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1.
PLoS One ; 15(4): e0230941, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32348311

RESUMO

We develop a method to identify statistically significant communities in a weighted network with a high proportion of self-looping weights. We use this method to find overlapping agglomerations of U.S. counties by representing inter-county commuting as a weighted network. We identify three types of communities; non-nodal, nodal and monads, which correspond to different types of regions. The results suggest that traditional regional delineations that rely on ad hoc thresholds do not account for important and pervasive connections that extend far beyond expected metropolitan boundaries or megaregions.


Assuntos
Meios de Transporte/métodos , Humanos , População Rural , Estados Unidos , População Urbana
2.
IEEE Trans Med Imaging ; 38(3): 697-709, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30235119

RESUMO

The 18F-AV-1451 PET tracer binds to tau, an Alzheimer's disease biomarker. The standardized uptake value ratio (SUVR) 80-100 min window is widely used to quantify tau binding, although 18F-AV-1451 continues increasing relative to a reference region in regions with tau deposition. Left uncorrected, acquisition time inaccuracies can lead to errors from -4% to 6% in 20-min SUVR measurements in subjects with Alzheimer's disease. In 40 subjects with scans from 75-115 min following 18F-AV-1451 injection, we created 20-min reconstructions (4×5 min) of start-times ranging from 75-85 min, as proxies of offset scans and calculated the mean in regions of interest (ROIs). We developed a segmented least squares (SLS) method to obtain error-minimizing weighting coefficients for 18F-AV-1451 ROIs that best predict SUVR 80-100 from weighted means of SUVRs from offset start-times. We compared residual errors of our SLS method to those in: 1) uncorrected offset 20-min-SUVRs; 2) the mean of five-min frames within the 80-100 window; and 3) a least-squares interpolation method. We evaluated errors induced by start-time offset on SUVRs for each method. TheSLS, which corrected using least-squares coefficients of 5-min components, consistently reduced errors across all offset starttimes. Effect size analysis for simulated clinical longitudinal 18F-AV-1451 drug trials showed that uncorrected 20-min offset SUVRs would require up to 20% more participants to detect treatment effects compared with using SLS. Correction of SUVR scan-time errors by SLS minimizes errors compared with other correction methods and may be extended to other scanners and tracers.


Assuntos
Doença de Alzheimer/diagnóstico por imagem , Biomarcadores/análise , Carbolinas/administração & dosagem , Cintilografia/métodos , Proteínas tau/análise , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Disfunção Cognitiva/diagnóstico por imagem , Simulação por Computador , Meios de Contraste , Humanos , Processamento de Imagem Assistida por Computador/métodos , Imageamento por Ressonância Magnética/métodos , Masculino , Método de Monte Carlo , Reprodutibilidade dos Testes
3.
J Nucl Med ; 58(2): 332-338, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27587706

RESUMO

The goal of this paper was to evaluate the in vivo kinetics of the novel tau-specific PET radioligand 18F-AV-1451 in cognitively healthy control (HC) and Alzheimer disease (AD) subjects, using reference region analyses. METHODS: 18F-AV-1451 PET imaging was performed on 43 subjects (5 young HCs, 23 older HCs, and 15 AD subjects). Data were collected from 0 to 150 min after injection, with a break from 100 to 120 min. T1-weighted MR images were segmented using FreeSurfer to create 14 bilateral regions of interest (ROIs). In all analyses, cerebellar gray matter was used as the reference region. Nondisplaceable binding potentials (BPNDs) were calculated using the simplified reference tissue model (SRTM) and SRTM2; the Logan graphical analysis distribution volume ratio (DVR) was calculated for 30-150 min (DVR30-150). These measurements were compared with each other and used as reference standards for defining an appropriate 20-min window for the SUV ratio (SUVR). Pearson correlations were used to compare the reference standards to 20-min SUVRs (start times varied from 30 to 130 min), for all values, for ROIs with low 18F-AV-1451 binding (lROIs, mean of BPND + 1 and DVR30-150 < 1.5), and for ROIs with high 18F-AV-1451 binding (hROIs, mean of BPND + 1 and DVR30-150 > 1.5). RESULTS: SRTM2 BPND + 1 and DVR30-150 were in good agreement. Both were in agreement with SRTM BPND + 1 for lROIs but were greater than SRTM BPND + 1 for hROIs, resulting in a nonlinear relationship. hROI SUVRs increased from 80-100 to 120-140 min by 0.24 ± 0.15. The SUVR time interval resulting in the highest correlation and slope closest to 1 relative to the reference standards for all values was 120-140 min for hROIs, 60-80 min for lROIs, and 80-100 min for lROIs and hROIs. There was minimal difference between methods when statistical significance between ADs and HCs was calculated. CONCLUSION: Despite later time periods providing better agreement between reference standards and SUVRs for hROIs, a good compromise for studying lROIs and hROIs is SUVR80-100. The lack of SUVR plateau for hROIs highlights the importance of precise acquisition time for longitudinal assessment.


Assuntos
Doença de Alzheimer/metabolismo , Encéfalo/metabolismo , Carbolinas/farmacocinética , Carbolinas/normas , Tomografia por Emissão de Pósitrons/métodos , Proteínas tau/metabolismo , Idoso , Doença de Alzheimer/diagnóstico por imagem , Biomarcadores/metabolismo , Encéfalo/diagnóstico por imagem , Simulação por Computador , Feminino , Humanos , Aumento da Imagem/normas , Cinética , Masculino , Taxa de Depuração Metabólica , Pessoa de Meia-Idade , Modelos Biológicos , Imagem Molecular/normas , Mapeamento de Interação de Proteínas/normas , Compostos Radiofarmacêuticos/farmacocinética , Compostos Radiofarmacêuticos/normas , Valores de Referência , Estados Unidos
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