| Summaries of the latest research concerning fish oils and mental health and depression |
CONTENTS |
| Depression/Anger |
| Post-partum Depression |
| Schizophrenia |
| Bipolar Disorder (Manic-depressive Illness |
|
Depression/Anger
Fish oils in anger management The double-blind, randomized trial involved 24 patients who had a lifelong history of aggressive behaviour and problems with the law, and had been admitted to substance abuse clinics. The average age of the patients was 51 years, 80% were unemployed, and 60% were either separated, divorced or widowed. Eight patients (4 in the treatment group and 4 in the placebo group) had a history of assaultive behaviour and 7 patients in each group had served jail sentences for various offences. Baseline fish intake was low at 36 grams a day average yielding about 150 mg/day of long-chain omega-3 fatty acids, predominantly EPA and DHA. The researchers made the interesting observation that patients with a history of assaultive behaviour consumed only about half the amount of fish consumed by those who had not exhibited this behaviour.
The study participants were randomly assigned to receive placebo capsules (soybean oil) or 5 fish oil capsules a
day providing a total of 2250 mg/day of EPA and 500 mg of DHA. All capsules contained vitamin E as an
antioxidant and lemon oil to mask their taste. At the end of the 3-month supplementation period, the anger score in
the group of patients given fish oil had dropped by over 50% and this improvement persisted for another 3 months
after ceasing supplementation. The anger score for those given the placebo did not change. The researchers
speculate that the beneficial effects of fish oils may be due to their ability to improve membrane fluidity and increase
brain levels of serotonin. They suggest that fish oil supplementation should be considered in treatment protocols for
patients displaying aggressive behaviours.
Fish oil helps combat childhood depression
After the first 4 weeks of supplementation the researchers noted that the children on fish oil had significantly improved their rating on the Childhood Depression Rating Scale (CDRS) with 7 out of 10 showing an improvement of greater than 50%. None of the children in the placebo group experienced a 50% or better improvement. Four of the 10 children in the fish oil group were classified as being no longer depressed whereas none of the children in the placebo group achieved this goal. The researchers conclude that fish oils may have therapeutic benefits in childhood depression.
Fish oil derivative reduces depression The standard medical therapy for depression involves the use of tricyclic antidepressants or selective serotonin reuptake inhibitors (SSRIs). These drugs, however, are not terribly effective. Prozac, for example, produces a 50% improvement in symptoms in only 38% of patients starting treatment. This is not much better than the placebo effect, which provides 50% improvement in about 25% of patients. A team of British and Scottish researchers has just completed a study aimed at determining if the ethyl ester of EPA, ethyl-eicosapentaenoate (EEP), would be effective in strengthening the beneficial effect of standard antidepressants. The study involved 60 patients who were already being treated with SSRIs or tricyclic antidepressants. Fourteen patients received a placebo while the remaining 46 received either 1, 2 or 4 grams/day of EEP. All participants were evaluated for depression using several different scales at the beginning of the experiment and after 12 weeks. At the end of the study it was clear that the 1gram/day dosage of EEP was highly effective in reducing depression and associated conditions such as sadness, pessimism, inability to work, sleep disturbances, and diminished sex drive. In most cases, 60- 70% of patients receiving 1 gram/day of EEP showed an improvement of 50% or better. This compares to only 25% of the patients on the placebo showing a 50% improvement. The degree of improvement was substantially less in the 2 grams/day and 4 grams/day groups. The researchers speculate that this could be due to the depletion of the omega-6 fatty acid, arachidonic acid, by an excess of omega-3 fatty acid (EPA), indicating that the balance between omega-3 and omega-6 is important when it comes to depression.
The researchers conclude that concurrent treatment with 1 gram/day of EEP is effective in reducing
depression in patients who are still depressed despite treatment with standard medications. They are
now planning on evaluating EEP on its own as a treatment for depression.
Fish oils: A cure for depression?
Fish consumption reduces suicide risk
Dieting and depression Epidemiologic studies have found a clear correlation between a low intake of EPA and DHA and the prevalence of depression. In two studies of population groups in the USA the incidence of depression was found to be 3.7% and 2.9%. Average intake of EPA and DHA in the USA is estimated to be about 0.1 gram per day. In two Japanese studies, on the other hand, the incidence of depression was only 0.9% and 0% and the intake of EPA plus DHA was 1.5 grams per day and 4.2 grams/day respectively. Other studies have shown that on-off dieting can produce a serious imbalance in the ratio of fatty acids and may lead to depression
The researchers conclude that an extremely low-fat diet may be counter-productive and have deleterious
psychological ramifications. They stress that dietary advice regarding cholesterol reduction, weight loss,
and cancer prevention should emphasize the importance of an adequate intake of omega-3 fatty acids.
