4.7 Article

Reproducible MRI measurement of adipose tissue volumes in genetic and dietary rodent obesity models

期刊

JOURNAL OF MAGNETIC RESONANCE IMAGING
卷 28, 期 4, 页码 915-927

出版社

WILEY-BLACKWELL
DOI: 10.1002/jmri.21481

关键词

obesity; small animal imaging; partial volume effect; image processing; chemical shift imaging; body composition

资金

  1. Ohio Wright Center of Innovation
  2. National Institutes of Health [1R24CA110943]
  3. National Center for Research Resources, National Institutes of Health [C06 RR12463-01]

向作者/读者索取更多资源

Purpose: To develop ratio MRI [lipid/(lipid+water)] methods for assessing lipid depots and compare measurement variability with biological differences among lean controls (spontaneously hypertensive rats [SHRs]), dietary obese rats (SHR-DOs), and genetic/dietary obese rats (SHROBs). Materials and Methods: Images with and without chemical shift-selective (CHESS) water suppression were processed using a semiautomatic method that accounts for relaxometry, chemical shift, receive coil sensitivity, and partial volume. Results: Partial volume correction improved results by 10% to 15%. Over six operators, volume variation was reduced to 1.9 mL from 30.6 mL for single-image-analysis with intensity inhomogeneity. For three acquisitions on the same animal, volume reproducibility was <1%. SHROBs had six times more visceral and eight times more subcutaneous adipose tissue than SHRs. SHR-DOs had enlarged visceral depots (three times larger than those in SHRs). SHROBs had significantly more subcutaneous adipose tissue, indicating a strong genetic component to this fat depot. Liver ratios in SHR-DO and SHROB were higher than in SHR, indicating elevated fat content. Among SHROBs, evidence suggested a phenotype SHROB* having elevated liver ratios and visceral adipose tissue volumes. Conclusion: Effects of diet and genetics on obesity were significantly larger than variations due to image acquisition and analysis, indicating that these methods can be used to assess accumulation/depletion of lipid depots in animal models of obesity.

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