Introduction
Psoriatic arthritis is an inflammatory disorder
of unknown aetiology that may affect peripheral and axial joints, correlated
with psoriasis.(1) It includes various designs of arthritis
and enthesitis in psoriatic patients or with a family history of psoriasis. It
is a progressive disease ranging from mild synovitis to intense progressive
erosive arthropathy. Psoriatic arthritis patients with oligoarthritis may
progress to polyarthritis and most of them experience articular involvement and
disfigurations which develop over time.
The clinical range of psoriatic arthritis has been nowadays widened
by recently introduced items such as: pustulosis palmoplantaris with
osteoarthritis sterno-clavicularis, psoriatic onycho-pachydermoperiostitis,
enthesopathy and osteo-periostitis. The clinical models of psoriatic arthritis
are different in different sites worldwide. The variable diversity of the
clinical designs of psoriatic arthritis may cause evolving and disfiguring
features if not identified and dealt with promptly.
Psoriatic arthritis occurs in 7-42% of psoriatic
patients. Psoriatic arthritis is an
inflammatory arthritis of joints and connective tissue and is correlated with
psoriasis of the skin or nails.(2) This is a reaction to
group A streptococci with an autoimmune reaction in psoriatic skin plaques.(3)
This disease is autoimmune-mediated with HLA correlation (HLA-B27,-B17,-CW6,-DR4
and -DR7).(4) Various subtypes of stimulated lymphocytes
migrate to skin or joint causing disease flaring at various times. Patients
with psoriasis can have one or more various types of arthritis with no
serological marker. Stimulated CD4 T lymphocytes are the lesion triggering,
producing cytokines (interleukin 1, TNF-beta and interferon).(5) Often, it can occur without skin lesions,
or with insignificant rash. The inflammatory disease may affect the synovium
and intra-articular ligaments, fascia and tendons.
The objective of our study was to determine
different clinical patterns of psoriatic arthritis in Jordanian patients
presenting to our rheumatology clinic at King Hussein medical center. Psoriatic
arthritis in Jordan is under diagnosed or misdiagnosed with osteoarthritis or
rheumatoid arthritis. To increase doctors and patients awareness, the clinical
models of psoriatic arthritis must be identified in a certain geographical
population.
Methods
Fifty patients with psoriatic arthritis and aged
18-75 years were studied. All patients were referred to the Rheumatology clinic
at King Hussein medical center and all patients with psoriatic arthritis were
diagnosed according to CASPAR (CAS stands for classification, P stands for
psoriatic and AR stands for arthritis) and referred to the Rheumatology clinic
at King Hussein medical center. Subjects with psoriatic arthritis were followed
up in terms of classification of psoriatic arthritis criteria (CASPAR) during
six years time period from August 2008 to August 2013 at our rheumatology
clinic at King Hussein medical center, Amman, Jordan. All patients signed an informed
consent. Exclusion criteria included patients with rheumatoid arthritis or
osteoarthritis .Inclusion criteria included patients with negative rheumatoid
factor. Demographics and psoriatic
arthritis frameworks were registered.
Clinical data was collected by a rheumatologist of
each patient in clinic according to standard protocol which includes age,
gender, and age of onset of psoriasis, age of onset of arthritis, types of
arthritis, types of psoriasis, Rheumatoid factor and family history. Patients
with an established diagnosis of psoriatic arthritis in earlier visits had a
registration of their articular condition, while patients with a newly
diagnosis of psoriatic arthritis had an examination of affected joints for the
presence of at least one item of articular symptoms for more than 6weeks of
tender joints, treatment for arthritis and earlier diagnosis of arthritis.
CASPAR classification criteria(6) included a confirmed
inflammatory joint, spine or enthesis disease with a score of 3 of: recent
psoriasis and family history of psoriasis (score of 2) but others (score of 1);
dactylitis; juxta-articular new bone formation; rheumatoid factor seronegative and specific nail changes. The
number of tender and swollen joints and the model of clinical arthritis were
registered as:oligoarthritis (<4 joints), polyarthritis (>5 joints), spondylitis
(inflammatory back pain +/-peripheral articular symptoms with at least one of: spine
tenderness, radiological sacroiliitis or spinal
syndesmophytes),enthesitis(spontaneous pain and tenderness at enthesis) and
dactylitis (spontaneous swelling +/- redness of fingers +/-toes beyond the
articular line with tenderness). Full
assessment included erythrocyte sedimentation rate, rheumatoid factor and
C-reactive protein in addition to radiography for diseased joints.
