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Subject:

Re: Can fish oils really improve your mind:- Is this 'bad-science and exploit...

From:

Eileen McGinn <[log in to unmask]>

Reply-To:

[log in to unmask]

Date:

Mon, 20 Aug 2007 13:33:50 EDT

Content-Type:

text/plain

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Yes, fish oil can improve your mind: cognition, mood and  behavior.  All this 
in addition to protection of heart, blood  vessels and other organs.  
 
Of course, if you eat a terrible diet and never do any physical activity at  
all and never try to learn anything and have no social support system, then  
just take some omega 3, it may not do much for you.  But even in controlled  
trials, just adding omega 3 without other changes has proven to be  beneficial 
for many medical and psychiatric illnesses, and even in aging and  healthy 
populations.  There is a massive literature on fish oil for  many medical 
conditions and for symptoms of psychiatric illnesses.   There is no need to create 
transgenic pigs.  In the US, there is a  pharmaceutical omega 3 called Omacor (at 
a high cost) which is approved by the  FDA for very high triglycerides (over 
500), one of the "bad fats".  Our  diets are so bad: the population of US is 
1/3 obese, 1/3 overweight and 1/3  normal weight. Many surveys have shown that 
people are deficient in many  nutrients.  
 
There are many articles now appearing in the press and in the medical  
literature about how "supplements" are no good, especially for people who are  not 
ill and that we are wasting money and possibly harming ourselves by  buying 
"supplements".  
Researchers think that they can test nutrients (supplements) like drugs,  one 
at a time.  If the supplement all by itself does not "work",  then it is no 
good.  Nutrients do not work that way, they work  together and that is why we 
need to eat food that is varied and supplies all our  nutrition needs.  Omega 3 
works on the cell membranes as well as  inside the cells and this seems to be 
why it helps so many body  systems.  
 
Some of the research about omega 3 is flawed: they are using only  EPA or 
only DHA,  not both together, so not really full omega 3  as used in some of the 
better research.  Then the conclusion is "omega  3 does not work".  But the 
study was not testing omega 3 to  begin with, only EPA or DHA alone.  They need 
to be together.   The whole idea of "active ingredient" from drug studies may 
not be  relevant to studies of nutrients, and certainly not to EPA or DHA 
alone.  

Is it better to eat fatty fish, wild from the ocean, twice a week or  more?  
Yes.  It is OK to take omega 3, if it is from a reputable  source?  Yes.  Go 
to foodforthebrain.org, a UK organization  that is helping to clarify 
information about diet and lifestyle and  health.  
 
I am enclosing some abstracts saved on my computer about omega 3 and the  
brain.  There are hundreds more in the medical literature, about many  medical 
and psychiatric illnesses.  Note that the conclusions are  sometimes rather 
tentative, saying more trials are needed, etc.  But we  have to keep in mind that 
in psychiatry, drugs are prescribed so  frequently "off-label" and in 
combinations of drugs never  studied.  Drugs are used commonly even when there have 
not even  been any trials to show any efficacy, especially in certain 
populations, like  elders, children, pregnant women, people with bipolar disorder,  etc. 
 Omega 3's adverse effect: since it thins the  blood, people already taking 
blood thinners should talk to their doctor  beforehand.      
 
Eileen
 
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Omega-3 Fatty Acids: Evidence Basis for Treatment and  Future Research in 
Psychiatry
Marlene P. Freeman, M.D.; Joseph R. Hibbeln, M.D.;  Katherine L. Wisner, 
M.D., M.S.; John M. Davis, M.D.; David Mischoulon,  M.D., Ph.D.; Malcolm Peet, 
M.B., F.R.C.Psych.; Paul E. Keck, Jr., M.D.;  Lauren B. Marangell, M.D.; 
Alexandra J. Richardson, Ph.D.; James Lake,  M.D.; and Andrew L. Stoll, M.D.  
 
