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Nutrition and psoriasis: is there any association between the severity of the disease and adherence to the Mediterranean diet?

Journal of Translational Medicine volume 13, Article number: 18 (2015) Cite this article

Abstract

Background

Many studies have evaluated the role of individual nutrients on the development of psoriasis. However, only few studies have investigated the effect of a healthy eating pattern, such as the Mediterranean diet. In this study, we aimed to investigate the relationship between adherence to the Mediterranean diet, the body composition and the severity of psoriasis in a group of naïve-treatment patients with psoriasis.

Methods

This is a cross-sectional case–control observational study. Sixty-two patients (49 males and 13 females, mean age: 50.2±10.5yrs) affected with mild-to-severe psoriasis were consecutively enrolled. Sixty-two age-, sex- and body mass index (BMI)-matched healthy subjects served as control group. A validated 14-item questionnaire (PREDIMED: PREvención con DIeta MEDiterránea) was used for the assessment of adherence to the Mediterranean diet. The severity of psoriasis was by assessed by standardized Psoriasis Area and Severity Index (PASI) score and C-reactive protein (CRP) levels. Body composition was analyzed with bioelectrical impedance analysis.

Results

A higher percentage of psoriatic patients had a lower PREDIMED score compared to the control group (30.6% vs 4.8%). PASI score was significantly associated with the percentage of fat mass (FM%) and CRP levels. PASI score and CRP levels were significantly associated with the dietary components included in the PREDIMED questionnaire or with the PREDIMED score. At multiple regression analysis, the major predictor of PASI score were FM among BIA parameters, (r2=0.537, β=0.740, p<0.001), and FM (r2=0.537, β=0.603, p<0.001) and PREDIMED score (r2=0.599, β=−0.296, p=0.007) among anthropometric measures, FM and PREDIMED score. Finally, among all items of the PREDIMED questionnaire, EVOO (r2=0.548, β=−0.741, p<0.001), and fish consumption (r2=0.139, β=−0.372, p=0.005) have an independent predictive value for PASI score and CRP levels.

Conclusions

This is the first study to evaluate the association between adherence to the Mediterranean diet and the severity of psoriasis. Moreover, our study highlights the usefulness of the assessment of body composition by bioelectrical impedance analysis in the evaluation of the psoriatic patients.

Background

Psoriasis is a chronic, immune-mediated inflammatory skin disease, associated with metabolic and cardiovascular disease [1,2]. Psoriasis is estimated to affect about 2–4% of the population in Western countries [3]. A number of risk factors have been recognized in the etiology and pathogenesis of psoriasis, including family history and environmental risk factors, such as diet, obesity, smoking, stress, and alcohol consumption [4]. Moreover, dietary factors can also affect both drug pharmacokinetics and pharmacodynamics. A number of single food components have been suggested to play a role in psoriasis. The ability of dietary of antioxidants, such as omega-3 polyunsaturated fatty acids from fish oil, some vitamins (A, E and C), and oligoelements (iron, copper, manganese, zinc and selenium), which decrease oxidative stress and the production of reactive oxygen species, might be of particular relevance mainly in a chronic systemic inflammatory diseases, like psoriasis [5]. In addition, due to its role in proliferation and maturation of keratinocytes, vitamin D has become an important therapeutic option in the treatment of psoriasis [6]. However, while many studies have evaluated the role of individual nutrients on the development of psoriatic disease [7], only few studies have investigated the effect of a healthful eating pattern. The psoriatic patients, in fact, often seek dietary advice, as they frequently link many of their health problems, including diseases of the skin, to their diet.

The Mediterranean diet is a healthy eating pattern, associated with reduced risk for metabolic [8], cardiovascular [9], and neoplastic diseases [10], that has consistently been shown to provide a degree of protection against chronic degenerative diseases [11]. One of the most accredited hypothesis of this association is that the high content of different beneficial compounds, such as antioxidants and polyphenols, largely present in Mediterranean foods, such as plant foods, fruits and red wine, have anti-inflammatory properties [12]. In particular, the monounsaturated fatty acids intake, whose major source is represented by extra virgin olive oil (EVOO), was found to be associated with a reduced prevalence of risk factors for major chronic inflammatory diseases [13].

