With advancing therapeutic options, achieving a state of remission has become the treatment goal in rheumatoid arthritis. Agreeing on what constitutes remission and what measures should be used to assess disease activity has remained a challenge. Multiple remission criteria have been devised and modified, all with different strengths and limitations. A consensus definition of remission will need to be achieved if we are to be able to evaluate outcomes of clinical trials and establish treatment targets for practice. Remission defined as the complete absence of disease currently may not be a realistic therapeutic goal.
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As new disease-modifying agents and biologic therapies are added to the treatment options in rheumatoid arthritis (RA), better outcomes are expected and reported. The current treatment goal for RA is to achieve a state of disease remission. The concept of remission at first glance seems simple. It has been defined as “an absence of articular and extra-articular inflammation and disease activity” . However, no consensus exists on what constitutes clinical remission and what indices should be used to assess disease activity. Presently, no gold standard can be uniformly applied in clinical trials or practice.
In clinical practice, a subjective definition of remission is commonly applied, one in which “we can recognize it when we see it.” Three clinical domains are usually considered in making this decision: signs and symptoms of inflammation, functional impairment, and structural joint damage . In a 2008 study evaluating physician and patient perspectives on remission, rheumatologists were asked, “Based on your experience, is your patient currently in remission?” while patients completed questionnaires regarding their disease activity. There was a 78.6% agreement (κ, 0.53) between patients and physicians regarding achievement of remission. However, most of these RA patients were found to have evidence of residual RA activity based on RA Disease Activity Index scores, which called into question whether subjective clinical remission is true absence of disease or a state of low disease activity .
One of the first descriptions of remission in RA came from Short and Bauer  in 1948, in which patients were classified as being in remission if they were asymptomatic and if examination of the joints was negative except for residual deformity. Since that time, various criteria have been developed to define remission using different clinical, laboratory, and radiographic measures. Clinical trials have used different definitions of remission, making it difficult to compare results between studies. To standardize the remission measure, the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) are currently collaborating to redefine remission in RA and to create a uniform definition that can be used in trials and clinical practice. They believe that a strict definition of remission is needed and should be validated against long-term outcomes [5••]. This review discusses current debates in remission, existing definitions, and their limitations.
Current Remission Criteria
One of the early attempts to define remission in RA was adopted by the American Rheumatism Association (now ACR) in 1981. Remission required fulfillment of 5 of 6 variables for at least 2 consecutive months: less than 15 min of morning stiffness, no fatigue, no joint pain by history, no joint tenderness, no swelling, and an erythrocyte sedimentation rate (ESR) of less than 30 mm/h for women and less than 20 mm/h for men . Three of these six variables rely on the patient’s history. It also should be noted that these criteria were established at a time when available treatment options did not provide the degree of improvement that is currently expected and possible .
Prevoo et al.  proposed modifying the ACR criteria because no specifications were provided on how to measure the variables, and because fatigue and morning stiffness are not currently recognized and accepted in a validated core set. Fatigue was removed, and having no joint pain by history was replaced by pain assessment on a Visual Analogue Scale (VAS). Remission required meeting four of the five variables of the revised criteria for 3 months . One criticism regarding the ACR remission criteria is that additional factors that may contribute to joint pain (eg, structurally damaged joints) may not necessarily reflect ongoing disease activity. Moreover, it would be possible to fulfill remission criteria while still having swollen joints . In addition, clinical trials do not routinely gather all data required to evaluate ACR remission criteria, and several studies have modified assessments of ACR remission criteria, excluding fatigue, stiffness, or modifying pain VAS measures . Despite these limitations, the ACR remission criteria are still viewed as reliable outcome measures.
The ACR remission criteria should not be confused with the ACR response criteria. Remission is a “status” measure (ie, an assessment of disease activity at a specific point in time), whereas a “response” measure is an assessment of how disease activity changes over time. The ACR 20%, 50%, and 70% improvement criteria are response measures and were developed to evaluate a response to therapy in the context of a clinical trial, not to determine remission .
