19
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The diagnostic value of [ 18F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          This study was undertaken to assess the diagnostic value of 2-[ 18F]-fluoro-2-deoxy-D-glucose positron emission tomography with computed tomography ([ 18F]-FDG-PET/CT) in the detection of radiation toxicity in normal bone marrow using Tibet minipigs as a model. Eighteen Tibet minipigs were caged in aseptic rooms and randomly divided into six groups. Five groups ( n = 3/group) were irradiated with single doses of 2, 5, 8, 11 and 14 Gy of total body irradiation (TBI) using an 8-MV X-ray linear accelerator. These pigs were evaluated with [ 18F]-FDG-PET/CT, and their marrow nucleated cells were counted. The data were initially collected at 6, 24 and 72 h after treatment and were then collected on Days 5–60 post-TBI at 5-day intervals. At 24 and 72 h post-TBI, marrow standardized uptake value (SUV) data showed a dose-dependent decrease in the radiation dose range from 2–8 Gy. Upon long-term observation, SUV and marrow nucleated cell number in the 11-Gy and 14-Gy groups showed a continuous and marked reduction throughout the entire time course, while Kaplan–Meier curves of survival showed low survival. In contrast, the SUVs in the 2-, 5- and 8-Gy groups showed early transient increases followed by a decline from approximately 72 h through Days 5–15 and then normalized or maintained low levels through the endpoint; marrow nucleated cell number and survival curves showed approximately the same trend and higher survival, respectively. Our findings suggest that [ 18F]-FDG-PET/CT may be helpful in quickly assessing the absorbed doses and predicting the prognosis in patients.

          Related collections

          Most cited references36

          • Record: found
          • Abstract: found
          • Article: not found

          Medical management of the acute radiation syndrome: recommendations of the Strategic National Stockpile Radiation Working Group.

          Physicians, hospitals, and other health care facilities will assume the responsibility for aiding individuals injured by a terrorist act involving radioactive material. Scenarios have been developed for such acts that include a range of exposures resulting in few to many casualties. This consensus document was developed by the Strategic National Stockpile Radiation Working Group to provide a framework for physicians in internal medicine and the medical subspecialties to evaluate and manage large-scale radiation injuries. Individual radiation dose is assessed by determining the time to onset and severity of nausea and vomiting, decline in absolute lymphocyte count over several hours or days after exposure, and appearance of chromosome aberrations (including dicentrics and ring forms) in peripheral blood lymphocytes. Documentation of clinical signs and symptoms (affecting the hematopoietic, gastrointestinal, cerebrovascular, and cutaneous systems) over time is essential for triage of victims, selection of therapy, and assignment of prognosis. Recommendations based on radiation dose and physiologic response are made for treatment of the hematopoietic syndrome. Therapy includes treatment with hematopoietic cytokines; blood transfusion; and, in selected cases, stem-cell transplantation. Additional medical management based on the evolution of clinical signs and symptoms includes the use of antimicrobial agents (quinolones, antiviral therapy, and antifungal agents), antiemetic agents, and analgesic agents. Because of the strong psychological impact of a possible radiation exposure, psychosocial support will be required for those exposed, regardless of the dose, as well as for family and friends. Treatment of pregnant women must account for risk to the fetus. For terrorist or accidental events involving exposure to radioiodines, prophylaxis against malignant disease of the thyroid is also recommended, particularly for children and adolescents.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            p53 controls radiation-induced gastrointestinal syndrome in mice independent of apoptosis.

            Acute exposure to ionizing radiation can cause lethal damage to the gastrointestinal (GI) tract, a condition called the GI syndrome. Whether the target cells affected by radiation to cause the GI syndrome are derived from the epithelium or endothelium and whether the target cells die by apoptosis or other mechanisms are controversial issues. Studying mouse models, we found that selective deletion of the proapoptotic genes Bak1 and Bax from the GI epithelium or from endothelial cells did not protect mice from developing the GI syndrome after sub-total-body gamma irradiation. In contrast, selective deletion of p53 from the GI epithelium, but not from endothelial cells, sensitized irradiated mice to the GI syndrome. Transgenic mice overexpressing p53 in all tissues were protected from the GI syndrome after irradiation. These results suggest that the GI syndrome is caused by the death of GI epithelial cells and that these epithelial cells die by a mechanism that is regulated by p53 but independent of apoptosis.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Hematologic consequences of exposure to ionizing radiation.

