complex I, can result in increased mitochondrial superoxide. Our inducible astrocytic MAO-B transgenic provides a novel model for exploring pathways involved in initiation and progression of several key features associated with PD pathology and for therapeutic drug testing