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Nutrition in Schizophrenia

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18 September 2023

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19 September 2023

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Abstract
Severe mental illness such as schizophrenia is associated with factors such as unemployment, meagre per capita income, and residence in disadvantaged, poorly resourced neighbourhoods. This means difficult access to healthy food and is particularly problematic for pregnant women and mothers with children to feed. Eating problems are also linked to the necessity of taking antipsychotic drugs that often lead to serious cognitive, psychological, and behavioural sequelae. Psychosis makes it extremely difficult to maintain a healthy diet; nutritional deficiencies result, as do medical complications. The results of present literature review confirm the gravity of the problem and suggest a number of potentially useful interventions.
Keywords: 
Subject: Biology and Life Sciences  -   Behavioral Sciences

1. Introduction

Clinical psychiatrists seldom ask schizophrenia patients what they eat. The evidence indicates that they probably should. What is widely known is that too many patients with schizophrenia, especially women, suffer from obesity, partly because of life style and partly as a result of treatment with antipsychotic drugs [1]. What is perhaps less well known is that eating disorders such as anorexia nervosa and schizophrenia can occur together [2,3,4]. As defined by the World Health Organization in 2020 [5], healthy eating refers not only to quantity, but also to the variety, balance, and safety of a person’s regular, day-in-day-out diet. Healthy eating is difficult for individuals diagnosed with schizophrenia and related disorders. In general, patients with any severe mental illness (SMI) eat high energy (sugar and saturated fat), relatively little fibre and fruit, and food that contains more salt than that of healthy controls [6,7]. The SMI diet is best characterized as high in easily accessible ready-to-eat food and low in fruit and vegetables [8,9]. A review of 822 studies of diet and psychosis in 2020 [10] found poor quality dietary patterns in individuals with psychosis, high intake of refined carbohydrates and total fat, and low intake of fibre, ω-3 and ω-6 fatty acids, vegetables, fruit, and important-to-health vitamins and minerals (vitamin B12 and B6, folate, vitamin C, zinc, and selenium). On average, individuals with SMI also exhibit considerably less knowledge about nutrition than their healthy peers [11]. Because this suggests that routine checks on patients’ food intake may need to become a routine component of psychiatric practice, I undertook a narrative review of the literature on A) the causes of poor diet in schizophrenia-related disorders, B) the presence of special dietary needs, C) the general health consequences of poor nutrition in this population, and D) potential interventions that show promise in ameliorating the situation.

2. Materials and Methods

In order to find the most current evidence available on the topics of interest to this review, I searched PubMed and Google Scholar titles and abstracts over the last ten years, using the following search terms: A) Diet OR Nutrition OR Food AND Schizophrenia OR Severe Mental Illness OR Psychosis AND Causes; B) Diet AND Needs AND Schizophrenia OR Severe Mental Illness OR Psychosis; C) Schizophrenia OR Severe Mental Illness OR Psychosis AND Consequences AND Nutrition OR Diet OR Food; D) Schizophrenia OR Severe Mental Illness OR Psychosis AND Intervention OR Treatment OR Prevention AND Nutrition AND Deficiency OR Lack. I included primary research and reviews and excluded papers in languages other than English. I then searched the reference lists of the full articles for potentially relevant paper published prior to 2013. My final selection of papers to review was based on clarity of writing, methodology, recency, and novelty of conclusions.

3. Results

3.1. Causes for Poor Diet in Schizophrenia

3.1.1. Poverty

Healthy diets are costly, which is a major reason why they are difficult to maintain by individuals with schizophrenia, most of whom are unemployed and living on disability or old age pensions in deprived urban environments. Majuri et al. [12] in 2023 published a study of 30 year employment trajectory patterns in schizophrenia based on the Northern Finland Birth Cohort of 1966 (number with schizophrenia = 62, ages 16-45). As had been shown in earlier work, most individuals with schizophrenia were not in the labour market and relied, instead, on a government pension. A 7 year study (2006-2013) from Sweden [13] had found employment to be rare (10%) among people with schizophrenia; over 80% were being supported on a disability pension. Writing about the finances of people with major psychiatric disorders, Eliason [14] summarizes the situation: “even in an advanced welfare state, people with SMI (severe mental illness), especially those with schizophrenia, have an extremely weak position on the labour market and an equally difficult financial situation.”
There are reasons beyond low income for poor nutrition in this population. Low income urban neighbourhoods, where people with schizophrenia tend to live, do not provide easy access to healthy food. In other words, supermarkets that offer fresh, good quality food at affordable prices are missing from these neighbourhoods [15,16]. Accessible grocery stores sell mostly processed food. The residential areas of individuals with schizophrenia are “food deserts, ” which means that one has to travel a fair distance to purchase healthy food, which, in turn, incurs unaffordable transportation costs [15], especially so for house-bound mothers.

3.1.2. Scizophrenia Symptoms

The comprehensive review of dietary habits associated with psychosis by Aucoin et al. [10] is quick to acknowledge that socio-economic status, but also psychotic symptoms, are responsible for the poor nutrition seen in this population. Positive symptoms (hallucinations, delusions), negative symptoms (apathy, social isolation, anhedonia), cognitive deficiencies (attention, short term memory), and mood problems (depression, anxiety) conspire in schizophrenia to reduce interest in food (anhedonia), and inhibit all motivation to prepare food (avolition). Furthermore, social isolation tends to make eating more of a chore than a pleasure. Food is best enjoyed in company; eating alone undermines appetite and makes shopping and preparing meals seem pointless [17,18]. Findings from a review of 42 studies suggest that eating with others significantly increases food intake relative to eating alone, but that this is moderated by the identity of a person’s meal companions. Human beings tend to imitate the food choices and preferences of frequent co-eaters [19]. Apathy, a common feature of schizophrenia [20], has been shown in one study to impede functional outcome in schizophrenia. In this study, apathy was measured using the Independent Living Skills Survey (ILSS) [21], which includes items relevant to food preparation. Semkovska et al. [22] examined three activities (choosing a menu, shopping for the ingredients, cooking a meal) performed by 27 patients with schizophrenia and 27 controls. Patients with schizophrenia committed significantly more omissions when choosing the menu, made more errors during the shopping task, and also during the cooking task. The degree of error was found to correlate significantly with the severity of the patient’s negative symptoms [22]. Cognitive problems have not been studied in relation to schizophrenia and food tasks, but probably contribute to the inability to budget for food and to prepare healthy meals, in the same way as they have been shown to do in Alzheimer’s disease [23].
The positive symptoms, delusions and hallucinations -e.g. hearing commands to desist from certain foods or avoid certain grocery stores for fear of danger, may deprive patients with schizophrenia of specific foods. Occasional case reports attest to this possibility – these are reports of Wernicke’s thiamine deficiency and encephalopathy associated with schizophrenia (and absence of alcohol consumption) [23,24,25,26,27,28]. Alcohol addiction may, nonetheless, in many cases of schizophrenia, be the main cause of Wernicke’s syndrome [29].

