TY - JOUR
T1 - Elevated CSF TDP-43 levels in amyotrophic lateral sclerosis
T2 - Specificity, sensitivity, and a possible prognostic value
AU - Noto, Yu Ichi
AU - Shibuya, Kazumoto
AU - Sato, Yasunori
AU - Kanai, Kazuaki
AU - Misawa, Sonoko
AU - Sawai, Setsu
AU - Mori, Masahiro
AU - Uchiyama, Tomoyuki
AU - Isose, Sagiri
AU - Nasu, Saiko
AU - Sekiguchi, Yukari
AU - Fujimaki, Yumi
AU - Kasai, Takashi
AU - Tokuda, Takahiko
AU - Nakagawa, Masanori
AU - Kuwabara, Satoshi
N1 - Funding Information:
This work was supported by grants-in-aid from the Research Committee of CNS Degenerative Diseases, the Ministry of Health, Labor and Welfare of Japan (MN and SK).
PY - 2011/3
Y1 - 2011/3
N2 - TAR DNA binding protein of 43 kDa (TDP-43) is likely to be the major pathogenetic protein in amyotrophic lateral sclerosis (ALS). A previous study has shown that levels of TDP-43 in CSF measured by an ELISA are significantly higher for ALS patients than for controls. The aim of this study was to investigate whether elevated CSF TDP-43 levels are specific to ALS, and are associated with clinical profiles in ALS patients. We measured CSF TDP-43 levels by the same ELISA in 27 ALS patients and 50 neurodegenerative or inflammatory disease controls such as Parkinson's disease, multiple sclerosis, and Guillain-Barré syndrome. Results showed that the CSF TDP-43 levels were increased only in ALS patients. Receiver operating characteristic (ROC) analyses showed a sensitivity of 59.3% and a specificity of 96.0%. We also found that lower CSF TDP-43 levels may be associated with shorter survival time. In conclusion, the CSF TDP-43 is a potential biomarker that supports a diagnosis of ALS. Moreover, among ALS patients, lower levels of CSF TDP-43 may reflect the accumulation of TDP-43 in the cortical and spinal motor neurons and thereby shorter survival time, although this should be confirmed in larger prospective studies.
AB - TAR DNA binding protein of 43 kDa (TDP-43) is likely to be the major pathogenetic protein in amyotrophic lateral sclerosis (ALS). A previous study has shown that levels of TDP-43 in CSF measured by an ELISA are significantly higher for ALS patients than for controls. The aim of this study was to investigate whether elevated CSF TDP-43 levels are specific to ALS, and are associated with clinical profiles in ALS patients. We measured CSF TDP-43 levels by the same ELISA in 27 ALS patients and 50 neurodegenerative or inflammatory disease controls such as Parkinson's disease, multiple sclerosis, and Guillain-Barré syndrome. Results showed that the CSF TDP-43 levels were increased only in ALS patients. Receiver operating characteristic (ROC) analyses showed a sensitivity of 59.3% and a specificity of 96.0%. We also found that lower CSF TDP-43 levels may be associated with shorter survival time. In conclusion, the CSF TDP-43 is a potential biomarker that supports a diagnosis of ALS. Moreover, among ALS patients, lower levels of CSF TDP-43 may reflect the accumulation of TDP-43 in the cortical and spinal motor neurons and thereby shorter survival time, although this should be confirmed in larger prospective studies.
KW - Amyotrophic lateral sclerosis
KW - ELISA
KW - TAR DNA binding protein of 43 kDa (TDP-43)
KW - cerebrospinal fluid (CSF)
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U2 - 10.3109/17482968.2010.541263
DO - 10.3109/17482968.2010.541263
M3 - Article
C2 - 21126161
AN - SCOPUS:79951764734
SN - 1748-2968
VL - 12
SP - 140
EP - 143
JO - Amyotrophic Lateral Sclerosis
JF - Amyotrophic Lateral Sclerosis
IS - 2
ER -