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  1. Article: ACPA Antibodies Titer at the Time of Rheumatoid Arthritis Diagnosis Is Not Associated with Disease Severity.

    Shpatz, Rotem / Braun-Moscovici, Yolanda / Balbir-Gurman, Alexandra

    The Israel Medical Association journal : IMAJ

    2021  Volume 23, Issue 10, Page(s) 646–650

    Abstract: Background: Rheumatoid arthritis (RA) is a chronic inflammatory and destructive joint disease with the presence of autoantibodies, rheumatoid factor (RF), and anti-citrullinated protein antibodies (ACPA). The presence of RF or ACPA predicts RA severity. ...

    Abstract Background: Rheumatoid arthritis (RA) is a chronic inflammatory and destructive joint disease with the presence of autoantibodies, rheumatoid factor (RF), and anti-citrullinated protein antibodies (ACPA). The presence of RF or ACPA predicts RA severity. Data on the influence of ACPA titer on RA course are limited.
    Objectives: To determine the correlation between ACPA titers at the time of RA diagnosis to RA features and severity during 3 years of follow-up.
    Methods: We performed a retrospective study of RA patients treated at our institution during the years 2006-2015 with known ACPA titers at RA diagnosis who completed at least 3 years of follow-up. Patients (N=133) were divided according to ACPA titer: seronegative (< 15 U/ml, n=55), weakly positive (15-49 U/ml, n=18), moderately positive (50-300 U/ml, n=29), and strongly positive (> 300 U/ml, n=31). Patient data, including disease activity score (DAS28), bone erosion on hand and/or foot X-rays, treatments with corticosteroids and disease-modifying-anti-rheumatic drugs (DMARDs), and hospitalizations, were recorded. Chi-square and Mann-Whitney method were used for statistical analysis. P < 0.05 was considered as statistically significant.
    Results: Male gender, smoking, and RF positivity correlated with ACPA positivity and higher ACPA titers. There was no correlation between ACPA titer and the variables defined as representing RA severity: higher DAS28, bone erosions, hospitalizations, need for corticosteroids, and conventional and biological DMARDs.
    Conclusions: Titer of ACPA was not identified as a predictive factor for RA severity.
    MeSH term(s) Adrenal Cortex Hormones/therapeutic use ; Anti-Citrullinated Protein Antibodies/blood ; Antirheumatic Agents/therapeutic use ; Arthritis, Rheumatoid/diagnosis ; Arthritis, Rheumatoid/drug therapy ; Arthritis, Rheumatoid/epidemiology ; Arthritis, Rheumatoid/immunology ; Correlation of Data ; Disease Progression ; Female ; Humans ; Israel/epidemiology ; Male ; Middle Aged ; Monitoring, Immunologic/methods ; Monitoring, Immunologic/statistics & numerical data ; Negative Results ; Patient Acuity ; Predictive Value of Tests ; Prognosis ; Radiography/methods ; Radiography/statistics & numerical data ; Retrospective Studies ; Rheumatoid Factor/blood ; Severity of Illness Index
    Chemical Substances Adrenal Cortex Hormones ; Anti-Citrullinated Protein Antibodies ; Antirheumatic Agents ; Rheumatoid Factor (9009-79-4)
    Language English
    Publishing date 2021-10-21
    Publishing country Israel
    Document type Journal Article
    ZDB-ID 2008291-5
    ISSN 1565-1088 ; 0021-2180
    ISSN 1565-1088 ; 0021-2180
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  2. Article ; Online: Is cyclophosphamide still the gold standard in early severe rapidly progressive systemic sclerosis?

    Campochiaro, Corrado / Allanore, Yannick / Braun-Moscovici, Yolanda / Matucci-Cerinic, Marco / Balbir-Gurman, Alexandra

    Autoimmunity reviews

    2023  Volume 23, Issue 1, Page(s) 103439

    Abstract: Cyclophosphamide (CYC) has been a gold standard of treatment for severe progressive Systemic Sclerosis (SSc), especially in patients with concomitant interstitial lung disease (ILD). This approach was based on results of several interventional studies, ... ...

