Literature DB >> 22744661

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy.

Luca Bello1, Luisa Piva, Andrea Barp, Antonella Taglia, Esther Picillo, Gessica Vasco, Marika Pane, Stefano C Previtali, Yvan Torrente, Elisabetta Gazzerro, Maria Chiara Motta, Gaetano S Grieco, Sara Napolitano, Francesca Magri, Adele D'Amico, Guja Astrea, Sonia Messina, Maria Sframeli, Gian Luca Vita, Patrizia Boffi, Tiziana Mongini, Alessandra Ferlini, Francesca Gualandi, Gianni Soraru', Mario Ermani, Giuseppe Vita, Roberta Battini, Enrico Bertini, Giacomo P Comi, Angela Berardinelli, Carlo Minetti, Claudio Bruno, Eugenio Mercuri, Luisa Politano, Corrado Angelini, Eric P Hoffman, Elena Pegoraro.   

Abstract

OBJECTIVE: To test the effect of the single nucleotide polymorphism -66 T>G (rs28357094) in the osteopontin gene (SPP1) on functional measures over 12 months in Duchenne muscular dystrophy (DMD).
METHODS: This study was conducted on a cohort of ambulatory patients with DMD from a network of Italian neuromuscular centers, evaluated longitudinally with the north star ambulatory assessment (NSAA) and the 6-minute walk test (6MWT) at study entry and after 12 months. Genotype at rs28357094 was determined after completion of the clinical evaluations. Patients were stratified in 2 groups according to a dominant model (TT homozygotes vs TG heterozygotes and GG homozygotes) and clinical data were retrospectively compared between groups.
RESULTS: Eighty patients were selected (age 4.1-19.3 years; mean 8.3 ± 2.7 SD). There were no differences in age or steroid treatment between the 2 subgroups. Paired t test showed a significant difference in both NSAA (p = 0.013) and 6MWT (p = 0.03) between baseline and follow-up after 12 months in patients with DMD carrying the G allele. The difference was not significant in the T subgroup. The analysis of covariance using age and baseline values as covariate and SPP1 genotype as fixed effect showed that these parameters are significantly correlated with the 12-month values.
CONCLUSIONS: These data provide evidence of the role of SPP1 genotype as a disease modifier in DMD and support its relevance in the selection of homogeneous groups of patients for future clinical trials.

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Year:  2012        PMID: 22744661      PMCID: PMC3390537          DOI: 10.1212/WNL.0b013e31825f04ea

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


  9 in total

1.  Predicting the severity of Duchenne muscular dystrophy: implications for treatment.

Authors:  Stanley F Nelson; Robert C Griggs
Journal:  Neurology       Date:  2010-12-22       Impact factor: 9.910

2.  Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study.

Authors:  E Mazzone; G Vasco; M P Sormani; Y Torrente; A Berardinelli; S Messina; A D'Amico; L Doglio; L Politano; F Cavallaro; S Frosini; L Bello; S Bonfiglio; E Zucchini; R De Sanctis; M Scutifero; F Bianco; F Rossi; M C Motta; A Sacco; M A Donati; T Mongini; A Pini; R Battini; E Pegoraro; M Pane; S Gasperini; S Previtali; S Napolitano; D Martinelli; C Bruno; G Vita; G Comi; E Bertini; E Mercuri
Journal:  Neurology       Date:  2011-07-06       Impact factor: 9.910

3.  SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy.

Authors:  E Pegoraro; E P Hoffman; L Piva; B F Gavassini; S Cagnin; M Ermani; L Bello; G Soraru; B Pacchioni; M D Bonifati; G Lanfranchi; C Angelini; A Kesari; I Lee; H Gordish-Dressman; J M Devaney; C M McDonald
Journal:  Neurology       Date:  2010-12-22       Impact factor: 9.910

4.  North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy.

Authors:  Elena Mazzone; Diego Martinelli; Angela Berardinelli; Sonia Messina; Adele D'Amico; Gessica Vasco; Marion Main; Luca Doglio; Luisa Politano; Filippo Cavallaro; Silvia Frosini; Luca Bello; Adelina Carlesi; Anna Maria Bonetti; Elisabetta Zucchini; Roberto De Sanctis; Marianna Scutifero; Flaviana Bianco; Francesca Rossi; Maria Chiara Motta; Annalisa Sacco; Maria Alice Donati; Tiziana Mongini; Antonella Pini; Roberta Battini; Elena Pegoraro; Marika Pane; Elisabetta Pasquini; Claudio Bruno; Giuseppe Vita; Chiara de Waure; Enrico Bertini; Eugenio Mercuri
Journal:  Neuromuscul Disord       Date:  2010-07-14       Impact factor: 4.296

Review 5.  Osteopontin: a multifunctional molecule regulating chronic inflammation and vascular disease.

