Objective: To compare the effectiveness of abatacept (ABA) in Rheumatoid Arthritis-associated Interstitial Lung Disease (RA-ILD) according to the radiological patterns of usual (UIP) or non-specific interstitial pneumonia (NSIP).

Methods: From an observational longitudinal multicentre study of 263 RA-ILD patients treated with ABA, those with UIP or NSIP were selected. Lung function, chest high resolution computerised tomography (HRCT) and dyspnoea were recorded and compared in both groups from baseline to the end of follow-up (progression definitions: improvement or worsening >10% of FVC or DLCO, changes in HRCT extension and 1-point change in the mMRC scale, respectively). Differences between final and baseline visits were calculated as the average difference (95% CI) through mixed effects models regression.

Results: We studied 190 patients with UIP (n=106) and NSIP (n=84). General features were similar in both groups except for older age, positive rheumatoid factor, and previous sulfasalazine therapy, which were more frequent in patients with UIP. ILD duration up to ABA initiation was relatively short: median 16 [4-50] and 11 [2-36] months (p=0.36) in UIP and NSIP, respectively. Mean baseline FVC and DLCO were 82% and 63% in UIP and 89% and 65% in NSIP, respectively. Both parameters remained stable during 24 months with ABA. HRCT lesions and dyspnoea improved/stabilized in 73.1% and 90.5% and 72.9% and 94.6% of UIP and NSIP patterns, respectively.

Conclusion: ABA seems equally effective in stabilizing dyspnoea, lung function and radiological impairment in both UIP and NSIP patterns of RA-ILD. Early administration of ABA may prevent RA-ILD progression, regardless of the radiological pattern.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejim.2023.08.025DOI Listing

Publication Analysis

Top Keywords

uip nsip
16
non-specific interstitial
8
interstitial pneumonia
8
uip
8
lung function
8
fvc dlco
8
patients uip
8
nsip patterns
8
aba
6
nsip
6

Similar Publications

: Anti-neutrophil cytoplasmic antibodies (ANCAs) have been found in interstitial lung disease (ILD) in recent years, although its impact on ILD prognosis is less known. To date, ANCAs are not included in the interstitial pneumonia with autoimmune features (IPAF) definition criteria. Therefore, ANCA-ILD, in the absence of known ANCA-associated vasculitis (AAV), could be underdiagnosed.

View Article and Find Full Text PDF

Background: This study aims to compare Lung Ultrasound (LUS) findings with High-Resolution Computerized Tomography (HRCT) and Pulmonary Function Tests (PFTs) to detect the severity of lung involvement in patients with Usual Interstitial Pneumonia (UIP) and Non-Specific Interstitial Pneumonia (NSIP).

Methods: A cross-sectional study was conducted on 35 UIP and 30 NSIP patients at a referral hospital. All patients underwent LUS, HRCT, and PFT.

View Article and Find Full Text PDF

Location of Fibroblastic Foci: Does the Lesion You Observe Really Suggest Usual Interstitial Pneumonia?

Mod Pathol

November 2024

Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan; Department of Diagnostic Pathology, Nara Medical University, Nara, Japan.

Article Synopsis
  • Fibroblastic foci (FF) are important indicators of usual interstitial pneumonia (UIP) but can also appear in various fibrotic interstitial lung diseases (ILDs), making them non-specific for UIP.
  • This study analyzed the spatial distribution of FF in different forms of ILDs in patients who underwent lung transplants, categorizing them by anatomical location.
  • Results showed that idiopathic pulmonary fibrosis (IPF) had more total and peripheral FF compared to other ILDs, while centrilobular FF was more prevalent in fibrotic hypersensitivity pneumonitis (FHP), suggesting distinct spatial patterns associated with different diseases.
View Article and Find Full Text PDF
Article Synopsis
  • - Early diagnosis of interstitial lung disease (ILD) and pulmonary hypertension (PH) in systemic sclerosis (SSc) is vital for effective management, but symptoms can be vague in the early stages, making diagnosis difficult.
  • - High-resolution computed tomography (HRCT) is the best imaging technique for evaluating SSc-ILD, showing key features like non-specific interstitial pneumonia (NSIP), ground-glass opacities, and traction bronchiectasis.
  • - Monitoring disease progression and treatment response through serial HRCT assessments is essential, as the extent of disease visible on scans correlates with patient prognosis.
View Article and Find Full Text PDF
Article Synopsis
  • This study aimed to see if a web-based application could help non-chest radiologists better diagnose pulmonary fibrosis by reviewing various chest CT scans.
  • Three radiologists examined multiple rounds of CT scans, initially diagnosing independently and later using suggested features from the application over time.
  • Results showed an increase in diagnostic accuracy from 63% to 74% over the rounds, with specific improvements when refining definitions of features used for diagnosis, particularly enhancing accuracy for a type of fibrosis called NSIP.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!