Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation

Systemic autoinflammatory disorders (SAIDs) are a growing spectrum of diseases in which the innate immune system is dysregulated. After the new concept of autoinflammation was first introduced in 1999, various previously known diseases have been attributed to a new genetic background or newly identified as monogenic autoinflammatory diseases. In addition, diseases with a clearly defined clinical picture, such as systemic juvenile idiopathic arthritis (SJIA), have been associated with an autoinflammatory pathophysiology without a monogenic background. Moreover, about half of the patients with recurrent inflammation do not fit the clinical picture of any well-defined SAIDs or do not have pathogenic mutations causing known hereditary SAIDs [1, 2].

Patients with recurrent fever without molecular diagnosis can often be diagnosed as Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA) syndrome, the most common pediatric autoinflammatory fever syndrome, with a high incidence in children up to 5 years of age. PFAPA may last up to adulthood with symptoms followed for years [3‐7]. Clinical diagnostic criteria are well described for the disease [8].

Nevertheless, there is a number of patients that do not fulfil current diagnostic criteria of PFAPA and have variably been called as atypical PFAPA, undefined autoinflammatory disease or disorder, or syndrome of undifferentiated recurrent fever (SURF) [9]. Due to the rarity of SAIDs, clinical characteristics of such patients are not extensively described in the current literature [8, 10, 11].

It is still unclear, whether these patients represent autoinflammatory gene variants of known syndromes, complex genetic autoinflammatory disorders, or independent entities [9, 12]. But over the last few years, SURF definition was proposed as a heterogeneous group of autoinflammatory diseases characterized by the presence of self-limiting episodes of systemic inflammation with multiple clinical presentations, without confirmed molecular diagnosis. SURF is progressively more diagnosed in patients with recurrent fever after excluding the known hereditary recurrent fevers (HRF) and PFAPA syndrome [12].

Physicians face a variety of challenges when dealing with recurrent fever in children that can be caused by a number of different conditions, ranging from benign viral infections to more serious underlying medical conditions, as inborn errors of immunity, oncologic and autoimmune diseases. Awareness of autoinflammatory syndromes, in particular the diagnosis of PFAPA and SURF, as well as a better discrimination of both syndromes are essential for general paediatricians, paediatric rheumatologists, and even adult clinical immunologists.

The aim of this work was to analyse the evolution of symptoms in recurrent fevers without molecular diagnosis in the context of undifferentiated AIDs, with special regard to PFAPA and SURF, in three European AID-registries.

In a project endorsed by PReS, supported by the EMERGE fellowship program, and performed in line with the Metadata registry for the ERN RITA (MeRITA) project, we analysed the clinical characteristics of PFAPA, SURF and undefined systemic autoinflammatory disease (uSAID) patients in three registries, Eurofever, JIRcohort and AID-net, that collect and hold the information on SAIDs patients in Europe and in extra-European countries. In total, the 3 registries cover 7825 patients with different AIDs from 278 participating centres from different parts of the world with in-between country distribution as reported earlier [13]. AID-Net is a national registry involving 36 main pediatric rheumatology centers in Germany. JIR and Eurofever are multi-national cohorts, covering about 40 countries in total. Data collection in AID-Net was completed in 2018, but JIR and Eurofever continue active recruitment and follow-up on children previously included.

Data of patients with PFAPA, SURF and uSAID were collected from all 3 registries including detailed epidemiological, demographic and clinical data, results of the genetic testing and additional laboratory investigations, as well as treatment.

Patients of whom epidemiological and clinical information was available were included in this study. The diagnosis of the SAID – PFAPA, uSAID or SURF, was made by judgement of treating physician and exported from the registry. Extraction of the data and exclusion process was conducted separately for PFAPA and uSAID/SURF groups. Patients were excluded from further analysis if there was failure to complete information about clinical outcome of the disease. Patients carrying known pathogenic mutations, classifying them into group of other well-defined AIDs were excluded.

Requested clinical characteristics included disease manifestations, activity of the laboratory markers and genetic testing, if available; treatment was an optional part to be completed in registries. Clinical manifestations were reported by the corresponding physician in a different way through the registries but counted as “present” or “absent” within the study. Information on molecular genetic analyses was collected and classified according to pathogenicity. Only pathogenic or likely pathogenic variants were regarded to be an exclusion criterion.

