Optimizing C-Type Natriuretic Peptide and Receptor Expression Analysis with Droplet Digital™ PCR: Advancing Biomarker Discovery for Brugada Syndrome?
Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using drop...
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Published in | Biomolecules (Basel, Switzerland) Vol. 15; no. 6; p. 792 |
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Abstract | Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect C-type natriuretic peptide (CNP) and its receptors, NPR-B and NPR-C, expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. CNP expression was detectable and lower in BrS patients than in the controls, although not significantly. NPR-B and NPR-C expression was significantly reduced in the same patients (p ≤ 0.05). Strong correlations were observed between CNP and NPR-B (p = 0.01) and NPR-C (p < 0.0001), as well as between NPR-B and NPR-C (p = 0.0002). Body weight correlated with CNP (p = 0.02), NPR-B (p = 0.03), and NPR-C (p = 0.02); meanwhile, NPR-B expression was related to height (p = 0.05). This study is the first to analyze CNP expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS. |
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AbstractList | Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect C-type natriuretic peptide (CNP) and its receptors, NPR-B and NPR-C, expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. CNP expression was detectable and lower in BrS patients than in the controls, although not significantly. NPR-B and NPR-C expression was significantly reduced in the same patients (p ≤ 0.05). Strong correlations were observed between CNP and NPR-B (p = 0.01) and NPR-C (p < 0.0001), as well as between NPR-B and NPR-C (p = 0.0002). Body weight correlated with CNP (p = 0.02), NPR-B (p = 0.03), and NPR-C (p = 0.02); meanwhile, NPR-B expression was related to height (p = 0.05). This study is the first to analyze CNP expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS. Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect C-type natriuretic peptide (CNP) and its receptors, NPR-B and NPR-C, expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. CNP expression was detectable and lower in BrS patients than in the controls, although not significantly. NPR-B and NPR-C expression was significantly reduced in the same patients (p ≤ 0.05). Strong correlations were observed between CNP and NPR-B (p = 0.01) and NPR-C (p < 0.0001), as well as between NPR-B and NPR-C (p = 0.0002). Body weight correlated with CNP (p = 0.02), NPR-B (p = 0.03), and NPR-C (p = 0.02); meanwhile, NPR-B expression was related to height (p = 0.05). This study is the first to analyze CNP expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS.Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect C-type natriuretic peptide (CNP) and its receptors, NPR-B and NPR-C, expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. CNP expression was detectable and lower in BrS patients than in the controls, although not significantly. NPR-B and NPR-C expression was significantly reduced in the same patients (p ≤ 0.05). Strong correlations were observed between CNP and NPR-B (p = 0.01) and NPR-C (p < 0.0001), as well as between NPR-B and NPR-C (p = 0.0002). Body weight correlated with CNP (p = 0.02), NPR-B (p = 0.03), and NPR-C (p = 0.02); meanwhile, NPR-B expression was related to height (p = 0.05). This study is the first to analyze CNP expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS. Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect ( ) and its receptors, and , expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. expression was detectable and lower in BrS patients than in the controls, although not significantly. and expression was significantly reduced in the same patients ( ≤ 0.05). Strong correlations were observed between and ( = 0.01) and ( < 0.0001), as well as between and ( = 0.0002). Body weight correlated with ( = 0.02), ( = 0.03), and ( = 0.02); meanwhile, expression was related to height ( = 0.05). This study is the first to analyze expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS. Brugada syndrome (BrS) is a cardiac disease associated with characteristic ECG abnormalities and a heightened risk of sudden cardiac death, especially in young individuals with structurally normal hearts. The primary aim of this study was to highlight, for the first time, the potential of using droplet digital PCR (ddPCR), a highly sensitive method, to detect C-type natriuretic peptide ( CNP ) and its receptors, NPR-B and NPR-C , expression in BrS. Whole-blood samples from 12 subjects