Differential Lipid Profiles of Normal Human Brain Matter and Gliomas by Positive and Negative Mode Desorption Electrospray Ionization – Mass Spectrometry Imaging

Desorption electrospray ionization-mass spectrometry (DESI-MS) imaging was used to analyze unmodified human brain tissue sections from 39 subjects sequentially in the positive and negative ionization modes. Acquisition of both MS polarities allowed more complete analysis of the human brain tumor lip...

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Published inPloS one Vol. 11; no. 9; p. e0163180
Main Authors Jarmusch, Alan K., Alfaro, Clint M., Pirro, Valentina, Hattab, Eyas M., Cohen-Gadol, Aaron A., Cooks, R. Graham
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 22.09.2016
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Abstract Desorption electrospray ionization-mass spectrometry (DESI-MS) imaging was used to analyze unmodified human brain tissue sections from 39 subjects sequentially in the positive and negative ionization modes. Acquisition of both MS polarities allowed more complete analysis of the human brain tumor lipidome as some phospholipids ionize preferentially in the positive and others in the negative ion mode. Normal brain parenchyma, comprised of grey matter and white matter, was differentiated from glioma using positive and negative ion mode DESI-MS lipid profiles with the aid of principal component analysis along with linear discriminant analysis. Principal component-linear discriminant analyses of the positive mode lipid profiles was able to distinguish grey matter, white matter, and glioma with an average sensitivity of 93.2% and specificity of 96.6%, while the negative mode lipid profiles had an average sensitivity of 94.1% and specificity of 97.4%. The positive and negative mode lipid profiles provided complementary information. Principal component-linear discriminant analysis of the combined positive and negative mode lipid profiles, via data fusion, resulted in approximately the same average sensitivity (94.7%) and specificity (97.6%) of the positive and negative modes when used individually. However, they complemented each other by improving the sensitivity and specificity of all classes (grey matter, white matter, and glioma) beyond 90% when used in combination. Further principal component analysis using the fused data resulted in the subgrouping of glioma into two groups associated with grey and white matter, respectively, a separation not apparent in the principal component analysis scores plots of the separate positive and negative mode data. The interrelationship of tumor cell percentage and the lipid profiles is discussed, and how such a measure could be used to measure residual tumor at surgical margins.
AbstractList Desorption electrospray ionization-mass spectrometry (DESI-MS) imaging was used to analyze unmodified human brain tissue sections from 39 subjects sequentially in the positive and negative ionization modes. Acquisition of both MS polarities allowed more complete analysis of the human brain tumor lipidome as some phospholipids ionize preferentially in the positive and others in the negative ion mode. Normal brain parenchyma, comprised of grey matter and white matter, was differentiated from glioma using positive and negative ion mode DESI-MS lipid profiles with the aid of principal component analysis along with linear discriminant analysis. Principal component-linear discriminant analyses of the positive mode lipid profiles was able to distinguish grey matter, white matter, and glioma with an average sensitivity of 93.2% and specificity of 96.6%, while the negative mode lipid profiles had an average sensitivity of 94.1% and specificity of 97.4%. The positive and negative mode lipid profiles provided complementary information. Principal component-linear discriminant analysis of the combined positive and negative mode lipid profiles, via data fusion, resulted in approximately the same average sensitivity (94.7%) and specificity (97.6%) of the positive and negative modes when used individually. However, they complemented each other by improving the sensitivity and specificity of all classes (grey matter, white matter, and glioma) beyond 90% when used in combination. Further principal component analysis using the fused data resulted in the subgrouping of glioma into two groups associated with grey and white matter, respectively, a separation not apparent in the principal component analysis scores plots of the separate positive and negative mode data. The interrelationship of tumor cell percentage and the lipid profiles is discussed, and how such a measure could be used to measure residual tumor at surgical margins.
Author Alfaro, Clint M.
Cohen-Gadol, Aaron A.
Pirro, Valentina
Hattab, Eyas M.
Jarmusch, Alan K.
Cooks, R. Graham
AuthorAffiliation West China Second Hospital, Sichuan University, CHINA
1 Department of Chemistry and Center for Analytical Instrument Development, Purdue University, West Lafayette, Indiana, United States of America
3 Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana, United States of America
2 Department of Pathology and Laboratory Medicine, University of Louisville School of Medicine, Louisville, Kentucky, United States of America
AuthorAffiliation_xml – name: 2 Department of Pathology and Laboratory Medicine, University of Louisville School of Medicine, Louisville, Kentucky, United States of America
– name: West China Second Hospital, Sichuan University, CHINA
– name: 3 Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana, United States of America
– name: 1 Department of Chemistry and Center for Analytical Instrument Development, Purdue University, West Lafayette, Indiana, United States of America
Author_xml – sequence: 1
  givenname: Alan K.
  surname: Jarmusch
  fullname: Jarmusch, Alan K.
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  givenname: Clint M.
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  givenname: Valentina
  surname: Pirro
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  fullname: Cohen-Gadol, Aaron A.
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  surname: Cooks
  fullname: Cooks, R. Graham
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27658243$$D View this record in MEDLINE/PubMed
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2016 Jarmusch et al 2016 Jarmusch et al
Copyright_xml – notice: 2016 Jarmusch et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Competing Interests: The authors have declared that no competing interests exist.
Conceptualization: AKJ CMA VP RGC. Data curation: VP. Formal analysis: AKJ CMA VP. Funding acquisition: RGC. Investigation: AKJ CMA. Methodology: AKJ CMA VP. Project administration: RGC EMH AAC. Resources: RGC. Software: AKJ CMA VP. Supervision: RGC EMH AAC. Validation: AKJ CMA VP EMH AAC RGC. Visualization: AKJ CMA VP. Writing – original draft: AKJ CMA RGC. Writing – review & editing: AKJ CMA VP EMH AAC RGC.
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Snippet Desorption electrospray ionization-mass spectrometry (DESI-MS) imaging was used to analyze unmodified human brain tissue sections from 39 subjects sequentially...
Desorption electrospray ionization—mass spectrometry (DESI-MS) imaging was used to analyze unmodified human brain tissue sections from 39 subjects sequentially...
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StartPage e0163180
SubjectTerms Biology and Life Sciences
Brain
Brain cancer
Brain tumors
Chemistry
Data integration
Desorption
Discriminant analysis
Electrospraying
Glioma
Histopathology
Human subjects
Ionization
Ions
Lipids
Mass spectrometry
Mass spectroscopy
Medical diagnosis
Medicine and Health Sciences
Metabolites
Multisensor fusion
Neuroimaging
Neurosciences
Parenchyma
Phospholipids
Physical Sciences
Principal components analysis
Research and Analysis Methods
Scientific imaging
Sensitivity
Spectroscopy
Substantia alba
Substantia grisea
Surgery
Tumors
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Title Differential Lipid Profiles of Normal Human Brain Matter and Gliomas by Positive and Negative Mode Desorption Electrospray Ionization – Mass Spectrometry Imaging
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http://dx.doi.org/10.1371/journal.pone.0163180
Volume 11
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