Evidence map›Paper›PMID 23769845›Full record

ReviewExperimental eye research2013

Lacritin and the tear proteome as natural replacement therapy for dry eye.

Roy Karnati, Diane E Laurie, Gordon W Laurie

Registry-linked trialAbstract readReview
In one paragraph

Review in Experimental eye research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04198740 (Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface), which is not on this map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.2field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04198740 recruitingnot on this mapstarted 2020, after this paper: background citation

Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface

TypeobservationalSponsorCentre hospitalier de l'Université de Montréal (CHUM)Ran2020 to 2035Enrolled300ConditionsDry Eye Syndrome, Infectious Keratoconjunctivitis, Mucous Membrane Pemphigoid, Allergic ConjunctivitisArmsTear sample collection via Schirmer strip and subsequent analysis by mass spectrometry
3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 70 citations in OpenAlex.

  1. Site-specific O-glycans influence lacritin structure and multimerization in tears.Protein science : a publication of the Protein Society · 2026
    Article
  2. Article
  3. Article
  4. Tear fluid proteomics: a comparative study of DIA and DDA mass spectrometry.Journal of mass spectrometry and advances in the clinical lab · 2025
    Article
  5. Review
  6. Translating Biomarker Discovery: From Bench to Bedside in Dry Eye Disease.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Unraveling the Intraday Variations in the Tear Fluid Proteome.Investigative ophthalmology & visual science · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Autophagy in the normal and diseased cornea.Experimental eye research · 2022
    Review
  18. Review
  19. Protein and polypeptide mediated delivery to the eye.Advanced drug delivery reviews · 2022
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

Roy KarnatiSchool of Life Sciences, University of Hyderabad, Hyderabad, India.
Diane E Laurie
Gordon W Laurie
University of Hyderabad · INUniversity of Virginia · USVirginia–Maryland College of Veterinary Medicine · US

Funding

Structure and Function of Ocular LacritinR01EY013143 · NEI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LAURIE, GORDON WILLIAM · 2002 to 2011
$2.8M
Modeling Novel Treatments for Dry EyeR01EY018222 · NEI · UNIVERSITY OF VIRGINIA · PI LAURIE, GORDON WILLIAM · 2007 to 2011
$1.9M
NEI NIH HHS EY018222NEI NIH HHS R01 EY013143NEI NIH HHS R01 EY018222
6 · The paper itself

Abstract

Tear proteins are potential biomarkers, drug targets, and even biotherapeutics. As a biotherapeutic, a recombinant tear protein might physiologically rescue the ocular surface when a deficiency is detected. Such a strategy pays more attention to the natural prosecretory and protective properties of the tear film and seeks to alleviate symptoms by addressing cause, rather than the current palliative, non-specific and temporary approaches. Only a handful of tear proteins appear to be selectively downregulated in dry eye, the most common eye disease. Lacritin and lipocalin-1 are two tear proteins selectively deficient in dry eye. Both proteins influence ocular surface health. Lacritin is a prosecretory mitogen that promotes basal tearing when applied topically. Levels of active monomeric lacritin are negatively regulated by tear tissue transglutaminase, whose expression is elevated in dry eye with ocular surface inflammation. Lipocalin-1 is the master lipid sponge of the ocular surface, without which residual lipids could interfere with epithelial wetting. It also is a carrier for vitamins and steroid hormones, and is a key endonuclease. Accumulation of DNA in tears is thought to be proinflammatory. Functions of these and other tear proteins may be influenced by protein-protein interactions. Here we discuss new advances in lacritin biology and provide an overview on lipocalin-1, and newly identified members of the tear proteome.

Indexed as

Dry Eye SyndromesEye ProteinsGlycoproteinsHumansLipocalin 1ProteomeEye ProteinsGlycoproteinsLACRT protein, humanLCN1 protein, humanLipocalin 1Proteometear proteinscorneadry eyelacrimal glandlacritintear lipocalintear proteome

Identifiers

PMID23769845
PMCPMC3844047
OpenAlexW2113189797

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.