DataSheet_1_The causal association between circulating cytokines with the risk of frailty and sarcopenia under the perspective of geroscience.zip

IntroductionCirculating cytokines were considered to play a critical role in the initiation and propagation of sarcopenia and frailty from observational studies. This study aimed to find the casual association between circulating cytokines and sarcopenia and frailty from a genetic perspective by two-sample Mendelian randomization (MR) analysis.MethodsData for 41 circulating cytokines were extracted from the genome-wide association study dataset of 8,293 European participants. Inverse-variance weighted (IVW) method, MR-Egger, and weighted median method were applied to assess the relationship of circulating cytokines with the risk of aging-related syndromes and frailty. Furthermore, MR-Egger regression was used to indicate the directional pleiotropy, and Cochran’s Q test was used to verify the potential heterogeneity. The “leave-one-out” method was applied to visualize whether there was a causal relationship affected by only one anomalous single-nucleotide polymorphisms.ResultsGenetic predisposition to increasing levels of interleukin-10 (IL-10), IL-12, and vascular endothelial growth factor (VEGF) was associated with the higher risk of low hand grip strength according to the IVW method [R = 1.05, 95% CI = 1.01–1.10, P = 0.028, false discovery rate (FDR)–adjusted P = 1.000; OR = 1.03, 95% CI = 1.00–1.07, P = 0.042, FDR-adjusted P = 0.784; OR = 1.02, 95% CI = 1.00–1.05, P = 0.038, FDR-adjusted P = 0.567]. Furthermore, genetically determined higher macrophage colony-stimulating factors (M-CSFs) were associated with a lower presence of appendicular lean mass (OR = 1.01, 95% CI = 1.00–1.02, P = 0.003, FDR-adjusted P = 0.103). Monokine induced by interferon-γ (MIG) and tumor necrosis factor–beta (TNF-β) were associated with a higher risk of frailty (OR = 1.03, 95% CI = 1.01–1.05, P ConclusionGenetic predisposition to assess IL-10, IL-12, and VEGF levels was associated with a higher risk of low hand grip strength and M-CSF with the presence of appendicular lean mass. The high levels of TNF-β and MIG were associated with a higher risk of frailty. More studies will be required to explore the molecular biological mechanisms underlying the action of inflammatory factors.</p

Supported Cu/Ni Bimetallic Cluster Electrocatalysts Boost CO₂ Reduction

Supported metal clusters with the integrated advantages of single-atom catalysts and conventional nanoparticles held great promise in the electrocatalytic carbon dioxide reduction (ECO2R) operated at low overpotential and high current density. However, its precise synthesis and the understanding of synergistically catalytic effects remain challenging. Herein, we report a facile method to synthesize the bimetallic Cu and Ni clusters anchored on porous carbon (Cu/Ni–NC) and achieve an enhanced ECO2R. The aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and synchrotron X-ray absorption spectroscopy were employed to verify the metal dispersion and the coordination of Cu/Ni clusters on NC. As a result of this route, the target Cu/Ni–NC exhibits excellent electrocatalytic performance including a stable 30 h electrolysis at 200 mA cm–2 with carbon monoxide Faradaic efficiency of ∼95.1% using a membrane electrode assembly electrolysis cell. Combined with the in situ analysis of the surface-enhanced Fourier transform infrared spectroelectrochemistry, we propose that the synergistic effects between Ni and Cu can effectively promote the H2O dissociation, thereby accelerate the hydrogenation of CO2 to *COOH and the overall reaction process