Prevalence and Determinants of Seborrhoeic Dermatitis in A Middle-Aged and Elderly Population: The Rotterdam Study
Prevalence and Determinants of Seborrhoeic Dermatitis in A Middle-Aged and Elderly Population: The Rotterdam Study
Prevalence and Determinants of Seborrhoeic Dermatitis in A Middle-Aged and Elderly Population: The Rotterdam Study
Summary
DOI 10.1111/bjd.15908
What’s already known about this topic?
• Seborrhoeic dermatitis is a common chronic relapsing inflammatory skin disease
with unclear pathophysiological mechanisms.
• Numerous host and environmental factors have been implicated in the pathogenesis
of seborrhoeic dermatitis, but most have not been validated.
Seborrhoeic dermatitis is a common relapsing inflammatory severe form of erythema and scaling on the scalp, face and
skin disease, characterized by poorly demarcated erythematous chest. Cross-sectional and retrospective studies using medical
patches with greasy scaling.1 The diagnosis is mainly clinical records show a prevalence between 2% and 8%,3 but the
and the disease spectrum is heterogeneous, ranging from a prevalence in prospective studies was found to be as high as
mild form of scaling limited to the scalp (dandruff),2 to a 23% in selected populations.4,5 Despite the high frequency of
148 British Journal of Dermatology (2018) 178, pp148–153 © 2017 British Association of Dermatologists
Prevalence and determinants of seborrhoeic dermatitis, M.G.H. Sanders et al. 149
seborrhoeic dermatitis in the population and the impaired alcohol misuse and smoking. Xerosis cutis was chosen as a
quality of life associated with seborrhoeic dermatitis,6 studies proxy for barrier dysfunction.
investigating the aetiology of seborrhoeic dermatitis are scarce. Age, sex, weight, height, blood pressure, presence of xero-
Both host and environmental determinants have been sis cutis (no, extensor-side extremities or generalized) and
implicated in the pathogenesis of seborrhoeic dermatitis. It skin colour24 were registered at the FBSE. Body mass index
has been postulated that overgrowth of commensal Malasse- (BMI) < 25 kg m 2 was defined as normal weight, 25–30 as
zia species, in a predisposed host (e.g. those with a overweight and > 30 as obese.25 Diastolic blood pressure of
decreased barrier function), is causal in the development of > 90 mmHg or systolic blood pressure of > 140 mmHg was
seborrhoeic dermatitis.7 Several other determinants have been defined as hypertension.26 The date of FBSE was used to deter-
studied as well, including older age,3,8,9 male sex,3,8–11 obe- mine the season. Other determinants were assessed at a home
sity,4,12 skin colour,4 stress,13–15 depression,13,16 winter cli- interview, including: education level (low: primary education;
mate,17,18 alcohol consumption,12,19 tobacco exposure, medium: lower-intermediate vocational education; high: gen-
hypertension,12 HIV20 and Parkinson disease.21,22 However, eral secondary education and higher), alcohol (glasses/week),
some of these studies were small (less than 100 partici- tobacco consumption (never and former vs. current), depres-
pants), or conducted in a selected population (e.g. dermatol- sion and anxiety. The home interviews were conducted before
ogy outpatients). Knowledge about determinants could the FBSE. The time between the home interview and the FBSE
provide new insights into the pathophysiology of seborrhoeic was less than 6 months for more than 95% of the participants.
dermatitis, which might lead to preventative strategies and/ To assess depression, the Center for Epidemiologic Studies
or new treatment regimens. Depression Scale was used and a score of ≥ 22 was taken as the
The aim of this study was to investigate the reported deter- cut-off point for depression.27 Anxiety disorders were used as a
minants of seborrhoeic dermatitis in a population-based study proxy of stress and were assessed by a slightly adapted version
of middle-aged and elderly people in the Netherlands (Rotter- of the Munich Composite International Diagnostic Interview.28
dam Study), in which people were diagnosed with sebor- Participants without any anxiety disorder were compared with
rhoeic dermatitis by a physician during skin examination. participants with one or more anxiety disorders.
