Posted 14 June 2006 - 04:16 AM
Funk, could you possible post a summary of MR's anti-DHA stand?
Some recent info...
Last year a workshop was held at the Institute of Human Nutrition, Columbia University, New York, NY (22 may 2005). The topic of the workshop "n-3 fatty acids: Recommendations for Therapeutics and Prevention". The quote function is not working so I'm going straight into this
Here is a summary of their discussion:
PREGNANCY
Current knowledge for which a general consensus exists
1.High fish oil consumption is associated with an increase in gestational length and may reduce the rates of postpartum depression.
2.Women should have 100–300 mg DHA/d.
Gaps and recommendations for research and policy
1.More work should be done to assess whether these doses are associated with any increased bleeding.
2. More extensive dose-response studies should be conducted.
3. Further assessment of specific effects of DHA and EPA should be conducted on neuropsychological function, immune response, and rates of infection in the infant.
INFANTS
Current knowledge for which a general consensus exists
1.High intake ratios of EPA to DHA can lead to a decreased growth rate.
2.Current levels of DHA:AA (1.4:1 to 2:1) are beneficial for the visual and cognitive development of low-birth-weight infants and likely also normal-birth-weight infants.
Gaps and recommendations for research and policy
1.The role of ALA is poorly understood and should be further examined, but ALA likely cannot substitute for DHA.
2.Dose responses of AA and DHA need to be more fully characterized.
3. Whether DHA is beneficial for immune and allergic response in older infants should be examined.
CARDIOVASCULAR DISEASE
Current knowledge for which a general consensus on EPA and DHA exists
1. Reduced overall mortality after onset of cardiovascular disease.
2. Reduced sudden death and arrhythmias, primarily in secondary prevention trials.
3. Reduced blood triacylglycerol concentrations with higher doses.
4. May slightly increase LDL, but the increase is not clinically significant.
5. Limited effect associated with increased ALA.
Gaps and recommendations for research and policy
1. Dose-response data for EPA and DHA are limited and should be studied.
2. Some data from small clinical trials suggest that DHA alone is similar to or better than a combination of EPA plus DHA; these studies should be replicated in larger trials.
3.A large trial on the effects of n–3 fatty acids in the primary prevention of cardiovascular disease should be conducted.
MENTAL HEALTH
Current knowledge for which a general consensus exists
1.EPA plus DHA appear to have better efficacy than either alone.
2. DHA alone has not been effective.
3. n–3 Fatty acids are likely to improve psychotic, depressive, and aggressive symptoms in severe patients.
Gaps and recommendations for research and policy
1. A clear body of treatment data on effects of EPA, DHA, or both has not yet been developed for either schizophrenia, depressive, or aggressive disorders; thus, recommendations should be cautious.
2. Dose-response data and primary prevention trials are lacking.
AGING: DEMENTIA AND MACULAR DEGENERATION
Current knowledge for which a general consensus exists
1. Increased fish and DHA intake are protective against cognitive decline.
2. Fish consumption and DHA are associated with a reduced risk of developing Alzheimer disease.
3. DHA may improve mental function and reduce aggression in patients with dementia.
4. Consuming fish and low linoleic acid is associated with reduced risk of age-related macular degeneration.
Gaps and recommendations for research and policy
1. Dose-response and primary prevention studies for both dementia and age-related macular degeneration are needed.
METABOLIC SYNDROME
Current knowledge for which a general consensus exists
1. To improve insulin sensitivity, n–3 fatty acids are more useful in prevention than in treatment.
2. EPA plus DHA effectively lowers blood triacylglycerol concentrations.
3. High doses tend to decrease small, dense LDL concentrations and may improve insulin sensitivity.
4. Inclusion of n–3 fatty acids should be considered along with other lifestyle interventions such as exercise, diet, and medication.
Gaps and recommendations for research and policy
1. Dose-response studies should be examined, especially because different individuals seem to be affected differently by n–3 fatty acids. 2. An upper level of intake for benefit needs to be established.
3. A primary intervention or prevention trial should be conducted.
INFLAMMATORY AND IMMUNE RESPONSE
Current knowledge for which a general consensus exists
1. For rheumatoid arthritis, there is a proven therapeutic benefit of EPA plus DHA. All studies that monitored use of nonsteroidal antiinflammatory agents reported a significant reduction in use, and n–3 fatty acids reduce requirements for corticosteroids.
2. Although evidence is weaker for treatment of Crohn disease and psoriasis, n–3 fatty acids prolong remission in Crohn disease and reduce the requirement for corticosteroids in both conditions.
-Linolenic acid is not antiinflammatory at intakes <10 g/d.
Gaps and recommendations for research and policy
1. Dose-response and primary prevention studies are needed in all areas of inflammatory and immune response.
2. Some evidence exists that n–3 fatty acids are therapeutic for childhood asthma; more studies are needed.
3. There is contradictory or no evidence that n–3 fatty acids are therapeutic in the treatment of ulcerative colitis, systemic lupus erythematosus, or adult asthma; more studies are needed.
GENERAL CONCLUSIONS RELEVANT TO ALL AREAS
Current knowledge for which a general consensus exists
1. Preformed long-chain n–3 fatty acids, derived from marine or algal sources, are more efficient biologically than are plant-derived n–3 ALA.
2. The efficiency of conversion of plant-derived ALA to EPA and DHA, where it has been shown to be beneficial, is dependent in large part on the n–6 fatty acid content of the diet.
Gaps and recommendations for research advancing policy
1. In almost every area, data are insufficient to make recommendations for intake of specific n–3 fatty acids, eg, EPA versus DHA versus EPA + DHA combined.
2. To develop more specific recommendations, more data will be needed that compare dose-response relations for both EPA and DHA.
3. Biological effects of n–3 fatty acids will be better elucidated when tissue concentrations of each n–3 fatty acid are measured. Wherever possible, tissue concentrations should be used to develop dose-response curves. Determining the appropriate tissue still requires more research, but at this time, plasma concentrations can be used as a reliable surrogate when the specific tissue level of interest cannot be obtained.
4. The intake of n–6 fatty acids may markedly affect the n–3 fatty acid intake required to achieve a desirable tissue n–3 fatty acid level. Future studies should consider that higher n–6 fatty acid intakes may lead to higher n–3 fatty acid requirements to achieve desired biological effects.
5. Intervention trials at a given dosage or form of an n–3 fatty acid are not necessarily going to have the same effect as more prolonged or lifelong intakes of n–3 fatty acids. Therefore, intakes required to prevent a specific disease may be different from intakes required to treat a disease, and research data should be interpreted with this in mind.
6. Data are lacking for primary prevention in almost every health area, and secondary prevention trials do not necessarily predict the usefulness of n–3 fatty acids for primary prevention.
7. National public health initiatives to increase n–3 fatty acid consumption are needed; the working group believes that data are currently sufficient to indicate that intake of n–3 fatty acids is suboptimal, and a national and international initiative should be launched to shift n–3 fatty acid intake upward.
8. Cross-disciplinary initiatives should be encouraged when studying the effects of n–3 fatty acids (eg, if a mental health study is being performed, include endpoints relevant to cardiovascular disease).
There are statements above that report the current knowledge and general consensus of supplementation with EPA plus DHA to be beneficial for various population groups