3.1.3. Circadian Rhythms in Schizophrenia

Disruption of circadian rhythm can interfere with mealtimes and interfere with eating. Both animal and human data point to sleep and circadian rhythm disturbance in schizophrenia, mediated perhaps by increasing dopamine release and sensitivity [30]. This affects sleep patterns such as day/night reversal, which, in turn, throw eating patterns into disarray. [31]. It has been suggested that a relationship exists between light exposure and mealtime regularity and that lack of light can have negative effects on metabolic health [32]. Being unemployed, as most persons with schizophrenia are, means few daytime obligations, which, in turn, means that sleeping by day and staying awake at night (night/day reversal) is a frequent mode of living for this population because it avoids social encounters, which many with this disorder find distressing. Avoiding social contact, however, impedes shopping for food and, thereby, negatively affects nutrition [33].

3.1.4. Substance Excess in Schizophrenia

Individuals who are socially isolated are particularly vulnerable to alcohol and drug dependency [34], while chronic substance abuse is known to be positively associated with food deficiencies and malnutrition. Ross et al. [35] conducted a study of 67 patients in an alcohol detoxification unit and assessed their nutritional status through questionnaires and blood tests. Twenty-four percent of the study participants qualified for a diagnosis of mild to moderate malnutrition, a percentage that the study authors considered an underestimate. Half the participants were found deficient in iron or vitamins. Alcohol consumption, especially in males, is highly prevalent in the schizophrenia population [36] and probably plays an important role in the extent of poor eating habits.

3.1.5. Living Circumstances

When not hospitalized, individuals with schizophrenia live with family or live alone or in communal living quarters. The living arrangements of over 1446 schizophrenia patients from 57 sites throughout the United States over a one year period were characterized by Tsai et al. [37]. At baseline, 46% were living with family members, 5% were living with nonrelatives, and 18% were living independently. Seventeen percent were housed in an institution, and 14% were living in unstable housing. In another study of 1825 participants with psychotic disorders, one half lived in public or private rented housing (48.6%) and 22.7% were waiting for public housing. Thirteen percent were living in their own home. One in 20 study participants was homeless at the time of the study; almost 13% had been homeless at some point within the previous 12 months [38]. Because of the close correlation between healthy eating and safe, stable housing [39], according to the results of these studies, between 12% and 14% of individuals with a psychotic disorder are precariously nourished [40,41].

3.1.6. Antipsychotics

Antipsychotic, antidepressant and mood-stabilising medications are all associated with substantial weight gain, which can result, over time, in obesity and cardiometabolic abnormalities. Elman et al. [42] have suggested that the mesolimbic hyperdopaminergic state that is hypothesized to exist in schizophrenia makes food taste bland unless extra salt or sugar is added. This, plus cognitive deficiencies, plus symptoms of psychosis, plus limited resources, plus alcohol help account for many of the unhealthy eating habits seen in schizophrenia. When treatment with antipsychotics is added to the mix, it lowers dopamine levels so that positive symptoms diminish, but appetite is increased. The result is overeating of unhealthy food. The findings of a study by Blouin et al. [43] are consistent with this view. Individuals taking second generation antipsychotic medication report increased appetite, decreased satiety levels and, in addition, increased cravings for sweet foods and beverages. Two more recent reviews of this topic confirm these results [44,45].
Mukherjee et al. [44] underscores the importance of a drug’s individual receptor binding profile to its impact on nutrition. Affinity for dopamine D2, serotonin 5HT2c, and histamine H1 receptors plays a critical role in a drug’s interaction with appetite regulation pathways in the brain.
Second generation antipsychotics are known to induce more metabolic ill effects than earlier drugs. In 2021, Rognoni et al. [46] conducted a review of 79 papers to determine the worst among the drug offenders, excluding clozapine, which was not part of their study. Olanzapine showed the largest BMI increase; paliperidone showed the highest increase in total cholesterol; quetiapine XR showed the highest decrease in fasting glucose and the highest increase in systolic and diastolic blood pressure. Lurasidone showed a reduction in BMI and a decrease in total cholesterol and triglycerides [46]. In another recent review, olanzapine and clozapine were reported as the antipsychotic drugs causing the greatest weight gain [47]. These drugs are, however, sedative, so that patients who, on other drugs, were snacking at night paradoxically lose weight on olanzapine and clozapine because they sleep more soundly!
Antagonistic effects on muscarinic and histaminergic receptors contribute to increased appetite. Additional variables are the drug’s effect on gut microbiota and the brain areas that regulate food intake. Antipsychotics change the balance of gut bacteria [48] and it may be this indirect route that leads to metabolic disturbance. The research groups of both Mukherjee et al. and Sankaranarayanan et al. [44,45] conclude their reviews of the effects of 2nd generation antipsychotics on disordered eating in schizophrenia by detailing the consequences of their use on a number of dietary and nutritional parameters, namely hunger, food craving and addiction, dietary restraint and disinhibition, satiety, caloric intake, eating habits and dietary composition.

