Effects of serial phlebotomy on vascular endothelial function: Results of a prospective double-blind randomized study. Academic Article uri icon

Overview

abstract

  • INTRODUCTION: Blood donation has been proposed as a potential therapy to reduce risk of cardiovascular disease, but the effects of phlebotomy on vascular function in human subjects have not been well characterized. AIMS: We conducted a prospective randomized double-blind study to determine the effects of serial phlebotomy on vascular endothelial function in the brachial artery. Eighty-four iron-replete, non-anemic subjects were randomly assigned to one of three study treatment groups: (a) four serial phlebotomy procedures each followed by intravenous infusion of placebo normal saline; (b) four serial phlebotomy procedures each followed by intravenous infusion to replete lost iron; and (c) four serial sham phlebotomy procedures each followed by intravenous infusion of placebo normal saline. Assigned phlebotomy procedures were conducted at 56-day intervals. We measured brachial artery reactivity (BAR, %) in response to transient oxidative stress induced by oral methionine with high-resolution duplex ultrasound imaging before and one week after the fourth study phlebotomy. RESULTS: Before phlebotomy, oral methionine decreased BAR by -2.04% (95% CI -2.58%, -1.50%), P < 0.001) with no significant difference between groups (P = 0.42). After phlebotomy, the BAR response to oral methionine did not significantly change between groups (P = 0.53). Brachial artery nitroglycerin-mediated dilation did not change in response to phlebotomy. CONCLUSIONS: Four serial phlebotomy procedures over six months with or without intravenous iron supplementation did not alter vascular endothelial function in the brachial artery when compared with sham phlebotomy.

publication date

  • November 13, 2018

Research

keywords

  • Blood Donors
  • Brachial Artery
  • Endothelium, Vascular
  • Phlebotomy
  • Vasodilation

Identity

PubMed Central ID

  • PMC6351195

Scopus Document Identifier

  • 85056424285

Digital Object Identifier (DOI)

  • 10.1111/1755-5922.12470

PubMed ID

  • 30341986

Additional Document Info

volume

  • 36

issue

  • 6