    Abstract Cyclophosphamide (CYC) has been a gold standard of treatment for severe progressive Systemic Sclerosis (SSc), especially in patients with concomitant interstitial lung disease (ILD). This approach was based on results of several interventional studies, including randomized control trials, which mainly addressed SSc-ILD as a primary end point and skin involvement as a second one. The use of CYC is time-limited due to significant adverse events. More recently, other immunosuppressive and biological agents showed efficacy but better safety profile in patients with SSc and SSc-ILD. With regards to other end-points, post-hoc analyses, systematic reviews and metalysis showed that CYC had limited influence on patients' quality of life, event-free survival and mortality. Comprehensive patient's stratification according to a molecular, cellular and phenotypic pattern may help in choosing of personalized medicine with more ambitious treatment effect and should be the future direction. According to the above available data and even if scientific evidence may be missing, experts' opinion has changed the attitude to CYC as an anchor drug in the management of severe SSc. Indeed, CYC has been pushed to the second and even third treatment option after mycophenolate mofetil, tocilizumab or rituximab. This position became obvious during debate on this topic at CORA meeting 2023.
    MeSH term(s) Humans ; Cyclophosphamide/therapeutic use ; Immunosuppressive Agents/therapeutic use ; Lung Diseases, Interstitial/etiology ; Lung Diseases, Interstitial/complications ; Quality of Life ; Scleroderma, Diffuse/chemically induced ; Scleroderma, Diffuse/complications ; Scleroderma, Diffuse/drug therapy ; Scleroderma, Systemic/complications
    Chemical Substances Cyclophosphamide (8N3DW7272P) ; Immunosuppressive Agents
    Language English
    Publishing date 2023-09-09
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2144145-5
    ISSN 1873-0183 ; 1568-9972
    ISSN (online) 1873-0183
    ISSN 1568-9972
    DOI 10.1016/j.autrev.2023.103439
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  3. Article ; Online: Clinical Images: The appearance of scurvy on magnetic resonance imaging.

    Giryes, Sami / Militianu, Daniela / Braun-Moscovici, Yolanda

    Arthritis & rheumatology (Hoboken, N.J.)

    2021  Volume 74, Issue 2, Page(s) 222

    MeSH term(s) Adult ; Female ; Humans ; Magnetic Resonance Imaging ; Scurvy/diagnostic imaging
    Language English
    Publishing date 2021-12-21
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.41932
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  4. Article: COVID-19 Infection in an Immunosuppressed Patient with Arthritis.

    Braun-Moscovici, Yolanda / Zisman, Devy / Balbir-Gurman, Alexandra

    The Israel Medical Association journal : IMAJ

    2020  Volume 22, Issue 8, Page(s) 523–524

    MeSH term(s) Antirheumatic Agents/therapeutic use ; Arthritis/complications ; Arthritis/drug therapy ; COVID-19/diagnosis ; COVID-19/therapy ; Female ; Humans ; Immunocompromised Host ; Middle Aged ; SARS-CoV-2
    Chemical Substances Antirheumatic Agents
    Language English
    Publishing date 2020-11-25
    Publishing country Israel
    Document type Case Reports ; Journal Article
    ZDB-ID 2008291-5
    ISSN 1565-1088 ; 0021-2180
    ISSN 1565-1088 ; 0021-2180
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  5. Article ; Online: Development and validation of Hebrew version of the UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract Instrument 2.0.

    Ozeri, David / Peretz, Shani / Oppenheim, Amit / Watad, Abdallah / Lidar, Merav / Braun-Moscovici, Yolanda

    Journal of scleroderma and related disorders

    2022  Volume 8, Issue 1, Page(s) 31–35

    Abstract: Aim: The aim of this study was to test the reliability of the University of California, Los Angeles Scleroderma Clinical Trial Consortium Gastrointestinal Tract (UCLA SCTC GIT) 2.0 questionnaire in Hebrew.: Methods: UCLA SCTC GIT 2.0 was translated ... ...