3.2. Special Dietary Needs

3.2.1. Schizophrenia and Diabetes

There are circumstances and health conditions that make good nutrition especially important. Comorbidity between schizophrenia and diabetes is one such condition and it is highly prevalent among individuals with schizophrenia. The rate of Type 2 diabetes is two to three times higher in schizophrenia than in the general population [49].
It has been hypothesized that the two disorders share common susceptibility genes [49]. Moreover, the antipsychotic drug treatment for schizophrenia is known to induce weight gain and metabolic abnormalities such as diabetes. Preventing diabetes and controlling diabetes means paying careful attention to what one eats in the context of a well-ordered lifestyle. This is difficult for persons with schizophrenia, in part because of cognitive defects, in part because of socioeconomic disadvantage. Focus groups held with individuals comorbid for diabetes and mental illness (not only schizophrenia) have uncovered many subjectively-reported challenges in this population, any of which can lead to poor diabetes self-care [50]. Qualitative interviews with psychiatric patients, family members, and primary care staff yielded similar results [51]. A wide range of factors are known to influence diabetes self-management, which refers not only to to dietary content and eating routines but also to motivation, knowledge, and skills, as well as to social support from family and friends, all of which are lacking in most patients with schizophrenia [52].

3.2.2. Schizophrenia and Pregnancy

Pregnancy incurs special nutritional needs in women. Although this has not been extensively studied, vitamin deficiency (especially Vitamin D deficiency) and mineral deficiencies (zinc and iron) have been reported and have been positively associated with intrauterine growth restriction in infants born to women with SMI [53]. Whereas, because of antipsychotic-induced obesity, pregnant women with schizophrenia need larger than average doses of routine prenatal folic acid supplements, in one study, folic acid was only being taken by 25% of pregnant schizophrenia women [54]. The same paper [54] reported iron deficiency in 73% of the women. A study of 38 pregnant women with SMI found high rates of obesity, with 82% showing gestational weight gain above recommendations. Almost one-third of the women failed to meet any of the Five Food Group serving recommendations for pregnancy and reported above-recommended levels in their diet of processed food (19%) and sugar snacks (51%) [54]. The likelihood of pregnant women with schizophrenia treated with antipsychotic medication developing gestational diabetes has been reported as 5-7 times that of women with schizophrenia not taking these drugs [55]. First generation antipsychotics were seen as the worst culprits [55]. Because of lack of education, high levels of misinformation, and the socio-economic status of women in low income countries, malnutrition during pregnancy remains an acute health problem in many regions of the world [56.]

3.2.3. Schizophrenia and Motherhood

Qualitative studies have addressed food access and healthy eating challenges in women with schizophrenia who are also mothers, most often single mothers. Lack of time (for shopping and cooking) and difficulties in finding transportation to and from food stores were reported by mothers in large urban centres to be major constraints to the provision of adequate nutrition for their children [15,57]. Low income mothers are known to often prioritize food pricing and shelf-stability when buying food, thereby sacrificing food quality [58]. Many environments, but especially poor environments, are plagued according to mothers, with street vendors selling non-nutritious high caloric food that is a magnet for children [58]. With respect to mothers’ own nutritional needs, during periods of food insecurity, mothers routinely compromise their own food needs in order to better feed their children [59]. This makes mothers with schizophrenia a particularly nutrition-vulnerable group.

3.2.4. Schizophrenia and Old Age

An even more nutrition-vulnerable group are the elderly, where the prevalence of severe malnutrition is reportedly very high [60] and has been attributed to “the nine ds” : dentition, dysgeusia, dysphasia, diarrhea, depression, disease, dementia, dysfunction, and drugs [61]. A recent study [62] has highlighted the functional impairments seen in older (mean age = 64) patients with schizophrenia. Because of physical, psychological, and cognitive morbidities, many participants in this study were unable to carry out their daily activities. Sixteen percent were underweight; 28% were overweight or obese. Authors of a study from Iran who recruited chronic psychiatric hospital patients aged 60-75 [63] reported that almost 60% were at risk for malnutrition. In a study of schizophrenia patients in the community (all ages), that percentage was 45% [64].

3.3. Health Consequences of Poor Nutrition

What one eats predicts the occurrence of many health conditions, including, among others, atherosclerosis, obesity, diabetes, hypertension, dyslipedemia, anemia, and sarcopenia [65,66,67,68]. These studies show that anemia can result from an inadequate diet even in the absence of blood loss. They refer to randomized controlled trials that show that intake of protein is critical for preservation of muscle strength, although the optimal dose and type of protein remains unknown. They demonstrate that inadequate nutrition, in addition to factors such as low amounts of physical activity and lack of hypertension control, are significant triggers of both cardiovascular and metabolic disease. Of specific importance to women, nutrition during pregnancy has been shown to importantly affect the health of the fetus [69].
Nutrition influences opportunities for employment; at work, it affects both productivity and performance [70]. Nutrition also affects the speed of the aging process and is a good predictor of longevity [71].

3.4. Interventions for Poor Nutrition in Schizophrenia

Interventions start with recognition of the problem and individual risk assessment. After a comprehensive review of disordered eating in schizophrenia, Sankaranarayanan et al. [72] conclude that clinicians need training in optimal ways to question severely ill psychiatric patients about their eating habits, assess their needs and manage their nutritional deficiencies. Smith et al. [73] also address the need to question patients with SMI about their ease of access to healthy food.
Using assessment measures such as the Geriatric Nutritional Risk Index (GNRI) and Onodera’s Prognostic Nutritional Index (OPNI) for long-term outcomes over a median period of 408 days, Tsai et al. [74] found that the GNRI predicted falls in hospitalized schizophrenia patients and the OPNI predicted both falls and infections. A scoping review of 17 nutrition screening methods for adults with severe mental disorder was recently identified [75]. Three had been validated specifically for this population.
After an appropriate assessment, which should ideally include a home visit, specific interventions are in order. Classes in meal planning, cooking, and eating behaviors have shown good results. Clark et al. [76] assessed 18 individuals with severe mental illnesses pre and post a 6-week nutrition education cooking class. They found that self-reported efficacy in cooking and grocery shopping skills improved and patients reported significant increases in calcium, vitamin D, grains, and fruit intake. Garcia and Privott [77] , in a N=1 qualitative study, discuss challenges and barriers to taking part in cooking classes in their description of one individual’s transition to independent community living after long-term hospitalization with SMI. They attribute recovery to the person’s sustained participation in meal preparation and cooking groups while in hospital.
Positive results with respect to healthy eating have been seen with both cognitive behavioral therapy and pharmacological intervention. Naltrexone prevents antipsychotic-induced weight gain by reducing food cravings [78]. The new anti-obesity drugs may, in the near future, be of great help to this population.
Providing patients with opportunities to socialize is another way to expose them to healthier eating habits. Successful online intervention has also been reported [79]. Food support (financed and delivered via a number of diverse ways) has been the way that many parts of the world utilize to help maintain adequate nutrition in individuals with schizophrenia and related disorders [80].