____________________________________
Objective: To determine if the available data support the  use of omega-3 
essential fatty acids (EFA) for clinical use in the  prevention and/or treatment 
of psychiatric disorders.  
Participants: The authors of this article were invited  participants in the 
Omega-3 Fatty Acids Subcommittee, assembled by the  Committee on Research on 
Psychiatric Treatments of the American  Psychiatric Association (APA).  
Evidence: Published literature and data presented at  scientific meetings 
were reviewed. Specific disorders reviewed included  major depressive disorder, 
bipolar disorder, schizophrenia, dementia,  borderline personality disorder and 
impulsivity, and  attention-deficit/hyperactivity disorder. Meta-analyses 
were conducted in  major depressive and bipolar disorders and schizophrenia, as 
sufficient  data were availableto conduct such analyses in these areas of 
interest.  
Consensus Process: The subcommittee prepared the  manuscript, which was 
reviewed and approved by the following APA  committees: the Committee on Research 
on Psychiatric Treatments, the  Council on Research, and the Joint Reference 
Committee.  
Conclusions: The preponderance of epidemiologic and  tissue compositional 
studies supports a protective effect of omega-3 EFA  intake, particularly 
eicosapentaenoic acid (EPA) and docosahexaenoic acid  (DHA), in mood disorders. 
Meta-analyses of randomized controlled trials  demonstrate a statistically 
significant benefit in unipolar and bipolar  depression (p = .02). The results were 
highly heterogeneous, indicating  that it is important to examine the 
characteristics of each individual  study to note the differences in design and 
execution. There is less  evidence of benefit in schizophrenia. EPA and DHA appear to 
have  negligible risks and some potential benefit in major depressive disorder 
 and bipolar disorder, but results remain inconclusive in most areas of  
interest in psychiatry. Treatment recommendations and directions for  future 
research are described. Health benefits of omega-3 EFA may be  especially important 
in patients with psychiatric disorders, due to high  prevalence rates of 
smoking and obesity and the metabolic side effects of  some psychotropic 
medications.  
(J Clin Psychiatry 2006;67:1954-1967) 
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1: _Asia Pac J Clin Nutr._ (javascript:AL_get(this, 'jour', 'Asia Pac J Clin 
Nutr.');)  2007;16  Suppl:391-7. _Links_ 
(javascript:PopUpMenu2_Set(Menu17392137);)  

Omega 3 fatty acids and the brain: review of studies in depression.
    *   _Sinclair AJ_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Sinclair+AJ"[Author]) ,  
    *   _Begg D_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Begg+D"[Author]) ,  
    *   _Mathai M_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Mathai+M"[Author]) ,  
    *   _Weisinger RS_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Weisinger+RS"[Author]) . 

School of Exercise and Nutrition Sciences, Deakin  University, 221 Burwood 
Highway, Burwood, Victoria 3125, Australia.  [log in to unmask] 
The brain is a lipid-rich organ containing mostly complex  polar 
phospholipids, sphingolipids, gangliosides and cholesterol. These lipids  are involved in 
the structure and function of cell membranes in the brain. The  
glycerophospholipids in the brain contain a high proportion of polyunsaturated  fatty acids 
(PUFA) derived from the essential fatty acids, linoleic acid and  
alpha-linolenic acid. The main PUFA in the brain are docosahexaenoic acid (DHA,  all cis 
4,7,10,13,16,19-22:6) derived from the omega 3 fatty acid,  alpha-linolenic 
acid, and arachidonic acid (AA, all cis 5,8,11,14-20:4) and  docosatetraenoic 
acid (all cis 7,10,13,16-22:4), both derived from the omega 6  fatty acid, 
linoleic acid. Experimental studies in animals have shown that diets  lacking omega 
3 PUFA lead to substantial disturbances in neural function, which  in most 
circumstances can be restored by the inclusion of omega 3 PUFA in the  diet. In 
the past 10 years there has been an emerging interest in treating  
neuropsychological disorders (depression and schizophrenia) with omega 3 PUFA.  This paper 
discusses the clinical studies conducted in the area of depression  and omega 
3 PUFA and the possible mechanisms of action of these PUFA. It is  clear from 
the literature that DHA is involved in a variety of processes in  neural 
cells and that its role is far more complex than simply influencing cell  membrane 
properties. 
PMID: 17392137 [PubMed - in process]
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1: J Nutr Health Aging._ (javascript:AL_get(this, 'jour', 'J Nutr Health 
Aging.');)   2005;9(1):31-8. _Links_ (javascript:PopUpMenu2_Set(Menu15750663);)  

