Literature DB >> 32938485

Clinical characteristics and quality of life in seborrheic dermatitis patients: a cross-sectional study in China.

Meiling Xuan1,2, Chuanjian Lu3,4,5, Zehui He6.   

Abstract

BACKGROUND: Seborrheic dermatitis (SD) is a common, chronic, inflammatory skin disorder, yet few studies have reported its clinical characteristics, or addressed its effect on quality of life (QoL). This study assesses the clinical characteristics and QoL of SD patients in China. It also identifies the clinical, demographic and environmental factors that may influence QoL.
METHODS: Three hundred twelve SD outpatients from 9 hospitals completed a survey. QoL was measured with the dermatology-specific instrument Skindex-29. We collected social demographic characteristics and disease severity, and conducted logistic regression to determine the factors associated with QoL impairment.
RESULTS: 67.3% of the patients were females. The mean Skindex-29 overall score was 33.97 (SD = 20.55). The breakdown was 40.79 (SD = 24.24) for emotions, 32.83 (SD = 19.84) for symptoms and 28.3 (SD = 23.24) for functioning. 48.1% had severe emotional problems. Logistic regression analysis showed that BMI less than 25 (OR = 0.223; 95% CI: 0.072-0.692; P = 0.009), skin disease-related hospitalization (OR = 6.882; 95% CI:1.767-26.795; P = 0.005), environmental PM 10 levels above 120 μg/m3 (OR = 3.386; 95% CI: 1.253-9.15; P = 0.016) and severe disease conditions (OR = 4.438; 95% CI:1.26-15.626; P = 0.02) were risk factors for severe emotional impairment. Moreover, skin disease-related hospitalization (OR = 6.057; 95% CI:1.351-27.149; P = 0.019), environmental PM 10 levels between 70 and 120 μg/m3 (OR = 6.317; 94% CI: 1.704-23.42; P = 0.006), moderate (OR = 2.388; 95% CI: 1.272-4.487; P = 0.007) and severe disease conditions (OR = 5.732; 95% CI: 1.838-17.88; P = 0.003) were each risk factors for overall severe impairment.
CONCLUSION: In China, nearly half of SD patients had severely emotional problems. Disease severity, BMI, dermatologic hospitalization, and ambient PM 10 levels are each risk factors for QoL impairment in SD patients. These implications are alarming, and warrant public health attention in SD disease management.

Entities:  

Keywords:  Quality of life; Seborrheic dermatitis; Skindex-29

Year:  2020        PMID: 32938485      PMCID: PMC7493366          DOI: 10.1186/s12955-020-01558-y

Source DB:  PubMed          Journal:  Health Qual Life Outcomes        ISSN: 1477-7525            Impact factor:   3.186


Background

Seborrheic dermatitis (SD) is a chronic, superficial, inflammatory skin disorder, characterized by scaling on an erythematous base [1]. It is considered one of the most frequent dermatoses. The etiology of SD is complex, and may be associated with several factors or internal diseases [2]. It also has high incidence and prevalence (1 to 3% in the immunocompetent adult population, 3 to 5% in young adults, and 40 to 80% in HIV-positive individuals) [3, 4] An Asian survey has shown that the prevalence of SD was 2.66, 2.85, 17.16 and 26.45% in Macao, Guangzhou, Malaysia and Indonesia, respectively [5]. The actual prevalence is probably much higher, and men are affected more frequently than women. Patients with SD have scaling scalps, and erythematous patches on the eyebrows, eyelids, nasolabial creases, lips, ears and sternal area. These symptoms affect patients’ social activities. SD co-occurs with depression, anxiety and other emotional symptoms, and has serious passive effects on patients’ Quality of Life (QoL). However, even though it is common and socially embarrassing, few studies have assessed SD patients’ QoL. SF-36, Dermatology Life Questionnaire Index (DLQI) and Skindex 29 have been used worldwide to investigate QoL [6-9]. Yet there is no data in systematic review studies concerning the effects of topical anti-inflammatory therapies on SD patients’ quality of life [10]. Some clinical trials of SD have reported QoL as a secondary outcome measure by using DLQI and Scalpdex [11, 12]. Likewise, a handful of studies have focused on QoL among patients suffering from this skin disorder in China. Recent evidence has indicated that particulate matter (PM) causes cutaneous damage not only directly, but also indirectly [13]. Systematic review has confirmed that particulate matter (PM) (PM 10 and PM 2.5) are associated with increased risks of human skin diseases [14]. It has also been suggested that other pollutants, such as O3, exert indirect toxic mechanisms on the skin [15, 16]. Whereas, there is lack of evidence about the effect of air pollution on QoL among SD patients in Asia. Therefore, this study investigates the clinical characteristics and QoL of patients with SD in China, and explores factors associated with QoL impairment.