Omega-3 fatty acids: the missing link?
Fish consumption and depression
Omega-3 fatty acid deficiency linked to depression Researchers at the University of Sheffield and the Efamol Research Institute in Nova Scotia now report that they have found a highly significant association between severity of depression and the levels of omega-3 fatty acids in both the diet and the red blood cell membranes. Their study involved 10 patients with major depression and 14 healthy control subjects with no history of psychiatric disorder (average age of participants was 39 years). All participants had blood samples taken and analyzed for essential fatty acid (EFA) content and also completed a questionnaire to determine their dietary intake of EFAs over the 7 days prior to enrollment.
The severity of depression was found to be inversely proportional with the red blood cell level and dietary
intake of omega-3 fatty acids. The correlation between a low level of alpha-linolenic acid in blood cells
and depression and between low blood cell levels of DHA and depression were particularly strong. No
correlation was found between red blood cell levels of omega-6 fatty acids and depression. However,
there was a slight positive correlation between dietary intake of omega-6s and severity of depression
when both patients and controls were considered in one group. The researchers conclude that low levels
of omega-3 fatty acids in cell membranes are associated with depression. They speculate that
supplementation with omega-3 fatty acids may be useful in alleviating depression.
DHA levels linked to suicide and violence
To test this hypothesis the researchers measured the levels of cerebrospinal 5-HIAA and the levels of
blood plasma polyunsaturated fatty acids in a group of 176 subjects. Forty-nine of the subjects were
healthy volunteers, 88 were early-onset alcoholics (excessive alcohol use prior to their 25th birthday), and
39 were late-onset alcoholics. None of the alcoholics had been drinking for at least 21 days prior to the
test. The researchers found a strong positive correlation between blood levels of docosahexaenoic acid
(DHA) and the level of 5-HIAA in the healthy volunteers. In other words, the higher the DHA levels the
higher the 5-HIAA levels and as a corollary, the lower the tendency to depression, violence and suicide.
In the early-onset alcoholics the situation was completely reversed. Higher DHA levels corresponded to
lower 5-HIAA levels and thus a possibly increased tendency to violence, suicide and depression. The
researchers found no correlation between 5-HIAA levels and total cholesterol levels. They conclude that
further studies are required to determine if supplementation with essential fatty acids, notably DHA, can
influence central nervous system serotonin and dopamine metabolism and modify impulsive behaviour
related to these neurotransmitters.
Your brain needs DHA
Fatty acid profile linked to depression Now researchers at the Royal Melbourne Institute of Technology report that the severity of depression is indeed directly associated with the ratio of LA- to ALA-type PUFAs in red blood cells. Their study involved 20 moderately to severely depressed patients. The severity of depression was determined using the 21-item Hamilton depression rating scale and a second scale which omitted anxiety symptoms. All patients had blood samples drawn and analyzed for arachidonic acid (AA) - the major metabolite of linoleic acid, and EPA - the major metabolite of alpha-linolenic acid and the main constituent of fish oils. The researchers found a clear correlation between a high AA/EPA ratio and increased severity of depression. There was also a significant association between a low level of EPA in the red blood cells and increased severity of depression.
The researchers conclude that there is a definite relationship between high AA/EPA ratios and increased
severity of depression, but are not certain whether the fatty acid imbalance causes depression or whether
depression results in a high AA/EPA ratio. They suggest that further studies be done to determine the
benefits of supplementation aimed at increasing tissue levels of EPA and thereby decreasing the AA/EPA
ratio.
Docosahexaenoic acid fights depression
Post-partum Depression
Pilot trial of fish oil for post-partum depression Their 8-week pilot study involved 16 women with PPD. The extent of depression was evaluated using the Edinburgh Postnatal Depression Scale (EPDS) and the Hamilton Rating Scale for Depression (HRSD). The EPDS scores ranged from 15.3 to 19.0 at the start of the study (a score equal to or greater than 9.0 indicates depression). The HRSD scores ranged from 18 to 20.3 with a score equal to or greater than 15 signifying depression.