Dietary omega-3 Fatty acids and psychiatry: mood, behaviour, stress,  
depression, dementia and aging.
    *   _Bourre JM_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Bourre+JM"[Author]) .
French Academy of Medicine, INSERM department of  Neuro-pharmaco-nutrition, 
Hopital Fernand Widal, 75475 Paris cedex 10.  
[log in to unmask] 
In view of the high omega-3 poly unsaturated fatty acid  content of the 
brain, it is evident that these fats are involved in brain  biochemistry, 
physiology and functioning; and thus in some neuropsychiatric  diseases and in the 
cognitive decline of ageing. Though omega-3 fatty acids  (from fatty fish in the 
human diet) appear effective in the prevention of  stress, their role as 
regulator of mood and of libido is a matter for  discussion pending experimental 
proof in animal and human models. Dietary  omega-3 fatty acids play a role in the 
prevention of some disorders including  depression, as well as in dementia, 
particularly Alzheimer's disease. Their  direct role in major depression, 
bipolar disorder (manic-depressive disease)  and schizophrenia is not yet 
established. Their deficiency can prevent the  renewal of membranes, and thus 
accelerate cerebral ageing; none the less, the  respective roles of the vascular 
component on one hand (where the omega-3's  are active) and the cerebral parenchyma 
itself on the other, have not yet been  clearly resolved. The role of omega-3 
in certain diseases such as dyslexia and  autism is suggested. In fact, 
omega-3 fatty acids participated in the first  coherent experimental demonstration 
of the effect of dietary substances  (nutrients) on the structure and function 
of the brain. Experiments were first  of all carried out one x-vivo cultured 
brain cells (1), then on in vivo brain  cells(2), finally on physiochemical, 
biochemical, physiological, neurosensory,  and behavioural parameters (3). These 
findings indicated that the nature of  poly unsaturated fatty acids(in 
particular omega-3) present in formula milks  for infants (both premature and term) 
determines the visual, cerebral,and  intellectual abilities, as described in a 
recent review (4). Indeed,the  insufficient dietary supply of omega-3 fatty 
acids in today's French and  occidental diet raises the problem of how to 
correct dietary habits so that  the consumer will select foods that are genuinely 
rich in omega-3/ the omega-3  family ; mainly rapeseed, (canola) and walnut 
oils on one hand and fatty fish  on the other. 
PMID: 15750663 [PubMed - indexed for MEDLINE]

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OMEGA 3 FATTY ACIDS  INFLUENCE MOOD, IMPULSIVITY AND PERSONALITY, STUDY 
INDICATES 
DENVER, March 3,  2006 — Omega-3 polyunsaturated fatty acids may influence 
mood,  personality and behavior, according to results of a study presented today 
by  University of Pittsburgh School of Medicine researchers at the 64th 
Annual  Scientific Meeting of the American Psychosomatic Society in Denver. 
In a study of 106 healthy  volunteers, researchers found that participants 
who had lower blood levels of  omega-3 polyunsaturated fatty acids were more 
likely to report mild or moderate  symptoms of depression, a more negative 
outlook and be more impulsive.  Conversely, those with higher blood levels of 
omega-3s were found to be more  agreeable. 
“A number of previous studies have  linked low levels of omega-3 to 
clinically significant conditions such as major  depressive disorder, bipolar disorder, 
schizophrenia, substance abuse and  attention deficit disorder,” said Sarah 
Conklin, Ph.D., a postdoctoral scholar  with the Cardiovascular Behavioral 
Medicine Program in the department of  psychiatry at the University of Pittsburgh 
School of Medicine. “However, few  studies have shown that these relationships 
also occur in healthy adults. This  study opens the door for future research 
looking at what effect increasing  omega-3 intake, whether by eating omega-3 
rich foods like salmon, or taking  fish-oil supplements, has on people’s mood.”
 
