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1.
Tohoku J Exp Med ; 251(2): 125-133, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32581186

RESUMEN

Polymyalgia rheumatica (PMR) is an inflammatory disorder in the elderly and is characterized by pain in the shoulders and lower back. Previous studies from western countries have shown that relapse is frequent; however, there are only a few reports on the relapse rate in Japan. Here we examined the relapse rate, and sought to identify factors that predict recurrence in patients with PMR. Of 110 patients who fulfilled the Bird's criteria for PMR between May 2011 and June 2019, 21 patients were excluded, and the remaining 89 patients were followed up until July 2019. Relapse was defined when clinical symptoms were exacerbated and serum C-reactive protein level increased. The relapse-free survival curves were plotted using the Kaplan-Meier method, and log-rank test was used for statistical analysis. The mean age of the 89 patients (50 males and 39 females) was 71.8 years. The mean dose of initial prednisolone (PSL) was 11.8 mg/day. The 1-, 3-, and 5-year relapse-free survival rates were 81.6%, 58.0%, and 52.3% (N = 59, 21, and 7), respectively. In patients who experienced recurrence, the 1- and 3-year second relapse-free survival rates were 58.3% and 27.3% (N = 18 and 3), respectively. Immunosuppressants, such as methotrexate and tacrolimus, were added to PSL in 19 of 30 patients who experienced relapse at the discretion of the attending physicians; however, none of the immunosuppressants worked for preventing second relapses and had steroid-sparing effects. These results indicate that effective immunosuppressants are required to suppress relapse in the treatment of PMR.


Asunto(s)
Inmunosupresores/administración & dosificación , Polimialgia Reumática/tratamiento farmacológico , Prednisolona/administración & dosificación , Anciano , Anciano de 80 o más Años , Supervivencia sin Enfermedad , Quimioterapia Combinada , Femenino , Estudios de Seguimiento , Humanos , Japón/epidemiología , Masculino , Persona de Mediana Edad , Polimialgia Reumática/mortalidad , Polimialgia Reumática/patología , Recurrencia , Estudios Retrospectivos , Tasa de Supervivencia , Resultado del Tratamiento
2.
Tohoku J Exp Med ; 250(3): 153-159, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32132324

RESUMEN

Recently, biological disease-modifying antirheumatic drugs (bDMARDs) have revolutionized the treatment of rheumatoid arthritis (RA) and provided patients with a higher chance of achieving clinical remission. Among them, abatacept (ABT), which selectively inhibits T cell activation through blocking costimulation signal, has been reported efficacious in controlling disease activity. Previous studies have shown that ABT has a high retention rate of up to three years with tolerable adverse events; however, it remains unclear whether this is maintained in the longer term. Here we conducted a retrospective five-year follow-up study to explore prognostic factors concerning better retention. In total, 98 patients who were treated with ABT from May 2011 to July 2019 in Osaki Citizen Hospital were enrolled, including 73 female patients (74.5%). The Kaplan-Meier method was used to estimate the retention rate of ABT. The mean age of ABT initiation was 72.1 years. Concomitant methotrexate was prescribed for 39 patients, and ABT was used as the first-line bDMARD for 65 patients. Rheumatoid factor (RF) was positive in 79 patients. One-, three-, and five-year retention rates of ABT were 83.3%, 66.2%, and 62.7%, respectively. Approximately two-thirds of discontinuation resulted from an inadequate response. Multivariate logistic regression analysis revealed that positive RF was associated with better drug retention. Receiver operating characteristics analysis showed that patients with high RF (≥ 45 IU/mL) had better retention rate of ABT. In conclusion, ABT shows high retention rate among patients with positive RF. The present study may provide better insights when selecting bDMARDs.


Asunto(s)
Abatacept/uso terapéutico , Artritis Reumatoide/sangre , Artritis Reumatoide/tratamiento farmacológico , Factor Reumatoide/sangre , Anciano , Femenino , Estudios de Seguimiento , Humanos , Modelos Logísticos , Masculino , Análisis Multivariante , Curva ROC , Privación de Tratamiento
3.
Tohoku J Exp Med ; 252(2): 133-141, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-33028756

RESUMEN

The reactivation of hepatitis B virus (HBV) in patients with rheumatoid arthritis (RA) is currently a social problem. Our hospital has established a project team, which consisted of medical staff including doctors, nurses, pharmacists, and technicians, to prevent HBV reactivation and subsequent de novo hepatitis B in 2015. To verify the usefulness of the team, we aimed to examine the implementation rate of HBV screening tests in patients with RA in 2011, 2015, and 2018. We also examined the rate of HBV infection, as well as the rate of HBV reactivation during the course. In this study, medical records of patients who visited our hospital in 2011, 2015, and 2018 were retrospectively reviewed. HBV screening was completed when hepatitis B surface antigen (HBsAg), hepatitis B surface antibody (HBsAb), and hepatitis B core antibody (HBcAb) were all examined. The prevalence of patients who completed HBV screening dramatically increased from 2.4% in 2011 to 79.1% in 2015 and 86.9% in 2018. Patients who completed the screening had significantly higher rates of liver dysfunction, methotrexate use, and use of biological disease-modifying antirheumatic drugs than those who did not. Of the 767 patients who completed HBV screening in 2018, 157 patients (20.5%) had previously resolved HBV infection (HBsAg-negative but HBsAb- and/or HBcAb-positive). During a mean follow-up of 41.0 months, reactivation of HBV was observed in 10 out of the 157 patients (6.4%); however, none developed de novo hepatitis B. In conclusion, our multidisciplinary approach to prevent de novo hepatitis B is considered useful.


