Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure

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Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure. / Vestergaard, Martin; Baaré, William F.C.; Holm, Sara K.; Madsen, Camilla G.; Paulson, Olaf B.; Born, Alfred P.; Uldall, Peter; Siebner, Hartwig R.; Madsen, Kathrine Skak.

In: Pediatric Research, Vol. 91, 2022, p. 879–887.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Vestergaard, M, Baaré, WFC, Holm, SK, Madsen, CG, Paulson, OB, Born, AP, Uldall, P, Siebner, HR & Madsen, KS 2022, 'Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure', Pediatric Research, vol. 91, pp. 879–887. https://doi.org/10.1038/s41390-021-01394-w

APA

Vestergaard, M., Baaré, W. F. C., Holm, S. K., Madsen, C. G., Paulson, O. B., Born, A. P., Uldall, P., Siebner, H. R., & Madsen, K. S. (2022). Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure. Pediatric Research, 91, 879–887. https://doi.org/10.1038/s41390-021-01394-w

Vancouver

Vestergaard M, Baaré WFC, Holm SK, Madsen CG, Paulson OB, Born AP et al. Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure. Pediatric Research. 2022;91:879–887. https://doi.org/10.1038/s41390-021-01394-w

Author

Vestergaard, Martin ; Baaré, William F.C. ; Holm, Sara K. ; Madsen, Camilla G. ; Paulson, Olaf B. ; Born, Alfred P. ; Uldall, Peter ; Siebner, Hartwig R. ; Madsen, Kathrine Skak. / Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure. In: Pediatric Research. 2022 ; Vol. 91. pp. 879–887.

Bibtex

@article{ce7ef47eb25c4cc6a2d570f223c68c22,
title = "Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure",
abstract = "Background: Evidence suggests that fronto-limbic brain regions and connecting white matter fibre tracts in the left hemisphere are more sensitive to glucocorticoids than in the right hemisphere. It is unknown whether treatment with glucocorticoids in childhood is associated with microstructural differences of the uncinate fasciculus and cingulum bundle, which connect fronto-limbic brain regions. Here, we tested the hypothesis that prior glucocorticoid treatment would be associated with differences in fractional anisotropy (FA) of the left relative to right uncinate fasciculus and cingulum bundle. Methods: We performed diffusion-weighted imaging in 28 children and adolescents aged 7–16 years previously treated with glucocorticoids for nephrotic syndrome or rheumatic disease and 28 healthy controls. Results: Patients displayed significantly different asymmetry in the microstructure of uncinate fasciculus with higher left but similar right uncinate fasciculus FA and axial diffusivity compared to controls. No apparent differences were observed for the cingulum. Notably, higher cumulative glucocorticoid doses were significantly associated with higher uncinate fasciculus FA and axial diffusivity bilaterally. Conclusions: Our findings indicate that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in the microstructure of the uncinate fasciculi, and that higher cumulative glucocorticoid doses have a proportional impact on the microstructure. Impact: It is unknown if treatment with glucocorticoids in childhood have long-term effects on fronto-limbic white matter microstructure.The study examined if children and adolescents previously treated with glucocorticoids for nephrotic syndrome or rheumatic disorder differed in fronto-limbic white matter microstructure compared to healthy controls.The nephrotic and rheumatic patients had higher left but similar right uncinate fasciculus FA and axial diffusivity.Higher bilateral uncinate fasciculus FA and axial diffusivity was associated with higher cumulative glucocorticoid doses.We revealed new evidence suggesting that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in uncinate fasciculi microstructure.",
author = "Martin Vestergaard and Baar{\'e}, {William F.C.} and Holm, {Sara K.} and Madsen, {Camilla G.} and Paulson, {Olaf B.} and Born, {Alfred P.} and Peter Uldall and Siebner, {Hartwig R.} and Madsen, {Kathrine Skak}",
note = "Correction: https://doi.org/10.1038/s41390-021-01736-8",
year = "2022",
doi = "10.1038/s41390-021-01394-w",
language = "English",
volume = "91",
pages = "879–887",
journal = "Pediatric Research",
issn = "0031-3998",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with differences in uncinate fasciculus microstructure

AU - Vestergaard, Martin

AU - Baaré, William F.C.

AU - Holm, Sara K.

AU - Madsen, Camilla G.

AU - Paulson, Olaf B.

