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  1. Article ; Online: Unveiling the clinical spectrum of relapsing polychondritis: insights into its pathogenesis, novel monogenic causes, and therapeutic strategies.

    Bica, Blanca E R G / de Souza, Alexandre Wagner S / Pereira, Ivânio Alves

    Advances in rheumatology (London, England)

    2024  Volume 64, Issue 1, Page(s) 29

    Abstract: Relapsing polychondritis is a rare multisystem disease involving cartilaginous and proteoglycan-rich structures. The diagnosis of this disease is mainly suggested by the presence of flares of inflammation of the cartilage, particularly in the ears, nose ... ...

    Abstract Relapsing polychondritis is a rare multisystem disease involving cartilaginous and proteoglycan-rich structures. The diagnosis of this disease is mainly suggested by the presence of flares of inflammation of the cartilage, particularly in the ears, nose or respiratory tract, and more rarely, in the presence of other manifestations. The spectrum of clinical presentations may vary from intermittent episodes of painful and often disfiguring auricular and nasal chondritis to an occasional organ or even life-threatening manifestations such as lower airway collapse. There is a lack of awareness about this disease is mainly due to its rarity. In 2020, VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome, a novel autoinflammatory syndrome, was described. VEXAS syndrome is attributed to somatic mutations in methionine-41 of UBA1, the major E1 enzyme that initiates ubiquitylation. This new disease entity connects seemingly unrelated conditions: systemic inflammatory syndromes (relapsing chondritis, Sweet's syndrome, and neutrophilic dermatosis) and hematologic disorders (myelodysplastic syndrome or multiple myeloma). Therefore, this article reviews the current literature on both disease entities.
    MeSH term(s) Humans ; Polychondritis, Relapsing/diagnosis ; Polychondritis, Relapsing/drug therapy ; Polychondritis, Relapsing/genetics ; Inflammation/complications ; Bone Diseases/complications
    Language English
    Publishing date 2024-04-16
    Publishing country England
    Document type Journal Article ; Review
    ISSN 2523-3106
    ISSN (online) 2523-3106
    DOI 10.1186/s42358-024-00365-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders.

    Salles Rosa Neto, Nilton / Pereira, Ivânio Alves / Sztajnbok, Flávio Roberto / Azevedo, Valderílio Feijó

    Advances in rheumatology (London, England)

    2024  Volume 64, Issue 1, Page(s) 32

    Abstract: Hereditary connective tissue disorders include more than 200 conditions affecting different organs and tissues, compromising the biological role of the extracellular matrix through interference in the synthesis, development, or secretion of collagen and/ ... ...

    Abstract Hereditary connective tissue disorders include more than 200 conditions affecting different organs and tissues, compromising the biological role of the extracellular matrix through interference in the synthesis, development, or secretion of collagen and/or its associated proteins. The clinical phenotype includes multiple signs and symptoms, usually nonspecific but of interest to rheumatologists because of musculoskeletal involvement. The patient´s journey to diagnosis is long, and physicians should include these disorders in their differential diagnoses of diseases with systemic involvement. In this review, insights for the diagnosis and treatment of osteogenesis imperfecta, hypermobility spectrum disorder/Ehlers-Danlos syndrome, Marfan, Loeys-Dietz, and Stickler syndromes are presented.
    MeSH term(s) Humans ; Osteogenesis Imperfecta/genetics ; Ehlers-Danlos Syndrome/genetics ; Ehlers-Danlos Syndrome/diagnosis ; Connective Tissue Diseases/genetics ; Connective Tissue Diseases/therapy ; Loeys-Dietz Syndrome/genetics ; Loeys-Dietz Syndrome/diagnosis ; Marfan Syndrome/genetics ; Marfan Syndrome/diagnosis ; Collagen/genetics ; Joint Instability/genetics ; Arthritis ; Hearing Loss, Sensorineural ; Retinal Detachment
    Chemical Substances Collagen (9007-34-5)
    Language English
    Publishing date 2024-04-25
    Publishing country England
    Document type Journal Article ; Review
    ISSN 2523-3106
    ISSN (online) 2523-3106
    DOI 10.1186/s42358-024-00373-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Lyme disease and Whipple's disease: a comprehensive review for the rheumatologist.

    Giardini, Henrique Ayres Mayrink / Neves, Fabricio Souza / Pereira, Ivanio Alves / Cordeiro, Rafael Alves

    Advances in rheumatology (London, England)

    2024  Volume 64, Issue 1, Page(s) 16

    Abstract: Despite their rarity, Lyme disease and Whipple's disease are of significant importance in rheumatology, as both can manifest as chronic arthritis, presenting challenges in the differential diagnosis of inflammatory arthropathies. In Lyme disease, ... ...

    Abstract Despite their rarity, Lyme disease and Whipple's disease are of significant importance in rheumatology, as both can manifest as chronic arthritis, presenting challenges in the differential diagnosis of inflammatory arthropathies. In Lyme disease, arthritis typically emerges as a late manifestation, usually occurring six months after the onset of erythema migrans. The predominant presentation involves mono- or oligoarthritis of large joints, with a chronic or remitting-recurrent course. Even with appropriate antimicrobial treatment, arthritis may persist due to inadequate immunological control triggered by the disease. In contrast, Whipple's disease may present with a migratory and intermittent seronegative poly- or oligoarthritis of large joints, preceding classic gastrointestinal symptoms by several years. Both disorders, particularly Whipple's disease, can be misdiagnosed as more common autoimmune rheumatic conditions such as rheumatoid arthritis and spondyloarthritis. Epidemiology is crucial in suspecting and diagnosing Lyme disease, as the condition is transmitted by ticks prevalent in specific areas of the United States, Europe, and Asia. On the contrary, the causative agent of Whipple's disease is widespread in the environment, yet invasive disease is rare and likely dependent on host genetic factors. In addition to erythema migrans in Lyme disease and gastrointestinal manifestations in Whipple's disease, neurological and cardiac involvement can further complicate the course of both. This article offers a comprehensive review of the epidemiological, pathophysiological, clinical, and therapeutic aspects of both diseases.
    MeSH term(s) Humans ; Rheumatologists ; Whipple Disease/diagnosis ; Whipple Disease/drug therapy ; Lyme Disease/diagnosis ; Lyme Disease/drug therapy ; Lyme Disease/epidemiology ; Arthritis, Rheumatoid ; Erythema
    Language English
    Publishing date 2024-03-04
    Publishing country England
    Document type Journal Article ; Review
    ISSN 2523-3106
    ISSN (online) 2523-3106
    DOI 10.1186/s42358-024-00359-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: IgG4-related disease-rare but you should not forget it.

    Pinheiro, Frederico Augusto Gurgel / Pereira, Ivanio Alves / de Souza, Alexandre Wagner Silva / Giardini, Henrique Ayres Mayrink / Cordeiro, Rafael Alves

    Advances in rheumatology (London, England)

    2024  Volume 64, Issue 1, Page(s) 35

    Abstract: Immunoglobulin G4-related disease is a systemic immune-mediated disease with insidious evolution characterized by fibroinflammatory lesions over virtually any organ system. Despite the remarkable progression of knowledge, its etiology remains undefined. ... ...

    Abstract Immunoglobulin G4-related disease is a systemic immune-mediated disease with insidious evolution characterized by fibroinflammatory lesions over virtually any organ system. Despite the remarkable progression of knowledge, its etiology remains undefined. Due to its relapse-remitting pattern, it could accumulate irreversible damage, increasing comorbidities and mortality. This paper emphasizes key concepts for diagnosing and treating patients with this condition.
    MeSH term(s) Humans ; Immunoglobulin G4-Related Disease/diagnosis ; Immunoglobulin G4-Related Disease/complications ; Rare Diseases ; Immunoglobulin G/blood
    Chemical Substances Immunoglobulin G
    Language English
    Publishing date 2024-05-03
    Publishing country England
    Document type Journal Article ; Review
    ISSN 2523-3106
    ISSN (online) 2523-3106
    DOI 10.1186/s42358-024-00374-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Rheumatoid arthritis: why to treat only arthritis, knowing that comorbidities are common and determine morbidity and mortality?

    Pereira, Ivânio Alves

    Revista brasileira de reumatologia

    2012  Volume 52, Issue 4, Page(s) 472–473

    MeSH term(s) Arthritis/drug therapy ; Arthritis, Rheumatoid/drug therapy ; Arthritis, Rheumatoid/epidemiology ; Comorbidity ; Humans
    Language Portuguese
    Publishing date 2012-08
    Publishing country Brazil
    Document type Editorial
    ISSN 1809-4570
    ISSN (online) 1809-4570
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Envolvimento ocular nas doenças reumáticas.

    Pereira, Ivânio Alves

    Revista brasileira de reumatologia

    2011  Volume 44, Issue 2, Page(s) 160–167

    Title translation Ocular involvement in patients with rheumatic diseases.
    Language Portuguese
    Publishing date 2011-04-15
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 2223192-4
    ISSN 1809-4570 ; 0482-5004
    ISSN (online) 1809-4570
    ISSN 0482-5004
    DOI 10.1590/s0482-50042004000200010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Artrite reumatoide

    Ivânio Alves Pereira

    Revista Brasileira de Reumatologia, Vol 52, Iss 4, Pp 472-

    por que tratar apenas a artrite, sabendo que comorbidades são comuns e determinam morbidade e mortalidade? Rheumatoid arthritis: why to treat only arthritis, knowing that comorbidities are common and determine morbidity and mortality?

    2012  Volume 473

    Keywords Diseases of the musculoskeletal system ; RC925-935 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language Portuguese
    Publishing date 2012-08-01T00:00:00Z
    Publisher Sociedade Brasileira de Reumatologia
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Interferon III-related IL28RA variant is associated with rheumatoid arthritis and systemic lupus erythematosus and specific disease sub-phenotypes.

    Drehmer, Manuela Nunes / Castro, Gabriel Vaisam / Pereira, Ivanio Alves / de Souza, Ilíada Rainha / Löfgren, Sara Emelie

    International journal of rheumatic diseases

    2020  Volume 24, Issue 1, Page(s) 49–55

    Abstract: Background: The interferon pathways have been commonly implicated in autoimmune disease development but the identity of the genes involved has not yet been fully clarified. Variation in genes involved in interferon pathways is expected to have a role in ...

    Abstract Background: The interferon pathways have been commonly implicated in autoimmune disease development but the identity of the genes involved has not yet been fully clarified. Variation in genes involved in interferon pathways is expected to have a role in the etiology of these diseases.
    Methods: The potential association of a polymorphism in the IL28RA gene, involved in these pathways, with susceptibility to systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) and disease-related phenotypes was investigated in 603 Brazilian individuals (354 well-characterized SLE and RA patients, and 249 controls). IL28RA (rs4649203) variant was genotyped by TaqMan assay. Statistical analysis was performed including both diseases and a comprehensive list of patient clinical manifestations.
    Results: The rs4649203-G (minor) allele was associated with SLE and RA occurrence and was shown to be a risk factor for serositis and anemia among SLE patients as well as a protective factor for rheumatoid vasculitis and rheumatoid nodules in RA patients, suggesting an association with a milder form of the disease.
    Conclusions: The IL28RA gene may contribute to SLE and RA susceptibility and to specific clinical manifestations of the diseases.
    MeSH term(s) Adolescent ; Adult ; Arthritis, Rheumatoid/diagnosis ; Arthritis, Rheumatoid/genetics ; Arthritis, Rheumatoid/immunology ; Case-Control Studies ; Disease Progression ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Humans ; Lupus Erythematosus, Systemic/diagnosis ; Lupus Erythematosus, Systemic/genetics ; Lupus Erythematosus, Systemic/immunology ; Male ; Phenotype ; Polymorphism, Single Nucleotide ; Receptors, Interferon/genetics ; Risk Assessment ; Risk Factors ; Young Adult
    Chemical Substances IFNLR1 protein, human ; Receptors, Interferon
    Language English
    Publishing date 2020-12-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 2426924-4
    ISSN 1756-185X ; 1756-1841
    ISSN (online) 1756-185X
    ISSN 1756-1841
    DOI 10.1111/1756-185X.14015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Resumos dos trabalhos brasileiros apresentados no Congresso do Colégio Americano de Reumatologia (ACR) 2004 Abstracts of the Brazilian studies presented at the American Collese of Rheumatology (ACR) 2004

    Ivânio Alves Pereira

    Revista Brasileira de Reumatologia, Vol 44, Iss 6, Pp 486-

    2004  Volume 503

    Keywords Diseases of the musculoskeletal system ; RC925-935 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language Portuguese
    Publishing date 2004-12-01T00:00:00Z
    Publisher Sociedade Brasileira de Reumatologia
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Envolvimento ocular nas doenças reumáticas Ocular involvement in patients with rheumatic diseases

    Ivânio Alves Pereira

    Revista Brasileira de Reumatologia, Vol 44, Iss 2, Pp 160-

    2004  Volume 167

    Keywords Diseases of the musculoskeletal system ; RC925-935 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Internal medicine ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language Portuguese
    Publishing date 2004-04-01T00:00:00Z
    Publisher Sociedade Brasileira de Reumatologia
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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