Obesity is an important risk factor for psoriasis [14]. The relationship between the two conditions is probably bidirectional, with obesity predisposing to psoriasis and psoriasis favoring obesity [15]. Several studies have been conducted to explore the association between obesity and psoriasis [16,17]. In particular, there was a 2-fold increased risk for psoriasis development in the setting of obesity as compared with normal weight subjects [18]. In addition, for each unit increment increase in body mass index (BMI) was reported a 9% higher risk for psoriasis onset and a 7% higher risk for increased of Psoriasis Area and Severity Index (PASI) score [19], currently the preferred method for the assessment of the disease severity and extent. A further evidence of a link between, obesity, inflammation and cardiovascular diseases in patients with psoriasis is provided by several studies reporting a correlation between PASI score and increased of C-reactive protein (CRP) levels [20], an acute phase protein significantly associated with obesity, representing the most sensitive markers of inflammation and an independent risk for cardiovascular disease. BMI is a commonly used surrogate for adiposity that is inexpensive and easily measured, although it evaluates excess weight rather than excess fat [21], does not measure body fat directly and poorly distinguishes between fat mass and lean or bone mass [22]. The National Heart, Lung and Blood Institute (NHLBI) Clinical Guidelines recognize this limitation of BMI [23]; thus, waist circumference (WC) is recommended as an additional surrogate measure of fat distribution, due to its high correlation with visceral fat [24], the main source of inflammatory cytokines in obesity [25]. Again, a number of studies have evidenced a strict association between WC and psoriasis [26], being the production of inflammatory cytokines in visceral obesity the link involved in the complex mechanisms leading to the exacerbation of psoriasis [27]. Nevertheless, only few studies have assessed body composition in psoriatic patients [28,29]. Bioelectrical impedance analysis (BIA) is a simple, safe, inexpensive and non-invasive method to estimate body composition. This method is particularly useful in determining body compartments in studies of large population samples [30].

The wake of this evidence, we aimed to investigate the relationship between adherence to the Mediterranean diet using a 14-item PREDIMED (PREvención con DIeta MEDiterránea) questionnaire [31], the body composition by BIA, and the severity of psoriasis evaluated by PASI score and CRP levels in a group of naïve-treatment patients with psoriasis.

Methods

This is a cross-sectional case control observational study carried out at the Department of Clinical Medicine and Surgery of the University of Naples Federico II (Italy), in accordance with the guidelines of the Helsinki Declaration on human experimentation. All participants gave their informed consent before enrolment.

Sixty-two patients affected by mild-to-severe psoriasis were consecutively enrolled from a pool of patients referred to the outpatient clinic of our University Hospital from January to August 2014. Patients aged more than 18 years and with a diagnosis of mild-to-severe psoriasis lasting for at least 6 months were enrolled, while patients with pustular, erythrodermic or arthropathic psoriasis or receiving any systemic treatment for psoriasis including acitretin, ciclosporin, methotrexate, phototherapy or biologics for at least 3 months were excluded. Exclusion criteria included smoking and alcohol abuse too. Furthermore they had not received any drug therapy known to affect carbohydrate or lipid metabolism for the 6 months before. All patients were checked and recorded. Data collected included age, gender, weight, height, BMI and WC. Severity of psoriasis and the age at onset of it (early psoriasis: age < 39 years and late psoriasis aged >40 years) were also noted. PASI score was used as measure of disease severity. PASI score was used to be recorded by measuring four body surface areas (head, chest, upper and lower limbs) with patient in a standing position according to the method described by Harari M et al. 2000 [32]. Sixty-two healthy subjects among clerks, and medical and paramedical personnel of the Department of Clinical & Surgical Medicine, Unit of Endocrinology of the University Federico II of Naples, matched for sex, age, and BMI with the patients agreed to participate in this study and were used as controls. Exclusion criteria for controls were the same as the patients. Blood samples were obtained between 08.00 h and 09.00 h from an antecubital vein after an overnight fast, with the patient in the resting position. CRP levels was determined with a nephelometric assay with CardioPhase high-sensitivity from Siemens Healthcare Diagnostics (Marburg, Germany); the intra-assay coefficient of variations was >4%.

All anthropometric measurements were taken with subjects wearing only light clothes and without shoes. In each subject, weight and height were measured to calculate the BMI [weight (kg) divided by height squared (m2), kg/m2]. Height was measured to the nearest 1 cm using a wall-mounted stadiometer. Body weight was determined to the nearest 50 g using a calibrated balance beam scale. The degree of obesity was established according to a scale based on BMI cut-off points: 30–34.9 (grade I obesity), 36–39.9 (grade II obesity) and ≥ 40 kg/m2 (grade III obesity or severe obesity), respectively.

WC was measured to the closest 0.1 cm with a non-extensible tape at the natural indentation or at a midway level between the iliac crest and the lower edge of the rib cage if no natural indentation was visible. The measurement was made with the subject standing upright, feet together and arms hanging freely at the sides.

