PIIS0022202X1536098X
PIIS0022202X1536098X
PIIS0022202X1536098X
ORIGINAL ARTICLE
INTRODUCTION
Psoriasis is a chronic, immune-mediated inflammatory skin
disease. It ranges in severity from a few scattered red, scaly
plaques to involvement of almost the entire body surface. It may
progressively worsen with age, or wax and wane in its severity;
the degree of severity depends on inheritance and environmental
factors (Lebwohl, 2003). Psoriasis causes considerable psychosocial disability and has a major impact on patients quality of life
(Rapp et al., 1999). The cost to both patients and health-care
systems is high (Javitz et al., 2002). Psoriasis is associated with
cardiovascular disease, depressive illness, and psoriatic arthritis
(Griffiths and Barker, 2007). The causes of psoriasis are not fully
understood, but a number of risk factors are recognized, including
family history and environmental risk factors, such as smoking,
stress, obesity, and alcohol consumption (Huerta et al., 2007).
Psoriasis is estimated to affect about 24% of the population
in western countries (Stern et al., 2004; Gelfand et al., 2005b;
1
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Global Epidemiology of Psoriasis
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Global Epidemiology of Psoriasis
Table 1. List of studies providing incidence rates in children, adults, and all ages
Study
Country
Time
Diagnostic
method
Age
19701999
N/D
o18
People
with Ps
Incidence rate
per 100,000
person-years
(95% CI) female
Incidence rate
per 100,000
person-years
(95% CI) male
40.8 (36.645.1)1,2
43.9 (37.650.2)1,2
37.9 (32.243.6)1,2
73.2 (68.078.4)1,3
85.5 (79.591.6)1,3
Children
Tollefson et al.
(2010)
USA
357
19701974
29.6 (20.938.3)
19751979
35.7 (25.945.5)
19801984
31.4 (22.040.8)
19851989
42.7 (31.853.7)
19901994
40.0 (29.750.3)
19951999
62.7 (50.465.0)
Adult
Icen et al. (2009);
Shbeeb et al. (1995)
USA
19702000
D/Ph
X18
1,633
78.9 (75.082.9)1,3
19701974
50.8 (41.959.6)
19751979
53.2 (44.861.6)
19801984
80.9 (70.891.1)
19851989
78.9 (69.588.4)
19901994
88.7 (79.198.3)
19951999
100.5 (90.8110.2)
USA
19912005
SR
2542
Italy
20012005
Ph
X18
82 (7789)1
892
5,792
2001
3211
2911
3571
2005
2301
2071
2541
63.6 (48.978.3)1,2
58.4 (42.874.1)1,2
All ages
o2070
132
59.9 (49.570.3)1,2
Ph
065
106
130 (120140)1,2
1995
Ph
065
24
120 (70190)1,2
19961997
Ph
080
3,994
USA
19801983
D/Ph
The
Netherlands
19871988
The
Netherlands
UK
1401
Abbreviations: CI, confidence interval; Ps, psoriasis; diagnostic methods: D, dermatologist; N, nurse; Ph, physician; SR, self-reported diagnosis.
1
Value reported from the study.
2
Age and/or sex adjusted.
3
Rate adjusted with linear interpolation between census years.
379
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Global Epidemiology of Psoriasis
Europe
Asia
Europe
Taiwan
Taiwan
0
Denmark
Norway
Norway
Croatia
ltaly
France
Uk
Uk
Uk
Australia
Australia
Australia
America
USA
USA
USA
USA
USA
4
6
8
Prevalence %
10
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Global Epidemiology of Psoriasis
Europe
North America
Latin America
Denmark
Sweden
Norway
Norway
Norway
Yugoslavia
Scotland
UK
UK
UK
UK
Spain
ltaly
Germany
Germany
Russia
USA
USA
USA
Tanzania
Egypt
Sri Lanka
China
China
Taiwan
Africa
Asia
0.5
1
1.5
2
Prevalence %
2.5
Figure 3. Studies providing information on the prevalence of psoriasis in all ages. Circle, period prevalence; diamond, not specified; square, lifetime prevalence;
triangle, point prevalence.
