Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: The purpose of this study was to investigate the association between clinical and unltrasonographic features of psoriatic nail disease and to identify specific nail features associated with psoriatic arthritis (PsA).
Methods: Patients with PsA and Psoriasis without arthritis (PsC) were recruited from prospective cohorts in a single centre. Healthy volunteers were also recruited. Subjects with co-existing OA or history of nail trauma were excluded. A detailed nail assessment according to the modified Nail Psoriasis Severity Index (mNAPSI) for the presence of onhycolysis, nail pitting, nail plate crumbling, leukonychia, splinter hemorrhages, nail bed hyperkeratosis and red spots in the lunula was completed for each participant. All participants underwent an ultrasound evaluation of the nail apparatus at each finger with detailed recording of loss of definition of the ventral or dorsal plates, thickness of the nail bed or matrix and the presence of increased vascularity in the nail bed or matrix using a 10-MHz linear array transducer. Doppler signal was standardized with a pulse repetition frequency of 400 Hz, a gain of 20 dB and a low wall filter. Descriptive analyses and comparisons were conducted using Kruskal Wallis for continuous variables and Fisher’s exact test for categorical variables. Logistic regression analyses using GEE model was used to compare between the groups due to repeated observations for each patient.
Table 1- Demographic Characteristics (n=30) between Controls, PsC and PsA
Frequency (%) or Mean (sd) |
||||
Controls |
Controls (n=10) |
PsC (n=10) |
PsA (n=10) |
p-value |
Gender (Males) |
3 (30.0%) |
9 (90.0%) |
7 (77.8%) |
0.02 |
Age |
29.0 (4.4) |
46.0 (16.1) |
54.7 (12.6) |
0.0006 |
Age at diagnosis of Psoriasis |
– |
33.0 (21.9) |
33.4 (13.8) |
0.60 |
Duration of Psoriasis |
– |
13.0 (13.9) |
21.1 (11.7) |
0.10 |
mNAPSI score |
0 |
6.2 (5.8) |
3.8 (4.6) |
0.01 |
Nail Feature |
Controls |
PsC |
PsA |
p-value* |
p-value** |
Loss of definition of the ventral plate |
6/100 |
24/100 |
29/100 |
<0.0001 |
0.42 |
Hyperechoioc focal involvement of the ventral plate |
0/100 |
23/100 |
16/100 |
<0.0001 |
0.21 |
Thickening of both the and dorsal and ventral plates |
0/100 |
8/100 |
2/100 |
0.005 |
0.052 |
Nail bed thickness (mm) |
14.1 (1.2) |
16.0 (2.9) |
15.9 (3.0) |
<0.0001 |
0.81 |
Nail matrix thickness (mm) |
15.8 (0.92) |
17.5 (2.9) |
18.8 (3.0) |
<0.0001 |
0.002 |
Nail bed vascularity |
2/100 |
14/100 |
18/100 |
0.001 |
0.44 |
Nail matrix vascularity |
16/100 |
30/100 |
34/100 |
0.01 |
0.54 |
Onycholysis and oil drop dyschromia (Some vs. none) |
0/100 |
13/100 |
5/100 |
0.0005 |
0.048 |
Pitting Some vs. none |
0/100 |
28/100 |
20/100 |
<0.0001 |
0.19 |
Nail bed crumbling (Some vs. none) |
0/100 |
8/100 |
0/100 |
0.0003 |
0.004 |
Leukonychia |
0/100 |
3/100 |
2/100 |
0.24 |
0.65 |
Splinter hemorrhage |
0/100 |
0/100 |
0/100 |
NS |
NS |
Nail bed hyperkeratosis |
0/100 |
0/100 |
0/100 |
NS |
NS |
Red spots in the lunula |
0/100 |
0/100 |
1/100 |
0.37 |
0.32 |
P-value* is between the 3 groups, p-value** is between the PsC and PsA.
None of the nail’s sonographic or clinical covariates were found to statistically different in between PsA and PsC groups after adjusting for repeated measurements.
Conclusion: This proof of concept study shows that ultrasounds can be used as a tool for assessment of psoriatic nail disease. Patients with psoriatic disease had increased nail bed and matrix thickness as well as vascularity compared to healthy controls. However, whether these microanatomical nail structures could be predictors for evolution of psoriatic arthritis is yet to be determined.
Disclosure:
A. Haddad,
None;
A. Thavaneswaran,
None;
V. Chandran,
Abbott Canada,
5;
D. D. Gladman,
Abbott Canada,
5.
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