Asunto(s)
Artritis Reumatoide/complicaciones , Hepatitis B/complicaciones , Hepatitis B/prevención & control , Anciano , Antirreumáticos/uso terapéutico , Antivirales/uso terapéutico , Artritis Reumatoide/tratamiento farmacológico , Femenino , Anticuerpos contra la Hepatitis B/uso terapéutico , Antígenos de Superficie de la Hepatitis B/inmunología , Virus de la Hepatitis B/fisiología , Humanos , Comunicación Interdisciplinaria , Hepatopatías/complicaciones , Masculino , Metotrexato/efectos adversos , Persona de Mediana Edad , Grupo de Atención al Paciente , Estudios Retrospectivos
5.
Mod Rheumatol Case Rep ; 8(2): 296-301, 2024 Jul 08.
Artículo en Inglés | MEDLINE | ID: mdl-38597870

RESUMEN

The induction of autoimmune diseases during tumour necrosis factor-alpha inhibitor (TNFi) usage has been described. Herein, we report a rare case of a 49-year-old woman with antimelanoma differentiation-associated gene 5 (MDA5) antibody (Ab)-positive dermatomyositis (DM), which developed 5 weeks after the introduction of an etanercept biosimilar to rheumatoid arthritis (RA). Four of the five known cases, including ours, of anti-MDA5Ab-positive DM complicated with RA revealed anti-MDA5Ab-positive DM following TNFi usage. When patients with RA are diagnosed with interstitial lung disease during TNFi usage, anti-MDA5 Ab-positive DM could be a differential diagnosis.


Asunto(s)
Artritis Reumatoide , Autoanticuerpos , Biosimilares Farmacéuticos , Dermatomiositis , Etanercept , Helicasa Inducida por Interferón IFIH1 , Humanos , Dermatomiositis/inmunología , Dermatomiositis/diagnóstico , Femenino , Artritis Reumatoide/tratamiento farmacológico , Artritis Reumatoide/diagnóstico , Persona de Mediana Edad , Etanercept/efectos adversos , Etanercept/uso terapéutico , Helicasa Inducida por Interferón IFIH1/inmunología , Autoanticuerpos/sangre , Autoanticuerpos/inmunología , Biosimilares Farmacéuticos/uso terapéutico , Biosimilares Farmacéuticos/efectos adversos , Antirreumáticos/uso terapéutico , Antirreumáticos/efectos adversos
6.
Int J Rheum Dis ; 25(3): 335-343, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-34989482

RESUMEN

OBJECTIVES: To investigate 6-year drug survival (median: 48.5 months) of golimumab and predictors for lack of efficacy leading to golimumab discontinuation in Japanese patients with rheumatoid arthritis (RA) in routine practice. METHODS: This retrospective single-center study included 60 patients with RA treated with golimumab from November 2011 to August 2020. Patients were divided into 2 groups (retention, n = 28; withdrawal due to lack of efficacy, n = 24). The retention rate was assessed using the Kaplan-Meier method, and variables associated with golimumab discontinuation were identified using the Cox proportional hazard model. RESULTS: The prevalence of concomitant methotrexate and no biologics use was significantly higher in the retention than in the withdrawal group. Overall drug survival of golimumab was 66.3%, 48.3%, and 24.5% at 12, 36, and 72 months, respectively. There were statistical differences in retention rates among groups stratified by initiation dose, methotrexate, and biologics use. Multivariate analysis revealed the factor associated with golimumab discontinuation as history of 1 (hazards ratio: 4.42, 95% CI: 1.35-19.93, P = .012) and ≥2 biologics use (7.49, 1.97-36.27, P = .003). CONCLUSIONS: Prior exposure of increasing number of biologics was identified as the most important factor negatively affecting long-term golimumab retention in Japanese patients with RA.


Asunto(s)
Anticuerpos Monoclonales/uso terapéutico , Predicción , Sistema de Registros , Literatura de Revisión como Asunto , Anciano , Artritis Reumatoide/tratamiento farmacológico , Femenino , Estudios de Seguimiento , Humanos , Japón/epidemiología , Masculino , Persona de Mediana Edad , Prevalencia , Estudios Retrospectivos , Inhibidores del Factor de Necrosis Tumoral/uso terapéutico
7.
Mod Rheumatol Case Rep ; 4(2): 289-295, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-33087019

RESUMEN

We report a case of polycythaemia vera (PV) associated with IgA vasculitis. A 45-year-old man was admitted for evaluation of abdominal pain and palpable purpura. IgA vasculitis was diagnosed, and oral prednisolone therapy (30 mg/day) was initiated. On day 6, the patient developed left hemiparesis, and magnetic resonance imaging revealed acute cerebral infarction. Bone marrow biopsy results and the identification of a Janus kinase 2 (JAK2) mutation led to the diagnosis of PV. Despite steroid therapy, urine protein levels increased to 15 g/g・Cre. Renal biopsy demonstrated mild mesangial proliferation with IgA deposits, but immunosuppressive therapy was partially effective. This case suggests that PV can be a complication of IgA vasculitis and that preventive measures for thrombosis should be taken in such cases.


Asunto(s)
Inmunoglobulina A/inmunología , Janus Quinasa 2/genética , Mutación , Síndrome Nefrótico/diagnóstico , Síndrome Nefrótico/etiología , Policitemia Vera/complicaciones , Policitemia Vera/genética , Vasculitis/etiología , Biopsia , Médula Ósea/patología , Manejo de la Enfermedad , Susceptibilidad a Enfermedades , Humanos , Inmunosupresores/administración & dosificación , Inmunosupresores/uso terapéutico , Masculino , Síndrome Nefrótico/tratamiento farmacológico , Policitemia Vera/tratamiento farmacológico , Vasculitis/tratamiento farmacológico
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