EULAR Criteria: Disease Activity Score
The Disease Activity Score (DAS) was proposed by EULAR in the early-1990 s. The DAS is a single-point, absolute measure of disease activity. The original DAS—the DAS44—uses four core set variables in a mathematical equation to quantify the level of disease activity. The variables include the Ritchie Tender Joint Index (a graded measurement of joint tenderness), the number of swollen joints (44 joints assessed), an acute-phase reactant (ESR or C-reactive protein [CRP]), and a general health score on a 100-mm VAS. A DAS44/ESR four-item score of less than 1.6 is considered remission. An abbreviated version, the DAS28, has been validated against the original version. A DAS28 score of less than 2.6 is considered remission .
The DAS28 is more time efficient, requiring the evaluation of fewer joints. However, the 28-joint count could lead to an underestimation of disease activity. Ankles and feet are commonly affected in RA but are not included in the assessment. Painful and/or swollen metatarsophalangeal joints have been detected in many patients classified as being in DAS28 remission [11•]. In a study comparing the DAS28 with a DAS32 that included ankles and a combined metatarsophalangeal joint count, the frequency of remission did not change between the two definitions (n = 767, 95% concordance). For those with ankle and foot involvement, abnormal acute-phase reactants or general health scores increased DAS28 scores to levels above remission . However, a substantial number of RA patients can have tender and swollen joints and still be considered in DAS remission . Thus, it can be argued that DAS remission reflects a measure of minimal RA disease activity rather than remission.
Another limitation of the DAS is that it relies heavily on acute-phase reactants. A subnormal ESR or CRP may artificially weigh the DAS score into remission despite objective evidence of disease activity in the joint count. Subnormal inflammatory markers may be possible given current biologic therapies that have been shown to drive down acute-phase reactants without necessarily having equivalent clinical improvement. On the flip side, ESR and CRP are nonspecific and may not accurately reflect the patient’s disease activity if they are elevated for other reasons (eg, age, comorbidities). When the DAS28 is used instead of the DAS44, the acute-phase reactant becomes more heavily weighted, further amplifying changes in this variable .
Derivatives of EULAR Criteria: Disease Activity Indices
The Simplified Disease Activity Index (SDAI) and the Clinical Disease Activity Index (CDAI) are less complex composite indices that have been derived from the DAS. The SDAI includes five components that are simply added together for a final score: 28 tender joint count, a 28 swollen joint count, CRP, and both a patient’s and a physician’s global disease activity based on a 10-cm VAS. The CDAI is exactly the same except that it excludes the CRP component and is therefore one of the few criteria that does not involve a laboratory value. Remission is defined as an SDAI score of less than 3.3 or a CDAI score of less than or equal to 2.8 .
An advantage of the SDAI and CDAI over the DAS is that they do not require a complex formula or a calculator and can be used more readily in clinical practice. As they are derived from the DAS, though, the disease activity indices carry similar limitations. Interestingly, RA patients who met SDAI remission criteria had less joint inflammation by power Doppler ultrasonography than patients who met DAS28 remission criteria . Patients with RA in CDAI remission also have been shown to have quality-of-life scores closer to those of the healthy population when compared with patients who meet DAS28 remission criteria . These studies suggest that SDAI and CDAI remission scores are stringent and may more accurately reflect a state of decreased disease activity than DAS28 remission scores.
When SDAI and CDAI were compared with the DAS28 in a clinical practice setting, significantly fewer RA patients met CDAI/SDAI remission than DAS28 remission . This highlights the point that there are different remission rates depending on the definition used. In a large, multinational, cross-sectional cohort of 5848 RA patients in 24 countries, 8.6% met ACR criteria for remission, 13.8% met CDAI remission criteria, and 19.6% achieved DAS28 remission—numbers that are consistent with the ACR criteria being the most difficult to fulfill and the DAS28 being more inclusive [18••]. Therefore, clinical trials must be interpreted carefully in light of the remission definitions being used.
The FDA criteria define remission as meeting the above ACR remission criteria plus radiographic arrest (defined by Larsen or Sharp scores) for 6 months after all antirheumatic therapy has been discontinued. This is the only definition that includes radiographic changes as well as a medication-free state. These is the most stringent of all the criteria, and no therapy to date has been able to fulfill the requirements (Fig. 1) .