A literature search for potential determinants of seborrhoeic Subgroup analysis was done to test whether previously
dermatitis was carried out using PubMed, Embase, Web of reported sex differences in seborrhoeic dermatitis were the
Science and Google Scholar and it was limited to observational result of hormonal differences. Hormone levels were available
studies on humans, published in English and updated until for a previous Rotterdam Study visit. On average, hormones
January 2016. The following determinants of seborrhoeic der- were measured 75 years before the FBSE. We tested the asso-
matitis were identified: elderly age, male sex, obesity, white ciation between seborrhoeic dermatitis and total testosterone
skin colour, stress, depression, hypertension, HIV infection, in men, using a logistic regression adjusting for age, skin col-
Parkinson disease, winter climate, high educational level, our, xerosis cutis and season. We used the same model in
© 2017 British Association of Dermatologists British Journal of Dermatology (2018) 178, pp148–153
150 Prevalence and determinants of seborrhoeic dermatitis, M.G.H. Sanders et al.
women, but replaced total testosterone with the Free Andro- Table 1 Characteristics of participants with and without seborrhoeic
gen Index (FAI). Also, we determined the P-value of the inter- dermatitis
action terms between sex and the other determinants in the
full model. Seborrhoeic No seborrhoeic
Coding dermatitis dermatitis P-valuea
Participants 788 (143) 4710 (857)
Results Sex
Male 466 (591) 1922 (408) < 0001
A total of 5498 participants from the Rotterdam Study under-
Age (years), 701 (631–774) 677 (617–763) 0027
went a FBSE (Table 1). The median age of participants at the
median (IQR)
date of the FBSE was 679 years [interquartile range (IQR) Body mass index (kg m 2)
619–764] and the proportion of women was 57%. Of the < 25 215 (273) 1418 (301) 0241
5498 participants, 788 participants were diagnosed with seb- 25–30 383 (486) 2165 (460)
orrhoeic dermatitis (point prevalence of 143%). The percent- > 30 189 (240) 1115 (237)
age of missing data per variable was low (< 5%), except for Missing 1 (01) 12 (03)
Skin colour
alcohol use (173%; Table 1).
Very white– 694 (881) 3858 (819) < 0001
In the univariable logistic regression we found significant
white
associations between an increased prevalence of seborrhoeic White–olive 81 (103) 650 (138)
dermatitis and age, male sex, a high education level, general- Light brown– 13 (16) 202 (43)
ized xerosis cutis and alcohol consumption, whereas darker black
skin colour and summer season were associated with a Education
decreased prevalence (Table 2). In the multivariable model, Low 74 (94) 477 (101) 0038
Average 454 (576) 2884 (612)
male sex (adjusted OR 209, 95% CI 177–247), a darker
High 250 (317) 1286 (273)
skin colour (white–olive and brown skin vs. white skin:
Missing 10 (13) 63 (13)
adjusted OR 039, 95% CI 022–069), season (summer vs. Depression
winter: adjusted OR 063, 95% CI 048–082) and generalized CESD ≥ 22 31 (39) 199 (42) 0687
xerosis cutis (adjusted OR 141, 95% CI 111–180) remained Missing 7 (09) 52 (11)
significant predictors for seborrhoeic dermatitis (Table 2). All Anxiety disorder(s)
significant variables remained significant in the model without Yes 43 (55) 234 (50) 0623
Missing 27 (34) 227 (48)
imputed data and the effect sizes were comparable (data not
Xerosis cutis
shown).
No 271 (344) 1815 (385) 0017
In the logistic regression analyses between seborrhoeic der- Extensor-side 390 (495) 2293 (487)
matitis and total testosterone in men (adjusted OR 100, 95% extremities
CI 098–102) and seborrhoeic dermatitis and the FAI in Generalized 121 (154) 557 (118)
women (adjusted OR 101, 95% CI 092–110) no significant Other 6 (08) 43 (09)
associations were found. Also, none of the interaction terms Missing 0 2 (004)
Hypertension
between sex and the other determinants were found to be sig-
Yes 418 (536) 2413 (512) 0329
nificant (data not shown).
Missing 8 (10) 43 (09)
Table 3 presents an overview of the determinants for sebor- Season
rhoeic dermatitis from previously published papers in compar- Winter 224 (284) 1091 (232) 0001
ison with the data in the current study. We replicated Spring 172 (218) 1056 (224)
previous associations between seborrhoeic dermatitis and sex, Summer 92 (117) 756 (161)
skin colour and season; however, we did not replicate several Autumn 300 (381) 1807 (384)
Smoking
other associations such as obesity, depression, hypertension,
Current 115 (146) 682 (145) 0937
alcohol consumption and tobacco use.
