Evidence map›Paper›PMID 25604658›Full record

ArticleAmerican journal of medical genetics. Part A2015

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, Marcin Szynkiewicz, Gabriella M A Forte, Hannah L Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman and 126 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 344 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
344citing papers in PubMed, 3 pooled it
22.4field-weighted citation impact, top 1% 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

344 citing papers in PubMed, 3 syntheses or guidelines pooled it, 601 citations in OpenAlex.

  1. Pooled it
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  4. Trial
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  8. Article
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  12. Autoinflammatory syndromes of STING and TREX1 dysfunction.The Journal of clinical investigation · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. HeterozygousiScience · 2026
    Article
  19. Article
  20. Article

284 more citing papers are in PubMed but not listed here.

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

136 authors at 20 institutions in 25 countries.

Yanick J CrowINSERM UMR 1163, Laboratory of Neurogenetics and Neuroinflammation, Paris Descartes - Sorbonne Paris Cité University, Institut Imagine, Hôpital Necker, Paris, France; Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
Diana S Chase
Johanna Lowenstein Schmidt
Marcin Szynkiewicz
Gabriella M A Forte
Hannah L Gornall
Anthony Oojageer
Beverley Anderson
Amy Pizzino
Guy Helman
Mohamed S Abdel-Hamid
Ghada M Abdel-Salam
Sam Ackroyd
Alec Aeby
Guillermo Agosta
Catherine Albin
Stavit Allon-Shalev
Montse Arellano
Giada Ariaudo
Vijay Aswani
Riyana Babul-Hirji
Eileen M Baildam
Nadia Bahi-Buisson
Kathryn M Bailey
Christine Barnerias
Magalie Barth
Roberta Battini
Michael W Beresford
Geneviève Bernard
Marika Bianchi
Thierry Billette de Villemeur
Edward M Blair
Miriam Bloom
Alberto B Burlina
Maria Luisa Carpanelli
Daniel R Carvalho
Manuel Castro-Gago
Anna Cavallini
Cristina Cereda
Kate E Chandler
David A Chitayat
Abigail E Collins
Concepcion Sierra Corcoles
Nuno J V Cordeiro
Giovanni Crichiutti
Lyvia Dabydeen
Russell C Dale
Stefano D'Arrigo
Christian G E L De Goede
Corinne De Laet
Liesbeth M H De Waele
Ines Denzler
Isabelle Desguerre
Koenraad Devriendt
Maja Di Rocco
Michael C Fahey
Elisa Fazzi
Colin D Ferrie
António Figueiredo
Blanca Gener
Cyril Goizet
Nirmala R Gowrinathan
Kalpana Gowrishankar
Donncha Hanrahan
Bertrand Isidor
Bülent Kara
Nasaim Khan
Mary D King
Edwin P Kirk
Ram Kumar
Lieven Lagae
Pierre Landrieu
Heinz Lauffer
Vincent Laugel
Roberta La Piana
Ming J Lim
Jean-Pierre S-M Lin
Tarja Linnankivi
Mark T Mackay
Daphna R Marom
Charles Marques Lourenço
Shane A McKee
Isabella Moroni
Jenny E V Morton
Marie-Laure Moutard
Kevin Murray
Rima Nabbout
Sheela Nampoothiri
Noemi Nunez-Enamorado
Patrick J Oades
Ivana Olivieri
John R Ostergaard
Belén Pérez-Dueñas
Julie S Prendiville
Venkateswaran Ramesh
Magnhild Rasmussen
Luc Régal
Federica Ricci
Marlène Rio
Diana Rodriguez
Agathe Roubertie
Elisabetta Salvatici
Karin A Segers
Gyanranjan P Sinha
Doriette Soler
Ronen Spiegel
Tommy I Stödberg
Rachel Straussberg
Kathryn J Swoboda
Mohnish Suri
Uta Tacke
Tiong Y Tan
Johann te Water Naude
Keng Wee Teik
Maya Mary Thomas
Marianne Till
Davide Tonduti
Enza Maria Valente
Rudy Noel Van Coster
Marjo S van der Knaap
Grace Vassallo
Raymon Vijzelaar
Julie Vogt
Geoffrey B Wallace
Evangeline Wassmer
Hannah J Webb
William P Whitehouse
Robyn N Whitney
Maha S Zaki
Sameer M Zuberi
John H Livingston
Flore Rozenberg
Pierre Lebon
Adeline Vanderver
Simona Orcesi
Gillian I Rice
Manchester Academic Health Science Centre · GBHôpital Necker-Enfants Malades · FRFondazione Istituto Neurologico Nazionale Casimiro Mondino · ITKU Leuven · BEFondazione IRCCS Istituto Neurologico Carlo Besta · ITGeorge Washington University · USNational Research Centre · EGAssistance Publique – Hôpitaux de Paris · FRBirmingham Women's Hospital · GBChildren's National · USDélégation Paris 5 · FREmek Medical Center · ILHospital for Sick Children · CAHospital Italiano de Buenos Aires · ARLeeds General Infirmary · GBNottingham University Hospitals NHS Trust · GBSchneider Children's Medical Center · ILSt Mary's Hospital · GBAarhus University Hospital · DKAlder Hey Children's NHS Foundation Trust · GB

