Effect of diets rich in oleic acid, stearic acid and linoleic acid on postprandial haemostatic factors in young healthy men
Hunter KA, Crosbie LC, Horgan GW, Miller GJ, Dutta-Roy AK
The British journal of nutrition · 21 citas
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Cómo se estudió
- Diseño
- Ensayo controlado aleatorizado (indexado por PubMed)
- Estudiado en
- Personas
- Resultado principal
- Marcadores de salud y funcionamiento
- Consumo medido con
- Comida provista por los investigadores
Quién lo pagó
- Financiación
- Financiación no declarada
Publicación
- Publicado
- 2001-08-01 · Br J Nutr · vol. 86 · número 2 · págs. 207–15
- Editorial
- National Institutes of Health
- Citado
- 35 citas · más que el 86% de estudios similares · 1.8× el promedio de su campo
- Referencias
- 43 trabajos
- Acceso
- De pago
- Áreas de investigación
- Fatty Acid Research and Health · Blood Coagulation and Thrombosis Mechanisms · Blood properties and coagulation
- Palabras clave
- oleic acid, stearic acid, linoleic acid, dietary fatty acids, factor VII activation, plasminogen activator inhibitor-1, tissue plasminogen activator, chylomicrons, palmitic acid, plasma lipids, fat load
- MeSH
- humans, factor viia, blood glucose, dietary fats, fatty acids, linoleic acid, oleic acid, stearic acids, chylomicrons, blood coagulation factors, analysis of variance, hemostasis, postprandial period, adult, male
5 autores
- Kirsty A. Hunter🇬🇧University of Aberdeen
- Lynn Crosbie
- Graham William Horgan
- George J. Miller
- Asim K. Duttaroy
Resumen
El texto original del estudio, en el idioma en que se publicó.
The aim of the present study was to investigate the effects of stearic acid-, oleic acid- and linoleic acid-rich meals on postprandial haemostasis in young healthy volunteers whose background diets had been controlled for 14 d in a residential study. Six healthy male volunteers were assigned randomly to consume diets rich in stearic acid, oleic acid or linoleic acid for 14 d. On day 15, plasma lipids and haematological variables were measured in the fasted state, and 3 and 7 h (factor VII and prothrombin activation peptide fragments, 1 and 2 only) after consumption of a test meal. Test meals provided 40 % of the subjects' daily energy requirement, with 41 % of the energy provided as fat, 17 % energy as protein and 42 % energy as carbohydrate. The mean fat content of the meal was 45 (sd 5) g. Significant alterations from fasted values were observed for activated factor VII after 7 h), factor VII antigen after 7 h), prothrombin activation peptide fragments 1 and 2 after 7 h) and plasminogen activator inhibitor type 1 activity after 3 h) after consumption of each of the three meals. No significant differences were observed in haemostatic values (factor VII coagulant activity, factor VII antigen, tissue plasminogen activator activity prothrombin activation peptide fragment and plasminogen activator inhibitor type-1) with regard to diet except for activated factor VII at 3 h; values were higher after the oleic acid- and linoleic acid-rich meals than after the stearic acid-rich meal After consumption of each of the three meals, chylomicrons contained proportionately more palmitic acid than the lipids ingested. The present study shows that there are demonstrable changes in postprandial haemostasis when young healthy volunteers with controlled dietary backgrounds are challenged with a physiological fat load. These changes are independent of the fatty acid composition of the test meals.
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