The concept that remission in RA should require a disease-free state after the discontinuation of medications is debatable. At present, the cause for the immune dysregulation that leads to RA is unknown. Current treatment aims to control the disease, not cure it. Thus, is it theoretically possible to achieve remission while being off treatment if the underlying immune pathology is still present? . It is also known, however, that a wide spectrum of possible disease outcomes exists for patients with RA, ranging from mild to rapidly destructive and debilitating disease. Drug-free remission has been previously reported in a small proportion of RA patients. Within this subset of patients, it is unclear whether current therapies are inducing a greater rate of drug-free remission or if the observed percentages represent the natural history of RA subtypes. The few studies addressing drug-free remission vary in how remission is defined, making them difficult to compare .
Tippana-Kinnunen et al. [22••] observed 87 patients with early RA for 15 years treated by the “sawtooth strategy.” Disease-modifying antirheumatic drugs (DMARDs) were discontinued in 29% of patients who met the modified ACR criteria of remission (excluding fatigue) or who had an undefined symptom-free period. However, 11 of the patients off medications (45%) had disease flares and had to be restarted on DMARDs. The mean DMARD-free period was 50 months overall (range, 3–137). None of the patients who had to restart DMARD therapy were in remission at the end of 15 years, suggesting that it may be more difficult to control RA after medications have been stopped and then restarted. The authors concluded that most patients with long-standing RA require continuous DMARD treatment, and if the treatment is discontinued, patients should be followed up closely to monitor for flares [22••].
A 4-year follow-up to the BeSt (Dutch acronym for Behandel–Strategieen treatment strategies) study looked at drug-free remission in 508 patients with recent-onset, active RA. Four different treatment strategies were adjusted every 3 months to achieve a DAS of less than 2.4. From year 2 onward, if the patient had a DAS less than 1.6 for at least 6 consecutive months, all antirheumatic treatment was discontinued. Between months 24 and 48, drug-free remission was achieved in 20% (n = 102). By the end of 4 years, 13% (n = 67) were still in drug-free remission, with the other patients requiring reinitiation of treatment. The mean duration of drug-free remission was 9 to 11 months. Treatment strategy was not associated with drug-free remission. Patients with milder RA at baseline, the absence of autoantibodies, male gender, and shorter symptom duration were associated with drug-free remission at year 4 .
Another study of the Leiden Early Arthritis Clinic (EAC) and the British Early Rheumatoid Arthritis Study (ERAS) also looked at the prevalence and predictive factors related to DMARD-free remission. Remission was defined as having no swollen joints, being off DMARDs, and classified as being in remission by a rheumatologist for a total duration of 1 year. Sustained DMARD-free remission was achieved in 15% of the EAC group (68 of 454 patients) and 9.4% of the ERAS group (84 of 895 patients). Factors associated with remission included acute onset, short symptom duration, nonsmokers, little radiographic damage at baseline, absence of rheumatoid factor, and absence of HLA shared epitope alleles [24•].
These studies suggest that a small proportion of early-RA patients (9%–15%) will be able to achieve medication-free remission for a sustained period of time and that certain factors may help predict in which RA patients this would be possible. However, up to 45% will require a reinitiation of therapy, and RA treatment may be more difficult when medications are restarted. These studies varied in how remission was defined, making it difficult to determine how to apply medication-free remission to clinical practice. There are no clear guidelines as to if and when medications should be stopped in RA.
Imaging in Remission
The purpose of having remission as a goal in RA treatment is to prevent joint damage and disability. Active inflammation in RA is generally correlated with progressive joint destruction. However, it has been shown that patients in clinical remission by ACR criteria  and by DAS28 criteria  can develop erosions and joint damage on radiographs of hands and feet when observed 2 to 5 years later. The progression of joint damage despite clinical remission suggests that traditional assessments of disease activity may not be sensitive enough, thereby leaving levels of RA activity undetected . This has led to the suggestion that radiographs, ultrasound, or MRI should be included in remission criteria to better assess disease activity. At present, the FDA definition of remission is the only criterion that requires the absence of radiographic progression.
In a study using data from the PREMIER (A Multicenter, Randomized, Double-Blind Clinical Trial of Combination Therapy With Adalimumab Plus Methotrexate Versus Methotrexate Alone or Adalimumab Alone in Patients With Early, Aggressive Rheumatoid Arthritis Who Had Not Had Previous Methotrexate Treatment) trial, 794 patients with early RA on three different treatment strategies were monitored for radiographic progression. Remission as defined by CDAI, SDAI, or DAS28 was achieved in 15% of patients (n = 119) by the second year of the trial. Radiographic progression was significantly different between patients with 3, 6, or 9 additional months of remission (P < 0.05) regardless of the type of treatment received. The shorter the duration of remission, the more likely radiographic progression was found. It was concluded that this was likely a carryover effect of past periods of inflammation and that this latency should be considered when evaluating radiographic outcomes in clinical trials and remission .
