Department of Radiology, Children's Hospital Los Angeles, 4650 Sunset Blvd, MS #81, Los Angeles, California 90027, USA.
AJR Am J Roentgenol. 2013 Jan;200(1):177-83. doi: 10.2214/AJR.12.8996.
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.
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.
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.
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.
本研究旨在利用化学位移水脂 MRI 对人体棕色脂肪组织(BAT)进行特征描述,并确定 BAT 和白色脂肪组织(WAT)之间的脂肪信号分数和 T2(*)弛豫时间趋势和差异是否在死后和体内的婴儿、青少年和成年人中一致观察到。
对一具尸体和八名患者进行了研究。在 3T 上进行了六回波扰相梯度回波化学位移水脂 MRI 序列,以联合定量肩胛颈上 BAT 和皮下 WAT 的脂肪信号分数和 T2(*)。为了确认 BAT 的身份,活检和组织学作为尸体研究的参考,而在需要医疗检查的八名患者中的五名中使用了 PET/CT。
在尸体标本和八名患者中的七名中,BAT 的脂肪信号分数和 T2(*)时间均低于 WAT。除了一个病例外,棕色和白色脂肪组织之间的名义比较均具有统计学意义(p<0.05)。在受试者之间,BAT 中观察到脂肪信号分数值的范围很大,但 WAT 中则没有。
我们已经表明,联合源自化学位移水脂 MRI 的脂肪信号分数和 T2(*)值在 BAT 中低于 WAT,这可能是由于细胞结构、甘油三酯含量和血管化的差异所致。这两个指标可以作为 BAT 检测的互补生物标志物。