Literature DB >> 28921817

Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation.

T Konno1,2, K Yoshida3, I Mizuta4, T Mizuno4, T Kawarai5, M Tada2, H Nozaki6, S-I Ikeda7, O Onodera2, Z K Wszolek1, T Ikeuchi8.   

Abstract

BACKGROUND AND
PURPOSE: To establish and validate diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) due to colony-stimulating factor 1 receptor (CSF1R) mutation.
METHODS: We developed diagnostic criteria for ALSP based on a recent analysis of the clinical characteristics of ALSP. These criteria provide 'probable' and 'possible' designations for patients who do not have a genetic diagnosis. To verify its sensitivity and specificity, we retrospectively applied our criteria to 83 ALSP cases who had CSF1R mutations (24 of these were analyzed at our institutions and the others were identified from the literature), 53 cases who had CSF1R mutation-negative leukoencephalopathies and 32 cases who had cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with NOTCH3 mutations.
RESULTS: Among the CSF1R mutation-positive cases, 50 cases (60%) were diagnosed as 'probable' and 32 (39%) were diagnosed as 'possible,' leading to a sensitivity of 99% if calculated as a ratio of the combined number of cases who fulfilled 'probable' or 'possible' to the total number of cases. With regard to specificity, 22 cases (42%) with mutation-negative leukoencephalopathies and 28 (88%) with CADASIL were correctly excluded using these criteria.
CONCLUSIONS: These diagnostic criteria are very sensitive for diagnosing ALSP with sufficient specificity for differentiation from CADASIL and moderate specificity for other leukoencephalopathies. Our results suggest that these criteria are useful for the clinical diagnosis of ALSP.
© 2017 EAN.

Entities:  

Keywords:  adult-onset leukoencephalopathy with axonal spheroids and pigmented glia; alanyl-transfer RNA synthetase 2; colony-stimulating factor 1 receptor; diagnostic criteria; hereditary diffuse leukoencephalopathy with spheroids; leukoencephalopathy; pigmented orthochromatic leukodystrophy

Mesh:

Substances:

Year:  2017        PMID: 28921817      PMCID: PMC5741468          DOI: 10.1111/ene.13464

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  14 in total

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Authors:  T Konno; D F Broderick; N Mezaki; A Isami; D Kaneda; Y Tashiro; T Tokutake; B M Keegan; B K Woodruff; T Miura; H Nozaki; M Nishizawa; O Onodera; Z K Wszolek; T Ikeuchi
Journal:  AJNR Am J Neuroradiol       Date:  2016-09-15       Impact factor: 3.825

2.  Novel AARS2 gene mutation producing leukodystrophy: a case report.

Authors:  Laszlo Szpisjak; Nora Zsindely; Jozsef I Engelhardt; Laszlo Vecsei; Gabor G Kovacs; Peter Klivenyi
Journal:  J Hum Genet       Date:  2016-10-13       Impact factor: 3.172

3.  Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.

Authors:  Alexandra Götz; Henna Tyynismaa; Liliya Euro; Pekka Ellonen; Tuulia Hyötyläinen; Tiina Ojala; Riikka H Hämäläinen; Johanna Tommiska; Taneli Raivio; Matej Oresic; Riitta Karikoski; Outi Tammela; Kalle O J Simola; Anders Paetau; Tiina Tyni; Anu Suomalainen
Journal:  Am J Hum Genet       Date:  2011-05-05       Impact factor: 11.025

4.  Invited article: an MRI-based approach to the diagnosis of white matter disorders.

Authors:  Raphael Schiffmann; Marjo S van der Knaap
Journal:  Neurology       Date:  2009-02-24       Impact factor: 9.910

5.  MRI characteristics and scoring in HDLS due to CSF1R gene mutations.

Authors:  Christina Sundal; Jay A Van Gerpen; Alexandra M Nicholson; Christian Wider; Elizabeth A Shuster; Jan Aasly; Salvatore Spina; Bernardino Ghetti; Sigrun Roeber; James Garbern; Anne Borjesson-Hanson; Alex Tselis; Russell H Swerdlow; Bradley B Miller; Shinsuke Fujioka; Michael G Heckman; Ryan J Uitti; Keith A Josephs; Matt Baker; Oluf Andersen; Rosa Rademakers; Dennis W Dickson; Daniel Broderick; Zbigniew K Wszolek
Journal:  Neurology       Date:  2012-07-25       Impact factor: 9.910

6.  CSF1R mutations link POLD and HDLS as a single disease entity.

Authors:  Alexandra M Nicholson; Matt C Baker; Nicole A Finch; Nicola J Rutherford; Christian Wider; Neill R Graff-Radford; Peter T Nelson; H Brent Clark; Zbigniew K Wszolek; Dennis W Dickson; David S Knopman; Rosa Rademakers
Journal:  Neurology       Date:  2013-02-13       Impact factor: 9.910

7.  A practical approach to diagnosing adult onset leukodystrophies.

Authors:  R M Ahmed; E Murphy; I Davagnanam; M Parton; J M Schott; C J Mummery; J D Rohrer; R H Lachmann; H Houlden; N C Fox; J Chataway
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-12-19       Impact factor: 10.154

8.  Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS.