The American Heart Association  recommends that all Americans consume fish, 
which is high in omega-3 fatty  acids, twice per week. This recommendation is 
based upon evidence that a diet  high in fish s associated with improved heart 
health and reduced risk for  heart-related problems. While the cardiovascular 
benefit of increasing omega-3  intake is well recognized, relatively little is 
known of the potential mental  health effects among the general public. 
Comparisons were made by analyzing  levels of omega-3 fatty acids in 
participants’ blood and comparing that data to  the participants’ scores on three 
accepted tests for depression, impulsiveness  and personality. The amount of 
omega-3 circulating in blood reflects dietary  intake of the fatty acid. The study 
did not require participants to make changes  in their normal diet habits. 
In addition to Dr. Conklin,  co-authors of the study, which was funded by the 
National Heart, Lung and Blood  Institute of the National Institutes of 
Health (NIH), include: Jennifer I.  Harris, M.D., psychiatry resident, department 
of psychiatry, Brown University;  Stephen B. Manuck, Ph.D., University 
Professor of Health Psychology and  Behavioral Medicine, department of psychology, 
University of Pittsburgh; Joseph  R. Hibbeln, M.D., chief of outpatient clinic, 
Lab of Membrane Biophysics and  Biochemistry, National Institute on Alcohol 
Abuse and Alcoholism, NIH; and  Matthew F. Muldoon, M.D., associate professor, 
department of medicine,  University of Pittsburgh School of Medicine.  
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1: _Am J Clin Nutr._ (javascript:AL_get(this, 'jour', 'Am J Clin Nutr.');)  
2006 Jun;83(6  Suppl):1483S-1493S. _Links_ 
(javascript:PopUpMenu2_Set(Menu16841858);)  

Healthy intakes of n-3 and n-6 fatty acids: estimations considering  
worldwide diversity.
    *   _Hibbeln JR_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Hibbeln+JR"[Author]) ,  
    *   _Nieminen LR_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Nieminen+LR"[Author]) ,  
    *   _Blasbalg TL_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Blasbalg+TL"[Author]) ,  
    *   _Riggs JA_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Riggs+JA"[Author]) ,  
    *   _Lands WE_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Lands+WE"[Author]) . 
Laboratory of Membrane Biochemistry and Biophysics and the  National 
Institute on Alcohol Abuse and Alcoholism, National Institutes of  Health, Bethesda, 
MD 20892-2088, USA. [log in to unmask] 
BACKGROUND: The worldwide diversity of dietary intakes of n-6  and n-3 fatty 
acids influences tissue compositions of n-3 long-chain fatty acids  (LCFAs: 
eicosapentaenoic, docosapentaenoic, and docosahexaenoic acids) and risks  of 
cardiovascular and mental illnesses. OBJECTIVE: We aimed to estimate healthy  
dietary allowances for n-3 LCFAs that would meet the nutrient requirements of  
97-98% of the population. DESIGN: Deficiency in n-3 LCFAs was defined as  
attributable risk from 13 morbidity and mortality outcomes, including all  causes, 
coronary heart disease, stroke, cardiovascular disease, homicide,  bipolar 
disorder, and major and postpartum depressions. Dietary availability of  n-3 LCFAs 
from commodities for 38 countries and tissue composition data were  
correlated by best fit to each illness in deficiency risk models. RESULTS: The  
potential attributable burden of disease ranged from 20.8% (all-cause mortality  in 
men) to 99.9% (bipolar disorder). n-3 LCFA intake for Japan (0.37% of energy,  
or 750 mg/d) met criteria for uniformly protecting >98% of the populations  
worldwide. n-3 LCFA intakes needed to meet a tissue target representative of  
Japan (60% n-3 in LCFA) ranged from 278 mg/d (Philippines, with intakes of 0.8%  
of energy as linoleate, 0.08% of energy as alpha-linolenate, and 0.06% of 
energy  as arachidonic acid) to 3667 mg/d (United States, with 8.91% of energy as 
 linoleate, 1.06% of energy as alpha-linolenate, and 0.08% of energy as  
arachidonic acid). CONCLUSIONS: With caveats inherent for ecologic, nutrient  
disappearance analyses, a healthy dietary allowance for n-3 LCFAs for current US  
diets was estimated at 3.5 g/d for a 2000-kcal diet. This allowance for n-3  
LCFAs can likely be reduced to one-tenth of that amount by consuming fewer n-6  
fats. 
PMID: 16841858 [PubMed - indexed for MEDLINE] 
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1: _Drugs._ (javascript:AL_get(this, 'jour', 'Drugs.');)  2005;65(8):1051-9. 
_Links_ (javascript:PopUpMenu2_Set(Menu15907142);)  

