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ORIGINAL RESEARCH article

Front. Nutr., 02 February 2023
Sec. Nutrition and Metabolism
Volume 10 - 2023 | https://doi.org/10.3389/fnut.2023.1092781

Associations of adherence to Mediterranean-like diet pattern with incident rosacea: A prospective cohort study of government employees in China

Peng Chen1,2,3 Ziye Yang1,2,3 Zhihua Fan1,2,3 Ben Wang1,2,3 Yan Tang1,2,3 Yi Xiao1 Xiang Chen1,4,5 Dan Luo6 Shuiyuan Xiao6 Ji Li1,2,3 Hongfu Xie1,2,3* Minxue Shen1,5,6*
  • 1Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China
  • 2Hunan Engineering Research Center of Skin Health and Disease, Xiangya Hospital, Central South University, Changsha, China
  • 3Hunan Key Laboratory of Aging Biology, Xiangya Hospital, Central South University, Changsha, China
  • 4National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China
  • 5Furong Laboratory, Changsha, China
  • 6Department of Social Medicine and Health Management, Xiangya School of Public Health, Central South University, Changsha, China

Background: Despite of growing evidence on gastrointestinal comorbidities of rosacea, there was a lack of literatures regarding the role of diet on rosacea.

Objectives: To investigate the relationship between adherence to a Mediterranean-like diet pattern and the risk of incident rosacea.

Methods: This was a prospective cohort study of government employees aged >20 years conducted between January 2018 and December 2021 from five cities of Hunan province of China. At baseline, participants completed a food frequency questionnaire and participated in a skin examination. Presence of rosacea was determined by certified dermatologists. Subsequent skin examinations during follow-up were performed every one-year interval since the entry of the study. The Mediterranean diet score (MDS) was generated based on seven food groups (whole grains, red meats, fish, raw vegetables, legumes, fruits and nuts). Binary logistic regression models adjusted for potential confounders were used to estimate risks for incident rosacea.

Results: Of the 3,773 participants who completed at least two consecutive skin examinations, 3,496 were eligible for primary analyses. With a total follow-up of 8,668 person-years, we identified 83 incident rosacea cases. After full adjustments for covariates, the MDS was associated a decreased risk of incident rosacea (aOR: 0.84, 95% CI: 0.72, 0.99; Ptrend = 0.037 for 1-point increment of MDS). In subgroup analyses by body mass index (BMI), this inverse association was consistently observed in the lowest and medium tertiles of BMI (<24.5 kg/m2), but not in the highest tertile of BMI (≥24.5 kg/m2), with a significant interaction effect (P < 0.001).

Conclusions: Our results suggested that adherence to a Mediterranean-like diet pattern might reduce the risk of incident rosacea among non-overweight individuals.

Introduction

Rosacea is recognized as a common chronic inflammatory skin syndrome encompassing a variety of signs or symptoms, which affects 5.46% of the general population over the world (1, 2). Although the exact pathogenesis of rosacea still remains unclear, it's found that both genetic and environmental factors contributed to development of the disease (3). In one survey conducted by the National Rosacea Society, several dietary factors including heat-related, alcohol-related, capsaicin-related, and cinnamaldehyde-related, were reported as rosacea triggers by patients (4), which suggested the diet might play an important role in rosacea. What's more, epidemiological studies have demonstrated that compared to healthy subjects, patients with rosacea had a higher prevalence of gastrointestinal (GI) disease, such as Helicobacter pylori infection (HPI), small intestinal bacterial overgrowth (SIBO), and irritable bowel syndrome (IBS) (5, 6). These findings further emphasized the importance of carrying out dietary interventions to decrease the risk of GI comorbidities. However, there was a lack of literatures regarding the role of dietary factors on the development of rosacea, (4) with few studies only focusing on effects of single nutrients or food groups (7, 8).

The Mediterranean diet (MD) is a healthy diet pattern characterized as high intake of fruits, vegetables, whole grains, fish, legumes, and nuts; moderate consumption of alcohol; low intake of red or processed meats, and using olive oil as the main source of fat (9, 10). A meta-analysis has shown that greater adherence to MD was associated with decreased incidence of many chronic diseases (e.g., cancer, Parkinson's disease, and Alzheimer's disease) (11, 12). Epidemiology studies also demonstrated that adherence to the MD pattern reduced the mortality caused by a series of metabolic diseases, such as cardiovascular disease and type 2 diabetes (1315). The underlying mechanisms could partially be explained by the anti-inflammatory capacity of MD (16). Meanwhile, the MD pattern had also shown protective roles on severity or development of certain inflammatory skin disorders like acne and psoriasis (1720). Similarly, higher levels of pro-inflammatory serum markers like C-reaction protein (CRP) in rosacea patients indicated the involvement of both cutaneous and systemic inflammation in the pathogenesis of rosacea (2123).

