Abstract
Objective
To determine if associations exist between a range of unsaturated fatty acid intakes and mental health outcomes.
Design
Cross-sectional data analysis of the Australian Longitudinal Study on Women’s Health (ALSWH) Young Cohort Survey 3 that included the validated seventy-four-item Dietary Questionnaire for Epidemiological Studies FFQ, validated mental health scales and self-report questions on depression and anxiety.
Setting
Australia, 2003.
Subjects
A nationally representative sample of young Australian women (25–30 years) from ALSWH. The 7635 women with plausible energy intakes (>4·5 but <20·0 MJ/d) were included in the analyses.
Results
Adjusted logistic regression analyses found statistically significant associations between higher intakes of α-linolenic acid and decreased likelihood of depressive symptoms indicated by the ten-item Center for Epidemiological Studies Depression Scale (CESD-10; OR=0·77; 95 % CI 0·60, 0·99; P=0·040) and the Short Form Health Survey (SF-36) mental health subscale (OR=0·73 95 % CI 0·56, 0·96; P=0·024). Furthermore, higher intakes of n-6 fatty acids (OR=0·96, 95 % CI 0·93, 0·99; P=0·019) and linoleic acid (OR=0·96, 95 % CI 0·93, 0·99; P=0·020) were associated with decreased likelihood of self-reported diagnosed anxiety and higher intakes of n-9 fatty acids (OR=1·02, 95 % CI 1·00, 1·04; P=0·041) and oleic acid (OR=1·02, 95 % CI 1·00, 1·05; P=0·046) were associated with increased likelihood of self-reported diagnosed anxiety.
Conclusions:
Increased intakes of α-linolenic acid were associated with a reduced likelihood of depressive symptoms, increased intakes of n-6 fatty acids and linoleic acid were associated with a reduced likelihood of self-reported anxiety, and increased intakes of n-9 fatty acids and oleic acid were associated with an increased likelihood of anxiety. Additional studies are needed to further elucidate associations between unsaturated fatty acids and depression and anxiety.
Keywords: Unsaturated fatty acids, FFQ, Women, Depression, Anxiety, Mental health
In recent years there has been an increase in the incidence of mental illnesses, with depression now being the leading cause of disability worldwide( 1 – 3 ). According to the 2007 National Survey of Mental Health and Wellbeing, approximately 45 % of the Australian population have experienced a mental illness in their lifetime and the incidence is increasing by approximately 20 000 cases per annum( 2 ). Women, in particular young women, were found to be more likely to experience anxiety and depression, the most common forms of mental illness( 2 ). The rise in mental illnesses has correlated with changes in dietary intake in Western countries, in particular a decreased consumption of n-3 fatty acids (FA) and concomitant increases in intakes of n-6 and most likely n-9 FA( 4 – 8 ).
The n-3, n-6 and n-9 FA are collectively referred to as unsaturated fats. Unsaturated FA are found in high concentrations in cell membranes and are thought to influence membrane fluidity and thus cell signalling, neurotransmitter release and receptor sensitivity( 10 – 13 ). Therefore higher concentrations of unsaturated FA in neural membranes are thought to improve the communication between brain neurons and the transport of neurotransmitters such as dopamine and serotonin, and thus play a role in mental health( 10 , 12 ). The focus of past research has been primarily on n-3 FA due to the particularly high concentration of long-chain (LC) n-3 FA found in the brain and nervous system tissues( 9 – 11 ).
The majority of experimental studies investigating the potential therapeutic effect of n-3 FA on pre-existing mental health issues have often used supplementation rather than a dietary source. The role of n-3 FA in the prevention of mental health issues in observational studies to date has yielded mixed results( 12 ). These studies commonly measure dietary sources of n-3 FA using fish consumption as a proxy measure, rather than individual n-3 FA, thereby excluding n-3 FA derived from non-fish sources. There are conflicting results about gender-specific differences in the association of n-3 FA and mental health. Also, the literature suffers as a variety of measures of mental health outcomes have been used, making direct comparison of the evidence base difficult. A longitudinal study by Yanfeng et al. (2011) found that among 5068 adults, infrequent fish consumption was a risk factor for severely depressed mood in men, but not in women, measured using the ten-item Center for Epidemiological Studies Depression Scale (CESD-10)( 13 ). However, a longitudinal cohort study of 3317 African-American and Caucasian young adults by Colangelo et al. (2009) found that fish intake and intakes of EPA, DHA and EPA + DHA were all significantly related to depressive symptoms, measured using the CESD-10, in women only( 14 ). Additionally Tanskanen et al. (2001) found that infrequent fish consumption was significantly associated with depressive symptoms measured using the Beck Depression Inventory scale among both genders, but especially in women, in a cross-sectional study of 3204 Finnish adults( 15 ). In contrast, a population-based study of 2416 New Zealand adults that measured EPA and DHA in serum phospholipids found inconsistent associations between the LC n-3 FA and mental well-being measured using the Short Form Health Survey questionnaire (SF-36)( 16 ).
There has been far less focus on anxiety than depression in relation to n-3 FA intakes in the research literature, despite the probability that mood and anxiety disorders are mechanistically related( 17 ). One prospective cohort study of 7903 university graduates showed that dietary n-3 fat intake provided a potential benefit to total mental disorders (anxiety, depression, stress) at baseline( 18 ). However, the study also found that participants who had a high fish consumption at baseline, which had then increased further by the 2-year follow-up, was then associated with an increased risk of mental disorders( 18 ).
