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. 2021 Sep 18;13:845–851. doi: 10.2147/CLEP.S323744

Prevalence and Associated Diseases of Seborrheic Skin in Adults

Natalia Kirsten 1,, Nicole Mohr 1, Aminah Alhumam 1,2, Matthias Augustin 1
PMCID: PMC8459174  PMID: 34566435

Abstract

Background

Seborrhea is a skin condition characterized by abundant production of sebum associated with typical dermatological conditions such as rosacea and acne. Little is known about the prevalence of seborrhea and the frequency of concurrent skin diseases in the general population.

Objective

To investigate the epidemiology and comorbidity of seborrhea in the adolescent and adult working population.

Methods

In large-scale examinations by dermatologists in 343 German companies, the seborrheic skin type and the occurrence of skin findings were documented electronically. Odds ratios (OR) and their 95% confidence intervals (95% CI) of further skin diseases were computed. Logistic regression analyses were conducted for each disease using seborrhea as dependent variable.

Results

A total of 48,630 employees were examined. About 6.0% showed seborrhea (6.6% in men, 5.4% in women). Seborrhea strongly predicted acne (OR 3.59; CI 3.18–4.05), trichilemmal cysts (OR 1.99; CI 1.25–3.18) and rosacea (OR 1.45; CI 1.17–1.81). Regression analyses controlling for age, gender and phototype confirmed significant associations of seborrhea with acne and rosacea.

Conclusion

Only a minor proportion of the working population shows meaningful seborrheic skin. However, this condition predicts distinct skin diseases and thus needs attention, in particular, with respect to consulting and secondary prevention.

Keywords: seborrhea, seborrheic skin, epidemiology, comorbidities

Introduction

Seborrhea is characterized by an overactivity of sebaceous glands, resulting in an excessive secretion of sebum.1,2 Seborrhea is also used as a synonym for seborrheic dermatitis, a skin disorder which is characterized by inflammatory scaling rush in seborrheic areas of the body. In this publication, the term seborrhea is used to describe the skin condition characterized by an oily skin due to hyperproduction of sebum without inflammatory reaction. Seborrhea has been shown to be a major pathogenetic factor for acne.3 Moreover, several other conditions like polycystic ovary syndrome4,5 or pityriasis versicolor6 are associated with increased sebum secretion. Seborrhea is more common in colored skin and in male people.7 Especially androgens seem to have a regulatory role in sebum secretion.8,9 The skin surface lipid film, derived by sebaceous glands, is an important part of skin barrier.10 Any alteration of lipid film of the skin can contribute to manifestation of common inflammatory skin diseases like acne vulgaris, rosacea or seborrheic dermatitis.10 Condition-adapted skin care has been shown to improve skin condition and patient well-being by restoring the disturbed barrier function and by re-establishing well-being and quality of life.11 Moreover, skin care adapted to the specific needs of the individuals can support the prevention of exacerbating skin inflammation and chronification.

In spite of the fact that seborrhea is a common condition, especially in young people, little is known about the population-based prevalence in Germany. For this, the objective of the current study was to gain robust data for the working-age population on the prevalence and comorbidity of dry skin across Germany. The research questions were as follows:

  1. Which is the prevalence of seborrhea in the German adult population?

  2. Which dermatologic comorbidities are associated with seborrhea?

  3. Which comedication profile is associated with seborrhea?

Materials and Methods

Centers and People

Dermatological whole-body exams were performed in 48,630 employed persons by dermatologists during voluntary company-based skin screenings in 343 German companies as described previously.12,13 To reduce selection bias, the screenings were conducted during the working hours, and every employee was asked to participate. Validity and sensitivity of the procedures have been shown previously.12,13

All procedures performed were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study has received a granted ethics vote from the ethics committee of the Medical Association Hamburg. All subjects included in the study have signed an informed consent.

Assessments

The whole-body exams were conducted by trained dermatologists and recorded in an electronic database by a research assistant. Seborrhea was evaluated both clinically and by interviewing the individual. The assessment of seborrhea was based on the validated six-item skin oiliness scale (SOS).14 Seborrhea was considered prevalent when alternatively meeting the following criteria as proposed by Baumann et al: a) Three hours after washing the face it appears shiny with reflection of bright light, b) the facial skin of the person is often or always oily at the latest one hour after washing the face on the T-zone, c) the person has clogged pores and b) the skin must be washed at least twice a day for seborrhea. Every other condition of the skin found by the dermatologist was recorded. Skin type was categorized according to the phototypes I–IV by Fitzpatrick.15 Furthermore, medical history, comorbidity and systemic comedication were obtained.