The study participants were randomized to receive placebo capsules (corn oil + 1% fish oil) or 0.5, 1.4 or 2.8 grams/day of a fish oil having an EPA:DHA ratio of 1.5:1 (EPAX 5500, Pronova, Lysker, Norway) for 8 weeks. The participants were followed up and checked for depression scores at weeks 1, 2, 4, 6, and 8. At week 8 the average EPDS score had decreased to 9.3 (a 51.5% reduction) and the HRSD score had fallen by 48.8% to an average of 10 in the fish oil groups. Improvement was most noticeable in the group receiving 1.4 grams/day of EPA + DHA and no advantage was seen by taking 2.8 grams/day. However, just 0.5 gram/day also was successful in reducing both EPDS scores and HRSD scores to normal (non-depressed) levels. The researchers conclude that fish oil supplementation in women with PPD is well tolerated and effective in reducing symptoms of depression.
Fatty acid status and post-partum depression Their study included 48 healthy, pregnant women who had blood samples taken shortly after delivery. These blood samples were analyzed to determine the fatty acid profile in serum phospholipids (PL) and cholesteryl esters (CE). The women were also interviewed within 6 to 10 months after delivery to ascertain whether they suffered from PPD. Ten of the women (21%) had indeed developed PPD with most reporting depressive symptoms immediately following delivery. Analyses of the blood samples showed that DHA concentration and total omega-3 level were significantly lower in both the PL and CE fractions of blood serum taken from women who developed PPD.
The Dutch researchers speculate that the milder form of PPD, post-partum blues, also is related to a fatty acid imbalance and is currently investigating this in a separate study involving 98 women. They conclude that pregnant women at risk for developing PPD may benefit from preventive supplementation with DHA, perhaps in combination with its precursor docosapentaenoic acid.
Post-partum depression and functional DHA status The Dutch study involved 112 pregnant women who had blood samples collected at week 36 of pregnancy, immediately following delivery, and 32 weeks post-partum. At week 32 post-delivery the women were assessed for the presence of PPD using the Edinburgh Postnatal Depression Scale (EPDS) questionnaire. Twenty-four of the women (21%) were found to suffer from depression (EPDS score equal to or greater than 10). Seventy-five percent of the depressed women rated themselves as “not healthy” in the months following delivery as compared to only 6% in the non-depressed group (EPDS score less than 10).
The researchers did not observe any statistically significant relationship between post-partum depression and DHA level as such; however, they did find a significant correlation between PPD and the increase in DHA:DPA ratio between delivery and 32 weeks post-partum. Women with a slower increase in this ratio had a 10% higher risk of PPD. There was no indication that breast-feeding increased the risk of PPD. The researchers recommend further studies, but suggest that women who have recently given birth increase their intake of DHA.
Post-partum depression linked to DHA deficiency Dr. Hibbeln evaluated the results of 41 relevant studies involving over 14,000 women located in 23 different countries. He compared the incidence of post-partum depression in new mothers in each country with the average seafood consumption and average DHA concentration in the mothers’ milk in the country. The results were remarkable. Dr. Hibbeln found a clear correlation between the incidence of PPD and seafood consumption. The highest incidence of PPD (24.5%) was found in South Africa, which also reported the lowest seafood intake at 8.6 lb/person/year. In comparison, Japan reported a PPD incidence of only 2% and an average seafood consumption of 147.7 lb/person/year. In the United States average seafood intake amounted to 48.1 lb/person/year with a corresponding PPD incidence of 11.5%. Numbers for Canada were similar at 50.7 lb/person/year seafood consumption and 12.7% PPD. Analyses of fatty acid content of mothers’ milk were available for 16 countries. While there was no correlation between PPD and the content of arachidonic acid and eicosapentaenoic acid, there was a clear correlation between PPD and low DHA level. South Africa reported the lowest DHA content (0.15% of total fats in mothers’ milk) and the highest PPD incidence at 24.5%. The average DHA level in mothers’ milk in Japan was 0.81% versus a PPD incidence of 2%. Average DHA level in the USA was 0.17% (PPD incidence of 11.5%).
Although there are clearly other factors predisposing to post-partum depression, Dr. Hibbeln found that the effects of low socioeconomic status, young maternal age, no partner, and poor education were minor when compared to the effect of seafood consumption and low DHA status. He points out that numerous studies have shown that DHA status can be safely and effectively improved by supplementation with fish oil. Specifically, studies have found that supplementation with 1.1 gram/day of DHA will increase breast milk concentration to 0.8% without any adverse effects. A level of 0.8% is equivalent to the average level observed in Japan and is associated with a low 2.0% risk of PPD.
