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: 1445

Gastrointestinal Manifestations in Systemic Lupus Erythematosus Are Associated with High Disease Activity and Mortality: A Nationwide Cohort Study from India

Pankti Mehta1, Akansha Srivastava2, Amita Aggarwal2, Liza Rajasekhar3, Vineetha Shobha4, Chengappa Kavadichanda5, ASHISH JACOB MATHEW6, Parasar Ghosh7, Bidyut Das8, Avinash Jain9, Ranjan Gupta10 and Manish Rathi11, 1King George's Medical University, Lucknow, India, 2Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 3Nizam's Institute of Medical Sciences, Madhapur, India, 4St. John’s Medical College Hospital, Bangalore, India, 5JIPMER, Pondicherry, Puducherry, India, 6Christian Medical College, Vellore, Vellore, India, 7Govt of West Bengal, Kolkata, India, Kolkata, West Bengal, India, 8SCB medical college, Cuttack, India, 9SMS Medical College, Lucknow, India, 10All India Institute of Medical Sciences, New Delhi, India, 11PGIMER Chandigarh, Chandigarh, India

Meeting: ACR Convergence 2022

Keywords: Systemic lupus erythematosus (SLE)

  • 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, November 13, 2022

Title: SLE – Diagnosis, Manifestations, and Outcomes Poster II: Manifestations

Session Type: Poster Session C

Session Time: 1:00PM-3:00PM

Background/Purpose: Gastrointestinal (GI) manifestations of Systemic Lupus Erythematosus (SLE) although rare are often severe. These are difficult to directly attribute to SLE as they can also be associated with drugs, infections and other organ manifestations of SLE. There is a paucity of prospective data on the prevalence, associations and outcomes of GI manifestations in SLE. Thus, we studied the GI manifestations in a prospectively enrolled nationwide cohort of SLE in India.

Methods: Cases with GI manifestations (defined as per BILAG) along with controls (one on either side of the case based on the serial number of recruitment into the cohort; one on either side of the block for consecutive cases) were selected from the database of a nationwide, prospective, multicenter cohort (INSPIRE) of patients with SLE (classified by SLICC classification criteria). Data on demographics, clinical features, investigations, disease activity at baseline and early outcomes were retrieved for analysis.

Data are expressed as mean ± standard deviation and SPSS was used for statistical analysis. Univariate analysis was done using the t-test and chi-square test based on the type of variables; those with a p-value of ≤0.1 were included for multivariate analysis using the forward likelihood test.

Results: Of 2210 patients with SLE enrolled in the INSPIRE registry, 254(11.5%) had GI manifestations, with more than one GI feature in 39 patients. The most common was ascites (193,76%) followed by lupus enteritis (35, 13.8%), lupus pancreatitis (32, 12.6), lupus hepatitis (19, 7.5), lupus peritonitis (6, 2.3), intestinal obstruction and lupus cholecystitis (3, 1.2%) with malabsorption and protein losing enteropathy being the least common (2, 0.7%). The majority were observed within 2.2±3.3 months of presentation with 97(38%) being present at the onset.

On univariate analysis, patients with GI manifestations were significantly younger; had a higher frequency of fever, lupus nephritis, psychosis, seizures and pleural effusion; were more likely to have anemia, lymphopenia, thrombocytopenia, elevated creatinine, low albumin and low complements as compared to controls. There was no difference in the serology between the two groups. SLEDAI 2K and the BILAG score were higher in the cases. (Table 1)

On multivariate analysis, younger age [p=0.03, 0.97(0.95-0.99,)]; high creatinine [0.001, 1.6(1.2-2.1)], low albumin [0.0001, 0.6(0.5-0.8)], presence of pleural effusion [0.0001, 3.3(1.9-5.2)], presence of thrombocytopenia [0.02, 1.6(1.1-2.5)] were significantly associated with GI features. (Figure 1)

Mortality was higher in the cases [10.3 and 5.5%, p=0.04, 1.9(1.1-3.7)] as compared to controls. (Table 1)

Conclusion: GI manifestations were observed in 11.5% of the cohort with ascites being the most common feature. GI involvement is associated with higher disease activity and mortality.

Supporting image 1

Supporting image 2

Figure 1: Association of gastrointestinal manifestations on multivariate analysis as compared with controls


Disclosures: P. Mehta, None; A. Srivastava, None; A. Aggarwal, None; L. Rajasekhar, None; V. Shobha, None; C. Kavadichanda, None; A. MATHEW, None; P. Ghosh, None; B. Das, None; A. Jain, None; R. Gupta, None; M. Rathi, None.

To cite this abstract in AMA style:

Mehta P, Srivastava A, Aggarwal A, Rajasekhar L, Shobha V, Kavadichanda C, MATHEW A, Ghosh P, Das B, Jain A, Gupta R, Rathi M. Gastrointestinal Manifestations in Systemic Lupus Erythematosus Are Associated with High Disease Activity and Mortality: A Nationwide Cohort Study from India [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/gastrointestinal-manifestations-in-systemic-lupus-erythematosus-are-associated-with-high-disease-activity-and-mortality-a-nationwide-cohort-study-from-india/. 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 ACR Convergence 2022

ACR Meeting Abstracts - https://acrabstracts.org/abstract/gastrointestinal-manifestations-in-systemic-lupus-erythematosus-are-associated-with-high-disease-activity-and-mortality-a-nationwide-cohort-study-from-india/

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