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The REAL study: a nationwide prospective study of rheumatoid arthritis in Brazil

Advances in Rheumatology volume 58, Article number: 9 (2018) Cite this article

Abstract

Background

There are few data on the epidemiology, clinical manifestations and management of RA in Brazil, even with the recognition of the high direct, indirect and societal costs of this disease. Herein, we report the formation of the REAL - Rheumatoid Arthritis in Real Life, the first nationally representative multicenter prospective observational study in Brazil.

Methods

The REAL study was designed to include a total of 1300 evaluable patients from 13 tertiary care public health centers specialized in RA management and representative of 5 regions of Brazil. Each center was expected to enroll ~ 100 consecutively seen patients and follow them prospectively in a systematic protocol-driven fashion with scheduled visits at baseline, 6 and 12 months. Core clinical, laboratory and patient-reported outcomes measures were required to be collected at each visit.

Results

A total of 1115 patients (89.4% female, mean age of 56.7 years and median disease duration of 12.7 years) were enrolled from 11 participating centers. Almost 80% of patients were of middle-low or low socioeconomic classes. The median educational time was 8 years, with 3.23% being below literacy level. The interval between symptoms and diagnosis varied from 1 to 457 months (median 12 months). Almost half of the patients were on glucocorticoids, 96.5% on DMARDs, with 35.7% on biologics. Median HAQ-DI was 0.875, ranging from 0 to 3. Median DAS28-ESR was 3.5, with 58.7% of patients presenting moderate or high disease activity.

Conclusions

The first large cohort of Brazilian patients with RA in a real-life setting shows several striking differences from previously published cohorts from other countries. The long delay for diagnosis and start of DMARDs may partly explain the high frequency of erosive disease. An elevated percentage of patients on moderate or high disease activity was seen, despite of the high frequency of corticosteroid and biologics utilization. Data from this cohort may enable public health managers of developing countries better allocate the limited resources available for the care of RA patients.

Background

Rheumatoid arthritis (RA) is a systemic, chronic and progressive disease, characterized by synovial inflammation of peripheral joints. Inadequate treatment often results in reduced health-related quality of life and excess mortality [1]. The current concept of RA management relies on early diagnosis, immediate initiation of a disease-modifying antirheumatic drug (DMARD) and effective suppression of inflammation [2]. Advances in diagnostic tools, the availability of new therapeutic options, mainly the biologic agents, and the adoption of a treat-to-target strategy have been of utmost importance for improving patient outcomes [3]. Despite all this progress, in many areas of the world, the diagnosis of RA is delayed and patients remain undertreated, resulting in great negative humanistic and socioeconomic impact [4, 5].

Brazil is the largest country in Latin America, with a multiethnic population of around 200 million inhabitants [6]. There are few data on the epidemiology and management of RA in Brazil, even with the recognition of the high direct, indirect and societal costs of this disease [7]. A better understanding of the profile of RA patients seen in public health care centers in Brazil can underpin public health policy, enabling a rational allocation of resources and the setting of priorities in this sector.

The REAL – Rheumatoid Arthritis in Real Life – is a multicenter prospective observational cohort study, with twelve-month follow-up period. The aims of this study were to describe the demographic, clinical and therapeutic features of Brazilian patients with RA, and to evaluate adherence to treatment, safety of pharmacologic treatment, and impact on quality of life, physical function and work capacity of these patients. In this first report of REAL study, we describe the methodology and the baseline characteristics of this cohort.

Methods

Setting

Thirteen tertiary care public healthcare centers (Appendix 1) specialized in RA management were selected to represent the five geographic regions in Brazil. Eventually, 11 centers from 4 regions enrolled in the program. The recruitment period started on August 12th, 2015 and ended on April 15th, 2016. Patients were followed for ~ 12 months, with systematic data collection at the initial visit (baseline), at the intermediate visit (6 months ±1 month) and at the final visit (12 months ±1 month), with additional descriptive report of any other unscheduled visit.

Participants

The inclusion criteria were 1) fulfillment of the 1987 American Rheumatism Association (ARA) or the 2010 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) classification criteria for rheumatoid arthritis [8, 9]; 2) age 18 years or older; and 3) documented medical record data of at least 6 months of follow up in their healthcare center prior to study enrollment.

Each center was expected to enroll ~ 100 patients consecutively. Since all centers were tertiary-care academic rheumatology practices, they were requested to limit the enrollment of biologic-treated patients to roughly the proportion of these patients being treated in their center.

Variables, data sources and data collection

Table 1 shows the study visit protocol, with all the items systematically evaluated and respective time of assessment. Most data were collected during the medical appointments, with previous medical records used as secondary sources. All data were collected on an electronic medical chart and gathered in a centralized dataset.