In addition, for each patient we performed body composition with bioelectrical impedance analysis (single-frequency 50 kHz BIA 101 RJL, Akern Bioresearch, Firenze) and biavector analysis, with resistance (R) and reactance (Xc) data plotted on an R/H Xc/H graph using a specific software [33]. All participants were supine with limbs slightly spread apart from the body, refrained from eating, drinking, and exercising for six hours before testing. Subjects were tested in the supine position with arms and legs abducted from the body. Shoes and socks were removed and contact areas were scrubbed with alcohol immediately before electrode placement. Electrodes (BIATRODES Akern Srl; Florence, Italy) were placed proximal to the phalangeal–metacarpal joint on the dorsal surface of the right hand and distal to the transverse arch on the superior surface of the right foot. Sensor electrodes were placed at the midpoint between the distal prominence of the radius and ulna of the right wrist, and between the medial and lateral malleoli of the right ankle.

A validated 14-item questionnaire for the assessment of adherence to the Mediterranean Diet (PREDIMED) [31] was recorded for all the enrolled subjects during a face-to-face interview between the patient and a certified nutritionist. Briefly, for each items was assigned score 1 and 0; PREDIMED score was calculated as follows: 0–5, lowest adherence; score 6–9, average adherence; score ≥10, highest adherence [31].

Results are expressed as mean ± SD. Differences between the two groups were analyzed by paired t test. Frequencies were analyzed by χ 2 test. Correlations between variables were performed using Pearson r correlation coefficient. Using PASI score and CRP levels as dependent variables, three multiple linear regression analysis models (stepwise method) were set up to estimate the predictive value of: a) body composition evaluated by BIA, b) BMI, WC, FM and PREDIMED score; c) each item included in PREDIMED questionnaire (expressed as r2, Beta (β) and t). In these analysis, we entered only those variables that had a p-value <0.05 in the univariate analysis. To avoid multicollinearity, variables with a variance inflation factor (VIP) >10 were excluded. Values ≤5% were considered statistically significant. Data were stored and analysed using the MedCalc® package (Version 12.3.0 1993–2012 MedCalc Software bvba - MedCalc Software, Mariakerke, Belgium).

Results

A total of 62 subjects (49 males and 13 females) for group completed the study. Among psoriatic patients PASI score was 7.9 ± 7.2 and CRP levels were 2.4 ± 5.4 ng/ml (control group: 0.7 ± 0.4 ng/ml; p = 0.040). In Table 1 are shown the differences in the anthropometric and BIA parameters of the psoriatic patients and the control group. No statistically significant differences in age was and BMI were observed between the two groups. Psoriatic patients exhibited statistically significant differences compared with control group for BIA parameters. In particular psoriatic patients have the lowest values of Na/K ratio, FFM (%), SMM (%), TBW (%), and higher values of FM (Kg) and FM (%). Moreover, in psoriatic patients WC were and FM were significantly higher and PREDIMED score was lower than in control group; Figure 1. In Table 2 are reported the responses of each item included in PREDIMED questionnaire in the two groups. Psoriatic patients exhibited statistically significant differences compared with controls for use of the following dietary components: EVOO, fruits, red processed meats, fish and nuts. The total PREDIMED score in the two groups is reported in Figure 2. A higher percentage of psoriatic patients had a lower/average adherence score compared to the control group (30.6% vs 4.8%, p < 0.001 and 51.7% vs 77.5%, p = 0.004, respectively) as assessed by the PREDIMED questionnaire, while there no significant differences with the high adherence score (17.7% vs 17.7%, p = 0.814).

Table 1 Anthropometric measures and body composition evaluated by BIA parameters of the psoriatic patients and control group
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Figure 1
figure 1

Anthropometric and nutritional differences between psoriatic patients and control group. In psoriatic patients BMI (a), WC (b) and FM (c) were significantly higher and PREDIMED score (d) was lower than in control group. Results are expressed as mean ± SD. Differences between groups were analyzed by paired t test. BMI, body mass index; WC, waist circumference; FM, Fat Mass; PREDIMED, PREvención con DIeta MEDiterránea.

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Table 2 Response frequency of dietary components included in the PREDIMED questionnaire of the psoriatic patients and control group
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Figure 2
figure 2

PREDIMED score of all participants. A higher percentage of psoriatic patients had a lower PREDIMED score compared with the control group (30.6% vs 4.8%). Frequencies were analyzed by χ 2 test. Score 0–5, lowest adherence to the Mediterranean diet; Score 6–9, average adherence to the Mediterranean diet; Score ≥10, highest adherence to the Mediterranean Diet. PREDIMED, PREvención con DIeta MEDiterránea.