Authors:  Marta Scatena; Lucy Liaw; Cecilia M Giachelli
Journal:  Arterioscler Thromb Vasc Biol       Date:  2007-08-23       Impact factor: 8.311

6.  The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy.

Authors:  Craig M McDonald; Erik K Henricson; Jay J Han; R Ted Abresch; Alina Nicorici; Gary L Elfring; Leone Atkinson; Allen Reha; Samit Hirawat; Langdon L Miller
Journal:  Muscle Nerve       Date:  2010-04       Impact factor: 3.217

7.  Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta.

Authors:  Sylvia A Vetrone; Encarnacion Montecino-Rodriguez; Elena Kudryashova; Irina Kramerova; Eric P Hoffman; Scot D Liu; M Carrie Miceli; Melissa J Spencer
Journal:  J Clin Invest       Date:  2009-05-18       Impact factor: 14.808

8.  Osteopontin and skeletal muscle myoblasts: association with muscle regeneration and regulation of myoblast function in vitro.

Authors:  Kitipong Uaesoontrachoon; Hyun-Jin Yoo; Elizabeth M Tudor; Robert N Pike; Eleanor J Mackie; Charles N Pagel
Journal:  Int J Biochem Cell Biol       Date:  2008-04-06       Impact factor: 5.085

9.  Reliability of the North Star Ambulatory Assessment in a multicentric setting.

Authors:  E S Mazzone; S Messina; G Vasco; M Main; M Eagle; A D'Amico; L Doglio; L Politano; F Cavallaro; S Frosini; L Bello; F Magri; A Corlatti; E Zucchini; B Brancalion; F Rossi; M Ferretti; M G Motta; M R Cecio; A Berardinelli; P Alfieri; T Mongini; A Pini; G Astrea; R Battini; G Comi; E Pegoraro; L Morandi; M Pane; C Angelini; C Bruno; M Villanova; G Vita; M A Donati; E Bertini; E Mercuri
Journal:  Neuromuscul Disord       Date:  2009-06-23       Impact factor: 4.296

  9 in total
  43 in total

1.  Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study.

Authors:  Luca Bello; Heather Gordish-Dressman; Lauren P Morgenroth; Erik K Henricson; Tina Duong; Eric P Hoffman; Avital Cnaan; Craig M McDonald
Journal:  Neurology       Date:  2015-08-26       Impact factor: 9.910

2.  Genetic Modifiers for Neuromuscular Diseases.

Authors:  Kay-Marie Lamar; Elizabeth M McNally
Journal:  J Neuromuscul Dis       Date:  2014

Review 3.  Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies.

Authors:  Elisabeth Le Rumeur
Journal:  Bosn J Basic Med Sci       Date:  2015-07-20       Impact factor: 3.363

Review 4.  Muscular dystrophy in a dish: engineered human skeletal muscle mimetics for disease modeling and drug discovery.

Authors:  Alec S T Smith; Jennifer Davis; Gabsang Lee; David L Mack; Deok-Ho Kim
Journal:  Drug Discov Today       Date:  2016-04-22       Impact factor: 7.851

5.  226th ENMC International Workshop:: Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands.

Authors:  Annemieke Aartsma-Rus; Alessandra Ferlini; Elizabeth M McNally; Pietro Spitali; H Lee Sweeney
Journal:  Neuromuscul Disord       Date:  2017-10-26       Impact factor: 4.296

6.  Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy.

Authors:  Luca Bello; Kevin M Flanigan; Robert B Weiss; Pietro Spitali; Annemieke Aartsma-Rus; Francesco Muntoni; Irina Zaharieva; Alessandra Ferlini; Eugenio Mercuri; Sylvie Tuffery-Giraud; Mireille Claustres; Volker Straub; Hanns Lochmüller; Andrea Barp; Sara Vianello; Elena Pegoraro; Jaya Punetha; Heather Gordish-Dressman; Mamta Giri; Craig M McDonald; Eric P Hoffman
Journal:  Am J Hum Genet       Date:  2016-10-13       Impact factor: 11.025

Review 7.  Genetic diagnosis as a tool for personalized treatment of Duchenne muscular dystrophy.

Authors:  Luca Bello; Elena Pegoraro
Journal:  Acta Myol       Date:  2016-12

Review 8.  Outside in: The matrix as a modifier of muscular dystrophy.

Authors:  Mattia Quattrocelli; Melissa J Spencer; Elizabeth M McNally
Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2016-12-21       Impact factor: 4.739

Review 9.  Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trials.

Authors:  Joe N Kornegay; Christopher F Spurney; Peter P Nghiem; Candice L Brinkmeyer-Langford; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  ILAR J       Date:  2014

10.  DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study.

Authors:  Luca Bello; Lauren P Morgenroth; Heather Gordish-Dressman; Eric P Hoffman; Craig M McDonald; Sebahattin Cirak
Journal:  Neurology       Date:  2016-06-24       Impact factor: 9.910

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