with type 1 BrS and 12 controls were analyzed. CNP expression was detectable and lower in BrS patients than in the controls, although not significantly. NPR-B and NPR-C expression was significantly reduced in the same patients ( p ≤ 0.05). Strong correlations were observed between CNP and NPR-B ( p = 0.01) and NPR-C ( p < 0.0001), as well as between NPR-B and NPR-C ( p = 0.0002). Body weight correlated with CNP ( p = 0.02), NPR-B ( p = 0.03), and NPR-C ( p = 0.02); meanwhile, NPR-B expression was related to height ( p = 0.05). This study is the first to analyze CNP expression and its specific receptors using ddPCR technology, showing for the first time their presence and activation in individuals with BrS. Although further research is needed to clarify CNP-related mechanisms, these findings offer a valuable starting point for exploring its role in BrS. |
Audience | Academic |
Author | Cabiati, Manuela Vozzi, Federico Solarino, Gianluca Morales, Maria Aurora Mazzocchetti, Lorenzo Guiducci, Letizia Cecchettini, Antonella Del Ry, Silvia Piacenti, Marcello Sgalippa, Agnese Zucchelli, Giulio Rossi, Andrea Persiani, Elisa Notarstefano, Pasquale |
AuthorAffiliation | 2 Fondazione Toscana Gabriele Monasterio, 56124 Pisa, Italy; marcello.piacenti@ftgm.it (M.P.); andrea.rossi@ftgm.it (A.R.) 5 University Cardiology Division, Versilia Hospital, 55041 Lido di Camaiore, Italy; gianluca.solarino@uslnordovest.toscana.it 7 Cardiovascular and Neurological Department, San Donato Hospital, 52100 Arezzo, Italy; pasqualenotarstefano@gmail.com 1 Laboratory of Biochemistry and Molecular Biology, CNR Institute of Clinical Physiology, Via Giuseppe Moruzzi 1, 56124 Pisa, Italy; manuela.cabiati@cnr.it (M.C.); federico.vozzi@cnr.it (F.V.); elisa.persiani@cnr.it (E.P.); agnese.sgalippa@santannapisa.it (A.S.); antonella.cecchettini@unipi.it (A.C.); letizia.guiducci@cnr.it (L.G.); auroramorales@icloud.com (M.A.M.) 3 Health Science Interdisciplinary Center, Sant’Anna School of Advanced Studies, 56100 Pisa, Italy 4 Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy 6 Second Division of Cardiology, Azienda Ospedaliero Universitaria Pisana, 56126 |
AuthorAffiliation_xml | – name: 3 Health Science Interdisciplinary Center, Sant’Anna School of Advanced Studies, 56100 Pisa, Italy – name: 4 Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy – name: 7 Cardiovascular and Neurological Department, San Donato Hospital, 52100 Arezzo, Italy; pasqualenotarstefano@gmail.com – name: 2 Fondazione Toscana Gabriele Monasterio, 56124 Pisa, Italy; marcello.piacenti@ftgm.it (M.P.); andrea.rossi@ftgm.it (A.R.) – name: 1 Laboratory of Biochemistry and Molecular Biology, CNR Institute of Clinical Physiology, Via Giuseppe Moruzzi 1, 56124 Pisa, Italy; manuela.cabiati@cnr.it (M.C.); federico.vozzi@cnr.it (F.V.); elisa.persiani@cnr.it (E.P.); agnese.sgalippa@santannapisa.it (A.S.); antonella.cecchettini@unipi.it (A.C.); letizia.guiducci@cnr.it (L.G.); auroramorales@icloud.com (M.A.M.) – name: 5 University Cardiology Division, Versilia Hospital, 55041 Lido di Camaiore, Italy; gianluca.solarino@uslnordovest.toscana.it – name: 6 Second Division of Cardiology, Azienda Ospedaliero Universitaria Pisana, 56126 Pisa, Italy; zucchelli76@gmail.com (G.Z.); info@aritmologomazzocchetti.it (L.M.) |
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Keywords | mRNA Brugada syndrome C-type natriuretic peptide NPR-B NPR-C droplet digital™ PCR |
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SubjectTerms | Adult Biomarkers Biomarkers - blood Blood Body weight Brugada syndrome Brugada Syndrome - blood Brugada Syndrome - diagnosis Brugada Syndrome - genetics Brugada Syndrome - metabolism C-Type natriuretic peptide Cardiac arrhythmia Cardiology Cardiovascular disease Cardiovascular diseases Case-Control Studies Coronary artery disease droplet digital™ PCR Electrocardiogram Electrocardiography Female Genes Heart Heart diseases Humans Inflammation Kinases Male Middle Aged mRNA Mutation Natriuretic Peptide, C-Type - blood Natriuretic Peptide, C-Type - genetics Natriuretic Peptide, C-Type - metabolism Natriuretic peptides NPR-B NPR-C Peptides Physiology Polymerase Chain Reaction - methods Precision medicine Public radio Receptors, Atrial Natriuretic Factor - blood Receptors, Atrial Natriuretic Factor - genetics Receptors, Atrial Natriuretic Factor - metabolism |
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Title | Optimizing C-Type Natriuretic Peptide and Receptor Expression Analysis with Droplet Digital™ PCR: Advancing Biomarker Discovery for Brugada Syndrome? |
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