Literature DB >> 26581299

Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome.

Roberta La Piana1, Carla Uggetti1, Federico Roncarolo1, Adeline Vanderver1, Ivana Olivieri1, Davide Tonduti1, Guy Helman1, Umberto Balottin1, Elisa Fazzi1, Yanick J Crow1, John Livingston2, Simona Orcesi2.   

Abstract

OBJECTIVE: To perform an updated characterization of the neuroradiologic features of Aicardi-Goutières syndrome (AGS).
METHODS: The neuroradiologic data of 121 subjects with AGS were collected. The CT and MRI data were analyzed with a systematic approach. Moreover, we evaluated if an association exists between the neuroradiologic findings, clinical features, and genotype.
RESULTS: Brain calcifications were present in 110 subjects (90.9%). Severe calcification was associated with TREX1 mutations and early age at onset. Cerebral atrophy was documented in 111 subjects (91.8%). Leukoencephalopathy was present in 120 children (99.2%), with 3 main patterns: frontotemporal, diffuse, and periventricular. White matter rarefaction was found in 54 subjects (50.0%), strongly associated with mutations in TREX1 and an early age at onset. Other novel radiologic features were identified: deep white matter cysts, associated with TREX1 mutations, and delayed myelination, associated with RNASEH2B mutations and early age at onset.
CONCLUSIONS: We demonstrate that the AGS neuroradiologic phenotype is expanding by adding new patterns and findings to the classic criteria. The heterogeneity of neuroradiologic patterns is partly explained by the timing of the disease onset and reflects the complexity of the pathogenic mechanisms.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 26581299      PMCID: PMC4731289          DOI: 10.1212/WNL.0000000000002228

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  33 in total

1.  Neuroimaging in Cockayne syndrome.

Authors:  M Koob; V Laugel; M Durand; H Fothergill; C Dalloz; F Sauvanaud; H Dollfus; I J Namer; J-L Dietemann
Journal:  AJNR Am J Neuroradiol       Date:  2010-06-03       Impact factor: 3.825

2.  Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke.

Authors:  Baozhong Xin; Stephen Jones; Erik G Puffenberger; Claas Hinze; Alicia Bright; Haiyan Tan; Aimin Zhou; Guiyun Wu; Jilda Vargus-Adams; Dimitris Agamanolis; Heng Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-14       Impact factor: 11.205

Review 3.  Cockayne syndrome: the expanding clinical and mutational spectrum.

Authors:  Vincent Laugel
Journal:  Mech Ageing Dev       Date:  2013-02-18       Impact factor: 5.432

4.  Aicardi-Goutieres syndrome: neuroradiologic findings and follow-up.

Authors:  C Uggetti; R La Piana; S Orcesi; M G Egitto; Y J Crow; E Fazzi
Journal:  AJNR Am J Neuroradiol       Date:  2009-07-23       Impact factor: 3.825

5.  Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.

Authors:  Gillian I Rice; Paul R Kasher; Gabriella M A Forte; Niamh M Mannion; Sam M Greenwood; Marcin Szynkiewicz; Jonathan E Dickerson; Sanjeev S Bhaskar; Massimiliano Zampini; Tracy A Briggs; Emma M Jenkinson; Carlos A Bacino; Roberta Battini; Enrico Bertini; Paul A Brogan; Louise A Brueton; Marialuisa Carpanelli; Corinne De Laet; Pascale de Lonlay; Mireia del Toro; Isabelle Desguerre; Elisa Fazzi; Angels Garcia-Cazorla; Arvid Heiberg; Masakazu Kawaguchi; Ram Kumar; Jean-Pierre S-M Lin; Charles M Lourenco; Alison M Male; Wilson Marques; Cyril Mignot; Ivana Olivieri; Simona Orcesi; Prab Prabhakar; Magnhild Rasmussen; Robert A Robinson; Flore Rozenberg; Johanna L Schmidt; Katharina Steindl; Tiong Y Tan; William G van der Merwe; Adeline Vanderver; Grace Vassallo; Emma L Wakeling; Evangeline Wassmer; Elizabeth Whittaker; John H Livingston; Pierre Lebon; Tamio Suzuki; Paul J McLaughlin; Liam P Keegan; Mary A O'Connell; Simon C Lovell; Yanick J Crow
Journal:  Nat Genet       Date:  2012-09-23       Impact factor: 38.330

6.  Dysregulation of the immune system in Aicardi-Goutières syndrome: another example in a TREX1-mutated patient.

Authors:  I Olivieri; M Cattalini; D Tonduti; R La Piana; C Uggetti; J Galli; A Meini; A Tincani; D Moratto; E Fazzi; U Balottin; S Orcesi
Journal:  Lupus       Date:  2013-08-05       Impact factor: 2.911

7.  Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.