Omega-3 fatty acids in the treatment of psychiatric disorders.
    *   _Peet M_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Peet+M"[Author]) ,  
    *   _Stokes C_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Stokes+C"[Author]) . 
Swallownest Court Hospital, Doncaster and South Humber  Healthcare NHS Trust, 
Sheffield, UK. [log in to unmask] 
The importance of omega-3 fatty acids for physical health is  now well 
recognised and there is increasing evidence that omega-3 fatty acids  may also be 
important to mental health. The two main omega-3 fatty acids in fish  oil, 
eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) have important  
biological functions in the CNS. DHA is a major structural component of neuronal  
membranes, and changing the fatty acid composition of neuronal membranes leads  to 
functional changes in the activity of receptors and other proteins embedded  
in the membrane phospholipid. EPA has important physiological functions that 
can  affect neuronal activity. Epidemiological studies indicate an association  
between depression and low dietary intake of omega-3 fatty acids, and  
biochemical studies have shown reduced levels of omega-3 fatty acids in red  blood 
cell membranes in both depressive and schizophrenic patients.Five of six  
double-blind, placebo-controlled trials in schizophrenia, and four of six such  
trials in depression, have reported therapeutic benefit from omega-3 fatty acids  
in either the primary or secondary statistical analysis, particularly when 
EPA  is added on to existing psychotropic medication. Individual clinical trials 
have  suggested benefits of EPA treatment in borderline personality disorder 
and of  combined omega-3 and omega-6 fatty acid treatment for 
attention-deficit  hyperactivity disorder. The evidence to date supports the adjunctive use of 
 omega-3 fatty acids in the management of treatment unresponsive depression 
and  schizophrenia. As these conditions are associated with increased risk of  
coronary heart disease and diabetes mellitus, omega-3 fatty acids should also  
benefit the physical state of these patients. However, as the clinical 
research  evidence is preliminary, large, and definitive randomised controlled 
trials  similar to those required for the licensing of any new pharmacological 
treatment  are needed. 
PMID: 15907142 [PubMed - indexed for MEDLINE] 
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1: _Biol Psychiatry._ (javascript:AL_get(this, 'jour', 'Biol Psychiatry.');)  
2006 Aug 18; [Epub ahead of  print] 

Omega-3 Fatty Acids Supplementation in Children with Autism: A Double-blind  
Randomized, Placebo-controlled Pilot Study.
    *   _Amminger GP_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Amminger+GP"[Author]) ,  
    *   _Berger GE_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Berger+GE"[Author]) ,  
    *   _Schafer MR_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Schafer+MR"[Author]) ,  
    *   _Klier C_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Klier+C"[Author]) ,  
    *   _Friedrich MH_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Friedrich+MH"[Author]) ,  
    *   _Feucht M_ 
(http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Search&itool=pubmed_AbstractPlus&term="Feucht+M"[Author]) . 
Department of Child and Adolescent Neuropsychiatry, Medical  University of 
Vienna; Vienna, Austria; and ORYGEN Research Centre, University of  Melbourne, 
Melbourne, Australia. 
BACKGROUND: There is increasing evidence that fatty acid  deficiencies or 
imbalances may contribute to childhood neurodevelopmental  disorders. METHODS: We 
conducted a randomized, double-blind, placebo-controlled  6-week pilot trial 
investigating the effects of 1.5 g/d of omega-3 fatty acids  (.84 g/d 
eicosapentaenoic acid, .7 g/d docosahexaenoic acid) supplementation in  13 children 
(aged 5 to 17 years) with autistic disorders accompanied by severe  tantrums, 
aggression, or self-injurious behavior. The outcome measure was the  Aberrant 
Behavior Checklist (ABC) at 6 weeks. RESULTS: We observed an advantage  of 
omega-3 fatty acids compared with placebo for hyperactivity and stereotypy,  each 
with a large effect size. Repeated-measures ANOVA indicated a trend toward  
superiority of omega-3 fatty acids over placebo for hyperactivity. No clinically  
relevant adverse effects were elicited in either group. CONCLUSIONS: The 
results  of this study provide preliminary evidence that omega-3 fatty acids may 
be an  effective treatment for children with autism. 
PMID: 16920077 [PubMed - as supplied by publisher]
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78/1/40&link_type=GOOGLESCHOLAR)      PubMed     _PubMed  Citation_ 
(file:///C:/cgi/external_ref?access_num=12816769&link_type=PUBMED)     _Articles by 
Tiemeier, H._ 
(file:///C:/cgi/external_ref?access_num=Tiemeier+H&link_type=AUTHORSEARCH)     _Articles by Breteler, M. M._ 
(file:///C:/cgi/external_ref?access_num=Breteler+MM&link_type=AUTHORSEARCH)      Agricola     _Articles by 
Tiemeier, H._ 
(http://agricola.nal.usda.gov/cgi-bin/Pwebrecon.cgi?DB=local&CNT=100&CMD=nkey+Tiemeier&STARTDB=AGRIDB)     _Articles by Breteler, M. M._ 
(http://agricola.nal.usda.gov/cgi-bin/Pwebrecon.cgi?DB=local&CNT=100&CMD=nkey+Breteler&STAR
TDB=AGRIDB)   


