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. 2021 Jul 24;8(3):1443–1450. doi: 10.1007/s40744-021-00343-7

The “Climb” Towards Minimal Disease Activity in Psoriatic Arthritis

Ennio Lubrano 1,✉,#, Silvia Scriffignano 1,#, Fabio Massimo Perrotta 1
PMCID: PMC8380617  PMID: 34302631

Abstract

Introduction

Minimal disease activity (MDA) is a validated outcome measure in psoriatic arthritis (PsA) defining a low disease activity state with a cutoff of 5/7. The main aim of the study was to look at the MDA divided into in the seven cutoffs, analyzing the more frequently achieved domains. The relationship between MDA, PASS, PsAID, DAPSA, and the PhGA in all cutoffs was also evaluated.

Methods

Cross-sectional analysis on PsA patients satisfying CASPAR criteria. An assessment of disease activity, treatment target, function, and impact of disease was performed. Patients achieving MDA were compared to patients not achieving MDA in order to evaluate the most frequent domain found.

Results

Ninety-three PsA patients were enrolled. MDA was satisfied in 44/93, while in 47 MDA ranged from 1/7 to 4/7. Among the seven domains, Leeds Enthesitis Index (LEI) was the most frequent domain found in all patients. In those not in MDA, BSA ≤ 3 (70%) and swollen joints count ≤ 1 (68%) were also well represented. The domains with a lower percentage of patients not in MDA were HAQ-DI ≤ 0.5 (38.8%), tender joint count ≤ 1 (23%), PtGA ≤ 20 (4.2%) and VAS pain ≤ 15 mm (2%). There was a growing trend, from MDA 1/7 to MDA 7/7 in the percentage of patients in PASS yes, in PsAID ≤ 4, and in DAPSA ≤ 14.

Conclusions

The present study detailed the domains more achieved also in those patients not in MDA showing that “physician-driven” domains are more frequently achieved in our patients.

Keywords: Psoriatic arthritis, Minimal disease activity, Assessment, Outcome measures

Key Summary Points

PsA is an inflammatory chronic disease with different clinical manifestations.
Minimal disease activity (MDA) is an achievable treatment target for PsA patients. However, even when MDA is not achieved, the disease state could be very different when the cut-off of 4 out of 7 criteria is reached, compared to a cut-off of 1 out of 7.
Our study demonstrated that some domains are frequently achieved even in patients not in MDA. In particular, swollen joints, enthesitis (by LEI) and BSA≤ 3 are frequently achieved even in those not in MDA.
The study showed that “physician-driven” domains are more frequently achieved in all enrolled patients. Moreover, a strong correlation was found with other outcome measures throughout the seven domains.

Introduction

Psoriatic arthritis (PsA) is a chronic inflammatory disease characterized by a variable clinical course [1, 2]. In the last 10 years, the achievement of clinical remission or low disease activity have been proposed as treatment targets for PsA patients [3, 4]. In particular, minimal disease activity (MDA) is a categorical and validated measure in PsA as treatment response criteria to capture a disease state: patients are in MDA when they satisfy 5/7 of previously published criteria [4]. More recently, a stringent definition of remission (very low disease activity, VLDA), in which all 7/7 criteria had to be satisfied, has been proposed [5].

MDA has been useful to define the disease state in randomized controlled trials [6] and in real-world evidence studies [7, 8]. However, even when MDA is not achieved, the disease state could be very different when the cutoff of 4 out of 7 criteria is reached, comparing to a cutoff of 1 out of 7. This could be interesting to be assessed in real life because the achievement of a cutoff of 4/7 criteria has, probably, a different clinical meaning compared to the achievement of only 1/7 criteria.

As potential lack in this field is the assessment of which domains are more frequently achieved in those patients non reaching the MDA 5/7 onwards 7/7. In other words, what are the more frequently missed/achieved domains in patients that do not achieve MDA?

Therefore, the aim of this clinical study was to look at the MDA divided into the seven cutoffs (from 1/7 to 7/7) and analyzing which domains were more frequently achieved, in particular in those not satisfying the MDA, namely from 1/7 to 4/7, in a group of PsA patients, as a “climb” towards MDA. A secondary aim was to assess the relationship between MDA, categorized into seven cutoffs, with the Patient Acceptable Symptoms State (PASS) [9], the Psoriatic Arthritis Impact of the Disease (PsAID) [10], the Disease Activity for Psoriatic Arthritis (DAPSA) [11], and the Physician Global Assessment (PhGA).

