👤 Lindsay Master

To compare components of the 24-hour movement behaviors (physical activity, sedentary behavior, sleep) across sex and race/ethnic groups among a diverse sample of adolescents to identity potential gaps and opportunities for intervention. The sample consisted of 704 adolescents (15.4 ± 0.6 years; 51% Black; 53% female) from year 15 of the Future of Families and Child Wellbeing Study. Twenty-four-hour movement behaviors were measured over a week-long period using waist- and wrist-worn accelerometry. Sex, racial, and ethnic differences in 24-hour movement behaviors were examined with chi-square and t-test analyses. Female adolescents, on average, spent less time in light physical activity (LPA) and in moderate-to-vigorous physical activity (MVPA) than male adolescents. Additionally, female adolescents spent more time in sedentary behavior and had longer daily total sleep time than adolescent males. Black adolescents had higher average LPA than White adolescents. Black adolescents also had higher average MVPA and LPA than Hispanic/Latino adolescents. Hispanic/Latino youth had longer total sleep time, and more sedentary time than Black youth. No other significant differences were observed across these demographic groups. There is a continued need for interventions to promote physical activity and sleep among adolescents, with a particular focus on increasing sleep duration among boys and physical activity among girls and Hispanic/Latino adolescents. Show less

Proteins involved in mitochondrial metabolic pathways engage in functionally relevant multi-enzyme complexes. We previously described an interaction between short-chain 3-hydroxyacyl-coenzyme A dehydrogenase (SCHAD) and glutamate dehydrogenase (GDH) explaining the clinical phenotype of hyperinsulinism in SCHAD-deficient patients and adding SCHAD to the list of mitochondrial proteins capable of forming functional, multi-pathway complexes. In this work, we provide evidence of SCHAD's involvement in additional interactions forming tissue-specific metabolic super complexes involving both membrane-associated and matrix-dwelling enzymes and spanning multiple metabolic pathways. As an example, in murine liver, we find SCHAD interaction with aspartate transaminase (AST) and GDH from amino acid metabolic pathways, carbamoyl phosphate synthase I (CPS-1) from ureagenesis, other fatty acid oxidation and ketogenesis enzymes and fructose-bisphosphate aldolase, an extra-mitochondrial enzyme of the glycolytic pathway. Most of the interactions appear to be independent of SCHAD's role in the penultimate step of fatty acid oxidation suggesting an organizational, structural or non-enzymatic role for the SCHAD protein. Show less