ArticleNeuroImage. Clinical2016
Data-driven regions of interest for longitudinal change in frontotemporal lobar degeneration.
Article in NeuroImage. Clinical, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
17 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Morphometric MRI as a diagnostic biomarker of frontotemporal dementia: A systematic review to determine clinical applicability.NeuroImage. Clinical · 2018Pooled it
- Longitudinal multimodal imaging and clinical endpoints for frontotemporal dementia clinical trials.Brain : a journal of neurology · 2019Trial
- Sexually dimorphic differences in angiogenesis markers are associated with brain aging trajectories in humans.Science translational medicine · 2024Article
- Classifying Alzheimer's disease and frontotemporal dementia using machine learning with cross-sectional and longitudinal magnetic resonance imaging data.Human brain mapping · 2023Article
- TDP-43-associated atrophy in brains with and without frontotemporal lobar degeneration.NeuroImage. Clinical · 2022Article
- A multicenter comparison of [European journal of nuclear medicine and molecular imaging · 2021Article
- Baseline neuropsychological profiles in prion disease predict survival time.Annals of clinical and translational neurology · 2020Article
- Association of Cognitive and Behavioral Features Between Adults With Tuberous Sclerosis and Frontotemporal Dementia.JAMA neurology · 2020Observational
- Data-driven approaches for tau-PET imaging biomarkers in Alzheimer's disease.Human brain mapping · 2019Article
- Multimodal imaging in familial FTLD: phenoconversion and planning for the future.Brain : a journal of neurology · 2019Article
- Peripheral Innate Immune Activation Correlates With Disease Severity inFrontiers in neurology · 2019Article
- Cerebrospinal fluid biomarkers predict frontotemporal dementia trajectory.Annals of clinical and translational neurology · 2018Article
- Effects of Time-Compressed Speech Training on Multiple Functional and Structural Neural Mechanisms Involving the Left Superior Temporal Gyrus.Neural plasticity · 2018Article
- An 8-week, open-label, dose-finding study of nimodipine for the treatment of progranulin insufficiency fromAlzheimer's & dementia (New York, N. Y.) · 2017Article
- Neuroimaging in Dementia.Seminars in neurology · 2017Review
- Data-driven regions of interest for longitudinal change in three variants of frontotemporal lobar degeneration.Brain and behavior · 2017Article
- Longitudinal white matter change in frontotemporal dementia subtypes and sporadic late onset Alzheimer's disease.NeuroImage. Clinical · 2017Article
Corrections and comments
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Authors and funding
11 authors.
Funding
Abstract
Current research is investigating the potential utility of longitudinal measurement of brain structure as a marker of drug effect in clinical trials for neurodegenerative disease. Recent studies in Alzheimer's disease (AD) have shown that measurement of change in empirically derived regions of interest (ROIs) allows more reliable measurement of change over time compared with regions chosen a-priori based on known effects of AD on brain anatomy. Frontotemporal lobar degeneration (FTLD) is a devastating neurodegenerative disorder for which there are no approved treatments. The goal of this study was to identify an empirical ROI that maximizes the effect size for the annual rate of brain atrophy in FTLD compared with healthy age matched controls, and to estimate the effect size and associated power estimates for a theoretical study that would use change within this ROI as an outcome measure. Eighty six patients with FTLD were studied, including 43 who were imaged twice at 1.5 T and 43 at 3 T, along with 105 controls (37 imaged at 1.5 T and 67 at 3 T). Empirically-derived maps of change were generated separately for each field strength and included the bilateral insula, dorsolateral, medial and orbital frontal, basal ganglia and lateral and inferior temporal regions. The extent of regions included in the 3 T map was larger than that in the 1.5 T map. At both field strengths, the effect sizes for imaging were larger than for any clinical measures. At 3 T, the effect size for longitudinal change measured within the empirically derived ROI was larger than the effect sizes derived from frontal lobe, temporal lobe or whole brain ROIs. The effect size derived from the data-driven 1.5 T map was smaller than at 3 T, and was not larger than the effect size derived from a-priori ROIs. It was estimated that measurement of longitudinal change using 1.5 T MR systems requires approximately a 3-fold increase in sample size to obtain effect sizes equivalent to those seen at 3 T. While the results should be confirmed in additional datasets, these results indicate that empirically derived ROIs can reduce the number of subjects needed for a longitudinal study of drug effects in FTLD compared with a-priori ROIs. Field strength may have a significant impact on the utility of imaging for measuring longitudinal change.
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