Methods

Study design

We conducted a cross-sectional survey involving Chinese adults with seborrheic dermatitis. The inclusion criteria were: at least 16 years of age; diagnosed with SD; provided signed informed consent.

Settings

This study was conducted in 9 general hospitals, in 6 Chinese cities, from 2013 to 2015. Four of the hospitals were located in subtropical Southern China. The other 5 hospitals were located in temperate climate zones. All participants gave signed informed consent. This study was approved by the ethics committee at the Guangdong Provincial Hospital of Chinese Medicine.

Sociodemographic characteristics

Patients were asked to provide their sociodemographic information such as age, sex, disease duration, body mass index (BMI), relationship status, education level, employment, smoking and alcohol consumption, exercise habits, hospitalizations and private insurance status.

Health-related characteristics

We assessed this group of patients’ QoL with Skindex-29. Skindex-29 is one of the best dermatological instruments for measuring dermatology-specific QoL. It is a 30-item dermatology-specific QoL instrument for adults with an unscored item no. 18, measuring 3 domains—emotions, functioning and symptoms. Each item is rated on a 5-point Likert scale (never, rarely, sometimes, often, all the time), with higher scores indicating worse health status. There is also a Chinese version of the Skindex-29. It has been shown to be reliable and valid for use as a QoL instrument for patients with skin disease in China [17]. In this study, data were collected during clinical visits for both outpatients and inpatients. After obtaining informed consent, experienced doctors rated SD severity with three grades (mild, moderate, severe). Then patients were asked to complete a survey questionnaire comprised of sociodemographic characteristics and Skindex-29 questions.

Urban air quality data

Nine hospitals participated in this study. They were located in Guangzhou, Beijing, Shanghai, Chengdu, Urumqi and Harbin. The environmental conditions from 2013 to 2015 (including annual average SO2, NO2, CO, PM2.5 and PM 10 levels) were gathered from China Statistical Yearbook [18-20]. The average environmental factors from 2013 to 2015 were as follows: SO2 29.8 ± 15.4 μg/m3; NO2 52.4 ± 4.3 μg/m3; CO 2.2 ± 1.2 μg/m3; O3 136.9 ± 36.2 μg/m3; PM 2.5 65.3 ± 14.9 μg/m3 and PM 10 99.8 ± 29.3 μg/m3. Environmental indexes for these six cities are shown in Additional file 1.

Sampling

This study employed convenience sampling, and patients visiting hospitals were recruited to participate in the survey study when they had satisfied the inclusion criteria. The sample size was determined according to a rule of thumb that the sample size must be 5–10 times the number of survey items. Since there were 30 items, we enrolled 300 patients in this study to satisfy the sample size estimation.

Statistical analysis

Data were statistically analyzed with PASW Statistics 18.0 (IBM SPSS Inc., Armonk, NY, USA). Patients’ sociodemographic characteristics are shown with descriptive statistics. Mean values and standard deviations were calculated for all QoL scores and compared between subgroups using a t-test, nonparametric test or ANOVA. Variables with P values ≤0.1 were incorporated into the logistic regression model. We conducted logistic regression analysis with dichotomized Skindex-29 (emotions, symptoms, functioning and overall) mild and moderate (coded 0) and severe (coded 1) as dependent variables, and demographic and disease-related variables as covariates. Severely impaired QoL was based on the Skindex-29 cut-off scores as follows: ≥44 on the overall score, ≥39 on emotions, ≥52 on symptoms and ≥ 37 on functioning [21]. Variables entered the models via the forward likelihood ratio method. P < 0.05 was considered statistically significant.