MRI and ultrasound are now being used more commonly to assess RA disease activity. Patients who have met the modified ACR criteria and DAS28 criteria for remission have ongoing synovitis by ultrasound . Brown et al.  studied ultrasound and MRI images of the hands of 107 RA patients who were considered to be in remission by their rheumatologist, the DAS28, or the modified ACR criteria. Regardless of which definition of remission was used, MRI showed that 96% of patients had synovitis and 46% had bone marrow edema, while ultrasound showed that 73% had synovial hypertrophy and 43% had increased power Doppler signal. No significant difference was noted in the number of patients with inflammation between those who met DAS28 or ACR remission criteria. These findings suggest that DAS28 and ACR criteria may not measure RA remission, in that “true remission” should show the absence of synovitis on imaging studies .
In a follow-up longitudinal study, 102 of the RA patients thought to be in remission underwent routine radiographs, ultrasound, and MRI at 12 months. Despite apparent clinical remission, 19% of patients (n = 17 [of 90 analyzed]) had continued deterioration in radiographic joint damage, although 11 satisfied ACR and DAS28 remission criteria. Inflammatory scores on ultrasound, especially power Doppler signals, and MRI synovitis scores at baseline were significantly associated with development of radiographic damage over 1 year. This study documents the association of subclinical inflammation with progressive structural damage in RA patients in clinical remission. It also supports the use of sensitive imaging techniques to more accurately evaluate disease status and define the remission state [30••].
Subclinical inflammation detected by ultrasound and MRI may predict which patients considered to be in remission are likely to experience disease progression. In another study of RA patients in remission by DAS less than 1.6, having a positive power Doppler signal on ultrasound was the main predictor of relapse within 6 months [31•]. Imaging could be valuable in therapeutic decisions, helping clinicians decide whether patients in clinical remission should continue, stop, or restart antirheumatic medications. Currently, no guidelines exist on how to incorporate imaging in clinical practice and trials.
Spontaneous remission is not uncommon in patients who present with very early arthritis, some of whom may meet criteria for RA over less than a few months. Spontaneous remission is thought of as a “natural remission,” in which disease activity essentially disappears, and medications are no longer required. Spontaneous remission may be seen in 13% to 55% of individuals presenting with undifferentiated arthritis, probably as a result of different underlying etiologies, such as a transient viral infection . About one third of patients with undifferentiated arthritis go on to develop RA. In a study of three cohorts of recent-onset undifferentiated arthritis from the United Kingdom, Germany, and the Netherlands, the severity of morning stiffness and presence of autoantibodies were the strongest predictors of progression to RA . Spontaneous remission can be seen not only in early undifferentiated arthritis but in RA pregnancy and juvenile idiopathic arthritis (JIA) as well.
Pregnancy has a beneficial effect on the signs and symptoms of RA to the point at which patients can appear to have spontaneous remission of disease activity. Prospective studies have shown improvement in joint involvement in RA in two thirds to three quarters of pregnancies . Improvement occurs for 50% to 76% of patients by the end of the first trimester and is usually sustained throughout pregnancy. However, within 3 months of delivery, relapse is observed in 90% of patients . Most pregnant women with RA have an uneventful course with no significant complications. Except for slight intrauterine growth restriction in patients with active disease (3.36 vs 3.52 kg birth weight in matched controls; P = 0.01), the outcome of pregnancy is favorable in patients with RA .
In a nationwide prospective study, 84 pregnant RA patients were observed during each trimester and postpartum. DAS28 scores decreased significantly (P = 0.035) during pregnancy and increased postpartum. In patients with DAS greater than 3.2 (n = 52), about 48% had moderate improvement based on EULAR-defined response criteria. In patients with DAS greater than 2.6 and less than 3.2 (n = 32), disease activity was stable during pregnancy. Before conception, 10% of patients were in DAS28 remission (DAS28 < 2.6). The number of patients in remission increased during the first trimester to 17%, and 27% achieved DAS28 remission by the third trimester. However, only 18% were in remission by the 12th week postpartum. Thirty-nine percent of patients had a moderate flare postpartum. Less medication was used during pregnancy compared with before conception and postpartum. The authors showed that RA disease activity can improve during pregnancy but that not as many patients achieved disease remission as previously thought [37••].
