178 findings · Molecular · published 2022+
- MolecularStrong
Metabolic dysregulation is linked to ectopic fat deposition and alterations in immune cell populations in adipose tissue among PWH.
Understanding these links can help in developing targeted interventions for obesity in PWH.
Supports 2023 - MolecularStrong
Post-exercise changes in proteins reflective of protein synthesis were similar between groups, though some mRNA exhibited exercise order-dependent responses.
Understanding the molecular responses can help tailor exercise programs for optimal protein synthesis.
Qualifies 2023 - MolecularStrong
There is a surge of interest in unimolecular peptide hormone-based polypharmacy for obesity management.
Practitioners should stay informed about developments in peptide hormone therapies for obesity.
Supports 2022 - MolecularStrong
Excessive consumption of industrial seed oils rich in linoleic acid contributes to mitochondrial dysfunction.
Reducing intake of linoleic acid-rich oils may be beneficial for mitochondrial health.
Supports 2025New - MolecularStrong
GLP-1 receptor agonists and GLP-1/GIP biagonists reduce the expression of genes involved in lipogenesis in adipose tissue.
These drugs may help in managing fat storage by altering gene expression.
Supports 2024 - MolecularStrong
L-aspartate may serve as a novel endogenous inducer of energy expenditure and suppressor of adipogenesis and lipogenesis along with activation of AMPK.
L-aspartate could be explored as a therapeutic agent for enhancing energy expenditure and reducing fat accumulation.
Supports 2024 - MolecularStrong
Higher adipose tissue GIP receptor mRNA expression is related to elevated glycerol release after GIP and GLP-1/GIP/glucagon receptor triagonist stimulation.
Increased GIP receptor expression may enhance fat mobilization, suggesting a focus for obesity treatments.
Supports 2025New - MolecularStrong
The engineered GLP-1 receptor agonist depot offers a more convenient and long-lasting therapeutic option for managing diabetes and treating metabolic disorders.
This approach could simplify treatment regimens for patients with diabetes.
Supports 2024 - MolecularStrong
Higher genetic GLP1R gene expression is associated with a lower risk of kidney disease progression (HR, 0.96; P = .02).
Practitioners may consider the role of GLP1R gene expression in managing kidney disease risk.
Supports 2024 - MolecularStrong
Higher GLP1R gene expression is associated with a small reduction in risk of kidney disease progression in fully adjusted models (HR, 0.96; P = .04).
This suggests that monitoring GLP1R gene expression could be relevant in kidney disease management.
Supports 2024 - MolecularStrong
Nutrients play a multifaceted role in cardiovascular health beyond their impact on cardiac events.
Practitioners should consider the diverse roles of nutrients in promoting cardiovascular health.
Supports 2024 - MolecularStrong
Dietary supplements may contribute to CVD risk reduction.
Incorporating dietary supplements may be beneficial for individuals at risk of CVD.
Supports 2024 - MolecularStrong
BGM1812 is a novel dual amylin and calcitonin receptor agonist with enhanced efficacy compared to petrelintide.
BGM1812 may be a promising option for obesity treatment.
Supports 2025New - MolecularStrong
BGM1812 exhibits excellent performance in terms of half-life, stability, and solubility.
These properties suggest BGM1812 could be a viable therapeutic option.
Supports 2025New - MolecularStrong
The interaction between hyperglycemia, endothelial dysfunction, inflammation, and thrombosis contributes to the progression of coronary artery disease (CAD) and its acute complications.
Understanding these interactions can help in developing targeted therapies for CAD.
Supports 2025New - MolecularStrong
GLP-1 receptor agonist patients had significantly lower serum albumin (4.06 g/dL) and prealbumin levels (23.52 mg/dL) compared to controls (4.22 g/dL and 25.55 mg/dL, respectively).
Monitoring nutritional status, including serum albumin and prealbumin, may be important for patients on GLP-1 receptor agonists.
Supports 2025New - MolecularStrong
Rational protein engineering and delivery innovations transformed incretin biology into global metabolic therapeutics.
Innovations in protein engineering can enhance therapeutic efficacy.
Supports 2025New - MolecularStrong
Genetic variation within the leptin-melanocortin pathway may predict response to endoscopic interventions and guide personalized treatment selection.
Understanding genetic factors can help tailor obesity treatments to individual patients.
Supports 2025New - MolecularStrong
The study aims to understand the use of semaglutide for treating obesity and its pharmacological mechanism.
The study may provide insights into how semaglutide works, aiding in treatment decisions.
Supports 2022 - MolecularStrong
The use of nano-based medications through transdermal delivery is important for effective obesity treatment.
Practitioners should consider incorporating nano-based medications for better treatment outcomes.
Supports 2025New - MolecularStrong
Coconut oil and kernel flakes failed to induce favorable lipid changes comparable to coconut milk supplementation.
Coconut oil and kernel flakes may not be effective for improving lipid profiles compared to coconut milk.
Supports 2024 - MolecularStrong
The MC4R gene variant rs17782313 is directly associated with the risk of metabolic syndrome (MetS) in obese adults (B = 0.010; P = 0.023).
Genetic testing for the MC4R variant may help identify individuals at higher risk for metabolic syndrome.
Supports 2022 - MolecularStrong
Glycemic index (GI) and glycemic load (GL) mediate the relationship between the MC4R variant and LDL cholesterol (LDL-C) levels.
Dietary management focusing on GI and GL may help mitigate LDL-C levels in genetically susceptible individuals.
Supports 2022 - MolecularStrong
Mitochondrial uncoupling promotes energy dissipation and may serve as a strategy for obesity treatment.
Practitioners may consider mitochondrial uncoupling as a potential target for obesity interventions.
Supports 2025New