Results

Patient characteristics

67.3% of the 312 patients were females, and the mean age was 30.51 years (standard deviation SD = 9.77). Disease duration ranged from 0.02 to 20.5 years (mean = 2.51 years; SD = 3.44). Two hundred seventy-one patients (86%) had normal weight, i.e., BMI was under 25. 26% had been hospitalized for various skin conditions over the past year (Table 1).
Table 1

Patient demographic characteristics, urban air quality and disease conditions

Total, n (%)Missing, n (%)
All patients312 (100)
Sex1 (0.3)
 Male101 (32.4)
 Female210 (67.3)
Age0
 < 24 years102 (32.7)
 ≥ 24 years210 (67.3)
Duration24 (7.7)
 < 3 years209 (67.0)
 ≥ 3 years79 (25.3)
BMIa10 (3.2)
 < 25271 (86.0)
 ≥ 2531 (9.8)
Relationship status9 (2.9)
 Married153 (49.0)
 Single150 (48.1)
Highest level of education4 (1.3)
 High school education or less103 (3.3)
 College or above205 (65.7)
Employment6 (1.9)
 Employed175 (56.1)
 Unemployed/student131 (42.0)
Diet preference136 (43.6)
 No59 (18.9)
 Yes117 (37.5)
Smoking5 (1.6)
 No197 (63.1)
 Yes110 (35.3)
Alcohol consumption4 (1.3)
 No174 (55.8)
 Yes134 (42.9)
Exercise7 (2.2)
 No134 (42.9)
 Yes171 (54.8)
Hospitalized for skin disease over the previous year7 (2.2)
 No224 (71.8)
 Yes81 (26.0)
Income
 ≤ 4000 yuan per month200 (64.1)
 > 4000 yuan per month112 (35.9)
Medical insurance24 (7.7)
 No80 (25.6)
 Yes213 (68.3)
SO2 level in the air
 < 20 μg/m3133 (42.6)
 20–40 μg/m385 (27.2)
 > 40 μg/m394 (30.1)
NO2 level in the air
 ≤50 μg/m3123 (39.4)
 > 50 μg/m3189 (60.6)
CO level in the air
 < 2 μg/m3199 (63.8)
 2–4 μg/m393 (29.8)
 > 4 μg/m320 (6.4)
O3 level in the air
 < 100 μg/m338 (12.2)
 100–160 μg/m3131 (42.0)
 > 160 μg/m3143 (45.8)
PM 2.5 level in the air
 < 60 μg/m3128 (41.0)
 60–80 μg/m3159 (51.0)
 > 80 μg/m325 (8.0)
PM 10 level in the air
 < 70 μg/m3112 (35.9)
 70–120 μg/m3141 (45.2)
 > 120 μg/m359 (18.9)
Disease severity9 (2.9)
 Mild144 (46.2)
 Moderate138 (44.2)
 Severe21 (6.7)

a The BMI classification is based on the World Health Organization’s obesity criteria

Patient demographic characteristics, urban air quality and disease conditions a The BMI classification is based on the World Health Organization’s obesity criteria

Skindex-29 scores across subgroups

All SD patients were divided into subgroups according to sex, age, disease duration, BMI, marital status, education level, employment, diet preference, smoking, alcohol consumption, routine exercise, hospitalization for skin problems, monthly income, medical insurance, urban air quality levels and disease severity. A comparison of these groups’ Skindex-29 scores showed a statistically significant difference between variable categories, including BMI (Z = − 2.418, P = 0.016), medical insurance (Z = − 2.146, P = 0.032), disease severity (F = 10.349, P < 0.001) in the emotion domain; sex (Z = − 2.477, P = 0.013) and disease severity (F = 13.785, P < 0.001) in the symptom domain; BMI (Z = − 2.515, P = 0.012), hospitalization (Z = − 2.745, P = 0.006), medical insurance (Z = − 2.147, P = 0.032), O3 levels (F = 6.47, P = 0.002), PM 2.5 levels (F = 7.1, P = 0.001), PM 10 levels (F = 3.387, P = 0.035) and disease severity (F = 18.049, P < 0.001) in the functioning domain; BMI (Z = − 2.277, P = 0.023), hospitalization (Z = − 2.432, P = 0.015) and disease severity (F = 16.531, P < 0.001) in the overall score (Table 2).
Table 2

Comparison of Skindex-29 domains across subgroups (mean ± SD)