Combining this evidence, we hypothesized that MD might also have an effect on the onset of rosacea. The objective of the current study was therefore to investigate the relationship between a score reflecting adherence to MD and the risk of incident rosacea in a prospective cohort of government employees. The traditional MD score was mainly applied in Mediterranean countries like Greece or for samples of elderly participants (24). To adapt the score to Chinese population, we selected the alternate Mediterranean Diet (aMed) score established by Fung et al. to evaluate adherence to MD in our study (25).

Materials and methods

Study design and population

This was a population-based prospective cohort study conducted from January 2018 to December 2021 in five cities (Changsha, Zhuzhou, Xiangtan, Huaihua, and Changde) of Hunan province, China. On the basis of informed consent, a total of 11,523 government employees aged >20 years from 25 organizations were enrolled. At baseline, they completed a questionnaire collecting information on demographic, socioeconomic, and lifestyle behaviors and participated in a dermatological physical examination at the same time. Subsequent skin examinations were performed every one-year interval since their enrollment of the study to update their skin health status during the follow-up period.

The follow up began on the date the questionnaires were returned or the first physical examinations were performed (baseline). Participants contributed person-time from baseline until the date of the first-time rosacea diagnosis during follow-up or the date of last-time physical examination (due to loss to follow up or the end of the study), whichever came first.

In the current study, we only included participants who completed at least two consecutive dermatological physical examinations (n = 3773). Thus, the follow-up time of participants ranged from 1 to 4 years. The study procedures were approved by the institutional research ethics boards of Xiangya School of Public Health, Central South University (XYGW-2016-10).

Outcome ascertainment

The presence of rosacea was determined by certified dermatologists from local tertiary hospitals in each dermatological physical examination. In the field survey, clinical manifestation, disease history, and family history of participants were inquired, and dermatologists made an accurate diagnosis of rosacea based on the diagnostic criteria established by the National Rosacea Society Expert Committee in 2017 (at least 1 diagnostic or 2 major phenotypes were required) (2).

Dietary assessment and Mediterranean diet score calculation

The weekly average frequency of dietary intake for different food groups over the preceding year of enrollments was assessed by a self-reported semi-quantitative food frequency questionnaire (FFQ) at baseline. Each food groups had 5 possible frequency of intake responses in the FFQ: rarely, <1 time/week, 1–3 days/week, 4–6 days/week and every day. The Mediterranean diet score (MDS) applied in this study was adopted from the aMed score posted by Fung et al. (25). As alcohol drinking was associated with increased risks of incident rosacea even under low doses of daily intake, it was not included in the MDS calculation (26). Due to the availability of data, ratio of monounsaturated to saturated fat was also excluded. Eventually, our MDS consisted of seven components of food groups: whole grains, red meats, fish, raw vegetables, legumes, fruits, and nuts. Each component was assigned with point 0 or 1 using sex-specific medians of food intake frequency categories as cut-offs. For presumed beneficial food groups (whole grains, fish, raw vegetables, legumes, fruits, and nuts), participants whose intake was below the median categories received a point of 0, and a point of 1 otherwise. For presumed detrimental food groups (red meats), participants whose intake was below the median categories received a point of 1, and a point of 0 otherwise. Thus, the possible MDS ranged from 0 to 7, with higher score representing closer adherence to the Mediterranean diet pattern. We additionally separated participants by approximately tertiles of MDS into three groups: low (0–3), medium (4–5), and high (6–7).

Covariates

Information on socioeconomic characteristics (education level, annual household income) and behaviors (smoking status, alcohol drinking status, frequency of sunbath, frequency of physical exercise) was collected by questionnaires at baseline. New variables were created when including cigarette smoking and alcohol drinking for adjustments in multivariable models by further including information on daily average consumption of cigarettes and frequency of drinking per week in current smokers and drinkers. The body mass index (BMI) was calculated by dividing individuals' weight in kilograms by the square of their height in meters which were obtained from physical examination.