Results
Eight patients (8/50=16%) were diagnosed
previously as confirmed psoriatic arthritis while 42 patients (42/50=84%) were
recently diagnosed. The male to female ratio was 1:1(25:25).The mean age of
onset of psoriasis. was 29.88+/-10.12 (range 21.4-36.3) years and the mean
duration of psoriasis was 8.67+/-8.99 years. The mean age of onset of psoriatic
arthritis was 35.34+/-10.22(range 27.6-43.7) years and the mean duration of
psoriatic arthritis was 1.29+/-0.5(range 0.8-1.7) years. The mean age of
patients was 46.5+/-26 years. Psoriatic
arthritis occurred between 30 and 45 years of age in 60% of patients with
psoriatic arthritis.
Family history of psoriasis was found in 60% of
patients and family history of psoriatic arthritis was found in 8% of
patients).Table I.
The most frequent significant pattern was
polyarticular arthritis (20/50=40%) (P<0.05), then in decreasing order comes
oligoarticular arthritis (10/50=20%), ankylosing spondylitis (9/50=18%),
enthesitis and dactylitis (6/50=12%) {enthesitis was found in 4
patients(4/50=8%) with Achiles tendinitis
affected frequently in 40% of patients} {dactylitis (1/50=2%), Table II.
Extra-articular involvement was shown in Table
III. Nails were affected by psoriasis in 30% of patients with psoriatic
arthritis. The most frequent nail feature is pitting in 60% of patients. Psoriatic
skin rash preceded arthritis in 80% of patients with psoriatic arthritis with a
mean interval of 8.4years. Arthritis preceded psoriatic skin rash in 20% of
patients with psoriatic arthritis with a mean interval of 3.1 years. Chronic
plaque psoriasis was the most frequent skin lesion found in 90% of psoriatic
arthritis patients. Aortic aneurysm was found in one patient with arthritis (2%).
The mean number of swollen joints was 2.4+/-2.3
and the mean number of tender joints was 6.5+/-4.8. All patients with articular swelling
experienced pain with tenderness. The most frequently affected joint was knee
in 70% of patients.
In our patients with psoriatic arthritis, the
erythrocyte sedimentation rate was increased in 90% of patients while
C-reactive protein was increased in 70% of patients. Rheumatoid factor was negative
in all patients. Abnormal radiological features were found in 30% of patients
with bony erosions as the most frequent finding in 20% of patients.
Discussion
Psoriasis is a chronic inflammatory disease. It
includes different co-morbidities which are induced by psoriatic arthritis and
by chronic inflammation of psoriasis as metabolic syndrome and cardiovascular
disease.(7) Psoriatic arthritis differs in various studies
because of patient’s geographical, ethnical and demographical variability and because
of diagnostic framework of psoriatic arthritis.(8) Yang
Q and Radtke MA agreed that patients with psoriatic arthritis experience more
intense psoriasis,(9,10) while Gladman DD and Elkayam O, showed
that there is no direct correlation between intensity of psoriasis and
articular symptoms.(11,12)
The study revealed that the mean age of onset
for psoriatic arthritis was 35.34years which was comparable to that of
rheumatoid arthritis.(4) Rajendran CP, et al, showed a
69% high frequency of psoriatic arthritis during the 4th and 5th
decades of life.(13) Yang Q, et al, demonstrated that
the mean age of onset of psoriatic arthritis was 39.2years (4th
decade) in China.(9) Other
studies showed that psoriatic arthritis affects males and females in equal
proportions.(14,15) Others
showed a higher female preponderance, while Kumar R, et al, showed a
higher male preponderance(16) comparable with other authors(2,17,18)
because of the higher percentage of male patients addressing the clinic.
In our study, psoriatic arthritis was not
observed in patients with long standing psoriasis (i.e.>8 years) on immunosuppressant’s.