    Abstract Aim: The aim of this study was to test the reliability of the University of California, Los Angeles Scleroderma Clinical Trial Consortium Gastrointestinal Tract (UCLA SCTC GIT) 2.0 questionnaire in Hebrew.
    Methods: UCLA SCTC GIT 2.0 was translated into Hebrew using the translation-retranslation method. The Hebrew version of the UCLA SCTC GIT 2.0 and the Hebrew version of the Short Form 36 (SF-36) were administered to 19 Hebrew-speaking patients with systemic sclerosis. Internal reliability was assessed using Cronbach's alpha. The Hebrew questionnaire was then tested for external validity using Spearman's correlation coefficient. Correlations (
    Results: A group of 19 patients treated at Sheba Medical Center meeting the ACR/EULAR classification system for systemic sclerosis were included in the study. The mean age of the participants was 60.4 ± 12 years with a female predominance (84%). Diffuse cutaneous scleroderma accounted for 10 of the participants (54%), 7 had limited cutaneous scleroderma (36%) with 2 having an overlap syndrome (10%). The Cronbach's alpha value for the UCLA SCTC GIT 2.0 scale was 0.908 showing reliability. In addition, the UCLA SCTC GIT 2.0 showed correlation to the SF-36.
    Conclusion: The translation of the Hebrew UCLA SCTC GIT 2.0 scale was reliable and valid with a total Cronbach's alpha score among the participants of 0.908. Cronbach's alpha was particularly reliable in reflux, bloating, social function, and emotional well-being. Our results suggest that our Hebrew version of the UCLA SCTC GIT 2.0 scale can be used as a tool in future studies with Hebrew-speaking patients. In the abstract conclusion, it states that "Cronbach's alpha was particularly reliable in reflux, bloating, social function, and emotional well-being." The related data should be listed in the results section and then an interpretation of the results should be listed in the conclusions section. Please revise.
    Language English
    Publishing date 2022-12-08
    Publishing country England
    Document type Journal Article
    ISSN 2397-1991
    ISSN (online) 2397-1991
    DOI 10.1177/23971983221138712
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  6. Article: Autoimmune Diseases in Systemic Sclerosis Patients and Their Relatives: Data from a Single Center.

    Balbir-Gurman, Alexandra / Shataylo, Vika / Braun-Moscovici, Yolanda

    The Israel Medical Association journal : IMAJ

    2019  Volume 21, Issue 1, Page(s) 29–34

    Abstract: Background: The aggregation of autoimmune diseases in relatives (AID-R) of patients with systemic sclerosis (SSc) has been reported.: Objectives: To analyze the prevalence of autoimmune diseases in SSc relatives and to compare their features to those ...

    Abstract Background: The aggregation of autoimmune diseases in relatives (AID-R) of patients with systemic sclerosis (SSc) has been reported.
    Objectives: To analyze the prevalence of autoimmune diseases in SSc relatives and to compare their features to those of SSc patients without AID-R (controls).
    Methods: A case-control analysis compared SSc patients with AID-R to those without AID-R (25 patients) with similar disease duration.
    Results: Among 322 patients, 25 (7.7%; 21 females, 41.4 ± 15.6 years of age, disease duration 11 ± 8.6 years) had AID-R (21 had a first-degree relative, 4 had a second-degree relative, and 2 had both). Fourteen patients (56%) and five controls (20%) had an additional autoimmune disease (P < 0.009). Diffuse SSc (48% vs. 24%) and arthritis (72% vs. 28%) were more frequent among the patients with AID-R than the controls (P < 0.05). No significant differences were found regarding lung, heart, vascular, and digestive system involvement. The mean number of additional autoimmune diseases was 0.84 ± 0.94 in AID-R vs. 0.24 ± 0.52 in controls (P < 0.038). The mean number of autoantibodies was 2.8 ± 1.5 and 2.2 ± 0.9 (P < 0.047). Five patients died during follow-up, four of whom had AID-R. Relatives of SSc patients had diverse autoimmune diseases; the prevalence of SSc in scleroderma relatives was 1.86% (2 in first-degree and 6 in second-degree relatives). SSc patients with AID-R had an obvious tendency to polyautoimmunity.
    Conclusions: A precise family history is an important clue in prognosis and prediction of autoimmune diseases in SSc patients and their relatives.
    MeSH term(s) Adolescent ; Adult ; Aged ; Autoantibodies/blood ; Autoimmune Diseases/complications ; Autoimmune Diseases/epidemiology ; Case-Control Studies ; Family ; Female ; Humans ; Male ; Middle Aged ; Prevalence ; Retrospective Studies ; Scleroderma, Systemic/complications ; Young Adult
    Chemical Substances Autoantibodies
    Language English
    Publishing date 2019-01-18
    Publishing country Israel
    Document type Journal Article
    ZDB-ID 2008291-5
    ISSN 1565-1088 ; 0021-2180
    ISSN 1565-1088 ; 0021-2180
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  7. Article ; Online: Hypocomplementemia during tocilizumab treatment: Long-term follow-up results.

