Introduction
The efficacy of psoriasis treatments has steadily improved over the last two decades [
1]. Systemic agents, including biologic agents that target inflammatory cytokines, have emerged as some of the most effective treatment options. As the efficacy of biologic agents has increased, clinical outcome measures for trials have become more stringent. A number of trials have incorporated clinical outcomes such as achieving a body surface area (BSA) ≤ 1%, and a 90% or 100% reduction in Psoriasis Area and Severity Index (PASI90, PASI100) [
2,
3].
As clinical outcomes for psoriasis have improved, dermatology organizations around the world have aimed to define successful treatment and remission. In the USA, the National Psoriasis Foundation (NPF) proposed that the target response to treatment is a BSA ≤ 1% at 3 months after initiating therapy and ≤ 1% every 6 months during the maintenance period [
4]. The Belgian consensus added on the concept of treat-to-target, emphasizing that both disease severity and quality of life measures are essential components of remission, and variables that capture the patient’s perspective of their condition should be considered as well [
5].
To further explore remission from a patient-centered view, the NPF aimed to identify demographic and clinical factors associated with patient-reported remission of psoriasis.
Methods
The National Psoriasis Foundation conducted a cross-sectional study using an online and telephone-based survey of a random, stratified sample of individuals with psoriasis in October and November 2019. The survey was approved by the Genetic Alliance Institutional Review Board. Participants included individuals living in the USA with a physician-given diagnoses of psoriasis and/or psoriatic arthritis, 18 years of age or older, who contacted the foundation between 2017 and 2019. The Patient Report of Extent of Psoriasis Involvement (PREPI) was used to assess severity of psoriasis at the time of data collection [
6]. Participants who reported a body surface area (BSA) of 3% or less were asked questions about their perspective on whether their psoriasis is in remission. Quality of life was assessed using a global quality of life question and the Dermatology Life Quality Index (DLQI). The DLQI is a well-established, validated tool to assess dermatology-specific quality of life [
7,
8]. The global quality of life question asked participants the following questions: “[c]onsidering all the ways your psoriasis and/or psoriatic arthritis may affect you at this time, please indicate you are doing” on a scale of 0–10 with 0 being “very well” and 10 being “very poorly.” The survey asked participants about their current and past treatments, physician diagnosed comorbidities (see Table
1), and demographics, including race, biological sex, height, and weight. Participant-reported height and weight were used to calculate body mass index (BMI) using the standard formula: weight (lb)/height (in)
2 × 703
Table 1
Comorbidities surveyed
Cardiovascular disease | Dyslipidemia | Chronic obstructive pulmonary disease (COPD) |
Stroke | Depression | Uveitis |
Hypertension | Anxiety | Liver disease |
High blood pressure | Sexual dysfunction | Fatty liver disease |
Heart attack | Crohn’s disease | Rheumatoid arthritis |
Adult onset diabetes (Type 2 diabetes) | Ulcerative colitis | Gout |
Metabolic syndrome | Cancer | Osteoarthritis |
High triglyceride levels | Cutaneous T-cell lymphoma | Fibromyalgia |
High cholesterol | Chronic kidney disease | Thyroid disease |
Coronary artery disease | Sleep apnea | Other (specify) |
Atherosclerosis | Hardening/narrowing of arteries | None of the above |
Descriptive statistics were used to report the number and percentage of respondents who believe their psoriasis is in remission. Chi-square tests of independence were conducted to explore characteristics associated with patient perception of psoriasis remission. Characteristics associated with remission were included in logistic regression models used to assess factors related to patient perception of psoriasis remission. For the logistic regression models, the continuous variable for age was used, race was collapsed into a dichotomous “white” and “non-white” variable due to the lack of racial diversity among participants, and a continuous variable for BSA was used for disease severity. The number of comorbidities reported by each participant was created by summing responses to the question about physician-given diagnoses of comorbid conditions (Table
1). Hypertension and high blood pressure were counted as one comorbidity for high blood pressure. Cardiovascular disease, stroke, and heart attack were counted as one comorbidity for cardiovascular disease. Atherosclerosis and narrowing of the arteries were counted as one question for atherosclerosis.
A total of 1570 individuals with psoriasis completed the survey, including 736 (46.9%) diagnosed by a physician with psoriasis, 76 (4.8%) diagnosed with psoriatic arthritis, and 758 (48.3%) with psoriasis and psoriatic arthritis. Among individuals with psoriasis, 783 (49.9%) reported mild psoriasis (BSA < 3%) and 787 (50.1%) reported moderate to severe psoriasis (BSA ≥ 3%). Individuals diagnosed with psoriatic arthritis without a concomitant diagnosis of psoriasis and individuals with a self-reported BSA > 3% at the time of data collection were excluded from the analyses.
