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Correspondence to Author: Elesis Vaass,
Lipids, Nutrition, and Cardiovascular Prevention Clinic of the Montreal Clinical Research Institute, 110 avenue des Pins Ouest, Montreal, Québec, Canada, H2W 1R7.
ABSTRACT:
Context : Apolipoprotein E malfunction caused by a genetic
mutation in combination with other metabolic variables
results in residual lipoproteins building up in the plasma,
a condition known as dysbetalipoproteinemia (DBL). An
elevated risk of peripheral vascular disease and coronary
heart disease (PVD) has been noted in these patients in
research conducted in the past.
Comparing the incidence of PVD and atherosclerotic
cardiovascular disease (ASCVD) in a cohort of patients with
DBL to normolipidemic controls was the main goal of the
study. The incidence of PVD and ASCVD was compared
between individuals with familial hypercholesterolemia (FH)
and patients with DBL as a secondary goal.
Methods : The study comprised 1481 normolipidemic
controls, 725 patients with FH, and 221 patients with DBL.
Medical records were examined in order to gather the data.
Results : Compared to normolipidemic controls, patients
with DBL had an overall increased risk of PVD (hazard ratio
[HR] 13.58, 95% CI 4.76-38.75) and ASCVD (HR 3.55, 95% CI
2.17-5.83) (P.0001). Patients with DBL showed an elevated
risk of PVD (HR 3.89, 95% CI 1.20-12.55, P=.02) in comparison
to those with FH.
conclusion : we showed that compared to normolipidemic
controls, DBL patients have >3-fold and >13-fold greater
risks of ASCVD and PVD, respectively. Moreover, DBL has a
roughly 4-fold higher risk of PVD than FH. In order to enhance
the clinical management of these patients by halting the
progression of ASCVD, adequate DBL screening is essential.
Citation:
Elesis Vaass. An Increased Risk of Coronary and Peripheral Vascular Disease Is Associated With Dysbetalipoproteinemia. Journal of Clinical Endocrinology and Metabolism 2024.
Journal Info
- Journal Name: Journal of Clinical Endocrinology and Metabolism
- Impact Factor: 1.9
- ISSN: 2998-9213
- DOI: 10.52338/jocem
- Short Name: JOCEM
- Acceptance rate: 55%
- Volume: 7 (2024)
- Submission to acceptance: 25 days
- Acceptance to publication: 10 days
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