Your browser doesn't support javascript.
loading
The geometry of arteriovenous fistulas using endothelial nitric oxide synthase mouse models.
Falzon, Isabelle; Northrup, Hannah; Guo, Lingling; Totenhagen, John; Lee, Timmy; Shiu, Yan-Ting.
Afiliação
  • Falzon I; Department of Biomedical Engineering, University of Utah, Salt Lake City, UT, USA.
  • Northrup H; Division of Nephrology and Hypertension, Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
  • Guo L; Department of Biomedical Engineering, University of Utah, Salt Lake City, UT, USA.
  • Totenhagen J; Division of Nephrology and Hypertension, Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
  • Lee T; Department of Medicine and Division of Nephrology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Shiu YT; Department of Radiology, University of Alabama at Birmingham, Birmingham, AL, USA.
Kidney360 ; 1(9): 925-935, 2020 Sep 24.
Article em En | MEDLINE | ID: mdl-33117991
BACKGROUND: Arteriovenous fistula (AVF) maturation failure is a significant clinical problem in the hemodialysis population. Geometric parameters of human AVFs were associated with AVF development, but causative studies are lacking. We characterized mouse AVF geometry using endothelial nitric oxide synthase (NOS3) mouse models. METHODS: Carotid-jugular AVFs were created in NOS3 overexpression (OE), knockout (KO), and wild type (WT) mice. At 7 and 21 days postcreation, black-blood magnetic resonance images of AVFs were acquired and used to build three-dimensional reconstructions of AVF lumens. We used these reconstructions to calculate the lumen area, lumen centerline, and centerline-derived parameters: anastomosis angle, tortuosity, nonplanarity angle, and location of maximal distance between the feeding artery and AVF vein. Inter- and intrauser variabilities were also determined. RESULTS: When all mice were considered, increased minimum AVF venous lumen area was accompanied by increased venous tortuosity and increased distance between the artery and vein, with both remaining in-plane with the anastomosis. At day 7, the lumen area of AVFs from all strains was 1.5- to 2.5-fold larger than native veins. Furthermore, at day 21, AVF lumen in NOS3 OE (4.04±1.43 mm2) was significantly larger than KO (2.74±1.34 mm2) (P<0.001) and WT (2.94±1.30 mm2) mice (p<0.001). At day 21, the location of maximal artery-vein distance on the vein was further away from the anastomosis in OE (4.49±0.66 mm) than KO (2.87±0.38 mm) (p=0.001). Other geometric parameters were not significantly different between mouse strains or time points. Inter- and intrauser variabilities were small, indicating the reliability and reproducibility of our protocol. CONCLUSIONS: Our study presents a detailed characterization of mouse AVF geometry, and a robust protocol for future mechanistic studies to investigate the role of molecular pathways in AVF geometry. Identifying a geometry related to desired AVF remodeling can help inform surgery to enhance AVF maturation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derivação Arteriovenosa Cirúrgica / Fístula Arteriovenosa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derivação Arteriovenosa Cirúrgica / Fístula Arteriovenosa Idioma: En Ano de publicação: 2020 Tipo de documento: Article