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Research Article| Volume 319, ISSUE 1-2, P96-101, August 15, 2012

Frontal dysfunctions of ALS-PBP patients in relation to their bulbar symptoms and rCBF decline

  • Nobutoshi Morimoto
    Affiliations
    Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
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  • Tomoko Kurata
    Affiliations
    Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
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  • Kota Sato
    Affiliations
    Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
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  • Yoshio Ikeda
    Affiliations
    Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
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  • Shuhei Sato
    Affiliations
    Department of Radiology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
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  • Koji Abe
    Correspondence
    Corresponding author at: Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, 2-5-1 Shikata-cho, Okayama 700-8558, Japan. Tel.: +81 86 235 7365; fax: +81 86 235 7368.
    Affiliations
    Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama University, Okayama, Japan
    Search for articles by this author

      Abstract

      Background

      Amyotrophic lateral sclerosis (ALS) is a progressive and fatal disease characterized by progressive degeneration of spinal and bulbar motor neurons. However up to 50% ALS patients may also have cognitive dysfunction which has not been fully examined.

      Methods

      35 ALS patients [23 patients presenting with limb-type ALS (ALS-limb) and 12 patients presenting with primary bulbar palsy (PBP)-type ALS (ALS-PBP)] and 5 Spinal and Bulbar Muscular Atrophy (SBMA) patients have participated. To assess cognitive function mini-mental state examination (MMSE), Hasegawa dementia scale—revised (HDS-R), and frontal assessment battery (FAB) were performed. Additionally the time to complete card flipping with a computerized touch panel-type screening test was also examined. To investigate regional cerebral blood flow (rCBF), single-photon emission computed tomography (SPECT) using a 99mTc labeled ethyl cysteinate dimer (99mTc-ECD) were performed. Statistical image analysis was performed using the easy Z-score imaging system (eZIS).

      Results

      HDS-R and FAB scores were significantly lower in the ALS-PBP group than in age- and gender-matched control subjects or ALS-limb groups (p<0.01). The time to complete card flipping was significantly longer in the ALS-PBP group than in the control and ALS-limb groups (p<0.01). Although MMSE, HDS-R and FAB scores and the time to complete card flipping had no correlation with ALS functional rating scale—revised (ALSFRS-R) or Norris-limb scale scores, FAB score (r=0.63, p <0.01) and the time to complete card flipping (r=0.66, p<0.01) were strongly correlated with Norris-bulbar score. The eZIS showed that rCBF of the frontal lobe was more severely declined in ALS-PBP patients than in ALS-limb patients (p<0.05).

      Conclusion

      These results suggest a selective decline of frontal cerebral functions in the ALS-PBP group in relation to their bulbar symptoms and rCBF decline.

      Abbreviations:

      AD (Alzheimer's disease), ALS (amyotrophic lateral sclerosis), ALSFRS-R (ALS functional rating scale—revised), AR (androgen receptor), SBMA (Spinal and bulbar muscular atrophy), CDR (Clinical Dementia Rating), eZIS (easy Z-score imaging system), FAB (frontal assessment battery), FTLD (frontotemporal lobar degeneration), HDS-R (Hasegawa dementia scale—revised), MMSE (mini-mental state examination), MND (motor neuron disease), rCBF (regional cerebral blood flow), ROI (region of interest), SOD1 (superoxide dismutase 1), SPM (statistical parametric mapping), SPECT (single-photon emission computed tomography), 99mTc-ECD (99mTc labeled ethyl cysteinate dimer), TDP-43 (transactivation responsive region (TAR)-DNA-binding protein of 43kDa)

      Keywords

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