4. Discussion

I do not cover in this review the possibility that nutrition and schizophrenia may be bidirectional in the sense that prenatal deficiency in mothers has been suspected of increasing the risk of schizophrenia in offspring [81,82]. Animal research has bolstered this hypothesis. For instance, Chen et al. [2020] compared hippocampus and prefrontal cortex transcriptomes in rats with and without prenatal nutritional deficiency. They identified genes involved in synaptic development, neuronal projection, cognitive function, and learning function in rat hippocampus (none in the prefrontal cortex) that responded to maternal prenatal nutritional deficiency; four of the genes were associated with schizophrenia. This work suggests that effective prenatal care of women with schizophrenia is of vital importance to their offspring.
After years of relative medical neglect, nutrition and its effect on mental health has become a topic of active current research. This research field, however, has tended to focus on aspects of diet related to depression. Examples are plans for interventional studies for dietary modification and nutraceuticals based on personalized biomarkers [84,85]. In the study of schizophrenia, older research advocated vitamins for schizophrenia [86] and dietary factors such as gluten have for decades been seriously investigated as potential schizophrenia causes [87]. Today, the schizophrenia and nutrition field is best summarized by the Aucoin et al. [10] review. Their review does not address the hypothesis that food deficiencies can cause psychosis but does conclude, on the basis of literature, that there is demonstrated benefit for people with psychosis eating a diet rich in vitamins and minerals (vitamin B12 and B6, folate, and zinc) and amino acids (serine, lysine, glycine, and tryptophan). The authors do acknowledge, however, that financial barriers, inadequate education and poor budgeting skills, as well as lack of motivation, make it very difficult for individuals with psychosis to achieve and sustain healthy diets. Aucoin and colleagues [10] advocate for the integration of nutrition experts into mental health teams.
The present review underscores the degree of poor nutrition seen in a sizable minority of patients with severe mental illness and attributes it to a host of factors working together: economic status, psychotic symptoms, life style effects, social isolation, and drug-induced effects. There is general agreement that nutritional deficiencies often result in a variety of serious medical disorders and that their prevention needs to become an inherent component of schizophrenia treatment.

5. Conclusions

Patients with severe mental illness live on very meagre incomes in under-resourced neighbourhoods and they struggle with serious cognitive, psychological, and behavioural symptoms as well as with the adverse effects of antipsychotic drugs. In circumstances such as these, it is extremely difficult to maintain a healthy diet. This results in a variety of nutritional deficiencies, which often lead to serious medical complications. The literature confirms the gravity of the problem and suggests a number of potentially useful interventions, which all begin with recognition of the issue and inclusion of dietary assessment in routine psychiatric evaluations. Traditionally, nutrition has been the concern of women more than of men. Women with disorders such as schizophrenia need particular attention because their long-term health affects not only themselves, but also their children.

Author Contributions

This is a solo-authored paper.

Funding

This research received no external funding.

Institutional Review Board Statement

Not required for a review.