Statistics

Statistical analyses were performed using SPSS for Windows 23.0 (IBM, Armonk, New York, US.). Seborrhea and further conditions were assessed as dichotomous variables and point prevalence rates of further dermatological conditions were calculated. Subgroup analyses were conducted to compare the prevalence rates between people with and without seborrhea. Odds ratios (OR) and their 95% confidence intervals (95% CI) were computed indicating the chance of people with seborrhea to also have the diagnosis of any further skin disease. To account for the influence of age, gender and skin phototype, logistic regression analyses were conducted for each disease using seborrhea as dependent variable.

Results

Centers and People

In n = 343 German companies, a total of n = 48,630 persons were examined. The mean age was 43.2 ± 11.4 years, 52.8% (n = 25,674) were male. In total, n = 2932 persons (6.0%) had seborrheic skin (men: 1700; 6.6%, women: 1232; 5.4%; p < 0.001). Prevalence decreased by age (Figure 1). The prevalence of seborrheic skin also differed between skin phototypes: Skin type I (n = 4235): 6.6%, skin type II (n = 36,542): 6.2%, skin type III (n = 7357): 5.0% skin type IV (n = 264): 8.7%. There was a significant difference between skin type III and IV (p = 0.007) but not between skin type I, II, III combined (6.2%) vs IV (8.7%).

Figure 1.

Figure 1

Flowchart of the materials and methods.

In group comparisons, a significantly higher rate of comorbidity among participants with seborrhea was found for the following dermatological conditions (Table 1): acne (OR 3.59; CI 3.18–4.05), trichilemmal cysts (OR 1.99; CI 1.25–3.18), seborrheic eczema (OR 1.94; CI 1.65–2.27), folliculitis (OR 1.74; CI 1.54–1.97), pyodermia (OR 1.69; CI 1.20–2.37), hypertrophic sebaceous glands (OR 1.66; CI 1.40–1.97), rosacea (OR 1.45; CI 1.17–1.81) and verruca vulgaris (OR 1.37; CI 1.01–1.86). Significantly less common in people with seborrhea were atopic eczema (OR 0.51; CI 0.33–0.78), other inflammatory skin diseases excluding rosacea (OR 0.67; CI 0.48–0.94), lentigo solaris (OR 0.69; CI 0.64–0.75) and atopic diathesis (OR 0.91; CI 0.83–0.99).

Table 1.

Frequency of Skin Conditions in People with versus without Seborrheic Skin (n = 48,630)

Total n = 48,630 Seborrhea n = 2932 No Seborrhea n = 45,698 OR (Occurrence Among People with Seborrhea)
n % n % n % OR (95% CI)
Atopic diathesis 12,273 25.24 689 23.50 11,584 25.35 0.905 (0.828–0.988)
Bacterial infections Folliculitis 3195 6.57 308 10.50 2887 6.32 1.741 (1.538–1.970)
Pyodermia 381 0.78 37 1.26 344 0.75 1.685 (1.198–2.370)
Other benign non-inflammatory skin conditions Lentigo solaris 24,357 50.09 1219 41.58 23,138 50.63 0.694 (0.643–0.748)
Fibroma 15,755 32.40 1050 35.81 14,705 32.18 1.176 (1.088–1.271)
Seborrheic keratosis 12,231 25.15 854 29.13 11,377 24.90 1.240 (1.142–1.346)
Hypertrophic sebaceous gland 1590 3.27 150 5.12 1440 3.15 1.657 (1.395–1.969)
Other benign non-inflammatory skin conditions 668 1.37 59 2.01 609 1.33 1.520 (1.161–1.992)
Cysts Epidermal cysts 662 1.36 47 1.60 615 1.35 1.194 (0.886–1.610)
Trichilemmal cysts 177 0.36 20 0.68 157 0.34 1.992 (1.249–3.178)
Other skin cysts 123 0.25 5 0.17 118 0.26 0.660 (0.269–1.616)
Inflammatory skin diseases Acne 2055 4.23 357 12.18 1698 3.72 3.593 (3.184–4.054)
Seborrheic dermatitis 1636 3.36 176 6.00 1460 3.19 1.935 (1.647–2.273)
Rosacea 1052 2.16 89 3.04 963 2.11 1.454 (1.167–1.813)
Atopic dermatitis 694 1.43 22 0.75 672 1.47 0.507 (0.331–0.776)
Psoriasis 1005 2.07 68 2.32 937 2.05 1.134 (0.884–1.455)
Other inflammatory skin diseases 843 1.73 35 1.19 808 1.77 0.671 (0.478–0.943)
Fungal skin infections Tinea corporis 229 0.47 16 0.55 213 0.47 1.172 (0.704–1.950)
Viral skin infections Verruca vulgaris 572 1.18 46 1.57 526 1.15 1.369 (1.010–1.855)
Herpes labialis 206 0.42 8 0.27 198 0.43 0.629 (0.310–1.276)

