HDL cholesterol efflux capacity and cholesterol loading capacity in long-term fasting: Evidence from a prospective, single-arm interventional study in healthy individuals

Atherosclerosis. 2024 Oct:397:118548. doi: 10.1016/j.atherosclerosis.2024.118548. Epub 2024 Aug 6.

Abstract

Background and aims: Long-term fasting (LF) is increasingly emerging as a non-pharmacological approach to modulate risk factors associated with the development of atherosclerotic cardiovascular diseases (ASCVD). However, protection from ASCVD is more tied to the functionality of high-density lipoprotein (HDL) than its plasma levels. Our prospective interventional study focuses on the functional properties of lipoproteins in modulating cholesterol homeostasis on peripheral cells and examines how LF may influence this and lipoprotein subclass composition. For that purpose, we investigated its impact on HDL-cholesterol efflux capacity (CEC), and on serum cholesterol loading capacity (CLC).

Methods: Forty healthy subjects (50 % females) underwent medically supervised 9-day fasting (250 kcal/day) in a specialised facility. Thirty-two subjects had a follow-up examination after one month of food reintroduction.

Results: LF was well tolerated and increased self-reported energy levels. Fasting reduced triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and HDL cholesterol (HDL-C). Very-low-density lipoprotein cholesterol (VLDL-C) and LDL3-C showed sustained reductions at follow-up. Only HDL-C, specifically HDL2-C levels, increased at follow-up. Total HDL-CEC decreased during LF and increased above baseline at follow-up. Fasting decreased ATP binding cassette (ABC)A1-mediated HDL-CEC whereas ABCG1-mediated HDL-CEC remained unaffected. Aqueous diffusion increased at follow up. LF decreased serum CLC and then returned to baseline levels.

Conclusions: LF not only maintains lipoprotein functionality but also contributes to a favorable shift in the atherogenic risk profile, which persists even after food reintroduction. This further emphasizes the importance of considering HDL functionality alongside traditional lipid measurements to understand the potential for non-pharmacological interventions like LF to promote cardiovascular prevention and health.

Trial registration number: NCT05031598.

Keywords: Cardiovascular health; Cholesterol loading capacity; HDL efflux capacity; Lipoprotein subclasses; Prolonged fasting; Weight loss.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 1 / metabolism
  • Adult
  • Atherosclerosis / blood
  • Atherosclerosis / prevention & control
  • Biomarkers / blood
  • Cholesterol / blood
  • Cholesterol, HDL* / blood
  • Fasting* / blood
  • Female
  • Healthy Volunteers*
  • Humans
  • Male
  • Middle Aged
  • Prospective Studies
  • Time Factors
  • Young Adult

Substances

  • ATP Binding Cassette Transporter, Subfamily G, Member 1
  • Biomarkers
  • Cholesterol
  • Cholesterol, HDL

Associated data

  • ClinicalTrials.gov/NCT05031598