Results
Among the 1570 individuals who completed the survey, 930 (63.7%) reported a BSA ≤ 3% and were asked if they believed their psoriasis was in remission. Of these, 479 (51.7%), believed that their psoriasis was in remission (Table
3). Participants with psoriasis and a BSA ≤ 3% were mostly white (89.4%), female (59.1%), over the age of 50 years (60.7%), and were overweight or obese (68.4%) (Table
2). Participants with psoriasis only (470, 50.5%) and psoriasis and psoriatic arthritis (460, 49.5%) were evenly represented (Table
3). Most participants with BSA ≤ 3% believed their psoriasis had a small (314, 38.8%) or no effect (282, 34.8%) on their quality of life, based on DLQI results (Table
3).
Table 2
Participant demographics
Race |
White or Caucasian | 819 (89.4%) |
Asian or Asian American | 37 (4.0%) |
Black or African American | 13 (1.4%) |
American Indian or Alaskan Native | 9 (1.0%) |
Native Hawaiian or other Pacific Island | 2 (0.2%) |
Two or more races | 19 (2.1%) |
Other | 8 (0.9%) |
Unsure | 9 (1.0%) |
Biological sex |
Male | 376 (40.9%) |
Female | 544 (59.1%) |
Age |
18–35 years | 98 (11.0%) |
36–50 years | 254 (28.4%) |
51–65 years | 325 (36.3%) |
Older than 65 years | 219 (24.4%) |
BMI categories |
Underweight | 15 (1.7%) |
Normal weight | 260 (29.8%) |
Overweight | 298 (34.2%) |
Obese | 298 (34.2%) |
Table 3
Descriptive statistics of participants
Disease diagnosed |
Psoriasis | 470 (50.5%) |
Psoriasis and psoriatic arthritis | 460 (49.5%) |
Disease severity |
0% BSA | 123 (13.2%) |
1% BSA | 439 (47.2%) |
2% BSA | 221 (23.7%) |
3% BSA | 147 (15.8%) |
DLQI interpretation |
No effect at all | 282 (34.8%) |
Small effect | 314 (38.8%) |
Moderate effect | 141 (17.4%) |
Very large effect | 67 (8.3%) |
Extremely large effect | 6 (0.7%) |
Perception of remission |
PsO not in remission | 448 (48.3%) |
PsO in remission | 479 (51.7%) |
Results from chi-square tests of independence suggest that type of disease diagnosed, BSA, biologic use, and DLQI score are related to perception of psoriasis in remission (Table
4). Compared with individuals with psoriasis, only (43.6%), a higher percentage of those with psoriasis and psoriatic arthritis (56.4%), perceived their psoriasis was in remission (
p < 0.001). The percentage of participants perceiving their psoriasis as in remission increased as BSA decreased. However, among those who perceived their psoriasis as being in remission, only 22.7% reported having full clear skin and 51.6% reported having 1% BSA. A higher percentage of those who perceived their psoriasis was in remission reported using a biologic therapy (65.2%) compared with those not using a biologic therapy (34.8%,
p < 0.001). Nearly 14% of participants who perceived their psoriasis was in remission reported their skin disease had a moderate to extremely large effect on their quality of life (
p < 0.001).