Informed Consent Statement

Not applicable

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Afzal, M.; Siddiqi, N.; Ahmad, B.; Afsheen, N.; Aslam, F.; Ali, A.; Ayesha, R.; Bryant, M.; Holt, R.; Khalid, H.; Ishaq, K.; Koly, K.N.; Rajan, S.; Saba, J.; Tirbhowan, N.; Zavala, G.A. Prevalence of overweight and obesity in people with severe mental illness: Systematic review and meta-analysis. Front Endocrinol 2021, 12, 769309. [Google Scholar] [CrossRef] [PubMed]
  2. Bang, L.; Bahrami, S.; Hindley, G.; Smeland, O.B.; Rødevand, L.; Jaholkowski, P.P.; Shadrin, A.; Connell, K.S.O.; Frei, O.; Lin, A.; Rahman, Z.; Cheng, W.; Parker, N.; Fan, C.C.; Dale, A.M.; Djurovic, S.; Bulik, C.M.; Andreassen, O.A. Genome-wide analysis of anorexia nervosa and major psychiatric disorders and related traits reveals genetic overlap and identifies novel risk loci for anorexia nervosa. Transl Psychiatry 2023, 13, 291. [Google Scholar] [CrossRef] [PubMed]
  3. Ganson, K.T.; Cuccolo, K.; Nagata, L.M. Associations between psychosis symptoms and eating disorders among a national sample of U.S. college students. S. college students. Eating Behav 2022, 45, 101622. [Google Scholar] [CrossRef] [PubMed]
  4. Seeman, M.V. Eating disorders and psychosis: Seven hypotheses. World J Psychiatry 2014, 4, 112–119. [Google Scholar] [CrossRef]
  5. W.H.O. Healthy diet. 2020. Available online: https://www.who.int/news-room/fact-sheets/detail/healthy-diet (accessed on 15 September 2023).
  6. Dipasquale, S.; Pariante, C.M.; Dazzan, P.; Aguglia, E.; McGuire, P.; Mondelli, V. The dietary pattern of patients with schizophrenia: A systematic review. J Psychiatr Res 2013, 47, 197–207. [Google Scholar] [CrossRef]
  7. Teasdale, S.B.; Ward, P.B.; Samaras, K.; Firth, J.; Stubbs, B.; Tripodi, E.; Burrows, T.L. Dietary intake of people with severe mental illness: Systematic review and meta-analysis. Br J Psychiatry 2019, 21, 251–259. [Google Scholar] [CrossRef] [PubMed]
  8. Głodek, M.; Skibinska, M.; Suwalska, A. Diet and physical activity and metabolic disorders in patients with schizophrenia and bipolar affective disorder in the Polish population. Peer J 2023, 11, e15617. [Google Scholar] [CrossRef] [PubMed]
  9. Tsuruga, K.; Sugawara, N.; Sato, Y.; Saito, M.; Furukori, H.; Nakagami, T.; Nakamura, K.; Takahashi, I.; Nakaji, S.; Yasui-Furukori, N. Dietary patterns and schizophrenia: A comparison with healthy controls. Neuropsychiatr Dis Treat 2015, 11, 1115–1120. [Google Scholar] [CrossRef]
  10. Aucoin, M.; Lachance, L.; Cooley, K.; Kidd, S. Diet and psychosis: A scoping review. Neuropsychopharmacol 2020, 79, 20–42. [Google Scholar] [CrossRef]
  11. Mötteli, S.; Provaznikova, B.; Vetter, S.; Jäger, M.; Seifritz, E.; Hotzy, F. Examining nutrition knowledge, skills, and eating behaviours in people with severe mental illness: A cross-sectional comparison among psychiatric inpatients, outpatients, and healthy adults. Nutrients 2023, 15, 2136. [Google Scholar] [CrossRef]
  12. Majuri, T.; Alakokkare, A.-E.; Haapea, M.; Nordström, T.; Miettunen, J.; Jääskeläinen, E.; Ala-Mursula, L. Employment trajectories until midlife in schizophrenia and other psychoses: The Northern Finland Birth Cohort 1966. Soc Psychiatry Psychiatr Epidemiol 2023, 58, 65–76. [Google Scholar] [CrossRef]
  13. Holm, M.; Taipale, H.; Tanskanen, A.; Tiihonen, J.; Mitterdorfer-Rutz, E. Employment among people with schizophrenia or bipolar disorder: A population-based study using nationwide registers. Acta Psychiatrica Scand 2021, 143, 61–71. [Google Scholar] [CrossRef]
  14. Eliason, M. The financial situation before and after first-time psychiatric in-patient diagnosis of schizophrenia spectrum, bipolar, and major depressive disorder. Econ Hum Biol 2023, 49, 101231. [Google Scholar] [CrossRef]
  15. Vilar-Compte, M.; Burrola-Méndez, S.; Lozano-Marrufo, A.; Ferré-Eguiluz, I.; Flores, D.; Gaitán-Rossi, P.; Teruel, G.; Pérez-Escamilla, R. Urban poverty and nutrition challenges associated with accessibility to a healthy diet: A global systematic literature review. Int J Equity Health 2021, 20, 40. [Google Scholar] [CrossRef]
  16. Walker, R.E.; Keane, C.R.; Burke, J.G. Disparities and access to healthy food in the United States: A review of food deserts literature. Health Place 2010, 16, 876–884. [Google Scholar] [CrossRef]
  17. Dunbar, R.I.M. Breaking bread: The functions of social eating. Adapt Hum Behav Physiol 2017, 3, 198–211. [Google Scholar] [CrossRef]
  18. Herman, C.P. The social facilitation of eating. A review. Appetite 2015, 86, 61–73. [Google Scholar] [CrossRef] [PubMed]
  19. Ruddock, H.K.; Brunstrom, J.M. A systematic review and meta-analysis of the social facilitation of eating. Am J Clin Nutrition 2019, 110, 842–861. [Google Scholar] [CrossRef] [PubMed]
  20. Kiang, M.; Christensen, B.K.; Remington, G.; Kapur, S. Apathy in schizophrenia: Clinical correlates and association with functional outcome. Schizophr Res 2003, 63, 79–88. [Google Scholar] [CrossRef]
  21. Wallace, C.J.; Liberman, R.P.; Tauber, R.; Wallace, J. The independent living skills survey: A comprehensive measure of the community functioning of severely and persistently mentally ill individuals. Schizophr Bull 2000, 26, 631–658. [Google Scholar] [CrossRef] [PubMed]
