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Intermuscular adipose tissue in Type 2 diabetes mellitus: Non-invasive quantitative imaging and clinical implications

  • Fuyao Yu
    ,
  • Yiping Fan
    ,
  • He Sun
    ,
  • Tianming Li
    ,
  • ,
  • Shinong Pan(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Intermuscular adipose tissue (IMAT) is an ectopic fat depot found beneath the fascia and within the muscles. IMAT modulates muscle insulin sensitivity and triggers local and systemic chronic low-grade inflammation by producing cytokines and chemokines, which underlie the pathogenesis of Type 2 diabetes mellitus (T2DM). Imaging techniques have been increasingly used to non-invasively quantify IMAT in patients with diabetes in research and healthcare settings. In this study, we systematically reviewed the cell of origin and definition of IMAT, and the use of quantitative and functional imaging technology pertinent to the etiology, risk factors, lifestyle modification, and therapeutic treatment of diabetes. The purpose of this article is to provide important insight into the current understanding of IMAT and future prospects of targeting IMAT for T2DM control.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

109881

Pages from-to (Number of pages)

Pages 109881

Journal (Volume, Issue Number)

Diabetes Research and Clinical Practice (Volume 187)

Publication milestones

  • Published - 05/2022

Publication status

Published - 05/2022

ISSN

0168-8227

Publication IDs

  • Scopus: 85129098120
  • PubMed: 35483545

Publication metrics

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1
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0.17
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5
Fractional count
0.83
Fractional count
1
Fractional count
1
Scopus
citations

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Mentions
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Funding Details

The authors wish to thank Pingchuan Wang, MS, for the pathological support. YU F wrote and edited the article. FAN Y and DONG Y contributed to the discussion and reviewed/edited the article. SUN H and LI T edited and revised the article. PAN S approved the final version of the manuscript. This work (Pan S) was supported by the National Natural Science Foundation of China-Research grant number (No.30871211 and No. 81271538). This work (Pan S) was supported by the National Natural Science Foundation of China-Research grant number (No.30871211 and No. 81271538).
FundersFunding numbers
Dong-A Pharmaceutical Company
-
NSFC
81271538, 30871211