Diurnal and acute patterns of postprandial apolipoprotein B-48 in VLDL, IDL, and LDL from normolipidemic humans.
Abstract
Smaller size particles of intestinal origin may be more relevant to atherosclerosis than larger particles because of easier transendothelial transport. We examined the diurnal pattern in response to low-fat high-carbohydrate meals and the effect of a single high-fat milkshake on apoB-48 in very light Sf degrees >400, light Sf degrees 60-400, and dense Sf degrees 20-60 VLDL, IDL, and LDL in 24 subjects (12 in each study). After the high-fat meal, apoB-48 concentrations peaked at 3 h for very light VLDL, 4 h for light VLDL, and 5 h for dense VLDL and IDL, suggesting a delipidation cascade. The diurnal pattern was characterized by a sharp increase in light and dense VLDL apoB-48 after breakfast, reaching the highest concentration 4-8h after breakfast. Less response was observed after lunch, dinner or snack, despite 75% of energy supplied by these meals. The proportion of apoB-48 in LDL in the fasting state ranged between 48 and 54%. LDL apoB-48 concentration decreased by 35% after the high-fat meal, and slowly recovered to near fasting concentrations after 10-12 h. In contrast, in the diurnal study, LDL apoB-48 concentration steady increased peaking 13 h after breakfast, followed by a sharp decrease. In sum, most intestinally synthesized apoB lipoproteins circulate in LDL, and are likely formed in the late postprandial period from larger VLDL-size particles. Although small apoB-48 lipoproteins may be atherogenic remnant particles, their very low concentration may diminish their clinical significance.
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The concentration of VLDL cholesterol and apoB is at least 10 times higher than the corresponding chylomicron concentration, even after consumption of a large amount of fat.
“The concentration of VLDL cholesterol and apoB is at least 10 times higher than the corresponding chylomicron concentration, even after consumption of a large amount of fat (56 -59).”
From Evaluation and Treatment of Hypertriglyceridemia: An Endocrine Society Clinical Practice Guideline (2012) · cites this paper as [58]
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- Authors
- Campos, H., Khoo, C., & Sacks, F. M.
- Affiliations
- Harvard University (US)
- Corresponding author
- Campos, Hannia
- Venue
- Atherosclerosis
- Publisher
- Elsevier BV
- Published
- 2005-08
- Volume
- 181
- Issue
- 2
- Pages
- 345-351
- ISSN
- 0021-9150 (ISSN-L)
- OpenAlex
- W2049419310
- Cited by
- 58
- References
- 32
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 3 · 2022: 2 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 2 · 2017: 5 · 2016: 2 · 2015: 5 · 2014: 6 · 2013: 5 · 2012: 2
- FWCI
- 2.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Atherosclerosis (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association
- National Heart, Lung, and Blood Institute (R01HL069376, R01HL056210, HL69376)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- apolipoprotein B-48, VLDL, IDL, low-density lipoprotein, postprandial lipemia, diurnal variation, high-fat meal, lipoprotein particle size
- MeSH terms
- Aged, Apolipoproteins B, Cholesterol, Circadian Rhythm, Dietary Carbohydrates, Female, Humans, Lipoproteins, Cholesterol, LDL, Middle Aged, Particle Size, Reference Values, Cholesterol, VLDL, Postprandial Period, Apolipoprotein B-48, Apolipoprotein B-100
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Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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