  22. Semkovska, M.; Bedard, M.A.; Godbout, L.; Limoge, F,; Stip, E. Assessment of executive dysfunction during activities of daily living in schizophrenia. Schizophr Res 2004, 69, 289–300. [Google Scholar] [CrossRef]
  23. Hall, G.R. Chronic dementia challenges in feeding a patient. J Gerontol Nurs 2013, 20, 21–30. [Google Scholar] [CrossRef] [PubMed]
  24. Çetin, A.B.; Güler, S.K. A paranoid schizophrenia patient presenting with Wernicke’s encephalopathy, case report. Asian J Med Case Rep 2023, 5, 1–5. Available online: https://globalpresshub.com/index.php/AJMCR/article/view/1723.
  25. Hargrave, D.D.; Schroeder, R.W.; Heinrichs, R.J.; Baade, L.E. Wernicke-Korsakoff syndrome as a consequence of delusional food refusal: A case study. Cogn Behav Neurol 2015, 28, 215–219. [Google Scholar] [CrossRef] [PubMed]
  26. He, J.; Li, J.; Li, Z.; Ren, H.; Chen, X.; Tang, J. A case report of Wernicke’s encephalopathy associated with schizophrenia. Front Psychiatry 2021, 12, 657649. [Google Scholar] [CrossRef]
  27. Ishida, M.; Uchida, N.; Yoshioka, A.; Sato, I.; Ito, H.; Sato, R.; Mizunuma, N.; Onishi, H. Thiamine deficiency in a patient with schizophrenia: Precautions and countermeasures for subclinical thiamine deficiency. Cureus 2023, 15, e38454. [Google Scholar] [CrossRef]
  28. Oudman, E.; Wijnia, J.W.; Oey, M.J.; van Dam, M.J.; Postma, A. Wernicke encephalopathy in schizophrenia: A systematic review. Int J Psychiatry Clin Pract 2021, 25, 233–237. [Google Scholar] [CrossRef]
  29. Barrio, P.; Seeman, M.V.; González-Rodríguez, A. Alcohol and psychosis: A narrative review of the prevalence, clinical manifestations, and management of alcohol-related psychotic symptoms. Curr Psychiatry Res Rev 2021, 17, 72–80. [Google Scholar] [CrossRef]
  30. Yates, N.J. Schizophrenia: The role of sleep and circadian rhythms in regulating dopamine and psychosis. Rev Neurosci 2016, 27, 669–687. [Google Scholar] [CrossRef]
  31. Zarrinpar, A.; Chaix, A.; Panda, S. Daily eating patterns and their impact on health and disease. Trends Endocrinol Metab 2016, 27, 69–83. [Google Scholar] [CrossRef]
  32. Ng, C.M.; Kaur, S. Environmental light exposure and mealtime regularity: Implications for human health. Chronobiol Int J Biol Med Rhythm Res 2022, 39, 1183–1194. [Google Scholar] [CrossRef] [PubMed]
  33. Bucher Della Torre, S.; Wild, P.; Dorribo, P.; Danuser, B.; Amati, F. Energy, nutrient and food intakes of male shift workers vary according to the schedule type but not the number of nights worked. Nutrients 2020, 12, 919. [Google Scholar] [CrossRef] [PubMed]
  34. Gregg, L.; Barrowclough, C.; Haddock, G. Reasons for increased substance use in psychosis. Clin Psychol Rev 2007, 27, 494–510. [Google Scholar] [CrossRef] [PubMed]
  35. Ross, L.J.; Wilson, M.; Banks, M.; Rezannah, F.; Daglish, M. Prevalence of malnutrition and nutritional risk factors in patients undergoing alcohol and drug treatment. Nutrition 2012, 28, 738–743. [Google Scholar] [CrossRef]
  36. Lv, M.; Wang, X.; Wang, Z.; Li, X.; Wang, L.; Tan, Y.; Zhang, X.Y. Alcohol drinking in male patients with chronic schizophrenia: Prevalence and its relationship to clinical symptoms. Front Psychiatry 2023, 14, 1164968. [Google Scholar] [CrossRef]
  37. Tsai, J.; Stroup, T.S.; Rosenheck, R.A. Housing arrangements among a national sample of adults with chronic schizophrenia living in the United States: A descriptive study. J Community Psychol 2011, 39, 76–88. [Google Scholar] [CrossRef]
  38. Harvey, C.; Killackey, E.; Groves, A.; Herrman, H. A place to live: Housing needs for people with psychotic disorders identified in the second Australian national survey of psychosis. Aust NZ J Psychiatry 2012, 46, 840–850. [Google Scholar] [CrossRef]
  39. Seale, J.; Fallaize, R.; Lovegrove, J. Nutrition and the homeless: The underestimated challenge. Nutrition Res Rev 2016, 29, 143–151. [Google Scholar] [CrossRef]
  40. Easton, C.; Oudshoorn, A.; Smith-Carrier, T.; Forchuk, C.; Marshall, C.A. The experience of food insecurity during and following homelessness in high-income countries: A systematic review and meta-aggregation. Health Soc Care 2022, 30, e3384–e3405. [Google Scholar] [CrossRef]
  41. Moynihan, P.J.; Mulvaney, C.E.; Adamson, A.J.; Seal, C.; Steen, N.; Mathers, J.C.; Zohouri, F.V. The nutrition knowledge of older adults living in sheltered housing accommodation. J Human Nutrition Dietetics 2007, 20, 446–458. [Google Scholar] [CrossRef]
  42. Elman, I.; Borsook, D.; Lukas, S.E. Food intake and reward mechanisms in patients with schizophrenia: Implications for metabolic disturbances and treatment with second-generation antipsychotic agents. Neuropsychopharmacol 2006, 31, 2091–2120. [Google Scholar] [CrossRef] [PubMed]
  43. Blouin, M.; Tremblay, A.; Jalbert, M.E.; Venables, H.; Bouchard, R.H.; Roy, M.A.; Alméras, N. Adiposity and eating behaviors in patients under second generation antipsychotics. Obesity 2008, 16, 1780–1787. [Google Scholar] [CrossRef] [PubMed]
  44. Mukherjee, S.; Skrede, S.; Milbank, E.; Andriantsitohaina, R.; López, M.; Fernø, J. Understanding the effects of antipsychotics on appetite control. Front Nutr 2022, 8, 815456. [Google Scholar] [CrossRef] [PubMed]