Missing 1 (01) 8 (02)
Alcohol (glasses/week)
Median (IQR) 58 (08–146) 44 (06–118) 0004
Discussion
Missing 119 (151) 831 (176)
In this middle-aged and elderly population, the point preva-
Data are n (%) unless otherwise specified. IQR, interquartile
lence of seborrhoeic dermatitis was 143%, which is higher
range; CESD, Center for Epidemiologic Studies Depression Scale.
than the 2–8% in previous studies.1,3,30 This difference may v -test for categorical and t-test for continuous variables.
a 2
British Journal of Dermatology (2018) 178, pp148–153 © 2017 British Association of Dermatologists
Prevalence and determinants of seborrhoeic dermatitis, M.G.H. Sanders et al. 151
Table 2 Associations between seborrhoeic dermatitis and reported men and seborrhoeic dermatitis and the FAI in women sug-
determinants gested no direct association between previously measured
hormone levels and presence of seborrhoeic dermatitis among
Crude odds Adjusted odds the participants of the Rotterdam Study.33 As the hormone
Variable, coding ratio (95% CI) ratio (95% CI)
measurements were taken several years before the FBSE, repli-
Sex, male 210 (18–245)** 209 (177–247)** cation of our findings with more recent data is recom-
Age at FBSE (years), 101 (100–102)* 101 (099–102) mended. Sex differences could also be explained in part by
continuous
cutaneous differences in pH and/or use of skin products,
BMI (kg m 2)
which might influence microbial colonization and barrier
< 25 Reference Reference
25–30 117 (097–140) 105 (087–127) integrity.34,35 Unfortunately, these variables were not avail-
> 30 112 (091–138) 112 (090–139) able in the Rotterdam Study and therefore were not investi-
Skin colour gated. Other studies will be needed to assess the behavioural
Very white–white Reference Reference or biological differences underlying the statistical associations
White–olive 069 (054–088)* 070 (053–086)* between sex and seborrhoeic dermatitis.
Light brown–black 036 (020–063)** 039 (022–069)*
In line with previous studies, the prevalence of seborrhoeic
Education
dermatitis was lowest during summer, which could be
Low 098 (076–128) 099 (075–129)
Average Reference Reference explained by increased ultraviolet (UV) radiation exposure.
High 123 (104–145)* 114 (085–153) UV-induced cutaneous immunosuppressive effects might
Depression, 103 (064–165) 106 (070–159) reduce the inflammatory response to environmental stimuli
CESD ≥ 22 and UV radiation has a direct effect on the microbiome,
Anxiety 124 (083–184) 133 (093–189) including on Malassezia yeast of the skin.36,37 The decreased
disorder(s), yes
risk of seborrhoeic dermatitis in people with coloured skin is
Xerosis cutis
again consistent with a previous study.4 Although this may be
No Reference Reference
Extensor-side 114 (097–134) 114 (096–135) because of a diagnostic bias in dark-skinned individuals,
extremities because erythema is less striking, it might also be the result of
Generalized 146 (117–181)* 141 (111–180)* a superior barrier function in more pigmented skin.38
Other 094 (060–146) 079 (033–189) Several studies underline the importance of skin-barrier
Hypertension, yes 097 (082–116) 099 (085–116) function in the pathogenesis of seborrhoeic dermatitis.2,7,32 In
Season
this study, xerosis cutis was taken as a proxy for skin-barrier
Winter Reference Reference
dysfunction and an association between generalized xerosis
Spring 079 (064–098)* 084 (067–105)
Summer 059 (046–077)** 063 (048–082)** cutis and seborrhoeic dermatitis was observed. Although we
Autumn 081 (067–098)* 081 (067–098)* cannot rule out overdiagnosis of seborrhoeic dermatitis
Smoker, 101 (081–125) 098 (078–122) because of excessive squamae that may accompany xerosis
yes (current) cutis of the scalp and face, the association implies that partici-
Alcohol 101 (101–102)** 101 (099–101) pants with seborrhoeic dermatitis more often have a skin-bar-
(glasses/week),
rier dysfunction and that this is not limited to the areas
continuous
affected by seborrhoeic dermatitis. Therefore, interventions
CI, confidence interval; FBSE, full-body skin examination; CESD, aiming to improve skin-barrier function may become a target
Center for Epidemiologic Studies Depression Scale. *P < 005, in the treatment of patients with seborrhoeic dermatitis.
