June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
Evaluation of systemic immune markers in dry eye disease and a comparison of subjects with and without Sjogren’s syndrome in the Dry Eye Assessment and Management (DREAM©) Study
Author Affiliations & Notes
  • Marium Hashemi
    The University of Tennessee Health Science Center College of Medicine, Memphis, Tennessee, United States
  • Gui-Shuang Ying
    University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States
  • Di Zhu
    University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States
  • Penny A Asbell
    The University of Tennessee Health Science Center College of Medicine, Memphis, Tennessee, United States
  • Footnotes
    Commercial Relationships   Marium Hashemi None; Gui-Shuang Ying None; Di Zhu None; Penny Asbell Regeneron, Code C (Consultant/Contractor)
  • Footnotes
    Support  National Eye Institute Grants U10EY022879, U10EY022881, R21EY031338, and R01EY026972; Immco Diagnostics Inc./Trinity Biotech (supplied and performed antibody testing for experiment)
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 3943. doi:
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    • Get Citation

      Marium Hashemi, Gui-Shuang Ying, Di Zhu, Penny A Asbell; Evaluation of systemic immune markers in dry eye disease and a comparison of subjects with and without Sjogren’s syndrome in the Dry Eye Assessment and Management (DREAM©) Study. Invest. Ophthalmol. Vis. Sci. 2023;64(8):3943.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Ocular surface inflammation is a well-described component of dry eye disease (DED). This study evaluated the positivity of 34 systemic inflammatory biomarkers in the serum of DED patients from the DREAM study and their associations with Sjogren’s syndrome (SS).

Methods : Baseline blood samples were collected and analyzed for biomarkers using line immunoassays (LIA). The ImmcoStripe ANA Advanced LIA (Immco Diagnostics Inc., Buffalo, NY) was used for detection of antibodies to Ro 60, Ro 52, PM-Scl100, PM-Scl75, AMA-M2, DFS70, CENP-B, PCNA, Ku, Mi2, SRP54, Histones, DNA, Sm, Jo1, U1SnRNP A, U1SnRNP68, U1SnRNP C, Scl70, La, and Ribo-P. The ImmcoStripe Myositis Advanced LIA (Immco Diagnostics Inc., Buffalo, NY) was used for detection of antibodies to PM-Scl100, PM-Scl75, Ku, Mi-2, Ro 52, Jo-1, Fibrillarin/U3 RNP, PL7, PL12, OJ, EJ, U1 SnRNP68, U1 SnRNP A, U1 SnRNP C, U2 SnRNP A’, U2SnRNP B’’, SRP54, SAE1, MDA5/CADM-140, CN-1A, MORC3, TIF1/TIF1a, and KS. At baseline, participants were categorized as SS or non-SS patients based on the 2012 American College of Rheumatology (ACR) criteria1. Comparison of biomarker positivity between Sjo vs. non-Sjo patients was performed using a Chi-square test.

1.Bunya et al. Prevalence of Novel Candidate Sjogren Syndrome Autoantibodies in the Dry Eye Assessment and Management (DREAM) Study. Cornea. 2018;37(11):1425-1430.

Results : 481 DREAM participants with moderate-to-severe DED had biomarker assessments at baseline. Table 1 shows the positivity of each inflammatory biomarker. Few subjects showed strongly positive results for any of the biomarkers. KS, U2SnRNP A’, OJ, PL-12, Ku, and PCNA were 0% strongly positive. The rest ranged from 0.2% (MORC-3, Sm, Histones, Ribo-P) to 11.4% (SAE-1). Table 2 compares the positivity of biomarkers with a significant difference between SS and non-SS patients. Compared to the latter, Sjo patients had significantly higher biomarker positivity in CN-1A (P=.004), PL-7 (P=.03), Ro 52 (P<.0001), and La (P<.0001).

Conclusions : Most systemic inflammation biomarkers were not positive in the majority of participants. Antibodies to CN-1A, PL-7, Ro-52, and La, biomarkers associated with pathologies such as inclusion body myositis, anti-synthetase syndrome, myositis with interstitial lung disease, and primary SS, respectively, were more highly expressed in SS patients.

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

 

 

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