Evidence map›Paper›PMID 38735647›Full record

SynthesisBrain : a journal of neurology2024

Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders.

James Liu, Yi He, Cara Lwin, Marina Han, Bin Guan, Amelia Naik, Chelsea Bender, Nia Moore, Laryssa A Huryn, Yuri V Sergeev and 35 more

Abstract readSystematic Review
In one paragraph

Synthesis in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The cyclic nucleotide binding sites of Swiss-Cheese, thebioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Novel variant inFrontiers in genetics · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

45 authors.

James LiuOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Yi HeFermentation Facility, Biochemistry and Biophysics Center, National Heart, Lung and Blood Institute, Bethesda, MD 20892, USA.
Cara LwinOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Marina HanOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Bin GuanOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Amelia NaikOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Chelsea BenderOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Nia MooreOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Laryssa A HurynOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Yuri V SergeevOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Haohua QianVisual Function Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-1114-4697
Yong ZengVisual Function Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Lijin DongGenetic Engineering Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Pinghu LiuGenetic Engineering Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jingqi LeiGenetic Engineering Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Carl J HaugenGenetic Engineering Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Lev PrasovDepartment of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan, Ann Arbor, MI 48105, USA.
Ruifang ShiDepartment of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, 100730 Beijing, China.
Hélène DollfusCentre de référence pour les Affections Rares Ophtalmologiques CARGO, Hôpitaux Universitaires de Strasbourg, Université de Strasbourg, UMRS_1112, Strasbourg 67091, France.
Petros AristodemouCyprus Institute of Neurology and Genetics, Nicosia 1683, Cyprus.
Yannik LaichUCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Andrea H NémethOxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, ACE Building, Nuffield Orthopaedic Centre, Oxford OX3 7HE, UK.
John TaylorOxford Regional Genetics Laboratory, Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, UK.
Susan DownesNuffield Department of Ophthalmology, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, UK.
Maciej R KrawczynskiDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznan 60-512, Poland.
Isabelle MeunierNational Referent Centre for Rare Sensory Diseases, Montpellier University Hospital, Montpellier University, Montpellier 34295, France.
Melissa StrassbergInvitae Corporation, San Francisco, CA 94103, USA.
Jessica TenneyDivision of Medical Genetics, Department of Pediatrics, UCSF School of Medicine, San Francisco, CA 94143, USA.
Josephine GaoDivision of Medical Genetics, Department of Pediatrics, UCSF School of Medicine, San Francisco, CA 94143, USA.
Matthew A ShearDivision of Medical Genetics, Department of Pediatrics, UCSF School of Medicine, San Francisco, CA 94143, USA.
Anthony T MooreUCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Jacque L DuncanDepartment of Ophthalmology, UCSF School of Medicine, San Francisco, CA 94143, USA.
Beatriz MenendezDepartment of Pediatrics, University of Illinois School of Medicine, Chicago, IL 60612, USA.
Sarah HullDepartment of Ophthalmology, University of Auckland, Auckland 1023, New Zealand.
Andrea L VincentDepartment of Ophthalmology, University of Auckland, Auckland 1023, New Zealand.
Carly E SiskindNeurology and Neurological Sciences, Stanford School of Medicine, Stanford, CA 94305, USA.
Elias I TraboulsiThe Center for Genetic Eye Diseases, The Cleveland Clinic Eye Institute, Cleveland, OH 44106, USA.
Craig BlackstoneMovement Disorders Division, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0003-1261-9655
Robert A SiskDepartment of Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Virginia Miraldi UtzDepartment of Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Andrew R WebsterUCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Michel MichaelidesUCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Gavin ArnoUCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Matthis SynofzikDivision Translational Genomics of Neurodegenerative Diseases Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen 72076, Germany.ORCID 0000-0002-2280-7273
Robert B HufnagelOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Funding

NEI Genetic Engineering CoreZICEY000458 · NEI · NATIONAL EYE INSTITUTE · PI DONG, LIJIN · 2009 to 2025
$22.6M
Proteins From Hereditary Eye Diseases: In-silico and Experimental StudiesZIAEY000476 · NEI · NATIONAL EYE INSTITUTE · PI SERGEEV, YURI · 2009 to 2025
$16.8M
National Ophthalmic Disease Genotyping and Phenotyping Network - eyeGENEZICEY000478 · NEI · NATIONAL EYE INSTITUTE · PI GOETZ, KERRY · 2009 to 2025
$14.8M
Visual Function CoreZICEY000503 · NEI · NATIONAL EYE INSTITUTE · PI QIAN, HAOHUA · 2011 to 2025
$12.3M
Genomic and epigenomic mechanisms of pediatric ocular disordersZIAEY000565 · NEI · NATIONAL EYE INSTITUTE · PI HUFNAGEL, ROBERT · 2019 to 2024
$11.4M
Clinical ophthalmic molecular diagnostics and discoveryZIAEY000564 · NEI · NATIONAL EYE INSTITUTE · PI GUAN, BIN · 2019 to 2025
$7.9M
Defining the genetic landscape of nanophthalmos and the role of MYRFK08EY032098 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PRASOV, LEV · 2021 to 2025
$1.2M
Fight for Sight UKGreat Ormond Street Hospital Institute for Child HealthMoorfields Eye HospitalNational Institute of Health Research Biomedical Research CentreNEI NIH HHS K08 EY032098Research to Prevent BlindnessSave sight society NZ, Retina NZ, and the Ombler trustUCL Institute of Ophthalmology
6 · The paper itself

Abstract

Biallelic pathogenic variants in the PNPLA6 gene cause a broad spectrum of disorders leading to gait disturbance, visual impairment, anterior hypopituitarism and hair anomalies. PNPLA6 encodes neuropathy target esterase (NTE), yet the role of NTE dysfunction on affected tissues in the large spectrum of associated disease remains unclear. We present a systematic evidence-based review of a novel cohort of 23 new patients along with 95 reported individuals with PNPLA6 variants that implicate missense variants as a driver of disease pathogenesis. Measuring esterase activity of 46 disease-associated and 20 common variants observed across PNPLA6-associated clinical diagnoses unambiguously reclassified 36 variants as pathogenic and 10 variants as likely pathogenic, establishing a robust functional assay for classifying PNPLA6 variants of unknown significance. Estimating the overall NTE activity of affected individuals revealed a striking inverse relationship between NTE activity and the presence of retinopathy and endocrinopathy. This phenomenon was recaptured in vivo in an allelic mouse series, where a similar NTE threshold for retinopathy exists. Thus, PNPLA6 disorders, previously considered allelic, are a continuous spectrum of pleiotropic phenotypes defined by an NTE genotype:activity:phenotype relationship. This relationship, and the generation of a preclinical animal model, pave the way for therapeutic trials, using NTE as a biomarker.

Indexed as

PhenotypeAcyltransferasesAnimalsCarboxylic Ester HydrolasesFemaleHumansMaleMiceMutation, MissensePhospholipasesRetinal DiseasesAcyltransferasesCarboxylic Ester Hydrolasesneurotoxic esterasePhospholipasesPNPLA6 protein, humanBoucher-Neuhäuser syndromeGordon-Holmes syndromeLaurence-Moon syndromeneurodegenerationOliver-McFarlane syndromespastic paraplegia type 39

Identifiers

PMID38735647
PMCPMC11146429

What OpenQuestion holds

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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.