Depletion of circulating progenitor cells precedes overt diabetes: A substudy from the VA enhanced fitness trial


Journal Article

Background One theory of aging and disease development is that chronic injury (pathology) results in activation of regenerative processes and initial repair, with overt disease arising only after exhaustion of reparative capability leads to inadequate repair. While depletion of circulating progenitor cells (CPCs) has been noted in diabetes, the degree to which CPC depletion predates and is associated with propensity to develop overt disease is unclear. Methods The Enhanced Fitness trial enrolled overweight/obese (body mass index > 25) sedentary patients with glucose intolerance but without overt diabetes. Baseline CPCs were measured in 129 patients based on the cell surface markers CD34, CD133, and aldehyde dehydrogenase (ALDH) activity. HgbA1C, fasting insulin and glucose levels, and HOMA calculations were ascertained. Results Lower counts of early angiogenic CPCs identified as CD34+, CD34+CD133+, and ALDH-bright (ALDHbr) cells were associated with impairments in glucose homeostasis as reflected by HgbA1C, but not fasting insulin, glucose, or HOMA-IR. These associations remained when corrected for age and cardiovascular risk factors. Conclusions/Interpretation The numbers of CD34+ and ALDHbr CPCs were significantly lower in patients with impaired glucose tolerance. Depletion of reparative capacity as reflected by loss of CPCs may presage overt disease as exemplified in this pre-diabetes model. © 2013 Elsevier Inc.

Full Text

Duke Authors

Cited Authors

  • Povsic, TJ; Sloane, R; Green, JB; Zhou, J; Pieper, CF; Pearson, MP; Peterson, ED; Cohen, HJ; Morey, MC

Published Date

  • November 1, 2013

Published In

Volume / Issue

  • 27 / 6

Start / End Page

  • 633 - 636

Electronic International Standard Serial Number (EISSN)

  • 1873-460X

International Standard Serial Number (ISSN)

  • 1056-8727

Digital Object Identifier (DOI)

  • 10.1016/j.jdiacomp.2013.08.004

Citation Source

  • Scopus