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pubmed-article:7762523pubmed:dateCreated1995-6-29lld:pubmed
pubmed-article:7762523pubmed:abstractTextWe examined the effects of replacing dietary fat with carbohydrates on high-density-lipoprotein (HDL) subclasses as measured by nondenaturing polyacrylamide-gradient-gel electrophoresis. One hundred five men received a 6-wk low-fat diet (24% of total energy) and a 6-wk high-fat diet (46% of energy) in a crossover design. Absorbency of protein stain was measured within five HDL subclasses: HDL3c (7.2-7.8 nm), HDL3b (7.8-8.2 nm), HDL3a (8.2-8.8 nm), HDL2a (8.8-9.7 nm), and HDL2b (9.7-12 nm). The low-density-lipoprotein-(LDL) subclass pattern was determined by gradient-gel electrophoresis, with pattern B men defined as having an LDL-predominant peak diameter < or = 25.5 nm and an LDL distribution skewed toward larger size particles. On the high-fat diet, 18 men exhibited LDL-subclass pattern B and 87 men exhibited the alternative LDL pattern A. Twelve men had the apolipoprotein (apo) epsilon 2 allele. Replacing dietary fat with carbohydrates 1) significantly decreased HDL3a, HDL2a, and HDL2b; 2) reduced HDL2b significantly more in pattern A than in pattern B men; and 3) increased plasma HDL3b concentrations significantly more in those men with the epsilon 2 allele. Our results suggest that unfavorable HDL changes were significantly more likely to occur in men who had LDL-subclass pattern A or the apo epsilon allele than in men who had pattern B or lacked the epsilon 2 allele.lld:pubmed
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pubmed-article:7762523pubmed:authorpubmed-author:KraussR MRMlld:pubmed
pubmed-article:7762523pubmed:authorpubmed-author:WilliamsP TPTlld:pubmed
pubmed-article:7762523pubmed:authorpubmed-author:DreonD MDMlld:pubmed
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pubmed-article:7762523pubmed:volume61lld:pubmed
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pubmed-article:7762523pubmed:pagination1234-40lld:pubmed
pubmed-article:7762523pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:7762523pubmed:year1995lld:pubmed
pubmed-article:7762523pubmed:articleTitleEffects of dietary fat on high-density-lipoprotein subclasses are influenced by both apolipoprotein E isoforms and low-density-lipoprotein subclass patterns.lld:pubmed
pubmed-article:7762523pubmed:affiliationLife Sciences Division, Lawrence Berkeley Laboratory, Berkeley, CA 94720, USA.lld:pubmed
pubmed-article:7762523pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7762523pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:7762523pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:7762523pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:7762523pubmed:publicationTypeRandomized Controlled Triallld:pubmed
pubmed-article:7762523pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed