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  1. Article ; Online: Comparing clinical features between males and females with VEXAS syndrome: data from literature analysis of patient reports.

    Echerbault, Robin / Bourguiba, Rim / Georgin-Lavialle, Sophie / Lavigne, Christian / Ravaiau, Camille / Lacombe, Valentin

    Rheumatology (Oxford, England)

    2024  

    Abstract: Objectives: VEXAS syndrome is an autoinflammatory disease associated with a somatic mutation of the X-linked UBA1 gene in haematopoietic progenitor cells. This disorder was originally described as a disease affecting men, but rare cases of VEXAS ... ...

    Abstract Objectives: VEXAS syndrome is an autoinflammatory disease associated with a somatic mutation of the X-linked UBA1 gene in haematopoietic progenitor cells. This disorder was originally described as a disease affecting men, but rare cases of VEXAS syndrome in women have since been reported. The theoretical existence of phenotypic sex differences in this X-linked disease is debated. We compared the features of VEXAS syndrome between males and females to better understand this disorder and to improve its diagnostic accuracy in females.
    Methods: From previously published clinical descriptions of VEXAS syndrome, we included studies that described patients with precise, individual VEXAS-related features. We formed a literature-based cohort of patients by collecting their clinical and biological data and compared the characteristics of male and female patients.
    Results: We gathered 224 patient descriptions from 104 articles: 9 women and 215 men. Among the women, 1 had a constitutional 45, X karyotype and 4 had an acquired X monosomy in the bone marrow karyotype, while the marrow karyotype was not provided for the others. No difference was observed in the clinical or biological features according to sex. We also observed no difference in the type of UBA1 mutation or the association with myelodysplastic syndrome.
    Conclusions: Our results supported that UBA1 mutation should be sought under the same conditions in both sexes. As UBA1 is not subject to X-chromosome inactivation, VEXAS syndrome in females requires both UBA1 mutation and X monosomy, thus explaining the similarity between male and female VEXAS-related features and the lower prevalence of VEXAS syndrome in females.
    Language English
    Publishing date 2024-02-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 1464822-2
    ISSN 1462-0332 ; 1462-0324
    ISSN (online) 1462-0332
    ISSN 1462-0324
    DOI 10.1093/rheumatology/keae123
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Malignant Peritoneal Mesothelioma Complicating Familial Mediterranean Fever on 18 F-FDG PET/CT.

    Fayand, Antoine / Kerrou, Khaldoun / Wendum, Dominique / Grateau, Gilles / Georgin-Lavialle, Sophie

    Clinical nuclear medicine

    2024  Volume 49, Issue 3, Page(s) e123–e124

    Abstract: Abstract: A 77-year-old man with a personal history of familial Mediterranean fever presented with a slowly enlarging tumefaction of the left abdominal wall and persistent inflammatory syndrome despite good adherence to colchicine. 18 F-FDG PET/CT ... ...

    Abstract Abstract: A 77-year-old man with a personal history of familial Mediterranean fever presented with a slowly enlarging tumefaction of the left abdominal wall and persistent inflammatory syndrome despite good adherence to colchicine. 18 F-FDG PET/CT showed a hypermetabolic muscular mass of the abdominal wall along with other hypermetabolic lesions including a peritoneal mass and several subcutaneous soft tissue nodules. CT-guided needle biopsy led to the diagnosis of a muscular localization of a malignant peritoneal mesothelioma, which is an extremely rare complication of familial Mediterranean fever. Six courses of chemotherapy with carboplatin and pemetrexed allowed an almost complete response.
    MeSH term(s) Male ; Humans ; Aged ; Familial Mediterranean Fever/complications ; Familial Mediterranean Fever/diagnostic imaging ; Familial Mediterranean Fever/drug therapy ; Positron Emission Tomography Computed Tomography ; Mesothelioma/complications ; Mesothelioma/diagnostic imaging ; Fluorodeoxyglucose F18 ; Mesothelioma, Malignant/complications ; Peritoneal Neoplasms/complications ; Peritoneal Neoplasms/diagnostic imaging ; Peritoneal Neoplasms/pathology
    Chemical Substances Fluorodeoxyglucose F18 (0Z5B2CJX4D)
    Language English
    Publishing date 2024-01-24
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 197628-x
    ISSN 1536-0229 ; 0363-9762
    ISSN (online) 1536-0229
    ISSN 0363-9762
    DOI 10.1097/RLU.0000000000005041
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Efficacy of canakinumab for mosaic tumor necrosis factor receptor associated periodic syndrome.

