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Sex differences and risk factors for bleeding in Alagille syndrome.

Authors :
Hankeova S
Van Hul N
Laznovsky J
Verboven E
Mangold K
Hensens N
Adori C
Verhoef E
Zikmund T
Dawit F
Kavkova M
Salplachta J
Sjöqvist M
Johansson BR
Hassan MG
Fredriksson L
Baumgärtel K
Bryja V
Lendahl U
Jheon A
Alten F
Fahnehjelm KT
Fischler B
Kaiser J
Andersson ER
Source :
EMBO molecular medicine [EMBO Mol Med] 2022 Dec 07; Vol. 14 (12), pp. e15809. Date of Electronic Publication: 2022 Nov 08.
Publication Year :
2022

Abstract

Spontaneous bleeds are a leading cause of death in the pediatric JAG1-related liver disease Alagille syndrome (ALGS). We asked whether there are sex differences in bleeding events in patients, whether Jag1 <superscript>Ndr/Ndr</superscript> mice display bleeds or vascular defects, and whether discovered vascular pathology can be confirmed in patients non-invasively. We performed a systematic review of patients with ALGS and vascular events following PRISMA guidelines, in the context of patient sex, and found significantly more girls than boys reported with spontaneous intracranial hemorrhage. We investigated vascular development, homeostasis, and bleeding in Jag1 <superscript>Ndr/Ndr</superscript> mice, using retina as a model. Jag1 <superscript>Ndr/Ndr</superscript> mice displayed sporadic brain bleeds, a thin skull, tortuous blood vessels, sparse arterial smooth muscle cell coverage in multiple organs, which could be aggravated by hypertension, and sex-specific venous defects. Importantly, we demonstrated that retinographs from patients display similar characteristics with significantly increased vascular tortuosity. In conclusion, there are clinically important sex differences in vascular disease in ALGS, and retinography allows non-invasive vascular analysis in patients. Finally, Jag1 <superscript>Ndr/Ndr</superscript> mice represent a new model for vascular compromise in ALGS.<br /> (© 2022 The Authors. Published under the terms of the CC BY 4.0 license.)

Details

Language :
English
ISSN :
1757-4684
Volume :
14
Issue :
12
Database :
MEDLINE
Journal :
EMBO molecular medicine
Publication Type :
Academic Journal
Accession number :
36345711
Full Text :
https://doi.org/10.15252/emmm.202215809