Table 4
Chi-square tests of independence comparing remission status
Disease diagnosed*** |
Psoriasis | 258 (57.6%) | 209 (43.6%) |
Psoriasis and psoriatic arthritis | 190 (42.4%) | 270 (56.4%) |
Disease severity*** |
0% BSA | 13 (2.9%) | 109 (22.7%) |
1% BSA | 190 (42.4%) | 247 (51.6%) |
2% BSA | 143 (31.9%) | 78 (16.3%) |
3% BSA | 102 (22.7%) | 45 (9.4%) |
Biologic use*** |
Not biologic user | 255 (59.1%) | 160 (34.8%) |
Biologic user | 176 (40.9%) | 300 (65.2%) |
DLQI interpretation*** |
No effect at all | 60 (15.4%) | 222 (52.9%) |
Small effect | 174 (44.6%) | 140 (33.3%) |
Moderate effect | 99 (25.4%) | 42 (10.0%) |
Very large effect | 53 (13.6%) | 14 (3.3%) |
Extremely large effect | 4 (1.0%) | 2 (.5%) |
Factors associated with perception of psoriasis remission were explored using logistic regression. Results from multivariate logistic regression suggest that skin specific [OR = 0.87, 95% CI (0.82–0.92)] and global quality of life [OR = 0.80, 95% CI (0.72–0.86)], BSA [OR = 0.71, 95% CI (0.57–0.88)], male sex [OR = 0.65, 95% CI (0.46–0.94)], biologic use [OR = 2.26, 95% CI (1.54–5.51)], and concomitant diagnosis of psoriatic arthritis [OR = 2.04, 95% CI (1.38–3.02)] are associated with increased likelihood of feeling psoriasis was in remission (Table
5). An increased impact of skin disease on quality of life was associated with a 13% decrease in likelihood of perceiving psoriasis was in remission. For each decrease in global quality of life, the likelihood of perceiving psoriasis was in remission decreased by 20%. Each percentage of BSA affected by psoriasis decreased perception of psoriasis in remission by 29%. Males were 35% less likely to perceive their psoriasis as being in remission than females. Using a biologic therapy to treat psoriasis increased the likelihood of perceiving psoriasis was in remission by 126%. Having a concomitant diagnosis of psoriatic arthritis increased the likelihood of perceiving psoriasis was in remission by 104%.
Table 5
Logistic regression models of factors associated with remission status
Model 1 |
DLQI Scale | 0.80 | 0.018 | 0.76–0.84 | < 0.001 |
Model 2 |
DLQI Scale | 0.83 | 0.020 | 0.79–0.87 | < 0.001 |
Global QoL | 0.83 | 0.028 | 0.77–0.89 | < 0.001 |
Model 3 |
DLQI Scale | 0.86 | 0.021 | 0.82–0.91 | < 0.001 |
Global QoL | 0.84 | 0.030 | 0.78–0.90 | < 0.001 |
BSA | 0.56 | 0.055 | 0.46–0.68 | < 0.001 |
Model 4 |
DLQI Scale | 0.85 | 0.021 | 0.81–0.90 | < 0.001 |
Global QoL | 0.83 | 0.030 | 0.77–0.89 | < 0.001 |
BSA | 0.58 | 0.058 | 0.48–0.71 | < 0.001 |
Male | 0.68 | 0.114 | 0.49–0.95 | 0.023 |
Model 5 |
DLQI Scale | 0.86 | 0.022 | 0.82–0.91 | < 0.001 |
Global QoL | 0.82 | 0.031 | 0.76–0.88 | < 0.001 |
BSA | 0.65 | 0.068 | 0.53–0.80 | < 0.001 |
Male | 0.67 | 0.115 | 0.47–0.93 | 0.019 |
Biologic user | 2.72 | 0.46 | 1.95–3.79 | < 0.001 |
Model 6 |
DLQI Scale | 0.87 | 0.022 | 0.83–0.91 | < 0.001 |
Global QoL | 0.78 | 0.032 | 0.73–0.85 | < 0.001 |
BSA | 0.65 | 0.069 | 0.53–0.81 | < 0.001 |
Male | 0.68 | 0.118 | 0.48–0.96 | 0.27 |
Biologic user | 2.19 | 0.398 | 1.53–3.13 | < 0.001 |
Has PsA | 1.88 | 0.358 | 1.29–2.73 | 0.001 |
Model 7 | | | | |
DLQI Scale | 0.87 | 0.023 | 0.82–0.92 | < 0.001 |
Global QoL | 0.80 | 0.033 | 0.72–0.86 | < 0.001 |
BSA | 0.71 | 0.079 | 0.57–0.88 | 0.002 |
Male | 0.65 | 0.121 | 0.46–0.94 | 0.023 |
Biologic user | 2.26 | 0.439 | 1.54–3.31 | < 0.001 |
Has PsA | 2.04 | 0.409 | 1.38–3.02 | < 0.001 |
Age | 1.00 | 0.007 | 0.99–1.01 | 0.624 |
White | 0.87 | 0.262 | 0.48–1.57 | 0.644 |
Obese | 0.74 | 0.147 | 0.50–1.09 | 0.129 |
Discussion
This study highlights several clinical and demographic factors associated with psoriasis remission from the perspective of patients.