The majority of the literature to date focuses on the association between n-3 FA and mental health, in particular depression; however, there are a few studies investigating n-6 and n-9 FA in relation to mental health. A prospective cohort study of 4856 adults aged 25–74 years by Wolfe et al. (2009) found that increased intake of oleic acid (OA; 18: 1n-9) was associated with a reduced risk of severe depressed mood in women, while an increased intake of linoleic acid (LA; 18: 2n-6) was associated with an increased risk of severe depressed mood in men( 19 ). Furthermore Yary and Aazami (2011) found an inverse association between total PUFA intake and depressive symptoms among 402 Iranian postgraduate students in Malaysia( 20 ).
Overall, the association between LC n-3 FA and depression is still unclear. In addition, despite being metabolically plausible, few studies exist that investigate a range of different FA in relation to depression and anxiety. The present study aimed to assess whether a range of dietary unsaturated FA are associated with mental health status in a cross-sectional analysis of data from the Australian Longitudinal Study on Women’s Health (ALSWH) Young Cohort Survey 3 (2003).
Methods
Study sample
The ALSWH is a population-based prospective longitudinal study funded by the Commonwealth Department of Health and Ageing. The study commenced in 1996 and was established to investigate the changes in the health of Australian women by distributing self-reported questionnaires over a 20-year period( 21 ). Approximately 45 000 women were recruited by random selection from the Australian Medicare database, which includes all permanent residents of Australia( 21 ). Women from three age groups were selected (‘younger’ women aged 8–23 years, ‘mid-age’ women aged 45–50 years, ‘older’ women aged 70–75 years)( 21 ). Women living in rural or remote areas were over-sampled to ensure adequate numbers for statistical analysis( 21 ). The respondents have been shown to be broadly representative of the national population of women in the target age groups, with a slight over-representation of Australian-born, better-educated non-smoking women( 21 , 22 ).
The present study is a cross-sectional data analysis of the Young Cohort Survey 3, which was distributed in 2003 when the participants were aged 25–30 years. At baseline (survey 1 in 1996) 14 247 women aged 18–23 years participated( 23 ). At survey 3 in 2003, 9067 women responded to the survey (retention rate of 64 %); however, this response rate compares well with other surveys of this highly mobile age group( 21 , 24 ). Survey 3 included an FFQ and questions that explore factors influencing the health of Australian women( 24 ).
The ALSWH has been approved by the Human Research Ethics Committees of the University of Newcastle and the University of Queensland.
Fatty acid measures
The Dietary Questionnaire for Epidemiological Studies (DQES) version 2, developed by the Cancer Council Victoria, is a seventy-four-item FFQ that assesses usual dietary intake for the previous 12 months, but does not include questions on vitamin or mineral supplement use( 25 ). This FFQ has previously been validated in a cohort of young to middle-aged Australian women( 26 ).
All FA intakes were estimated from the analysis of the FFQ responses, using the NUTTAB95 and Royal Melbourne Institute of Technology FA databases that have been shown to give accurate indications of intake levels( 25 – 27 ). The n-9 FA are MUFA that are synthesised in the body, but can also be obtained from dietary sources such as olive, rapeseed and peanut oils( 11 ). The main n-9 FA is OA (18: 1n-9). The n-3 and n-6 FA are PUFA. The main n-6 FA, LA (18: 2n-6), is an essential FA found primarily in seed oils( 11 ). The essential n-3 FA is α-linolenic acid (ALA; 18: 3n-3) found in plant-based foods such as rapeseed, linseed and walnuts( 11 ). ALA can be converted within the body into the LC n-3 FA, EPA (20: 5n-3), docosapentaenoic acid (DPA; 22: 5n-3) and DHA (22: 6n-3); evidence suggests that 9 % of ALA is converted to LC n-3 FA in women( 11 , 27 ). The LC n-3 FA are mostly found in oily fish, seafood and in red meats (especially DPA) in the Australian diet( 28 ).
Unsaturated FA variables used in the present analysis included: (i) individual n-3 FA intakes (ALA, EPA, DPA, DHA); (ii) total n-3 FA intake; (iii) total LC n-3 FA acid intake (EPA+DPA+DHA); (iv) total n-6 FA intake; (v) intake of the individual n-6 FA, LA; (vi) total n-9 FA intake; and (vii) intake of the individual n-9 FA, OA.
Mental health outcome measures
The CESD-10 tool was used to measure depressive symptoms experienced ‘during the last week’. CESD-10 has good internal consistency and validity and was specifically designed to identify depressive symptoms by self-report in non-clinical population research( 29 ). Responses are converted to a score out of 30, where higher scores indicate increased depressive symptomatology. Scores ≥10 were used to indicate depression( 30 ).
The five-item mental health (MH) subscale of the Medical Outcomes Study SF-36 specifically targets depression and anxiety experienced ‘during the past 4 weeks’( 31 ). Responses are converted to a score out of 100, with higher scores indicating better mental health. The scales of the SF-36 have high internal consistency and have been tested extensively for reliability and validity with adults of all ages( 32 ). The MH subscale was used as it is highly correlated with other measures of depression and is a validated screening tool for depression, at a cut-off point of ≤52( 33 – 35 ).
Participants were asked if they had been diagnosed with or treated for depression or anxiety (self-reported data) in the last 3 years (yes/no). The responses to these items were both also used as separate mental health outcome variables in the present analysis.