AU - Born, Alfred P.

AU - Uldall, Peter

AU - Siebner, Hartwig R.

AU - Madsen, Kathrine Skak

N1 - Correction: https://doi.org/10.1038/s41390-021-01736-8

PY - 2022

Y1 - 2022

N2 - Background: Evidence suggests that fronto-limbic brain regions and connecting white matter fibre tracts in the left hemisphere are more sensitive to glucocorticoids than in the right hemisphere. It is unknown whether treatment with glucocorticoids in childhood is associated with microstructural differences of the uncinate fasciculus and cingulum bundle, which connect fronto-limbic brain regions. Here, we tested the hypothesis that prior glucocorticoid treatment would be associated with differences in fractional anisotropy (FA) of the left relative to right uncinate fasciculus and cingulum bundle. Methods: We performed diffusion-weighted imaging in 28 children and adolescents aged 7–16 years previously treated with glucocorticoids for nephrotic syndrome or rheumatic disease and 28 healthy controls. Results: Patients displayed significantly different asymmetry in the microstructure of uncinate fasciculus with higher left but similar right uncinate fasciculus FA and axial diffusivity compared to controls. No apparent differences were observed for the cingulum. Notably, higher cumulative glucocorticoid doses were significantly associated with higher uncinate fasciculus FA and axial diffusivity bilaterally. Conclusions: Our findings indicate that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in the microstructure of the uncinate fasciculi, and that higher cumulative glucocorticoid doses have a proportional impact on the microstructure. Impact: It is unknown if treatment with glucocorticoids in childhood have long-term effects on fronto-limbic white matter microstructure.The study examined if children and adolescents previously treated with glucocorticoids for nephrotic syndrome or rheumatic disorder differed in fronto-limbic white matter microstructure compared to healthy controls.The nephrotic and rheumatic patients had higher left but similar right uncinate fasciculus FA and axial diffusivity.Higher bilateral uncinate fasciculus FA and axial diffusivity was associated with higher cumulative glucocorticoid doses.We revealed new evidence suggesting that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in uncinate fasciculi microstructure.

AB - Background: Evidence suggests that fronto-limbic brain regions and connecting white matter fibre tracts in the left hemisphere are more sensitive to glucocorticoids than in the right hemisphere. It is unknown whether treatment with glucocorticoids in childhood is associated with microstructural differences of the uncinate fasciculus and cingulum bundle, which connect fronto-limbic brain regions. Here, we tested the hypothesis that prior glucocorticoid treatment would be associated with differences in fractional anisotropy (FA) of the left relative to right uncinate fasciculus and cingulum bundle. Methods: We performed diffusion-weighted imaging in 28 children and adolescents aged 7–16 years previously treated with glucocorticoids for nephrotic syndrome or rheumatic disease and 28 healthy controls. Results: Patients displayed significantly different asymmetry in the microstructure of uncinate fasciculus with higher left but similar right uncinate fasciculus FA and axial diffusivity compared to controls. No apparent differences were observed for the cingulum. Notably, higher cumulative glucocorticoid doses were significantly associated with higher uncinate fasciculus FA and axial diffusivity bilaterally. Conclusions: Our findings indicate that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in the microstructure of the uncinate fasciculi, and that higher cumulative glucocorticoid doses have a proportional impact on the microstructure. Impact: It is unknown if treatment with glucocorticoids in childhood have long-term effects on fronto-limbic white matter microstructure.The study examined if children and adolescents previously treated with glucocorticoids for nephrotic syndrome or rheumatic disorder differed in fronto-limbic white matter microstructure compared to healthy controls.The nephrotic and rheumatic patients had higher left but similar right uncinate fasciculus FA and axial diffusivity.Higher bilateral uncinate fasciculus FA and axial diffusivity was associated with higher cumulative glucocorticoid doses.We revealed new evidence suggesting that previous glucocorticoid treatment for non-cerebral diseases in children and adolescents is associated with long-term changes in uncinate fasciculi microstructure.

U2 - 10.1038/s41390-021-01394-w

DO - 10.1038/s41390-021-01394-w

M3 - Journal article

C2 - 33790412

AN - SCOPUS:85103925077

VL - 91

SP - 879

EP - 887

JO - Pediatric Research

JF - Pediatric Research

SN - 0031-3998

ER -

ID: 260301110