Table 1 Variables assessed in study visits
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Initial visit

At the initial visit the study physician formally assessed the RA classification criteria fulfillment and collected demographic and contact data, socioeconomic profile, family history of RA, other autoimmune diseases or associated conditions, personal history of comorbidities and lifestyle habits (smoking, alcohol consumption and physical activity). For the socioeconomic classification we used the Brazilian Economic Classification Criterion (BECC), a score system updated in 2015 that includes variables such as the number of household electrical appliances, level of education of the householder and access to public services [10]. The score range is stratified from A to D-E, with each stratum corresponding to an estimated household income (Table 2).

Table 2 Brazilian Economic Classification Criterion (BECC): relation between socioeconomic strata and estimated household income
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The study physician also assessed the following RA aspects: disease duration, time between symptoms onset and diagnosis, time to first DMARD prescription, health facility and physician specialty at first contact with healthcare due to RA symptoms, presence of extra-articular manifestations, positive rheumatoid factor (RF) and anti-citrullinated protein antibody (ACPA), and presence of bone erosions on radiographic study on both hands and feet. Erosive disease was defined when an erosion (defined as a cortical break) was seen in at least three separate joints at any of the following sites: the proximal interphalangeal, the metacarpophalangeal, the wrist (counted as one joint) and the metatarsophalangeal joints. In addition, prior pharmacologic treatments for RA were described (with respective reasons for discontinuation), history of orthopedic surgery and history of intra-articular or periarticular steroid injections.

Clinical evaluation included vital signs, anthropometric measures, tender and swollen joint counts, and physician score on the visual analogue scale (VAS) of disease activity. Patient reported outcomes included pain (VAS), global health (VAS), current and previous 6 months disease activity (VAS), fatigue (VAS), morning stiffness (VAS) and articular index, in which the patient evaluates the presence of pain and respective intensity in 16 joints. All laboratory tests, including erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were recorded. Compliance to prescribed medications as well as scheduled medical appointments and laboratory tests were also recorded.

The disease activity score-28 joints (DAS28), clinical disease activity index (CDAI), simplified disease activity index (SDAI) and the rheumatoid arthritis disease activity index (RADAI) were also calculated for each appointment [11,12,13].

The translated and validated versions of the Health Assessment Questionnaire-Disability Index (HAQ-DI), Short Form-12 (SF-12) and SF-6D evaluated, respectively, physical function, functional capacity and wellbeing, and health status from the patient’s perspective [14,15,16].

In this report, we summarize important demographic and clinical data at the baseline visit of all enrolled patients.

Intermediate and final visits

At the intermediate and the final visits, some variables from the medical history, such as change in the marital and employment status, onset of new extra-articular manifestations or comorbidities and medical intercurrences were reassessed. All the items within the physical exam domain, the patient reported outcomes, the lab tests ESR and CRP along with the disease activity indexes, were evaluated at the three scheduled visits (Table 1). Additionally, at the final visit, physicians were requested to describe their therapeutic plan.

Ethical aspects

This study was approved by the National Commission of Ethics in Research (CONEP - Comissão Nacional de Ética em Pesquisa) – Ministry of Health. The coordinating center was the Rio de Janeiro State University, and the approval number was 45781015.8.1001.5259. Each of the centers also obtained approval from the respective Institutional Review Boards. All patients signed the informed consent form.

Results

A total of 1115 patients were enrolled in the study. The general demographic and clinical data of the population at the time of the initial evaluation are presented in Tables 3 and 4. Approximately 90% were female, with a mean age of 56.7 years and median disease duration of 12.7 years. The majority of subjects were white, with minorities from Asian and Brazilian-Indian origins making up 1% of the sample. Almost 80% of patients were classified as pertaining to middle-low or low socioeconomic classes. Median BMI was 27 kg/m2, with 64% of the patients classified as overweight or obese. The median educational time was 8 years, with 3.23% being below literacy level. About 40% were either current or former smokers.

Table 3 Baseline demographic data of patients enrolled in the REAL study
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Table 4 Baseline clinical data of patients enrolled in the REAL study
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The interval between symptoms and diagnosis varied from 1 to 457 months (median 12 months). The gap between symptoms onset and first DMARD initiation was wider, ranging from 1 to 624 months, but the same median value of 12 months.

The seropositivity rate was similar between RF (78%) and ACPA (77%), but it is important to highlight that the latter was assessed in less than half of the patients.

Interestingly, similar numbers of patients fulfilled the ARA 1987 and the 2010 ACR-EULAR classification criteria for RA, with 80.8% of subjects meeting both criteria. All patients met at least one criteria.

Almost half of the patients were on glucocorticoids, 96.5% on DMARDs, with 35.7% on biologics. Of those on biologics (n = 398), 15.6% were on monotherapy.