**P < 0001. In contrast to previous studies,12,19 we did not find associa-
tions for other determinants, including smoking, alcohol and
education (Table 3). None of these previous studies adjusted
higher vulnerability to external stimuli in this age group.31,32 for the important seborrhoeic dermatitis predictors such as
In contrast to other studies, age was not significant in the sex, age or skin colour, leading to residual confounding and
multivariable analysis, most likely because of the advanced age spurious associations, especially because differences in smok-
of the entire study population. ing and alcohol consumption between men and women are
Of the reported determinants of seborrhoeic dermatitis, well known.39 In addition, the definition of determinants
sex, skin colour and season were seen in the Rotterdam between studies differed and might explain the lack of replica-
Study, whereas obesity, depression, hypertension, alcohol tion of other determinants such as obesity, stress and depres-
consumption and tobacco use were not (Table 3). We found sion. A large study with 9255 seborrhoeic dermatitis cases and
that men were twice as likely to develop seborrhoeic der- 9246 controls suggested that seborrhoeic dermatitis and
matitis than women. Hormonal differences between men and hypertension were associated (adjusted OR 123, 95% CI
women may explain this association, as seborrhoeic dermati- 112–135), but we did not replicate this finding.12
tis has an incidence peak during puberty, where the levels of We did not investigate the association between seborrhoeic
androgens in men are high.1,30 However, logistic regression dermatitis and Parkinson disease and HIV, because the data
analyses on seborrhoeic dermatitis and total testosterone in were incomplete and/or not available. Another limitation lies
© 2017 British Association of Dermatologists British Journal of Dermatology (2018) 178, pp148–153
152 Prevalence and determinants of seborrhoeic dermatitis, M.G.H. Sanders et al.
Table 3 A summary of reported and tested risk factors for seborrhoeic dermatitis
Previous studies
Rotterdam Study
Determinants References Summary Measurements Summary (Table 2)
3, 8–11
Male sex Higher prevalence for males in adult Ratio, male: female Seborrhoeic dermatitis
population 14 : 1 has a strong association
with male sex
3, 8, 9
Age Peak between 30 and 50, which Prevalence graphs No association. Relatively
mostly persists in old age high prevalence in this
elderly cohort
4, 12
Obesity Increased triceps skinfold in male Adjusted PR 156, 95% No association
adolescents CI 112–218
Higher percentage of obesity in adult 163% vs. 153%,
population P = 0014
4
Skin colour Higher prevalence in white skinned Adjusted PR (white skin) Decreased risk in white–
male adolescents 142, 95% CI 106–192 olive and brown skin vs.
white skin
Education 4, 12
No significant effect of socio- – No association
economic status in two studies
Higher prevalence with high socio- 254% vs. 191%,
economic status in one study P = 0001
12
Hypertension One study found an association Adjusted OR 123, 95% No association
between hypertension and CI 112–135
seborrhoeic dermatitis
Depression 13, 16
Increased prevalence in depressive 36% vs. 9%, P < 001 No association
patients, not adjusted
Stress 13–15
Self-reported triggering factor – No association
More stressful life events in Mean SD: 547 392
seborrhoeic dermatitis patients vs. 327 296,
P < 005
Higher perceived stress scale Adjusted OR 1065 95%
CI 1021–1110,
P = 0003
17, 18
Season Self-reported seasonal influences: 52% reported seasonal Lowest risk for
higher disease severity in winter influences: more skin seborrhoeic dermatitis
and lowest in summer problems in winter in summer
(50%), fewer in
summer (77%)
Visits for the diagnosis of Spring 42%, summer 7%,
seborrhoeic dermatitis to the autumn 25%, winter
outpatient clinic 25%
4, 12
Smoking One study showed no effect of Adjusted PR (smoking) No association
smoking 106, 95% CI 075–
Another study showed a slightly 150, P = 07
lower incidence of smokers in the 162% vs. 196%,
seborrhoeic dermatitis group, not P = 0001
adjusted
12, 19
Alcohol No study with a control group Alcohol misuse 03% No association
shows an association (seborrhoeic dermatitis)
vs. 05% (control),
P = 013
in the cross-sectional design of the analysis as this means it is epidemiological determinants that allowed us to control for
not possible to make causal inferences between seborrhoeic potential confounders.
dermatitis and determinants. Further, this study covers a mid- In conclusion, one out of seven people had seborrhoeic der-
dle-aged and elderly population, which limits the generaliz- matitis, and men and those with generalized xerosis cutis were
ability to younger patients. The strength of our study is the even more likely to have seborrhoeic dermatitis. Participants
population-based setting, the large sample size, the physician- with a darker complexion and those assessed during the sum-
based diagnosis and the availability of different mer period were less likely to have the condition. The
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