<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-29T04:10:24Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18265" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18265</identifier><datestamp>2024-11-28T15:07:51Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec><setSpec>col_20.500.12105_16982</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Mena-Vázquez, Natalia</subfield>
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      <subfield code="a">Rojas-Gimenez, Marta</subfield>
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      <subfield code="a">Romero-Barco, Carmen María</subfield>
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      <subfield code="a">Manrique-Arija, Sara</subfield>
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      <subfield code="a">Francisco, Espildora</subfield>
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      <subfield code="a">Aguilar-Hurtado, María Carmen</subfield>
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      <subfield code="a">Añón-Oñate, Isabel</subfield>
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      <subfield code="a">Pérez-Albaladejo, Lorena</subfield>
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      <subfield code="a">Ortega-Castro, Rafaela</subfield>
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      <subfield code="a">Godoy-Navarrete, Francisco Javier</subfield>
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      <subfield code="a">Ureña-Garnica, Inmaculada</subfield>
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      <subfield code="a">Velloso-Feijoo, Maria Luisa</subfield>
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      <subfield code="a">Redondo-Rodriguez, Rocio</subfield>
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      <subfield code="a">Jimenez-Núñez, Francisco Gabriel</subfield>
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      <subfield code="a">Panero Lamothe, Blanca</subfield>
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      <subfield code="a">Padin-Martín, María Isabel</subfield>
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      <subfield code="a">Fernández-Nebro, Antonio</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2021-02-20</subfield>
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      <subfield code="a">Objectives: To describe a prospective cohort of patients with rheumatoid arthritis associated with interstitial lung disease (RA-ILD) and identify risk factors associated with disease progression and mortality in this cohort. Patients and methods: We performed a multicenter, prospective, observational study of patients with RA-ILD receiving disease-modifying antirheumatic drugs (DMARDs) between 2015 and 2020. The patients were assessed using high-resolution computed tomography and pulmonary function tests at baseline and at 60 months. The main endpoint was “Progression to ILD at the end of follow-up” in terms of the following outcomes: (1) improvement (i.e., improvement in forced vital capacity (FVC) ≥10% or diffusing capacity of the lungs for carbon monoxide (DLCO) ≥15% and absence of radiological progression); (2) nonprogression (stabilization or improvement in FVC ≤10% or diffusing capacity of the lungs for carbon monoxide (DLCO) &lt;15% and absence of radiological progression); (3) progression (worsening of FVC >10% or DLCO >15% and radiological progression); or (4) death. We recorded demographic and clinical characteristics, lung function, and the incidence of adverse events. A Cox regression analysis was performed to identify factors associated with the worsening of ILD. Results: After 60 months, lung disease had stabilized in 66 patients (56.9%), improved in 9 (7.8%), and worsened in 23 (19.8%). Eighteen patients (15.5%) died, with a mean survival of 71.8 (1.9) months after diagnosis of ILD. The Cox multivariate analysis revealed the independent predictors of worsening of RA-ILD to be usual interstitial pneumonia (hazard ratio (HR), 2.6 (95%CI, 1.0–6.7)), FVC &lt;80% (HR, 3.8 (95%CI, 1.5–6.7)), anticitrullinated protein antibody titers (HR, 2.8 (95%CI, 1.1–6.8)), smoking (HR, 2.5 (95%CI, 1.1–6.2)), and treatment with abatacept, tocilizumab, or rituximab (HR, 0.4 (95%CI, 0.2–0.8)). During follow-up, 79 patients (68%) experienced an adverse event, mostly infection (61%). Infection was fatal in 10/18 patients (55.5%) during follow-up. Conclusions: Lung function is stable in most patients with RA-ILD receiving treatment with disease-modifying anti-rheumatic drugs (DMARDs), although one-third worsened or died. Identifying factors associated with worsening in RA-ILD is important for clinical management.</subfield>
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      <subfield code="a">http://hdl.handle.net/10668/4143</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18265</subfield>
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      <subfield code="a">33672699</subfield>
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      <subfield code="a">10.3390/jcm10040874</subfield>
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      <subfield code="a">2077-0383</subfield>
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      <subfield code="a">Journal of Clinical Medicine</subfield>
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      <subfield code="a">Rheumatoid arthritis</subfield>
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      <subfield code="a">Interstitial lung disease</subfield>
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      <subfield code="a">Biologics</subfield>
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      <subfield code="a">Non-anti-TNF biologics</subfield>
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      <subfield code="a">Antirheumatic drug</subfield>
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      <subfield code="a">Vital capacity</subfield>
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      <subfield code="a">Smoking</subfield>
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      <subfield code="a">Tomography</subfield>
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      <subfield code="a">Artritis reumatoide</subfield>
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      <subfield code="a">Enfermedades pulmonares intersticiales</subfield>
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      <subfield code="a">Productos biológicos</subfield>
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      <subfield code="a">Antirreumáticos</subfield>
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      <subfield code="a">Capacidad vital</subfield>
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      <subfield code="a">Fumar</subfield>
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      <subfield code="a">Tomografía</subfield>
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      <subfield code="a">Estudios de cohortes</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Predictors of Progression and Mortality in Patients with Prevalent Rheumatoid Arthritis and Interstitial Lung Disease: A Prospective Cohort Study</subfield>
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