Methods

Patient Selection

In this cross-sectional analysis of a longitudinal cohort, patients were enrolled at the Rheumatology Unit, Department of Medicine and Health Science-University of Molise. From the June 30, 2019 until December 31, 2019, all PsA patients who were on at least 6-month follow-up treatment with conventional synthetics (cs) and biologic (b) disease-modifying anti-rheumatic drugs (DMARDs) were considered potentially eligible for the study.

Inclusion criteria were:

  1. PsA classified with the ClASsification criteria for Psoriatic ARthritis (CASPAR) criteria [12],

  2. Age ≥ 18 years,

  3. AT least 6 months of follow-up at the study visit,

  4. Stable treatment with a csDMARDs or bDMARDs for at least 6 months.

Data Collection

Patients’ data collection included a medical history, physical examination, current use of medications, and laboratory assessment. Demographics and disease characteristics including age, sex, body mass index, and disease duration were taken into account. The clinical assessment encompassed the number of tender and swollen joints (68/66), enthesitis by the Leeds Enthesitis Index (LEI) [13], and dactylitis. Psoriasis was quantified by the body surface area (BSA) [14]. The Health Assessment Questionnaire-Disability Index (HAQ-DI) [15] was used to assess function. Patient Global Assessment (PtGA) and pain on Visual Analogic Scale (VAS) were performed by all patients. PhGA of disease activity on a VAS [16] and C-reactive protein (CRP) were also collected.

MDA, VLDA, DAPSA, PASS, and PsAID

MDA was defined according to Coates et al. [4]. Patients were considered in MDA when they satisfied 5/7 of the following criteria: tender joint count ≤ 1; swollen joint count ≤ 1; BSA ≤ 3; pain on VAS ≤ 15 mm; PtGA ≤ 20 mm; HAQ-DI ≤ 0.5; LEI ≤ 1. VLDA was satisfied when all seven criteria were met [5].

DAPSA was calculated by adding the number of tender and swollen joints, pain on VAS, PtGA, and CRP (mg/dl) [17]. The PASS is a single question tool to evaluate the level of symptoms at which patients consider themselves well [9]. The PsAID was also assessed [10].

The study protocol was in compliance with the Declaration of Helsinki; written consent was obtained from each participant. The study was approved by the Institutional Review Board of the University of Molise (protocol no. 0001–09-2017).

Statistical Analysis

Statistical analysis was performed using SPSS (version 27). All demographical and clinical characteristics were summarized by using descriptive statistics. Parametric variables were reported by mean ± standard deviation (SD), and non-parametric ones by median and inter-quartile range (IQR). Categorical data are shown as number and percentage. Spearman’s correlation was used to assess the relationship between MDA divided in the seven cutoffs and DAPSA, PhGA, PsAID. A Spearman’s coefficient rho ≤ 0.2 = very weak, < 0.4 = weak, < 0.6 = moderate, < 0.8 strong and ≤ 1 very strong correlation, respectively. A significance level was accepted at p ≤ 0.05.

Results

Patient characteristics and overall disease activity

In the study period, 93 PsA satisfied the inclusion criteria and were enrolled. Table 1 shows the main clinical characteristics of the enrolled patients. In particular, in Table 1 are reported the different proportions of patients achieving the different MDA cutoffs; 44/93 (47.3%) patients were in MDA.

Table 1.

Demographic and clinical disease characteristics of the 93 PsA patients

93 PsA patients
Sex (M), n (%) 61 (65.6)
Age, mean (SD) 55.3 (13.1)
Disease duration (months), median (IQR) 72 (24–156)
Weight (kg), median (IQR) 75 (66–85)
Height (m), median (IQR) 1.70 (1.64–1.75)
BMI (kg/h2), median (IQR) 26.12 (22.85–29.72)
BSA, median (IQR) 1 (0–3)
Dactylitis, n (%)
 Never 61
 Present 11
 Past 19
PtGA, median (IQR) 4 (2–6)
VAS pain, median (IQR) 4 (1–7)
VAS physician, median (IQR) 3 (1–5)
TJ/68, median (IQR) 1 (0–3)
SwJ/66, median (IQR) 0 (0–1)
LEI, median (IQR) 0 (0–1)
CRP (mg/dl), median (IQR) 0.2 (0.18–0.50)
HAQ-DI, median (IQR) 0.500 (0.125–0.750)
DAPSA, median (IQR) 10.40 (4.40–16.83)
PsAID, median (IQR) 2.60 (1.00–4.75)
PASS yes, n (%) 59/87 (67.8)
MDA 5/7 n (%) 44 (47.3)
MDA n (%)
 7/7 14 (15.05)
 0/7 2 (2.15)
 1/7 5 (5.37)
 2/7 13 (14.0)
 3/7 16 (17.2)
 4/7 13 (14.0)
 5/7 12 (12.9)
 6/7 18 (19.35)
Therapy, n (%)
 NSAIDs 10/91 (11)
 Oral steroids 5/91 (5.5)
 Methotrexate 16/91(17.6)
 Anti-TNF-α 38/91 (41.7)
 Anti-IL 17 17/90 (18.9)
 Anti-IL-12/23 9/90 (10)
 Apremilast 5/90 (5.5)

