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DOI 10.1002/mdc3.14319

Медицинская библиотека · Movement disorders clinical practice · 2024

Gastrointestinal Dysfunction Bears on the Clinical-Biological Profile of Parkinson's Disease.

Bissacco Jacopo, Bovenzi Roberta, Conti Matteo, Simonetta Clara, Mascioli Davide, Cerroni Rocco, Sancesario Giulia Maria, Grillo Piergiorgio, Pierantozzi Mariangela, Stefani Alessandro, Mercuri Nicola Biagio, Camacho Marta, Schirinzi Tommaso

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Аннотация

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.

Для цитирования: Bissacco Jacopo, Bovenzi Roberta, Conti Matteo, Simonetta Clara, Mascioli Davide, Cerroni Rocco, Sancesario Giulia Maria, Grillo Piergiorgio, Pierantozzi Mariangela, Stefani Alessandro, Mercuri Nicola Biagio, Camacho Marta, Schirinzi Tommaso. Gastrointestinal Dysfunction Bears on the Clinical-Biological Profile of Parkinson's Disease.. Movement disorders clinical practice. 2024. DOI: 10.1002/mdc3.14319.

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