background: gastrointestinal dysfunction (GID) accompanies any phase of parkinson's disease (PD), underlying differential clinical-pathological trajectories. objective: to investigate associations between GID and peripheral immune or neurodegeneration-related markers in PD. methods: one-hundred-and-fourteen patients (n = 55 de novo, DN; n = 59 middle-advanced, MA) completed the gastrointestinal dysfunction scale for PD (GIDS-PD), and other motor and non-motor scales; paired measurement of amyloid-β42, amyloid-β42β/β40, total-tau, phosphorylated-181-tau, total α-synuclein CSF levels, albumin ratio, and peripheral blood cell count were collected. group and correlation analyses were performed. results: MA patients had greater GID than DN. GIDS-PD scores directly correlated with MDS-UPDRS-III and non-motor scores in both groups, although more in DN. GIDS-PD scores were directly associated with α-synuclein and inversely with lymphocytes only in DN; conversely, they were positively associated with tau proteins and albumin ratio, and negatively with amyloid-β-peptides in both groups. conclusions: the burden of GID increases along the PD course with associated stage-specific clinical-biological patterns.
Bissacco, J., Bovenzi, R., Conti, M., Simonetta, C., Mascioli, D., Cerroni, R., et al. (2024). Gastrointestinal Dysfunction Bears on the Clinical‐Biological Profile of Parkinson's Disease. MOVEMENT DISORDERS CLINICAL PRACTICE [10.1002/mdc3.14319].
Gastrointestinal Dysfunction Bears on the Clinical‐Biological Profile of Parkinson's Disease
Jacopo Bissacco;Roberta Bovenzi;Matteo Conti;Clara Simonetta;Davide Mascioli;Rocco Cerroni;Piergiorgio Grillo;Mariangela Pierantozzi;Alessandro Stefani;Nicola Biagio Mercuri;Tommaso Schirinzi
2024-01-01
Abstract
background: gastrointestinal dysfunction (GID) accompanies any phase of parkinson's disease (PD), underlying differential clinical-pathological trajectories. objective: to investigate associations between GID and peripheral immune or neurodegeneration-related markers in PD. methods: one-hundred-and-fourteen patients (n = 55 de novo, DN; n = 59 middle-advanced, MA) completed the gastrointestinal dysfunction scale for PD (GIDS-PD), and other motor and non-motor scales; paired measurement of amyloid-β42, amyloid-β42β/β40, total-tau, phosphorylated-181-tau, total α-synuclein CSF levels, albumin ratio, and peripheral blood cell count were collected. group and correlation analyses were performed. results: MA patients had greater GID than DN. GIDS-PD scores directly correlated with MDS-UPDRS-III and non-motor scores in both groups, although more in DN. GIDS-PD scores were directly associated with α-synuclein and inversely with lymphocytes only in DN; conversely, they were positively associated with tau proteins and albumin ratio, and negatively with amyloid-β-peptides in both groups. conclusions: the burden of GID increases along the PD course with associated stage-specific clinical-biological patterns.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


