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JCL Roundtable: European perspective on comprehensive lipid management and cardiovascular health
Triglycerides and Remnant Cholesterol Need More Focus:The discussion highlighted the need for more potent therapies target...
Meta-analysis: Lipids, Vascular Function, Cardio-Cerebrovascular Events after Previous Kawasaki Disease in Children
Kawasaki disease (KD) is an acute multisystem vasculitis that is the leading cause of acquired heart disease in children i...
SEX DIFFERENCES IN INFLAMMATORY BIOMARKERS DURING LONG-TERM EVOLOCUMAB THERAPY
Introduction and objectivesAtherosclerotic cardiovascular disease remains a predominant cause of morbidity and mortality w...
DHCR24-Related Desmosterolosis in the First Reported Turkish Patient: Expanding the Genotypic and Phenotypic Spectrum
Desmosterolosis (OMIM #602398) is a ultra-rare autosomal recessive disorder characterized by multiple congenital anomalies...
Response to letter to the editor by Matsubara and colleagues
Available online 27 November 2025Author links open overlay panel, , , Section snippetsUse of AI and AI-assisted technologi...
Improvement of severe hypertriglyceridaemia in atypical subtype 4 partial lipodystrophy with volanesorsen
Lipodystrophy is a rare metabolic disorder resulting from adipose tissue abnormalities. Lipodystrophy can be divided by ae...
Sequencing and Functional Characterization of SCARB1 Variants in subjects with Extreme HDL cholesterol levels
Available online 1 December 2025Author links open overlay panel, , , , , , , , Highlights•SCARB1 was sequenced in 96 extre...
Lipoprotein(a) at the Crossroads of Inflammation and Atherosclerosis in Rheumatoid Arthritis: A Narrative Review
Rheumatoid arthritis (RA; Table 1) is a chronic systemic autoimmune disorder primarily affecting synovial joints, characte...
Examining Barriers and Facilitators to Testing Lipoprotein (a): Understanding At-Risk Individual and Clinician Perspectives
Objective: Lipoprotein(a), or Lp(a), is a significant risk factor for cardiovascular disease, yet is infrequently measured...
Severe Hypercholesterolemia in a Pediatric Cohort: Familial Homozygous and Autosomal Recessive Hypercholesterolemia
Familial hypercholesterolemia (FH) arises from variants in genes critical to the receptor-mediated removal of low-density ...
Gender Differences in Lipid Management, LDL-C Goal Attainment, and Prescribing Practices
Cardiovascular disease (CVD) is the leading cause of death in men and women worldwide. Meta-analyses of the Cholesterol Tr...
Developing a national implementation strategy for enhancing the detection of familial hypercholesterolemia: An Australian experience
Available online 20 March 2025Author links open overlay panel, , , , , , , , , , , , , , , , , , , Highlights•Developed a ...
Prevention of Acute Systemic Reaction During LDL apheresis post COVID-19 by Icatibant Pre-Treatment
Familial hypercholesteremia (FH) is a genetic disorder that is due to LDLR, APOB, and PCSK9 gene mutations resulting in ve...
IS TANGIER DISEASE A RARE CAUSE OF PREMATURE OVARIAN INSUFFICIENCY? – A CASE REPORT
Tangier disease (TD) is a rare inherited disorder of lipoprotein metabolism, characterised by the accumulation of choleste...
Familial chylomicronemia syndrome: An expert clinical review from the National Lipid Association
Familial chylomicronemia syndrome (FCS) is a rare Mendelian autosomal recessive disorder (MIM 238600) characterized by ext...
Triglyceride-rich lipoprotein sphingolipids are altered in primary hypertension: A pilot case-control study
Available online 26 March 2025Author links open overlay panel, , , , , , , , , , , Highlights•Patients with primary hypert...
Epidemiology and longitudinal course of chylomicronemia: Insights from NHANES and a large health care system
BACKGROUNDChylomicronemia is characterized by fasting triglyceride (TG) ≥1000 mg/dL; its longitudinal course is not well s...