Serum asymmetric dimethylarginine level correlates with the progression and prognosis of amyotrophic lateral sclerosis

  • Kensuke Ikenaka
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Yasuhiro Maeda
    Center for Joint Research Facilities Support Fujita Health University Toyoake Japan
  • Yuji Hotta
    Department of Hospital Pharmacy Nagoya City University Graduate School of Pharmaceutical Sciences Nagoya Japan
  • Seiichi Nagano
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Shinichiro Yamada
    Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan
  • Daisuke Ito
    Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan
  • Ryota Torii
    Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan
  • Keita Kakuda
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Harutsugu Tatebe
    T & T Brothers Corporation Chiba Japan
  • Naoki Atsuta
    Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan
  • Cesar Aguirre
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Yasuyoshi Kimura
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Kousuke Baba
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan
  • Takahiko Tokuda
    T & T Brothers Corporation Chiba Japan
  • Masahisa Katsuno
    Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan
  • Kazunori Kimura
    Department of Hospital Pharmacy Nagoya City University Graduate School of Pharmaceutical Sciences Nagoya Japan
  • Gen Sobue
    Research Division of Dementia and Neurodegenerative Disease Nagoya University Graduate School of Medicine Nagoya Japan
  • Hideki Mochizuki
    Department of Neurology Osaka University Graduate School of Medicine Suita Japan

Abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Background and purpose:</jats:title></jats:sec><jats:sec><jats:label /><jats:p>The aim was to investigate the association between serum asymmetric dimethylarginine (ADMA) levels and the progression and prognosis of amyotrophic lateral sclerosis (ALS), and to compare cerebrospinal fluid (CSF) and serum ADMA levels with other biomarkers of ALS.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Serum ADMA levels of sporadic ALS patients (<jats:italic>n</jats:italic> = 68), disease control patients (<jats:italic>n</jats:italic> = 54) and healthy controls (<jats:italic>n</jats:italic> = 20) were measured using liquid chromatography tandem mass spectrometry. Correlations of the ADMA level and other markers (nitric oxide and neurofilament light chain levels) were analyzed. Changes in the ALS Functional Rating Scale Revised (ALSFRS‐R) score from the onset of disease (ALSFRS‐R pre‐slope) was used to assess disease progression. Survival was evaluated using the Cox proportional hazards model and Kaplan–Meier analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The serum ADMA level was substantially higher in patients with ALS than in healthy controls and disease controls. Serum ADMA level correlated with CSF ADMA level (<jats:italic>r</jats:italic> = 0.591, <jats:italic>p</jats:italic> < 0.0001) and was independently associated with the ALSFRS‐R pre‐slope (<jats:italic>r</jats:italic> = 0.505, <jats:italic>p</jats:italic> < 0.0001). Patients with higher serum ADMA levels had less favorable prognoses. CSF ADMA level significantly correlated with CSF neurofilament light chain level (<jats:italic>r</jats:italic> = 0.456, <jats:italic>p</jats:italic> = 0.0002) but not with nitric oxide level (<jats:italic>r</jats:italic> = 0.194, <jats:italic>p</jats:italic> = 0.219).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Serum ADMA level is an independent biomarker of ALS disease progression and prognosis and reflects the degree of motor neuron degeneration.</jats:p></jats:sec>

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