% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{OrosPeusquens:16489,
author = {Oros-Peusquens, A.M. and Matusch, A. and Becker, J.S. and
Shah, N.J.},
title = {{A}utomatic segmentation of tissue sections using the
multielement information provided by {LA}-{ICP}-{MS} imaging
and k-means cluster analysis},
journal = {International journal of mass spectrometry},
volume = {307},
issn = {1387-3806},
address = {[S.l.]},
publisher = {Elsevier Science},
reportid = {PreJuSER-16489},
year = {2011},
note = {Record converted from VDB: 12.11.2012},
abstract = {Laser Ablation Inductively Coupled Plasma Mass Spectrometry
(LA-ICP-MS) is an established and powerful tool to analyse
the distribution of elements in tissue sections. Among other
applications, the technique is expected to play a central
role in the understanding of normal and pathological element
distributions in brain tissue.In order to interpret the
distribution of elements such as the bio-metals Cu, Zn, Fe
and Mn and proceed to an element-based comparison between
groups of samples, it is necessary to anatomically parcel
the tissue section into regions-of-interest and to average
element signals across these regions. This categorization,
also termed segmentation, can be done manually, but the
support of automated procedures is highly desirable,
especially in order to (1) identify groups of pixels with
similar elemental fingerprint, termed clusters, and to
determine which degree of discrimination is reasonable; (2)
segment anatomical structures known to exhibit substructure
but without clearly defined borders, such as the healthy
cortex, zones of tumours or ischemic lesions, in an
observer-independent way; and (3) to investigate correlation
between the distribution of elements in tissue and phenomena
which incorporate contributions from several elements in a
convoluted way, such as the origin of contrast in magnetic
resonance imaging (MRI) experiments.The multi-parametric
information provided by LA-ICP-MS lends itself naturally to
multivariate analysis. This study provides a new way to
synthesise the information distributed over many element
images by demonstrating the possibility to segment tissue
sections into biologically meaningful substructures. This
data-driven, observer-independent categorization was based
on k-means clustering. The optimal number of clusters was
determined based on the silhouette method.Segmentation of
healthy tissue resulted in a set of substructures in perfect
congruence to the anatomical architecture. Segmentation of
ischemic lesions identified a number of regions with
different fingerprints of C, P. Fe, Cu and Zn deposits.
Clustering provides a promising way of combining the
information present in several element images and reveals
structure which is not entirely present in any isolated
image.As a useful by-product of this study we have found a
promising method for investigating the optimal line length
within the process of image reconstruction from the
continuous stream of raw data points. Images were
characterized by their tensor of inertia, in image- as well
as in Fourier dual-space (k-space) and changes in the ratio
of the intrinsic moments of inertia or the orientation of
the principal axes were found to closely describe the
optimum orientation. The first results look very
encouraging, but the method must be extensively tested
before it can be used as an automatic procedure.In
conclusion, cluster analysis of mass spectrometric imaging
data allows one to define the fingerprint element
distribution of different anatomically or functionally
distinct regions and opens a new way for the study of
correlation between the element distribution and related
phenomena. (C) 2011 Elsevier B.V. All rights reserved.},
keywords = {J (WoSType)},
cin = {ZCH / INM-4 / INM-2},
ddc = {530},
cid = {I:(DE-Juel1)ZCH-20090406 / I:(DE-Juel1)INM-4-20090406 /
I:(DE-Juel1)INM-2-20090406},
pnm = {Funktion und Dysfunktion des Nervensystems (FUEK409) /
89573 - Neuroimaging (POF2-89573)},
pid = {G:(DE-Juel1)FUEK409 / G:(DE-HGF)POF2-89573},
shelfmark = {Physics, Atomic, Molecular $\&$ Chemical / Spectroscopy},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000295864100034},
doi = {10.1016/j.ijms.2011.03.014},
url = {https://juser.fz-juelich.de/record/16489},
}