ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 529

Chest Computed Tomography Abnormalities in Patients with Rheumatoid Arthritis By Serologic Status

Sicong Huang1, Tracy Doyle2, Allison Marshall3, Christine K Iannaccone4, Jie Huang1, Michael E Weinblatt2, Paul F. Dellaripa5, Elizabeth Karlson5, Nancy A. Shadick2 and Jeffrey A. Sparks1, 1Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston, MA, 3Rheumatology, Brigham and Women's Hospital, Boston, MA, 4Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 5Brigham and Women's Hospital and Harvard Medical School, Boston, MA

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: respiratory disease and rheumatoid arthritis (RA)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Sunday, October 21, 2018

Title: Rheumatoid Arthritis – Diagnosis, Manifestations, and Outcomes Poster I: Comorbidities

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose:

Lung involvement in rheumatoid arthritis (RA) has been recognized as an important contributor to morbidity and mortality. While interstitial lung disease (ILD) is a well-recognized manifestation more common in seropositive RA, the association between RA and other respiratory outcomes such as chronic obstructive pulmonary disease (COPD) and bronchiectasis are less understood. The purpose of this study was to describe imaging abnormalities in clinically-indicated chest computed tomography (CTs) of patients with RA and compare abnormalities based on serologic status.

 

Methods:

We identified patients within a single-center registry composed of 1,500 RA patients with prospective measures of RA characteristics and detailed clinical data who had clinically-indicated chest CTs. We extracted data by reviewing the initial clinically-indicated chest CT report occurring after baseline study visit. We described the proportion of patients with imaging findings and impression in the report from the attending radiologist. We further stratified the characteristics by RA serostatus (seropositive as rheumatoid factor and/or anti-cyclic citrullinated peptide positivity; seronegative as both negative). We compared patients with seropositive RA to seronegative RA using t-tests or Wilcoxon rank-sum tests for continuous variables and chi-square tests or Fisher’s exact tests for categorical variables.

 

Results:

We analyzed 188 patients with chest CTs performed after study baseline. The mean age was 64.3 years (SD 11.9), 79.8% were female, mean RA duration was 21.4 years (SD 13.3), mean body mass index (BMI) was 27.5 kg/m2 (SD 6.3), 60.1% were ever smokers, and 73.4% were seropositive. Most CTs were obtained to rule out respiratory illness (43.1%), followed by malignancy (24.5%). The most common chest CT pattern abnormalities were: pulmonary nodules (38.8%), opacities (24.5%), and pleural effusions/thickening (18.1%). The most common final impressions for the chest CTs were: pulmonary nodules (30.3%), atelectasis (21.3%), and ILD (16.0%). Only 11.7% of chest CTs had completely normal final impressions. There were no statistically significant differences between seropositive and seronegative RA, including ILD (p=1.0), bronchiectasis (p=0.21), and COPD (p=0.78).

 

Conclusion:

A wide variety of chest CT abnormalities were present at high prevalence in both seropositive and seronegative RA patients with few having normal findings. While we found no differences based on serostatus in these clinically-indicated chest CTs, there may be differences in the subclinical natural history of lung disease based on RA serostatus and disease activity. The pathogenesis, clinical manifestations, and outcomes of patients with pulmonary abnormalities warrant further research.

 

 

Table. Chest computed tomography (CT) findings in patients with seronegative vs. seropositive rheumatoid arthritis (RA)

 

All patients

(n = 188)

Seronegative RA

(n = 50)

Seropositive RA

(n = 138)

p value

Demographics

Age (Mean, SD), years

64.3 (11.9)

63.6 (13.7)

64.5 (11.2)

0.90

Female (n, %)

150 (79.8)

37 (74.0)

113 (81.9)

0.33

RA duration (mean, SD), years

21.4 (13.3)

16.8 (14.4)

23.1 (12.5)

<0.001

BMI (mean, SD), kg/m2

27.5 (6.3)

27.6 (6.0)

27.5 (6.4)

1.00

Ever smoker (n, %)

113 (60.1)

29 (58.0)

84 (60.9)

0.85

 

CT Patterns (n, %)

Normal

24 (12.8)

9 (18.0)

15 (10.9)

0.30

Pulmonary nodules

73 (38.8)

18 (36.0)

55 (39.9)

0.76

Consolidation

46 (24.5)

8 (16.0)

38 (27.5)

0.15

Pleural abnormalities

34 (18.1)

8 (16.0)

26 (18.8)

0.82

Ground-glass opacities

32 (17.0)

11 (22.0)

21 (15.2)

0.38

Bronchiectasis

31 (16.5)

7 (14.0)

24 (17.4)

0.74

Lymph node enlargement

26 (13.8)

6 (12.0)

20 (14.5)

0.84

Fibrotic changes

24 (12.8)

7 (14.0)

17 (12.3)

0.95

Emphysema

21 (11.2)

6 (12.0)

15 (10.9)

1.00

Pulmonary embolism

7 (3.7)

3 (6.0)

4 (2.9)

0.39

 

CT Diagnosis per Report (n, %)

Normal

22 (11.7)

8 (16.0)

14 (10.1)

0.40

Pulmonary nodules

57 (30.3)

15 (30.0)

42 (30.4)

1.00

Atelectasis

40 (21.3)

14 (28.0)

26 (18.8)

0.25

ILD

30 (16.0)

8 (16.0)

22 (15.9)

1.00

Bronchiectasis

27 (14.4)

4 (8.0)

23 (16.7)

0.21

Infection

24 (12.8)

5 (10.0)

19 (13.8)

0.66

Pleural effusion

18 (9.6)

5 (10.0)

13 (9.4)

1.00

COPD

17 (9.0)

5 (10.0)

12 (8.7)

0.78

Lymphadenopathy

16 (8.5)

2 (4.0)

14 (10.1)

0.24

Malignancy

10 (5.3)

1 (2.0)

9 (6.5)

0.30

Pulmonary embolism

7 (3.7)

3 (6.0)

4 (2.9)

0.39

Other

32 (17)

6 (12.0)

26 (18.8)

0.38

BMI: body mass index

COPD: chronic obstructive pulmonary disease

ILD: interstitial lung disease

 

 


Disclosure: S. Huang, None; T. Doyle, None; A. Marshall, None; C. K. Iannaccone, None; J. Huang, None; M. E. Weinblatt, Amgen Inc., 5,Bristol-Myers Squibb, 5,Crescendo Bioscience, 5,UCB, Inc., 5,Amgen Inc., 2,Bristol-Myers Squibb, 2,Crescendo Bioscience, 2,Sanofi/Regeneron, 2; P. F. Dellaripa, up to date, 7,Genentech, Inc., 9; E. Karlson, None; N. A. Shadick, Bristol-Myers Squibb, 5,Amgen Inc., 2,Mallinckrodt, 2,UCB, Inc., 2,Crescendo Biosciences, 2,Sanofi, 2,Bristol-Myers Squibb, 2,DxTerity, 2; J. A. Sparks, None.

To cite this abstract in AMA style:

Huang S, Doyle T, Marshall A, Iannaccone CK, Huang J, Weinblatt ME, Dellaripa PF, Karlson E, Shadick NA, Sparks JA. Chest Computed Tomography Abnormalities in Patients with Rheumatoid Arthritis By Serologic Status [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/chest-computed-tomography-abnormalities-in-patients-with-rheumatoid-arthritis-by-serologic-status/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2018 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/chest-computed-tomography-abnormalities-in-patients-with-rheumatoid-arthritis-by-serologic-status/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology