Dysbetalipoproteinemia: differentiating multifactorial remnant cholesterol disease from genetic apoE deficiency.
Martine PaquetteSophie BernardGuillaume ParéAlexis BaassPublished in: The Journal of clinical endocrinology and metabolism (2021)
In the largest cohort of DBL worldwide, we demonstrated that the presence of E2/E2 was associated with a more severe DBL phenotype. We suggest that two dysbetalipoproteinemia phenotypes should be distinguished: the multifactorial remnant cholesterol disease and the genetic apoE deficiency disease.