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Abstract Number: 7

Predictive Value for Thrombosis of Double or Triple Positivity in Secondary APS Depends on the Component Assays and the Type of Thrombosis

Michelle Petri1, Daniel Goldman2 and Laurence S Magder3, 1Medicine (Rheumatology), Division of Rheumatology, Johns Hopkins University School of Medicine, MD, USA, Baltimore, MD, 2Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 3Epidemiology and Public health, University of Maryland School of Medicine, Baltimore, MD

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Antiphospholipid antibodies, Antiphospholipid syndrome and thrombosis

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Session Information

Date: Sunday, November 5, 2017

Title: Antiphospholipid Syndrome Poster

Session Type: ACR Poster Session A

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

Background/Purpose: The lupus anticoagulant (LAC) is individually the antiphospholipid antibody (aPL) most associated with thrombotic risk in both primary and secondary APS. Anticardiolipin (aCL) and anti-beta2 glycoprotein 1 may further increase the risk. We investigated the risk for thrombosis in SLE of double or triple positivity for these different aPLs.

Methods: The analysis is based on 1508 SLE patients, (92% female, 51% white, 40% black, and with a mean age at end of follow-up of 46.4 [SD=14.2]). Thrombosis was defined as: arterial thrombosis (CVA, MI, other arterial thrombosis or digital gangrene); and venous thrombosis (DVT, PE or other venous thrombosis).

Results: We looked at the risk of lifetime occurrence of thrombosis as a function of the history of LAC (RVVT confirm), aCL, or anti-beta2 glycoprotein 1 (anti-Beta2). The OR’s in the tables are adjusted for age.

Table 1. History of thrombosis by history of APS.

Specific Components

Proportion (%) of patients with a history of any thrombosis

Odds Ratio (relative to those without any APS components)

P-value

Any Thrombosis

No aPL

None

100/488 (20%)

1.0 (Ref Group)

Single Positive

aCL alone

66/369 (18%)

0.8 (0.6, 1.2)

0.31

LAC alone

26/74 (35%)

2.1 (1.2, 3.6)

0.0063

anti-Beta2 alone

10/82 (12%)

0.6 (0.3, 1.1)

0.095

Double Positive

Any double positive

105/315 (33%)

1.9 (1.4, 2.6)

0.0002

aCL + LAC

61/138 (44%)

2.9 (1.9, 4.4)

<0.0001

aCL + anti-Beta2

29/147 (20%)

0.9 (0.6, 1.5)

0.71

LAC + anti-Beta2

15/30 (50%)

4.1 (1.9, 8.8)

0.0002

Triple positive

All three

89/180 (49%)

3.7 (2.6, 5.4)

<0.0001

Arterial Thrombosis

No aPL

None

55/488 (11%)

1.0 (Ref)

Single Positive

aCL alone

40/369 (11%)

0.9 (0.6, 1.5)

0.78

LAC alone

12/74 (16%)

1.5 (0.7, 3.0)

0.26

anti-Beta2 alone

6/82 (7%)

0.6 (0.3, 1.5)

0.31

Double Positive

Any double positive

59/315 (19%)

1.7 (1.1, 2.5)

0.013

aCL + LAC

37/138 (27%)

2.6 (1.6, 4.2)

<0.0001

aCL + anti-Beta2

18/147 (12%)

1.0 (0.6, 1.9)

0.89

LAC + anti-Beta2

4/30 (13%)

1.3 (0.4, 3.8)

0.66

Triple positive

All three

54/180 (30%)

3.2 (2.1, 5.0)

<0.0001

Venous Thrombosis

No aPL

None

54/488 (11%)

1.0 (Ref)

Single Positive

aCL alone

39/369 (11%)

0.9 (0.6, 1.5)

0.79

LAC alone

19/74 (26%)

2.8 (1.5, 5.1)

0.0008

anti-Beta2 alone

5/82 (6%)

0.5 (0.2, 1.4)

0.19

Double Positive

Any double positive

72/315 (23%)

2.4 (1.6, 3.5)

<0.0001

aCL + LAC

42/138 (31%)

3.5 (2.2, 5.6)

<0.0001

aCL + anti-Beta2

17/147 (12%)

1.0 (0.6, 1.8)

0.93

LAC + anti-Beta2

12/30 (40%)

5.5 (2.5, 12.0)

<0.0001

Triple positive

All three

60/180 (33%)

3.9 (2.6, 6.0)

<0.0001

The findings in the table confirm that there can be an increase in the point estimate from single, to double positivity. However, it clearly depends on which components are considered, and whether it is arterial or venous thrombosis. The strongest finding is that LAC is the most important component. For arterial thrombosis, however, double positivity with LAC and aCL leads to increased risk.

Conclusion: In SLE, lupus anticoagulant is the most important single antiphospholipid test predictive of any thrombosis and venous thrombosis. For arterial thrombosis, aCL and LAC together outperform single tests. For venous thrombosis, the point estimates increase for double positives containing LAC, and for triple positive, although the confidence intervals overlap. In SLE, double, and possibly triple, positivity show promising results. However, different combinations of “double positive” aPLs are important, and differ in arterial vs. venous thrombosis.


Disclosure: M. Petri, Anthera Inc, 5,GlaxoSmithKline, 5,EMD Serono, 5,Eli Lilly and Company, 5,Bristol Meyer Squibb, 5,Amgen, 5,United Rheumatology, 5,Global Academy, 5,Exagen, 2; D. Goldman, None; L. S. Magder, None.

To cite this abstract in AMA style:

Petri M, Goldman D, Magder LS. Predictive Value for Thrombosis of Double or Triple Positivity in Secondary APS Depends on the Component Assays and the Type of Thrombosis [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/predictive-value-for-thrombosis-of-double-or-triple-positivity-in-secondary-aps-depends-on-the-component-assays-and-the-type-of-thrombosis/. Accessed .
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