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Marzi, C.

Publications and source records attributed to Marzi, C..

2 recordsLinked to original sources

Cerebrovascular response dynamics to hypercapnia in healthy aging

Cerebrovascular dysfunction is an early and underrecognized contributor to cognitive decline. Standard measures such as cerebrovascular reactivity (CVR) during hypercapnia capture only the amplitude of flow responses, providing limited insight into the timing of vascular adaptation. Temporal features, such as delay (onset latency) and time constant (rate of adjustment), together with gain (response amplitude) may serve as more sensitive indicators of vascular health, but cannot be directly obtained from conventional imaging. Here, we investigated cerebral blood flow (CBF), cerebral blood volume (CBV), and blood oxygenation level dependent (BOLD) signal dynamics during hypercapnic challenge in healthy aging. Using a physiologically validated computational model, we estimated delay, time constant, and gain by optimizing the mapping of end-tidal gases to their arterial counterparts in a region-of-interest framework. Once parametrized using CBF, the model successfully predicted CBV and BOLD responses in independent experimental sessions. Across subjects, aging was associated with widespread heterogeneous region-specific changes in delay and substantial reductions in gain and time constant, indicating that cerebrovascular responses become weaker and less adaptable with age. These results demonstrate that calibrated simulations have the ability to track vascular aging, allowing the extraction of parameters that may represent novel biomarkers of cerebrovascular dysfunction. Unlike conventional CVR, temporal hemodynamic parameters capture the dynamics of vascular adaptation, providing a complementary dimension for early detection and therapeutic monitoring in aging and disease.

neuroscience↗

The Pattern and Staging of Brain Atrophy in Spinocerebellar Ataxia Type 2 (SCA2): MRI Volumetrics from ENIGMA-Ataxia

ObjectiveSpinocerebellar ataxia type 2 (SCA2) is a rare, inherited neurodegenerative disease characterised by progressive deterioration in both motor coordination and cognitive function. Atrophy of the cerebellum, brainstem, and spinal cord are core features of SCA2, however the evolution and pattern of whole-brain atrophy in SCA2 remain unclear. We undertook a multi-site, structural magnetic resonance imaging (MRI) study to comprehensively characterize the neurodegeneration profile of SCA2. MethodsVoxel-based morphometry analyses of 110 participants with SCA2 and 128 controls were undertaken to assess groupwise differences in whole-brain volume. Correlations with clinical severity and genotype, and cross-sectional profiling of atrophy patterns at different disease stages, were also performed. ResultsAtrophy in SCA2 relative to controls was greatest (Cohens d>2.5) in the cerebellar white matter (WM), middle cerebellar peduncle, pons, and corticospinal tract. Very large effects (d>1.5) were also evident in the superior cerebellar, inferior cerebellar, and cerebral peduncles. In cerebellar grey matter (GM), large effects (d>0.8) mapped to areas related to both motor coordination and cognitive tasks. Strong correlations (|r|>0.4) between volume and disease severity largely mirrored these groupwise outcomes. Stratification by disease severity showed a degeneration pattern beginning in cerebellar and pontine WM in pre-clinical subjects; spreading to the cerebellar GM and cerebro-cerebellar/corticospinal WM tracts; then finally involving the thalamus, striatum, and cortex in severe stages. InterpretationThe magnitude and pattern of brain atrophy evolves over the course of SCA2, with widespread, non-uniform involvement across the brainstem, cerebellar tracts, and cerebellar cortex; and late involvement of the cerebral cortex and striatum.

neuroscience↗