Publications by authors named "Gennaro L"

Major depressive disorder (MDD) and Insomnia disorder (ID) are characterized by sleep alterations. To define their polysomnographic profiles, we conducted a Network Meta-Analysis comparing MDD and ID patients versus healthy controls (HCs). The literature search, conducted from 2008 up to January 2023 and following PRISMA guidelines, covered PubMed, Web of Science, Scopus, and Embase databases.

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The crab-eating macaques (Macaca fascicularis) and rhesus macaques (Macaca mulatta) are pivotal in biomedical and evolutionary research. However, their genomic complexity and interspecies genetic differences remain unclear. Here, we present a complete genome assembly of a crab-eating macaque, revealing 46% fewer segmental duplications and 3.

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Heart failure (HF) is a clinical syndrome with high morbidity and mortality, characterized by periods of relative clinical stability and exacerbations of HF, known as worsening heart failure (WHF). WHF is currently defined as a deterioration of HF signs and symptoms, necessitating an intensification of medical therapy, often identified by an increase in diuretic therapy. Episodes of WHF, whether they result in patient hospitalization or outpatient management, suggest clinical progression of HF with significant worsening of the prognosis.

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Fusion proteins constitute a class of engineered therapeutics and have emerged as promising candidates for disease treatment. However, the structural complexity and heterogeneity of fusion proteins make their characterization extremely challenging, and thus, an innovative and comprehensive analytical toolbox is needed. Here, for the first time, we demonstrate a novel and robust workflow to evaluate charge variants for a highly glycosylated fusion protein with heavy sialylation using imaged capillary isoelectric focusing (icIEF).

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Over the past decades, the number of therapeutic protein pipelines in early-phase clinical studies has increased dramatically. The rapid growth in the pipeline underscores the need to accelerate early-stage development and enable fast first-in-human (FIH) trials to bring novel therapies to patients. Across the industry, various efforts have been developed to achieve this goal.

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Insomnia disorder (ID) is characterized by electroencephalographic indexes of hyperarousal, often associated with the underestimation of sleep duration (i.e., sleep state misperception).

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The history of human populations has been strongly shaped by admixture events, contributing to patterns of observed genetic diversity across populations. In this study, we introduce the Principal component Ancestry proportions using NNLS Estimation (PANE) method that leverages principal component analysis and non-negative least squares to assess the ancestral compositions of admixed individuals given a large set of populations. Our results show its ability to reliably estimate ancestry across several scenarios, even those with a significant proportion of missing genotypes, in a fraction of the time required when using other tools.

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Introduction: Brain and sleep development in childhood shapes emotional and cognitive growth, including the ability to recall dreams. In line with the continuity hypothesis of dreaming, several findings suggest a link between clinical symptoms and nightmare frequency. Sleep disorders and anxiety are among the most frequently co-occurring conditions in children and adolescents with autism spectrum disorder (ASD).

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The aim of the present study is to investigate differences in brain networks modulation during the pre- and post-sleep onset period, both within and between two groups of young and older individuals. Thirty-six healthy elderly and 40 young subjects participated. EEG signals were recorded during pre- and post-sleep onset periods and functional connectivity analysis, specifically focusing on the small world (SW) index, applied to EEG data (i.

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Mineralocorticoid receptor antagonists (MRAs) represent one of the cornerstones of treatment for heart failure with reduced ejection fraction. Post-hoc data from the TOPCAT trial, conducted in patients with heart failure mildly reduced or preserved ejection fraction (HFmrEF/HFpEF), suggest the possible clinical benefit of MRAs, particularly for slightly reduced ejection fraction values. The advent of non-steroidal MRAs, including finerenone, seems to represent a turning point in the treatment for HFmrEF/HFpEF.

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Article Synopsis
  • - The study explores how pregnancy-related factors, emotional awareness (alexithymia), and depression impact dream experiences in women during their first trimester, suggesting that dreaming helps with emotional regulation during this sensitive period.
  • - 118 pregnant women participated in various questionnaires measuring their dream characteristics, emotional awareness, and depression, revealing that older age, prior pregnancies, and depressive symptoms influenced dream recall and nightmares.
  • - Findings indicate that higher alexithymia and depressive symptoms are linked to more frequent and distressing nightmares, suggesting a need for targeted support to improve emotional coping strategies in pregnant women; future studies should look into the content of these nightmares for better understanding.
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Background: Early reconstruction of the skull represents the gold standard after resection of bone infiltrating cranial tumors. Customized hydroxyapatite porous ceramics are an excellent option for covering skull bone defects. The authors illustrate the surgical technique and investigate the effectiveness of the "one-step" procedure in terms of aesthetic results and early degree of osteointegration.

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Background: The Italic Iron Age is characterized by the presence of various ethnic groups partially examined from a genomic perspective. To explore the evolution of Iron Age Italic populations and the genetic impact of Romanization, we focus on the Picenes, one of the most fascinating pre-Roman civilizations, who flourished on the Middle Adriatic side of Central Italy between the 9 and the 3 century BCE, until the Roman colonization.