Statistical analysis

Descriptive statistics were performed to summarize participants' characteristics at baseline stratified by categories of MDS. Continuous variables were presented as mean ± standard deviation (SD) and categorical variables were presented as number (%). Between-group differences were tested by ANOVA or chi-square test for continuous and categorical variables. We used binary logistic regression models to assess the association between incident rosacea and variables of interests and calculated the odds ratio (OR) and 95% confidence interval (CI).

First, we evaluated the association of incident rosacea with each component of food groups in the MDS separately. Those food intake frequency groups with small sample sizes were merged into one group where appropriate to achieve approximately tertiles and the lowest tertiles were treated as reference groups. Then, we investigated the association of MDS with risks of incident rosacea using MDS categories with lowest (0–3) adherence to MD as reference. A P-value for trend across MDS categories was calculated by treating MDS as a continuous variable. We also applied natural cubic splines to examine potential non-linear or linear relationships between MDS and incidence of rosacea. As the obesity was reported as a risk factor for incident rosacea in previous study, (27) we additionally tested effect modification by BMI by adding an interaction term between MDS and BMI into logistic models. We then stratified the analyses by tertiles of BMI. Subgroup analyses by other potential covariates were also performed.

To test the robustness of the primary analyses, we performed sensitivity analyses by (1) excluding participants who made significant changes on dietary or lifestyle habits last year before the entry of the study, or (2) excluding participants with prevalent or incident acne vulgaris, contact dermatitis or seborrheic dermatitis which were considered as differential diagnoses of rosacea for patients with skin of color (28).

We used principal component analysis (PCA) to extract components of intake frequency of other dietary factors not associated with calculation of MDS in our FFQ (rice, pasta, poultry, eggs, dairy products, pickles, deserts, and marinated or smoked fish) with eigenvalues >1, for the purpose of addressing the collinearity issues among dietary factors when being included in multivariate models. All basic models were adjusted by age and sex, and the fully adjusted models were further adjusted by education level, annual household income, BMI, cigarette smoking, alcohol drinking, sunbath, physical exercise, and specially, the principal components of other dietary factors not associated with calculation of MDS to reduce residual confounding. Participants with missing data on dietary intake frequency associated with calculation of MDS was eliminated, while missing data on covariates was imputed by multiple imputation.

All statistical analyses were performed using R software (version 4.1.3). A P < 0.05 was considered significant.

Results

Baseline characteristics stratified by MDS categories

After excluding participants with unavailable follow-up time (n = 68), prevalent rosacea (n = 51), and missing data on dietary intake frequency (n = 158), there were a total of 3,496 participants included in the primary analyses (Supplementary Figure S1). During a median follow-up of 2 years (interquartile range: 2–3 years; 8,668 total person-years), we identified 83 incident rosacea cases (incidence rate: 9.58 per 1,000 person-years). The baseline characteristics of participants stratified by MDS categories were shown in Table 1. Among 3,496 eligible participants, 23.3, 45.8, and 30.9% of them were categorized into low, medium, and high adherence to Mediterranean diet pattern groups. Compared to participants with either low or medium adherence to MD, those in the high adherence group had older age, higher education level, annual household income, and frequency of physical exercise, and lower rate of current smokers (all p-values <0.05). We extracted three components from other dietary factors not associated with calculation of MDS, accounting for 33.6, 16, and 13% of the total variance, respectively (Supplementary Figure S2).

TABLE 1
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Table 1. Baseline characteristics of the study population according to MDS categories (n = 3496).

Food groups and incident rosacea

Associations between intakes of each food groups from MDS and incident rosacea were reported in Table 2. Taken individually, we observed that the intake of whole grains with ≥4 days/week was associated with a decreased risk of incident rosacea compared to the lowest intake frequency group (<1 time/week) in both basic model and fully adjusted model (aOR: 0.37; 95%CI: 0.17, 0.84). However, no significant association was found for other food groups in fully adjusted models.

TABLE 2
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Table 2. Associations of each food groups from MDS with incident rosacea (n = 3496).