Median HAQ-DI was 0.875, ranging from 0 to 3. Median DAS28-ESR was 3.5, with 58.7% of patients presenting moderate or high disease activity. When assessed by CDAI, the median score represented low disease activity (CDAI = 9), with 46.7% of subjects classified as presenting moderate to high disease activity.

Discussion

We describe the formation of the first large cohort of Brazilian patients with RA in a real-life setting, with consecutive enrollment of subjects and systematic data collection. The demographic, clinical, serological and radiographic characteristics of the patients being followed have several similar but some divergent characteristics from previously published North American, European and Latin American cohorts [17,18,19,20,21]. Particularly notable are the long delay for diagnosis, the high frequency of corticosteroid use and of erosive disease, as well as, the elevated percentage of patients on moderate or high disease activity. The high frequency of biologic DMARD use, considering the economic limitations in Brazil, is also remarkable. The fact that most patients were either RF or ACPA positive and had a delay in the initiation of DMARD may explain the observed high frequency (almost 60%) of moderate or high disease activity and erosive disease. The ethnic and socioeconomic class distribution reflects the Brazilian population in general, and is considerably different from other international cohorts [17,18,19,20,21,22]. It is important to note that the socioeconomic class distribution likely reflects the patients seen at the participating centers, which provide free health care within the Brazilian Public Health System -Sistema Único de Saúde (SUS). In Brazil, three quarters of the population is served by this public and free system, with the others using various private and paid health plans [23] and the latter were likely not represented to a significant degree in this study. About 11% of REAL patients were currently smokers, a number lower than that published in previous RA studies from other parts of the world (25–33%), but consistent with the relatively low rates of smoking in the Brazilian population (females: 8.2% and males: 12.6%) [24,25,26,27]. Subsequent publications will explore the relationship of these differences with clinical and outcome variables.

We recognize several limitations of the REAL study. All the sites enrolled in the study are “reference centers”, and thus are unlikely to represent the broader management of RA across the country. It is probable that these patients present more severe disease, with a less favorable prognosis. REAL study was designed to be representative of the entire Brazilian population, but one center in the Northeast (representing 27.9% of population) could not participate because of delays in the Ethics Committee approval. Also, our cohort does not include patients from among the 25% of Brazilian population receiving their healthcare outside of the public health system. On the other hand, the REAL study data reflects perhaps a more optimal standard of care possibly resulting in better outcomes in comparison with those treated in less prepared facilities. Further publications will study multiple management strategies and their effects on patient outcomes.

Conclusions

The first large cohort of Brazilian patients with RA in a real-life setting shows several striking differences from previously published cohorts from other countries. The long delay for diagnosis and start of DMARDs may partly explain the high frequency erosive disease. An elevated percentage of patients on moderate or high disease activity was seen, despite of the high frequency of corticosteroid and biologics utilization. Data from this cohort may enable public health managers of developing countries better allocate the limited resources available for the care of RA patients.

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Acknowledgements

Gurkirpal Singh, MD and Leticia Rocha provided technical and writing assistance.

Funding

This work was supported by the Brazilian Society of Rheumatology (BSR). For this project, BSR received specific grant support from the following companies: Bristol-Myers Squibb Farmacêutica Ltda; Eli Lilly do Brasil Ltda; Janssen-Cilag Farmacêuticos Ltda; Laboratórios Pfizer Ltda; Produtos Roche Químicos e Farmacêuticos S.A. and UCB Biopharma Ltda. The funding body or the companies had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Author information

Authors and Affiliations

  1. Departamento de Medicina Interna, Disciplina de Reumatologia, Universidade do Estado do Rio de Janeiro, Avenida Nossa Senhora de Copacabana, 978, sala 508, Copacabana, Rio de Janeiro, RJ, 22060-002, Brazil

    Geraldo da Rocha Castelar-Pinheiro

  2. Serviço de Reumatologia, Hospital Universitário Pedro Ernesto - Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

    Ana Beatriz Vargas-Santos

  3. Serviço de Reumatologia, Hospital Universitário de Brasília - Universidade de Brasília, Brasília, Brazil

    Cleandro Pires de Albuquerque & Licia Maria Henrique da Mota

  4. Disciplina de Reumatologia, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, Brazil

    Manoel Barros Bértolo

  5. Disciplina de Reumatologia, Faculdade de Medicina da Universidade de Ribeirao Preto, Universidade de Sao Paulo, Ribeirão Preto, Brazil

    Paulo Louzada Júnior

  6. Serviço de Reumatologia, Instituto de Assistência Médica ao Servidor Público Estadual, Hospital do Servidor Público Estadual de São Paulo, São Paulo, Brazil

    Rina Dalva Neubarth Giorgi

  7. Disciplina de Reumatologia, Faculdade de Medicina da Universidade Federal do Paraná, Universidade Federal do Paraná, Curitiba, Brazil

