Current and Potential Approaches for Defining Disease Signatures: a Systematic Review.
Disease signature
Parkinson’s disease
Systematic review
Journal
Journal of molecular neuroscience : MN
ISSN: 1559-1166
Titre abrégé: J Mol Neurosci
Pays: United States
ID NLM: 9002991
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
16
12
2018
accepted:
22
01
2019
pubmed:
20
2
2019
medline:
30
5
2019
entrez:
20
2
2019
Statut:
ppublish
Résumé
Identifying disease signatures in order to facilitate accurate diagnosis/treatment has been the focus of research efforts in the last decade. However, the term "disease signature" has not been properly defined, resulting in inconsistencies between studies, as well as limited ability to fully utilize the tools/information available in the evolving field of healthcare big data. Research was conducted according to the Preferred Reporting Items for Systematic Review and Meta-analyses (PRISMA) guidelines. The search (in PubMed, Cochrane, and Web of Science) was limited to English articles published up to 31/12/2016. The search string was "disease signature" OR "disease signatures" OR "disease fingerprint" OR "disease fingerprints" OR "subtype signature" OR "subtype signatures" OR "subgroup signature" OR "subgroup signatures." The full text of the articles was reviewed to determine the meaning of the phrase "disease signature" as well as the context of its use. Of 285 articles identified in the search, 129 were included in the final analysis. The term disease signature was first found in an article from 2001. In the last 10 years, the use of the term increased by approximately ninefold, which is double the general increase in the number of published articles. Only one article attempted to define the term. The two major medical fields where the term was used were oncology (31%) and neurology (20%); 71% of the identified articles used a single biomarker to define the term, 13% of the articles used a pair of biomarkers, and 16% used signatures with multiple biomarker; in 42% of the identified articles, genomic biomarkers were used for the signature, in 17% measurements of biochemical compounds in body fluids, and in 10%, changes in imaging studies were used for the signature. Our findings identified a lack of consistency in defining the term disease signature. We suggest a novel hierarchical multidimensional concept for this term that would combine both current approaches for identifying diseases (one focusing on undesired effects of the disease and the other on its causes). This model can improve disease signature definition consistency which will enable to generalize and classify diseases, resulting in more precise treatments and better outcomes. Ultimately, this model could lead to developing a statistical confidence in a disease signature that would allow physicians/patients to estimate the precision of the diagnosis, which, in turn, may have important implications on patients' prognosis and treatment.
Identifiants
pubmed: 30778835
doi: 10.1007/s12031-019-01269-0
pii: 10.1007/s12031-019-01269-0
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
550-558Subventions
Organisme : European Union Seventh Framework Programme
ID : 604102
Références
Clin Pharmacol Ther. 2001 Mar;69(3):89-95
pubmed: 11240971
EMBO Rep. 2004 Jul;5(7):650-3
pubmed: 15229637
Ann Clin Microbiol Antimicrob. 2005 Oct 31;4:17
pubmed: 16262889
Dialogues Clin Neurosci. 2008;10(1):29-38
pubmed: 18472482
Cereb Cortex. 2009 Mar;19(3):497-510
pubmed: 18632739
Pediatr Nephrol. 2009 Aug;24(8):1525-32
pubmed: 19280229
J Clin Epidemiol. 2009 Oct;62(10):e1-34
pubmed: 19631507
Lancet. 2010 Mar 20;375(9719):1030-47
pubmed: 20304247
Arch Neurol. 2010 May;67(5):542-7
pubmed: 20457952
Curr Opin HIV AIDS. 2010 Nov;5(6):463-6
pubmed: 20978388
Pract Neurol. 2011 Apr;11(2):91-7
pubmed: 21385966
Physiol Rev. 2011 Oct;91(4):1161-218
pubmed: 22013209
Brain Res. 2012 Aug 21;1469:114-28
pubmed: 22750125
BMJ Open. 2012 Dec 02;2(6):null
pubmed: 23204142
Nat Med. 2013 Mar;19(3):249
pubmed: 23467220
JAMA Neurol. 2014 Apr;71(4):499-504
pubmed: 24514863
Mol Neurodegener. 2014 Nov 12;9:47
pubmed: 25391693
Parkinsonism Relat Disord. 2015 May;21(5):494-9
pubmed: 25840672
J Natl Compr Canc Netw. 2015 Jul;13(7):880-915
pubmed: 26150582
Mov Disord. 2016 Oct;31(10):1527-1534
pubmed: 27430880
Clin Gastroenterol Hepatol. 2017 Jun;15(6):809-819
pubmed: 27712984
Mov Disord. 2017 Mar;32(3):319-324
pubmed: 28233927
Cancer Discov. 2017 Jul;7(7):656
pubmed: 28583911
Crit Rev Oncol Hematol. 2018 Sep;129:133-145
pubmed: 30097232
N Engl J Med. 1968 Mar 14;278(11):593-600
pubmed: 5637758