10-Year Comparative Follow-up of Familial versus Multifactorial Chylomicronemia Syndromes

J Clin Endocrinol Metab. 2021 Mar 8;106(3):e1332-e1342. doi: 10.1210/clinem/dgaa838.

Abstract

Context: The relative incidence of acute pancreatitis, ischemic cardiovascular disease, and diabetes in hyperchylomicronemic patients exhibiting familial chylomicronemia syndrome (FCS) or multifactorial chylomicronemia syndrome (MCS) is unknown.

Objective: The objective was to study the occurrence of these events in FCS and MCS patients compared with the general population.

Methods: Twenty-nine FCS and 124 MCS patients, with genetic diagnosis, in 4 lipid clinics were matched with 413 controls. Individual hospital data linked to the national claims database were collected between 2006 and 2016. The occurrence of complications was retrospectively assessed before follow-up and during a median follow-up time of 9.8 years, for 1500 patient years of follow-up.

Results: Patients with FCS were younger than those with MCS (34.3 ± 13.6 vs 45.2 ± 12.6 years, P < 0.01). During the study period, 58.6% of the FCS patients versus 19.4% of the MCS patients had at least 1 episode of acute hypertriglyceridemic pancreatitis (AHP) (hazard ratio [HR] = 3.6; P < 0.01). Conversely, the ischemic risk was lower in FCS than in MCS (HR = 0.3; P = 0.05). The risk of venous thrombosis was similar in both groups. The incidence of diabetes was high in both groups compared with matched controls (odds ratio [OR] = 22.8; P < 0.01 in FCS and OR = 30.3; P < 0.01 in MCS).

Conclusion: The incidence of AHP was much higher in FCS than in MCS patients, whereas the incidence of ischemic cardiovascular events was found to be increased in MCS versus FCS patients and a representative matched control group. Differences in both triglyceride-rich lipoproteins metabolism and comorbidities in MCS versus FCS drive the occurrence of different patterns of complications.

Trial registration: ClinicalTrials.gov NCT03912181.

Keywords: diabetes; hyperchylomicronemia; ischemic cardiovascular events; pancreatitis.

Publication types

  • Multicenter Study
  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • DNA Mutational Analysis
  • Female
  • Follow-Up Studies
  • France / epidemiology
  • Genetic Predisposition to Disease / epidemiology
  • Humans
  • Hyperlipoproteinemia Type I / classification
  • Hyperlipoproteinemia Type I / diagnosis
  • Hyperlipoproteinemia Type I / epidemiology*
  • Hyperlipoproteinemia Type I / etiology*
  • Male
  • Middle Aged
  • Prognosis
  • Retrospective Studies
  • Risk Factors
  • Syndrome
  • Time Factors
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT03912181