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Mercè Boada

Possible papers associated with this exact author name in Arrow. This page groups case-insensitive exact name matches and is not a full identity disambiguation profile.

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YNICL Journal 2025 Journal Article

Amyloid PET predicts atrophy in older adults without dementia: Results from the AMYPAD Prognostic & Natural History study

  • Leonard Pieperhoff
  • Luigi Lorenzini
  • Sophie Mastenbroek
  • Mario Tranfa
  • Mahnaz Shekari
  • Alle Meije Wink
  • Robin Wolz
  • Sylke Grootoonk

Highlights • Aβ-PET predicts atrophy in key brain regions in older adults without dementia.• Fusiform volumetric loss is linked to Aβ independent of CSF tau levels.• Temporal atrophy is stronger in women with higher Aβ burden.• APOE-ε4 carriers show larger Aβ-driven frontal & hippocampal atrophy.

YNICL Journal 2020 Journal Article

The combined effect of amyloid-β and tau biomarkers on brain atrophy in dementia with Lewy bodies

  • Carla Abdelnour
  • Daniel Ferreira
  • Ketil Oppedal
  • Lena Cavallin
  • Olivier Bousiges
  • Lars Olof Wahlund
  • Jakub Hort
  • Zuzana Nedelska

BACKGROUND: Alzheimer's disease (AD)-related pathology is frequently found in patients with dementia with Lewy bodies (DLB). However, it is unknown how amyloid-β and tau-related pathologies influence neurodegeneration in DLB. Understanding the mechanisms underlying brain atrophy in DLB can improve our knowledge about disease progression, differential diagnosis, drug development and testing of anti-amyloid and anti-tau therapies in DLB. OBJECTIVES: We aimed at investigating the combined effect of CSF amyloid-β42, phosphorylated tau and total tau on regional brain atrophy in DLB in the European DLB (E-DLB) cohort. METHODS: 86 probable DLB patients from the E-DLB cohort with CSF and MRI data were included. Random forest was used to analyze the association of CSF biomarkers (predictors) with visual rating scales for medial temporal lobe atrophy (MTA), posterior atrophy (PA) and global cortical atrophy scale-frontal subscale (GCA-F) (outcomes), including age, sex, education and disease duration as extra predictors. RESULTS: DLB patients with abnormal MTA scores had abnormal CSF Aβ42, shorter disease duration and older age. DLB patients with abnormal PA scores had abnormal levels of CSF Aβ42 and p-tau, older age, lower education and shorter disease duration. Abnormal GCA-F scores were associated with lower education, male sex, and older age, but not with any AD-related CSF biomarker. CONCLUSIONS: This study shows preliminary data on the potential combined effect of amyloid-β and tau-related pathologies on the integrity of posterior brain cortices in DLB patients, whereas only amyloid-β seems to be related to MTA. Future availability of α-synuclein biomarkers will help us to understand the effect of α-synuclein and AD-related pathologies on brain integrity in DLB.

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