Statistical analysis
All analyses were performed using the JMP statistical software package (version 9·0, 2010). To improve the validity of the dietary analyses, women with reported daily energy intakes <4·5 or >20·0 MJ/d were excluded (n 1432) as energy values outside this range were considered biologically improbable and indicative of misreporting( 36 ). Therefore a total of 7635 women were included in the analysis. Logistic regression analyses were conducted as the outcome variables are binary.
First, unadjusted logistic regression analyses were conducted using all unsaturated FA listed above as continuous variables. Each FA value was compared with each categorical outcome variable; self-reported diagnosed depression, self-reported diagnosed anxiety, CESD-10 (cut-off point ≥10) and SF-36 MH subscale (cut-off point ≤52).
Adjusted analyses were then conducted using logistic regression models. The association was reported after the following confounders were adjusted for after consideration of their potential influence on mental health outcomes: BMI( 37 ) (<18·5 kg/m2 underweight, 18·5–24·99 kg/m2 normal weight, 25·0–29·99 kg/m2 overweight, ≥30·0 kg/m2 obese); energy intake (kJ); physical activity categorised in total metabolic equivalent (MET) minutes( 38 ) (<40 none, 40–600 low, 600–1200 moderate, >1200 high); whether they had been diagnosed with/treated for any of seventeen medical conditions in the previous 3 years such as type 2 diabetes, heart disease, postnatal depression, anxiety, a sexually transmitted infection, hepatitis B or C or cancer (anxiety and depression conditions were excluded from this count in models as appropriate); whether they had experienced any of twenty-one symptoms ‘often’, such as severe tiredness, leaking urine, back pain and skin problems (anxiety and depression symptoms were excluded from this count in models as appropriate); alcohol status (low risk, non-drinker, rare drinker, risky/high risk drinker); highest qualification completed (high school, trade/apprenticeship/certificate/diploma, university degree or higher); pattern of drug use (no use of any drugs in the last 12 months/ever, only used marijuana in last 12 months, used multiple/single drug other than marijuana in last 12 months); smoking status (never smoked, ex-smoker, >10/d, 10–19/d, ≥20/d); pregnancy status (yes/no, ‘don’t know’ was replaced with missing); experienced any kind of abuse in last 3 years (yes/no); area of residence (major city, inner regional, outer regional, remote/very remote); ability to manage on income (impossible/difficult all the time, difficult some of the time, not too bad, easy); marital status (never married, married/de facto, separated/divorced/widowed); whether they had experienced any of twenty-eight major life events in the last 12 months (e.g. major personal injury, illness, surgery, having a child with a serious disability or illness, divorce/separation, becoming a sole parent, death of partner/close family member, loss of job, natural disaster, involvement in a serious accident, sexual abuse, legal troubles). Additionally, participants taking antidepressant medications were also adjusted for in the analyses involving CESD-10 and SF-36 MH subscale. P values of <0·05 were considered statistically significant and odds ratios and their 95 % confidence intervals were calculated.
Results
In survey 3, 9067 women completed and returned the questionnaire. Of these, 1432 (15·8 %) were excluded as they had implausible energy intakes of <4·5 or >20·0 MJ/d( 36 ). Overall, 7635 young Australian women between the ages of 25 and 30 years were included in the analyses. The mean energy intake for this population was 7526 (sd 2389) kJ/d, 51 % were of a healthy weight and 52 % were moderately-highly active. In terms of education, 43 % had a university degree or higher, 55 % lived in a major city and 76 % had never smoked or were an ex-smoker.
Mean FA intakes for the ALSWH young women are presented in Table 1. The 1995 National Nutrition Survey data on FA intakes( 39 ) (for Australian adults) and the Nutrient Reference Value recommendations( 11 ) (for women 19+ years) are also presented here for comparison (Table 1). Unadjusted mean intakes of each explanatory FA variable for each categorisation of the mental health outcomes are shown in Table 2.
Table 1.
ALSWH (n 7635) | 1995 NNS (n 10 851) (mean intake, Australian adults aged 19+ years) | Australian NRV recommendations (AI, women aged 19+ years) | ||
---|---|---|---|---|
Mean | sd | |||
Total n-3 (g) | 1·43 | 0·66 | 1·36 | – |
ALA (g) | 1·05 | 0·45 | 1·17 | 0·80 |
EPA (g) | 0·11 | 0·13 | – | – |
DPA (g) | 0·04 | 0·04 | – | – |
DHA (g) | 0·24 | 0·25 | – | – |
LC n-3 (g) | 0·39 | 0·41 | 0·19 | 0·09 |
Total n-6 (g) | 8·73 | 4·09 | 10·85 | 8·00 |
LA (g) | 8·63 | 4·06 | 10·80 | – |
Total n-9 (g) | 28·79 | 11·99 | 20·31 | – |
OA (g) | 25·63 | 10·78 | – | – |
AI, Adequate Intake; ALA, α-linolenic acid; DPA, docosapentaenoic acid; LC, long chain; LA, linoleic acid; OA, oleic acid.
Table 2.
