Camilo E. Jaimes

Dr. Camilo E. Jaimes


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 May 2020 in Human Brain Mapping
Verified
Journal Article
Open access
PDF file
CJCamilo E. Jaimes
Camilo E. Jaimes
FMFedel Machado‐Rivas
Fedel Machado‐Rivas
OAOnur Afacan
Onur Afacan
SKShadab Khan
Shadab Khan
BMBahram Marami
Bahram Marami
AGAli Gholipour
Ali Gholipour
The third trimester of pregnancy is a period of rapid development of fiber bundles in the fetal white matter. Using a recently developed motion‐tracked slice‐to‐volume registration (MT‐SVR) method, we aimed to quantify tract‐specific developmental changes in apparent diffusion coefficient (ADC), fractional anisotropy (FA), and volume in third trimester healthy fetuses. To this end, we reconstructed diffusion tensor images from motion corrected fetal diffusion magnetic resonance imaging data. With an approved protocol, fetal MRI exams were performed on healthy pregnant women at 3 Tesla and included multiple (2–8) diffusion scans of the fetal head (1–2 b = 0 s/mm2 images and 12 diffusion‐sensitized images at b = 500 s/mm2). Diffusion data from 32 fetuses (13 females) with median gestational age (GA) of 33 weeks 4 days were processed with MT‐SVR and deterministic tractography seeded by regions of interest corresponding to 12 major fiber tracts. Multivariable regression analysis was used to evaluate the association of GA with volume, FA, and ADC for each tract. For all tracts, the volume and FA increased, and the ADC decreased with GA. Associations reached statistical significance for: FA and ADC of the forceps major; volume and ADC for the forceps minor; FA, ADC, and volume for the cingulum; ADC, FA, and volume for the uncinate fasciculi; ADC of the inferior fronto‐occipital fasciculi, ADC of the inferior longitudinal fasciculi; and FA and ADC for the corticospinal tracts. These quantitative results demonstrate the complex pattern and rates of tract‐specific, GA‐related microstructural changes of the developing white matter in human fetal brain.

21 December 2021 in Radiology
Verified
Journal Article
Closed access
FMFedel Machado-Rivas
Fedel Machado-Rivas
JGJasmine Gandhi
Jasmine Gandhi
JCJungwhan John Choi
Jungwhan John Choi
CVClemente Velasco-Annis
Clemente Velasco-Annis
OAOnur Afacan
Onur Afacan
CJCamilo E. Jaimes
Camilo E. Jaimes
MRI volumetric growth of the emerging fetal brain followed a complex trajectory dependent on structure, gestational age, sex, and laterality; recognition of this pattern may aid prenatal diagnosis. Background Tools in image reconstruction, motion correction, and segmentation have enabled the accurate volumetric characterization of fetal brain growth at MRI. Purpose To evaluate the volumetric ...

20 October 2022 in Pediatric Radiology
Verified
Journal Article
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SGSebastian Gallo-Bernal
Sebastian Gallo-Bernal
MBM. Alejandra Bedoya
M. Alejandra Bedoya
MGMichael S. Gee
Michael S. Gee
CJCamilo E. Jaimes
Camilo E. Jaimes

19 October 2017 in Pediatric Radiology
Verified
Journal Article
Closed access
PDF file
CJCamilo E. Jaimes
Camilo E. Jaimes
DMDiana J. Murcia
Diana J. Murcia
KMKaren Miguel
Karen Miguel
CDCathryn DeFuria
Cathryn DeFuria
PSPallavi Sagar
Pallavi Sagar
MGMichael S. Gee
Michael S. Gee

1 June 2020 in Radiology
Verified
Journal Article
Closed access
CBChristian A. Barrera
Christian A. Barrera
MFMichael L. Francavilla
Michael L. Francavilla
SSSuraj Dilip Serai
Suraj Dilip Serai
JEJ. Christopher Edgar
J. Christopher Edgar
CJCamilo E. Jaimes
Camilo E. Jaimes
TVTeresa Victoria
Teresa Victoria
Fetal MRI can be performed and optimized to deliver an equivalent amount of energy at 3.0 and 1.5 T. Background MRI performed at 3.0 T offers greater signal-to-noise ratio and better spatial resolution than does MRI performed at 1.5 T; however, for fetal MRI, there are concerns about the potential...

9 July 2020 in American Journal of Neuroradiology
Verified
Journal Article
Closed access
PDF file
CJCamilo E. Jaimes
Camilo E. Jaimes
VRV. Rofeberg
V. Rofeberg
CSC. Stopp
C. Stopp
COC.M. Ortinau
C.M. Ortinau
AGA. Gholipour
A. Gholipour
CRC.K. Rollins
C.K. Rollins
BACKGROUND AND PURPOSE: Brain MRI of newborns with congenital heart disease show signs of immaturity relative to healthy controls. Our aim was to determine whether the semiquantitative fetal total maturation score can detect abnormalities in brain maturation in fetuses with congenital heart disease in the second and third trimesters. MATERIALS AND METHODS: We analyzed data from a prospective study of fetuses with and without congenital heart disease who underwent fetal MR imaging at 25–35 weeks’ gestation. Two independent neuroradiologists blinded to the clinical data reviewed and scored all images using the fetal total maturation score. Interrater reliability was evaluated by the intraclass correlation coefficient using the individual reader scores, which were also used to calculate an average score for each subject. Comparisons of the average and individual reader scores between affected and control fetuses and relationships with clinical variables were evaluated using multivariable linear regression. RESULTS: Data from 69 subjects (48 cardiac, 21 controls) were included. High concordance was observed between readers with an intraclass correlation coefficient of 0.98 (95% CI, 0.97–0.99). The affected group had significantly lower fetal total maturation scores than the control group (β-estimate, –0.9 [95% CI, –1.5 to –0.4], P = .002), adjusting for gestational age and sex. Averaged fetal total maturation, germinal matrix, myelination, and superior temporal sulcus scores were significantly delayed in fetuses with congenital heart disease versus controls (P < .05 for each). The fetal total maturation score was not significantly associated with any cardiac, anatomic, or physiologic variables. CONCLUSIONS: The fetal total maturation score is sensitive to differences in brain maturation between fetuses with isolated congenital heart disease and healthy controls.