Evidence map›Paper›PMID 32146219›Full record

ArticleOphthalmology. Retina2020

Symmetric Age Association of Retinal Degeneration in Patients with CLN2-Associated Batten Disease.

Kyle D Kovacs, Samir Patel, Anton Orlin, Keunpyo Kim, Sherri Van Everen, Therese Conner, Dolan Sondhi, Stephen M Kaminsky, Donald J D'Amico, Ronald G Crystal and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Ophthalmology. Retina, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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.

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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. The Role of Visual Electrophysiology in Systemic Hereditary Syndromes.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Visual perception and macular integrity in non-classical CLN2 disease.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Observational
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
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

11 authors at 2 institutions in 1 country.

Kyle D KovacsDepartment of Ophthalmology, Retina Service, Weill Cornell Medical College, New York, New York.
Samir PatelRegenxbio Inc, Rockville, Maryland.
Anton OrlinDepartment of Ophthalmology, Retina Service, Weill Cornell Medical College, New York, New York.
Keunpyo KimRegenxbio Inc, Rockville, Maryland.
Sherri Van EverenRegenxbio Inc, Rockville, Maryland.
Therese ConnerRegenxbio Inc, Rockville, Maryland.
Dolan SondhiDepartment of Genetic Medicine, Weill Cornell Medical College, New York, New York.
Stephen M KaminskyDepartment of Genetic Medicine, Weill Cornell Medical College, New York, New York.
Donald J D'AmicoDepartment of Ophthalmology, Retina Service, Weill Cornell Medical College, New York, New York.
Ronald G CrystalDepartment of Genetic Medicine, Weill Cornell Medical College, New York, New York.
Szilárd KissDepartment of Ophthalmology, Retina Service, Weill Cornell Medical College, New York, New York. Electronic address: szk7001@med.cornell.edu.
Cornell University · USRegenxbio (United States) · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Training & EducationU54NS065768 · NINDS · UNIVERSITY OF MINNESOTA · PI WHITLEY, CHESTER B. · 2009 to 2024
$17.7M
Gene Therapy for Batten Disease Using AAVrh.10 Expressing Human CLN2 cDNAR01NS061848 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G · 2010 to 2013
$3.7M
NCATS NIH HHS UL1 TR001863NEI NIH HHS L30 EY023847NIH HHS 1R01NS061848NINDS NIH HHS R01 NS061848NINDS NIH HHS U54 NS065768
6 · The paper itself

Abstract

purposeMutations in the CLN2 gene lead to a neurodegenerative and blinding lysosomal storage disorder: late infantile neuronal ceroid lipofucinosis, also known as "CLN2 disease." The purpose of the current study was to characterize the evolution of CLN2-associated retinal manifestations using the Weill Cornell Batten Scale (WCBS) and the age association of the retinal degeneration using central subfield thickness (CST) measurements and then correlate these findings with fundus photography and OCT to determine a critical period for retinal intervention.

designRetrospective, single-center cohort.

participantsEighty-four eyes of 42 treatment-naïve patients with CLN2 disease.

methodsClinical records, fundus photographs, and OCT imaging for patients with CLN2 disease collected during examinations under anesthesia were reviewed. Imaging was categorized per WCBS criteria by 3 masked graders.

main outcome measuresCLN2-associated retinopathy assessed using WCBS scores, fundus photographs, and OCT imaging, correlated with patient age.

resultsEighty-four eyes of 42 patients had baseline fundus photographs, with baseline OCT in 31 eyes of 16 patients. Fundus photographs were obtained serially for 26 eyes of 13 patients, and serial OCT scans were obtained in 10 eyes of 5 patients. At baseline, bilateral WCBS scores were highly correlated for OCT and fundus photographs (r = 0.96 and 0.82, respectively). Central subfield thickness was negatively correlated with left and right eye WCBS OCT scores (r = -0.92 and -0.83, respectively; P < 0.001) and fundus photograph scores (r = -0.80 and -0.83, respectively; P < 0.001). OCT thickness was symmetrical between each eye. Baseline OCT data with age fit using a sigmoid function demonstrated a period of accelerated loss between 48 and 72 months of age.

conclusionsRetinal degeneration associated with CLN2 disease manifests as a progressive, symmetrical decline, which appears to accelerate during a critical period at 48 to 72 months of age, suggesting intervention with retina-specific CLN2 gene therapy should occur ideally before or as early as possible within this critical period. The WCBS is a valuable tool and is highly correlated with the extent of retinal degeneration observed in OCT or fundus photographs; by using the fellow eye as a control, this grading scale can be used to monitor the effect of CLN2 gene therapy in future trials.

Indexed as

MutationVisual AcuityAminopeptidasesChild, PreschoolDipeptidyl-Peptidases and Tripeptidyl-PeptidasesDNADNA Mutational AnalysisFluorescein AngiographyFundus OculiHumansInfantMacular DegenerationNeuronal Ceroid-LipofuscinosesRetinaRetrospective StudiesSerine ProteasesAminopeptidasesDipeptidyl-Peptidases and Tripeptidyl-PeptidasesDNASerine ProteasesTPP1 protein, humanTripeptidyl-Peptidase 1

Identifiers

PMID32146219
PMCPMC7354207
OpenAlexW3000747477

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.