              From the early 1900s, it has been known that ionizing radiation (IR) impairs hematopoiesis through a variety of mechanisms. IR exposure directly damages hematopoietic stem cells and alters the capacity of bone marrow stromal elements to support and/or maintain hematopoiesis in vivo and in vitro. Exposure to IR induces dose-dependent declines in circulating hematopoietic cells not only through reduced bone marrow production, but also by redistribution and apoptosis of mature formed elements of the blood. Recently, the importance of using lymphocyte depletion kinetics to provide a "crude" dose estimate has been emphasized, particularly in rapid assessment of large numbers of individuals who may be exposed to IR through acts of terrorism or by accident. A practical strategy to estimate radiation dose and triage victims based upon clinical symptomatology is presented. An explosion of knowledge has occurred regarding molecular and cellular pathways that trigger and mediate hematologic responses to IR. In addition to damaging DNA, IR alters gene expression and transcription, and interferes with intracellular and intercellular signaling pathways. The clinical expression of these disturbances may be the development of leukemia, the most significant hematologic complication of IR exposure among survivors of the atomic bomb detonations over Japan. Those at greatest risk for leukemia are individuals exposed during childhood. The association of leukemia with chronic, low-dose-rate exposure from nuclear power plant accidents and/or nuclear device testing has been more difficult to establish, due in part to lack of precision and sensitivity of methods to assess doses that approach background radiation dose. Nevertheless, multiple myeloma may be associated with chronic exposure, particularly in those exposed at older ages.
                Bookmark

                Author and article information

                Journal
                J Radiat Res
                J. Radiat. Res
                radres
                jrr
                Journal of radiation research
                Oxford University Press
                0449-3060
                1349-9157
                July 2012
                6 June 2012
                : 53
                : 4
                : 537-544
                Affiliations
                [1 ]Department of Hematology, Zhujiang Hospital, Southern Medical University, 253# Industry Road, 510282, Guangzhou, Guangdong, China
                [2 ]Department of Ophthalmology, Zhujiang Hospital, Southern Medical University, 253# Industry Road, 510282, Guangzhou, Guangdong, China
                [3 ]Department of Laboratory Animal Center, Southern Medical University, 1838# Guangzhou North Road, 510282, Guangzhou, Guangdong, China
                [4 ]Center of Laboratory Medicine, Affiliated Hospital of The Medical College of Guiyang, 2# Beijing Road, 550001, Guiyang, Guizhou, China
                [5 ]School of Hygiene and Tropical Medicine, Southern Medical University, 1838# Guangzhou North Road, 510282, Guangzhou, Guangdong, China
                Author notes
                [* ]Corresponding author. Department of Laboratory Animal Center, Southern Medical University, 1838# Guangzhou North Road, 510282, Guangzhou, Guangdong, China School of Hygiene and Tropical Medicine, Southern Medical University, 1838# Guangzhou North Road, 510282, Guangzhou, Guangdong, China. Tel: +8613076872147; Fax: +86(20)61360033; Email: doctorwangyujue@ 123456yahoo.com.cn
                [†]

                These authors contributed equally to this work. Li-Meng Yan was considered as co-first author.

                Article
                rrs006
                10.1093/jrr/rrs006
                3393352
                22843618
                f4355a96-35a4-4075-bdd3-fafbbe47f90b
                © The Author 2012. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 5 January 2012
                : 3 March 2012
                : 6 March 2012
                Page count
                Pages: 16
                Categories
                Biology

                Oncology & Radiotherapy
                [18f]-fdg-pet/ct,total body irradiation,bone marrow,tibet minipigs
                Oncology & Radiotherapy
                [18f]-fdg-pet/ct, total body irradiation, bone marrow, tibet minipigs

                Comments

                Comment on this article