Literature DB >> 27261500

Defining SOD1 ALS natural history to guide therapeutic clinical trial design.

Taha Bali1, Wade Self1, Jingxia Liu2, Teepu Siddique3, Leo H Wang4, Thomas D Bird4,5, Elena Ratti6, Nazem Atassi6, Kevin B Boylan7, Jonathan D Glass8, Nicholas J Maragakis9, James B Caress10, Leo F McCluskey11, Stanley H Appel12, James P Wymer13, Summer Gibson14, Lorne Zinman15, Tahseen Mozaffar16, Brian Callaghan17, April L McVey18, Jennifer Jockel-Balsarotti1, Peggy Allred19, Elena R Fisher1, Glenn Lopate1, Alan Pestronk1, Merit E Cudkowicz6, Timothy M Miller1.   

Abstract

IMPORTANCE: Understanding the natural history of familial amyotrophic lateral sclerosis (ALS) caused by SOD1 mutations (ALSSOD1) will provide key information for optimising clinical trials in this patient population.
OBJECTIVE: To establish an updated natural history of ALSSOD1. DESIGN, SETTING AND PARTICIPANTS: Retrospective cohort study from 15 medical centres in North America evaluated records from 175 patients with ALS with genetically confirmed SOD1 mutations, cared for after the year 2000. MAIN OUTCOMES AND MEASURES: Age of onset, survival, ALS Functional Rating Scale (ALS-FRS) scores and respiratory function were analysed. Patients with the A4V (Ala-Val) SOD1 mutation (SOD1A4V), the largest mutation population in North America with an aggressive disease progression, were distinguished from other SOD1 mutation patients (SOD1non-A4V) for analysis.
RESULTS: Mean age of disease onset was 49.7±12.3 years (mean±SD) for all SOD1 patients, with no statistical significance between SOD1A4V and SOD1non-A4V (p=0.72, Kruskal-Wallis). Total SOD1 patient median survival was 2.7 years. Mean disease duration for all SOD1 was 4.6±6.0 and 1.4±0.7 years for SOD1A4V. SOD1A4V survival probability (median survival 1.2 years) was significantly decreased compared with SOD1non-A4V (median survival 6.8 years; p<0.0001, log-rank). A statistically significant increase in ALS-FRS decline in SOD1A4V compared with SOD1non-A4V participants (p=0.02) was observed, as well as a statistically significant increase in ALS-forced vital capacity decline in SOD1A4V compared with SOD1non-A4V (p=0.02). CONCLUSIONS AND RELEVANCE: SOD1A4V is an aggressive, but relatively homogeneous form of ALS. These SOD1-specific ALS natural history data will be important for the design and implementation of clinical trials in the ALSSOD1 patient population. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

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Year:  2016        PMID: 27261500      PMCID: PMC5136332          DOI: 10.1136/jnnp-2016-313521

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  30 in total

Review 1.  Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis.

Authors:  Susan Byrne; Cathal Walsh; Catherine Lynch; Peter Bede; Marwa Elamin; Kevin Kenna; Russell McLaughlin; Orla Hardiman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2010-11-03       Impact factor: 10.154

2.  Rapid disease progression correlates with instability of mutant SOD1 in familial ALS.

Authors:  T Sato; T Nakanishi; Y Yamamoto; P M Andersen; Y Ogawa; K Fukada; Z Zhou; F Aoike; F Sugai; S Nagano; S Hirata; M Ogawa; R Nakano; T Ohi; T Kato; M Nakagawa; T Hamasaki; A Shimizu; S Sakoda
Journal:  Neurology       Date:  2005-11-16       Impact factor: 9.910

3.  SOD1 in cerebral spinal fluid as a pharmacodynamic marker for antisense oligonucleotide therapy.

Authors:  Leah Winer; Dushyanth Srinivasan; Seung Chun; David Lacomis; Matthew Jaffa; Anne Fagan; David M Holtzman; Ed Wancewicz; C Frank Bennett; Robert Bowser; Merit Cudkowicz; Timothy M Miller
Journal:  JAMA Neurol       Date:  2013-02       Impact factor: 18.302

4.  Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS.

Authors:  Cédric Raoul; Toufik Abbas-Terki; Jean-Charles Bensadoun; Sandrine Guillot; Georg Haase; Jolanta Szulc; Christopher E Henderson; Patrick Aebischer
Journal:  Nat Med       Date:  2005-03-13       Impact factor: 53.440

5.  Small-molecule-mediated stabilization of familial amyotrophic lateral sclerosis-linked superoxide dismutase mutants against unfolding and aggregation.

Authors:  Soumya S Ray; Richard J Nowak; Robert H Brown; Peter T Lansbury
Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-28       Impact factor: 11.205

6.  In vivo kinetic approach reveals slow SOD1 turnover in the CNS.

Authors:  Matthew J Crisp; Kwasi G Mawuenyega; Bruce W Patterson; Naveen C Reddy; Robert Chott; Wade K Self; Conrad C Weihl; Jennifer Jockel-Balsarotti; Arun S Varadhachary; Robert C Bucelli; Kevin E Yarasheski; Randall J Bateman; Timothy M Miller
Journal:  J Clin Invest       Date:  2015-06-15       Impact factor: 14.808

7.  Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.