Psoriasis skin rash preceded psoriatic arthritis in 80%of patients and in 20%
of patients, the psoriatic arthritis preceded skin rash. This pattern was
comparable to others.(9) Onset of articular pain after onset
of skin rash was found in 50.8%, preceded in 12.1% and in the same time in 37%
of patients.(13)
In our investigation, 30% of patients with
psoriatic arthritis had nail changes although Prasad PV and Reich K,demonstrated
that nail changes percentage was between 65% and 97%.(2,3) Although there was no relation between nail
changes and intensity of psoriatic arthritis,nevertheless nail changes in a
patient with psoriasis must guide the physician to search for articular
involvement. McGonagle D reported a significant anatomical relation between
psoriatic arthritis and nail inflammation.(5) Enthesitis is found in distal
interphalangeal disease in patients with psoriatic arthritis. Jajic Z ,found
that wrists and small joints of the hands and feet are most frequently affected.(17) The same previous authors showed that
chronic plaque skin lesion was the most frequent feature in patients with
psoriatic arthritis with an incidence of 72%-92%.(2,9,10,14)
We found that polyarthritis was the most
frequent pattern of psoriatic arthritis (40%) with an average of psoriatic
arthritis duration of 8.99 years. Other
authors found similar results such as 48.3%(13) and 58.3%.(3)
This was not the case in Yang Q and Prasad PV studies who showed that
oligoarthritis was the most frequent model in 42-67% of patients, while
Jamshidi F reported polyarticular arthritis in 48.3% as the prevalent type.(2,9,19)
Although spondylitis is not frequent worldwide
and occurs with peripheral arthritis, Baek HJ , found that it was the most
common model accounting for 50% of
patients(20) and Kumar R,found its percentage of 49%.(16) This increased frequency of spondylitis
is attributed to genetic predisposition. Oligoarthritis is predominant with
shorter disease duration while Jajic Z, reported that polyarthritis is
prevalent with longer disease duration.(17) Oligoarthritis
may progress to polyarthritis in 63% of patients with psoriatic arthritis over
12.2 years. Wide variability in clinical models is attributed to genetics,
epidemiology and population.
Important findings of psoriatic arthritis are
dactylitis and enthesitis with a frequency of 16-40% in the first and 40-45% in
the second.(20) Eight
percent of patients had enthesitis which is almost comparable to other
studies. It is equal to others (7.8%)
and lower than others (26.8%).(9,10,13,20) It is caused by trauma, bare foot walking
and genetics. We found dactylitis in a frequency of 6%, which was comparable to
others(9,20) and lower than others.(10)
In early psoriatic arthritis, radiological
examination is not helpful. All our group of patients had negative
rheumatoid factor, though it is mentioned in some studies that 3%of patients
might have positive rheumatoid factor. Al-Heresh AM, et al(21)
addressed the possibility that certain polymorphisms within the IL10 gene could
influence the development of PsA. Although they found no significant
correlation with any of the three IL10 polymorphisms studied, there was an
increase in the incidence of homozygosity for an IL10 haplotype (-1082A / -819C
/ -592C) independently of any correlation with either HLA-Cw*0602 or TNFA-238A.
We believe that our investigation has some limitations. First, it is
descriptive analysis and second, it includes small group of patients. In
future, we aim to compare our data with data in other Arab countries. Among patients with psoriasis, 6-42% from
Europe, USA and South Africa were found to experience PsA. PsA was recorded in 9% of the patients with
psoriasis in Iran, Korea and India; 5% in China; 2% in Turkey and 1% in Japan. Various
ethnicities may influence the development of PsA.(22) Unfortunately,
we did not find in the literature any data regarding its frequency in Arab
countries to make comparison with ours.
Conclusion
Polyarticular arthritis was
the commonest clinical pattern in our Jordanian patients. Psoriatic arthritis
might affect a patient with chronic plaque skin lesions of hands preceding the
arthritis.
References
1.Amer
E, Arshi I, Nadia I. Patterns of psoriatic arthritis. Journal of
the College of Physicians and Surgeons Pakistan 2009; 19(9): 553-556.