Symptoms of depression | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Self-reported depression | Self-reported anxiety | (CESD-10 ≥10) | (SF-36 MH subscale ≤52) | |||||||||||||
Yes | No | Yes | No | Yes | No | Yes | No | |||||||||
(n 927) | (n 6590) | (n 452) | (n 7065) | (n 1949) | (n 5570) | (n 1310) | (n 6311) | |||||||||
Mean | sd | Mean | sd | Mean | sd | Mean | sd | Mean | sd | Mean | sd | Mean | sd | Mean | sd | |
Total n-3 (g) | 1·47 | 0·63 | 1·43 | 0·66 | 1·49 | 0·68 | 1·43 | 0·66 | 1·51 | 0·75 | 1·41 | 0·64 | 1·49 | 0·70 | 1·42 | 0·65 |
ALA (g) | 1·09 | 0·46 | 1·04 | 0·44 | 1·09 | 0·47 | 1·04 | 0·44 | 1·12 | 0·49 | 1·02 | 0·43 | 1·11 | 0·50 | 1·03 | 0·43 |
EPA (g) | 0·11 | 0·12 | 0·11 | 0·13 | 0·12 | 0·13 | 0·11 | 0·13 | 0·11 | 0·15 | 0·11 | 0·12 | 0·11 | 0·13 | 0·11 | 0·13 |
DPA (g) | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 | 0·04 |
DHA (g) | 0·23 | 0·23 | 0·24 | 0·25 | 0·25 | 0·25 | 0·23 | 0·25 | 0·24 | 0·29 | 0·23 | 0·25 | 0·23 | 0·25 | 0·24 | 0·25 |
LC n-3 (g) | 0·38 | 0·38 | 0·39 | 0·41 | 0·41 | 0·42 | 0·38 | 0·41 | 0·39 | 0·48 | 0·38 | 0·40 | 0·38 | 0·41 | 0·39 | 0·41 |
Total n-6 (g) | 9·09 | 4·37 | 8·66 | 4·03 | 9·22 | 4·21 | 8·68 | 4·07 | 9·14 | 4·24 | 8·57 | 4·01 | 9·10 | 4·37 | 8·65 | 4·02 |
LA (g) | 8·99 | 4·35 | 8·57 | 4·01 | 9·12 | 4·18 | 8·57 | 4·04 | 9·04 | 4·22 | 8·47 | 3·98 | 9·00 | 4·34 | 8·55 | 4·00 |
Total n-9 (g) | 29·72 | 12·76 | 28·61 | 11·83 | 29·27 | 12·37 | 28·72 | 11·93 | 30·7 | 13·60 | 28·09 | 11·27 | 30·32 | 13·57 | 28·46 | 11·62 |
OA (g) | 26·52 | 11·56 | 25·46 | 10·62 | 26·08 | 11·13 | 25·56 | 10·73 | 27·34 | 12·24 | 24·99 | 10·13 | 27·01 | 12·20 | 25·32 | 10·44 |
CESD-10, ten-item Center for Epidemiological Studies Depression Scale; SF-36 MH subscale, Medical Outcomes Study Short Form Health Survey mental health subscale; ALA, α-linolenic acid; DPA, docosapentaenoic acid; LC, long chain; LA, linoleic acid; OA, oleic acid.
The prevalence of mental health outcomes is presented in Table 3. In the previous 3 years in this cohort, the prevalence of self-reported diagnosed or treated depression was 12·1 % (n 927) and anxiety was 5·9 % (n 452). The number experiencing symptoms of depression in the previous week, indicated by the CESD-10 screening tool, was 25·5 % (n 1949). The SF-36 MH subscale, which considers the previous 4 weeks, identified 17·2 % (n 1310) with risk of depressive symptoms.
Table 3.
Yes | No | Missing | ||||
---|---|---|---|---|---|---|
n | % | n | % | n | % | |
Self-reported diagnosed depression | 927 | 12·1 | 6590 | 86·3 | 118 | 1·6 |
Self-reported diagnosed anxiety | 452 | 5·9 | 7065 | 92·5 | 118 | 1·6 |
CESD-10 ≥10 | 1949 | 25·5 | 5570 | 72·9 | 116 | 1·6 |
SF-36 MH subscale ≤52 | 1310 | 17·2 | 6311 | 82·7 | 14 | 0·1 |
CESD-10, ten-item Center for Epidemiological Studies Depression Scale; SF-36 MH subscale, Medical Outcomes Study Short Form Health Survey mental health subscale.
Table 4 shows the results of the adjusted logistic regression analyses between dietary intake of unsaturated FA and mental health outcomes. There were no statistically significant associations between self-reported diagnosed depression and the intake of any of the unsaturated FA. There was a statistically significant association between the individual n-3 FA, ALA, and the CESD-10 score (OR=0·77; 95 % CI 0·60, 0·99; P=0·040; Table 4). Additionally, there was a statistically significant association between increased ALA and the SF-36 MH subscale (OR=0·73; 95 % CI 0·56, 0·96; P=0·024). There was also a statistically significant association between higher intakes of total n-6 FA and LA and decreases in self-reported diagnosed anxiety, although the effect was considerably smaller (OR=0·96; 95 % CI 0·93, 0·99 for both; P=0·019 and P=0·020, respectively). Small, but statistically significant associations were also found between self-reported diagnosed anxiety and intakes of total n-9 FA (OR=1·02; 95 % CI 1·00, 1·04; P=0·041) and OA (OR=1·02; 95 % CI 1·00, 1·05; P=0·046), although these were in the opposite direction.
Table 4.
