Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation. / Ebbesen, Maria; Weischendorff, Sarah; Kielsen, Katrine; Kammersgaard, Marte; Juul, Anders; Müller, Klaus Gottlob.

I: Bone Marrow Transplantation, Bind 56, Nr. 5, 2021, s. 1021-1030.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ebbesen, M, Weischendorff, S, Kielsen, K, Kammersgaard, M, Juul, A & Müller, KG 2021, 'Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation', Bone Marrow Transplantation, bind 56, nr. 5, s. 1021-1030. https://doi.org/10.1038/s41409-020-01127-3

APA

Ebbesen, M., Weischendorff, S., Kielsen, K., Kammersgaard, M., Juul, A., & Müller, K. G. (2021). Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation. Bone Marrow Transplantation, 56(5), 1021-1030. https://doi.org/10.1038/s41409-020-01127-3

Vancouver

Ebbesen M, Weischendorff S, Kielsen K, Kammersgaard M, Juul A, Müller KG. Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation. Bone Marrow Transplantation. 2021;56(5):1021-1030. https://doi.org/10.1038/s41409-020-01127-3

Author

Ebbesen, Maria ; Weischendorff, Sarah ; Kielsen, Katrine ; Kammersgaard, Marte ; Juul, Anders ; Müller, Klaus Gottlob. / Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation. I: Bone Marrow Transplantation. 2021 ; Bind 56, Nr. 5. s. 1021-1030.

Bibtex

@article{cb91733a0f664285bdabbf77ec6f84c9,
title = "Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation",
abstract = "Sinusoidal obstruction syndrome (SOS) is a potentially fatal complication of hematopoietic stem cell transplantation (HSCT) initiated through damage of sinusoidal endothelium and inflammation. Insulin-like growth factor-l (IGF-l) maintains and repairs endothelium and intestinal mucosa. We hypothesized that low IGF-l levels may increase the risk of inflammatory complications, such as SOS, in HSCT-patients. We prospectively measured IGF-l concentrations in 121 pediatric patients before, during, and after allogeneic HSCT. Overall, IGF-l levels were significantly reduced compared with healthy sex- and age-matched children. IGF-I levels pre-HSCT and at day 0 were inversely associated with C-reactive protein levels, hyperbilirubinemia, and number of platelet transfusions within the first 21 days post-transplant. Low levels of IGF-I before conditioning and at day of transplant were associated with increased risk of SOS diagnosed by the modified Seattle criteria (pre-HSCT: OR = 1.7 (95% CI: 1.2–2.6, p = 0.01), and the pediatric EBMT criteria (pre-HSCT: 1.7 (1.2–2.5, p = 0.009) and day 0: 1.7 (1.3–2.5, p = 0.001)/SDS decrease in IGF-1). These data suggest that IGF-I is protective against cytotoxic damage and SOS, most likely through trophic effects on endothelial cells and anti-inflammatory properties, and may prove useful as a predictive biomarker of SOS.",
author = "Maria Ebbesen and Sarah Weischendorff and Katrine Kielsen and Marte Kammersgaard and Anders Juul and M{\"u}ller, {Klaus Gottlob}",
note = "Publisher Copyright: {\textcopyright} 2020, The Author(s), under exclusive licence to Springer Nature Limited.",
year = "2021",
doi = "10.1038/s41409-020-01127-3",
language = "English",
volume = "56",
pages = "1021--1030",
journal = "Bone Marrow Transplantation",
issn = "0268-3369",
publisher = "nature publishing group",
number = "5",

}

RIS

TY - JOUR

T1 - Insulin-like growth factor-I predicts sinusoidal obstruction syndrome following pediatric hematopoietic stem cell transplantation

AU - Ebbesen, Maria

AU - Weischendorff, Sarah

AU - Kielsen, Katrine

AU - Kammersgaard, Marte

AU - Juul, Anders

AU - Müller, Klaus Gottlob

N1 - Publisher Copyright: © 2020, The Author(s), under exclusive licence to Springer Nature Limited.

PY - 2021

Y1 - 2021

N2 - Sinusoidal obstruction syndrome (SOS) is a potentially fatal complication of hematopoietic stem cell transplantation (HSCT) initiated through damage of sinusoidal endothelium and inflammation. Insulin-like growth factor-l (IGF-l) maintains and repairs endothelium and intestinal mucosa. We hypothesized that low IGF-l levels may increase the risk of inflammatory complications, such as SOS, in HSCT-patients. We prospectively measured IGF-l concentrations in 121 pediatric patients before, during, and after allogeneic HSCT. Overall, IGF-l levels were significantly reduced compared with healthy sex- and age-matched children. IGF-I levels pre-HSCT and at day 0 were inversely associated with C-reactive protein levels, hyperbilirubinemia, and number of platelet transfusions within the first 21 days post-transplant. Low levels of IGF-I before conditioning and at day of transplant were associated with increased risk of SOS diagnosed by the modified Seattle criteria (pre-HSCT: OR = 1.7 (95% CI: 1.2–2.6, p = 0.01), and the pediatric EBMT criteria (pre-HSCT: 1.7 (1.2–2.5, p = 0.009) and day 0: 1.7 (1.3–2.5, p = 0.001)/SDS decrease in IGF-1). These data suggest that IGF-I is protective against cytotoxic damage and SOS, most likely through trophic effects on endothelial cells and anti-inflammatory properties, and may prove useful as a predictive biomarker of SOS.

AB - Sinusoidal obstruction syndrome (SOS) is a potentially fatal complication of hematopoietic stem cell transplantation (HSCT) initiated through damage of sinusoidal endothelium and inflammation. Insulin-like growth factor-l (IGF-l) maintains and repairs endothelium and intestinal mucosa. We hypothesized that low IGF-l levels may increase the risk of inflammatory complications, such as SOS, in HSCT-patients. We prospectively measured IGF-l concentrations in 121 pediatric patients before, during, and after allogeneic HSCT. Overall, IGF-l levels were significantly reduced compared with healthy sex- and age-matched children. IGF-I levels pre-HSCT and at day 0 were inversely associated with C-reactive protein levels, hyperbilirubinemia, and number of platelet transfusions within the first 21 days post-transplant. Low levels of IGF-I before conditioning and at day of transplant were associated with increased risk of SOS diagnosed by the modified Seattle criteria (pre-HSCT: OR = 1.7 (95% CI: 1.2–2.6, p = 0.01), and the pediatric EBMT criteria (pre-HSCT: 1.7 (1.2–2.5, p = 0.009) and day 0: 1.7 (1.3–2.5, p = 0.001)/SDS decrease in IGF-1). These data suggest that IGF-I is protective against cytotoxic damage and SOS, most likely through trophic effects on endothelial cells and anti-inflammatory properties, and may prove useful as a predictive biomarker of SOS.

U2 - 10.1038/s41409-020-01127-3

DO - 10.1038/s41409-020-01127-3

M3 - Journal article

C2 - 33219341

AN - SCOPUS:85096314494

VL - 56

SP - 1021

EP - 1030

JO - Bone Marrow Transplantation

JF - Bone Marrow Transplantation

SN - 0268-3369

IS - 5

ER -

ID: 269671890