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Abstract Number: 714

Prolonged Antimalarial Treatment Is Associated with Increased Risk for Elevated Myocardial Biomarkers in Systemic Lupus Erythematosus

Konstantinos Tselios1, Dafna D Gladman2, Paula Harvey3, Shadi Akhtari3, Jiandong Su4 and Murray Urowitz2, 1Medicine, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3Cardiology, Women's College Hospital, University of Toronto, Toronto, ON, Canada, 4University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Antimalarial drugs, Biomarkers, myocardial involvement and systemic lupus erythematosus (SLE)

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Session Information

Date: Sunday, November 5, 2017

Title: Systemic Lupus Erythematosus – Clinical Aspects and Treatment Poster I: Biomarkers and Outcomes

Session Type: ACR Poster Session A

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

Background/Purpose: Antimalarial (AM)-induced cardiomyopathy (AMIC) has been rarely reported in systemic lupus erythematosus (SLE). However, given the large number of patients treated, it seems possible that AMIC is under-recognized and may run undiagnosed as an ill-defined heart failure syndrome. Specific cardiac biomarkers may identify patients at risk. We sought to investigate the prevalence and associated factors for such biomarkers in systemic lupus erythematosus (SLE).

Methods: One hundred sixty eight consecutive patients (153 females) attending a large lupus clinic, without past history of cardiac disease (heart failure, coronary artery disease, valvulopathy etc.) and/or pulmonary hypertension, were enrolled. None had chest pain or electrocardiographic (ECG) abnormalities suggestive of acute coronary syndrome. High-sensitivity cardiac troponin I (cTnI) and B-natriuretic peptide (BNP) were measured simultaneously in serum and plasma samples, respectively. Patients were categorized according to normal or abnormal BNP and/or cTnI. For the assessment of the impact of AM duration on abnormal cardiac biomarkers, patients were divided in two groups according to the median duration of use, which was calculated at 5.6 years in the current cohort. Statistical analysis was performed with SAS 9.0 software; p<0.05 was considered significant.

Results: Sixteen patients (9.5%) had elevated BNP and/or cTnI. Compared to subjects with normal biomarkers, they were older, had longer disease and AM use duration and more frequently persistent creatine phosphokinase (CPK) elevation. Details are shown in Table 1.

Table 1. Comparison between BNP/cTnI abnormal and BNP/cTnI normal patients

VARIABLE

(At assessment)

BNP/cTnI abnormal (no history of heart disease or PAH) (n=16)

BNP/cTnI normal

(n=152)

P

Age (y)

54.7 ±15.1

47.83 ± 12.15

0.037

SLE duration (y)

22.54 ± 10.44

15.45 ± 10.05

0.008

SLEDAI-2K

1.88 ± 2.47

2.79 ± 3.64

0.329

Adjusted Mean SLEDAI-2K for 2 years prior

2.52±2.96

3.02±3.18

0.549

eGFR < 30ml/min

0 (0%)

3 (2%)

0.571

Hypertension

10 (62.5%)

54 (35.5%)

0.035

Diuretics treatment

5 (31.3%)

8 (5.3%)

<0.001

Systolic BP at test (mmHg)

118.4 ± 21.7

113.5 ± 16.9

0.28

Diastolic BP at test (mmHg)

71.9 ± 10.1

69.5 ± 11.8

0.444

Abnormal CPK ⌘

7 (43.8%)

24 (15.8%)

0.008

Cumulative years on AM

13.66 ± 9.14

7.88 ± 8.02

0.008

AM duration>5.6 years

14 (87.5%)

69 (45.4%)

0.001

Corticosteroids

8 (50%)

70 (46.1%)

0.763

Mean prednisone (mg/day)

9.4 ± 4.2

7.53 ± 5.1

0.326

Immunosuppressives

10 (62.5%)

87 (57.2%)

0.685

eGFR: estimated glomerular filtration rate, PAH: pulmonary arterial hypertension, BP: blood pressure, CPK: creatine phosphokinase, AM: antimalarials, CQ: chloroquine, HCQ: hydroxychloroquine, ⌘ Three abnormal measurements during the last two years

Multivariable regression analysis showed prolonged AM treatment (>5.6 years) and persistent CPK elevation to be important predictors for elevated cardiac biomarkers [HR=5.43, 95%CI=1.14-25.9, p=0.034 and HR=4.62, 95%CI=1.22-17.51, p=0.024, respectively]. Two patients were diagnosed with AMIC on endomyocardial biopsy; both had CPK and BNP/cTnI elevation.

Conclusion: Approximately 9% of SLE patients had elevated myocardial biomarkers, in the absence of prior cardiac disease or pulmonary arterial hypertension. Prolonged AM therapy and persistent CPK elevation conferred an increased risk for abnormal BNP and cTnI, which might predict AMIC.


Disclosure: K. Tselios, None; D. D. Gladman, None; P. Harvey, None; S. Akhtari, None; J. Su, None; M. Urowitz, None.

To cite this abstract in AMA style:

Tselios K, Gladman DD, Harvey P, Akhtari S, Su J, Urowitz M. Prolonged Antimalarial Treatment Is Associated with Increased Risk for Elevated Myocardial Biomarkers in Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/prolonged-antimalarial-treatment-is-associated-with-increased-risk-for-elevated-myocardial-biomarkers-in-systemic-lupus-erythematosus/. Accessed .
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