Abbreviations: OR, odds ratio; CI, confidence interval.

Dermatologic Conditions Predicted by Seborrhea

In the regression analyses controlling for age, gender and skin phototype IV, seborrhea was a significant predictor for: acne (3.45; CI 3.03–3.91), contact dermatitis (OR 2.15; CI 1.33–3.48), trichilemmal cysts (OR 1.98; CI 1.24–3.17), seborrheic eczema (OR 1.87; CI 1.59–2.20), folliculitis (OR 1.62; CI 1.43–1.84), pyodermia (OR 1.55; CI 1.10–2.19), rosacea (OR 1.54; CI 1.23–1.92), other benign non-inflammatory skin conditions (OR 1.52; CI 1.16–2.00) and verruca vulgaris (OR 1.38; CI 1.02–1.87) (Table 2).

Table 2.

Odds Ratio (OR) of the Occurrence of Different Skin Conditions Among People with Seborrhea, Controlling for Age and Gender and Skin Phototype IV (n = 48,630)

Skin Disease OR 95% CI of OR
Folliculitis 1.624 1.432–1.843
Pyodermia 1.554 1.103–2.189
Lentigo solaris 0.709 0.655–0.767
Fibroma 1.220 1.126–1.322
Seborrheic keratosis 1.461 1.329–1.605
Hypertrophic sebaceous gland 1.687 1.417–2.009
Other benign non-inflammatory skin conditions 1.523 1.162–1.995
Epidermoid cysts 1.209 0.896–1.632
Trichilemmal cysts 1.984 1.243–3.167
Other cysts 0.674 0.275–1.652
Acne 3.445 3.033–3.913
Seborrheic eczema 1.870 1.589–2.201
Rosacea 1.537 1.229–1.921
Other inflammatory skin diseases 0.671 0.478–0.944
Atopic dermatitis 0.494 0.323–0.758
Psoriasis 0.379 0.094–1.525
Contact dermatitis 2.149 1.328–3.477
Pityriasis versicolor 1.141 0.781–1.669
Tinea corporis 1.088 0.643–1.841
Verruca vulgaris 1.381 1.019–1.871

Abbreviation: CI, confidence interval.

By contrast, seborrhea was a negative predictor for atopic eczema (OR 0.50; CI 0.32–0.76), other inflammatory skin diseases (OR 0.67; CI 0.47–0.94) and lentigo solaris (OR 0.71; CI 0.66–0.77).

Comedication Profile in People with Seborrhea

People with seborrhea used more frequently steroids (OR 1.59; CI 1.12–2.09). Less commonly used were hormones (OR 0.82; CI 0.74–0.91) and other drugs (OR 0.90; CI 0.81–0.99; Table 3). Stratified by gender, there was no difference for hormone intake as comedication between people with versus without seborrhea. Male people with seborrhea more frequently used steroids as comedication (OR 1.76; CI 1.21–2.55). Female people with seborrhea more frequently used antidiabetics (OR 2.19; CI 1.43–3.37) and psychotropic drugs (OR 1.68; CI 1.10–2.56) compared to those without seborrhea.

Table 3.