CRP C-reactive protein, LEI Leeds Enthesitis Index, BSA body surface area, PtGA patient global assessment, VAS Visual Analogue Scale, DAPSA disease activity for psoriatic arthritis, PsAID psoriatic arthritis impact of the disease, PASS patient acceptable symptoms state, MDA minimal disease activity, HAQ-DI Health Assessment Questionnaire-Disability Index, NSAIDs non-steroid anti-inflammatory drugs, anti-TNF-α anti-tumor necrosis factor alfa, IL interleukin, SD standard deviation, IQR interquartile range

Analysis of Different Domains

LEI ≤ 1 was the most frequently achieved domain either in the 47 patients not achieving MDA, or in those 44 patients in MDA. On the other hand, pain on VAS ≤ 15 mm was the most frequently missed domain in patients achieving or not MDA. Beyond LEI, the other domains frequently achieved in patients not in MDA were BSA ≤ 3 (70%) and swollen joints count ≤ 1 (68%). On the contrary, the domains with a lower percentage of achievement in patients not in MDA were: HAQ-DI ≤ 0.5 (38.8%), tender joint count ≤ 1 (23%), PtGA ≤ 20 (4.2%), and pain on VAS ≤ 15 mm (2%). All data are shown in Fig. 1. It also shows the “climb” of MDA, divided into the seven cutoffs. There was a growing trend, from MDA 1/7 to MDA 7/7, in the percentage of patients in PASS yes, in PsAID ≤ 4 and in DAPSA ≤ 4 and ≤ 14. In particular, in those MDA 4/7, more than 80% were in PASS yes, 75% in PsAID ≤ 4 and more than 90% in DAPSA ≤ 14.

Fig. 1.

Fig. 1

Numbers and percentage of patients that achieved each MDA domain, divided into the seven cutoffs. For both the 47 patients that did not meet the MDA status (MDA 1/7, 2/7, 3/7,4/7) and the 44 patients in MDA status (MDA5/7, 6/7, 7/7) the cumulative percentage of each MDA domain achieved is shown. PASS patient acceptable symptoms state, PsAID psoriatic arthritis impact of the disease, DAPSA disease activity for psoriatic arthritis, MDA minimal disease activity, LEI Leeds Enthesitis Index, BSA body surface area, PtGA Patient Global Assessment, Pain Pain on Visual Analogue Scale, HAQ-DI Health Assessment Questionnaire-Disability Index, Sw J swollen joints count, TJ tender joints count

An inverse correlation (Fig. 2) was found between MDA categories with DAPSA, (rho = − 0.91, p < 0.001), PhGA (rho = − 0.76, p < 0.001) and PsAID (rho = − 0.78, p < 0.001).

Fig. 2.

Fig. 2

Liner graph to show the correlation between the MDA divided in seven cutoffs with Disease Activity for Psoriatic Arthritis (DAPSA), Physician Global Assessment on VAS (PhGA), and Psoriatic Arthritis Impact of the Disease (PsAID). The relationship between MDA categorized in seven cutoffs (as continuous variable) and DAPSA, PhGA, and PsAID is shown by Spearman’s rho value. DAPSA disease activity for psoriatic arthritis, PhGA physician global assessment, PsAID psoriatic arthritis impact of the disease, MDA minimal disease activity. *All the correlations had a p < 0.001

Discussion

To our knowledge, this was the first study to detail the achievement of each single domain included in the MDA and divided by the seven categories. In particular, it seems that some domains are frequently achieved in patients not in MDA, as well as in those in MDA. In fact, in those 47 patients not achieving MDA 5/7, LEI ≤ 1, BSA ≤ 3 and swollen joints count ≤ 1 were satisfied in more than 60%. On the other hand, in the same group of 47 patients, there was a drop of the other domains which were ranging from HAQ-DI ≤ 0.5 in 38% until pain on VAS ≤ 15 mm in 2%. Overall, this study showed that the “objective” or “physician-driven” domains were more frequently reached in all PsA patients enrolled, MDA or not; on the other hand, the most frequently missed domains are those “patient-driven”. Moreover, if we look at those 13 patients in MDA 4/7, 81.8% were in PASS yes, 75% in PsAID ≤ 4 and 92.3% in DAPSA ≤ 14. As a further element to consider, the correlation found between MDA with DAPSA, PhGA, and PsAID might support the view of MDA as an instrument capable of complying with disease activity, physician, and patient’s perspective throughout the seven cutoffs.

