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: The aim of this secondary analysis is to determine the baseline characteristics that are associated with a higher likelihood of weight-loss success in a personalized nutrition intervention. : Data were analyzed in adults with abnormal glucose metabolism and obesity from a 6-month behavioral counseling randomized clinical trial. Participants were randomized to two calorie-restricted diets: a low-fat diet () or a personalized nutrition diet leveraging a machine learning algorithm (). The gradient boosting machine method was used to determine the baseline variables (i.e., age, weight-loss self-efficacy) that predicted successful weight loss (≥5%) at 6 months in each study arm separately, using repeated five-fold cross-validation with 100 repetitions. : A total of 155 participants (: n = 84 vs. : n = 71) contributed data (mean [standard deviation]: age, 59 [10] y; 66.5% female; 56.1% White; body mass index (BMI), 33.4 [4.6] kg/m). In both arms, higher baseline self-efficacy for weight loss was a predictor of weight-loss success. Participants with a higher BMI ( < 0.0001) in the arm and those who were older ( < 0.0001) in the arm were more likely to achieve successful weight loss. : Future weight-loss interventions may consider providing tailored behavioral support for individuals based on weight-loss self-efficacy, BMI, and age.
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http://dx.doi.org/10.3390/nu17132178 | DOI Listing |
Cureus
August 2025
Department of Internal Medicine, Local Health Unit of Santa Maria, Lisbon, PRT.
Polyarteritis nodosa (PAN) rarely affects both intracranial and mesenteric arteries. Evidence on optimal timing of revascularisation and the role of interleukin-6 blockade remains limited. A 73-year-old man with longstanding ankylosing spondylitis presented with weight loss and elevated inflammatory markers.
View Article and Find Full Text PDFJ Metab Bariatr Surg
August 2025
Division of Gastrointestinal Surgery, Department of Surgery, Seoul National University Hospital, Seoul, Korea.
Prader-Willi Syndrome (PWS) is a genetic disorder characterized by insatiable hyperphagia, resulting in severe, early-onset obesity that is often refractory to conventional management. The associated comorbidities and reduced life expectancy in PWS present a significant therapeutic challenge. This review synthesizes the existing literature on the controversial role, outcomes, and complexities of bariatric surgery in patients with PWS.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China. Electronic address:
Environmentally friendly food packaging has emerged as a viable strategy to replace traditional plastic films. In this study, eugenol Pickering emulsion was constructed with konjac glucomannan (KGM) and tragacanth gum (GT) as stabilizers, and was introduced into the KGM/chitosan (CS) composite film by electrostatic action to develop a new type of active packaging film. Interfacial characterization revealed optimal emulsion stability at a 1:5 KGM-to-GT mass ratio.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
School of Biosciences, Mahatma Gandhi University, Kottayam, Kerala 686560, India. Electronic address:
This study presents the design and functional evaluation of a biodegradable nanocomposite film (CPZG) composed of chitosan, polyvinyl alcohol (PVA), zinc oxide nanoparticles (ZnONPs), and garlic extract (GE) for active fish packaging. The film was fabricated via solvent casting and characterized using FTIR, SEM, XPS, and EDX, confirming successful molecular-level integration and uniform dispersion of ZnONPs and phytochemicals. GC-MS profiling revealed key organosulfur compounds such as diallyl disulfide and allyl trisulfide, with evidence of both sustained release and long-term retention within the polymer matrix.
View Article and Find Full Text PDFJIMD Rep
September 2025
Manchester Centre for Genomic Medicine, St Mary's Hospital Manchester University NHS Foundation Trust, Health Innovation Manchester Manchester UK.
We report the case of an 11-year-old girl who developed hepatopulmonary syndrome (HPS) as a rare complication of Zellweger spectrum disorder and was successfully treated with liver transplantation. Our patient presented with neonatal sensorineural hearing loss. Muscular hypotonia, global developmental delay, and pigmentary retinopathy in infancy led to a diagnosis of peroxisomal biogenesis disorder due to compound heterozygous variants.
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