    Sebastião Cezar Radominski

  8. Serviço de Reumatologia, Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil

    Maria Fernanda B. Resende Guimarães

  9. Disciplina de Reumatologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil

    Karina Rossi Bonfiglioli

  10. Disciplina de Reumatologia, Faculdade de Medicina, Universidade Federal do Pará, Belém, Brazil

    Maria de Fátima Lobato da Cunha Sauma

  11. Serviço de Reumatologia, Hospital Universitário, Universidade Federal de Santa Catarina, Florianópolis, Brazil

    Ivânio Alves Pereira

  12. Serviço de Reumatologia, Departamento de Medicina Interna, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

    Claiton Viegas Brenol

  13. Departamento de Epidemiologia e Métodos Quantitativos em Saúde, Fundação Osvaldo Cruz, Rio de Janeiro, Brazil

    Evandro Silva Freire Coutinho

Authors
  1. Geraldo da Rocha Castelar-Pinheiro
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  2. Ana Beatriz Vargas-Santos
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  4. Manoel Barros Bértolo
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  5. Paulo Louzada Júnior
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  7. Sebastião Cezar Radominski
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  13. Evandro Silva Freire Coutinho
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  14. Licia Maria Henrique da Mota
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Contributions

All authors made substantial contributions to the acquisition of data, have been involved in drafting the manuscript or revising it critically for important intellectual content, gave final approval of the version to be published and have participated sufficiently in the work to take public responsibility for appropriate portions of the content; and agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

In addition, GRCP, ABVS and LMHM also made substantial contributions to conception and design of the study.

Corresponding author

Correspondence to Geraldo da Rocha Castelar-Pinheiro.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the National Commission of Ethics in Research (CONEP - Comissão Nacional de Ética em Pesquisa) – Ministry of Health. The coordinating center was the University of the State of Rio de Janeiro, and the approval number was 45781015.8.1001.5259. Each of the centers also obtained approval from the respective Institutional Review Boards. All patients signed the informed consent form.

Competing interests

GRCP: Has received consulting fees from AbbVie, Bristol-Myers Squibb, Eli Lilly, Glaxosmithkline, Janssen, Pfizer, Sanofi Genzyme and Roche; ABVS: Has received supporting for international medical events from AbbVie and Janssen; CPA: Has received personal fees and/or non-financial support from Pfizer, AbbVie, AstraZeneca, Janssen, Bristol-Myers Squibb, Roche, Novartis and UCB, outside the submitted work; MBB: Has participated in clinical and/or experimental studies related to this work and sponsored by Roche; has delivered speeches at events related to this work and sponsored by AbbVie and Pfizer; PLJ: Has received supporting for internationals congresses from Bristol-Myers Squibb, UCB and consulting fees from Pfizer; RDNG: Has received consulting fees, speaking fees and supporting for internationals congresses from Roche, Pfizer, Bristol-Myers Squibb, UCB, Eli-Lilly, AbbVie, Abbott and EMS; SCR: Has received consulting and speaking fees from Abbvie, Janssen, Pfizer, Roche and UCB; MFBRG: Has received speaking fees and supporting for congresses from AbbVie, Bristol-Myers Squibb, Janssen, Novartis, Pfizer, Roche and UCB; KRB: Has received speaking fees and supporting for international congresses from Roche, Pfizer, Bristol-Myers Squibb, Abbvie and Janssen; MFLCS: No financial disclosures; CVB: Has participated in clinical and/or experimental studies related to this work and sponsored by AbbVie, BMS, Janssen, Pfizer and Roche; has received personal or institutional support from AbbVie, BMS, Janssen, Pfizer and Roche; has delivered speeches at events related to this work and sponsored by AbbVie, Janssen, Pfizer and Roche; IAP: Has received consulting fees, speaking fees and supporting for internationals congresses from Roche, Pfizer, UCB Pharma, Eli-Lilly, Abbvie and Janssen; ESFC: No financial disclosures; LMHM: Has received personal or institutional support from AbbVie, Janssen, Pfizer and Roche; has delivered speeches at events related to this work and sponsored by AbbVie, Janssen, Pfizer, Roche and UCB.

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Appendix 1

Appendix 1

Table 5 Thirteen tertiary care public healthcare centers specialized in RA management representing the five geographic regions in Brazil
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da Rocha Castelar-Pinheiro, G., Vargas-Santos, A.B., de Albuquerque, C.P. et al. The REAL study: a nationwide prospective study of rheumatoid arthritis in Brazil. Adv Rheumatol 58, 9 (2018). https://doi.org/10.1186/s42358-018-0017-9

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Keywords

Advances in Rheumatology

ISSN: 2523-3106