Funding

UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
European Research Council 309449NCRR NIH HHS UL1 RR025764
6 · The paper itself

Abstract

Aicardi-Goutières syndrome is an inflammatory disease occurring due to mutations in any of TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR or IFIH1. We report on 374 patients from 299 families with mutations in these seven genes. Most patients conformed to one of two fairly stereotyped clinical profiles; either exhibiting an in utero disease-onset (74 patients; 22.8% of all patients where data were available), or a post-natal presentation, usually within the first year of life (223 patients; 68.6%), characterized by a sub-acute encephalopathy and a loss of previously acquired skills. Other clinically distinct phenotypes were also observed; particularly, bilateral striatal necrosis (13 patients; 3.6%) and non-syndromic spastic paraparesis (12 patients; 3.4%). We recorded 69 deaths (19.3% of patients with follow-up data). Of 285 patients for whom data were available, 210 (73.7%) were profoundly disabled, with no useful motor, speech and intellectual function. Chilblains, glaucoma, hypothyroidism, cardiomyopathy, intracerebral vasculitis, peripheral neuropathy, bowel inflammation and systemic lupus erythematosus were seen frequently enough to be confirmed as real associations with the Aicardi-Goutieres syndrome phenotype. We observed a robust relationship between mutations in all seven genes with increased type I interferon activity in cerebrospinal fluid and serum, and the increased expression of interferon-stimulated gene transcripts in peripheral blood. We recorded a positive correlation between the level of cerebrospinal fluid interferon activity assayed within one year of disease presentation and the degree of subsequent disability. Interferon-stimulated gene transcripts remained high in most patients, indicating an ongoing disease process. On the basis of substantial morbidity and mortality, our data highlight the urgent need to define coherent treatment strategies for the phenotypes associated with mutations in the Aicardi-Goutières syndrome-related genes. Our findings also make it clear that a window of therapeutic opportunity exists relevant to the majority of affected patients and indicate that the assessment of type I interferon activity might serve as a useful biomarker in future clinical trials.

Indexed as

MutationPhenotypeAdenosine DeaminaseAutoimmune Diseases of the Nervous SystemDEAD-box RNA HelicasesExodeoxyribonucleasesGenetic Association StudiesGenotypeHumansInterferon-Induced Helicase, IFIH1InterferonsMonomeric GTP-Binding ProteinsNervous System MalformationsPhosphoproteinsPterinsRibonuclease HAdenosine DeaminaseDEAD-box RNA HelicasesExodeoxyribonucleasesIFIH1 protein, humanInterferon-Induced Helicase, IFIH1InterferonsMonomeric GTP-Binding ProteinsPhosphoproteinsPterinsRibonuclease Hribonuclease HIISAM Domain and HD Domain-Containing Protein 1SAMHD1 protein, humanthree prime repair exonuclease 1Aicardi-Goutières syndromebilateral striatal necrosisinterferon signaturespastic paraparesistype I interferon

Identifiers

PMID25604658
PMCPMC4382202
OpenAlexW2063675796

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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.