Identifying the individual metabolic abnormities from a systemic perspective using whole-body PET imaging
Creators
- 1. Paul C. Lauterbur Research Center for Biomedical Imaging, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen (China)
- 2. Department of Medical Imaging, Henan Provincial People's Hospital and People's Hospital of Zhengzhou University, Zhengzhou (China)
- 3. Department of Statistics, School of Mathematical Sciences, University College Cork, Cork (Ireland)
- 4. Central Research Institute, United Imaging Healthcare Group Co., Ltd, Shanghai (China)
- 5. Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA (United States)
- 6. School of Biomedical Engineering, Shanghai Tech University, Shanghai (China)
Description
Distinct physiological states arise from complex interactions among the various organs present in the human body. PET is a non-invasive modality with numerous successful applications in oncology, neurology, and cardiology. However, while PET imaging has been applied extensively in detecting focal lesions or diseases, its potential in detecting systemic abnormalities is seldom explored, mostly because total-body imaging was not possible until recently. In this context, the present study proposes a framework capable of constructing an individual metabolic abnormality network using a subject's whole-body F-FDG SUV image and a normal control database. The developed framework was evaluated in the patients with lung cancer, the one discharged after suffering from Covid-19 disease, and the one that had gastrointestinal bleeding with the underlying cause unknown. The framework could successfully capture the deviation of these patients from healthy subjects at the level of both system and organ. The strength of the altered network edges revealed the abnormal metabolic connection between organs. The overall deviation of the network nodes was observed to be highly correlated to the organ SUV measures. Therefore, the molecular connectivity of glucose metabolism was characterized at a single subject level. The proposed framework represents a significant step toward the use of PET imaging for identifying metabolic dysfunction from a systemic perspective. A better understanding of the underlying biological mechanisms and the physiological interpretation of the interregional connections identified in the present study warrant further research.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-022-05832-7Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 49
- Journal Issue
- 8
- Journal Page Range
- p. 2994-3004
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 53085616
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; CORONAVIRUSES; CORRELATIONS; FLUORINE 18; FLUORODEOXYGLUCOSE; GASTROINTESTINAL TRACT; GLUCOSE; IMAGE PROCESSING; LUNGS; METABOLISM; NEUROLOGY; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS
- Descriptors DEC
- ALDEHYDES; ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CARBOHYDRATES; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DIGESTIVE SYSTEM; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; HEXOSES; HOURS LIVING RADIOISOTOPES; INFECTIOUS DISEASES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MEDICINE; MICROORGANISMS; MONOSACCHARIDES; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PARASITES; PROCESSING; RADIOACTIVE MATERIALS; RADIOISOTOPES; RESPIRATORY SYSTEM; SACCHARIDES; TOMOGRAPHY; VIRAL DISEASES; VIRUSES; ZOONOTIC DISEASES
Optional Information
- Notes
- Oncology #En Dash# General