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: 2689

Troponinemia Independently Associates with Mortality in Systemic Sclerosis

Julie J. Paik1, Debbie Choi1, Fredrick M. Wigley2, Laura K. Hummers3 and Ami A. Shah1, 1Johns Hopkins University, Baltimore, MD, 2Rheum Div/Mason F Lord, Johns Hopkins University, Baltimore, MD, 3Medical and Rheumatology, Johns Hopkins University, Baltimore, MD

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Cardiovascular disease, Morbidity and mortality and systemic sclerosis

  • Tweet
  • Email
  • Print
Session Information

Date: Tuesday, November 7, 2017

Title: Systemic Sclerosis, Fibrosing Syndromes and Raynaud's – Clinical Aspects and Therapeutics Poster III

Session Type: ACR Poster Session C

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

Title: Troponinemia independently associates with mortality in systemic sclerosis

Background/Purpose: Cardiac involvement is common in systemic sclerosis (SSc) and in the early asymptomatic stages, elevated troponin, or troponinemia, may be the only sign of ongoing myocardial disease. 

Methods: This retrospective, cross-sectional study included SSc patients with any troponin measurement in the past 10 years, as identified using our institution¡¯s electronic medical record system. Elevated troponin was defined as any value above or at the cut off of normal value in a commercially available laboratory. Clinical data including SSc subtype, disease duration, maximum modified Rodnan skin score (mRSS), maximum serum creatine kinase, aldolase, pro-B-type natriuretic peptide (BNP), echocardiographic and right heart catheterization data were compared between those with elevated troponin and normal troponin. Survival analyses including Cox proportional hazards regression analyses were used to compare both groups.

Results: 272 patients were identified with a troponin evaluated during the study period. 83 (31%) had an elevated troponin. Compared to those with a normal troponin, SSc patients with troponinemia were more likely to have the diffuse SSc subtype (55% vs. 37%, p=0.004), shorter disease duration since first non-Raynaud¡¯s symptom (5.8 ± 8.4 vs. 6.1 ± 7.6 years; p=0.30), lower ejection fraction (EF) (49.8 ± 12 vs. 54.8 ± 7.3, p=<0.0001), lower FVC (61.2 ± 18.8 vs. 66.8 ± 20.4, p=0.03), higher RVSP( 51.7 ± 21.2 vs. 43.8 ± 16.2, p=0.002), more renal crisis (8.4% vs. 2.6%, p=0.04), higher Medsger muscle (p=0.001) and heart severity scores (p=0.001). Patients with troponinemia also have higher CK values (514 ± 783 vs. 300 ± 553, p=0.01) and higher aldolase (15 ± 11 vs. 11.3 ± 6.3, p=0.002). There was higher frequency of death (28% vs. 9.5%, p=<0.0001). Cox proportional regression analyses demonstrated that patients with troponinemia are 3.2 times (95% confidence interval, 1.33 to 7.7, p=0.009) more likely to have death than those without an elevated troponin even after controlling for SSc subtype, age, gender, race, duration of disease, diabetes, coronary artery disease, smoking, CK, BNP, and World Health Organization dyspnea classification.

Conclusion: SSc patients with troponinemia have increased all-cause mortality when compared to those without an elevated troponin even after controlling for demographic and disease-specific confounders.

Clinical Characteristics

Troponin Positive (N=83)

Troponin negative (N=189)

p-value

Disease duration defined by 1st non-Raynaud¡¯s (at first visit)

5.8 ± 8.4 years

6.1 ± 7.6 years

0.79

Age at SSc diagnosis defined by 1st non-Raynaud¡¯s

45.7 ± 14.2 years

44 ± 13.9 years

0.34

Female

60 (72.3%)

154 (81.5%)

0.06

Diffuse skin subtype

46 (55.4%)

70 (37%)

0.004

Renal crisis

7 (8.4%)

5 (2.6%)

0.04

Race

Caucasian

African-American

Other

46 (55.4%)

34 (41%)

3 (3.6%)

122 (64.6%)

59 (31%)

8 (4.2%)

0.30

Maximum Heart Severity Score

0

1

2

3

4

25 (30.9%)

4 (4.9%)

10 (12.4%)

2 (2.5%)

40 (49.4%)

102 (55.1%)

11 (6.0%)

22 (11.9%)

5 (2.7%)

45 (24.3%)

0.001

Maximum Muscle Severity Score

0

1

2

3

4

32 (38.6%)

37 (44.6%)

10 (12.1%)

2 (2.4%)

2 (2.4%)

123 (65.1%)

48 (25.4%)

12 (6.4%)

2 (1.1%)

4 (2.1%)

0.001

Maximum RVSP

51.7 ± 21.2

43.8 ±16.2

0.002

Max pro-BNP

6205 ± 22110

896 ± 1833

0.003

Lowest Ejection Fraction

49.8 ± 12

54.8 ± 7.3

<0.0001

Lowest FVC

61.2 ± 18.8

66.8 ± 20.4

0.03

Coronary Artery Disease

16 (19.5%)

21 (11.2%)

0.06

Ever Smoker

34 (41%)

74 (39.2%)

0.44

Dyslipidemia

30 (37%)

68(37%)

0.53

Diabetes

9 (10.8%)

8(4.3%)

0.04

Peripheral artery disease

10 (12.2%)

12 (6.5%)

0.09

History of myopathy

48 (52%)

57(30.2%)

0.001

Maximum CK

514 ± 783

300 ± 553

0.01

Maximum aldolase

15.0 ± 11

11.3 ± 6.3

0.002

Deceased

23 (27.7%)

18 (9.5%)

<0.0001

Anti-centromere

12 (23.5%)

32 (23.9%)

0.56

Anti-topoisomerase 1

13 (26.5%)

27 (21.3%)

0.29

Anti-U1RNP

4 (10.8%)

9 (8.9%)

0.50

Anti-RNA Poly III

7 (21.2%)

10 (13.2%)

0.22


Disclosure: J. J. Paik, None; D. Choi, None; F. M. Wigley, None; L. K. Hummers, None; A. A. Shah, None.

To cite this abstract in AMA style:

Paik JJ, Choi D, Wigley FM, Hummers LK, Shah AA. Troponinemia Independently Associates with Mortality in Systemic Sclerosis [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/troponinemia-independently-associates-with-mortality-in-systemic-sclerosis/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/troponinemia-independently-associates-with-mortality-in-systemic-sclerosis/

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