EmotionsSymptomsFunctioningOverall
Mean40.79 ± 24.2432.83 ± 19.8428.3 ± 23.2433.97 ± 20.55
Sex
 Male38.71 ± 25.0728.72 ± 19.17*27.57 ± 23.9531.56 ± 20.74
 Female41.8 ± 23.934.75 ± 19.95*28.66 ± 22.9935.12 ± 20.46
Age
 < 2444.78 ± 25.5331.05 ± 19.4229.66 ± 24.0235.08 ± 20.8
 ≥ 2438.82 ± 23.3933.71 ± 20.0327.63 ± 22.8733.42 ± 20.46
Duration
 < 3 year39.24 ± 24.5232.13 ± 19.8126.9 ± 23.4832.79 ± 20.54
 ≥ 3 years44.32 ± 24.1235.02 ± 20.6831.41 ± 23.3136.95 ± 21.19
BMI
 < 2541.72 ± 24.23*33.01 ± 20.1829.17 ± 23.49*34.67 ± 20.74*
 ≥ 2531.38 ± 24.95*28.83 ± 17.9519.32 ± 20.99*25.94 ± 19.28*
Marital status
 Married38.44 ± 2333.9 ± 20.827.56 ± 22.8633.27 ± 20.42
 Single42.87 ± 25.2331.64 ± 19.0328.77 ± 23.7234.43 ± 20.76
Education level
 Primary school or high school40.32 ± 24.3633.13 ± 17.6728.84 ± 22.9934.01 ± 20.42
 University40.97 ± 24.2632.71 ± 20.8828.1 ± 23.4833.97 ± 20.7
Occupation
 Employed39.43 ± 22.8632.08 ± 19.3828.16 ± 2233.2 ± 19.84
 Unemployed/student42.52 ± 25.8933.85 ± 20.5328.48 ± 24.9434.95 ± 21.51
Taste preferences
 No47.29 ± 27.4233.87 ± 19.2633.9 ± 24.8938.25 ± 22.23
 Yes41.04 ± 22.7331.86 ± 20.2928.84 ± 23.9333.92 ± 20.15
Smoking
 No39.12 ± 23.8632.22 ± 19.7626.47 ± 21.8232.58 ± 19.81
 Yes43.58 ± 25.0133.72 ± 20.2931.75 ± 25.4836.35 ± 21.92
Alcohol consumption
 No39.51 ± 23.8932.21 ± 19.6626.88 ± 22.1732.84 ± 19.83
 Yes42.27 ± 24.8233.52 ± 20.2830.33 ± 24.5735.39 ± 21.58
Exercises
 No39.66 ± 25.2132.36 ± 20.0125.93 ± 22.7332.65 ± 21.05
 Yes41.16 ± 23.6732.89 ± 19.8329.85 ± 23.7934.68 ± 20.31
Skin disease hospitalization
 No38.25 ± 23.3332.01 ± 18.9925.63 ± 21.08*31.99 ± 19.13*
 Yes47.62 ± 25.6235.45 ± 21.4835.24 ± 26.91*39.37 ± 23.02*
Income
 ≤ 4000 yuan/month41.32 ± 24.4333.32 ± 20.1827.55 ± 22.434.07 ± 20.21
 >4000 yuan/month39.86 ± 23.9931.95 ± 19.2729.64 ± 24.733.8 ± 21.25
Medical insurance
 No46 ± 25.22*37.46 ± 23.0234.01 ± 26.83*39.16 ± 23.18*
 Yes39.07 ± 23.99*31.41 ± 18.2426.29 ± 21.69*32.29 ± 19.35*
Disease severity
 Slight or mild35.98 ± 22.19*29.1 ± 17.66*23.92 ± 19.25*29.67 ± 17.67*
 Moderate43.15 ± 24.6*33.86 ± 20.36*29.18 ± 23.14*35.41 ± 20.7*
 Severe59.76 ± 27.46*52.38 ± 21.62*54.96 ± 32.64*55.7 ± 25.78*
Urban air quality (SO2)
 < 20 μg/m342.58 ± 21.9631.71 ± 18.730.69 ± 21.8634.99 ± 19.01
 20–40 μg/m338.72 ± 27.0633.25 ± 20.5528.73 ± 26.1733.44 ± 22.31
 > 40 μg/m340.08 ± 24.8234.08 ± 20.9124.48 ± 22.1332.96 ± 21.25
Urban air quality (NO2)
 ≤ 50 μg/m342.78 ± 22.3431.16 ± 18.7830.62 ± 22.1934.85 ± 19.3
 > 50 μg/m339.47 ± 25.433.96 ± 20.526.76 ± 23.8433.38 ± 21.39
Urban air quality (CO)
 < 2 μg/m341.63 ± 22.5132.34 ± 20.0428.87 ± 22.6834.32 ± 19.95
 2–4 μg/m339.56 ± 27.834.22 ± 19.6127.31 ± 24.4833.71 ± 21.9
 > 4 μg/m338.03 ± 24.3231.15 ± 19.5527.08 ± 24.0031.47 ± 21.05
Urban air quality (O3)
 < 100 μg/m341.64 ± 25.132.71 ± 18.5425.56 ± 20.21*33.33 ± 19.97
 100–160 μg/m336.78 ± 23.7333.41 ± 20.5423.58 ± 22.39*31.2 ± 20.34
 > 160 μg/m344.24 ± 24.132.35 ± 19.6633.35 ± 23.84*36.64 ± 20.69
Urban air quality (PM 2.5)
 < 60 μg/m342.62 ± 22.5231.94 ± 19.2631.94 ± 22.79*35.5 ± 19.87
 60–80 μg/m338.66 ± 24.333.39 ± 19.9223.18 ± 21.21*31.78 ± 19.93
 > 80 μg/m342.8 ± 28.6633.57 ± 21.6835.26 ± 27.64*37.04 ± 24.23
Urban air quality (PM 10)
 < 70 μg/m343.1 ± 23.0231.44 ± 19.0131.75 ± 22.74*35.43 ± 19.93
 70–120 μg/m341.88 ± 24.7334.05 ± 21.0328.13 ± 23.92*34.76 ± 21.4
 > 120 μg/m333.75 ± 24.4932.64 ± 18.622.05 ± 21.52*29.23 ± 19.31

