Abstract | BACKGROUND: METHODS: RESULTS: Serum IGF-1 levels (mean ± standard error) were not significantly different among the patients with different neurodegenerative diseases: Parkinson's disease (PD; n = 73), 112.1 ± 5.1 ng/mL; progressive supranuclear palsy (n = 15), 102.9 ± 8.3 ng/mL; multiple system atrophy (n = 22), 103.1 ± 37.6 ng/mL; Alzheimer's disease (AD; n = 18), 102.2 ± 9.4 ng/mL; amyotrophic lateral sclerosis (n = 6), 105.5 ± 27.4 ng/mL; dementia with Lewy bodies (n = 14), 82.4 ± 7.4 ng/mL; frontotemporal dementia (n = 6), 90.0 ± 17.0 ng/mL; and corticobasal syndrome (n = 2), 118.0 ± 14.0 ng/mL. In patients with PD, serum IGF-1 levels were negatively correlated with age and modified Rankin scale (mRS) scores and positively correlated with the striatal dopamine transporter-specific binding ratio and the frontal assessment battery score. In patients with AD, serum IGF-1 levels were negatively correlated with age, disease duration, and mRS scores. CONCLUSION: We found correlations of serum IGF-1 levels with frontal lobe and striatal dopaminergic function and disability in PD patients and with disability in AD patients. The usefulness of measuring serum IGF-1 levels for monitoring disease progression in neurodegenerative diseases requires further studies.
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Authors | Keisuke Suzuki, Shiho Suzuki, Yuko Ishii, Hiroaki Fujita, Takeo Matsubara, Madoka Okamura, Hirotaka Sakuramoto, Koichi Hirata |
Journal | Acta neurologica Scandinavica
(Acta Neurol Scand)
Vol. 139
Issue 6
Pg. 563-567
(Jun 2019)
ISSN: 1600-0404 [Electronic] Denmark |
PMID | 30903695
(Publication Type: Journal Article)
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Copyright | © 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- Biomarkers
- IGF1 protein, human
- Insulin-Like Growth Factor I
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Topics |
- Aged
- Biomarkers
(blood)
- Female
- Humans
- Insulin-Like Growth Factor I
(analysis, metabolism)
- Male
- Middle Aged
- Neurodegenerative Diseases
(blood)
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