Analysis of Genetic and MRI Changes, Blood Markers, and Risk Factors in a Twin Pair Discordant of Progressive Supranuclear Palsy

Medicina (Kaunas). 2023 Sep 22;59(10):1696. doi: 10.3390/medicina59101696.

Abstract

Background and Objectives: Progressive supranuclear palsy (PSP) is a neurodegenerative disease, a tauopathy, which results in a wide clinical spectrum of neurological symptoms. The diagnosis is mostly based on clinical signs and neuroimaging; however, possible biomarkers for screening have been under investigation, and the role of the gut microbiome is unknown. The aim of our study was to identify potential blood biomarkers and observe variations in the gut microbiome within a PSP discordant monozygotic twin pair. Materials and Methods: Anthropometric measurements, neuropsychological tests, and the neurological state were evaluated. Blood was collected for metabolic profiling and for the detection of neurodegenerative and vascular biomarkers. Both the gut microbiome and brain MRI results were thoroughly examined. Results: We found a relevant difference between alpha-synuclein levels and moderate difference in the levels of MMP-2, MB, Apo-A1, Apo-CIII, and Apo-H. With respect to the ratios, a small difference was observed for ApoA1/SAA and ApoB/ApoA1. Using a microbiome analysis, we also discovered a relative dysbiosis, and the MRI results revealed midbrain and frontoparietal cortical atrophy along with a reduction in overall brain volumes and an increase in white matter lesions in the affected twin. Conclusions: We observed significant differences between the unaffected and affected twins in some risk factors and blood biomarkers, along with disparities in the gut microbiome. Additionally, we detected abnormalities in brain MRI results and alterations in cognitive functions.

Keywords: alpha diversity; dementia; environment; genetics; magnetic resonance; plasma biomarker; risk factor.

MeSH terms

  • Biomarkers
  • Humans
  • Magnetic Resonance Imaging / methods
  • Neurodegenerative Diseases*
  • Risk Factors
  • Supranuclear Palsy, Progressive* / diagnostic imaging
  • Supranuclear Palsy, Progressive* / pathology

Substances

  • Biomarkers

Grants and funding

This research was funded by the Semmelweis Science and Innovation Fund—Research and Development Application; Bólyai scholarship of the Hungarian Academy of Sciences; and ÚNKP-20-5 and ÚNKP-21-5 New National Excellence Program of the Ministry for Innovation and Technology, sourced from the National Research, Development, and Innovation Fund. The sequencing and bioinformatics analysis was supported by Semmelweis University-Eötvös Lóránd Research Network, Human Microbiota Study Group No. “0272”. Measurements performed on the CytoFlex device were supported by VEKOP-2.3.3-15-2017-00016.