A systematic review of the effects of increasing arachidonic acid intake on PUFA status, metabolism and health-related outcomes in humans

Autor: Ans Eilander, Bert J. M. van de Heijning, Szimonetta Lohner, Cristina Campoy, Per-Olof Larsson, Stewart Forsyth, Aliz Szommer, Mathilde Fleith, Ronald P. Mensink, Bettina Schelkle, Philip C. Calder
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
Male
BLOOD
Medicine (miscellaneous)
Physiology
Blood lipids
ARA arachidonic acid
law.invention
chemistry.chemical_compound
Randomized controlled trial
LC-PUFA long-chain PUFA
law
Medicine
DGLA dihomo-γ-linolenic acid
heterocyclic compounds
RESISTANCE EXERCISE
PLATELET
LA linoleic acid
Randomized Controlled Trials as Topic
POLYUNSATURATED FATTY-ACIDS
chemistry.chemical_classification
FA fatty acid
Nutrition and Dietetics
Arachidonic Acid
n-6 Fatty acids
PL phospholipid
food and beverages
RCT randomised controlled trial
CE cholesteryl ester
Middle Aged
Arachidonic acid
Fatty Acids
Unsaturated

Female
lipids (amino acids
peptides
and proteins)

DIETARY SUPPLEMENTATION
Polyunsaturated fatty acid
Adult
LONG-CHAIN N-3
EICOSANOIDS
Linoleic acid
Nutritional Status
03 medical and health sciences
Humans
CELL
Fatty acids
Adverse effect
Aged
Inflammation
030109 nutrition & dietetics
Dihomo-γ-linolenic acid
business.industry
Human health
Fatty acid
DOCOSAHEXAENOIC ACID
biochemical phenomena
metabolism
and nutrition

carbohydrates (lipids)
030104 developmental biology
chemistry
Dietary Supplements
business
Zdroj: Digibug. Repositorio Institucional de la Universidad de Granada
instname
Popis: We conducted a systematic review of randomised controlled trials (RCT) of increased intake of arachidonic acid (ARA) on fatty acid status and health outcomes in humans. We identified twenty-two articles from fourteen RCT. Most studies were conducted in adults. These used between 80 and 2000 mg ARA per d and were of 1–12 weeks duration. Supplementation with ARA doses as low as 80 mg/d increased the content of ARA in different blood fractions. Overall there seem to be few marked benefits for adults of increasing ARA intake from the typical usual intake of 100–200 mg/d to as much as 1000 mg/d; the few studies using higher doses (1500 or 2000 mg/d) also report little benefit. However, there may be an impact of ARA on cognitive and muscle function which could be particularly relevant in the ageing population. The studies reviewed here suggest no adverse effects in adults of increased ARA intake up to at least 1000–1500 mg/d on blood lipids, platelet aggregation and blood clotting, immune function, inflammation or urinary excretion of ARA metabolites. However, in many areas there are insufficient studies to make firm conclusions, and higher intakes of ARA are deserving of further study. Based on the RCT reviewed, there are not enough data to make any recommendations for specific health effects of ARA intake.
Databáze: OpenAIRE