Mediterranean diet score and risks of incident rosacea

In the whole study population, we observed an inverse association between MDS and the risk of incident rosacea in both basic and fully-adjusted models (aOR: 0.84, 95%CI: 0.72, 0.99; Ptrend = 0.037 for 1-point increment of MDS) (Table 3). Cubic splines revealed a negative linear relationship between MDS and the incidence of rosacea (Figure 1).

TABLE 3
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Table 3. Associations of Mediterranean diet score with incident rosacea (n = 3496).

FIGURE 1
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Figure 1. The negative linear relationship between the Mediterranean diet score and incidence of rosacea in cubic splines.

Subgroup analysis

Since an interaction effect between BMI and MDS was detected (Pinteraction <0.001), we further stratified the analyses by tertiles of BMI shown in Table 4 (two participants eliminated with missing value or extremely low value on BMI). Among participants in tertile 1 (BMI <21.8) and tertile 2 (BMI range: 21.8–24.5), we consistently found inverse associations between MDS and incident rosacea in fully-adjusted models (Ptrend = 0.018 and 0.023, respectively). However, no significant protective effects of MDS were observed in those with highest tertile of BMI (tertile 3: BMI ≥ 24.5) in both the basic model and fully-adjusted model. Subgroup analysis by other covariates was presented in Figure 2.

TABLE 4
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Table 4. Subgroup analysis for the associations of MDS with incident rosacea by tertiles of BMI (n = 3494).

FIGURE 2
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Figure 2. Subgroup analysis for the association of Mediterranean diet score and incident rosacea by potential covariates.

Sensitivity analysis

The results of primary analyses remained stable when excluding participants with significant lifestyle or dietary modifications over the preceding year, or excluding participants with skin disorders that were differential diagnoses of rosacea (Supplementary Table S1).

Discussion

In this population-based prospective cohort of Chinese government employees, we observed an inverse association between adherence to MD and risks of incident rosacea. This association was consistently present in groups with lowest and medium tertiles of BMI (BMI <24.5 Kg/m2), but not in group with highest tertile of BMI (BMI ≥ 24.5 Kg/m2). To our knowledge, this was the first study to report a positive association between MD and rosacea.

In this study, the incidence rate of rosacea was 9.58 per 1,000 person-years. Previously, only one study from U.K.-based General Practice Research Database had reported an incidence rate of rosacea (1.65 per 1,000 person-years), which was notably lower than our study (1, 29). However, the ascertainment of rosacea from this database was performed by general practitioners in primary care and diagnoses were primarily based on visible symptoms due to lacking diagnostic guidelines, thus leading to underestimate of the incidence rate for missing cases with mild rosacea (29). By contrast, presence of rosacea in this study was determined by certified dermatologists in field survey for all enrolled participants based on the latest diagnostic criteria combining presenting cutaneous signs and personal history, which allowed us to assume a higher diagnostic accuracy (2). Moreover, to address the concern of misdiagnosis, we also performed sensitivity analysis by excluding participants with skin disorders that were considered as differential diagnoses of rosacea.

As mentioned before, prior studies investigating the role of diet on rosacea mainly focused on single nutrients or food components. For instance, a case-control study with 1,347 rosacea patients and 1,290 controls reported a positive correlation between high-frequency intake of fatty food and tea and risks of rosacea, while high-frequency intake of dairy products showed a negative correlation (7). In our analyses of single food components, we only observed a significant inverse association between intakes of whole grains and incident rosacea. However, there seemed to be a negative but non-significant correlation between higher intake frequency of other beneficial components of MD and the incidence of rosacea. This could partially be explained that the effect of single food components might be too small to detect among individuals, while a dietary pattern approach examining cumulative effects of multiple nutrients or food components was feasible to identify overall effects. What's more, dietary pattern analysis considered the issues of complex interactions and correlations among nutrients (30).