One-way ANOVA/t-test/nonparametric described the mean Skindex-29 for various demographics and clinical and environmental variables

*P < 0.05

Comparison of Skindex-29 domains across subgroups (mean ± SD) One-way ANOVA/t-test/nonparametric described the mean Skindex-29 for various demographics and clinical and environmental variables *P < 0.05 The comparison of whether or not there was severe impairment, defined by Skindex-29 cutoff scores for the subgroups, are shown in Additional file 2. 130 (42.2%), 75 (24.4%), 66 (21.4%) and 86 (27.9%) patients had severe impairment on emotion, symptoms, functioning and the overall realm, respectively. The high Skindex-29 scores in each of the domains was significantly different in terms of SD severity (emotion: P = 0.001; symptoms: P < 0.001; functioning: P < 0.001; overall: P < 0.001). Emotion and overall scores differed for hospitalization (P = 0.011; P = 0.002) and medical insurance (P = 0.016; P = 0.048) subgroups. The emotion score was also significantly different for several variables, including patient’s BMI and the concentration of PM 10 in the air (P = 0.014; P = 0.025). Also, the functional impact differed on O3 concentration in the air (P = 0.035). Moreover, those severely impaired based on their overall score also varied on smoking and alcohol consumption (P = 0.023; P = 0.034) subgroups.

Skindex-29 impairment risk factors

Variables with P value < 0.1 in Additional file 2 were included in a multivariate logistic regression model (emotions: duration, BMI, smoking, hospitalization, medical insurance, PM 10 level and disease severity; symptoms: disease severity; functioning: diet preference, smoking, hospitalization, PM 2.5 levels, O3 levels and disease severity; overall: BMI, smoking, alcohol consumption, hospitalization, medical insurance, O3 level, PM 10 level and disease severity). They were selected by the forward likelihood ratio method in the model. Significant variables for the multiple logistic model are shown in Table 3.
Table 3

Logistic regression analysis with Skindex scores as the dependent variable

VariableEmotionSymptomsFunctioningOverall
Exp(B)95% CIExp(B)95% CIExp(B)95% CIExp(B)95% CI
BMI
 < 25Ref
 ≥ 250.2230.072–0.692
Skin disease-related hospitalization
 NoRefRef
 Yes6.8821.767–26.7956.0571.351–27.149
PM 10 level in the air
 < 70 μg/m3RefRef
 70–120 μg/m30.8980.202–3.9956.3171.704–23.42
 > 120 μg/m33.3861.253–9.153.7420.674–20.77
Disease severity
 MildRefRefRefRef
 Moderate1.6860.953–2.9821.8721.049–3.3412.010.844–4.7892.3881.272–4.487
 Severe4.4381.26–15.6268.0573.012–21.55210.8852.676–44.2775.7321.838–17.88