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Correlation studies

The correlations among PASI score, CRP levels and BIA parameters were reported in Table 3. In particular, PASI score was negatively correlated with Xc, PA, BCMI, FFM%, BCM (Kg and%), SMM (Kg and%), TBW%, TBW/BW, and ICW%. Moreover, there was a significant positive association among PASI score and BMI, FM, WC and PREDIMED score (Figure 3). The correlations between PASI score and CRP levels with each item of the PREDIMED questionnaire are showed in Table 4. At multiple regression analysis, the major predictor of PASI score were FM among BIA parameters, (r2 = 0.537, β = 0.740, t = 7.457, p < 0.001), and FM (r2 = 0.537, β = 0.603, t = 5.790, p < 0.001) and PREDIMED score (r2 = 0.599, β = −0.296, t = −2.839, p = 0.007) among anthropometric measures. Finally, among all items of the PREDIMED questionnaire, EVOO (r2 = 0.548, β = −0.741, t = −7.636, p < 0.001), and fish consumption (r2 = 0.139, β = −0.372, t = −2.922, p = 0.005) have an independent predictive value for PASI score and CRP levels, respectively.

Table 3 Correlations among body composition evaluated by BIA, PASI score and CRP levels in psoriatic patients
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Figure 3
figure 3

Correlation among PASI score and anthropometric parameters, body composition and PREDIMED score. There was a significant positive association among PASI score and BMI (a), FM (b), WC (c), and PREDIMED score (d). Correlations among variables were analyzed using Pearson r correlation coefficient. BMI, body mass index; WC, waist circumference; FM, Fat Mass; PREDIMED, PREvención con DIeta MEDiterránea.

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Table 4 Correlations between PASI score and CRP levels with dietary components included in the PREDIMED questionnaire in the psoriatic patients
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Discussion

Psoriasis is a chronic, immune-mediated inflammatory skin disease. Beyond the skin, psoriasis is associated with a systemic inflammatory state that has been linked to obesity, cardiovascular diseases, and type 2 diabetes. The causes of psoriasis are not fully understood, but a number of risk factors are recognized, including family history and environmental risk factors, such as diet, smoking, stress, obesity, and alcohol consumption [34].

The novel finding of this study is the association between the severity of psoriasis, assessed by PASI score and CRP levels, and the degree of adherence to the Mediterranean diet. In particular, the results of our study show that a higher percentage of psoriatic patients have a low adherence to the Mediterranean diet compared with the age- sex- and BMI-matched control group. In line with the current literature, we found that BMI and abdominal obesity, as measured by WC, were associated with psoriasis [26]. In addition, as also very recently reported [35] in a series of psoriatic patients (treated and untreated) compared with normal weight controls, we found that psoriatic patients exhibited statistically significant differences in body composition evaluated by BIA also compared with BMI-matched control group. In particular, we found that psoriatic patients have lower values of the ratio of TBW to body weight, greater amounts of adiposity and lower muscle mass compared with the obese counterpart without psoriasis. Although in obese patients, subtle variations of the hydration of soft tissues can propagate errors in BIA measures, BIA shows a good agreement with Dual-energy X-ray absorptiometry (DXA) [36], and the role of BIA to estimate body water and for predicting body cell mass is largely demonstrated [37]. These findings might suggest the presence of a form of sarcopenic obesity in psoriatic patients, likely linked to their chronic inflammatory disease, and let us also to hypothesize a worsening effect of psoriasis on body composition among equally obese individuals. Furthermore, after including all BIA parameters as predictive variables in the multiple regression model, FM remained the major predictor of the severity of the psoriasis. Thus, the usefulness of a careful assessment of body composition in the evaluation of the psoriatic patients of both genders is conceivable suggested.

Single food components have been suggested to play a role in aetiology and pathogenesis of psoriasis. Previous studies of the relationship of diet and nutrition with psoriasis have focused on either individual nutrients (eg, fish oil, omega 3, vitamin B12, vitamin D, vitamin A, selenium, inositol and zinc and antioxidants) or individual food groups (eg, fruit, vegetables, and fish) [5]. However, diet is a complex combination of foods from various groups and nutrients, and some nutrients are highly correlated. Thus, it is challenging to separate the effect of a single nutrient or food group from that of others in free-living populations [38].

One of the most frequently asked questions by patients with psoriasis is whether dietary changes could improve their disease. Given the negative impact of psoriasis on quality of life, patients often seek information about dietary and lifestyle modifications to assist in clearing their skin lesions [18]. Modifying diet is an accessible and self-empowering method that many patients are eager to embrace in treating their disease. However, despite the fact that nutrition might be considered an adjunctive tool for the treatment of psoriasis, there are no national or international guidelines that recommend an adequate diet for such patients [39]. With increasing awareness that psoriasis is associated with cardiovascular disease and metabolic syndrome, patients may also seek to improve diet to prevent these comorbidities. To the best of our knowledge, this is the first study to look at the association between adherence Mediterranean diet and psoriasis. In particular, the psoriatic patients consumed less EVOO, fruit, fish and nuts, while consumed more red meat compared to the control group.