Although the mechanism of health benefits of MD had not been fully understood, several hypotheses could be considered when interpreting our results. First, the MD exerted antioxidative properties. It's known that oxidative stress plays a role in the pathogenesis of rosacea. Individuals with rosacea were confirmed to have higher serum peroxide levels and lower serum antioxidative potential levels (31). Takci et al. (32) also demonstrated that rosacea patients had decreased activity of Paraoxonase-1 (PON1), an antioxidant enzyme, and higher levels of serum lipid hydroperoxide (32). Multiple components of MD, including nuts, fruits, and vegetables, have been proven effective in increasing PON1 activity and reducing lipid peroxidation (33). Second, the MD pattern exhibited an anti-inflammatory capacity. The elevated levels of chemokines and CRP in serum (21, 34). and pro-inflammatory cytokines (IL-8, IL-1β, TNF-α) in skin lesions implied that rosacea was not only a cutaneous inflammatory skin disorder but also with low-grade systemic inflammation (22, 35). Interestingly, diet intervention studies revealed inverse associations between MD and almost all inflammatory biomarkers which indicated the capacity of MD to reduce low-grade inflammation (36). This was potentially mediated by modulation of the gastrointestinal (GI) microbiota. Altered GI microbiota, a pivotal element of gut-skin axis, has been observed by emerging studies in rosacea and might be responsible for increased risks of GI comorbidities in rosacea (37, 38). Multiple nutrients from MD, including polyphenols, polyunsaturated fatty acids (PUFAs) and fiber, contribute to modulations of the gut microbiota both in the aspects of diversity and inflammatory response (39). For example, the ω-3 PUFAs, rich in fish and nuts, could induce increases of several short-chain fatty acid-producing intestinal bacteria thus leading to suppression of inflammation, (40, 41) and was reported effective in the treatment of ocular rosacea (42). In addition, the MD was also associated with an increased abundance of fiber-degrading bacteria in GI microbiota and lower levels of intestinal inflammation (43). We hypothesized that a chronic subclinical inflammation caused by obesity might counterbalance the anti-inflammatory capacity of MD, which could explain the interaction effects between BMI and MDS (16, 27).

Our study encompassed several strengths and limitations. The strengths included the prospective study design, the dermatologists-based rosacea diagnoses, annually-renewable skin health status, and the availability of various epidemiological factors which allowed us to adjust for potential confounders and performed sensitivity analyses based on multiple conditions. In the meanwhile, we also acknowledged the existence of several limitations in our study. First, this study had a high rate of loss to follow-up (referring to those excluded for only attending skin examinations at baseline) and this population represented a lower level of education and income compared to those included in primary analyses (Supplementary Table S2). As a result, even though we adjusted the models with education, income and lifestyle factors, the selection bias was inevitable, and it should be interpreted with caution when generalizing our results to the public population. Second, our study was limited by short periods of follow-up and few cases of incident rosacea. However, a short-time study duration ensured the stability of dietary habits of participants during follow-up. Moreover, we also applied sensitivity analyses by excluding participants with dietary modifications to minimize the measurement error of dietary intake by FFQ. Third, it's worth noting that due to the availability of data, our MDS didn't include the variable of monounsaturated fat (MUFA) to saturated fat (SFA) ratio thus only representing a Mediterranean-like diet pattern. Nevertheless, this parameter could partially be reflected by the intakes of nuts and meat products which were rich in MUFA and SFA, respectively (44, 45). The efficacy of unsaturated fat in rosacea treatment also allowed us to assume an underestimate of protective effects of the Mediterranean diet on rosacea (42).

Conclusion

In summary, this study indicated that adherence to a Mediterranean-like diet pattern was associated with lower risks of incident rosacea among non-overweight individuals. Our results needed to be verified in other population-based prospective cohort studies with larger sample sizes, longer follow-up periods and quantitative measurement on foods or nutrients intake.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by the Ethics Committee of Xiangya Hospital, Central South University. The patients/participants provided their written informed consent to participate in this study.

Author contributions

PC drafted the manuscript and analyzed the data. ZY, ZF, BW, YT, YX, DL, and SX participated in the field investigation. MS and HX designed the study. MS, HX, XC, and JL obtained the funding. All authors participated in the data collection, critically revised the manuscript, and gave final approval to the version submitted for publication.

Funding

This work was supported by the National Key Research and Development Program of China (2021YFF1201205 and 2016YFC0900802), the National Natural Science Funds for Distinguished Young Scholars (82225039), and Hunan Science and Technology Program for Young Scholars (2022RC1014).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2023.1092781/full#supplementary-material

References

1. Gether L, Overgaard LK, Egeberg A, Thyssen JP. Incidence and prevalence of rosacea: a systematic review and meta-analysis. Br J Dermatol. (2018) 179:282–9. doi: 10.1111/bjd.16481

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Gallo RL, Granstein RD, Kang S, Mannis M, Steinhoff M, Tan J, et al. Standard classification and pathophysiology of rosacea: The 2017 update by the national rosacea society expert committee. J Am Acad Dermatol. (2018) 78:148–55. doi: 10.1016/j.jaad.2017.08.037

