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Maternal glycemic status and longitudinal fetal body composition and organ volumes based on three-dimensional ultrasonography

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posted on 2024-10-16, 19:53 authored by Kathryn A. Wagner, Jessica L. Gleason, Zhen Chen, Cuilin Zhang, Stefanie N. Hinkle, Dian He, Wesley Lee, Roger B. Newman, John Owen, Daniel W. Skupski, William A. Grobman, Seth Sherman, Fasil Tekola-Ayele, Jagteshwar Grewal, Katherine L. Grantz

Objective: Gestational diabetes mellitus (GDM) increases the risk of fetal overgrowth, as measured by two-dimensional (2D) ultrasonography. Whether fetal 3D soft tissue and organ volumes provide additional insight into fetal overgrowth is unknown.

Research Design & Methods: We prospectively evaluated longitudinal 3D fetal body composition and organ volumes in a diverse US singleton pregnancy cohort (2015-2019). Women were diagnosed with GDM, impaired glucose tolerance (IGT), or normal glucose tolerance (NGT). Up to five 3D ultrasound scans measured fetal body composition and organ volumes; trajectories were modeled using linear mixed models. Overall and weekly mean differences in fetal 3D trajectories were tested across glycemic status, adjusted for covariates.

Results: In this sample (N=2427), 5.2% of women had GDM and 3.0% had IGT. Fetuses of women who developed GDM, compared to NGT, had larger fractional arm and fractional fat arm volumes from 26-35 weeks, smaller fractional lean arm volume from 17-22 weeks, and larger abdominal area from 24-40 weeks. Fetuses of women with IGT had similar growth patterns, but manifested later in gestation and with larger magnitudes, and had larger fractional lean arm volume. No overall differences were observed among thigh or organ volumes across glycemic status.

Conclusions: Body composition differed in fetuses of GDM pregnancies, including larger arm and abdominal measures across the second and third trimesters. Patterns were similar in IGT pregnancies except occurred later in gestation and with larger magnitudes. Future research should explore how lifestyle and medication may alter fetal fat accumulation trajectories among hyperglycemic pregnancies.

Funding

This research was supported, in part, by the Division of Population Health Research, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health; and, in part, with Federal funds for the Fetal 3D Study (Contract Numbers: HHSN275201300026I; HHSN275201500002C) and, in part, the NICHD Fetal Growth Studies – Singletons (Contract Numbers: HHSN275200800013C; HHSN275200800002I; HHSN27500006; HHSN275200800003IC; HHSN275200800014C; HHSN275200800012C; HHSN275200800028C; HHSN275201000009C). Jessica Gleason, Zhen Chen, Fasil Tekola-Ayele, Jagteshwar Grewal, and Katherine Grantz have contributed to this work as part of their official duties as employees of the United States Federal Government.

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