Symptoms of depression | ||||||||||||
Self-reported depression | Self-reported anxiety | CESD-10 ≥10 | SF-36 MH subscale ≤52 | |||||||||
OR | 95 % CI | P value | OR | 95 % CI | P value | OR | 95 % CI | P value | OR | 95 % CI | P value | |
Total n-3 (g) | 1·05 | 0·87, 1·26 | 0·637 | 0·93 | 0·74, 1·19 | 0·564 | 0·98 | 0·85, 1·14 | 0·128 | 0·96 | 0·82, 1·16 | 0·629 |
ALA (g) | 0·90 | 0·66, 1·24 | 0·519 | 0·98 | 0·65, 1·49 | 0·928 | 0·77 | 0·60, 0·99 | 0·040* | 0·73 | 0·56, 0·96 | 0·024* |
EPA (g) | 1·38 | 0·68, 2·89 | 0·379 | 0·78 | 0·34, 1·90 | 0·564 | 1·31 | 0·75, 2·34 | 0·353 | 1·29 | 0·69, 2·49 | 0·433 |
DPA (g) | 6·97 | 0·58, 93·3 | 0·134 | 0·41 | 0·02, 9·14 | 0·562 | 3·35 | 0·45, 25·89 | 0·241 | 3·43 | 0·37, 34·16 | 0·285 |
DHA (g) | 1·21 | 0·84, 1·77 | 0·326 | 0·87 | 0·57, 1·37 | 0·535 | 1·20 | 0·89, 1·61 | 0·234 | 1·21 | 0·87, 1·70 | 0·262 |
LC n-3 (g) | 1·12 | 0·90, 1·41 | 0·316 | 0·92 | 0·71, 1·22 | 0·544 | 1·11 | 0·93, 1·33 | 0·265 | 1·11 | 0·91, 1·36 | 0·308 |
Total n-6 (g) | 0·98 | 0·95, 1·00 | 0·091 | 0·96 | 0·93, 0·99 | 0·019* | 0·99 | 0·97, 1·02 | 0·597 | 0·99 | 0·97, 1·01 | 0·443 |
LA (g) | 0·98 | 0·95, 1·00 | 0·093 | 0·96 | 0·93, 0·99 | 0·020* | 0·99 | 0·97, 1·02 | 0·603 | 0·99 | 0·97, 0·99 | 0·444 |
Total n- 9 (g) | 1·00 | 0·98, 1·02 | 0·917 | 1·02 | 1·00, 1·04 | 0·041* | 0·99 | 0·98, 1·01 | 0·287 | 1·00 | 0·99, 1·01 | 0·799 |
OA (g) | 1·00 | 0·98, 1·01 | 0·523 | 1·02 | 1·00, 1·05 | 0·046* | 0·99 | 0·98, 1·01 | 0·224 | 1·00 | 0·98, 1·01 | 0·790 |
CESD-10, ten-item Center for Epidemiological Studies Depression Scale; SF-36 MH subscale, Medical Outcomes Study Short Form Health Survey mental health subscale; ALA, α-linolenic acid; DPA, docosapentaenoic acid; LC, long chain; LA, linoleic acid, OA, oleic acid.
Adjusted for BMI, energy intake, physical activity, chronic illnesses, alcohol intake, education, drug use, smoking status, pregnancy status, abuse, area of residence, managing on income, marital status, major life events, symptoms, depression medications (for CESD-10 and SF-36 MH subscale only).
Statistically significant (P<0·05).
Discussion
Despite the acknowledged metabolically plausible role of unsaturated fats in mental health, the present study appears to be the first to compare a range of unsaturated FA derived from dietary intake data with various mental health outcomes using a large nationally representative cohort of young women.
Our findings demonstrated that women with higher consumptions of ALA were less likely to have depressive symptoms. A study by Panagiotakos et al. (2010) in 853 healthy adults from the province of Attica found that increases in plasma total PUFA, total MUFA, total n-3 FA, DHA, EPA, LA and ALA were all associated with lower scores on Zung’s Self-rating Depression Scale( 40 ). To the authors’ knowledge, no one has previously shown an association between dietary intakes of ALA and reduced risk of depression using the SF-36 MH subscale and CESD-10 validated screening measures. Despite the significant relationship with the validated screening tools, our analyses showed no significant relationship between ALA intake and self-reported diagnosed depression. This is possibly due to the wording in the ALSWH survey, which asked women to report if they had been ‘treated or diagnosed’ for depression in the ‘last 3 years’. This is a much longer timeframe than for the FFQ, and therefore the outcome has really been measured before the exposure, and it may be expected that anyone diagnosed and undertaking treatment for depression would not currently be experiencing depressive symptoms. However, the SF-36 and the CESD-10 ask about depressive symptoms experienced over the previous 4 weeks and 1 week, respectively, which are within the timeframe for the FFQ.
Contrary to much of the existing literature which shows an inverse association between LC n-3 FA and/or fish intake, there were no significant associations found between the LC n-3 FA and the mental health outcomes in the present analyses( 14 , 15 , 41 ). ALA is the primary n-3 FA consumed in a Western diet, but it is generally believed that the conversion rate of ALA to the LC n-3 FA is very limited, at approximately 8 % in adults( 27 , 42 , 43 ). However, there is recent evidence to suggest that ALA may be more efficiently converted to LC n-3 FA in women, in particular women of reproductive age, as a result of a variation in their metabolic capacity to meet the DHA demands of a fetus and neonate during pregnancy and lactation( 42 , 44 , 45 ). As the literature focuses primarily on fish consumption as a marker of LC n-3 FA, there is little reported in the literature about ALA and depression in young women. It is possible that the association with ALA but not with LC n-3 is a result of the FFQ more effectively assessing ALA in the diet compared with LC n-3, as the coverage of fish intake is limited.
