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Abstract Number: 2192

Phenotypic Features of Sjögren’s Syndrome Among Patients with Low-Titer SSA/B Antibodies

Mara McAdams DeMarco1, Mi Y. Lam2, Stephen Shiboski2, Lindsey A. Criswell3, Caroline Shiboski4 and Alan N. Baer5, 1Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 2University of California, San Francisco, San Francisco, CA, 3Department of Medicine, University of California, San Francisco, Rosalind Russell Medical Research Center for Arthritis, San Francisco, CA, 4Orofacial Sciences, University of California, San Francisco, San Francisco, CA, 5Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Sjogren's syndrome

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Session Information

Title: Sjögren's Syndrome - Clinical

Session Type: Abstract Submissions (ACR)

Background/Purpose: The significance of a low titer of SSA and/or SSB antibodies (SSA/B-Ab) in individuals with clinical or other laboratory findings suggestive of Sjögren’s syndrome (SS) is unclear. Low titers may represent false positive immunoassay results, seropositivity in the absence of clinical disease, or true markers of a connective tissue disease, such as SS. It is unclear whether low titers represent a distinct phenotype or one more similar to those with negative titers. We sought to explore the association between SSA/B titer levels and phenotypic features of SS, including histopathological characteristics.

Methods: The Sjögren’s International Collaborative Clinical Alliance (SICCA) is an NIH-funded registry of individuals with suspected or established SS. Each participant undergoes a uniform and protocol-driven evaluation for SS, including rheumatologic, oral, and ophthalmologic examinations, serologic testing, labial salivary gland biopsy, and ocular staining. SSA/B-Ab testing was performed by Quest Laboratories, using an automated multiplex flow immunoassay. Positive results were expressed in “antibody index” (AI) units and provided as continuous variables measure up to a level of 8 AI.  Levels more than >8 AI were not quantified. We compared the mean and prevalence of phenotypic features of SS by category of SSA/B-Ab (High: both SSA-Ab and/or SSB-Ab>8; Low: SSA-Ab and/or SSB-Ab≥1 but both ≤8; Negative: both SSA-Ab and SSB-Ab<1).

Results: Among the SICCA participants, low titers of SSA/B-Ab were present in 277 (14.1%), high titer SSA/B-Ab in 434 (22.1%) and negative SSA/B-Ab in 1256 (63.8%). The associations between these three strata of SSA/B-Ab titers and phenotypic features of SS are shown in the Table. Mean age decreased while focus score increased as SSA/B-Ab titers increased. The percentage of participants with each phenotypic feature was greater for those with high SSA/B-Ab compared with those with low titers and greater for those with low titers compared with negative titers.

Table: Phenotypic Features of Sjogren’s Syndrome by SSA/B Antibody Titer

 

High

Low

Negative

p

 

N

Mean or %

N

Mean or %

N

Mean or %

 

Age (years)

454

50.79

287

51.33

1270

54.48

<.0001

Focus score (foci/4 mm2)

367

3.32

204

2.79

527

1.50

<.0001

ANA≥1:320

455

69.5%

287

44.3%

1276

16.1%

<.0001

Rheumatoid factor ≥ 30 IU/ml

454

49.8%

287

34.2%

1275

10.0%

<.0001

IgG>1445 mg/dl

455

62.0%

285

49.5%

1273

12.1%

<.0001

C4<16 mg/dl

455

22.6%

285

17.2%

1273

10.6%

<.0001

WBC ≤ 4000/mm3

448

27.5%

283

19.4%

1266

7.4%

<.0001

FLS or F/SLS focus score ≥ 1*

434

74.0%

277

57.4%

1256

19.1%

<.0001

Germinal centers in lip biopsy

454

23.8%

285

7.4%

1273

4.2%

<.0001

Schirmer’s ≤5 mm either eye

454

46.0%

286

37.8%

1276

24.3%

<.0001

Ocular surface staining ≥ 3

454

94.1%

286

83.2%

1275

67.2%

<.0001

Unstimulated saliva ≤0.5 ml/5 min

455

64.4%

286

61.2%

1274

48.0%

<.0001

*FLS=focal lymphocytic sialadenitis; F/SLS=focal /sclerosing lymphocytic sialadenitis

Conclusion: There is a higher prevalence of all phenotypic features of SS among those with higher SSA/B-Ab titer. Low antibody titers occur in approximately 14% of patients suspected of having SS and may represent an intermediary phenotype distinct from those with high or negative titers.


Disclosure:

M. McAdams DeMarco,
None;

M. Y. Lam,
None;

S. Shiboski,
None;

L. A. Criswell,
None;

C. Shiboski,
None;

A. N. Baer,
None.

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