Evidence map›Paper›PMID 42162158›Full record

Trial reportScientific reports2026

Tear biomarker changes and ocular surface recovery with low-level light therapy after cataract surgery: a double-masked randomized controlled clinical trial.

Mihaela-Madalina Timofte-Zorila, Mariana Pavel-Tanasa, Giuseppe Giannaccare, Nicoleta Vlas, Filippo Lixi, Mario Troisi, Daniela Constantinescu, Radu Tanasa, Diana Alecu, Sabina Turcas and 4 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Mihaela-Madalina Timofte-ZorilaGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Mariana Pavel-TanasaGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania. mariana.pavel-tanasa@umfiasi.ro.ORCID http://orcid.org/0000-0002-2802-5993
Giuseppe GiannaccareDepartment of Surgical Sciences, Eye Clinic, University of Cagliari, 09124, Cagliari, Italy.
Nicoleta VlasGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Filippo LixiDepartment of Surgical Sciences, Eye Clinic, University of Cagliari, 09124, Cagliari, Italy.
Mario TroisiDepartment of Neurosciences, Reproductive and Odontostomatological Sciences, Eye Clinic, Federico II University, 80131, Naples, Italy.
Daniela ConstantinescuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Radu TanasaFaculty of Physics, Alexandru Ioan Cuza University, 700506, Iasi, Romania.
Diana AlecuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Sabina TurcasGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Sinziana IstrateCarol Davila University of Medicine and Pharmacy, 050474, Bucharest, Romania.
Daciana Elena BranisteanuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Cristina PredaGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.
Daniel Constantin BranisteanuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115, Iasi, Romania.

Funding

The Health Program (PS) 2021-2027, Policy Objective 1, Priority 5, project title "Development of translational research for vaccines, serums and other biological drugs-Acronym CANTAVAC 2.0" SMIS code 326920
6 · The paper itself

Abstract

Dry eye disease (DED) is a common complication following cataract-surgery, potentially impairing visual recovery. Low-level light therapy (LLLT) has emerged as a noninvasive approach to improve ocular surface status. This study evaluated the perioperative effects of LLLT on ocular surface modulation by correlating clinical outcomes with tear biomarker dynamics and developing predictive models to identify patients most likely to benefit from LLLT. Of the 98 patients initially randomized, 88 were included in the final analysis, with 44 allocated to the LLLT group and 44 to the sham treatment group. Clinical evaluation-including Ocular Surface Disease Index (OSDI) as the primary outcome, and tear breakup time, Schirmer test, and tear osmolarity as secondary endpoints-was performed preoperatively and one month postoperatively to classify patients as preclinical or having DED. Tear levels of biomarkers involved in tissue repair and neurotrophic-signaling (GDF-15,β-NGF, VEGFA, PDGF-AB, PDGF-CC) and inflammation (OPN, OPG, TNF-α) were assessed as exploratory endpoints and quantified using Luminex-FlexMap3D technology. LLLT-treated patients showed significantly higher clinical improvement post-cataract surgery than sham controls (44.2% vs. 4.4%; p < 0.0001). In DED patients, LLLT significantly increased GDF-15 (77.6 ± 7.2 to 95.5 ± 7.4 pg/mL; p = 0.0112) and PDGF-CC (711.4 ± 76.6 to 1024 ± 130.8 pg/mL; p = 0.0473). The LLLT-induced β-NGF increase was more pronounced in preclinical cases than in those with baseline DED (10.1 ± 3.02 vs. 5.8 ± 0.55 pg/mL; p = 0.0271). Biomarker profiles indicated inflammatory resolution post-LLLT, whereas sham-treated eyes showed persistent inflammation. Finally, integrative modeling of clinical and molecular data yielded a LASSO-adjusted AUC of 0.886, underscoring high discriminative performance. LLLT accelerates ocular surface recovery after cataract surgery by modulating reparative, neurotrophic, and inflammatory pathways. Tear biomarkers assessed at baseline and through one-month dynamics (GDF-15, PDGF-CC, β-NGF) and integrated with clinical parameters, may help predict treatment response and guide personalized postoperative management.

Indexed as

BiomarkersCataract ExtractionDry Eye SyndromesTearsAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedBiomarkersCataract surgeryDry eye diseaseGDF-15Low-level light therapyOPNOSDIPDGF-CCSchirmer testTBUTβ-NGF

Identifiers

PMID42162158
PMCPMC13391487

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Registered trials

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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.