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Aldrich N, Gerstenblith M, Fu P, Tuttle MS, Varma P, Gotow E, et al. Genetic vs environmental factors that correlate with rosacea: a cohort-based survey of twins. JAMA Dermatol. (2015) 151:1213–9. doi: 10.1001/jamadermatol.2015.2230

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Weiss E, Katta R. Diet and rosacea: the role of dietary change in the management of rosacea. Dermatol Pract Concept. (2017) 7:31–7. doi: 10.5826/dpc.0704a08

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Egeberg A, Weinstock LB, Thyssen EP, Gislason GH, Thyssen JP. Rosacea and gastrointestinal disorders: a population-based cohort study. Br J Dermatol. (2017) 176:100–6. doi: 10.1111/bjd.14930

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Gallo RL, Granstein RD, Kang S, Mannis M, Steinhoff M, Tan J, et al. Rosacea comorbidities and future research: the 2017 update by the national rosacea society expert committee. J Am Acad Dermatol. (2018) 78:167–70. doi: 10.1016/j.jaad.2017.06.150

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Yuan X, Huang X, Wang B, Huang YX, Zhang YY, Tang Y, et al. Relationship between rosacea and dietary factors: a multicenter retrospective case-control survey. J Dermatol. (2019) 46:219–25. doi: 10.1111/1346-8138.14771

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Searle T, Ali FR, Carolides S, Al-Niaimi F. Rosacea and diet: What is new in 2021? J Clin Aesthet Dermatol. (2021) 14:49–54.

Google Scholar

9. Sofi F, Abbate R, Gensini GF, Casini A. Accruing evidence on benefits of adherence to the Mediterranean diet on health: an updated systematic review and meta-analysis. Am J Clin Nutr. (2010) 92:1189–96. doi: 10.3945/ajcn.2010.29673

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Serra-Majem L, Roman-Vinas B, Sanchez-Villegas A, Guasch-Ferre M, Corella D, La Vecchia C. Benefits of the Mediterranean diet: Epidemiological and molecular aspects. Mol Aspects Med. (2019) 67:1–55. doi: 10.1016/j.mam.2019.06.001

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Sofi F, Cesari F, Abbate R, Gensini GF, Casini A. Adherence to Mediterranean diet and health status: meta-analysis. BMJ. (2008) 337:a1344. doi: 10.1136/bmj.a1344

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Gnagnarella P, Maisonneuve P, Bellomi M, Rampinelli C, Bertolotti R, Spaggiari L, et al. Red meat, Mediterranean diet and lung cancer risk among heavy smokers in the COSMOS screening study. Ann Oncol. (2013) 24:2606–11. doi: 10.1093/annonc/mdt302

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Knoops KT, de Groot LC, Kromhout D, Perrin AE, Moreiras-Varela O, Menotti A, et al. Mediterranean diet, lifestyle factors, and 10-year mortality in elderly European men and women: the HALE project. JAMA. (2004) 292:1433–9. doi: 10.1001/jama.292.12.1433

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Brunner EJ, Mosdol A, Witte DR, Martikainen P, Stafford M, Shipley MJ, et al. Dietary patterns and 15-y risks of major coronary events, diabetes, and mortality. Am J Clin Nutr. (2008) 87:1414–21. doi: 10.1093/ajcn/87.5.1414

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Li J, Guasch-Ferre M, Chung W, Ruiz-Canela M, Toledo E, Corella D, et al. The Mediterranean diet, plasma metabolome, and cardiovascular disease risk. Eur Heart J. (2020) 41:2645–56. doi: 10.1093/eurheartj/ehaa209

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Bailey MA, Holscher HD. Microbiome-mediated effects of the mediterranean diet on inflammation. Adv Nutr. (2018) 9:193–206. doi: 10.1093/advances/nmy013

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Skroza N, Tolino E, Semyonov L, Proietti I, Bernardini N, Nicolucci F, et al. Mediterranean diet and familial dysmetabolism as factors influencing the development of acne. Scand J Public Health. (2012) 40:466–74. doi: 10.1177/1403494812454235