The Mediterranean diet it is characterized by a high intake of fruit and vegetables, legumes, grains and cereals, fish and seafood and nuts; a low intake of dairy products, meat and meat products; and a moderate ethanol intake mainly in the form of wine and during meals [40]. EVOO is the main added lipid and its increased consumption is reflected in the high monounsaturated to saturated fatty acid intake [41]. The most interesting aspect of this study is that adherence to the Mediterranean diet is appraised using only a brief 14-item questionnaire (PREDIMED questionnaire) [31] which is less time-demanding, less expensive and requires less collaboration from participants than the usual full-length food frequency questionnaire (FFQ) or other more comprehensive methods [12]. Moreover, this questionnaire allows to provide feedback to the participant immediately after the interview is completed. In fact, this 14-item tool is a key element in the intervention conducted in the PREDIMED trial and has been previously validated against the FFQ used in the study [42]. In addition, we reported the specific association of each of the 14 individual items included in the PREDIMED score with the PASI score and CRP levels. In particular, PASI score and CRP levels were both negatively correlated not only with the PREDIMED score, but also the consumption of EVOO, vegetables, fruit, legumes, fish and nuts, and positively correlated with the consumption of red meat. Among these food components, EVOO and fish were independent predictors of PASI score and CRP levels, respectively. EVOO is one of many components of the Mediterranean diet. The decarboxy methyl ligstroside aglycone (also known as oleocanthal), a phenolic compound contained in EVOO, has been reported to provide per se both sensory and anti-inflammatory attributes of EVOO, thus contributing to the health benefits associated with the Mediterranean dietary pattern [43]. Oleocanthal is homologous with the non-steroidal anti-inflammatory drug ibuprofen [44] for both perceptual and anti-inflammatory properties. Therefore, it is tempting to speculate that long term consumption of EVOO containing this compound may contribute to significantly reduce the development and/or the progression of chronic inflammatory diseases and to increase the response to biological agents, thus representing a nutritional marker of responsiveness to Tumor Necrosis Factor-α blockers in psoriasis, in association with genetic marker, such as Interleukin 6 gene promoter polymorphism [45]. In this context, we evaluated also the relationship between the CRP levels, produced by the liver under the influence of IL-6 as one of the links between the altered cytokine milieu and psoriasis, and the consumption of EVOO. Indeed, we found higher consumption of EVOO and lower CRP levels in the control group compared with psoriatic patients.

Conclusions

This is the first study to evaluate the association between adherence to the Mediterranean diet and the severity of psoriasis, with a strict relationship between a higher consumption of EVOO and a lower psoriasis severity. Although we are aware that the reduced sample size and the validity of BIA in predicting the FM might be a limitation of our study, the association between the Mediterranean Diet and psoriasis severity suggests the possible beneficial effects of nutritional interventions promoting a Mediterranean food pattern rich in EVOO, fruits, vegetables, fish, chicken and whole grains, as an inexpensive and safe adjuvant treatment for psoriatic patients. Moreover, our study highlights the usefulness of the assessment of body composition by BIA in the evaluation of the psoriatic patients. Further researches on larger sample size are needed to unravel the individual role of the nutrients in the diet on the severity of psoriasis, particularly regarding the naturally occurring anti-inflammatory properties of olecanthal. The Nutritionists should play a central role in the evaluation and management of psoriatic patients.

Abbreviations

EVOO:

Extra virgin olive oil

BMI:

Body mass index

PASI:

Psoriasis area and severity index

CRP:

C-reactive protein

WC:

Waist circumference

BIA:

Bioelectrical impedance analysis

PREDIMED:

PREvención con DIeta MEDiterránea

R:

Resistance

Xc:

Reactance

R/H:

Resistance/Height

Xc/H:

Reactance/Height

PA:

Phase angle

Na/K:

Sodium/Potassium

BCMI:

Body cell mass index

FM:

Fat mass

FFM:

Fat-free mass

BCM:

Body cell mass

SMM:

Skeletal muscle mass

TBW:

Total body water

ECW:

Extra-cellular water

ICW:

Intra-cellular water

FFQ:

Food frequency questionnaire

References

  1. Grozdev I, Korman N, Tsankov N. Psoriasis as a systemic disease. Clin Dermatol. 2014;32:343–50.

    Article  PubMed  Google Scholar 

  2. Balato N, Balato A, Gallo L, Napolitano M, Patruno C, Ayala F. Psoriasis and osteoporosis: data from a Southern Italian population. Arch Osteoporos. 2012;7:321–3.