2. Prasad
PV, Bikku B, Kaviarasan PK, et al. A clinical study of psoriatic
arthropathy. Indian J Dermatol
Venereol Leprol 2007; 73: 166-170.
3.Reich
K, Kruger K, Mossner R, et al. Epidemiology and clinical pattern of
psoriatic arthritis in Germany: A prospective interdisciplinary epidemiological
study of 1511 patients with plaque-type psoriasis. Br J Dermatol 2009; 160:1040-1047.
4.Wilson
FC, Icen M, Crowsen CS, et al. Time trends in epidemiology and characteristics of
psoriatic arthritis over 3 decades:A population-based study. J Rheumatol
2009; 36: 361-367.
5.McGonagle
D, Tan Al, Benjamin M. The nail as a musculoskeletal
appendage-implications for an improved understanding of the link between
psoriasis and arthritis. Dermatology
2009; 218(2):97-102.
6.Taylor
W, Gladman D, Helliwell P, et al. CASPAR
study group. Classification criteria for psoriatic arthritis:Development of new
criteria from a large international study. Arthritis Rheum 2006 Aug; 54(8):
2665-2673.
7.Christophers
E. Comorbidities
in psoriasis. J Eur Acad Dermatol Venereol 2006; 20(supplement S2):
52-55.
8.Helliwell
PS, Taylor WJ. Classification and diagnostic criteria for
psoriatic arthritis. Ann Rheum Dis 2005; 64:3-8.
9. Yang
Q, Qu L, Tian H, et al. Prevalence and characteristics of psoriatic
arthritis in Chinese patients with psoriasis.
J Eur Acad Dermatol Venereol 2011; 25:1409-1414.
10. Radtke MA, Reich K, Blome
C, et al. Prevalence
and clinical features of psoriatic arthritis and joint complaints in 2009
patients with psoriasis of a Germannational survey. J Eur Acad Dermatol
Venereol 2009; 23: 683-691.
11.Gladman DD. Psoriatic arthritis. Dermatol Ther 2004; 17:350-363.
12.Elkayam O, Ophir J, Yaron
M, et al. Psoriatic
arthritis: Interrelationships between skin and joint manifestations related to
onset, course and distribution. Clin Rheumatol 2000; 19: 301-305.
13.Rajendran CP, Ledge SG, Rani
KP, et al. Psoriatic arthritis. J Assoc Physicians
India 2003; 51:1065-1068.
14. Ruderman EM, Tambar S. Psoriatic arthritis: Prevalence, diagnosis
and review of therapy for the dermatologist. Dermatol Clin 2004; 22:477-486.
15.Aslanian FM, Lisboa FF, Iwamoto
A, et al. Clinical
and epidemiological evaluation of psoriasis:Clinical variants and articular
manifestations. J Eur Acad Dermatol Venereol 2005; 19: 141-142.
16. Kumar R, Sharma A, Dogra
S. Prevalence and clinical patterns of psoriatic
arthritis in Indian patients with psoriasis. Indian J Dermatol Venereol
Leprol 2014; 80: 15-23.
17. Jajic Z, el Assadi G. Prevalence of psoriatic arthritis in a
population of patients with psoriasis. Acta
Med Croatica 2003; 57: 323-326.
18.Nadkar MY, Kalgikar A, Samant
RS, et al. Clinical profile of psoriatic arthritis. J Indian Rheumat Assoc 2000; 8:40.
19. Jamshidi F, Bouzari N, Seirafi
H, et al. The
prevalence of psoriatic arthritis in psoriatic patients in Tehran, Iran. Arch
Iran Med 2008; 2:162-165.
20.Baek HJ, Yoo CD, Shin
KC, et al.
Spondylitis is the most common pattern of psoriatic arthritis in Korea. Rheumatol
Int 2000; 19: 89-94.
21. Al-Heresh AM, Proctor J,
Jones SM, et al.
Tumour necrosis factor – alpha polymorphism and the HLA-Cw*0602 allele in
psoriatic arthritis. Rheumatology
2002; 41: 525-530.
22.Tam LS, Leung YY, Edmund
KLi. Psoriatic arthritis in Asia. Rheumatology 2009; 48(12):1473-1477.