Results: More than 50 samples are reported, spanning more than 1000 years of history from the Iron Age to Late Antiquity.

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Haemophilia is associated with reduced bone mass and mineral density. Due to the rarity of the disease and the heterogeneity among the studies, the pathogenesis of bone loss is still under investigation. We studied the effects of coagulation factors on bone cells and characterized in a pilot study the osteoclastogenic potential of patients' osteoclast precursors.

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Article Synopsis
  • Disorders of sexual development (DSDs) in dogs, especially prevalent in French Bulldogs, stem from genetic issues and breeding practices affecting genetic diversity.
  • A study on a French Bulldog with ambiguous genitalia utilized advanced genetic techniques and identified a potential connection to a known mutation linked to sex reversal syndrome, along with unusual genetic variants.
  • The results emphasize a higher level of homozygosity in the affected dog, suggesting inbreeding, and call for improved dog genome annotations and responsible breeding practices to manage genetic health.
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Study Objectives: Obstructive sleep apnea is considered a risk factor for sleepiness at the wheel and near-miss accidents (NMA). To date, there are subjective and objective methods such as the Maintenance of Wakefulness Test (MWT) to investigate sleepiness. However, these methods have limitations.

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Article Synopsis
  • Charge heterogeneity is essential for the quality of therapeutics like antibody-drug conjugates (ADCs), but creating effective methods for high drug-to-antibody ratios (DAR) is difficult due to increased complexity.
  • The study focuses on optimizing imaged capillary isoelectric focusing (icIEF) methods by analyzing various parameters such as solubilizers and focusing time to improve resolution and stability for high DAR ADCs.
  • This research is the first thorough investigation into icIEF method development for charge variant assessment in high DAR ADCs, offering valuable insights into their unique properties.
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  • The study presents detailed genomes of six ape species, achieving high accuracy and complete sequencing of all their chromosomes.
  • It addresses complex genomic regions, leading to enhanced understanding of evolutionary relationships among these species.
  • The findings will serve as a crucial resource for future research on human evolution and our closest ape relatives.
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  • - The study investigates Sleep State Misperception (SSM) in Insomnia Disorder (ID) patients, who tend to misjudge their sleep latency (how long it takes to fall asleep) and total sleep time compared to healthy individuals.
  • - The research involved twenty ID patients and eighteen healthy controls undergoing polysomnography (PSG) and analyzing their sleep diaries, with a focus on alterations in brain wave patterns during sleep onset and throughout the night.
  • - Results indicated significant differences in brain wave activity, with ID patients showing a low delta/beta ratio and distinctive power changes in certain brain regions, suggesting a relationship between sleep misperception and altered sleep EEG topography.
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  • The study analyzed sleep disturbances in 242 children and adolescents with Autism Spectrum Disorder (ASD) to identify predictors of sleep disorders and explore co-sleeping behaviors.
  • Approximately 33% of participants showed clinically relevant sleep disorders, with the most common issues related to difficulty falling and staying asleep.
  • Results indicated that higher IQ/DQ, internalizing problems, and parental stress contributed to sleep disturbances, while co-sleeping children tended to be younger with lower IQ/DQ scores and reduced well-being compared to non-co-sleepers.
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Article Synopsis
  • * It discusses how new research has shifted towards understanding the brain's activity related to dreams, revealing inconsistencies in traditional models of dream recall and highlighting emotions and social simulations in dreams during stressful times.
  • * The summary emphasizes that dreaming is a complex process involving different brain regions and serves various purposes, from reflecting real-life experiences to preparing for future challenges, indicating the need for more research in this area.
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Background: Dissection of genotype-phenotype relationships in hemophilia B (HB) is particularly relevant for challenging (mild HB) or for HB-associated but unclassified factor (F)IX missense variants.

Objective: To contribute elements to interpret unclassified HB-associated FIX missense variants by a multiple-level approach upon identification of a reported, but uncharacterized, FIX missense variant associated with mild HB.

Methods: Molecular modeling of wild-type and V92A FIX variants, expression studies in HEK293 cells with evaluation of protein (ELISA, western blotting) and activity (activated partial thromboplastin time-based/chromogenic assays) levels after recombinant expression, and multiple prediction tools.

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We investigated if children with Long Covid (n=14) have activated platelets compared with healthy controls (n=14). Platelet activation and secretion markers were investigated by flow cytometry using MoAbs directed against P-selectin, CD63, and PAC-1 in quiescent platelets and in platelets stimulated with 10-µM adenosine diphosphate and 25-µM protease activated receptor 1-activating peptide. Circulating platelets of patients with Long Covid had significantly increased expression of the activation marker cytometry using MoAbs directed against P-selectin (P = 0.

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