2014, Number 3
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Med Sur 2014; 21 (3)
Estudio de las proteínas 14-3-3 y Tau como biomarcadores en pacientes con enfermedades neurodegenerativas de origen no determinado. Experiencia en el Laboratorio de Patología Clínica de Médica Sur
Briones-Torres CA, Echeverría-Vargas JA, García-Ramos GS, Noffal-Nuño V, Pérez-Jáuregui J
Language: Spanish
References: 15
Page: 116-119
PDF size: 132.25 Kb.
ABSTRACT
Introduction. The gold standard for diagnosis of neurodegenerative
diseases of undetermined origin is brain biopsy; however, new
techniques have been developed that supports its diagnosis. The
detection of protein markers in cerebrospinal fluid, such as 14-3-3
protein, and Tau protein is vital for diagnosis.
Objective. Determine
the relationship between 14-3-3 and Tau testing in patients
referred to the Laboratory of Clinical Pathology with a probable
diagnosis of neurodegenerative diseases associated with undetermined
origin.
Material and methods. It was conducted a retrospective
observational-search using the database of the information
system of the Laboratory of Clinical Pathology Medical Sur from
January 2008 through December 2013 for all requested tests of 14-
3-3 and tau Protein in cerebrospinal fluid.
Results. Forty-two of 89
requested tests were positive (14-3-3) (47.2%) of which 69% were
women with a mean age of 55.7 years (29-73). 31% were men with
a mean age of 59.76 (36-72). The average value of the Tau protein
in the positive patients was 9,640 pg/mL (SD ± 18,184 pg/mL).
Discussion. In Mexico there is no well-documented information
about incidence of these diseases, however, these biochemical
markers are very helpful by not being post-mortem procedures.
These markers can be elevated in vascular, neoplastic, inflammatory
and metabolic diseases of the central nervous system, which are
associated with a rapid neuronal destruction.
Conclusion. In the
context of patients with dementia of undetermined origin, it should
be considered the detection of 14-3-3 and Tau protein, since its
presence is highly correlated with prion disease.
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