TY - JOUR
T1 - Identification of serum microRNAs as potential biomarkers in Pompe disease
AU - Carrasco-Rozas, Ana
AU - Fernández-Simón, Esther
AU - Lleixà, Maria Cinta
AU - Belmonte, Izaskun
AU - Pedrosa-Hernandez, Irene
AU - Montiel-Morillo, Elena
AU - Nuñez-Peralta, Claudia
AU - Llauger Rossello, Jaume
AU - Segovia, Sonia
AU - De Luna, Noemí
AU - Suarez-Calvet, Xavier
AU - Illa, Isabel
AU - Díaz-Manera, Jordi
AU - Gallardo, Eduard
N1 - © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. Objective: To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). Methods: We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expression levels of microRNAs that were deregulated were further studied in 35 AOPD patients and 10 controls using Real-Time PCR. Additionally, the skeletal muscle expression of microRNAs which showed significant increase levels in serum samples was also studied. Correlations between microRNA serum levels and muscle function test, spirometry, and quantitative muscle MRI were performed (these data correspond to the study NCT01914536 at ClinicalTrials.gov). Results: We identified 14 microRNAs that showed different expression levels in serum samples of AOPD patients compared to controls. We validated these results in a larger cohort of patients and we found increased levels of three microRNAs, the so called dystromirs: miR-1-3p, miR-133a-3p, and miR-206. These microRNAs are involved in muscle regeneration and the expression of these was increased in patients' muscle biopsies. Significant correlations between microRNA levels and muscle function test were found. Interpretation: Serum expression levels of dystromirs may represent additional biomarkers for the follow-up of AOPD patients.
AB - © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. Objective: To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). Methods: We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expression levels of microRNAs that were deregulated were further studied in 35 AOPD patients and 10 controls using Real-Time PCR. Additionally, the skeletal muscle expression of microRNAs which showed significant increase levels in serum samples was also studied. Correlations between microRNA serum levels and muscle function test, spirometry, and quantitative muscle MRI were performed (these data correspond to the study NCT01914536 at ClinicalTrials.gov). Results: We identified 14 microRNAs that showed different expression levels in serum samples of AOPD patients compared to controls. We validated these results in a larger cohort of patients and we found increased levels of three microRNAs, the so called dystromirs: miR-1-3p, miR-133a-3p, and miR-206. These microRNAs are involved in muscle regeneration and the expression of these was increased in patients' muscle biopsies. Significant correlations between microRNA levels and muscle function test were found. Interpretation: Serum expression levels of dystromirs may represent additional biomarkers for the follow-up of AOPD patients.
KW - DYSTROPHY
KW - ENZYME REPLACEMENT THERAPY
KW - EXPRESSION
KW - FEATURE-SELECTION
KW - MIR-206
KW - PLASMA MICRORNAS
KW - QUANTITATIVE PCR
KW - SKELETAL-MUSCLE
UR - http://www.mendeley.com/research/identification-serum-micrornas-potential-biomarkers-pompe-disease
U2 - 10.1002/acn3.50800
DO - 10.1002/acn3.50800
M3 - Article
C2 - 31353854
SN - 2328-9503
VL - 6
SP - 1214
EP - 1224
JO - Annals of Clinical and Translational Neurology
JF - Annals of Clinical and Translational Neurology
IS - 7
ER -