Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN Registry.

Arteriosclerosis, thrombosis, and vascular biology - 1 Dec 2025

D'Erasmo Laura, Tramontano Daniele, Di Costanzo Alessia, Casula Manuela, Galimberti Federica, Baratta Francesco, Cefalù Angelo Baldassare, Tarugi Patrizia Maria, Calandra Sebastiano, Zambon Alberto, Averna Maurizio, Catapano Alberico Luigi, Arca Marcello

Abstract excerpt

BACKGROUND: We aimed to compare the molecular and clinical characteristics of patients identified in Italy as affected by either familial chylomicronemia syndrome (FCS) or multifactorial chylomicronemia syndrome (MCS) and to assess the overall benefit of novel triglyceride-lowering therapies prescribed to these patients within the routine clinical care. METHODS: From the national LIPIGEN-sHTG (Lipid Transport...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Apolipoprotein A-V
Share to Hyperlipoproteinemia Type I

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypolipidemic Agents

Share to Lipoprotein Lipase

Share to Oligonucleotides

Share to Receptors, Lipoprotein

Share to Registries

Share to Triglycerides

Source

Open in PubMed Open full text

Identifiers

PMID: 41099101
DOI: 10.1161/ATVBAHA.125.323340
PMCID: PMC12643564

Genes

LPL
APOA5
GPD1
GPIHBP1
LMF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN Registry.PMID 41099101Read ↗

Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia SyndromesSemantic proximity Read ↗

Clinical identification of familial chylomicronemia syndrome and novel therapeutic options.Semantic proximity Read ↗

Comprehensive analysis of Chinese patients with non-LPL familial chylomicronemia syndrome: Genetic variants, dietary interventions, and clinical insights.Semantic proximity Read ↗

Rare Variants in Triglycerides-Related Genes Increase Pancreatitis Risk in Multifactorial Chylomicronemia Syndrome.Semantic proximity Read ↗

Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.Semantic proximity Read ↗

Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score".Semantic proximity Read ↗

Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE.Semantic proximity Read ↗

Understanding Hypertriglyceridemia: Integrating Genetic InsightsSemantic proximity Read ↗

Molecular and functional characterization of familial chylomicronemia syndrome.Semantic proximity Read ↗

Familial Chylomicronemia Syndrome (FCS): Recent Data on Diagnosis and Treatment.Semantic proximity Read ↗

Causes, clinical findings and therapeutic options in chylomicronemia syndrome, a special form of hypertriglyceridemia.Semantic proximity Read ↗

Assessment of Pediatric Hypertriglyceridemia Etiology: Insights from Next-Generation Sequencing Panels and Identification of Novel Variants.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.