Authors:  Gillian I Rice; Jacquelyn Bond; Aruna Asipu; Rebecca L Brunette; Iain W Manfield; Ian M Carr; Jonathan C Fuller; Richard M Jackson; Teresa Lamb; Tracy A Briggs; Manir Ali; Hannah Gornall; Lydia R Couthard; Alec Aeby; Simon P Attard-Montalto; Enrico Bertini; Christine Bodemer; Knut Brockmann; Louise A Brueton; Peter C Corry; Isabelle Desguerre; Elisa Fazzi; Angels Garcia Cazorla; Blanca Gener; Ben C J Hamel; Arvid Heiberg; Matthew Hunter; Marjo S van der Knaap; Ram Kumar; Lieven Lagae; Pierre G Landrieu; Charles M Lourenco; Daphna Marom; Michael F McDermott; William van der Merwe; Simona Orcesi; Julie S Prendiville; Magnhild Rasmussen; Stavit A Shalev; Doriette M Soler; Marwan Shinawi; Ronen Spiegel; Tiong Y Tan; Adeline Vanderver; Emma L Wakeling; Evangeline Wassmer; Elizabeth Whittaker; Pierre Lebon; Daniel B Stetson; David T Bonthron; Yanick J Crow
Journal:  Nat Genet       Date:  2009-06-14       Impact factor: 38.330

8.  Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

Authors:  Gillian I Rice; Gabriella M A Forte; Marcin Szynkiewicz; Diana S Chase; Alec Aeby; Mohamed S Abdel-Hamid; Sam Ackroyd; Rebecca Allcock; Kathryn M Bailey; Umberto Balottin; Christine Barnerias; Genevieve Bernard; Christine Bodemer; Maria P Botella; Cristina Cereda; Kate E Chandler; Lyvia Dabydeen; Russell C Dale; Corinne De Laet; Christian G E L De Goede; Mireia Del Toro; Laila Effat; Noemi Nunez Enamorado; Elisa Fazzi; Blanca Gener; Madli Haldre; Jean-Pierre S-M Lin; John H Livingston; Charles Marques Lourenco; Wilson Marques; Patrick Oades; Pärt Peterson; Magnhild Rasmussen; Agathe Roubertie; Johanna Loewenstein Schmidt; Stavit A Shalev; Rogelio Simon; Ronen Spiegel; Kathryn J Swoboda; Samia A Temtamy; Grace Vassallo; Catheline N Vilain; Julie Vogt; Vanessa Wermenbol; William P Whitehouse; Doriette Soler; Ivana Olivieri; Simona Orcesi; Mona S Aglan; Maha S Zaki; Ghada M H Abdel-Salam; Adeline Vanderver; Kai Kisand; Flore Rozenberg; Pierre Lebon; Yanick J Crow
Journal:  Lancet Neurol       Date:  2013-10-30       Impact factor: 44.182

9.  Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression.

Authors:  Holger Thiele; Marcel du Moulin; Katarzyna Barczyk; Christel George; Wolfram Schwindt; Gudrun Nürnberg; Michael Frosch; Gerhard Kurlemann; Johannes Roth; Peter Nürnberg; Frank Rutsch
Journal:  Hum Mutat       Date:  2010-11       Impact factor: 4.878

10.  Recognizable phenotypes associated with intracranial calcification.

Authors:  John H Livingston; Stavros Stivaros; Marjo S van der Knaap; Yanick J Crow
Journal:  Dev Med Child Neurol       Date:  2012-11-01       Impact factor: 5.449

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  22 in total

1.  Aicardi goutières syndrome is associated with pulmonary hypertension.

Authors:  Laura A Adang; David B Frank; Ahmed Gilani; Asako Takanohashi; Nicole Ulrick; Abigail Collins; Zachary Cross; Csaba Galambos; Guy Helman; Usama Kanaan; Stephanie Keller; Dawn Simon; Omar Sherbini; Brian D Hanna; Adeline L Vanderver
Journal:  Mol Genet Metab       Date:  2018-09-07       Impact factor: 4.797

2.  Comment on: Diagnosis of Aicardi-Goutières Syndrome in Adults.

Authors:  Eduardo R Pereira; Gustavo L Franklin; Salmo Raskin; Hélio A G Teive
Journal:  Mov Disord Clin Pract       Date:  2020-04-27

Review 3.  Dermatologic Manifestations of Monogenic Autoinflammatory Diseases.

