Numerical method for the interpolation of digitized lines (unrolling method).

M R Voegelin; G Paoli

Home/Archive/PubMed

PubMed · 8075175

Numerical method for the interpolation of digitized lines (unrolling method).

M R Voegelin·G Paoli

View original source ↗Export metadata ↓

Abstract

The proposed method can be used for reconstructing, from n not necessarily equidistant points of a digitized polydrome line, a set of n1 equidistant points (with n1 > n) interpolating the original points. This method is based on a transformation of the original line into a digitized monodrome function D(1i) (unrolling function), where 1i is the line length between the origin and the ith point (i = 1,..., n1). Advantage of this method consists in reducing the two-dimensional interpolation problem to the one-dimensional field. In scintigraphic imaging, it is possible to achieve interpolation and coding of ROI's (Regions Of Interest) edges. For n samples of a monodrome line this method can also be applied, representing a possible alternative to splines. The numerical procedure is developed to reduce the noise on the points.

Explore related subjects

Heart Humans Image Processing, Computer-Assisted Radionuclide Imaging Signal Processing, Computer-Assisted Journal Article

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

M R Voegelin, G Paoli. 1994. Numerical method for the interpolation of digitized lines (unrolling method).. https://pubmed.ncbi.nlm.nih.gov/8075175/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed2007

Cardiac stem cells: isolation, expansion and experimental use for myocardial regeneration.

Cellular cardiomyoplasty (myogenic cell grafting) is actively being explored as a novel method to regenerate damaged myocardium. The adult human heart contains small populations of indigenous committed cardiac stem cells or multipotent cardiac progenitor cells, identified by their cell-surface expression of c-kit (the receptor for stem cell factor), P-glycoprotein (a member of the multidrug resistance protein family), and Sca-1 (stem cell antigen 1, a mouse hematopoietic stem cell marker) or a Sca-1-like protein. Cardiac stem cells represent a logical source to exploit in cardiac regeneration therapy because, unlike other adult stem cells, they are likely to be intrinsically programmed to generate cardiac tissue in vitro and to increase cardiac tissue viability in vitro. Cardiac stem cell therapy could, therefore, change the fundamental approach to the treatment of heart disease.

Heart↗

PubMed2007

Growth-factor-mediated cardiac stem cell activation in myocardial regeneration.

The concept of an intrinsic regenerative capacity of the adult mammalian myocardium owing to the presence of cardiac stem cells (CSCs) in the atria and ventricles is starting to be accepted by the cardiovascular research community. The identification of this cell population has improved the prospects for developing successful clinical protocols for human myocardial regeneration. In the normal adult myocardium, only a small fraction of CSCs undergo amplification and differentiation to replace the parenchymal cells lost by normal wear and tear. Physiological or pathological stimuli cause substantial activation of CSCs, which is mediated by a paracrine feedback loop between myocytes and CSCs. In response to stress, the myocytes produce growth factors and cytokines, for which CSCs have receptors, and autocrine, self-sustaining activation of growth-factor production is simultaneously triggered in the CSCs. These findings from human and animal studies led us to test whether in situ activation of CSCs by growth factors would be as effective as transplantation of CSCs into the regenerating myocardium after ischemia in an animal model that has relevance to humans. In a porcine model, we produced extensive and functionally relevant myocardial regeneration. Here, we discuss the properties of endogenous myocardial stem cells that might be exploited to produce clinical myocardial regeneration without the need for cell transplantation.

Heart↗

PubMed2006

Myocardial strain and torsion quantified by cardiovascular magnetic resonance tissue tagging: studies in normal and impaired left ventricular function.

Accurate quantification and timing of regional myocardial function allows early identification of dysfunction, and therefore becomes increasingly important for clinical risk assessment, patient management, and evaluation of therapeutic efficacy. For this purpose, the application of tissue Doppler echocardiography has rapidly increased. However, echocardiography has some major inherent limitations. Cardiovascular magnetic resonance imaging with tissue tagging provides highly reproducible data on myocardial function, not only in longitudinal and radial directions, but also in the circumferential direction. Because of the development of faster imaging protocols, improved temporal resolution, less time-consuming postprocessing procedures, and the potential of quantifying myocardial deformation in 3 dimensions at any point in the heart, this technique may serve as an alternative for tissue Doppler echocardiography and is now ready for more widespread clinical use. This review discusses the clinical use of cardiovascular magnetic resonance tissue tagging for quantitative assessment of regional myocardial function, thereby underlining the specific features and emerging role of this technique.

Heart↗