    Bieber, Amir / Markovits, Doron / Toledano, Kohava / Tavor, Yonit / Mader, Reuven / Balbir-Gurman, Alexandra / Braun-Moscovici, Yolanda

    Medicine

    2022  Volume 101, Issue 24, Page(s) e29528

    Abstract: Abstract: Hypocomplementemia has been reported in patients with rheumatoid arthritis treated with tocilizumab (TCZ), but its long-term consequences are unknown. We assessed the long-term outcome of patients treated with TCZ who developed ... ...

    Abstract Abstract: Hypocomplementemia has been reported in patients with rheumatoid arthritis treated with tocilizumab (TCZ), but its long-term consequences are unknown. We assessed the long-term outcome of patients treated with TCZ who developed hypocomplementemia regarding serious bacterial infections or autoimmune diseases (AID).The charts of patients treated with TCZ at two rheumatology centers were reviewed retrospectively. Data regarding patients' age, gender, disease duration, autoantibodies status, previous or concomitant treatments, blood counts, liver enzymes, C3 and C4 levels at baseline and during TCZ treatment, episodes of infections, allergic reactions, and AID were analyzed. Univariate analysis was used to compare patients with low C3, C4 levels versus patients with normal C3, C4 levels. Variables that were statistically significant associated or tended to be associated with low C3 or C4 were included in multiple variable logistic regression.Of 132 patients treated with TCZ, 108 had serial measurements of serum complement concentration. Thirty-three (30%) patients developed low C4 levels and 23 (21%) had also low C3. Mean TCZ treatment period was 4.9 years (range, 1-14 years). All patients had normal complement levels at baseline. Leukopenia occurred in 18 (16.7%) patients, 14 of whom (77%) had low complement. Persistent leukopenia was observed in 8% and 5.3% of patients with normal C3 and C4 levels, respectively, as opposed to 47% and 42% of patients with low C3 or low C4, respectively. Low C3, C4 levels correlated with prolonged TCZ treatment retention time and effectiveness. There were no serious bacterial infections or new onset AID.Hypocomplementemia during TCZ treatment was accompanied by leukopenia that correlated with treatment duration. Hypocomplementemia was not associated with serious bacterial infections or new onset AID. Decreased complement levels were associated with treatment longevity. The role of monitoring complement level in predicting treatment response or assessing disease activity deserves further investigation.
    MeSH term(s) Antibodies, Monoclonal, Humanized ; Complement C3 ; Follow-Up Studies ; Hematologic Diseases ; Humans ; Leukopenia ; Retrospective Studies ; Treatment Outcome
    Chemical Substances Antibodies, Monoclonal, Humanized ; Complement C3 ; tocilizumab (I031V2H011)
    Language English
    Publishing date 2022-06-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80184-7
    ISSN 1536-5964 ; 0025-7974
    ISSN (online) 1536-5964
    ISSN 0025-7974
    DOI 10.1097/MD.0000000000029528
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  8. Article: Switching from intravenous tocilizumab to subcutaneous administration during COVID-19 pandemic: impact on treatment efficacy and patient satisfaction.

    Daood, Rula / Toledano, Kochava / Markovits, Doron / Tavor, Yonit / Giryes, Samy / Dolnikov, Katya / Jeries, Helani / Balbir-Gurman, Alexandra / Braun-Moscovici, Yolanda

    Clinical and experimental rheumatology

    2022  Volume 41, Issue 3, Page(s) 744–746

    Abstract: Objectives: We aimed to assess the efficacy and patient satisfaction of subcutaneous tocilizumab (SC TCZ) in patients previously treated with intravenous tocilizumab (IV TCZ) during the COVID-19 pandemic.: Methods: We conducted a single-centre ... ...

