4.5 Article

Characterization of Human Brown Adipose Tissue by Chemical-Shift Water-Fat MRI

Journal

AMERICAN JOURNAL OF ROENTGENOLOGY
Volume 200, Issue 1, Pages 177-183

Publisher

AMER ROENTGEN RAY SOC
DOI: 10.2214/AJR.12.8996

Keywords

brown adipose tissue; chemical-shift water-fat MRI; fat fraction; T2*relaxation; white adipose tissue

Funding

  1. National Institutes of Health [NIDDK-K25DK087931, NIDDK-R21DK090778]
  2. Zumberge Fund from the Office of the Provost at the University of Southern California
  3. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [K25DK087931, R21DK090778] Funding Source: NIH RePORTER

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OBJECTIVE. The purpose of this study was to characterize human brown adipose tissue (BAT) with chemical-shift water-fat MRI and to determine whether trends and differences in fat-signal fractions and T2* relaxation times between BAT and white adipose tissue (WAT) are consistently observed postmortem and in vivo in infants, adolescents, and adults. MATERIALS AND METHODS. A postmortem body and eight patients were studied. A six-echo spoiled gradient-echo chemical-shift water-fat MRI sequence was performed at 3 T to jointly quantify fat-signal fraction and T2* in interscapular-supraclavicular BAT and subcutaneous WAT. To confirm BAT identity, biopsy and histology served as the reference in the postmortem study and PET/CT was used in five of the eight patients who required examination for medical care. RESULTS. Fat-signal fractions and T2* times were lower in BAT than in WAT in the postmortem example and in seven of eight patients. With the exception of one case, nominal comparisons between brown and white adipose tissues were statistically significant (p < 0.05). Between subjects, a large range of fat-signal fraction values was observed in BAT but not in WAT. CONCLUSION. We have shown that fat-signal fractions and T2* values jointly derived from chemical-shift water-fat MRI are lower in BAT than in WAT likely because of differences in cellular structures, triglyceride content, and vascularization. The two metrics can serve as complementary biomarkers in the detection of BAT.

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