    Terré, Alexandre / Vautier, Mathieu / Kahn, Jean-Emmanuel / Georgin-Lavialle, Sophie / Boursier, Guilaine

    European journal of internal medicine

    2024  

    Language English
    Publishing date 2024-02-01
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 1038679-8
    ISSN 1879-0828 ; 0953-6205
    ISSN (online) 1879-0828
    ISSN 0953-6205
    DOI 10.1016/j.ejim.2024.01.034
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Diagnosis traps for patients with acquired NLRP3 mutation.

    Cescato, Margaux / Cuisset, Laurence / Le Corre, Laurent / Rodero, Mathieu P / Georgin-Lavialle, Sophie

    European journal of internal medicine

    2024  

    Language English
    Publishing date 2024-03-20
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 1038679-8
    ISSN 1879-0828 ; 0953-6205
    ISSN (online) 1879-0828
    ISSN 0953-6205
    DOI 10.1016/j.ejim.2024.01.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Waldenstrom macroglobulinaemia with AA amyloidosis reveals a B-cell-restricted NLRP2 variant.

    Terré, Alexandre / Buob, David / Cez, Alexandre / Rodero, Mathieu P / Georgin-Lavialle, Sophie

    British journal of haematology

    2024  

    Language English
    Publishing date 2024-03-10
    Publishing country England
    Document type Letter
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.19383
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Physical fitness in adolescent patients with familial Mediterranean fever.

    Elhani, Inès / Heydacker, Pascal / Tavernier, Anne-Sophie / Georgin-Lavialle, Sophie / Hentgen, Véronique

    Rheumatology international

    2024  

    Abstract: Introduction: Familial Mediterranean fever (FMF) is the most frequent monogenic auto-inflammatory disease worldwide responsible for episodes of fever, serositis and musculoskeletal symptoms. Inflammatory attacks are responsible for sedentary behavior ... ...

    Abstract Introduction: Familial Mediterranean fever (FMF) is the most frequent monogenic auto-inflammatory disease worldwide responsible for episodes of fever, serositis and musculoskeletal symptoms. Inflammatory attacks are responsible for sedentary behavior and FMF patients may be at increased cardiovascular risk. Cardiorespiratory Fitness (CRF) and physical capacities during adolescence are associated with cardiovascular mortality in adulthood. In this study, we aimed to describe the physical fitness of FMF adolescents.
    Methods: A monocentric retrospective study at the Versailles Hospital between January 2020 and June 2023. All FMF patients over 14-year-old who had completed a routine physical test were included. Clinical and physical data including results of the 6-minute walking test, timed unipedal stance test, Ruffier-Dickson index, 30-seconds chair-stand test and sit-and-reach test were extracted from medical records. Results were compared with previously published normative reference values and criterion-referenced standards for healthy subjects.
    Results: Eighteen FMF patients (12 girls, 6 boys) were included. The median age was 16 years old [14-18]. Clinical history included joint symptoms (n = 11), chest pleuritis (n = 8), and leg pain (n = 11). Estimated VO2max was below the recommended thresholds in 13 patients, which predicts cardiovascular risk. Cardiovascular adaptation was poor in 11 patients. Low VO2max was associated with CRP > 5 mg/l on test day and history of joint symptoms.
    Conclusion: FMF patients displayed altered physical capacities compared to normative values of healthy subjects. History of musculoskeletal pain, systemic inflammation and sedentary behavior may participate in impaired physical abilities and promote cardiovascular diseases in adulthood. Specific exercise programs could benefit patients for disease control and cardiovascular risk reduction.
    Language English
    Publishing date 2024-04-24
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 8286-7
    ISSN 1437-160X ; 0172-8172
    ISSN (online) 1437-160X
    ISSN 0172-8172
    DOI 10.1007/s00296-024-05598-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Commentary: 'Case Report: A Rare Case of Elderly-Onset Adult Onset Still's Disease in a Patient With Systemic Lupus Erythematous'.

    Delplanque, Marion / Mekinian, Arsène / Georgin-Lavialle, Sophie

    Frontiers in immunology

    2022  Volume 13, Page(s) 876477

    MeSH term(s) Adult ; Aged ; Humans ; Immunotherapy ; Lupus Erythematosus, Systemic/complications ; Lupus Erythematosus, Systemic/diagnosis ; Still's Disease, Adult-Onset/complications ; Still's Disease, Adult-Onset/diagnosis
    Language English
    Publishing date 2022-04-07
    Publishing country Switzerland
    Document type Journal Article ; Comment
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.876477
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Response letter to "Latent class analysis of 216 patients with adult-onset Still's disease" by Sugiyama et al.