However, the achievement of some treatment targets is not always agreed with the patient’s perception of the disease [18] and this is still an unmet need. In fact, it is possible to observe some residual disease activity in PsA patients and this, possibly, might imply some therapeutic decisions [19]. Furthermore, our study showed that residual activity is detectable in PsA patients even in a condition of MDA showing the importance to know what that remaining activity consists of.

Our study has strengths as well as limitations: the study was performed in a group of patients in a stable treatment and with a cross-sectional design. At the same time, we did not perform any analysis on potential treatment implications in those patients (such as change therapy) due to the study design. However, our study tried to look at the differences in the MDA domains and, as far as we know, this is a novelty in this intriguing topic. Moreover, our patients seem to have a good control of the disease, with most patients having less than three swollen/tender joints and very mild skin involvement. This might explain why skin criteria and enthesis criteria were two of the most frequently fulfilled domains in every category of criteria fulfilled. Other studies partially agree with our results, in particular, Marin J et al. showed that skin was one of the major domains that stopped patients from achieving MDA. In our clinic, patients are followed up regularly and treated to target, and this could explain the results obtained. However, as a possible further explanation is that at least 30% of patients of our group were under IL-12/23, Il-17 inhibitors [20].

Conclusions

In conclusion, this study detailed which domains are more frequently achieved on MDA divided into the seven cutoffs, underlying that “physician-driven” domains are more frequently achieved in all patients enrolled. Moreover, a strong correlation was found with other outcome measures throughout the seven domains.

Acknowledgements

We want to thank the participants in the study.

Funding

No funding or sponsorship was received for this study or publication of this article. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Authorship Contributions

All authors have made substantial contributions to all of these sections: conception and design of the study, acquisition of data, analysis and interpretation of data, drafting the article, revising it critically for important intellectual content and final approval of the version to be submitted.

Disclosures

Ennio Lubrano, Silvia Scriffignano, and Fabio Massimo Perrotta have nothing to disclose.

Compliance with Ethics Guidelines

All procedures performed in studies involving human participants 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. Informed consent was obtained from all individual participants included in the study. The study was approved by the Institutional Review Board of the University of Molise.

Data Availability

The datasets generated during and/or analyzed during the current study are not publicly available but are available from the corresponding author on reasonable request.

Footnotes

Ennio Lubrano and Silvia Scriffignano contributed equally to this work.