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Barrea L, Donnarumma M, Cacciapuoti S, Muscogiuri G, De Gregorio L, Blasio C, et al. Phase angle and mediterranean diet in patients with acne: two easy tools for assessing the clinical severity of disease. J Transl Med. (2021) 19:171. doi: 10.1186/s12967-021-02826-1

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Phan C, Touvier M, Kesse-Guyot E, Adjibade M, Hercberg S, Wolkenstein P, et al. Association between mediterranean anti-inflammatory dietary profile and severity of psoriasis: results from the nutrinet-sante cohort. JAMA Dermatol. (2018) 154:1017–24. doi: 10.1001/jamadermatol.2018.2127

PubMed Abstract | CrossRef Full Text | Google Scholar

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

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Duman N, Ersoy Evans S, Atakan N. Rosacea and cardiovascular risk factors: a case control study. J Eur Acad Dermatol Venereol. (2014) 28:1165–9. doi: 10.1111/jdv.12234

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Sinikumpu SP, Huilaja L, Auvinen J, Jokelainen J, Puukka K, Ruokonen A, et al. The Association between low grade systemic inflammation and skin diseases: a cross-sectional survey in the northern finland birth cohort 1966. Acta Derm Venereol. (2018) 98:65–9. doi: 10.2340/00015555-2795

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Ertekin SS, Koku Aksu AE, Kocyigit A, Guler EM, Baykara Ulusan M, Gurel MS. Carotid intima-media thickness and serum proinflammatory cytokine levels in rosacea patients without cardiovascular risk factors. Dermatol Ther. (2021) 34:e14733. doi: 10.1111/dth.14733

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Trichopoulou A, Costacou T, Bamia C, Trichopoulos D. Adherence to a mediterranean diet and survival in a Greek population. N Engl J Med. (2003) 348:2599–608. doi: 10.1056/NEJMoa025039

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Fung TT, Rexrode KM, Mantzoros CS, Manson JE, Willett WC, Hu FB. Mediterranean diet and incidence of and mortality from coronary heart disease and stroke in women. Circulation. (2009) 119:1093–100. doi: 10.1161/CIRCULATIONAHA.108.816736

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Li S, Cho E, Drucker AM, Qureshi AA, Li WQ. Alcohol intake and risk of rosacea in US women. J Am Acad Dermatol. (2017) 76:1061-7 e2. doi: 10.1016/j.jaad.2017.02.040

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Li S, Cho E, Drucker AM, Qureshi AA, Li WQ. Obesity and risk for incident rosacea in US women. J Am Acad Dermatol. (2017) 77:1083-7 e5. doi: 10.1016/j.jaad.2017.08.032

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Alexis AF, Callender VD, Baldwin HE, Desai SR, Rendon MI, Taylor SC. Global epidemiology and clinical spectrum of rosacea, highlighting skin of color: review and clinical practice experience. J Am Acad Dermatol. (2019) 80:1722-9 e7. doi: 10.1016/j.jaad.2018.08.049

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Spoendlin J, Voegel JJ, Jick SS, Meier CR, A. study on the epidemiology of rosacea in the U. K Br J Dermatol. (2012) 167:598–605. doi: 10.1111/j.1365-2133.2012.11037.x

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Hu FB. Dietary pattern analysis: a new direction in nutritional epidemiology. Curr Opin Lipidol. (2002) 13:3–9. doi: 10.1097/00041433-200202000-00002

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Tisma VS, Basta-Juzbasic A, Jaganjac M, Brcic L, Dobric I, Lipozencic J, et al. Oxidative stress and ferritin expression in the skin of patients with rosacea. J Am Acad Dermatol. (2009) 60:270–6. doi: 10.1016/j.jaad.2008.10.014

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Takci Z, Bilgili SG, Karadag AS, Kucukoglu ME, Selek S, Aslan M. Decreased serum paraoxonase and arylesterase activities in patients with rosacea. J Eur Acad Dermatol Venereol. (2015) 29:367–70. doi: 10.1111/jdv.12556

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Lou-Bonafonte JM, Gabas-Rivera C, Navarro MA, Osada J. PON1 and Mediterranean Diet. Nutrients. (2015) 7:4068–92. doi: 10.3390/nu7064068

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Liu T, Li J, Deng Z, Chen M, Sha K, Xiao W, et al. Increased serum levels of CCL3, CXCL8, CXCL9, and CXCL10 in rosacea patients and their correlation with disease severity. J Dermatol. (2022) 49:525–33. doi: 10.1111/1346-8138.16329

