Objective: The aim of this study was to test proportional-integral-derivative (PID) control of air inflow rate in a whole-room indirect calorimeter to improve accuracy in measuring oxygen (O ) consumption ( ) and carbon dioxide (CO ) production ( ).
Methods: A precision gas blender infused nitrogen (N ) and CO into the calorimeter over 24 hours based on static and dynamic infusion profiles mimicking and patterns during resting and non-resting conditions. Constant (60 L/min) versus time-variant flow set by a PID controller based on the CO concentration was compared based on errors between measured versus expected values for respiratory exchange ratio, and metabolic rate.
Results: Compared with constant inflow, the PID controller allowed both a faster rise time and long-term maintenance of a stable CO concentration inside the calorimeter, resulting in more accurate estimates (mean hourly error, PID: -0.9%, 60 L/min = -2.3%, p < 0.05) during static infusions. During dynamic infusions mimicking exercise sessions, the PID controller achieved smaller errors for (mean: -0.6% vs. -2.7%, p = 0.02) and respiratory exchange ratio (mean: 0.5% vs. -3.1%, p = 0.02) compared with constant inflow conditions, with similar (p = 0.97) and metabolic rate (p = 0.76) errors.
Conclusions: PID control in a whole-room indirect calorimeter system leads to more accurate measurements of substrate oxidation during dynamic metabolic studies.
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http://dx.doi.org/10.1002/oby.23683 | DOI Listing |
Food Environ Virol
January 2025
Ōmura Satoshi Memorial Institute, Kitasato University, 5-9-1 Shirokane, Minato-Ku, Tokyo, 108-8641, Japan.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza A virus are primarily transmitted through droplets or aerosols from patients. The inactivation effects of existing virus control techniques may vary depending on the environmental factors. Therefore, it is important to establish a suitable evaluation system for assessing virus control techniques against airborne viruses for further real-world implementation.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Stanford University, Stanford, CA, USA.
Background: APOE*4 is the strongest genetic risk for late-onset Alzheimer's disease (AD), but other genetic loci may counter its detrimental effect, providing therapeutic avenues. Expanding beyond non-Hispanic White subjects, we sought to additionally leverage genetic data from non-Hispanic and Hispanic subjects of admixed African ancestry to perform trans-ancestry APOE*4-stratified GWAS, anticipating that allele frequency differences across populations would boost power for gene discovery.
Method: Participants were ages 60+, of European (EU; ≥75%) or admixed African (AFR; ≥25%) ancestry, and diagnosed as cases or controls.
J Air Waste Manag Assoc
January 2025
Center for Applied Climate Sciences, University of Southern Queensland, Toowoomba, Australia.
Densification of biomass through pelletizing offers a promising approach to producing clean biofuels from renewable resources. This study, which investigates the impact of additive blends on wheat straw pellet making and upgrading the physiochemical properties, has revealed exciting possibilities. Five additives, including sawdust (SD), bentonite clay (BC), corn starch (S), crude glycerol (CG), and biochar (BioC), were chosen for this study.
View Article and Find Full Text PDFBackground: There is a strong genetic component to Alzheimer's disease (AD), as evidenced in genome-wide association studies (GWASs) that have identified new variants associated with the disease. This is particularly true for the apolipoprotein E (APOE) gene and its neighboring genes on chromosome 19q13.3.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
Background: Several studies have indicated sex-specific genetic risk for Alzheimer's disease (AD), but these were centered on non-Hispanic White individuals of European ancestry. We sought to identify sex-specific genetic variants for AD in non-Hispanic and Hispanic subjects of admixed African ancestry.
Method: Participants were ages 60+, of African ancestry (≥25%), and diagnosed as cases or controls.
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