American Journal of Clinical Nutrition, Vol. 78, No. 1, 40-46, July  2003
© 2003 _American Society for  Clinical Nutrition_ 
(file:///C:/misc/terms.shtml)  
 
____________________________________
ORIGINAL RESEARCH COMMUNICATION
Plasma fatty acid composition and depression are associated in the elderly:  
the Rotterdam Study1,2,3 
<NOBR>Henning Ti, , <NOBR>H  Ruud v, , <NOBR>Alber,  ,  <NOBR>Amanda and  and 
<NOBR>Monique MB  
1 From the Departments of Epidemiology &  Biostatistics (HT, AH, and MMBB) 
and Psychiatry (HRvT), Erasmus Medical Centre,  Rotterdam, Netherlands, and 
Numico Research, Wageningen, Netherlands (AJK).  
Background: It has been hypothesized that n-3  polyunsaturated fatty acids 
(PUFAs) are involved in mood regulation,  but epidemiologic evidence for such a 
link in the general population  is lacking.  
Objective: This study examined whether community-dwelling elderly persons 
with depression have a fatty acid composition that is different from that of 
nondepressed persons.  
Design: We screened 3884 adults aged ≥ 60 y for depressive symptoms as part 
of the Rotterdam Study. Subjects who screened positive had a psychiatric 
interview to diagnose depressive disorders. All eligible subjects had their blood  
drawn for measurement of plasma phospholipid concentrations. We  compared 
percentages of n-3 and n-6 PUFAs and their ratios between  264 subjects with 
depressive symptoms, including 106 subjects with  depressive disorders, and 461 
randomly selected reference  subjects. We also investigated whether 
atherosclerosis or the  inflammatory response as measured by C-reactive protein underlies 
the  relation between fatty acid composition and depression.  
Results: Subjects with depressive disorders had a higher ratio of n-6 to  n-3 
PUFAs, but differences in individual PUFAs were mostly small.  However, 
depressed subjects with normal CRP concentrations (< 1.5  mg/L) had a substantially 
altered fatty acid composition; percentages  of n-3 PUFAs and ratios of n-6 
to n-3 PUFAs were significantly lower  and higher, respectively, in subjects 
with depressive disorders than in control subjects [5.2%  compared with 5.9% (P 
= 0.02) and 7.2 compared with 6.6  (P = 0.01), respectively]. This relation 
was not due to  atherosclerosis.  
Conclusions: In community-dwelling persons, fatty acid  composition is 
related to depression. Because this relation was not  secondary to inflammation, 
atherosclerosis, or possible confounders,  it suggests a direct effect of fatty 
acid composition on mood.  
Key Words: Lipid composition • depression • polyunsaturated  fatty acids • 
phospholipids • inflammatory response • population-based study •  elderly • 
Rotterdam Study 
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