    Article  CAS  PubMed  Google Scholar 

  3. Kurd SK, Gelfand JM. The prevalence of previously diagnosed and undiagnosed psoriasis in US adults: results from NHANES 2003–2004. J Am Acad Dermatol. 2009;60:218–24.

    Article  PubMed  Google Scholar 

  4. Huerta C, Rivero E, Rodriguez LA. Incidence and risk factors for psoriasis in the general population. Arch Dermatol. 2007;143:1559–65.

    Article  PubMed  Google Scholar 

  5. Millsop JW, Bhatia BK, Debbaneh M, Koo J, Liao W. Diet and psoriasis, part III: role of nutritional supplements. J Am Acad Dermatol. 2014;71:561–9.

    Article  CAS  PubMed  Google Scholar 

  6. Augustin M, Mrowietz U, Bonnekoh B, Rosenbach T, Thaci D, Reusch M, et al. Topical long-term therapy of psoriasis with vitamin D(3) analogues, corticosteroids and their two compound formulations: position paper on evidence and use in daily practice. J Deutschen Dermatologischen Gesellschaft = J German Soc Dermatol: JDDG. 2014;12:667–82.

    Google Scholar 

  7. Wilson PB. Is dietary supplementation more common among adults with psoriasis? Results from the National Health and Nutrition Examination Survey. Complement Ther Med. 2014;22:159–65.

    Article  PubMed  Google Scholar 

  8. Steffen LM, Van Horn L, Daviglus ML, Zhou X, Reis JP, Loria CM, et al. A modified Mediterranean diet score is associated with a lower risk of incident metabolic syndrome over 25 years among young adults: the CARDIA (Coronary Artery Risk Development in Young Adults) study. The British journal of nutrition. 2014;112:1654–61.

    Article  CAS  PubMed  Google Scholar 

  9. Esposito K, Giugliano D. Mediterranean diet for primary prevention of cardiovascular disease. N Engl J Med. 2013;369:674–5.

    PubMed  Google Scholar 

  10. Schwingshackl L, Hoffmann G. Adherence to Mediterranean diet and risk of cancer: a systematic review and meta-analysis of observational studies. Int J Canc J Int Canc. 2014;135:1884–97.

    Article  CAS  Google Scholar 

  11. Esposito K, Di Palo C, Maiorino MI, Petrizzo M, Bellastella G, Siniscalchi I, et al. Long-term effect of mediterranean-style diet and calorie restriction on biomarkers of longevity and oxidative stress in overweight men. Cardiol Res Pract. 2011;2011:293916.

    PubMed Central  Google Scholar 

  12. Tresserra-Rimbau A, Rimm EB, Medina-Remon A, Martinez-Gonzalez MA, Lopez-Sabater MC, Covas MI, et al. Polyphenol intake and mortality risk: a re-analysis of the PREDIMED trial. BMC Med. 2014;12:77.

    Article  PubMed Central  PubMed  Google Scholar 

  13. Loued S, Berrougui H, Componova P, Ikhlef S, Helal O, Khalil A. Extra-virgin olive oil consumption reduces the age-related decrease in HDL and paraoxonase 1 anti-inflammatory activities. Br J Nutr. 2013;110:1272–84.

    Article  CAS  PubMed  Google Scholar 

  14. Santos M, Fonseca HM, Jalkh AP, Gomes GP, Cavalcante Ade S. Obesity and dyslipidemia in patients with psoriasis treated at a dermatologic clinic in Manaus. An Bras Dermatol. 2013;88:913–6.

    Article  PubMed Central  PubMed  Google Scholar 

  15. Carrascosa JM, Rocamora V, Fernandez-Torres RM, Jimenez-Puya R, Moreno JC, Coll-Puigserver N, et al. Obesity and psoriasis: inflammatory nature of obesity, relationship between psoriasis and obesity, and therapeutic implications. Actas Dermosifiliogr. 2014;105:31–44.

    Article  CAS  PubMed  Google Scholar 

  16. Kim CR, Lee JH. An observational study on the obesity and metabolic status of psoriasis patients. Ann Dermatol. 2013;25:440–4.

    Article  PubMed Central  PubMed  Google Scholar 

  17. Ni C, Chiu MW. Psoriasis and comorbidities: links and risks. Clin Cosmet Investig Dermatol. 2014;7:119–32.

    PubMed Central  PubMed  Google Scholar 

  18. Debbaneh M, Millsop JW, Bhatia BK, Koo J, Liao W. Diet and psoriasis, part I: impact of weight loss interventions. J Am Acad Dermatol. 2014;71:133–40.