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Global Epidemiology of Psoriasis
Children
Tollefson et al. (2010)
357
USA
03
47
13.5 42.2
52.2
53.1
44
49.6
61.9
54.6
44.7
Adults
Icen et al. (2009)
1,633
USA
77.4
81.1
71.3
88.0
94.2
73.8
51.4
75.6
69.2
69
90.7
76.2
71.2
39.8
79.4
93.3
73.6
85.2
115.3
77.9
80
70
All ages
Bell et al. (1991)
USA
o20
132
T
30.9
49.1
71.7
51.4
94.6
112.6
47.1
41.3
61.2
58.6
109.1
126.5
54.9
14.8
59.5
82.9
43.8
78.3
93.8
130.6
3,994
UK
019
77.4
116
134
155
116
167
164
163
100
121
155
131
105
172
144
118
82
110
111
174
128
161
186
224
173
population (e.g., employed), but underrepresented other subgroups (e.g., unemployed, retired, and disabled people).
Although there were a number of studies on the prevalence
of psoriasis, research on incidence was limited. Incidence
appeared to be higher in Europe than in the United States and
increased with age. Studies reporting age-specific incidence
rates showed a dual peak of psoriasis around 3039 years of
age and a second peak around 5059 or 6069 years of age
(Bell et al., 1991; Huerta et al., 2007; Icen et al., 2009). It is
believed that the bimodal distribution of psoriasis incidence
represents two clinical presentations of the disease, type I
(early-onset) and type II (late-onset), which are defined as
presenting at p40 and 440 years of age, respectively
(Henseler and Christophers, 1985). Furthermore, on combining the results of the two studies using the Rochester
Epidemiology Project database, it appeared that the incidence
of psoriasis was higher in females o18 years old, but was
higher in males X18 years old (Icen et al., 2009; Tollefson
et al., 2010). The same studies reported an increasing
incidence in children and adults over a 30-year period (Icen
et al., 2009; Tollefson et al., 2010). However, it was unclear
whether this represented a real increase, probably because
of a concomitant increase in risk factors (obesity, stress,
psychological conditions) for psoriasis, or improved
diagnostic methods, better collection of data, and more
R Parisi et al.
Global Epidemiology of Psoriasis
Data extraction
In the first stage, all study titles and abstracts obtained from the
database searches were reviewed for eligibility by one of the authors
(RP); papers successfully passing through into the second stage were
appraised and those meeting the inclusion criteria were selected for
data extraction. The references of all included studies and review
articles identified were also screened to identify any additional
eligible studies.
Data analysis
Measures of prevalence and/or incidence presented are those
reported in the individual studies; however, rates are presented as
percentage values for prevalence and rate/100,000 person-years for
incidence. Values were checked for potential errors (when possible)
on the basis of the number of cases of psoriasis and population
sample size. Missing information, such as prevalence and/or incidence rate and CIs were calculated when not reported in the study.
However, it was not possible to estimate CIs for some studies because
of lack of sufficient information. In addition, negative lower bounds of
CIs were replaced by zero.
Results were analyzed by country and age category (children, adult,
or all ages). Children were defined as being in the age group o18
years old. Within each country and category, study design (case
definition (self-reported vs dermatologist vs general practitioner diagnosis) and type of prevalence (point vs period vs lifetime prevalence))
were explored for possible differences. When multiple studies collected data from the same data set and time period, only the most
recent or the most complete articles were reported. When the same
study presented measures of prevalence and/or incidence of psoriasis
from different databases or populations, all results were reported.
CONFLICT OF INTEREST
The authors state no conflict of interest.
ACKNOWLEDGMENTS
This paper presents independent research funded by the National Institute for
Health Research (NIHR) under its Programme Grants for Applied Research
Programme (grant reference number RP-PG-0608-10163). The views expressed
are those of the author(s) and not necessarily those of the NHS, the NIHR, or
the Department of Health. We are grateful to Dr Elena Bichenkova, Dr
Suzanne Verstappen, and Dr Yu-Mei Chang for translation of articles in
Russian, Dutch, and Chinese, respectively.
SUPPLEMENTARY MATERIAL
Supplementary material is linked to the online version of the paper at http://
www.nature.com/jid
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