    Delplanque, Marion / Mekinian, Arsène / Georgin-Lavialle, Sophie

    Arthritis research & therapy

    2022  Volume 24, Issue 1, Page(s) 285

    Abstract: Sugiyama et al. recently described in "Latent class analysis of 216 patients with adult-onset Still's disease," baseline characteristics, laboratory tests, treatment, relapse, and death of adult-onset Still's disease (AOSD) patients from a Japanese ... ...

    Abstract Sugiyama et al. recently described in "Latent class analysis of 216 patients with adult-onset Still's disease," baseline characteristics, laboratory tests, treatment, relapse, and death of adult-onset Still's disease (AOSD) patients from a Japanese hospital. They identified two subgroups: Class 1 (n=155) with a younger age and typical symptoms of AOSD and Class 2 (n=61) with older patients and fewer typical symptoms of AOSD. In 2022, VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome, an established X-linked disease associated with a somatic mutation in UBA1, is considered as a differential diagnosis for AOSD particularly in elderly. These patients from Class 2 could benefit from more explorations for mild myelodysplasia and VEXAS.
    MeSH term(s) Adult ; Humans ; Aged ; Still's Disease, Adult-Onset/diagnosis ; Still's Disease, Adult-Onset/genetics ; Latent Class Analysis ; Myelodysplastic Syndromes/complications ; Syndrome
    Language English
    Publishing date 2022-12-28
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 2107602-9
    ISSN 1478-6362 ; 1478-6354
    ISSN (online) 1478-6362
    ISSN 1478-6354
    DOI 10.1186/s13075-022-02984-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Break down the barriers of auto-inflammation: How to deal with a monogenic auto-inflammatory disease and immuno-haematological features in 2022?

    Vergneault, Hélène / Picard, Capucine / Georgin-Lavialle, Sophie

    Immunology

    2022  Volume 168, Issue 1, Page(s) 1–17

    Abstract: In the past few years, the spectrum of monogenic systemic auto-inflammatory diseases (MSAID) has widely expanded beyond the typical recurrent fever. Immuno-haematological features, as cytopenias, hypogammaglobulinemia, hypereosinophilia, ... ...

    Abstract In the past few years, the spectrum of monogenic systemic auto-inflammatory diseases (MSAID) has widely expanded beyond the typical recurrent fever. Immuno-haematological features, as cytopenias, hypogammaglobulinemia, hypereosinophilia, lymphoproliferation and immunodeficiency, have been described in association of several MSAID. The objective of this review was to describe these particular MSAID. MSAID must be suspected in front of immuno-haematological features associated with non-infectious recurrent fever, chronic systemic inflammation, inflammatory cutaneous manifestations, arthritis or inflammatory bowel disease. Genes and cellular mechanisms involved are various but some of them are of special interest. Defects in actine regulation pathway are notably associated with cytopenia and immune deficiency. Because of their frequency, ADA2 deficiency and Vacuoles, E1-Enzyme, X-linked, auto-inflammatory, Somatic (VEXAS) syndrome deserve to be noticed. ADA2 deficiency results in polyarteritis nodosa-like presentation with a wide panel of manifestations including cytopenia(s), lymphoproliferation and immune deficiency. Neutrophilic dermatosis or chondritis associated with macrocytic anaemia or myelodysplasia should lead to screen for VEXAS. Of note, most of MSAID are associated with inflammatory anaemia. We proposed here a clinical and pragmatic approach of MSAID associated with immuno-haematological features.
    MeSH term(s) Humans ; Adenosine Deaminase/genetics ; Intercellular Signaling Peptides and Proteins/genetics ; Inflammation ; Immunologic Deficiency Syndromes/genetics ; Mutation
    Chemical Substances Adenosine Deaminase (EC 3.5.4.4) ; Intercellular Signaling Peptides and Proteins
    Language English
    Publishing date 2022-10-03
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 80124-0
    ISSN 1365-2567 ; 0019-2805 ; 0953-4954
    ISSN (online) 1365-2567
    ISSN 0019-2805 ; 0953-4954
    DOI 10.1111/imm.13579
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Vivre avec une amylose AL.

    Georgin-Lavialle, Sophie / Marciano, Sebastian

    La Revue du praticien

    2020  Volume 70, Issue 5, Page(s) 525–526

    Title translation Living with AL amyloidosis.
    MeSH term(s) Amyloidosis/diagnosis ; Humans ; Immunoglobulin Light-chain Amyloidosis/diagnosis
    Language French
    Publishing date 2020-10-15
    Publishing country France
    Document type Journal Article
    ZDB-ID 205365-2
    ISSN 2101-017X ; 0035-2640
    ISSN (online) 2101-017X
    ISSN 0035-2640
    Database MEDical Literature Analysis and Retrieval System OnLINE

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