References

  • 1.Ritchlin CT, Colbert RA, Gladman DD. Psoriatic arthritis. N Engl J Med. 2017;376:957–970. doi: 10.1056/NEJMra1505557. [DOI] [PubMed] [Google Scholar]
  • 2.Lubrano E, Scriffignano S, Perrotta FM. Psoriatic arthritis, psoriatic disease, or psoriatic syndrome? J Rheumatol. 2019;46:1428–1430. doi: 10.3899/jrheum.190054. [DOI] [PubMed] [Google Scholar]
  • 3.Tucker LJ, Coates LC, Helliwell PS. Assessing disease activity in psoriatic arthritis: a literature review. Rheumatol Ther. 2019;6:23–32. doi: 10.1007/s40744-018-0132-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Coates LC, Fransen J, Helliwel PS. Defining disease activity in psoriatic arthritis: a proposed objective target for treatment. Ann Rheum Dis. 2010;69:48–53. doi: 10.1136/ard.2008.102053. [DOI] [PubMed] [Google Scholar]
  • 5.Coates LC, Helliwell PS. Defining low disease activity states in psoriatic arthritis using novel composite disease instruments. J Rheumatol. 2016;43:371–375. doi: 10.3899/jrheum.150826. [DOI] [PubMed] [Google Scholar]
  • 6.Coates LC, Nash P, Kvien TK, et al. Comparison of remission and low disease activity states with DAPSA, MDA and VLDA in a clinical trial setting in psoriatic arthritis patients: 2-year results from the FUTURE 2 study. Semin Arthritis Rheum. 2020;4:709–718. doi: 10.1016/j.semarthrit.2020.03.015. [DOI] [PubMed] [Google Scholar]
  • 7.Lubrano E, De Socio A, Perrotta FM. Comparison of composite indices tailored for psoriatic arthritis treated with csDMARD and bDMARD: a cross-sectional analysis of a longitudinal cohort. J Rheumatol. 2017;44:1159–1164. doi: 10.3899/jrheum.170112. [DOI] [PubMed] [Google Scholar]
  • 8.de Vlam K, Steinfeld S, Toukap AN, BEPAS Study Investigators et al. The burden of psoriatic arthritis in the biological era: data from the Belgian Epidemiological Psoriatic Arthritis Study (BEPAS) Rheumatology (Oxford) 2021 doi: 10.1093/rheumatology/keab233. [DOI] [PubMed] [Google Scholar]
  • 9.Lubrano E, Scriffignano S, Azuaga AB, Ramirez J, Cañete JD, Perrotta FM. Assessment of the Patient Acceptable Symptom State (PASS) in psoriatic arthritis: association with disease activity and quality of life indices. RMD Open. 2020;6:e001170. doi: 10.1136/rmdopen-2020-001170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Gossec L, de Wit M, Kiltz U, EULAR PsAID Taskforce et al. A patient-derived and patient-reported outcome measure for assessing psoriatic arthritis: elaboration and preliminary validation of the Psoriatic Arthritis Impact of Disease (PsAID) questionnaire, a 13-country EULAR initiative. Ann Rheum Dis. 2014;73:1012–1019. doi: 10.1136/annrheumdis-2014-205207. [DOI] [PubMed] [Google Scholar]
  • 11.Schoels M, Aletaha D, Funovits J, Kavanaugh A, Baker D, Smolen JS. Application of the DAREA/DAPSA score for assessment of disease activity in psoriatic arthritis. Ann Rheum Dis. 2010;69:1441–1447. doi: 10.1136/ard.2009.122259. [DOI] [PubMed] [Google Scholar]
  • 12.Taylor W, Gladman D, Helliwell P, Marchesoni A, Mease P, Mielants H. Classification criteria for psoriatic arthritis: development of new criteria from a large international study. Arthritis Rheum. 2006;54:2665–2673. doi: 10.1002/art.21972. [DOI] [PubMed] [Google Scholar]
  • 13.Healy PJ, Helliwell PS. Measuring clinical enthesitis in psoriatic arthritis: assessment of existing measures and development of an instrument specific to psoriatic arthritis. Arthritis Rheum. 2008;59:686–691. doi: 10.1002/art.23568. [DOI] [PubMed] [Google Scholar]
  • 14.Fredriksson T, Pettersson U. Severe psoriasis–oral therapy with a new retinoid. Dermatologica. 1978;157:238–244. doi: 10.1159/000250839. [DOI] [PubMed] [Google Scholar]
  • 15.Ranza R, Marchesoni A, Calori G, et al. The Italian version of the Functional Disability Index of the Health Assessment Questionnaire. A reliable instrument for multicenter studies on rheumatoid arthritis. Clin Exp Rheumatol. 1993;11:123–128. [PubMed] [Google Scholar]
  • 16.Lubrano E, Perrotta FM, Parsons WJ, Marchesoni A. Patient’s global assessment as an outcome measure for psoriatic arthritis in clinical practice: a surrogate for measuring low disease activity? J Rheumatol. 2015;42:2332–2338. doi: 10.3899/jrheum.150595. [DOI] [PubMed] [Google Scholar]
  • 17.Schoels MM, Aletaha D, Alasti F, Smolen JS. Disease activity in psoriatic arthritis (PsA): defining remission and treatment success using the DAPSA score. Ann Rheum Dis. 2016;75:811–818. doi: 10.1136/annrheumdis-2015-207507. [DOI] [PubMed] [Google Scholar]
  • 18.Gorlier C, Orbai AM, Puyraimond-Zemmour D, et al. Comparing patient-perceived and physician-perceived remission and low disease activity in psoriatic arthritis: an analysis of 410 patients from 14 countries. Ann Rheum Dis. 2019;78:201–208. doi: 10.1136/annrheumdis-2018-214140. [DOI] [PubMed] [Google Scholar]
  • 19.Lubrano E, Scriffignano S, Perrotta FM. Residual disease activity and associated factors in psoriatic arthritis. J Rheumatol. 2020;47:1490–1495. doi: 10.3899/jrheum.190679. [DOI] [PubMed] [Google Scholar]
  • 20.Marin J, Acosta Felquer ML, FerreyraGarrot L, Ruta S, Rosa J, Soriano ER. Patients with psoriatic arthritis fulfilling the minimal disease activity criteria do not have swollen and tender joints, but have active skin. J Rheumatol. 2016;43:907–910. doi: 10.3899/jrheum.151101. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets generated during and/or analyzed during the current study are not publicly available but are available from the corresponding author on reasonable request.


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