  45. Sankaranarayanan, A.; Johnson, K.; Mammen, S.J.; Wilding, H.E.; Vasani, D.; Murali, V.; Mitchison, D.; Castle, D.J.; Hay, P. Disordered eating among people with schizophrenia spectrum disorders: A systematic review. Nutrients 2021, 13, 3820. [Google Scholar] [CrossRef] [PubMed]
  46. Rognoni, C.; Bertolani, A.; Jommi, C. Second-generation antipsychotic drugs for patients with schizophrenia: Systematic literature review and meta-analysis of metabolic and cardiovascular side effects. Clin Drug Investigation 2021, 41, 303–319. [Google Scholar] [CrossRef] [PubMed]
  47. Correll, C.U.; Kane, J.M. Ranking antipsychotics for efficacy and safety in schizophrenia. JAMA Psychiatry 2020, 77, 225–226. [Google Scholar] [CrossRef]
  48. Seeman, M.V. What is the significance of the impact of antipsychotics on the gut microbiome? Expert Opin Drug Metabol Toxicol 2023, 19, 125–127. [Google Scholar] [CrossRef]
  49. Mizuki, Y.; Sakamoto, S.; Okahisa, Y.; Yada, Y.; Hashimoto, N.; Takaki, M.; Yamada, N. Mechanisms underlying the comorbidity of schizophrenia and type 2 diabetes mellitus. Int J Neuropsychopharmacol 2021, 24, 367–382. [Google Scholar] [CrossRef]
  50. Cimo, A.; Dewa, C.S. Symptoms of mental illness and their impact on managing type 2 diabetes in adults. Can J Diabetes 2018, 42, 372–381. [Google Scholar] [CrossRef]
  51. Bellass, S.; Lister, J.; Wray Kitchen, C.E.; Kramer, L.; Alderson, S.L.; Doran, T.; Gilbody, S.; Han, L.; Hewitt, C.; Holt, R.I.G.; Rowena Jacobs, R.; Prady, S.L.; Shiers, D.; Siddiqi, N.; Taylor, J. Living with diabetes alongside a severe mental illness: A qualitative exploration with people with severe mental illness, family members and healthcare staff. Diabetic Med 2021, 38, e14562. [Google Scholar] [CrossRef]
  52. Alexandre, K.; Campbell, J.; Bugnon, M.; Henry, C.; Schaub, C.; Serex, M.; Elmers, J.; Desrichard, O.; Peytremann-Bridevaux, I. Factors influencing diabetes self-management in adults: An umbrella review of systematic reviews. JBI Evidence Synthesis 2021, 19, 1003–1118. [Google Scholar] [CrossRef] [PubMed]
  53. McColl, H.; Dhillon, M.; Howard, L. A systematic review of the nutritional status of women of a childbearing age with severe mental illness. Arch Womens Ment Health 2012, 16, 39–46. [Google Scholar] [CrossRef] [PubMed]
  54. Frayne, J.; Hauck, Y.; Nguyen, T.; Liira, H.; Morgan, V.A. Reproductive planning, vitamin knowledge and use, and lifestyle risks of women attending pregnancy care with a severe mental illness. Scand J Primary Health Care 2021, 39, 60–66. [Google Scholar] [CrossRef] [PubMed]
  55. Kulkarni, J.; Gurvich, C.; Gilbert, H.; Worsley, R.; Li, Q.; Karimi, L. The use of first and second-generation antipsychotic drugs and the potential to develop gestational diabetes mellitus among perinatal patients with psychosis. Schizophr Res 2023, 254, 22–26. [Google Scholar] [CrossRef]
  56. Levay, A.V.; Mumtaz, Z.; Faiz Rashid, S.; Willows, N. Influence of gender roles and rising food prices on poor, pregnant women’s eating and food provisioning practices in Dhaka, Bangladesh. Reprod Health 2013, 10, 53. [Google Scholar] [CrossRef]
  57. Dubowitz, T.; Acevedo-Garcia, D.; Salkeld, J.; Lindsay, A.C.; Subramanian, S.V.; Peterson, K.E. Lifecourse, immigrant status and acculturation in food purchasing and preparation among low-income mothers. Pub Health Nutr 2007, 10, 396–404. [Google Scholar] [CrossRef]
  58. de Morais, S.P.; Unsain, R.F.; Gittelsohn, J.; Sanches Tavares da Silva, J.G.; Gonçalves Perez, I.C.; Baeza Scagliusi, F. Strategies used by overweight and obese low income mothers to feed their families in urban Brazil. Appetite 2017, 111, 63–70. [Google Scholar] [CrossRef]
  59. McIntyre, L.; Glanville, N.; Kim, T.; Raine, D.; Dayle, J.B.; Anderson, B.; Battaglia, N. Do low-income lone mothers compromise their nutrition to feed their children? CMAJ 2003, 168, 686–691. [Google Scholar]
  60. Corcoran. C.; Murphy, C.; Culligan, E.P.; Walton, J.; Sleator, R.D. Malnutrition in the elderly. Sci Prog 2019, 102, 171–180. [Google Scholar] [CrossRef]
  61. Poulia, K.A.; Yannakoulia, M.; Karageorgou, D.; Gamaletsou, M.; Panagiotakos, D.B.; Sipsas, N.V.; Zampelas, A. Evaluation of the efficacy of six nutritional screening tools to predict malnutrition in the elderly. Clin Nutr 2012, 31, 378–385. [Google Scholar] [CrossRef]
  62. Wu, C.; Ye, J.; Li, S.; Wu, J.; Wang, C.; Yuan, L.; Wang, H.; Pan, Y.; Huang, X.; Zhong, X.; Huang, M.; Guo, J.; Ning, Y.; Xiao, A. Predictors of everyday functional impairment in older patients with schizophrenia: A cross-sectional study. Front Psychiatry 2023, 13, 1081620. [Google Scholar] [CrossRef] [PubMed]
  63. Rezaei, O.; Fattah Moghaddam, L.; Banihashem, S.; Arab Ghahestany, D.; Akhavan Zanjani, H.; Mansouri, P.; et al. Relationship of health status and micronutrients level with nutritional status of the elderly with psychological disorders. Salmand: Iran J Ageing 2022, 17, 218–231. [Google Scholar] [CrossRef]
  64. Kim, S.R.; Kim, J.Y.; Kim, H.Y.; Nho, J.H.; Kim, Y.H.; Min, S.Y. Factors related to malnutrition in community-dwelling patients with schizophrenia. Perspect Psychiatr Care 2019, 55, 415–423. [Google Scholar] [CrossRef] [PubMed]
