A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Brain Plasticity Modulator p75 Neurotrophin Receptor in Human Urine after Different Acute Brain Injuries: A Prospective Cohort Study
Tekijät: Hellström, Santtu; Sajanti, Antti; Srinath, Abhinav; Bennett, Carolyn; Girard, Romuald; Cao, Ying; Frantzén, Janek; Koskimäki, Fredrika; Falter, Johannes; Lyne, Seán B.; Rantamäki, Tomi; Takala, Riikka; Posti, Jussi P.; Roine, Susanna; Puolitaival, Jukka; Jänkälä, Miro; Kolehmainen, Sulo; Rahi, Melissa; Rinne, Jaakko; Castrén, Eero; Koskimäki, Janne
Kustantaja: Multidisciplinary Digital Publishing Institute (MDPI)
Julkaisuvuosi: 2024
Journal: Biomedicines
Tietokannassa oleva lehden nimi: Biomedicines
Artikkelin numero: 112
Vuosikerta: 12
Numero: 1
eISSN: 2227-9059
DOI: https://doi.org/10.3390/biomedicines12010112
Verkko-osoite: https://www.mdpi.com/2227-9059/12/1/112
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/386856998
Acute brain injuries (ABIs) pose a substantial global burden, demanding effective prognostic indicators for outcomes. This study explores the potential of urinary p75 neurotrophin receptor (p75NTR) concentration as a prognostic biomarker, particularly in relation to unfavorable outcomes. The study involved 46 ABI patients, comprising sub-cohorts of aneurysmal subarachnoid hemorrhage, ischemic stroke, and traumatic brain injury. Furthermore, we had four healthy controls. Samples were systematically collected from patients treated at the University Hospital of Turku between 2017 and 2019, at early (1.50 ± 0.70 days) and late (9.17 ± 3.40 days) post-admission time points. Urinary p75NTR levels, measured by ELISA and normalized to creatinine, were compared against patients’ outcomes using the modified Rankin Scale (mRS). Early urine samples showed no significant p75NTR concentration difference between favorable and unfavorable mRS groups. In contrast, late samples exhibited a statistically significant increase in p75NTR concentrations in the unfavorable group (p = 0.033), demonstrating good prognostic accuracy (AUC = 70.9%, 95% CI = 53–89%, p = 0.03). Assessment of p75NTR concentration changes over time revealed no significant variation in the favorable group (p = 0.992) but a significant increase in the unfavorable group (p = 0.009). Moreover, p75NTR concentration was significantly higher in ABI patients (mean ± SD 40.49 ± 28.83–65.85 ± 35.04 ng/mg) compared to healthy controls (mean ± SD 0.54 ± 0.44 ng/mg), irrespective of sampling time or outcome (p < 0.0001). In conclusion, late urinary p75NTR concentrations emerged as a potential prognostic biomarker for ABIs, showing increased levels associated with unfavorable outcomes regardless of the specific type of brain injury. While early samples exhibited no significant differences, the observed late increases emphasize the time-dependent nature of this potential biomarker. Further validation in larger patient cohorts is crucial, highlighting the need for additional research to establish p75NTR as a reliable prognostic biomarker across various ABIs. Additionally, its potential role as a diagnostic biomarker warrants exploration. © 2024 by the authors.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