Our results also showed that women with higher consumptions of total n-6 FA or LA were less likely to have self-reported anxiety. The agreement between these two explanatory variables is not surprising as for the present analysis LA comprised approximately 98 % of total n-6 intake. To the authors’ knowledge, this is the first comparison of dietary intake of n-6 FA and anxiety in an observational study of a large cohort. There is some evidence for total dietary PUFA and decreases in anxiety in a study by Yehuda et al. (2005), which found that higher intakes of PUFA in a group of college students reduced previously elevated cortisol levels and improved sleep quality, thereby reducing test anxiety( 46 ). Similarly, a randomised control trial by Williams et al. (1992) found that individuals who exhibited more psychological stress had altered proportions of total plasma esterified n-6 FA compared with their less stressed counterparts, although n-3 FA were found in similar proportions in both groups( 47 ). This suggests that stress-related metabolic processes may bypass n-3 FA pathways, and higher intakes of n-6 FA may prevent metabolism of n-3 FA within the body( 47 ).
The results of our study showed that young women with lower consumptions of total n-9 FA or OA were less likely to have self-reported diagnosed anxiety. Again, for this analysis, OA comprises 89 % of the total n-9 intake. The authors are not aware of any studies that have previously investigated n-9 FA and anxiety; however, there has been some research into the relationship between MUFA and depression. Unlike the present analysis, the results of these studies suggest that increased MUFA are associated with decreased risk of depression( 19 , 40 ). While these studies were not directly measuring anxiety, it is thought that depression and anxiety are mechanistically related( 17 ) and this justified the current investigation.
The strengths of the present study are the large population-based sample, the ability to control for multiple confounding variables, and the inclusion of validated dietary intake and depression-screening tools in the analysis. The dietary intake data used in the study were plausible with regard to energy intake( 36 ) and comparable with other Australian data( 3 ), and the outcome variables were not dissimilar to similar population data, making the results of the study meaningful to the population of interest( 3 , 48 ). Furthermore, having the data that enabled the study to be designed to include numerous markers of mental health and both total and individual FA strengthen the study as this allowed a unique and more comprehensive examination of the association between dietary FA intake and mental health measures.
The findings are limited by a potential for measurement error associated with the use of a self-reported FFQ, with a reduced range of foods included in the dietary evaluation. It should be noted however that all methods of dietary data collection have some form of measurement error. While this FFQ is a validated dietary intake tool for this population, it has not been validated for FA intakes( 26 ). However, data analysis was limited to plausible energy ranges using a previously published method( 36 ) and average intakes of FA were within realistic ranges of national dietary averages( 11 , 39 ). Participants may have been taking supplementary sources of various FA (n-3 in particular), which would impact the analyses, but this information was not available from the ALSWH survey. Data from the 1995 National Health Survey demonstrate that over 9 % of the Australian population uses natural/herbal medications (including fish-oil supplements), and women were almost twice as likely to use them than men( 49 ). Finally, the cross-sectional study design means that causal relationships and the direction of those relationships cannot be determined; therefore longitudinal studies are needed to assess temporal associations.
The findings of the present study were unexpected as no associations were revealed between the LC n-3 FA and anxiety or depression. While most of the recent research has been conducted in this area, the present findings suggest that further studies are needed of all dietary unsaturated FA as they may be associated with these common and debilitating mental health issues.
Overall, there is limited knowledge about the preventive potential of each type, source, dose or combination of unsaturated FA and the mental health outcomes of depression and anxiety due to a limited literature( 50 ). Further well-designed, large cohort studies are needed that use comparable measures of mental health and validated tools to measure unsaturated FA to ensure consistency in results. This in turn will strengthen the current evidence base to be able to confidently confirm or refute an association.
Conclusion
The current study demonstrated that among a nationally representative sample of young Australian women, an increased intake of ALA but not other n-3 FA was associated with a decreased likelihood of experiencing depressive symptoms. Furthermore, increased intakes of n-6 FA and LA and decreased intakes of n-9 FA and OA were associated with a decreased likelihood of having self-reported diagnosed anxiety. These findings deviate from the current literature and indicate that further studies are needed into the relationship between all unsaturated FA and the mental health outcomes of depression and anxiety.
Acknowledgements
Acknowledgements: The research on which this paper is based was conducted as part of the Australian Longitudinal Study on Women’s Health (ALSWH), the University of Newcastle and the University of Queensland. The authors are grateful to the Australian Government Department of Health and Ageing for funding the ALSWH and to the women who provided the survey data. The authors also thank Professor Graham Giles of the Cancer Epidemiology Centre of Cancer Council Victoria, for permission to use the Dietary Questionnaire for Epidemiological Studies (Version 2). Financial support: The research reported in this paper received no specific grant from any funding agency in the public, commercial or non-for-profit sectors. Conflict of interest: None. Authorship: This study was conducted as an honours research project by C.D. under the supervision of L.M.-W., A.P. and D.S., who designed the study. L.M.-W. and A.P. had the dietary and fatty acid expertise while D.S. assisted with the statistical analysis. C.D. conducted the data analysis, under the supervision of D.S., and drafted the first version of the manuscript. All authors contributed to reviewing, editing and approving of the final version of the paper. Ethics of human subject participation: The ALSWH has been approved by the Human Research Ethics Committees of the University of Newcastle and the University of Queensland.
