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Identification of novel plasma proteomic biomarkers of Dupuytren disease
by
Sebastiani, Paola
, Gurinovich, Anastasia
, Hummer, Blake
, Bager, Cecilie
, Leshchyk, Anastasia
, Karsdal, Morten
, Nielsen, Signe
, Eaton, Charles
in
Aged
/ Aptamers
/ Biological markers
/ Biology and Life Sciences
/ Biomarkers
/ Biomarkers - blood
/ Blood plasma
/ Blood Proteins - metabolism
/ Case-Control Studies
/ Collagen
/ Collagen (type I)
/ Collagen Type I - blood
/ Collagen Type I - metabolism
/ Computer and Information Sciences
/ Data collection
/ Degradation
/ Diagnosis
/ Disease
/ Disease Progression
/ Drug development
/ Dupuytren Contracture - blood
/ Dupuytren Contracture - diagnosis
/ Dupuytren's contracture
/ Enrollments
/ Family medical history
/ Female
/ Gender differences
/ Health aspects
/ Health risk assessment
/ Humans
/ Hypotheses
/ Informed consent
/ Laboratories
/ Male
/ Mass spectrometry
/ Medicine and Health Sciences
/ Middle Aged
/ Peptides
/ Physiological aspects
/ Pilot Projects
/ Plasma
/ Proteins
/ Proteomics
/ Proteomics - methods
/ Research and Analysis Methods
/ Scientific imaging
/ Serum proteins
/ Statistical analysis
/ Synthesis
2026
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Identification of novel plasma proteomic biomarkers of Dupuytren disease
by
Sebastiani, Paola
, Gurinovich, Anastasia
, Hummer, Blake
, Bager, Cecilie
, Leshchyk, Anastasia
, Karsdal, Morten
, Nielsen, Signe
, Eaton, Charles
in
Aged
/ Aptamers
/ Biological markers
/ Biology and Life Sciences
/ Biomarkers
/ Biomarkers - blood
/ Blood plasma
/ Blood Proteins - metabolism
/ Case-Control Studies
/ Collagen
/ Collagen (type I)
/ Collagen Type I - blood
/ Collagen Type I - metabolism
/ Computer and Information Sciences
/ Data collection
/ Degradation
/ Diagnosis
/ Disease
/ Disease Progression
/ Drug development
/ Dupuytren Contracture - blood
/ Dupuytren Contracture - diagnosis
/ Dupuytren's contracture
/ Enrollments
/ Family medical history
/ Female
/ Gender differences
/ Health aspects
/ Health risk assessment
/ Humans
/ Hypotheses
/ Informed consent
/ Laboratories
/ Male
/ Mass spectrometry
/ Medicine and Health Sciences
/ Middle Aged
/ Peptides
/ Physiological aspects
/ Pilot Projects
/ Plasma
/ Proteins
/ Proteomics
/ Proteomics - methods
/ Research and Analysis Methods
/ Scientific imaging
/ Serum proteins
/ Statistical analysis
/ Synthesis
2026
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Identification of novel plasma proteomic biomarkers of Dupuytren disease
by
Sebastiani, Paola
, Gurinovich, Anastasia
, Hummer, Blake
, Bager, Cecilie
, Leshchyk, Anastasia
, Karsdal, Morten
, Nielsen, Signe
, Eaton, Charles
in
Aged
/ Aptamers
/ Biological markers
/ Biology and Life Sciences
/ Biomarkers
/ Biomarkers - blood
/ Blood plasma
/ Blood Proteins - metabolism
/ Case-Control Studies
/ Collagen
/ Collagen (type I)
/ Collagen Type I - blood
/ Collagen Type I - metabolism
/ Computer and Information Sciences
/ Data collection
/ Degradation
/ Diagnosis
/ Disease
/ Disease Progression
/ Drug development
/ Dupuytren Contracture - blood
/ Dupuytren Contracture - diagnosis
/ Dupuytren's contracture
/ Enrollments
/ Family medical history
/ Female
/ Gender differences
/ Health aspects
/ Health risk assessment
/ Humans
/ Hypotheses
/ Informed consent
/ Laboratories
/ Male
/ Mass spectrometry
/ Medicine and Health Sciences
/ Middle Aged
/ Peptides
/ Physiological aspects
/ Pilot Projects
/ Plasma
/ Proteins
/ Proteomics
/ Proteomics - methods
/ Research and Analysis Methods
/ Scientific imaging
/ Serum proteins
/ Statistical analysis
/ Synthesis
2026
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Identification of novel plasma proteomic biomarkers of Dupuytren disease
Journal Article
Identification of novel plasma proteomic biomarkers of Dupuytren disease
2026
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Overview
Dupuytren Disease (DD) is a chronic progressive disease that can cause disabling hand deformities. The most common treatments have either high complication rates or high early recurrence rates. Dupuytren lacks a staging biomarker profile to inform the development of preventive therapeutics to improve long-term outcomes. This multi-omic study aimed to create a DD blood proteomic biomarker profile by comparing DD plasma with that of a healthy control group. We measured circulating collagen metabolism peptides and found normal Collagen I synthesis but impaired Collagen I degradation in DD. We measured 6995 serum protein aptamers and identified 68 proteins that showed statistically significant differences compared with the control group. We developed two Diagnostic Proteomic Risk Scores (DPRS) based on hypothesis-free and hypothesis-based analyses. In independent data, our hypothesis-free and hypothesis-based DPRS distinguished Dupuytren from control subjects with accuracies of 76.5% and 70.6%, respectively. Our hypothesis-based DPRS also distinguished DD subjects with different disease progression rates by age at their first corrective procedure (p = 0.0018). This pilot study is the first to provide evidence to suggest that Collagen I accumulation in DD results from impaired degradation rather than increased collagen synthesis. It also describes novel DPRS that have potential use as diagnostic and staging biomarker panels for Dupuytren disease.
Publisher
Public Library of Science,PLOS,Public Library of Science (PLoS)
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