  65. Bays, H.E.; Taub, P.R.; Epstein, E.; Michos, E.D.; Ferraro, R.A.; Bailey, A.L.; Kelli, H.M.; Ferdinand, K.C.; Echols, M.R.; Weintraub, H.; Bostrom, J.; Johnson, H.M.; Hoppe, K.K.; Shapiro, M.D.; German, C.A.; Virani, S.S.; Hussain, A.; Ballantyne, C.M.; Agha, A.M.; Toth, P.P. Ten things to know about ten cardiovascular disease risk factors. Am J Prevent Cardiol 2021, 5, 100149. [Google Scholar] [CrossRef]
  66. Bhadra, P.; Deb, A. A review on nutritional anemia. Indian J Natural Sci 2020, 10, 18674–18681. [Google Scholar]
  67. Ganapathy, G.; Nieves, J.W. Nutrition and sarcopenia – what do we know? Nutrients 2020, 12, 1755. [Google Scholar] [CrossRef]
  68. Peña-Jorquera, H.; Cid-Jofré, V.; Landaeta-Díaz, L.F.; Petermann-Rocha, F.; Martorell, M.; Zbinden-Foncea, H.; Ferrari, G.; Jorquera-Aguilera, C.; Cristi-Montero, C. Plant-based nutrition: Exploring health benefits for atherosclerosis, chronic diseases, and metabolic syndrome—A comprehensive review. Nutrients 2023, 15, 3244. [Google Scholar] [CrossRef] [PubMed]
  69. Naik, V.D.; Lee, J.; Wu, G.; Washburn, S.; Ramadoss, J. Effects of nutrition and gestational alcohol consumption on fetal growth and development. Nutrition Rev 2022, 80, 1568–1579. [Google Scholar] [CrossRef]
  70. Shearer, J.; Graham, T.E.; Skinner, T.L. Nutra-ergonomics: Influence of nutrition on physical employment standards and the health of workers. Applied Physiol Nutrit Metabol 2016, 41. [Google Scholar] [CrossRef]
  71. Leitao, C.; Mignano, A.; Estrela, M.; Fardiha, M.; Figueiras, A.; Roque, F.; Herdeiro, M.T. The effect of nutrition on aging – a systematic review focusing on aging-related biomarkers. Nutrients 2022, 14, 554. [Google Scholar] [CrossRef]
  72. Sankaranarayanan, A.; Johnson, K.; Mammen, S.J.; Wilding, H.E.; Vasani, D.; Murali, V.; Mitchison, D.; Castle, D.J.; Hay, P. Disordered eating among people with schizophrenia spectrum disorders: A systematic review. Nutrients 2021, 13, 3820. [Google Scholar] [CrossRef]
  73. Smith, J.; Ker, S.; Archer, D.; Gilbody, S.; Peckham, E.; Hardman, C. Food insecurity and severe mental illness: Understanding the hidden problem and how to ask about food access during routine healthcare. BJPsych Advances 2023, 29, 204–212. [Google Scholar] [CrossRef]
  74. Tsai, M-T. ; Chang, T-H.; Wu, B-J. Prognostic impact of nutritional risk assessment in patients with chronic schizophrenia. Schizophr Res 2018, 192, 137–141. [Google Scholar] [CrossRef] [PubMed]
  75. Hancox, L.E.; Lee, P.S.; Armaghanian, N.; Hirani, V.; Wakefield, G. Nutrition risk screening methods for adults living with severe mental illness: A scoping review. Nutrition Dietetics 2022, 79, 349–363. [Google Scholar] [CrossRef] [PubMed]
  76. Clark, A.; Bezyak, J.; Testerman, N. Individuals with severe mental illnesses have improved eating behaviors and cooking skills after attending a 6-week nutrition cooking class. Psychiatr Rehab J 2015, 38, 276–278. [Google Scholar] [CrossRef]
  77. Garcia, A.; Privott, C. Meal preparation and cooking group participation in mental health: A community transition. Food Studies 2023, 13, 85–101. [Google Scholar] [CrossRef]
  78. Guglielmi, V.; Bettini, S.; Sbraccia, P.; Busetto, L.; Pellegrini, M.; Yumuk, V.; Colao, A.M.; El Ghoch, M.; Muscogiuri, G. Beyond weight loss: Added benefits could guide the choice of anti-obesity medications. Curr Obesity Rep 2023, 12, 127–146. [Google Scholar] [CrossRef]
  79. O’Keeffe, D.; Clarke, M. A qualitative evaluation of a telehealth healthy lifestyle intervention for people with serious mental illness. Irish J Psychol Med 2023. [CrossRef]
  80. Mulrooney, H.M.; Ranta, R.; Nancheva, N.; Bhakta, D.; Lake, S. Social supermarkets, nutritional implications and healthy eating: Exploration of members and their views. J Human Nutrition Dietetics 2023. [Google Scholar] [CrossRef] [PubMed]
  81. Brown, A.S.; Susser, E.S. Prenatal nutritional deficiency and risk of adult schizophrenia. Schizophr Bull 2008, 34, 1054–1063. [Google Scholar] [CrossRef]
  82. Xu, M.Q.; Sun, W.S.; Liu, B.X.; Feng, G.Y.; Yu, L.; Yang, L.; He, G.; Sham, P.; Susser, E.; St Clair, D.; He, L. Prenatal malnutrition and adult schizophrenia: Further evidence from the 1959-1961 Chinese famine. Schizophr Bull 2009, 35, 568–576. [Google Scholar] [CrossRef] [PubMed]
  83. Chen, J.; Zhao, X.; Cui, L.; He, G.; Wang, X.; Wang, F.; Duan, S.; He, L.; Li, Q.; Yu, X.; Zhang, F.; Xu, M. Genetic regulatory subnetworks and key regulating genes in rat hippocampus perturbed by prenatal malnutrition: Implications for major brain disorders. Aging 2020, 12, 8434–8458. [Google Scholar] [CrossRef] [PubMed]
  84. Adan, R.A.H.; van der Beek, E.M.; Buitelaar, J.K.; Cryan, J.F.; Hebebrand, J.; Higgs, S.; Schellekens, H.; Dickson, S.L. Nutritional psychiatry: Towards improving mental health by what you eat. Eur Neuropsychopharmacol 2019, 29, 1321–1332. [Google Scholar] [CrossRef] [PubMed]
  85. Sarris, J. Nutritional psychiatry: From concept to the clinic. Drugs 2019, 79, 929–934. [Google Scholar] [CrossRef]
  86. Hoffer, A.; Osmond, H.; Callbeck, M.J.; Kahan, I. Treatment of schizophrenia with nicotinic acid and nicotinamide. J Clin Exp Psychopathol 1957, 18, 131–158. [Google Scholar]
  87. Dohan, F.C. Wheat “consumption” and hospital admissions for schizophrenia during World War II. A preliminary report. Am J Clin Nutr 1966, 18, 7–10. [Google Scholar] [CrossRef]
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