Clinical Factors and Biomarkers Associated with Depressive Disorders in Older Patients Affected by Chronic Kidney Disease (CKD): Does the Advanced Glycation End Products (AGEs)/RAGE (Receptor for AGEs) System Play Any Role?

Depressive disorders are highly prevalent among subjects suffering from chronic kidney disease (CKD). The aim of the present study is to evaluate clinical and biochemical factors associated with depressive disorders in a sample of older CKD patients, with a focus on advanced glycation end products (AGEs) and their soluble receptors (sRAGEs). A total of 115 older subjects affected by CKD (stages 3 to 5, not in dialysis) were selected for this study.

New Molecular Mechanisms and Markers in Inflammatory Disorders.

Inflammation is the primary response of different disorders, and these encompass a wide range of conditions in various tissues and organs [...

Circulating perturbation of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) is associated to cardiac remodeling and NLRP3 inflammasome in cardiovascular patients with insulin resistance risk.

Lipidome perturbation occurring during meta-inflammation is associated to left ventricle (LV) remodeling though the activation of the NLRP3 inflammasome, a key regulator of chronic inflammation in obesity-related disorders. Little is known about phosphatidylcholine (PC) and phosphatidylethanolamine (PE) as DAMP-induced NLRP3 inflammasome. Our study is aimed to evaluate if a systemic reduction of PC/PE molar ratio can affect NLRP3 plasma levels in cardiovascular disease (CVD) patients with insulin resistance (IR) risk.

DenRAM: neuromorphic dendritic architecture with RRAM for efficient temporal processing with delays.

An increasing number of studies are highlighting the importance of spatial dendritic branching in pyramidal neurons in the neocortex for supporting non-linear computation through localized synaptic integration. In particular, dendritic branches play a key role in temporal signal processing and feature detection. This is accomplished thanks to coincidence detection (CD) mechanisms enabled by the presence of synaptic delays that align temporally disparate inputs for effective integration.