References
- 1. World Health Organization (WHO) (2003) Investing in Mental Health. Geneva: WHO, Department of Mental Health and Substance Dependence. [Google Scholar]
- 2. Slade T, Johnston A, Teesson M et al. (2009) The Mental Health of Australians 2: Report on the 2007 National Survey of Mental Health and Wellbeing. Canberra: Department of Health and Ageing. [Google Scholar]
- 3. Australian Insitute of Health and Welfare (2008) Australia's Health 2008. Canberra: AIHW. [Google Scholar]
- 4. Klerman G & Weissman M (1989) Increasing rates of depression. JAMA 261, 2229–2235. [PubMed] [Google Scholar]
- 5. Drewnowski A & Popkin B (1997) The nutrition transition: new trends in the global diet. Nutr Rev 55, 31–43. [DOI] [PubMed] [Google Scholar]
- 6. Hibbeln J & Salem Jr N (1995) Dietary polyunsaturated fatty acids and depression: when cholesterol does not satisfy. Am J Clin Nutr 62, 1–9. [DOI] [PubMed] [Google Scholar]
- 7. Hidaka B (2012) Depression as a disease of modernity: explanations for increasing prevalence. J Affect Disord 140, 205–214. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Goldney D, Eckert K, Hawthorne G et al. (2010) Changes in the prevalence of major depression in an Australian community. Aust N Z J Psychiatry 44, 901–910. [DOI] [PubMed] [Google Scholar]
- 9. Wainwright P (2002) Dietary essential fatty acids and brain function: a developmental perspective on mechanisms. Proc Nutr Soc 61, 61–69. [DOI] [PubMed] [Google Scholar]
- 10. Jumpsen J & Clandinin MT (1995) Brain Development: Relationship to Dietary Lipid and Lipid Metabolism. Champaign, IL: AOCS Press. [Google Scholar]
- 11. Australian National and Health Medical Research Council (2006) Nutrient Reference Values for Australia and New Zealand Including Recommended Dietary Intakes. Canberra: Commonwealth of Australia. [Google Scholar]
- 12. Appleton K, Rogers P & Ness A (2010) Updated systematic review and meta-analysis of the effects of n-3 long-chain polyunsaturated fatty acids on depressed mood. Am J Clin Nutr 91, 757–770. [DOI] [PubMed] [Google Scholar]
- 13. Yanfeng L, Qi D, Ekperi L et al. (2011) Fish consumption and severely depressed mood, findings from the first national nutrition follow-up study. Psychiatry Res 190, 103–109. [DOI] [PubMed] [Google Scholar]
- 14. Colango L, Whooley M, Daviglus M et al. (2009) Higher dietary intake of long-chain omega-3 polyunsaturated fatty acids is inversely associated with depressive symptoms in women. Nutrition 25, 1011–1019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Tanskanen A, Hibbeln J, Tuomilehto J et al. (2001) Fish consumption and depressive symptoms in the general population in Finland. Psychiatr Serv 52, 529–531. [DOI] [PubMed] [Google Scholar]
- 16. Crowe F, Skeaff M, Green T et al. (2007) Serum phospholipid n-3 long-chain polyunsaturated fatty acids and physical and mental health in a population-based survey of New Zealand adolescents and adults. Am J Clin Nutr 86, 1278–1285. [DOI] [PubMed] [Google Scholar]
- 17. Ross B (2009) Omega-3 polyunsaturated fatty acids and anxiety disorders. Prostaglandins Leukot Essent Fatty Acids 81, 309–312. [DOI] [PubMed] [Google Scholar]
- 18. Sanchez-Villegas A, Henriquez P, Figueiras A et al. (2007) Long chain omega-3 fatty acids intake, fish consumption and mental disorders in the SUN cohort study. Eur J Nutr 46, 337–346. [DOI] [PubMed] [Google Scholar]
- 19. Wolfe A, Ogbonna E, Lim S et al. (2009) Dietary linoleic and oleic fatty acids in relation to severe depressed mood: 10 years follow-up of a national cohort. Prog Neuropsychopharmacol Biol Psychiatry 33, 972–977. [DOI] [PubMed] [Google Scholar]
- 20. Yary T & Aazami S (2011) The association between polyunsaturated fatty acids and depression among Iranian postgraduate students in Malaysia. Lipids Health Dis 10, 151. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Lee C, Dobson A, Brown W et al. (2005) Cohort profile: the Australian Longitudinal Study on Women’s Health. Int J Epidemiol 34, 987–991. [DOI] [PubMed] [Google Scholar]
- 22. Brown W, Bryson L, Byles J et al. (1996) Women’s health Australia: establishment of the Australian Longitudinal Study on Women’s Health. J Womens Health 5, 467–472. [Google Scholar]
- 23. Brown W, Bryson L, Byles J et al. (1998) Women’s Health Australia: recruitment for a national longitudinal cohort study. Womens Health 28, 23–40. [DOI] [PubMed] [Google Scholar]
- 24. University of Newcastle & University of Queensland (2012) Women’s Health Australia. www.alswh.org.au/
- 25. Giles G & Ireland P (1996) Dietary Questionnaire for Epidemiological Studies (version 2). Melbourne: The Cancer Council Victoria. [Google Scholar]
