Parkinson disease and progressive supranuclear palsy: protein expression in skin
I Rodríguez‐Leyva, EG Chi‐Ahumada… - Annals of clinical …, 2016 - Wiley Online Library
I Rodríguez‐Leyva, EG Chi‐Ahumada, J Carrizales, M Rodríguez‐Violante…
Annals of clinical and translational neurology, 2016•Wiley Online LibraryObjective This study characterizes the expression of tau (p‐tau) and α‐synuclein (α‐syn) by
immunohistochemistry in the skin of three different populations: healthy control (HC),
Parkinson disease (PD), and progressive supranuclear paralysis (PSP) subjects, with the
purpose of finding a biomarker that could differentiate between subjects with PD and PSP.
Material and Methods We evaluated the presence of p‐tau and α‐syn in a pilot study in the
skin of three distinct groups of patients: 17 healthy subjects, 17 patients with PD, and 10 …
immunohistochemistry in the skin of three different populations: healthy control (HC),
Parkinson disease (PD), and progressive supranuclear paralysis (PSP) subjects, with the
purpose of finding a biomarker that could differentiate between subjects with PD and PSP.
Material and Methods We evaluated the presence of p‐tau and α‐syn in a pilot study in the
skin of three distinct groups of patients: 17 healthy subjects, 17 patients with PD, and 10 …
Objective
This study characterizes the expression of tau (p‐tau) and α‐synuclein (α‐syn) by immunohistochemistry in the skin of three different populations: healthy control (HC), Parkinson disease (PD), and progressive supranuclear paralysis (PSP) subjects, with the purpose of finding a biomarker that could differentiate between subjects with PD and PSP.
Material and Methods
We evaluated the presence of p‐tau and α‐syn in a pilot study in the skin of three distinct groups of patients: 17 healthy subjects, 17 patients with PD, and 10 patients with PSP. Four millimeters punch biopsies were obtained from the occipital area and analyzed by immunohistochemistry using antibodies against α‐syn and phosphorylated species of tau. PHF (paired helical filaments) antibody identifies p‐tau in both normal and pathological conditions and AT8 recognizes p‐tau characteristic of pathological conditions. Differences between the three groups were assessed by quantification of immunopositive areas in the epidermis.
Results
The immunopositivity pattern of p‐tau and α‐syn was significantly different among the three groups. Healthy subjects showed minimal staining using AT8 and α‐syn. The PD group showed significantly higher α‐syn and AT8 immunopositivity, while the PSP group only expressed higher AT8 immunopositivity than HCs.
Conclusion
These data suggest that the skin reflects brain pathology. Therefore, immunohistochemical analysis of p‐tau and α‐syn in the skin can be useful for further characterization of PD and PSP.
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