PubMed Health⌕ Search

PubMed · 12201410

Material-specific analysis using coherent-scatter imaging.

Abstract

Coherent-scatter computed tomography (CSCT) is a novel imaging method we are developing to produce cross-sectional images based on the low-angle (<10 degrees) scatter properties of tissue. At diagnostic energies, this scatter is primarily coherent with properties dependent upon the molecular structure of the scatterer. This facilitates the production of material-specific maps of each component in a conglomerate. Our particular goal is to obtain quantitative maps of bone-mineral content. A diagnostic x-ray source and image intensifier are used to acquire scatter patterns under first-generation CT geometry. An accurate measurement of the scatter patterns is necessary to correctly identify and quantify tissue composition. This requires corrections for exposure fluctuations, temporal lag in the intensifier, and self-attenuation within the specimen. The effect of lag is corrected using an approximate convolution method. Self-attenuation causes a cupping artifact in the CSCT images and is corrected using measurements of the transmitted primary beam. An accurate correction is required for reliable density measurements from material-specific images. The correction is shown to introduce negligible noise to the images and a theoretical expression for CSCT image SNR is confirmed by experiment. With these corrections, the scatter intensity is proportional to the number of scattering centers interrogated and quantitative measurements of each material (in g/cm3) are obtained. Results are demonstrated using both a series of poly(methyl methacrylate) (PMMA) sheets of increasing thickness (2-12 mm) and a series of 5 acrylic rods containing varying amounts of hydroxyapatite (0-0.400 g/cm3), simulating the physiological range of bone-mineral density (BMD) found in trabecular bone. The excellent agreement between known and measured BMD demonstrates the viability of CSCT as a tool for densitometry.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Deidre L Batchelar, Ian A Cunningham. 2002. Material-specific analysis using coherent-scatter imaging.. https://doi.org/10.1118/1.1493216

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

KEEP EXPLORING

Related citations

Pregnancy in women with Marfan's Syndrome.

Marfan's Syndrome (MFS) is an autosomal dominant condition resulting in a generalised weakness of the supporting tissues of the body. In its classical form it is associated with abnormalities of the eye, the skeletal system and the cardiovascular system. The prevalence of classical Marfan's Syndrome is 4-6 per 100,000 people. It has significant implications for affected women who are contemplating pregnancy. A multidisciplinary approach involving the specialities of maternal fetal medicine, cardiology and clinical genetics is optimal for provision of care to women with Marfan's Syndrome.

Bone and Bones↗

Cardiovascular abnormalities associated with the Stuve-Wiedemann syndrome.

The Stuve-Wiedemann syndrome (SWS) is a congenital bone dysplasia characterized by camptodactyly with ulnar deviation and congenital bowing of the long bones. Affected patients present with respiratory difficulties in the neonatal period or later and recurrent episodes of hyperthermia. The typical radiological findings are bowing of the long bones of the lower limbs, wide metaphyses with decreased density, and abnormal trabecular pattern. Generally, respiratory insufficiency and hyperthermia are reported to be the cause of death. We report on two sibs with SWS, who died from severe pulmonary hypertension with pulmonary artery wall abnormality. We suggest a common pathophysiological process, which could explain the cardiovascular findings that we observed immediately after birth in the two affected sibs. We hypothesize that the severe pulmonary hypertension due to the arterial wall abnormality could explain the neonatal death of these two children.

Bone and Bones↗

Dimerization of SOX9 is required for chondrogenesis, but not for sex determination.

The SRY-related SOX9 gene is involved in both chondrogenesis and the early steps of mammalian sex determination. Mutations in the human SOX9 gene cause campomelic dysplasia, a severe skeletal malformation syndrome associated with male-to-female sex reversal in most, but not all, XY individuals. Here we show that SOX9 contains a dimerization domain, and binds co-operatively as a dimer in the presence of the DNA enhancer element in genes involved in chondrocyte differentiation, such as Col11a2 and Col9a2, but binds as a monomer to the regulatory region of the sex-determining gene SF1. Frameshift SOX9 mutations truncate its two activation domains, while all missense mutations reported to date lie in the high mobility group (HMG) DNA-binding domain. We identify a missense mutation (A76E), the first outside the HMG domain, in an XY patient presenting with campomelic dysplasia but without sex reversal. This mutation disrupts the dimerization capability of SOX9, interfering with both the DNA binding and consequent transactivation of both the Col11a2 and Col9a2 enhancers. Consistent with the patient's phenotype, the A76E mutation does not affect DNA binding and activation of the SF1 enhancer. DNA-dependent cooperative dimerization could represent a novel mechanism to achieve tissue-specific regulation of gene expression by a SOX transcription factor. These results establish that SOX9 cooperative dimerization is required for chondrogenesis but not for sex determination and may explain why campomelic dysplasia need not be associated with XY sex reversal.

Bone and Bones↗