Authors:  C Gellera; B Castellotti; M C Riggio; V Silani; L Morandi; D Testa; C Casali; F Taroni; S Di Donato; M Zeviani; C Mariotti
Journal:  Neuromuscul Disord       Date:  2001-05       Impact factor: 4.296

8.  Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutase.

Authors:  T Juneja; M A Pericak-Vance; N G Laing; S Dave; T Siddique
Journal:  Neurology       Date:  1997-01       Impact factor: 9.910

Review 9.  Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Authors:  R G Miller; C E Jackson; E J Kasarskis; J D England; D Forshew; W Johnston; S Kalra; J S Katz; H Mitsumoto; J Rosenfeld; C Shoesmith; M J Strong; S C Woolley
Journal:  Neurology       Date:  2009-10-13       Impact factor: 9.910

10.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Authors:  D R Rosen; T Siddique; D Patterson; D A Figlewicz; P Sapp; A Hentati; D Donaldson; J Goto; J P O'Regan; H X Deng
Journal:  Nature       Date:  1993-03-04       Impact factor: 49.962

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  24 in total

Review 1.  Emerging antisense oligonucleotide and viral therapies for amyotrophic lateral sclerosis.

Authors:  Cindy V Ly; Timothy M Miller
Journal:  Curr Opin Neurol       Date:  2018-10       Impact factor: 5.710

2.  SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis.

Authors:  Julien H Park; Christiane Elpers; Janine Reunert; Michael L McCormick; Julia Mohr; Saskia Biskup; Oliver Schwartz; Stephan Rust; Marianne Grüneberg; Anja Seelhöfer; Ulrike Schara; Eugen Boltshauser; Douglas R Spitz; Thorsten Marquardt
Journal:  Brain       Date:  2019-08-01       Impact factor: 13.501

Review 3.  Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy.

Authors:  Naoki Suzuki; Ayumi Nishiyama; Hitoshi Warita; Masashi Aoki
Journal:  J Hum Genet       Date:  2022-06-13       Impact factor: 3.172

4.  Occupational lead exposure and survival with amyotrophic lateral sclerosis.

Authors:  Te-Wei Wang; Joanne Wuu; Anne Cooley; Tian-Shin Yeh; Michael Benatar; Marc Weisskopf
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2022-04-09       Impact factor: 3.528

5.  Antisense oligonucleotides extend survival and reverse decrement in muscle response in ALS models.

Authors:  Alex McCampbell; Tracy Cole; Amy J Wegener; Giulio S Tomassy; Amy Setnicka; Brandon J Farley; Kathleen M Schoch; Mariah L Hoye; Mark Shabsovich; Linhong Sun; Yi Luo; Mingdi Zhang; Nicole Comfort; Bin Wang; Jessica Amacker; Sai Thankamony; David W Salzman; Merit Cudkowicz; Danielle L Graham; C Frank Bennett; Holly B Kordasiewicz; Eric E Swayze; Timothy M Miller
Journal:  J Clin Invest       Date:  2018-07-16       Impact factor: 14.808

Review 6.  Antisense Drugs Make Sense for Neurological Diseases.

Authors:  C Frank Bennett; Holly B Kordasiewicz; Don W Cleveland
Journal:  Annu Rev Pharmacol Toxicol       Date:  2020-10-09       Impact factor: 13.820

Review 7.  Differentiating lower motor neuron syndromes.

Authors:  Nidhi Garg; Susanna B Park; Steve Vucic; Con Yiannikas; Judy Spies; James Howells; William Huynh; José M Matamala; Arun V Krishnan; John D Pollard; David R Cornblath; Mary M Reilly; Matthew C Kiernan
Journal:  J Neurol Neurosurg Psychiatry       Date:  2016-12-21       Impact factor: 10.154

8.  Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutations.

Authors:  Dale J Lange; Mona Shahbazi; Vincenzo Silani; Albert C Ludolph; Jochen H Weishaupt; Senda Ajroud-Driss; Kara G Fields; Rahul Remanan; Stanley H Appel; Claudia Morelli; Alberto Doretti; Luca Maderna; Stefano Messina; Ulrike Weiland; Stefan L Marklund; Peter M Andersen
Journal:  Ann Neurol       Date:  2017-06-09       Impact factor: 10.422

9.  Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus.

Authors:  Yongwang Zhong; Jiou Wang; Mark J Henderson; Peixin Yang; Brian M Hagen; Teepu Siddique; Bruce E Vogel; Han-Xiang Deng; Shengyun Fang
Journal:  Elife       Date:  2017-05-02       Impact factor: 8.140

10.  Fingerprint analysis of Huolingshengji Formula and its neuroprotective effects in SOD1G93A mouse model of amyotrophic lateral sclerosis.

Authors:  Qinming Zhou; Youjie Wang; Jingjing Zhang; Yaping Shao; Song Li; Yuan Wang; Huaibin Cai; Yi Feng; Weidong Le
Journal:  Sci Rep       Date:  2018-01-26       Impact factor: 4.379

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