Authors:  Takuya Konno; Masayoshi Tada; Mari Tada; Akihide Koyama; Hiroaki Nozaki; Yasuo Harigaya; Jin Nishimiya; Akiko Matsunaga; Nobuaki Yoshikura; Kenji Ishihara; Musashi Arakawa; Aiko Isami; Kenichi Okazaki; Hideaki Yokoo; Kyoko Itoh; Makoto Yoneda; Mitsuru Kawamura; Takashi Inuzuka; Hitoshi Takahashi; Masatoyo Nishizawa; Osamu Onodera; Akiyoshi Kakita; Takeshi Ikeuchi
Journal:  Neurology       Date:  2013-12-13       Impact factor: 9.910

9.  Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.

Authors:  David S Lynch; Wei Jia Zhang; Rahul Lakshmanan; Justin A Kinsella; Günes Altiokka Uzun; Merih Karbay; Zeynep Tüfekçioglu; Hasmet Hanagasi; Georgina Burke; Nicola Foulds; Simon R Hammans; Anupam Bhattacharjee; Heather Wilson; Matthew Adams; Mark Walker; James A R Nicoll; Jeremy Chataway; Nick Fox; Indran Davagnanam; Rahul Phadke; Henry Houlden
Journal:  JAMA Neurol       Date:  2016-12-01       Impact factor: 18.302

10.  Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.

Authors:  T Konno; K Yoshida; T Mizuno; T Kawarai; M Tada; H Nozaki; S-I Ikeda; M Nishizawa; O Onodera; Z K Wszolek; T Ikeuchi
Journal:  Eur J Neurol       Date:  2016-09-29       Impact factor: 6.089

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  29 in total

1.  Biopsy histopathology in the diagnosis of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP).

Authors:  Chenhui Mao; Liangrui Zhou; Lixin Zhou; Yingmai Yang; Jingwen Niu; Jie Li; Xinying Huang; Haitao Ren; Yanhuan Zhao; Bin Peng; Jing Gao
Journal:  Neurol Sci       Date:  2019-11-08       Impact factor: 3.307

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Authors:  Mariko L Bennett; F Chris Bennett
Journal:  Nat Neurosci       Date:  2019-12-02       Impact factor: 24.884

3.  A novel dominant-negative mutation of the CSF1R gene causes adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.

Authors:  Cuihua Leng; Likui Lu; Guoping Wang; Yingying Zhang; Yan Xu; Xiaoqian Lin; Nana Shen; Xingshun Xu; Sen Qun; Miao Sun; Wei Ge
Journal:  Am J Transl Res       Date:  2019-09-15       Impact factor: 4.060

4.  Altered structural and functional connectivity in CSF1R-related leukoencephalopathy.

Authors:  Fei-Xia Zhan; Ze-Yu Zhu; Qing Liu; Hai-Yan Zhou; Xing-Hua Luan; Xiao-Jun Huang; Xiao-Li Liu; Wo-Tu Tian; Shi-Ge Wang; Xiao-Xuan Song; Guang Chen; Ming-Liang Zhao; Ying Wang; Hui-Dong Tang; Jiong Hu; Sheng-Di Chen; Bin-Yin Li; Li Cao
Journal:  Brain Imaging Behav       Date:  2021-06       Impact factor: 3.978

5.  Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities.

Authors:  T Konno; T Miura; A M Harriott; N Mezaki; E S Edwards; R Rademakers; O A Ross; J F Meschia; T Ikeuchi; Z K Wszolek
Journal:  Eur J Neurol       Date:  2018-04-03       Impact factor: 6.089

6.  Case Report: Novel CSF1R Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching Behavior.

Authors:  Adit Friedberg; Eliana Marisa Ramos; Zhongan Yang; Luke W Bonham; Jennifer S Yokoyama; Peter A Ljubenkov; Kyan Younes; Daniel H Geschwind; Bruce L Miller
Journal:  Front Neurol       Date:  2022-06-22       Impact factor: 4.086

7.  CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!

Authors:  Neeharika Sriram; Hansashree Padmanabha; Sadanandavalli R Chandra; Rohan Mahale; Bevinahalli Nandeesh; Maya D Bhat; Rita Christopher; Manisha Gupta; Gautham A Udupi; Pooja Mailankody; Pavagada S Mathuranath
Journal:  Ann Indian Acad Neurol       Date:  2021-11-10       Impact factor: 1.714

8.  Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Authors:  Jingying Wu; Yikang Cao; Mengting Li; Binyin Li; Xize Jia; Li Cao
Journal:  Brain Imaging Behav       Date:  2022-04-07       Impact factor: 3.224

9.  Clinical features and genetic characteristics of hereditary diffuse leukoencephalopathy with spheroids due to CSF1R mutation: a case report and literature review.

Authors:  Lv-Ping Zhuang; Chang-Yun Liu; Yuan-Xiao Li; Hua-Ping Huang; Zhang-Yu Zou
Journal:  Ann Transl Med       Date:  2020-01

10.  A proposed synergistic effect of CSF1R and NMUR2 variants contributes to binge eating in hereditary diffuse leukoencephalopathy with spheroids.

Authors:  Qing Liu; Xia-Nan Guo; Cai-Yan Liu; Wei-Hai Xu
Journal:  Ann Transl Med       Date:  2020-01
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