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Monika Sas-Wyżykowska

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Review Open access Jul 2026

The Role of the Gut-Brain Axis in the Pathogenesis and Treatment of Irritable Bowel Syndrome in Children and Adolescents: A Review of Current Research with Focus on Dietary and Psychoneurogastroenterological Interventions

Background. Irritable bowel syndrome (IBS) is a prevalent disorder of gut-brain interaction (DGBI) affecting 5-20% of children worldwide, with the microbiota-gut-brain axis (MGBA) playing a central pathophysiological role [7, 8, 21].   Aim. This narrative review evaluates MGBA-targeted therapeutic interventions in pediatric IBS.   Materials and methods. A systematic search of PubMed/MEDLINE (2021-2025) following PRISMA guidelines identified 31 eligible studies from 45 initially screened articles.   Results. Pediatric IBS pathophysiology involves intestinal dysmotility, visceral hypersensitivity, dysbiosis, and altered central processing of visceral signals [14, 15, 26]. The low-FODMAP diet has demonstrated efficacy in adults; however, pediatric evidence remains limited to five randomized trials with inconsistent results [25]. Probiotic supplementation with Lactobacillus rhamnosus GG and Limosilactobacillus reuteri DSM 17938 shows strain-specific efficacy [3, 4]. Cognitive-behavioral therapy and gut-directed hypnotherapy effectively target central signal processing [5, 21]. Pharmacological options, including neuromodulators, remain understudied in pediatric populations, with off-label use predominating [2, 12]. Psychological comorbidities, particularly anxiety and depression, significantly influence treatment response [1, 18].   Conclusions. The MGBA represents the primary therapeutic target in pediatric IBS, supporting multimodal approaches, but limitations in pediatric-specific evidence suggest the need for high-quality randomized controlled trials with standardized outcome measures and adequate long-term follow-up [6, 31].

J. Grygorowicz, Monika Maruszak, A. Wyżykowska et al. · 0 citations
Review Open access Jul 2026

Modern Directions in Early Biomarker Diagnostics of Parkinson's Disease

Background: Parkinson’s disease (PD) is the fastest-growing neurological disorder globally. Traditional diagnosis, which relies on motor symptoms, is associated with a 15–24% error rate and occurs after significant loss of dopaminergic neurons. Early biomarker identification is essential for biological redefinition of PD and timely intervention.Objective: To synthesize evidence from the past five years on minimally invasive biomarkers and assess whether multimodal panels offer greater diagnostic precision than single tests.Methods: A systematic review of PubMed and Scopus (January 2021–January 2026) was conducted per PRISMA guidelines, including meta-analyses and original studies on α-synuclein seed amplification assays (SAA), neuronally derived extracellular vesicles (LIEVs), neurofilament light chain (NfL), and advanced imaging (OCT-A, MRI).Results: SAA exhibited 96% sensitivity in GBA1 mutation carriers and 98.6% in hyposmic individuals with dopaminergic deficits, but only 67.5% in LRRK2 carriers. Serum LIEV-associated α-synuclein distinguished prodromal cases with high precision (AUC=0.91). NfL predicted functional decline (OR=2.54) up to five years before diagnosis. Advanced neuroimaging and skin RT-QuIC tests showed diagnostic accuracies from 82% to 100%.Conclusion: PD diagnosis is shifting from clinical observation to biological profiling. Multimodal biomarker panels integrating molecular, microvascular, and imaging data provide the most precise risk stratification, enabling timely, targeted neuroprotective interventions by rehabilitation specialists.

Aliaksandr Kryshtofik, J. Grygorowicz, Gabriela Faria et al. · 0 citations