- 26. Hodge A, Patterson A, Brown W et al. (2000) The Anti Cancer Council of Victoria FFQ: relative validity of nutrient intakes compared with weighed food records in young to middle-aged women in a study of iron supplementation. Aust N Z J Public Health 24, 576–583. [DOI] [PubMed] [Google Scholar]
- 27. Williams C & Burdge G (2006) Long-chain n-3 PUFA: plant v. marine sources. Proc Nutr Soc 65, 42–50. [DOI] [PubMed] [Google Scholar]
- 28. Howe P, Meyer B, Record S et al. (2006) Dietary intake of long chain n-3 polyunsaturated fatty acids: contribution of meat sources. Nutrition 22, 47–53. [DOI] [PubMed] [Google Scholar]
- 29. Roberts R & Vernon S (1983) The Center for Epidemiologic Studies Depression Scale: its use in a community sample. Am J Psychiatry 140, 41–46. [DOI] [PubMed] [Google Scholar]
- 30. Boey K (1999) Cross validation of a short form of the CESD-10 in Chinese elderly. Int J Geriatr Psychiatry 14, 608–617. [DOI] [PubMed] [Google Scholar]
- 31. Mishra G & Schofield M (1998) Norms for the physical and mental health component summary scores of the SF-36 for young, middle-aged and older Australian women. Qual Life Res 7, 215–220. [DOI] [PubMed] [Google Scholar]
- 32. McCallum J (1995) The SF-36 in an Australian sample: validating a new, generic health status measure. Aust J Public Health 19, 160–166. [DOI] [PubMed] [Google Scholar]
- 33. Byles J, Robinson I, Gibson R et al. (2007) Depression Among Women in the Australian Longitudinal Study on Women’s Health. Newcastle: Research Centre for Gender, Health and Ageing, University of Newcastle. [Google Scholar]
- 34. Silveira E, Taft C, Sundh V et al. (2005) Performance of the SF-36 Health Survey in screening for depressive and anxiety disorders in an elderly female Swedish population. Qual Life Res 14, 1263–1274. [DOI] [PubMed] [Google Scholar]
- 35. Berwick D, Murphy J, Goldman P et al. (1991) Performance of a 5-item mental health screening test. Med Care 29, 169–176. [DOI] [PubMed] [Google Scholar]
- 36. Hure A, Young A, Smith R et al. (2009) Diet and pregnancy status in Australian women. Public Health Nutr 12, 853–861. [DOI] [PubMed] [Google Scholar]
- 37. World Health Organization (2006) WHO Global Database on Body Mass Index. Geneva: WHO. [Google Scholar]
- 38. Brown W & Bauman A (2000) Comparison of estimates of population levels of physical activity using two measures. Aust N Z J Public Health 24, 52–55. [DOI] [PubMed] [Google Scholar]
- 39. McLennan W & Podger A (1995) National Nutrition Survey, Selected Highlights, Australia. Canberra: Australian Government Publishing Services. [Google Scholar]
- 40. Panagiotakos D, Mamplekou E, Pitsavos C et al. (2010) Fatty acid intake and depressive symptomatology in a Greek sample: an epidemiological analysis. J Am Coll Nutr 29, 586–594. [DOI] [PubMed] [Google Scholar]
- 41. Silvers K & Scott K (2002) Fish consumption and self-reported physical and mental health status. Public Health Nutr 5, 427–431. [DOI] [PubMed] [Google Scholar]
- 42. Burdge G & Wootton S (2002) Conversion of α-linolenic acid to eicosapentaenoic, docosapentaenoic and docosahexaenoic acids in young women. Br J Nutr 88, 411–420. [DOI] [PubMed] [Google Scholar]
- 43. Pawlosky R, Hibbeln J, Novotny J et al. (2001) Physiological compartmental analysis of α-linolenic acid metabolism in adult humans. J Lipid Res 42, 1257–1265. [PubMed] [Google Scholar]
- 44. Burdge G (2004) α-Linolenic acid metabolism in men and women: nutritional and biological implications. Curr Opin Clin Nutr Metab Care 7, 137–144. [DOI] [PubMed] [Google Scholar]
- 45. Burdge G & Calder P (2005) Conversion of α-linolenic acid to longer-chain polyunsaturated fatty acids in human adults. Reprod Nutr Dev 45, 581–597. [DOI] [PubMed] [Google Scholar]
- 46. Yehuda S, Rabinovitz S & Mostofsky D (2005) Mixture of essential fatty acids lowers test anxiety. Nutr Neurosci 8, 265–267. [DOI] [PubMed] [Google Scholar]
- 47. Williams L, Kiecolt-Glaser J, Horrocks L et al. (1992) Quantitative association between altered esterified omega-6 fatty acid proportions and psychological stress. Prostaglandins Leukot Essent Fatty Acids 47, 165–170. [DOI] [PubMed] [Google Scholar]
- 48. Taylor A, Wilson D, Grande E et al. (1999) Mental health status of the South Australian population. Aust N Z J Public Health 24, 29–34. [DOI] [PubMed] [Google Scholar]
- 49. Australian Bureau of Statistics (1999) National Health Survey: Use of Medications, Australia, 1995. Catalogue no. 4377.0. Canberra: Australian Government Publishing Service. [Google Scholar]
- 50. Schachter H, Kourad K, Merali Z et al. (2005) Effects of Omega-3 Fatty Acids on Mental Health. Evidence Report/Technology Assessment no. 116. Rockville, MD: Agency for Healthcare Research and Quality and University of Ottawa Evidence-based Practice Center. [PMC free article] [PubMed] [Google Scholar]