Retrospectively, modified Marshall and PRINTO/Eurofever classification criteria were applied on the cohort of PFAPA patients [5, 6]. Preliminary case definition of SURF proposed by Papa et al. were applied for SURF and uSAID patients [12]. Evaluation of the extracted information was descriptive, more than comparative, as far as aggregated data from all three cohorts was not merged, yet analysed successively.

The management of pediatric or young adult patients with SAIDs poses significant challenges for healthcare professionals across multiple specialties, including paediatricians, rheumatologists, and adult clinical immunologists. Among the various autoinflammatory disorders, PFAPA syndrome stands out as a common and well-recognized clinical entity in the pediatric population, while hereditary fever disorders are less frequently diagnosed in the United States and Western Europe. Despite the existence of approved classification criteria for PFAPA, diagnosing this syndrome remains a considerable challenge. Since its initial description in 1987, PFAPA has often been misinterpreted as upper respiratory infections, leading to inappropriate treatment strategies, including unnecessary antibiotic prescriptions. The non-specific nature of PFAPA symptoms, such as recurrent fever, pharyngitis, and cervical adenopathy, complicates diagnosis, which is primarily based on the exclusion of other infectious and autoinflammatory diseases. As a result, definitive diagnosis is typically reserved for specialists with extensive experience in managing this patient population [14]. It is increasingly recognized that a subset of children presenting with non-infectious recurrent fever cannot be classified within existing diagnostic categories. These patients, often referred to as having uSAID or syndrome of SURF, pose unique challenges for clinical management. The current landscape of managing these patients is characterized by the need for updating definitions and classification categories to better characterize and understand this heterogeneous group [8, 12, 15, 16, 17]

The distinction between patients falling into the PFAPA category versus those categorized as uSAID/SURF presents a significant challenge, particularly when considering the clinical patterns and associated symptoms. While some patients may meet criteria for SURF due to variations in periodicity and symptomatology, they could alternatively be classified as PFAPA depending on the criteria used. Our study sheds light on this potential overlap and aims to elucidate the evolving nature of PFAPA and its relationship with uSAID/SURF. PFAPA patients that were evaluated through the registries performed incomplete response towards applied criteria, in which it demonstrated a separate group of non-responders that potentially may perform overlapping group with SURF (Fig. 3). PFAPA is a self-limiting disease that has a favourable prognosis. Usually, it resolves spontaneously before adolescence without impairment of growth and development, yet, with less knowledge about the long-term outcomes of this disease. There are very few data on the prognosis of PFAPA lasting up to adolescence and beyond [18‐22].

The re-evaluation of the patients enrolled in the three registries as PFAPA and undefined recurrent fever according to the available PFAPA clinical criteria or case definition for SURF prompted rather heterogeneous results. In routine clinical practice, the diagnosis of PFAPA is based on summary of clinical judgements – with stereotypical attacks and prompt steroid response. Conversely uSAID/SURF should be defined by the absence of clinical manifestation typical for PFAPA in the absence of pathogenic mutations for genes associated with inherited recurrent fever, display a good response to colchicine treatment [23]. Globally up to 67% of patients enrolled as PFAPA fulfilled at least one PFAPA criteria only and up to 77% patients enrolled as undefined recurrent fever fulfilled the preliminary case definition for SURF only. Conversely, up to 17% of PFAPA and up to 37% of patients enrolled as undefined recurrent fever patients fulfilled at least one criteria associated to the alternative condition. Finally, up to 19% of PFAPA and 35% of SURF patients did not fulfil any clinical criteria.

The heterogeneity observed among patients diagnosed with PFAPA and SURF in the registries underscores the need for further evaluation and differentiation within these groups. This diversity in clinical presentation raises concerns regarding the potential for misdiagnosis and highlights the importance of refining diagnostic criteria to better characterize these conditions. The phenotypic heterogeneity observed in our study suggests that the current diagnostic labels may not fully capture the spectrum of presentations seen in patients with recurrent fever syndromes. As such, there is a pressing need for more precise classification criteria that can accurately distinguish between different subtypes of autoinflammatory diseases. This study clearly shows the existence of a large gray zone of overlap between these two conditions, at least looking into the retrospective data of three large international registries.