    Article  PubMed  Google Scholar 

  19. Wolk K, Mallbris L, Larsson P, Rosenblad A, Vingard E, Stahle M. Excessive body weight and smoking associates with a high risk of onset of plaque psoriasis. Acta Derm Venereol. 2009;89:492–7.

    Article  PubMed  Google Scholar 

  20. Beygi S, Lajevardi V, Abedini R. C-reactive protein in psoriasis: a review of the literature. J Eur Acad Dermatol Venereol: JEADV. 2014;28:700–11.

    Article  CAS  PubMed  Google Scholar 

  21. Okorodudu DO, Jumean MF, Montori VM, Romero-Corral A, Somers VK, Erwin PJ, et al. Diagnostic performance of body mass index to identify obesity as defined by body adiposity: a systematic review and meta-analysis. Int J Obes (Lond). 2010;34:791–9.

    Article  CAS  Google Scholar 

  22. De Lorenzo A, Bianchi A, Maroni P, Iannarelli A, Di Daniele N, Iacopino L, et al. Adiposity rather than BMI determines metabolic risk. Int J Cardiol. 2013;166:111–7.

    Article  PubMed  Google Scholar 

  23. The National Institute of Health. Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults--The Evidence Report. National Institutes of Health. Obes Res. 1998;6 Suppl 2:51S–209.

    Google Scholar 

  24. Bosy-Westphal A, Booke CA, Blocker T, Kossel E, Goele K, Later W, et al. Measurement site for waist circumference affects its accuracy as an index of visceral and abdominal subcutaneous fat in a Caucasian population. J Nutr. 2010;140:954–61.

    Article  CAS  PubMed  Google Scholar 

  25. Jensen MD. Role of body fat distribution and the metabolic complications of obesity. J Clin Endocrinol Metab. 2008;93:S57–63.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  26. Tobin AM, Hackett CB, Rogers S, Collins P, Richards HL, O’Shea D, et al. Body mass index, waist circumference and HOMA-IR correlate with the Psoriasis Area and Severity Index in patients with psoriasis receiving phototherapy. Br J Dermatol. 2014;171:436–8.

    Article  CAS  PubMed  Google Scholar 

  27. Toussirot E, Aubin F, Dumoulin G. Relationships between Adipose Tissue and Psoriasis, with or without Arthritis. Front Immunol. 2014;5:368.

    Article  PubMed Central  PubMed  Google Scholar 

  28. Di Renzo L, Saraceno R, Schipani C, Rizzo M, Bianchi A, Noce A, et al. Prospective assessment of body weight and body composition changes in patients with psoriasis receiving anti-TNF-alpha treatment. Dermatol Ther. 2011;24:446–51.

    Article  PubMed  Google Scholar 

  29. Pedreira PG, Pinheiro MM, Szejnfeld VL. Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis. Arthritis Res Ther. 2011;13:R16.

    Article  PubMed Central  PubMed  Google Scholar 

  30. Bohm A, Heitmann BL. The use of bioelectrical impedance analysis for body composition in epidemiological studies. Eur J Clin Nutr. 2013;67 Suppl 1:S79–85.

    Article  PubMed  Google Scholar 

  31. Martinez-Gonzalez MA, Garcia-Arellano A, Toledo E, Salas-Salvado J, Buil-Cosiales P, Corella D, et al. A 14-item Mediterranean diet assessment tool and obesity indexes among high-risk subjects: the PREDIMED trial. PLoS One. 2012;7:e43134.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  32. Harari M, Shani J, Hristakieva E, Stanimirovic A, Seidl W, Burdo A. Clinical evaluation of a more rapid and sensitive Psoriasis Assessment Severity Score (PASS), and its comparison with the classic method of Psoriasis Area and Severity Index (PASI), before and after climatotherapy at the Dead-Sea. Int J Dermatol. 2000;39:913–8.

    Article  CAS  PubMed  Google Scholar 

  33. Piccoli A, Brunani A, Savia G, Pillon L, Favaro E, Berselli ME, et al. Discriminating between body fat and fluid changes in the obese adult using bioimpedance vector analysis. Int J Obes Relat Metabol Disord: J Int Assoc Stud Obes. 1998;22:97–104.

    Article  CAS  Google Scholar 

  34. Balato N, Megna M, Ayala F, Balato A, Napolitano M, Patruno C. Effects of climate changes on skin diseases. Expert Rev Anti Infect Ther. 2014;12:171–81.

    Article  CAS  PubMed  Google Scholar 

  35. Engin B, Kutlubay Z, Yardimci G, Vehid HE, Ambarcioglu P, Serdaroglu S, et al. Evaluation of body composition parameters in patients with psoriasis. Int J Dermatol. 2014;53:1468–73.