    Abstract Objectives: We aimed to assess the efficacy and patient satisfaction of subcutaneous tocilizumab (SC TCZ) in patients previously treated with intravenous tocilizumab (IV TCZ) during the COVID-19 pandemic.
    Methods: We conducted a single-centre retrospective study at the Rheumatology Day Care at the Rheumatology Institute, Rambam Health Care Campus, Israel. Clinical and laboratory data of IV TCZ treated patients who switched to SC TCZ were retracted and analysed. Data were collected from the last two visits before switching to SC treatment and two visits afterwards. A telephone call conversation was conducted for all patients who continued SC treatment and did not come to follow-up visits.
    Results: Forty patients (age 53.03 (± 15.7)) treated with IV TCZ were switched to SC TCZ in April-May 2020. Three patients were excluded from the study. Most of the patients were treated with TCZ for 6.35 (±2.89) years and had low disease activity. 26/37 (70%) patients discontinued SC TCZ therapy and switched back to IV TCZ. The majority of discontinuations were due to flare up of the underlying disease reflected by increased number of tender and/or swollen joints, prolongation of morning stiffness or increased pain VAS score. Two patients were hospitalised for IV glucocorticoids and 1 patient underwent knee arthrocentesis. 11/37 (30%) patients continued SC TCZ treatment. 3/11 (27%) expressed less satisfaction with SC TCZ therapy.
    Conclusions: More than half of the patients who switched from IV TCZ to SC TCZ showed signs of flare of their underlying disease or were less satisfied with SC treatment.
    MeSH term(s) Humans ; Middle Aged ; Antibodies, Monoclonal, Humanized/administration & dosage ; Antibodies, Monoclonal, Humanized/therapeutic use ; Antirheumatic Agents/therapeutic use ; Arthritis, Rheumatoid/drug therapy ; COVID-19 ; Injections, Subcutaneous ; Pandemics ; Patient Satisfaction ; Retrospective Studies ; Treatment Outcome
    Chemical Substances Antibodies, Monoclonal, Humanized ; Antirheumatic Agents ; tocilizumab (I031V2H011)
    Language English
    Publishing date 2022-08-31
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 605886-3
    ISSN 1593-098X ; 0392-856X
    ISSN (online) 1593-098X
    ISSN 0392-856X
    DOI 10.55563/clinexprheumatol/lxfy2v
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  9. Article: [THE EMERGENCE OF RHEUMATOID ARTHRITIS AT THE AGE OF OVER 60 - A COMPARISON OF CLINICAL MANIFESTATIONS AND ACCESS TO TREATMENT PATTERN COMPARED TO YOUNGER PATIENTS].

    Balbir-Gurman, Alexandra / Arabi-Zuhabi, Amal / Braun-Moscovici, Yolanda

    Harefuah

    2019  Volume 158, Issue 9, Page(s) 563–567

    Abstract: Introduction: The aging process of rheumatoid arthritis (RA) requires re-assessment of diagnostic and treatment approaches in patients who developed RA at 60-69 years (EORA-Elderly-Onset RA), 70 years and older (LORA-Late Onset RA) compared with CORA ... ...

    Abstract Introduction: The aging process of rheumatoid arthritis (RA) requires re-assessment of diagnostic and treatment approaches in patients who developed RA at 60-69 years (EORA-Elderly-Onset RA), 70 years and older (LORA-Late Onset RA) compared with CORA patients - Common Onset RA (35 - 50 years).
    Methods: Comparing data of CORA, EORA and LORA patients: gender, nationality; swollen and tender joints (out of 28 joints), Disease Activity Score (DAS28), inflammatory markers, rheumatoid factor (RF) and anti-cyclic citrullinated peptide antibodies (ACPA); treatment with corticosteroids and disease modifying anti rheumatic drugs (DMARDs).
    Results: Patients' files were examined: CORA (39, 33.5%), EORA (37, 30.8%) and LORA (44, 36.7%). No differences were observed between swollen and tender joints, inflammatory markers, DAS28, RF, and ACPA. Methotrexate was introduced in 94.9% of CORA patients versus EORA (77.3%) and LORA (78.4%); 88.6% LORA-patients received corticosteroids versus 69.2% CORA; 43.2% of LORA patients and 92.3% CORA received synthetic disease-modifying antirheumatic drugs (DMARDs); 43.6% CORA versus 16.2% EORA and 9.3% LORA patients received biologics.
    Conclusions: No clinical and laboratory differences were found between CORA, EORA, and LORA groups. EORA and LORA patients received less synthetic and biological DMARDs. It is necessary to change the attitude to EORA and LORA and to promote advanced optimal treatments. Prospective studies on the efficacy and safety of novel drugs in EORA and LORA patients are needed.
    MeSH term(s) Age of Onset ; Aged ; Antirheumatic Agents ; Arthritis, Rheumatoid ; Health Services Accessibility ; Humans ; Prospective Studies
    Chemical Substances Antirheumatic Agents
    Language Hebrew
    Publishing date 2019-09-10
    Publishing country Israel
    Document type Journal Article
    ZDB-ID 953872-0
    ISSN 0017-7768
    ISSN 0017-7768
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