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Gamboa-Cárdenas  Rocio V  Ugarte-Gil  Manuel F.  Loreto  Massardo  Sacnun  Mónica P.  Saurit  Verónica  Cardiel  Mario H.  Soriano  Enrique R.  Pisoni  Cecilia  Galarza-Maldonado  Claudio M.  Rios  Carlos  Radominski  Sebastião C.  Castelar-Pinheiro  Geraldo da R.  Bianchi  Washington Alves  Appenzeller  Simone  da Silveira  Inés Guimarães  de Freitas Zerbini  Cristiano A.  Caballero-Uribe  Carlo V.  Rojas-Villarraga  Adriana  Guibert-Toledano  Marlene  Ballesteros  Francisco  Montufar  Rubén  Vázquez-Mellado  Janitzia  Esquivel-Valerio  Jorge  De La Torre  Ignacio García  Barile-Fabris  Leonor A.  Palezuelos  Fedra Irazoque  Andrade-Ortega  Lilia  Monge  Pablo  Teijeiro  Raquel  Achurra-Castillo  Ángel F.  Esteva Spinetti  María H.  Alarcón  Graciela S.  Pons-Estel  Bernardo A. 《Clinical rheumatology》2019,38(10):2737-2746
Objectives

To identify baseline predictors of remission and low disease activity (LDA) in early rheumatoid arthritis (RA) from the GLADAR (Grupo Latino Americano De estudio de la Artritis Reumatoide) cohort.

Methods

Patients with 1- and 2-year follow-up visits were included. Remission and LDA were defined by DAS28-ESR (< 2.6 and ≤ 3.2, respectively). Baseline predictors examined were gender, ethnicity, age at diagnosis, socioeconomic status, symptoms’ duration, DMARDs, RF, thrombocytosis, anemia, morning stiffness, DAS28-ESR (and its components), HAQ-DI, DMARDs and corticosteroid use, and Sharp-VDH score. Multivariable binary logistic regression models (excluding DAS28-ESR components to avoid over adjustment) were derived using a backward selection method (α-level set at 0.05).

Results

Four hundred ninety-eight patients were included. Remission and LDA/remission were met by 19.3% and 32.5% at the 1-year visit, respectively. For the 280 patients followed for 2 years, these outcomes were met by 24.3% and 38.9%, respectively. Predictors of remission at 1 year were a lower DAS28-ESR (OR 1.17; CI 1.07–1.27; p = 0.001) and HAQ-DI (OR 1.48; CI 1.04–2.10; p = 0.028). At 2 years, only DAS28-ESR (OR 1.40; CI 1.17–1.6; p < 0.001) was a predictor. Predictors of LDA/remission at 1 year were DAS28-ESR (OR 1.42; CI 1.26–1.61; p < 0.001), non-use of corticosteroid (OR 1.74; CI 1.11–2.44; p = 0.008), and male gender (OR 1.77; CI 1.2–2.63; p = 0.036). A lower baseline DAS28-ESR (OR 1.45; CI 1.23–1.70; p < 0.001) was the only predictor of LDA/remission at 2 years.

Conclusions

A lower disease activity consistently predicted remission and LDA/remission at 1 and 2 years of follow-up in early RA patients from the GLADAR cohort.

Key Points

In patients with early RA, a lower disease activity at first visit is a strong clinical predictor of achieving remission and LDA subsequently.

Other clinical predictors of remission and LDA to keep in mind in these patients are male gender, non-use of corticosteroids and low disability at baseline.

Not using corticosteroids at first visit is associated with a lower disease activity and predicts LDA/remission at 1 year in these patients.

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Previous studies have demonstrated that in admixed populations, West African ancestry is associated with an increased prevalence of systemic lupus erythematosus (SLE). In the current study, the effect of Amerindian ancestry in SLE was examined in an admixed population in Argentina. The Argentine population is predominantly European with approximately 20% Amerindian admixture, and a very small (<2%) contribution from West Africa. The results indicate that Amerindian admixture in this population is associated with a substantial increase in SLE susceptibility risk (Odds Ratio=7.94, P=0.00006). This difference was not due to known demographic factors, including site of collection, age and gender. In addition, there were trends towards significance for Amerindian ancestry influencing renal disease, age of onset and anti-SSA antibodies. These studies suggest that populations with Amerindian admixture, like those with West African admixture, should be considered in future studies to identify additional allelic variants that predispose to SLE.  相似文献   
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Pulmonary complications of primary antiphospholipid syndrome are common and diverse, with thromboembolic events counting as the most frequent manifestation. We present the case of a female patient with a diagnosis of primary antiphospholipid syndrome, pulmonary thromboembolism and infarction followed by lung cavitation.  相似文献   
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