Ref indicates reference variable

Logistic regression analysis with Skindex scores as the dependent variable Ref indicates reference variable BMI less than 25, skin disease-related hospitalization, environmental PM 10 concentration greater than 120 μg/m3 and disease severity of moderate to severe were risk factors for severe emotional impairment (P = 0.009, P = 0.005, P = 0.04, P = 0.03). The odds ratios were 0.223 (< 25 versus ≥25), 6.882 (yes versus no), 3.386 (> 120 μg/m3 versus < 70 μg/m3), 1.686 and 4.438 (moderate versus mild, severe versus mild) respectively. Disease severity for moderate to severe was the only factor associated with symptoms and severely impaired functioning (P < 0.01). The odds ratios were 1.872 and 8.057 (moderate versus mild, severe versus mild) in the symptom domain, 2.01 and 10.885 (moderate versus mild, severe versus mild) in the function domain. Moreover, skin disease-related hospitalization, environmental PM 10 concentration around 70–120 μg/m3 and disease severity of moderate to severe were risk factors for overall severe impairment (P = 0.019, P = 0.011, P = 0.006). The odds ratios were 6.057 (yes versus no), 6.317 (70–120 μg/m3 versus < 70 μg/m3), 2.388 and 5.732 (moderate versus mild, severe versus mild), respectively.

Discussion

This study has demonstrated that the presence of SD has a negative effect on QoL, and that disease severity influences QoL in all domains, and in the overall score. This study’s sample size was larger than previous studies conducted in Asia [8, 22]. In addition to disease severity, hospitalization and BMI, the environment was also found to influence QoL. Individuals were most influenced in the emotion domain. Also, skin disease-related hospitalization influenced individual feelings, which incurs substantial costs for both patients and the healthcare system. Obese or overweight people suffered less from emotional problems. This may have been because they pay less attention to appearance than those who stay in shape. In addition, dermatologic hospitalization and PM 10 concentration also negatively affected overall QoL scores. Several instruments have been used to evaluate SD patients’ QoL, such as the SF-36, DLQI and Skindex-29. Dai et al. used the SF-36 to assess QoL impairment in Chinese patients, which revealed that QoL was poor and was related to depression, alcohol consumption, smoking, exercise, and spicy food consumption [6]. We also demonstrated that alcohol consumption and smoking influenced patients’ QoL. A previous study found that SD patients’ mean DLQI score was 7.73, and that female, younger patients with higher education levels were the independent factors influencing QoL in Poland [7]. On the contrary, neither sex, age, nor education levels were independent QoL factors in this study. Furthermore, our data indicated that Chinese patients have a lower QoL than patients in other countries. A Korean study of soldiers with seborrheic dermatitis reported lower Skindex-29 scores for emotional and functioning than the scores in our study (E: 27.8 vs. 40.79; F: 19.6 vs. 28.29) [8]. This may have been due to disparities between military and common people in terms of social environment and physical health conditions. Compared to patients in Spain, patients in this study had worse QoL along all three Skindex domains (E: 20.54, S: 30.14 vs. 32.91, F: 15.45 vs. 28.29) [9]. Unlike previous studies, we analyzed the factors associated with the Skindex-29 cut-off score. This provides a better definition for the severe impairment in each domain. We found a statistically significant correlation between ambient PM 10 levels and patients’ QoL in our study. When outdoor air quality worsens (PM 10 levels over 120 μg/m3), individuals suffer more emotional torture than ever (OR:3.386; 95% CI: 1.253–9.15). Furthermore, higher air O3 levels have a negative functional effect on SD patients (P = 0.035). Existing studies have found air pollution to be causally linked to respiratory and allergic health problems [23, 24]. Over a decade ago, dermatologist Jean Krutmann began postulating how pollutants in the environment affect the skin. Evidence has shown that airborne pollutants harm the skin, and may even be deadly [13, 25, 26]. A recent epidemiological study has reported that indoor and outdoor air pollution also increase the risk of asthma, wheezing, rhinitis and eczema among pre-school children in China [27]. Due to the deleterious effects of airborne pollutants on both the skin and QoL, clinicians and seborrheic dermatitis patients may need to pay more attention to environmental air quality. One limitation of this study should be mentioned. Owing to this non-random sampling design, there may have been selection bias. A larger sample size and random sampling are needed to collect more representative data for further research.