Authors:  Kyawt Win Shwin; Chyi-Chia Richard Lee; Raphaela Goldbach-Mansky
Journal:  Dermatol Clin       Date:  2017-01       Impact factor: 3.478

Review 4.  Cockayne syndrome: Clinical features, model systems and pathways.

Authors:  Ajoy C Karikkineth; Morten Scheibye-Knudsen; Elayne Fivenson; Deborah L Croteau; Vilhelm A Bohr
Journal:  Ageing Res Rev       Date:  2016-08-06       Impact factor: 10.895

5.  Aicardi-Goutières syndrome: unusual neuro-radiological manifestations.

Authors:  Ghada M H Abdel-Salam; Mohamed S Abdel-Hamid; Shaimaa A Mohammad; Sherif F Abdel-Ghafar; Doaa R Soliman; Hala T El-Bassyouni; Laila Effat; Maha S Zaki
Journal:  Metab Brain Dis       Date:  2017-03-23       Impact factor: 3.584

Review 6.  Characterizing the Pattern of Anomalies in Congenital Zika Syndrome for Pediatric Clinicians.

Authors:  Cynthia A Moore; J Erin Staples; William B Dobyns; André Pessoa; Camila V Ventura; Eduardo Borges da Fonseca; Erlane Marques Ribeiro; Liana O Ventura; Norberto Nogueira Neto; J Fernando Arena; Sonja A Rasmussen
Journal:  JAMA Pediatr       Date:  2017-03-01       Impact factor: 16.193

7.  Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.

Authors:  Gillian I Rice; Naoki Kitabayashi; Magalie Barth; Tracy A Briggs; Annabel C E Burton; Maria Luisa Carpanelli; Alfredo M Cerisola; Cindy Colson; Russell C Dale; Federica Rachele Danti; Niklas Darin; Begoña De Azua; Valentina De Giorgis; Christian G L De Goede; Isabelle Desguerre; Corinne De Laet; Atieh Eslahi; Michael C Fahey; Penny Fallon; Alex Fay; Elisa Fazzi; Mark P Gorman; Nirmala Rani Gowrinathan; Marie Hully; Manju A Kurian; Nicolas Leboucq; Jean-Pierre S-M Lin; Matthew A Lines; Soe S Mar; Reza Maroofian; Laura Martí-Sanchez; Gary McCullagh; Majid Mojarrad; Vinodh Narayanan; Simona Orcesi; Juan Dario Ortigoza-Escobar; Belén Pérez-Dueñas; Florence Petit; Keri M Ramsey; Magnhild Rasmussen; François Rivier; Pilar Rodríguez-Pombo; Agathe Roubertie; Tommy I Stödberg; Mehran Beiraghi Toosi; Annick Toutain; Florence Uettwiller; Nicole Ulrick; Adeline Vanderver; Amy Waldman; John H Livingston; Yanick J Crow
Journal:  Neuropediatrics       Date:  2017-04-10       Impact factor: 1.947

8.  Late diagnosis and atypical brain imaging of Aicardi-Goutières syndrome: are we failing to diagnose Aicardi-Goutières syndrome-2?

Authors:  Leah Svingen; Mitchell Goheen; Rena Godfrey; Colleen Wahl; Eva H Baker; William A Gahl; May Christine V Malicdan; Camilo Toro
Journal:  Dev Med Child Neurol       Date:  2017-08-01       Impact factor: 5.449

9.  Childhood-Onset Dystonia Attributed to Aicardi-Goutières Syndrome and Responsive to Deep Brain Stimulation.

Authors:  Udit Saraf; Mitesh Chandarana; Divya Kalikavil Puthenveedu; Krishnakumar Kesavapisharady; Syam Krishnan; Asha Kishore
Journal:  Mov Disord Clin Pract       Date:  2021-04-19

10.  Ruxolitinib in Aicardi-Goutières syndrome.

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Journal:  Metab Brain Dis       Date:  2021-03-15       Impact factor: 3.584

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