Juvenile Inflammatory Arthritis
Spontaneous remission also has been reported in JIA (a heterogeneous group of childhood diseases that involve chronic idiopathic inflammation of one or more joints). JIA has three general subgroups: oligoarthritis, polyarthritis, and systemic disease. Frequencies of remission range from 29% to 78% depending on the subtype of disease, the definition of remission, and the study being reviewed .
The patterns of clinical remission within categories of JIA were studied in 437 JIA patients for at least 4 years. Patients were evaluated for episodes of inactive disease, clinical remission on medication, and clinical remission off medication. A total of 89% of patients (n = 391) experienced episodes of inactive disease with a median length of 12.7 months. Those with oligoarticular JIA (n = 258) spent 60% of their time in a state of inactive disease, whereas those with polyarticular or systemic JIA spent on average 30% to 36% of their time in a state of inactive disease. Twenty-six percent of patients (n = 228) had clinical remission off medication, with 68% of this group having oligoarticular JIA. Thirty-six percent of these episodes of remission off medication persisted for 2 years, but only 6% persisted for 5 years. This study shows that spontaneous remission in JIA is not as common and sustainable as previously reported and more likely to occur in the oligoarticular subtype .
RA is a complex inflammatory disorder with a wide spectrum of manifestations and outcomes ranging from mild, limited disease to severe, debilitating disease. We may be dealing with distinct diseases leading to different probabilities of remission. The exact etiology of RA is unknown, but further insights are being made continuously. New disease-modifying and biologic therapies are being introduced to suppress RA-associated inflammation. With more effective treatment options, the goal of treatment has become to achieve “remission.” Defining remission, however, has remained a challenge. With varying definitions of what constitutes remission, it is difficult to compare results of current drug trials and to know how to apply these results to clinical practice.
The current definitions of remission have major limitations. A patient can have tender and swollen joints and still meet most criteria for remission. Furthermore, it also has been shown that subclinical inflammation may be present on imaging despite the absence of clinical findings of disease activity, which could explain continuing joint damage despite a remission state. This continued progression of disease suggests that RA patients are not achieving true remission. If remission is defined as the complete absence of disease activity, these findings question whether remission is currently an achievable target. A more realistic treatment expectation in clinical practice may be to achieve minimal disease activity rather than complete absence of disease. Telling patients with RA that they are in remission may lead to periods of undertreatment and give patients (and physicians) a false sense of security, as patients are still at risk of developing deformities. With improved therapeutic management and medication development, perhaps remission can be a realistic goal in the future.
Many questions remain unanswered. Should remission be defined as the complete absence of disease, including signs, symptoms, inflammatory markers, and imaging? Should it apply to a moment in time or require a defined duration or permanent cure? Should remission permit treatment or require a drug-free state? As previously mentioned, a combined ACR and EULAR committee is attempting to redefine remission in RA and to reach a consensus as to how to apply the definition to clinical trials and practice. Many of these same questions were proposed and discussed. The committee concluded that the new definition should be strict, based on no or very low disease activity, and that remission should be defined independent of treatment, time course, and long-term outcomes such as radiographic damage. Variables deemed to be most important were tender joint count (with more joints being included), swollen joint count, and acute-phase reactants. A research agenda and subsequent meetings were planned to further investigate how to define remission [5••].
At the present time, when planning or evaluating RA therapeutic outcomes, it is important to carefully assess the precise definition of what is considered to be remission. A consensus definition of remission will help us evaluate outcomes of clinical trials and to establish treatment targets for practice.
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Dr. Ranganath is supported by ACR Research and Education Foundation Career Development Bridge funding awards and has received grant funding from the National Institutes of Health.
Dr. Paulus is supported by an ACR Research and Education Foundation Within Our Reach grant.
Dr. Ranganath has received gifts/grants from UCB, Roche, Amgen, and CycLex.
Dr. Paulus has served as a consultant for Amgen and has received grant support from Amgen and Abbott Laboratories. No other potential conflicts of interest relevant to this article were reported.
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