scholarly journals In vivo lung morphometry with hyperpolarized 3He diffusion MRI in canines with induced emphysema: disease progression and comparison with computed tomography

2007 ◽  
Vol 102 (1) ◽  
pp. 477-484 ◽  
Author(s):  
Tariq S. K. Tanoli ◽  
Jason C. Woods ◽  
Mark S. Conradi ◽  
Kyongtae Ty Bae ◽  
David S. Gierada ◽  
...  

Despite a long history of development, diagnostic tools for in vivo regional assessment of lungs in patients with pulmonary emphysema are not yet readily available. Recently, a new imaging technique, in vivo lung morphometry, was introduced by our group. This technique is based on MRI measurements of diffusion of hyperpolarized 3He gas in lung air spaces and provides quantitative in vivo tomographic information on lung microstructure at the level of the acinar airways. Compared with standard diffusivity measurements that strongly depend on pulse sequence parameters (mainly diffusion time), our approach evaluates a “hard number,” the average acinar airway radius. For healthy dogs, we find here a mean acinar airway radius of ∼0.3 mm compared with 0.36 mm in healthy humans. The purpose of the present study is the application of this technique for quantification of emphysema progression in dogs with experimentally induced disease. The diffusivity measurements and resulting acinar airway geometrical characteristics were correlated with the local lung density and local lung-specific air volume calculated from quantitative computed tomography data obtained on the same dogs. The results establish an important association between the two modalities. The observed sensitivity of our method to emphysema progression suggests that this technique has potential for the diagnosis of emphysema and tracking of disease progression or improvement via a pharmaceutical intervention.

2004 ◽  
Vol 83 (2) ◽  
pp. 222-229 ◽  
Author(s):  
D.R. Korver ◽  
J.L. Saunders-Blades ◽  
K.L. Nadeau

Endocrinology ◽  
2008 ◽  
Vol 150 (4) ◽  
pp. 1570-1579 ◽  
Author(s):  
David E. Komatsu ◽  
Kellie A. Brune ◽  
Hong Liu ◽  
Allen L. Schmidt ◽  
Bomie Han ◽  
...  

PTH has been shown to enhance fracture repair; however, exactly when and where PTH acts in this process remains to be elucidated. Therefore, we conducted a longitudinal, region-specific analysis of bone regeneration in mature, osteopenic rats using a cortical defect model. Six-month-old rats were ovariectomized, and allowed to lose bone for 2 months, before being subjected to bilateral 2-mm circular defects in their femoral diaphyses. They were then treated for 5 wk with hPTH1–38 at doses of 0, 3, 10, or 30 μg/kg · d and scanned weekly by in vivo quantitative computed tomography. Quantitative computed tomography analyses showed temporal, dose-dependent increases in mineralization in the defects, intramedullary (IM) spaces, and whole diaphyses at the defect sites. Histomorphometry confirmed PTH stimulation of primarily woven bone in the defects and IM spaces, but not the periosteum. After necropsy, biomechanical testing identified an increase in strength at the highest PTH dose. Serum procollagen type I N-terminal propeptide concentration showed a transient increase due to drilling, but procollagen type I N-terminal propeptide also increased with PTH treatment, whereas tartrate-resistant acid phosphatase unexpectedly decreased. Analyses of lumber vertebra confirmed systemic efficacy of PTH at a nonfracture site. In summary, PTH dose dependently induced new bone formation within defects, at endocortical surfaces, and in IM spaces, resulting in faster and greater bone healing, as well as efficacy at other skeletal sites. The effects of PTH were kinetic, region specific, and most apparent at high doses that may not be entirely clinically relevant; therefore, clinical studies are necessary to clarify the therapeutic utility of PTH in bone healing.


2004 ◽  
Vol 39 (7) ◽  
pp. 385-393 ◽  
Author(s):  
G??raldine Le Duc ◽  
St??phanie Corde ◽  
Anne-Marie Charvet ◽  
H??l??ne Elleaume ◽  
R??gine Farion ◽  
...  

2019 ◽  
Author(s):  
Nadège Corbin ◽  
Julio Acosta-Cabronero ◽  
Shaihan J. Malik ◽  
Martina F. Callaghan

AbstractPurposeQuantitative MRI applications, such as mapping the T1 time of tissue, puts high demands on the accuracy and precision of transmit field (B1+) estimation. A candidate approach to satisfy these requirements exploits the difference in phase induced by the Bloch-Siegert Shift (BSS) of two acquisitions with opposite off-resonance frequency RF pulses. Interleaving these RF pulses ensures robustness to motion and scanner drifts, however, here we demonstrate that doing so also introduces a bias in the B1+ estimates.MethodsWe show via simulation and experiments that the amplitude of the error depends on MR pulse sequence parameters, such as TR and RF spoiling increment, but more problematically, on the intrinsic properties, T1 and T2, of the investigated tissue. To solve these problems, we present a new approach to BSS-based B1+ estimation that uses a multi-echo acquisition and a general linear model (GLM) to estimate the correct BSS-induced phase.ResultsIn line with simulations, phantom and in-vivo experiments confirmed that the GLM-based method removed the dependency on tissue properties and pulse sequence settings. It also showed greater robustness to hardware imperfections.ConclusionThe GLM-based method is recommended as a more accurate approach to BSS-based B1+ mapping.


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