Patients were more likely to report remission status in relation to having a lower BSA of psoriasis disease. Interestingly, a significant subset of patients who reported not having clear skin or a BSA of 1% indicated that they believed they were in remission. A treat-to-target consensus performed by the National Psoriasis Foundation within the USA, published in 2017, established BSA as the most preferred outcome for establishing a treatment target among dermatologists [
4]. This study indicates that having completely clear skin or a BSA ≤ 1%, though a very important factor for remission, does not fully correlate with remission status from the perspective of all patients.
Quality of life was another significant factor associated with patient-reported remission. A treat-to-target consensus performed by the Belgian consensus added upon the United States concept of treat-to-target, indicating that quality of life be included within the definition in addition to disease severity measures [
5]. The consensus, published in 2020, incorporates clinical severity, quality of life, tolerability of side effects, and comorbidity in their definition for treat-to-target [
5]. Quality of life strongly correlates with disease severity, but our study further highlights that quality of life also independently contributes to patients’ perception of remission.
Furthermore, biologic use was significantly associated with patients reporting remission. Many biologic agents can improve both joint and skin symptoms with very few serious side effects [
1], and this favorable benefit-to-risk ratio may lead to improvements in patient satisfaction and perception of remission.
Our study highlighted some additional interesting factors associated with remission status. Patients who self-identified as male were less likely to report remission, while females were more likely to report remission. A recent study conducted by Murer et al. surveyed 1979 psoriasis patients and compared differences between patient gender and psoriasis symptoms [
9]. They found that pruritus was identified as the most significant symptom in relation to quality of life and that females reported higher rates of psoriatic pruritus, as well as lower satisfaction with treatment [
9]. A study conducted by Mabuchi et al. in Japan also reported that female patients reported worse quality of life scores than men [
10]. Moreover, studies have shown that females report higher intensities of experimentally induced itch compared with males and have higher plasma levels of drugs used to treat itch compared with males [
11,
12]. Therefore, it is possible that, compared with males, females may experience more intense psoriasis symptoms and improved treatment responses.
Interestingly, patients who reported a concomitant diagnosis of psoriatic arthritis were also more likely to report remission status. Psoriatic arthritis results in a substantial functional impact on quality of life in patients [
13]. In a study evaluating psoriasis patients with skin and joint symptoms, patients prioritized the burden of joint over skin symptoms [
14]. Our study may indicate that psoriatic arthritis patients, who have a large combined burden of skin and joint disease, may view improvement in skin or joint symptoms more favorably than those with skin symptoms alone.
Conclusion
Remission in psoriasis is an evolving concept that is actively being developed. Capturing the perspectives of patients on remission will ultimately assist in the shared decision-making process between patients and providers in discussing treatment goals. Using a large national survey, our study identified several factors related to remission in psoriasis. Among surveyed patients, we found that that psoriasis BSA and quality of life were significant factors, which have previously been highlighted in other treat-to-target initiatives. New factors including, sex, biologic use, and diagnosis of psoriatic arthritis, were also significant regarding patient-reported remission status. Ultimately, our study provides further evidence that remission may encompass multiple domains.
Acknowledgments
Disclosures
April W. Armstrong serves as a research investigator and/or scientific advisor to AbbVie, Almirall, Arcutis, ASLAN, BI, BMS, EPI, Incyte, Leo, UCB, Janssen, Lilly, Nimbus, Novartis, Ortho Dermatologics, Sun, Dermavant, Dermira, Sanofi, Regeneron, Pfizer, and Modmed. George Gondo is an employee of the National Psoriasis Foundation and Stacie J. Bell was an employee of the National Psoriasis Foundation at the time of this work. Wilson Liao has received research grant funding from Abbvie, Amgen, Janssen, Leo, Novartis, Pfizer, Regeneron, and TRex Bio. Joseph F. Merola serves as a consultant or investigator for Merck, Abbvie, Dermavant, Eli Lilly, Novartis, Janssen, UCB, Celgene, Sanofi, Regeneron, Arena, Sun Pharma, Biogen, Pfizer, EMD Serono, Avotres, and Leo Pharma. Tina Bhutani is a principal investigator for trials sponsored by Abbvie, Castle, CorEvitas, Dermavant, Galderma, Mindera, and Pfizer. She has received research grant funding from Novartis and Regeneron. She has been an advisor for Abbvie, Arcutis, Boehringer-Ingelheim, Bristol Myers Squibb, Janssen, Leo, Lilly, Novartis, Pfizer, Sun, and UCB. Edward Hadeler, Emanual Maverakis, and Nicholas Brownstone state no conflict of interest.
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