Jonathan P Dyke1, Kevin Oh1, Amanda Garfinkel2, Alan M Groves3, and Arzu Kovanlikaya1
1Radiology, Weill Cornell Medicine, New York, NY, United States, 2Pediatrics, Weill Cornell Medicine, New York, NY, United States, 3Pediatrics, Mount Sinai School of Medicine, New York, NY, United States
Synopsis
Whole
body fat fraction was previously published by our group in term and preterm infants
using Dixon CSI MRI. Advanced semi-automated
regional fat quantification was performed yielding: subcutaneous adipose tissue(SAT), visceral adipose tissue(VAT), brown adipose tissue (BAT) volumes and hepatic
fat fraction (HFF). Whole body VAT
volume (cc) was increased in preterm infants (3.4%±1.5%) compared to term (2.4%±0.9%)
(p=0.079) when normalized to total body volume (cc). HFF and BAT did not differ between term and
preterm infants (p>0.25). CSI MRI allows quantification of regional fat
depots in preterm infants which may potentially help
optimize nutritional management and monitor growth.
Introduction
Preterm birth and body
composition have demonstrable effects on growth and later health outcomes.[1] Previously, we reported that preterm infants at
term corrected age (TCA) have a lower proportion of lean body mass than their
term counterparts.[2] Weight and length do
not give an accurate assessment of body composition. Tracking body composition
rather than just weight is a fundamental part of improving nutritional outcomes.
Body composition and hepatic fat correlate with future risk for metabolic
syndrome.[3] In children, many
conventional techniques for quantifying body composition and hepatic fat have
limitations. MRI is a noninvasive
research tool to study body composition and hepatic fat in infants.
In the present study, we used
chemical shift MRI, a rapid, detailed, and robust method of body composition
analysis that can be feasibly implemented into the routine clinical care of
newborns. Further, we aimed to show that
chemical shift MRI has the sensitivity to detect differential growth patterns
in preterms at TCA versus term controls by semiautomatic quantification of
regional fat depots.Methods
Patient Demographics: Twenty-five infants were
enrolled in the study [10 Males/15 Females, median (range) postnatal age 69
(1-138) days, median (range) corrected gestational age 39.4 (36.4-44.7) weeks]
with 15 former preterm and 10 term infants. 5 of the 10 term infants were
infants of diabetic mothers and were excluded from this analysis. Infants were prepared for the MRI examination
using a “feed and wrap” technique.
MRI Acquisition Methods: High resolution (1 mm3
isotropic) whole body fat and water images [Figure 1] were acquired on a 3.0
Tesla MRI scanner (GE Healthcare) using the adult Head/Neck 48-Channel Array
coil and the Liver Acquisition with Volume Acceleration flex (LAVA-Flex) pulse
sequence. A coronal 3D slab was acquired during free-breathing with 160
images using: TR/TE 4.0ms/1.7ms, flip angle of 12°, 48 cm (FOV), a 288x288
matrix reconstructed to 512x512 yielding a scan time of only 42 seconds.
MRI Analysis Methods: SAT/VAT: A fully
automated ImageJ Macro produced a preliminary SAT map for each coronal slice in
the whole body [Figure 1]. Manual elimination of minor VAT deposits such as
those in the perirenal areas that were connected to the SAT were removed. An inverse mask of the SAT was multiplied by
the fat fraction map which resulted in the VAT map. Voxels > 50% fat fraction were categorized
as VAT.
HFF: An ROI was drawn on the Dixon water only
image which allowed the best anatomic delineation of the liver structure at the
level of the portal hilum avoiding vasculature and ducts [Figure 2]. The same ROI was overlaid onto the fat
fraction image and the process repeated in three consecutive slices. A fat
fraction histogram was calculated for all voxels in the three ROI’s and the
mean HFF of the typically asymmetric distribution reported.
BAT: Segmentation
of the brown adipose tissue (BAT) was determined by fixing the level of the fat
fraction map at 35% with a window of 10% [Figure 3]. ROI’s were drawn on three
consecutive slices outlining the supraclavicular and axillary BAT clusters
which were more readily identified in the VAT maps.
Statistics Methods: A two-tailed t-test was used assuming unequal
variances (heteroscedastic) and significance levels of p<0.05. Results
Whole
body VAT volume (cc) was mildly increased in preterm infants (3.4%±1.5%)
compared to term (2.4%±0.9%) when normalized to total volume (cc) (p=0.079). HFF did not significantly differ between
term (2.9%±1.4%) and preterm (3.3%±1.0%) infants (p=0.60) as measured in three
consecutive slices. Likewise, BAT
normalized to total volume was also similar between term (0.08%±0.01%) and
preterm (0.09%±0.03%) infants (p=0.25) as measured in three consecutive
slices. Discussion
Chemical
shift MRI is a rapid, accurate and repeatable method of body composition
analysis that may be feasible for implementation in routine nutritional
management of preterm infants. In seeking to better understand the
differential growth of preterm versus full-term infants, it may be important to
track not just whole body fat accumulation but also the fat distribution in
different compartments.Conclusion
In summary, semiautomated regional fat quantification
using chemical shift MRI represents a safe, rapid, robust method which may potentially
help optimize nutritional management of preterm infants and monitor their
growth.Acknowledgements
No acknowledgement found.References
1) Andrews
ET, Beattie RM, Johnson MJ. Measuring
body composition in the preterm infant: Evidence base and practicalities. Clin Nutr 2019:38:2521-2530.
2) Dyke
JP, Garfinkel AC, Groves AM, Kovanlikaya A. High-resolution rapid neonatal
whole-body composition using 3.0 Tesla chemical shift magnetic resonance
imaging. Pediatr Res. 2018;83:638-644.
3) Armstrong
T, Ly VL, Ghahremani S, Calkins KL, Wu HH.
Free breathing 3-D quantification of infant body composition and hepatic
fat using a stack-of-radial magnetic resonance imaging technique. Ped Radiol 2019;49:876-888.