Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 12;21(1):540.
doi: 10.1186/s12891-020-03559-w.

Magnetic resonance imaging at 7.0 T for evaluation of early lesions of epiphyseal plate and epiphyseal end in a rat model of Kashin-Beck disease

Affiliations

Magnetic resonance imaging at 7.0 T for evaluation of early lesions of epiphyseal plate and epiphyseal end in a rat model of Kashin-Beck disease

Yong Li et al. BMC Musculoskelet Disord. .

Abstract

Background: Kashin-Beck disease (KBD) is a disabling osteoarticular disease involving growth and joint cartilage. Early diagnosis can effectively prevent the progress of the disease. However, the early diagnosis of it is still very difficult. Our aim was to study the knee joint lesions of a rat KBD model using ultra-high field magnetic resonance imaging (MRI) and compare it with X-ray imaging to analyze the possible MRI manifestations of KBD, and to further explore ways to determine the pathological damage of KBD in the early stage.

Methods: A total of 96 Wistar rats were selected and randomly divided into 4 groups: normal diet (Group A), KBD-affected diet (Group B), normal diet+T-2 toxin (Group C), and KBD-affected diet+T-2 toxin (Group D). T-2 toxin was administered at a dose of 0.1 mg/kg/day. In the 4th week, 8th week, and 12th week, eight rats randomly selected in each group were sacrificed by cervical dislocation after undergoing X-ray and 7.0 T MRI imaging, and then knee joints were harvested, sliced, and subjected to hematoxylin-eosin (H&E) staining.

Results: Characteristic image changes including of continuity interruption and early closure and fusion of epiphyseal plates were observed on T1WI in rat model of KBD. The total necrosis rates in the H&E stain of group A to group D were 4.35, 52.38, 33.3, and 73.68%, respectively. The positive rate of image change under 7.0 T MRI was 0.833 VS. that under X-ray was 0.33 (P = 0.001).

Conclusions: MRI at 7.0 T is highly sensitive to the early pathological changes of the epiphysis, epiphyseal plate, and metaphyseal end, which can improve imaging positive rate of KBD and decrease the rate of missed diagnosis. This imaging modality can be used for research on early joint lesions and for early diagnosis of KBD.

Keywords: Epiphyseal plate; Kashin-Beck disease; Knee joint; Magnetic resonance imaging; Rat.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Results of X-ray examination of the rat knee joints. Arrow “a and “c”: sparseness of metaphyseal bone trabecula; arrow “b” and “g”: blurring or premature closure of the epiphyseal plate; Arrow “d”: abnormal sclerosis of the epiphyseal plate; arrow “e”: a developmental deformity of the femoral condyle; arrow “f”: defect and irregularity of the femoral condyle
Fig. 2
Fig. 2
Results of 7.0 T MRI coronal scan of the rat knee joint. Arrow “a”: clear structure and uniform signal in epiphysis, epiphyseal plate and metaphysis; arrow “b”: abnormally high signal in epiphysis; arrow “c”: abnormally high signal in epiphyseal plate; arrow “d” abnormally high signal in metaphysis
Fig. 3
Fig. 3
Histological observation of the proximal tibial epiphyseal plate of the rat. Group A: the chondrocytes of the epiphyseal plate are arranged orderly with a clear cytoplasm and nucleus. Groups B and C: focal necrosis of mast cells was found. Group D: the chondrocytes of the epiphyseal plate are disordered with a short cell column, focal necrosis and penetrating necrosis

References

    1. Wang Y, Yang Z, Gilula LA, Zhu C. Kashin-Beck disease: radiographic appearance in the hands and wrists. Radiology. 1996;201(1):265–270. - PubMed
    1. Yamamuro T. Kashin-Beck disease: a historical overview. Int Orthop. 2001;25(3):134–137. - PMC - PubMed
    1. Duan C, Guo X, Zhang XD, Yu HJ, Yan H, Gao Y, Ma WJ, Gao ZQ, Xu P, Lammi M. Comparative analysis of gene expression profiles between primary knee osteoarthritis and an osteoarthritis endemic to northwestern China, Kashin-Beck disease. Arthritis Rheum. 2010;62(3):771–780. - PubMed
    1. Wang LH, Fu Y, Shi YX, Wang WG. T-2 toxin induces degenerative articular changes in rodents: link to Kaschin-Beck disease. Toxicol Pathol. 2011;39(3):502–507. - PubMed
    1. Hinsenkamp M, Mathieu F, Claus W, Collard JF, de Maertelaer V. Effects of physical environment on the evolution of Kashin-Beck disease in Tibet. Int Orthop. 2009;33(4):1085–1088. - PMC - PubMed

LinkOut - more resources