Schizophrenia
EPA cures schizophrenia Researchers at the Imperial College School of Medicine now report that fatty acid levels can be restored to normal and schizophrenia symptoms eliminated or at least vastly diminished by oral supplementation with EPA, the major component of fish oils. Their experiment involved a 30-year-old man who had suffered from schizophrenia for over 10 years. He had frequent (at least daily) hallucinations and also suffered from persecutory delusions and thought disorder. The patient was put on 2 grams/day of EPA and was evaluated for schizophrenia symptoms and blood plasma and red blood cell membrane levels of fatty acids at monthly intervals for 6 months. The results were spectacular. After 6 months the overall score for schizophrenia symptoms had dropped by a factor of 6 (an 85% reduction in severity). Episodes of delusions were completely eliminated and there was an 88% reduction in the number of hallucinatory episodes.
The remarkable clinical improvement in symptoms was associated with substantial increases in the levels
of EPA, DHA and AA in red blood cell membranes and with significant increases in EPA and DHA levels
in blood plasma. The researchers conclude that EPA supplementation is able to reverse the abnormal
fatty acid profiles found in schizophrenics and that this reversal is associated with, and is likely to be the
cause of, the clinical improvement.
Fish oil supplementation helps schizophrenia patients Another study (Peet 1997) compared evening primrose oil supplementation with placebo in 43 schizophrenics. The patients' mental state was not improved in either the placebo or the treatment group after 12 weeks. A third study involving 29 schizophrenics compared supplementation with fish oil to evening primrose oil and found fish oil superior.
The researchers conclude that fish oils may be useful in the treatment of schizophrenia and that medical
doctors should not discourage their patients from taking fish oil supplements. They add that fish oils
seem to be well tolerated and free of adverse effects.
Fish oils alleviate schizophrenia symptoms
A more recent study by the same researchers evaluated the effect of fish oil supplementation on the
severity of schizophrenic symptoms in a group of 24 patients. They were given 10 grams/day of
concentrated fish oil for a six-week period. The supplementation resulted in a marked increase in EPA
and other omega-3 fatty acids in the red blood cell membranes and a concomitant decrease in omega-6
fatty acid levels. The researchers also noted a significant decrease in the severity of symptoms during
the supplementation period. Interestingly enough, none of the patients were clinically deficient in fatty
acid intake prior to supplementation, but a correlation between higher EPA intake and less severe
symptoms was clearly evident. The researchers conclude that schizophrenia is somehow related to an
abnormal fatty acid metabolism and urge larger clinical trials to evaluate the potential benefits of omega-3
fatty acid supplementation in the treatment of this disorder.
Bipolar Disorder (Manic-Depressive Illness)
Fish oils and manic-depressive illness
The double-blind, placebo-controlled study involved 30 patients (men and women 18 to 65 years of age)
who had all been diagnosed with bipolar disorder. Half the patients were given seven fish oil capsules
twice a day while the placebo group were given seven olive oil capsules twice a day. Each fish oil
capsule contained 440 mg of eicosapentaenoic acid and 240 mg of docosahexaenoic acid. All of the
participants except four in the fish oil group and four in the placebo group also continued to receive a
standard mood-stabilizing drug prescribed previously. The mental state of the participants was measured
using four scales (Clinical Global Impression Scale, Global Assessment Scale, Young Mania Rating
Scale, and the Hamilton Rating Scale for Depression) at the start of the study and after two, four, six,
eight, twelve and sixteen weeks. Twelve of the 14 participants in the fish oil group completed the four-
month study without major episodes of mania or depression as compared to only six out of 16 participants
in the placebo group. Also, while nine of the placebo group members experienced worsening depression
none of the fish oil group members did. The four patients in the fish oil group who had not been
prescribed mood-stabilizing drugs all completed the study without major episodes, but only one member
in the placebo group not on mood-stabilizing drugs did. The average decline in depression rating on the
Hamilton Scale was almost 50 per cent in the fish oil group as compared to an increase of 25 per cent in
the control group. The Harvard researchers urge further trials of fish oils in the treatment of depression
and manic-depressive illness.
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Additional References
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