Literature DB >> 24503592

Biomarkers in rare diseases.

A Ferlini1, C Scotton, G Novelli.   

Abstract

BACKGROUND: Nowadays 7,000 rare diseases (RDs) have been identified with a prevalence less than 5/10,000. Despite of the enormous effort the European Union (EU) has already invested in this field, still 4,000 RDs remain orphan of genetic diagnosis and causative gene identification. The genetic definition of RDs represents a prerequisite for being diagnosed, for having a robust prevention, for entering in a specific standard of care, and ultimately, for being included in clinical trials, often via personalized medicine. It is well established that biomarkers can offer a way to speed up research by understanding the pathophysiological mechanisms of diseases. In particular, biomarkers will offer an invaluable tool for monitoring disease progression, prognosis and response to drug treatment.
METHODS: In this review, we summarize the different types of biomarkers and their importance as well as their translational applications in RDs. We have reviewed the current knowledge on biomarkers state-of-the-art via literature data, specific websites and EU sources regarding past, pending and current projects.
RESULTS: Here we provide a comprehensive scenario of biomarkers research, its applications in clinical practice, with special emphasis on translational research applicable to diagnostic and clinical trials. The experience of the EU project BIO-NMD is also mentioned.
CONCLUSION: Biomarkers represent key features in both diagnostics and research on rare diseases and will encounter wide exploitation in translational and personalized medicine.
© 2013 S. Karger AG, Basel

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24503592     DOI: 10.1159/000355938

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  10 in total

1.  Orphan diseases: state of the drug discovery art.

Authors:  Claude-Henry Volmar; Claes Wahlestedt; Shaun P Brothers
Journal:  Wien Med Wochenschr       Date:  2016-01-27

2.  Use of the "Exposome" in the Practice of Epidemiology: A Primer on -Omic Technologies.

Authors:  D Gayle DeBord; Tania Carreón; Thomas J Lentz; Paul J Middendorf; Mark D Hoover; Paul A Schulte
Journal:  Am J Epidemiol       Date:  2016-08-15       Impact factor: 4.897

Review 3.  Translating rare-disease therapies into improved care for patients and families: what are the right outcomes, designs, and engagement approaches in health-systems research?

Authors:  Beth K Potter; Sara D Khangura; Kylie Tingley; Pranesh Chakraborty; Julian Little
Journal:  Genet Med       Date:  2015-04-09       Impact factor: 8.822

Review 4.  Discovery of biomarkers in rare diseases: innovative approaches by predictive and personalized medicine.

Authors:  Basri Gülbakan; Rıza Köksal Özgül; Ayşe Yüzbaşıoğlu; Matthias Kohl; Hans-Peter Deigner; Meral Özgüç
Journal:  EPMA J       Date:  2016-12-08       Impact factor: 6.543

Review 5.  Can composite digital monitoring biomarkers come of age? A framework for utilization.

Authors:  Christopher Kovalchick; Rhea Sirkar; Oliver B Regele; Lampros C Kourtis; Marie Schiller; Howard Wolpert; Rhett G Alden; Graham B Jones; Justin M Wright
Journal:  J Clin Transl Sci       Date:  2017-12

Review 6.  Experimental and Clinical Biomarkers for Progressive Evaluation of Neuropathology and Therapeutic Interventions for Acute and Chronic Neurological Disorders.

Authors:  Doodipala Samba Reddy; Hasara Nethma Abeygunaratne
Journal:  Int J Mol Sci       Date:  2022-10-03       Impact factor: 6.208

7.  Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy.

Authors:  Chiara Scotton; Matteo Bovolenta; Elena Schwartz; Maria Sofia Falzarano; Elena Martoni; Chiara Passarelli; Annarita Armaroli; Hana Osman; Carmelo Rodolico; Sonia Messina; Elena Pegoraro; Adele D'Amico; Enrico Bertini; Francesca Gualandi; Marcella Neri; Rita Selvatici; Patrizia Boffi; Maria Antonietta Maioli; Hanns Lochmüller; Volker Straub; Katherine Bushby; Tiziana Castrignanò; Graziano Pesole; Patrizia Sabatelli; Luciano Merlini; Paola Braghetta; Paolo Bonaldo; Paolo Bernardi; Reghan Foley; Sebahattin Cirak; Irina Zaharieva; Francesco Muntoni; Daniele Capitanio; Cecilia Gelfi; Ekaterina Kotelnikova; Anton Yuryev; Michael Lebowitz; Xiping Zhang; Brian A Hodge; Karyn A Esser; Alessandra Ferlini
Journal:  J Cell Sci       Date:  2016-03-04       Impact factor: 5.285

8.  Properties of beta oscillations in Dup15q syndrome.

Authors:  Vidya Saravanapandian; Joel Frohlich; Joerg F Hipp; Carly Hyde; Aaron W Scheffler; Peyman Golshani; Edwin H Cook; Lawrence T Reiter; Damla Senturk; Shafali S Jeste
Journal:  J Neurodev Disord       Date:  2020-08-13       Impact factor: 4.025

Review 9.  The Progression of Hemophilic Arthropathy: The Role of Biomarkers.

Authors:  Gianluigi Pasta; Salvatore Annunziata; Alberto Polizzi; Laura Caliogna; Eugenio Jannelli; Alessandro Minen; Mario Mosconi; Francesco Benazzo; Matteo Nicola Dario Di Minno
Journal:  Int J Mol Sci       Date:  2020-10-02       Impact factor: 5.923

Review 10.  Biomarkers in Hereditary Angioedema.

Authors:  Grzegorz Porebski; Mateusz Kwitniewski; Avner Reshef
Journal:  Clin Rev Allergy Immunol       Date:  2021-02-09       Impact factor: 8.667

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.