Diagnosis of a model of Duchenne muscular dystrophy in blood serum of mdx mice using Raman hyperspectroscopy

被引:0
|
作者
Nicole M. Ralbovsky
Paromita Dey
Andrew Galfano
Bijan K. Dey
Igor K. Lednev
机构
[1] University At Albany,Department of Chemistry
[2] SUNY,The RNA Institute
[3] University At Albany,Department of Biological Sciences
[4] SUNY,undefined
[5] University At Albany,undefined
[6] SUNY,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy and affects boys in infancy or early childhood. Current methods for diagnosing DMD are often laborious, expensive, invasive, and typically diagnose the disease late in its progression. In an effort to improve the accuracy and ease of diagnosis, this study focused on developing a novel method for diagnosing DMD which combines Raman hyperspectroscopic analysis of blood serum with advanced statistical analysis. Partial least squares discriminant analysis was applied to the spectral dataset acquired from blood serum of a mouse model of Duchenne muscular dystrophy (mdx) and control mice. Cross-validation showed 95.2% sensitivity and 94.6% specificity for identifying diseased spectra. These results were verified via external validation, which achieved 100% successful classification accuracy at the donor level. This proof-of-concept study presents Raman hyperspectroscopic analysis of blood serum as an easy, fast, non-expensive, and minimally invasive detection method for distinguishing control and mdx model mice, with a strong potential for clinical diagnosis of DMD.
引用
收藏
相关论文
共 50 条
  • [41] Respiratory Control and Diaphragm Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Burns, D.
    O'Halloran, K. D.
    IRISH JOURNAL OF MEDICAL SCIENCE, 2016, 185 : S18 - S18
  • [42] Cerebellar dysfunction in the mdx mouse model of Duchenne muscular dystrophy: An electrophysiological and behavioural study
    Prigogine, Cynthia
    Ruiz, Javier Marquez
    Cebolla, Ana Maria
    Deconinck, Nicolas
    Servais, Laurent
    Gailly, Philippe
    Dan, Bernard
    Cheron, Guy
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2024, 60 (10) : 6470 - 6489
  • [43] Proteomic analysis of cardiomyopathic tissue from the aged mdx model of Duchenne muscular dystrophy
    Holland, A.
    Ohlendieck, K.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 812 - 812
  • [44] Sildenafil Ameliorates Skeletal Muscle Pathology in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Percival, Justin
    Whitehead, Nicholas
    Siegel, Michael
    Gray, Heidi
    Adamo, Candace
    Marcinek, David
    Beavo, Joseph
    Froehner, Stanley
    FASEB JOURNAL, 2011, 25
  • [45] Body-wide gene therapy of Duchenne muscular dystrophy in the mdx mouse model
    Denti, MA
    Rosa, A
    D'Antona, G
    Sthandier, O
    De Angelis, FG
    Nicoletti, C
    Allocca, M
    Pansarasa, O
    Parente, V
    Musarò, A
    Auricchio, A
    Bottinelli, R
    Bozzoni, I
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (10) : 3758 - 3763
  • [46] Autophagic dysfunction and autophagosome escape in the mdx mus musculus model of Duchenne muscular dystrophy
    Spaulding, H. R.
    Kelly, E. M.
    Quindry, J. C.
    Sheffield, J. B.
    Hudson, M. B.
    Selsby, J. T.
    ACTA PHYSIOLOGICA, 2018, 222 (02)
  • [47] Resveratrol ameliorates skeletal muscle function in the mdx mouse, a model of Duchenne muscular dystrophy
    Sebori, Rio
    Kuno, Atsushi
    Hayashi, Takashi
    Hosoda, Ryusuke
    Hori, Yusuke
    Horio, Yoshiyuki
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2013, 121 : 69P - 69P
  • [48] Naproxcinod shows significant advantages over naproxen in the mdx model of Duchenne Muscular Dystrophy
    Miglietta, Daniela
    De Palma, Clara
    Sciorati, Clara
    Vergani, Barbara
    Pisa, Viviana
    Villa, Antonello
    Ongini, Ennio
    Clementi, Emilio
    ORPHANET JOURNAL OF RARE DISEASES, 2015, 10
  • [49] Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy
    Salgueiro Barboni, Mirella Telles
    Passos Liber, Andre Mauricio
    Joachimsthaler, Anneka
    Saoudi, Amel
    Goyenvalle, Aurelie
    Rendon, Alvaro
    Roger, Jerome E.
    Ventura, Dora Fix
    Kremers, Jan
    Vaillend, Cyrille
    NEUROBIOLOGY OF DISEASE, 2021, 152
  • [50] Ventilatory Chemosensory Drive Is Blunted in the mdx Mouse Model of Duchenne Muscular Dystrophy (DMD)
    Mosqueira, Matias
    Baby, Santhosh M.
    Lahiri, Sukhamay
    Khurana, Tejvir S.
    PLOS ONE, 2013, 8 (07):