Mineral density volume gradients in normal and diseased human tissues.

Clinical computed tomography provides a single mineral density (MD) value for heterogeneous calcified tissues containing early and late stage pathologic formations. The novel aspect of this study is that, it extends current quantitative methods of mapping mineral density gradients to three dimension...

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Main Authors: Sabra I Djomehri, Susan Candell, Thomas Case, Alyssa Browning, Grayson W Marshall, Wenbing Yun, S H Lau, Samuel Webb, Sunita P Ho
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4391782?pdf=render
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spelling doaj-a2222d268815411e96c32ffc9ece3f552020-11-24T21:35:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012161110.1371/journal.pone.0121611Mineral density volume gradients in normal and diseased human tissues.Sabra I DjomehriSusan CandellThomas CaseAlyssa BrowningGrayson W MarshallWenbing YunS H LauSamuel WebbSunita P HoClinical computed tomography provides a single mineral density (MD) value for heterogeneous calcified tissues containing early and late stage pathologic formations. The novel aspect of this study is that, it extends current quantitative methods of mapping mineral density gradients to three dimensions, discretizes early and late mineralized stages, identifies elemental distribution in discretized volumes, and correlates measured MD with respective calcium (Ca) to phosphorus (P) and Ca to zinc (Zn) elemental ratios. To accomplish this, MD variations identified using polychromatic radiation from a high resolution micro-computed tomography (micro-CT) benchtop unit were correlated with elemental mapping obtained from a microprobe X-ray fluorescence (XRF) using synchrotron monochromatic radiation. Digital segmentation of tomograms from normal and diseased tissues (N=5 per group; 40-60 year old males) contained significant mineral density variations (enamel: 2820-3095 mg/cc, bone: 570-1415 mg/cc, cementum: 1240-1340 mg/cc, dentin: 1480-1590 mg/cc, cementum affected by periodontitis: 1100-1220 mg/cc, hypomineralized carious dentin: 345-1450 mg/cc, hypermineralized carious dentin: 1815-2740 mg/cc, and dental calculus: 1290-1770 mg/cc). A plausible linear correlation between segmented MD volumes and elemental ratios within these volumes was established, and Ca/P ratios for dentin (1.49), hypomineralized dentin (0.32-0.46), cementum (1.51), and bone (1.68) were observed. Furthermore, varying Ca/Zn ratios were distinguished in adapted compared to normal tissues, such as in bone (855-2765) and in cementum (595-990), highlighting Zn as an influential element in prompting observed adaptive properties. Hence, results provide insights on mineral density gradients with elemental concentrations and elemental footprints that in turn could aid in elucidating mechanistic processes for pathologic formations.http://europepmc.org/articles/PMC4391782?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sabra I Djomehri
Susan Candell
Thomas Case
Alyssa Browning
Grayson W Marshall
Wenbing Yun
S H Lau
Samuel Webb
Sunita P Ho
spellingShingle Sabra I Djomehri
Susan Candell
Thomas Case
Alyssa Browning
Grayson W Marshall
Wenbing Yun
S H Lau
Samuel Webb
Sunita P Ho
Mineral density volume gradients in normal and diseased human tissues.
PLoS ONE
author_facet Sabra I Djomehri
Susan Candell
Thomas Case
Alyssa Browning
Grayson W Marshall
Wenbing Yun
S H Lau
Samuel Webb
Sunita P Ho
author_sort Sabra I Djomehri
title Mineral density volume gradients in normal and diseased human tissues.
title_short Mineral density volume gradients in normal and diseased human tissues.
title_full Mineral density volume gradients in normal and diseased human tissues.
title_fullStr Mineral density volume gradients in normal and diseased human tissues.
title_full_unstemmed Mineral density volume gradients in normal and diseased human tissues.
title_sort mineral density volume gradients in normal and diseased human tissues.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Clinical computed tomography provides a single mineral density (MD) value for heterogeneous calcified tissues containing early and late stage pathologic formations. The novel aspect of this study is that, it extends current quantitative methods of mapping mineral density gradients to three dimensions, discretizes early and late mineralized stages, identifies elemental distribution in discretized volumes, and correlates measured MD with respective calcium (Ca) to phosphorus (P) and Ca to zinc (Zn) elemental ratios. To accomplish this, MD variations identified using polychromatic radiation from a high resolution micro-computed tomography (micro-CT) benchtop unit were correlated with elemental mapping obtained from a microprobe X-ray fluorescence (XRF) using synchrotron monochromatic radiation. Digital segmentation of tomograms from normal and diseased tissues (N=5 per group; 40-60 year old males) contained significant mineral density variations (enamel: 2820-3095 mg/cc, bone: 570-1415 mg/cc, cementum: 1240-1340 mg/cc, dentin: 1480-1590 mg/cc, cementum affected by periodontitis: 1100-1220 mg/cc, hypomineralized carious dentin: 345-1450 mg/cc, hypermineralized carious dentin: 1815-2740 mg/cc, and dental calculus: 1290-1770 mg/cc). A plausible linear correlation between segmented MD volumes and elemental ratios within these volumes was established, and Ca/P ratios for dentin (1.49), hypomineralized dentin (0.32-0.46), cementum (1.51), and bone (1.68) were observed. Furthermore, varying Ca/Zn ratios were distinguished in adapted compared to normal tissues, such as in bone (855-2765) and in cementum (595-990), highlighting Zn as an influential element in prompting observed adaptive properties. Hence, results provide insights on mineral density gradients with elemental concentrations and elemental footprints that in turn could aid in elucidating mechanistic processes for pathologic formations.
url http://europepmc.org/articles/PMC4391782?pdf=render
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