Conclusion

Those who suffer from SD in China experience severe effects on all realms of daily life. We found that disease severity, dermatologic hospitalization and PM 10 level each had negative effects on patients’ QoL. These implications are alarming. Public health concerns for SD disease management, and its associated environmental factors, may see new emphasis in future SD mental health management. Additional file 1. Environmental data in research sites between 2013 and 2015. Additional file 2. Comparisons of the Skindex-29 cut-off score across subgroups.
  21 in total

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Review 2.  Role of antifungal agents in the treatment of seborrheic dermatitis.

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Review 3.  Outdoor air pollution and asthma.

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4.  Comparison of different regimens of pimecrolimus 1% cream in the treatment of facial seborrheic dermatitis.

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Journal:  J Cosmet Dermatol       Date:  2017-06-07       Impact factor: 2.696

5.  [Clinical and therapeutic profile and quality of life of patients with seborrheic dermatitis].

Authors:  J Peyrí; M Lleonart
Journal:  Actas Dermosifiliogr       Date:  2007-09

6.  Skin Damage Mechanisms Related to Airborne Particulate Matter Exposure.

Authors:  Natalia D Magnani; Ximena M Muresan; Giuseppe Belmonte; Franco Cervellati; Claudia Sticozzi; Alessandra Pecorelli; Clelia Miracco; Timoteo Marchini; Pablo Evelson; Giuseppe Valacchi
Journal:  Toxicol Sci       Date:  2015-10-26       Impact factor: 4.849

7.  Health-related quality of life assessment in dermatology: interpretation of Skindex-29 scores using patient-based anchors.

Authors:  Cecilia A C Prinsen; Robert Lindeboom; Mirjam A G Sprangers; Catharina M Legierse; John de Korte
Journal:  J Invest Dermatol       Date:  2009-12-24       Impact factor: 8.551

Review 8.  Systematic Review and Meta-Analysis of Human Skin Diseases Due to Particulate Matter.

Authors:  Le Thi Nhu Ngoc; Duckshin Park; Yongil Lee; Young-Chul Lee
Journal:  Int J Environ Res Public Health       Date:  2017-11-25       Impact factor: 3.390

9.  Antimicrobial and antioxidant activities of Cortex Magnoliae Officinalis and some other medicinal plants commonly used in South-East Asia.

Authors:  Lai Wah Chan; Emily L C Cheah; Constance L L Saw; Wanyu Weng; Paul W S Heng
Journal:  Chin Med       Date:  2008-11-28       Impact factor: 5.455

10.  Development and psychometric validation of the Chinese version of Skindex-29 and Skindex-16.

Authors:  Zehui He; Chuanjian Lu; Mary-Margaret Chren; Zhongzhao Zhang; Yan Li; Xiaojia Ni; Henry A Buchtel V; Paul F Ryan; Guo-Zheng Li
Journal:  Health Qual Life Outcomes       Date:  2014-12-24       Impact factor: 3.186

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  2 in total

1.  Tanshinone Capsules Combined With Prednisone for Facial Seborrheic Dermatitis: A Systematic Review and Meta-Analysis of Randomized Clinical Trials.

Authors:  Qiang Fu; Mengya Huang; Lei Tang; Qi Zheng; Fujun Huang; Xun Zhou; Shumei Wang
Journal:  Front Med (Lausanne)       Date:  2022-04-29

2.  Global Burden, Incidence and Disability-Adjusted Life-Years for Dermatitis: A Systematic Analysis Combined With Socioeconomic Development Status, 1990-2019.

Authors:  Yi Xue; Wu Bao; Jie Zhou; Qing-Liang Zhao; Su-Zhuang Hong; Jun Ren; Bai-Cheng Yang; Peng Wang; Bin Yin; Cheng-Chao Chu; Gang Liu; Chi-Yu Jia
Journal:  Front Cell Infect Microbiol       Date:  2022-04-12       Impact factor: 6.073

  2 in total

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