    Article  PubMed  Google Scholar 

  36. Savastano S, Belfiore A, Di Somma C, Mauriello C, Rossi A, Pizza G, et al. Validity of bioelectrical impedance analysis to estimate body composition changes after bariatric surgery in premenopausal morbidly women. Obes Surg. 2010;20:332–9.

    Article  PubMed  Google Scholar 

  37. De Lorenzo A, Andreoli A, Matthie J, Withers P. Predicting body cell mass with bioimpedance by using theoretical methods: a technological review. J Appl Physiol. 1997;82:1542–58.

    PubMed  Google Scholar 

  38. Hu FB. Dietary pattern analysis: a new direction in nutritional epidemiology. Curr Opin Lipidol. 2002;13:3–9.

    Article  CAS  PubMed  Google Scholar 

  39. Solis MY, de Melo NS, Macedo ME, Carneiro FP, Sabbag CY, Lancha Junior AH, et al. Nutritional status and food intake of patients with systemic psoriasis and psoriatic arthritis associated. Einstein. 2012;10:44–52.

    PubMed  Google Scholar 

  40. Bach-Faig A, Berry EM, Lairon D, Reguant J, Trichopoulou A, Dernini S, et al. Mediterranean diet pyramid today. Science and cultural updates. Public Health Nutr. 2011;14:2274–84.

    Article  PubMed  Google Scholar 

  41. Tapsell LC. Foods and food components in the Mediterranean diet: supporting overall effects. BMC Med. 2014;12:100.

    Article  PubMed Central  PubMed  Google Scholar 

  42. Schroder H, Fito M, Estruch R, Martinez-Gonzalez MA, Corella D, Salas-Salvado J, et al. A short screener is valid for assessing Mediterranean diet adherence among older Spanish men and women. J Nutr. 2011;141:1140–5.

    Article  CAS  PubMed  Google Scholar 

  43. Parkinson L, Keast R. Oleocanthal, a phenolic derived from virgin olive oil: a review of the beneficial effects on inflammatory disease. Int J Mol Sci. 2014;15:12323–34.

    Article  PubMed Central  PubMed  Google Scholar 

  44. Cicerale S, Breslin PA, Beauchamp GK, Keast RS. Sensory characterization of the irritant properties of oleocanthal, a natural anti-inflammatory agent in extra virgin olive oils. Chem Senses. 2009;34:333–9.

    Article  CAS  PubMed  Google Scholar 

  45. Di Renzo L, Bianchi A, Saraceno R, Calabrese V, Cornelius C, Iacopino L, et al. −174G/C IL-6 gene promoter polymorphism predicts therapeutic response to TNF-alpha blockers. Pharmacogenet Genomics. 2012;22:134–42.

    Article  PubMed  Google Scholar 

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    Authors and Affiliations

    1. I.O.S. & COLEMAN Srl, Naples, Italy

      Luigi Barrea & Maria Cristina Savanelli

    2. Dipartimento di Medicina Clinica e Chirurgia, Unit of Dermatology, Federico II University Medical School of Naples, Via Sergio Pansini 5, Naples, 80131, Italy

      Nicola Balato & Maddalena Napolitano

    3. IRCCS SDN, Napoli Via Gianturco 113, Naples, 80143, Italy

      Carolina Di Somma

    4. Department of Clinical and Experimental Medicine, Second University of Naples, Via Costantinopoli, Naples, 84-80138, Italy

      Katherine Esposito

    5. Dipartimento di Medicina Clinica e Chirurgia, Unit of Endocrinology, Federico II University Medical School of Naples, Via Sergio Pansini 5, Naples, 80131, Italy

      Paolo Emidio Macchia, Annamaria Colao & Silvia Savastano

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    1. Luigi Barrea
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    Correspondence to Luigi Barrea.

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    The authors declare that they have no competing interests.

    Authors’ contributions

    LB, NB and SS. designed the study; LB. and SS. have drafted the manuscript; CDS. and PEM. have all contributed substantially to the manuscript and have carried out the statistical analysis of the data; MN. collected the data; MCS performed laboratory analyses; AC. and KE. carefully revised the text. All authors read and approved the final manuscript.

    Luigi Barrea and Nicola Balato contributed equally to this work.

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    Barrea, L., Balato, N., Di Somma, C. et al. Nutrition and psoriasis: is there any association between the severity of the disease and adherence to the Mediterranean diet?. J Transl Med 13, 18 (2015). https://doi.org/10.1186/s12967-014-0372-1

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    Journal of Translational Medicine

    ISSN: 1479-5876

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