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Casas C, Paul C, Lahfa M, Livideanu B, Lejeune O, Alvarez-Georges S, et al. Quantification of Demodex folliculorum by PCR in rosacea and its relationship to skin innate immune activation. Exp Dermatol. (2012) 21:906–10. doi: 10.1111/exd.12030

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Barbaresko J, Koch M, Schulze MB, Nothlings U. Dietary pattern analysis and biomarkers of low-grade inflammation: a systematic literature review. Nutr Rev. (2013) 71:511–27. doi: 10.1111/nure.12035

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Tutka K, Zychowska M, Reich A. Diversity and composition of the skin, blood and gut microbiome in rosacea-a systematic review of the literature. Microorganisms. (2020) 8:756. doi: 10.3390/microorganisms8111756

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Moreno-Arrones OM, Ortega-Quijano D, Perez-Brocal V, Fernandez-Nieto D, Jimenez N, de Las Heras E, et al. Dysbiotic gut microbiota in patients with inflammatory rosacea: another clue towards the existence of a brain-gut-skin axis. Br J Dermatol. (2021) 185:655–7. doi: 10.1111/bjd.20411

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Merra G, Noce A, Marrone G, Cintoni M, Tarsitano MG, Capacci A, et al. Influence of mediterranean diet on human gut microbiota. Nutrients. (2020) 13:9–25. doi: 10.3390/nu13010007

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Sivaprakasam S, Prasad PD, Singh N. Benefits of short-chain fatty acids and their receptors in inflammation and carcinogenesis. Pharmacol Ther. (2016) 164:144–51. doi: 10.1016/j.pharmthera.2016.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Watson H, Mitra S, Croden FC, Taylor M, Wood HM, Perry SL, et al. A randomised trial of the effect of omega-3 polyunsaturated fatty acid supplements on the human intestinal microbiota. Gut. (2018) 67:1974–83. doi: 10.1136/gutjnl-2017-314968

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Bhargava R, Chandra M, Bansal U, Singh D, Ranjan S, Sharma S, et al. Randomized controlled trial of omega 3 fatty acids in rosacea patients with dry eye symptoms. Curr Eye Res. (2016) 41:1274–80. doi: 10.3109/02713683.2015.1122810

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Turpin W, Dong M, Sasson G, Raygoza Garay JA, Espin-Garcia O, Lee SH, et al. Mediterranean-like dietary pattern associations with gut microbiome composition and subclinical gastrointestinal inflammation. Gastroenterology. (2022) 163:685–98. doi: 10.1053/j.gastro.2022.05.037

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Bojkova B, Winklewski PJ, Wszedybyl-Winklewska M. Dietary fat and cancer-which is good, which is bad, and the body of evidence. Int J Mol Sci. (2020) 21:4114. doi: 10.3390/ijms21114114

PubMed Abstract | CrossRef Full Text | Google Scholar

45. de Oliveira Otto MC, Mozaffarian D, Kromhout D, Bertoni AG, Sibley CT, Jacobs DR. et al. Dietary intake of saturated fat by food source and incident cardiovascular disease: the multi-ethnic study of atherosclerosis. Am J Clin Nutr. (2012) 96:397–404. doi: 10.3945/ajcn.112.037770

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: rosacea, Mediterranean diet, incidence rate, diet pattern analysis, anti-inflammatory

Citation: Chen P, Yang Z, Fan Z, Wang B, Tang Y, Xiao Y, Chen X, Luo D, Xiao S, Li J, Xie H and Shen M (2023) Associations of adherence to Mediterranean-like diet pattern with incident rosacea: A prospective cohort study of government employees in China. Front. Nutr. 10:1092781. doi: 10.3389/fnut.2023.1092781

Received: 15 November 2022; Accepted: 16 January 2023;
Published: 02 February 2023.

Edited by:

Mireille Serhan, University of Balamand, Lebanon

Reviewed by:

Joanne Karam, University of Balamand, Lebanon
Berna Rahi, Sam Houston State University, United States

Copyright © 2023 Chen, Yang, Fan, Wang, Tang, Xiao, Chen, Luo, Xiao, Li, Xie and Shen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Hongfu Xie, yes xiehongfu1964@aliyun.com; Minxue Shen, yes shenmx1988@csu.edu.cn

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