Our study has several limitations that should be acknowledged. Firstly, most of the patients were enrolled in the registries before the development and the publication of the evidence-based Eurofever PFAPA criteria and the proposed case definition for SURF. This issue clearly explains the high phenotypic variability observed in the study, since the patients were enrolled in the registries according to the clinical diagnosis proposed by the enrolling centres. It should also be noted that the proposed case definition for SURF by PAPA et al. was not developed with an evidence-based approach comparing different conditions but simply derived from the critical revision of the literature. Additionally, the lack of prospective follow-up data limits our ability to draw definitive conclusions regarding therapeutic response and long-term outcomes.

Another relevant limitation of the present study was the lack of extensive genetic analysis in the entire population of included patients. Hence, genetic diagnosis might have been missed, due to the absence of the relevant genes testing. Genetic screening was often limited in this particular group of the patients for following reasons: large geographical distribution of the enrolling centres and limited availability of molecular screening; enrolment of the patients since 2009 before the availability of Next Generation Sequencing and routine use of gene panels; real-life diagnosing of PFAPA without genetic testing, based exclusively on clinical criteria.

Despite these limitations it should be underlined that a relevant number of patients with undefined autoinflammatory disease does not find a genetic definition even after an extensive genetic analysis with whole exome or genome sequencing [24]. The relevant number of patients presenting signs of undefined recurrent fevers, even after genetic testing, requires further evaluation and follow-up, that generally suggests a need for further discoveries in the field [7, 25]. The most important point for the clinician is to distinguish self-limiting disease from long-term conditions with high risk of damage and significant impact on future well-being of the patient. The development of evidence-based classification criteria for SURF based on the comparison of the most frequent causes of recurrent fever (PFAPA and inherited recurrent fevers) could help to identify a more homogeneous subset of patients with undefined recurrent fever; the acronym of uSAID may be more appropriate for patients without the criteria of PFAPA. In any case, patients whose clinical presentation is uncertain, recommended to be followed with gene panels of next generation sequencing and whole genome sequencing in case if the first one is negative [26, 27]. We want to stress the importance of the thorough diagnostic of patients with undefined autoinflammatory phenotype and if necessary, re-evaluate them with a time new information and updates are available. Such results potentially may improve treatment outcomes, as far most of defined SAIDs present favourable response to steroids, colchicine or IL1-blocking therapy [28‐30]. Contrary to the favourable effect observed in PFAPA to tonsillectomy, or aberrant effect of steroids, patients with undefined SAIDs rarely will perform the same response. But uSAID/SURF patients perform a favourable response to colchicine therapy, where in severe cases IL-1 therapy may dramatically resolve clinical presentation [31]. Early differentiation between these conditions will be beneficial for further follow-up management.

Further prospective studies are required to delineate fully the manifestations, diagnostic and treatment outcomes of children and adult patients with PFAPA and uSAID/SURF.

The study provides insights into the clinical heterogeneity of undefined recurrent fever through the analysis of data from three European AID registries, that aimed to unravel the evolving symptomatology of patients with undifferentiated AIDs, focusing on PFAPA and SURF. Our findings underscore the complexity of diagnosing and classifying patients with recurrent fevers without a clear genetic etiology with a significant proportion of patients did not fit neatly into existing diagnostic criteria for PFAPA or SURF, highlighting the need for refined classification criteria and updated definitions. The study elucidated a spectrum of clinical presentations among patients diagnosed with PFAPA, SURF/uSAID and revealed overlaps in symptomatology between groups, suggesting potential misclassification and emphasizing the importance of accurate diagnosis for tailored treatment strategies.

Finally, this study underscores the necessity of refining diagnostic criteria, updating classification categories, and improving our understanding of the clinical heterogeneity of autoinflammatory diseases. By addressing these challenges, we can advance patient care, enhance prognostic accuracy, and facilitate the development of targeted therapeutic interventions for individuals with recurrent fevers of unknown origin.