Frequency of Comedications in People with versus without Seborrhea

Total (n = 48,630) No Seborrhea (n = 45,698) Seborrhea (n = 2932) OR (Comedication in Participants with Seborrhea)
Drug n % n % n % OR (95% CI)
Analgetics 1013 2.08 966 2.11 47 1.60 0.754 (0.562–1.012)
Antibiotics 194 0.40 185 0.40 9 0.31 0.757 (0.388–1.480)
Antidiabetics 664 1.37 617 1.35 47 1.60 1.190 (0.883–1.605)
Cardiovascular drugs 5167 10.63 4838 10.59 329 11.22 1.067 (0.948–1.202)
Hormones 9358 19.24 8874 19.42 484 16.51 0.820 (0.742–0.907)
Psychotropic drugs 439 0.90 403 0.88 36 1.23 1.397 (0.991–1.969)
Hypnotics 58 0.12 54 0.12 4 0.14 1.155 (0.418–3.191)
Steroids 631 1.30 573 1.25 58 1.98 1.589 (1.210–2.088)
Other 8035 16.52 7590 16.61 445 15.18 0.898 (0.810–0.997)

Abbreviations: OR, odds ratio; CI, confidence interval.

Discussion

The aim of the current study was to address the prevalence of seborrhea as a typical dysfunctional skin pattern in the normal adult population. Furthermore, potential predictors were to be identified. Investigations were conducted during large-scale skin examinations including a large and largely representative proportion of the adult working population. No technology-based evaluation to detect seborrhea was possible to perform. This is one of the limitations. However, all exams were conducted by trained dermatologists with considerable experience in clinical dermatological examinations who used a clinical scoring system. Within these limitations, the prevalence of seborrhea of 6% can be assumed as robust. It corresponds to numbers reported in smaller and more selective cohorts.16,17

The skin-related comorbidity and the triggering factors determined, support the experience from clinical care and from the few studies published,3,18,19 suggesting that acne, seborrheic eczema, folliculitis and rosacea are associated with seborrhea.

Increased sebogenesis is crucial for the pathogenesis of acne and predisposes the skin to deregulated inflammatory reactions. The quantitative as well as the qualitative differences in sebum composition play a role here.18,20,21 This also appears comprehensible, since the increased sebum production alters the microenvironment, favoring colonization with Propionibacterium acnes.22,23 This leads to dysbiosis followed by an inflammatory reaction. The association found between seborrhea and acne seems plausible. It must be assumed that seborrhea precedes acne vulgaris and that appropriate skin care could stop the progress into an inflammatory condition.

In most cases, folliculitis is caused by Staphylococcus aureus.24 Here, too, it is conceivable that seborrhea favors the proliferation of Staphylococcus aureus and, similar to acne vulgaris, favors the disease.

Any change in the lipid film can lead to the manifestation of inflammatory skin disease.18 This may confirm the observation in the current study that people with seborrhea were more likely to develop rosacea.25 We also observed that people with seborrhea used more frequently systemic glucocorticosteroids reported to have a strong enhancing effect on the regulation of the pilosebaceous unit. Recent evidence suggests that steroid-induced inflammation may contribute to the development of acne by activating toll-like receptor 2.26 It remains unclear whether patients treated with systemic steroids are more likely to develop seborrhea or whether seborrhea may be associated with other inflammatory diseases requiring steroid therapy. Further research is needed to better understand these relationships.

Our data show a significantly higher prevalence of seborrhea in skin phototype IV compared to type III. It was reported about differences in sebum level in different ethnic population groups.27 Although this subgroup is small (n = 264), such finding should be further explored.

Overall, the current study indicates that a small but relevant part of the general population suffers from seborrhea and associated diseases. Timely initiated adapted skin care could prevent the manifestation of inflammatory skin diseases and thus improve the persons’ quality of life.

Conclusion

Our study shows that seborrhea is a non-negligible skin condition in the German working population especially in darker skin types. Seborrhea can promote other inflammatory skin diseases; therefore, this skin condition should not be neglected in daily practice.

Acknowledgments

We thank Heigel GmbH for providing the data. The authors thank the Scientific Communication Team of the IVDP, in particular Sara Tiedemann and Mario Gehoff, for copy editing.

Funding Statement

There is no funding to report.

Data Sharing Statement

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to restrictions, eg, their containing information that could compromise the privacy of research participants.

Author Contributions

All authors contributed to data analysis, drafting or revising the article, gave final approval of the version to be published, agreed to the submitted journal, and agreed to be accountable for all aspects of the work.

Disclosure

The authors declare no conflicts of interest.

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