TY - JOUR
T1 - Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis
AU - Volpato, Eleonora
AU - Gualerzi, Anna
AU - Meloni, Anna Maria
AU - Carlomagno, C.
AU - Banfi, P. I.
AU - Gualerzi, A.
AU - Picciolini, S.
AU - Meloni, M.
AU - Lax, A.
AU - Colombo, E.
AU - Ticozzi, N.
AU - Verde, F.
AU - Silani, V.
AU - Bedoni, M.
PY - 2020
Y1 - 2020
N2 - Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease leading to progressive and
irreversible muscle atrophy. The diagnosis of ALS is time-consuming and complex, with the clinical
and neurophysiological evaluation accompanied by monitoring of progression and a long procedure
for the discrimination of similar neurodegenerative diseases. The delayed diagnosis strongly slows
the potential development of adequate therapies and the time frame for a prompt intervention. The
discovery of new biomarkers could improve the disease diagnosis, as well as the therapeutic and
rehabilitative effectiveness and monitoring of the pathological progression. In this work saliva collected
from 19 patients with ALS, 10 affected by Parkinson’s disease, 10 affected by Alzheimer’s disease
and 10 healthy subjects, was analysed using Raman spectroscopy, optimizing the parameters for
detailed and reproducible spectra. The statistical multivariate analysis of the data revealed a significant
difference between the groups, allowing the discrimination of the disease onset. Correlation of Raman
data revealed a direct relationship with paraclinical scores, identifying multifactorial biochemical
modifications related to the pathology. The proposed approach showed a promising accuracy in ALS
onset discrimination, using a fast and sensitive procedure that can make more efficient the diagnostic
procedure and the monitoring of therapeutic and rehabilitative processes in ALS.
AB - Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease leading to progressive and
irreversible muscle atrophy. The diagnosis of ALS is time-consuming and complex, with the clinical
and neurophysiological evaluation accompanied by monitoring of progression and a long procedure
for the discrimination of similar neurodegenerative diseases. The delayed diagnosis strongly slows
the potential development of adequate therapies and the time frame for a prompt intervention. The
discovery of new biomarkers could improve the disease diagnosis, as well as the therapeutic and
rehabilitative effectiveness and monitoring of the pathological progression. In this work saliva collected
from 19 patients with ALS, 10 affected by Parkinson’s disease, 10 affected by Alzheimer’s disease
and 10 healthy subjects, was analysed using Raman spectroscopy, optimizing the parameters for
detailed and reproducible spectra. The statistical multivariate analysis of the data revealed a significant
difference between the groups, allowing the discrimination of the disease onset. Correlation of Raman
data revealed a direct relationship with paraclinical scores, identifying multifactorial biochemical
modifications related to the pathology. The proposed approach showed a promising accuracy in ALS
onset discrimination, using a fast and sensitive procedure that can make more efficient the diagnostic
procedure and the monitoring of therapeutic and rehabilitative processes in ALS.
KW - Amyotrophic Lateral Sclerosis (ALS)
KW - Human salivary fingerprint
KW - Amyotrophic Lateral Sclerosis (ALS)
KW - Human salivary fingerprint
UR - http://hdl.handle.net/10807/157516
U2 - 10.1038/s41598-020-67138-8
DO - 10.1038/s41598-020-67138-8
M3 - Article
VL - 10
SP - 1
EP - 13
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
ER -