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: 61

Predictors of Mortality Among Patients with Sarcoidosis: A Population-Based Study

Patompong Ungprasert1, Eva M. Carmona Porquera2, James P. Utz2, Jay H. Ryu3, Cynthia S. Crowson4 and Eric L. Matteson5, 1Rheumatology, Mayo Clinic, Rochester, MN, 2Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, 3Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, 4Health Sciences Research, Mayo Clinic, Rochester, MN, 5Division of Rheumatology, Department of Internal Medicine and Department of Health Sciences Research, Mayo Clinic, Rochester, MN

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Morbidity and mortality and sarcoidosis

  • 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 8, 2015

Title: Epidemiology and Public Health Poster I: Comorbidities and Outcomes of Systemic Inflammatory Diseases

Session Type: ACR Poster Session A

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

Background/Purpose: The epidemiology and natural history of sarcoidosis is not well-characterized as only coding-based studies without detailed clinical information from individual medical record review have been reported. This study aimed to assess the predictors of mortality of sarcoidosis, using data from a population-based cohort.

Methods: An inception cohort of patients who were diagnosed with sarcoidosis in 1976-2013 in a geographically well-defined population was identified based on comprehensive individual medical record review. Diagnosis required histopathological confirmation and diagnostic radiologic features of intrathoracic sarcoidosis, compatible clinical presentation, and exclusion of other known causes of granulomatous inflammation. Histopathological confirmation required presence of non-caseating granuloma without evidence of acid-fast bacilli or fungi. The only exception to the requirement of histopathological confirmation was stage I pulmonary sarcoidosis that required only radiographic evidence of symmetric bilateral hilar adenopathy with or without mediastinal lymphadenopathy. Cases of isolated granulomatous disease of the skin without other features of sarcoidosis were not included. Data were collected on demographic, clinical presentation, laboratory investigations and mortality. Univariable Cox models were used to identify prognostic factors of death.

Results: In 1976-2013, 345 incident cases of sarcoidosis were identified. 50.4% of the cohort was female and the mean age of the cohort was 45.6 years. During follow-up (median: 12.2 years; 5002 total person-years), 50 patients died.

Age, male sex, absence of intra-thoracic disease, and hepatic, cardiac, splenic or neurological involvement in conjunction with intra-thoracic disease were predictive factors for mortality in univariable models after adjustment for age, sex and calendar year of sarcoidosis diagnosis (Table 1).

Conclusion: Age, male sex, absence of intra-thoracic disease, and hepatic, cardiac, splenic or neurological involvement in conjunction with intra-thoracic disease were prognostic factors associated with mortality in patients with sarcoidosis.

Table 1: Predictors of mortality among patients with sarcoidosis

Characteristic

Hazard ratio*

(95% CI)

p-value

Age, per 10 year increase

2.48 (1.97, 3.13)

<0.001

Male sex

1.98 (1.04, 3.79)

0.038

Calendar year of diagnosis, per 1 year increase

0.98 (0.94, 1.02)

0.25

Black (vs white ethnicity)

3.16 (0.72, 13.81)

0.29

Other (vs white ethnicity)

1.33 (0.32, 5.58)

Former smoker (vs never)

1.80 (0.76, 4.30)

0.36

Current smoker (vs never)

0.94 (0.42, 2.11)

Presence of intrathoracic involvement

0.28 (0.08, 0.93)

0.038

Presence of parenchymal involvement

0.92 (0.51, 1.63)

0.77

Symptomatic from intrathoracic involvement

1.27 (0.705, 2.33)

0.44

Eye

0.46 (0.13, 1.57)

0.22

Nervous system

4.18 (1.44, 12.11)

0.008

Skin

0.84 (0.35, 2.03)

0.70

Liver

5.37 (1.90, 15.21)

0.002

Spleen

11.54 (4.05, 32.91)

<0.001

Heart

12.35 (2.76, 55.18)

0.001

Kidney

2.46 (0.72, 8.39)

0.15

Exocrine gland

0.43 (0.06, 3.15)

0.40


Disclosure: P. Ungprasert, None; E. M. Carmona Porquera, None; J. P. Utz, None; J. H. Ryu, None; C. S. Crowson, None; E. L. Matteson, Novartis/Sanofi/Centocor-Jansen/Celgene/Amgen/Roche/Genentech/Mesoblast/Pfizer, 2.

To cite this abstract in AMA style:

Ungprasert P, Carmona Porquera EM, Utz JP, Ryu JH, Crowson CS, Matteson EL. Predictors of Mortality Among Patients with Sarcoidosis: A Population-Based Study [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/predictors-of-mortality-among-patients-with-sarcoidosis-a-population-based-study/. 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 2015 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/predictors-of-mortality-among-patients-with-sarcoidosis-a-population-based-study/

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